Background-Description of the Prior Art Opioid agonist analgesics have long been a cornerstone of pharmaceutical management of pain and other medical maladies such as loose stool or diarrhea.

However, use of opioid agonist analgesics may be accompanied by feeling euphoria as a reaction apart from relief of pain, or may be accompanied by other pharmaceutical effects as to create a wanting of the opioid agonist analgesic as an issue separate and distinct from the issue of pain relief. It is undesirable for a human patient to want to be administered an opioid agonist analgesic for reasons other than relief of pain or prescribed treatment of licit medical maladies such as loose stool. Such a wanting could result in the opioid agonist analgesic being administered in quantities greater than that required to treat pain and other licit medical maladies, which would result in waste of opioid agonist analgesic, and an increase in spending for opioid agonist analgesics. This is of great societal significance in managing the allocation of scarce resources available in the treating health care system in general. Any wastage of money on a pharmaceutical or medication results in less money available for other needed resources, be they other medications or health care services. In and of itself, a decrease in wanting of opioids apart from pain relief and other licit uses (hereafter"any licit use") would be of great of

great utility, whether it be in an opioid na ve individual (i. e. , one that has not been previously exposed to opioid analgesics) or an individually chronically exposed to opioid agonist analgesics (e. g. , a chronic pain patient, as one who is long suffering from malignant or cancer-related pain).

There have been attempts to reduce the effective amount of opioid agonist analgesic for any licit use. Such attempts have included the co-administration of opioids with NMDA-receptor antagonists or relatively low doses of opioid antagonist. These methods, if effective, could theoretically serve the desired purpose of reducing wastage of opioids, however these methods have not been demonstrated to decrease the wanting of the opioid apart from any licit use, and in fact, could theoretically potentiate the opioid agonist effect to possibly increase the wanting desire of the opioid agonist analgesic, which would have the opposite of the desired effect to decrease wastage and optimize management of scare health care resources.

Crain et al. teach that very small doses of opioid antagonists may potentiate the analgesic effect of opioid agonist analgesics (U. S. Patent Nos. 5,580, 876 and 5,767, 125).

Crain does not mention nicotinic receptors of any sort, including ot3ß4 nicotinic receptors or their antagonists. Crain also does not teach decreasing the wanting desire of opioid analgesics apart from any licit use.

The present author teaches that a pharmaceutical composition comprising nalmefene and an opioid agonist analgesic may optimize dopamine homeostasis while dissuading a human from abusing the opioid agonist analgesic (U. S. Patent No.

6,103, 258, hereafter"'258"). This invention, however, does not utilize nicotinic receptors, and it has a ceiling effect for any given combination of nalmefene and opioid.

Further, specific drug combinations in varying ratios of nalmefene to opioid must be formulated to effectively deliver therapeutic doses of a particular opioid agonist analgesic.

Mayer, et al. teach that NMDA (N-methyl-D-aspartate) receptor antagonists such as dextromethorphan or dextrophan may be combined with opioid agonist analgesics for

the prevention of opioid tolerance (U. S. Patent No. 5,654, 281). However, this may make the opioid agonist effectively more potent, and Mayer does not teach that this invention will decrease the wanting or desire for being administered opioids apart from the effect of any licit use.

Caruso teaches that NMDA receptor antagonists administered with narcotic agonist/antagonists increase the analgesic effect of the agonist/antagonist (U. S. Patent 6,007, 841). Again, this may render the opioid agonist more potent and does not speak to decreasing the wanting of the opioid apart from the effect of any licit use. Caruso makes no mention of a3 (34 nicotinic receptors or its antagonists.

Palermo, et al. (U. S. Patent No. 6,228, 863) and Kaiko, et al. (U. S. Patent No.

6,277, 384) teaching compositions for oral administration containing opioid agonist analgesics and opioid antagonists in varying amounts depending upon the particular opioid agonist and antagonist used. These formulations, however, have the potential to produce precipitated abstinence syndrome in susceptible individuals, unlike the present invention. Unintentional precipitated abstinence syndrome ("withdrawal") can have serious deleterious effects on humans, such as precipitation of catecholamine release, exaggerated stress response and myocardial ischemia. Unmonitored, as may occur with an unintentional withdrawal, this could be life threatening.

Smith, et al. teach that a kappa-2 opioid receptor agonist may be combined with a mu opioid receptor agonist such that relatively low sub-therapeutic doses of each may result in therapeutic analgesia (U. S. Patent No. 6,310, 072). However, Smith does not teach that this invention reduces wanting for the combined drug combination apart from any licit use.

Hamann teaches a composition comprising mecamylamine and naltrexone for the treatment of pain, where mecamylamine is a nicotinic receptor antagonist (U. S. Patent No. 6,153, 621, hereafter"'621"). It is doubtful and highly unlikely that the invention claimed by Hamann could produce comparable analgesia as an opioid agonist analgesic as is contained in the present invention. Though Hamann does make mention in one

broad stroke of"using nicotinic, opioid, adrenergic and/or seratonergic antagonists with agonists, "he describes the"agonists"used as both opioid and nicotinic agonists: "Suitable opioid agonists... include... morphine, "etc., and"Suitable nicotinic agonists include... (-) -nicotine,"etc."It is not at all clear that Hamann means to teach a combination of an opioid agonist analgesic combined with a nicotine receptor antagonist.

In fact, his accepted claims speak to just the opposite,. i. e. , his first and subsequent claims claim an opioid antagonist (e. g. naltrexone) in combination with a nicotinic antagonist. Further, '621 does not purport to teach the decrease for wanting of an opioid agonist analgesic, as is taught in the present invention.

Glick, et al. teach the manufacture of ibogaine congeners, including oc3 ß4 nicotinic receptor antagonists (U. S. Patent No. 6,211, 360, hereafter"'360").'360 claims various methods"of treating a subject's addiction"comprising the administration of the claimed manufactured ibogaine congener for various addictions"wherein the addictive substance is an opiate. "Glick does not teach administering a3 (34 receptor antagonists in combination with opioid agonist analgesics for any licit use in those that are not addicted, as does the present invention. In fact, '360 does not teach a composition combining an opioid agonist analgesic with a a3 (34 nicotinic receptor antagonist at all.

'360 is specifically modeled after Lotsof (U. S. Patent Nos. 4,499, 096; 4,587, 243; 5,152, 994) where"a single oral treatment with ibogaine or its salts"is administered to treat a particular addiction. Glick quite clearly describes the method of'360 as "administering to the addicted subject an effective amount of a compound [ibogaine congener] having the... formula"without co-administration of the drug to which the subject is addicted. Thus, even to someone as expert and skilled in the art of Glick and colleagues, the present invention was not appreciated.

Though stereospecificity of ct3 ß4 receptors for ibogamine, ibogaine and their congeners may not (or may) be clinically relevant, the sterospecificity of opioid receptors for ibogamine, ibogaine and their congeners does seem to be important. For instance, the (+) -enantiomer of 18-MC has a 10-fold higher affinity for mu-and delta- opioid receptors than does the corresponding (-)-enantiomer (Bioorganic & Medicinal Chemistry Letters 10 (2000) 473-476).'360 specifically states that the'360'invention

includes compounds... without regard to the stereochemistry..."This is further evidence that'360 did not encompass, consider or teach the present invention that is a composition containing both opioids acting at mu-and delta-opioid receptors and ibogamine, ibogaine or their congeners that are a3p4 nicotinic receptor antagonists. It cannot be presumed otherwise that a single composition containing both opioid agonists and compounds whose stereoisomer orientation alters competition with binding at opioid receptors would not fit the definition of an invention that is"without regard to the stereochemistry." Glick, Maisonneuve, Kitchen and Fleck (European Journal of Pharmacology 438 (2002) 99-105) describe"antagonism off3 (34 nicotinic receptors as a strategy to reduce opioid and stimulant self-administration."The prototypical oc3 (34-antagonist is 18- methoxycoronaridine ("18-MC"). They teach that 18-MC is a"potential treatment for multiple forms of drug abuse"and they do not distinguish the utility of decreasing the wanting of opioid agonist analgesics specifically, as does the present invention. Further, nowhere is it suggested to compound or formulate a pharmaceutical composition containing both opioid agonist analgesic and (x3p4 nicotinic receptor antagonist. This article references other works by the same authors where 18-MC is specifically administered as a pre-treatment 19 hours prior to the administration of morphine (European Journal of Pharmacology 383 (1999) 15-21). That 18-MC is administered as a separate and distinct pre-treatment, not possibly administered as a single composition containing both 18-MC and active drug (where"active drug"is meant to mean opioid agonist analgesic or metamphetamine) is again evidence by an article written by Szumlinski, Haskew, Balogun, Maisonneuve and Glick (Pharmacology, Biochemistry and Behavior 69 (2001) 485-491) that again describes the pretreatment with ibogaine or its congener 19 hours prior to administration of active drug, which in this case was methamphetamine. Even in the article titled"The potential ant-addictive agent, 18- methoxycoronaridine, blocks the sensitized locomotor and dopamine responses produced by repeated morphine treatment"authored by Szumlinski, Maisonneuve and Glick (Brain Research 864 (2000) 13-23), 18-MC is always administered as a pretreatment 19 hours prior to morphine administration, again giving no evidence or suggestion that these authors teach a single pharmaceutical composition comprising both a3 ? 4 nicotinic

receptor antagonist and opioid agonist analgesic, as is taught in the present invention. In fact, the authors concluded in this article that"it appeared that 18-MC pretreatment [emphasis added] blocked the expression of sensitization in rats sensitized by previous morphine exposure" (without previous co-administration of 18-MC).

In Opioids In Pain Control : Basic and Clinical Aspects (ISBN 0 521 62269 7), a diagram labeled Figure 6.3 is shown, marked herein as FIGURE 1. FIGURE 1 demonstrates that dopamine is increased in striato-pallidal regions of the brain with administration of a prototypical opioid, as is morphine. Other explanations of opioid- induced increase in brain dopamine is offered by Garcia and Harlan in The Neurobiology of Opiates (ISBN 0-8493-7932-6) : it explains beta-endorphin infusion into the nucleus accumbens induces dopamine release there, and morphine infusion into the ventral tegmental area induces dopamine release there. In the same book (ISBN 0 52162269 7), Unterwald and Kornetsky state as a theory that"opiates activate opiate receptors located in the ventral tegmental area, which in turn stimulate dopaminergic activity in the mesolimbic system, which mediates reinforcement. "It is dopamine increase in response to opioids in the mesolimbic system that is responsible for wanting the drug again apart from any licit use of the opioid agonist analgesic. Antagonism of oc3 (34 nicotinic receptors indirectly alter dopamine in the nucleus accumbens and ventral tegmental area by communication via the habenulointerpedunclular pathway as explained by Glick (Ibid). Any licit use of an opioid agonist analgesic is mediated via opioid receptors, e. g. analgesia, which may occur independent of interactions involving wanting of the drug.

It would be of very great utility to separate the wanting or reinforcing effect of being administered an opioid agonist analgesic from any licit use of the opioid agonist as taught in the present invention.

There are at least three general mechanisms by which opioid agonist analgesics effect the relief of pain: 1) supraspinal mechanisms of opioid analgesia; 2) spinal mechanisms of opioid analgesia; and, 3) peripheral mechanisms of opioid analgesia.

Supraspinal opioid analgesia occurs primarily in areas of the brain apart from the pleasure-reward center in the mesolimbic system, such as the midbrain periaqueductal

grey ("PAG) area, and rostral ventromedial medulla ("RVM"). The anatomic organization of this pain modulating network is shown schematically in FIGURE 2 (labeled Figure 3.1 from Opioids In Pain Control : Basic and Clinical Aspects (ISBN 0 521 62269 7). Opioid actions within the RVM are mediated by GABA as a major neurotransmitter. Yaksh and Rudy demonstrated that if opioid actions are blocked in only the spinal cord (and not the brain) by an opioid antagonist, opioid-like effects of systemically administered morphine is completely blocked. Though this may be due to complex interactions among and between spinal and supraspinal sites, this demonstrates that any licit use of an opioid agonist analgesic can be separated from the wanting or reinforcing effects of opioid administration that occurs primarily in an anatomical location within the brain (the"pleasure-reward center"). Pain is mediated mostly by mu receptors in the spinal cord, and diarrhea is mediated by opioid receptors located within the gastrointestinal track. Further, many actions of analgesia and tolerance involving both opioid and NMDA receptors are mediated in the spinal cord and peripheral sites in the body, away from the actions of (x3 4 receptor antagonists in the pleasure-reward center of the brain (see for example, Science 1976 Jun 25 ; 192 (4246). 1357-8 and Anesthesiology 1996 May ; 84 (5) : 11 77-88 and Anesthesiology 1996 Oct ; 85 (4) : 808-16 and Neurosci Lett 1992 Jan 20; 135 (1):67-70 and J Pain Symptom Manage 1992 Aug ; 7 (6) : 356-61 and J Pharmacol Exp Ther 1999 Apr ; 289 (1) : 494-502).

Opioid agonist analgesics prescribed to reduce or alleviate pain working at the level of the spinal cord apart and away from the pleasure-reward center of the brain work by way of interaction of multiple neurotransmitters. Primarily, neurotransmitters in the spinal cord are in the dorsal horn of the spinal cord and include excitatory amino acids and certain neuropeptides (e. g. substance P and calcitonin gene-related peptide also known as CGRP), cholecystokinin ("CCK"), and Met-enkephalin. These are not known to be affected in the dorsal horn of the spinal cord by oc3ß4 nicotinic receptor antagonists.

FIGURE 3 (labeled Figure 4.3 in Opioids In Pain Control : Basic and Clinical Aspects (ISBN D 52162269 7) is a schematic representation of interactions among and between neurotransmitters in the spinal cord.

From Substance Abuse : A Comprehensive Textbook (ISBN 0-683-18179-3), it is stated"opiate-induced enhancement of the firing of reward-relevant mesotelencephalic dopamine neurons is well established. Mesolimbic dopamine neurons originating in the ventral tegmental area and projecting to the nucleus accumbens are preferentially sensitive to this opiate-induced activation. "The homeostatic control of dopamine in this area of the brain is under opposing tonic control by mu-and kappa-opioid receptors as taught in'258. Nevertheless, "the action of mu-opioid receptor agonists on the firing rate of mesotelencephalic dopamine neurons in reward-relevant brain loci is primarily an activating one" (ISBN 0-683-18179-3). For all intent and purpose, opioid agonist analgesics administered to treat pain are essentially mu-opioid agonists. "Nicotine also acutely activates mesotelencephalic dopamine neurons.. The same range of doses [of nicotine] was more than three times as effective on mesolimbic dopamine neurons as on mesostriatal dopamine neurons, and all nicotine-induced activation of dopamine neurons was prevented or reversed by intravenous mecamylamine" (ISBN 0-683-18179-3).

Objects and Advantages Accordingly, besides the objects and advantages of formulating or compounding a pharmaceutical composition containing both an opioid agonist analgesic and a oc3 ß4 receptor antagonist described in my invention, above, several objects and advantages of the present invention are: (a) to allow an opioid to be administered to a human effective to relieve pain while simultaneously not allowing for increased dopamine in regions of the brain that would effect wanting of an opioid or euphoria, in a single pharmaceutical composition; (b) to decrease the tendency of a human to self-administer opioid agonist analgesics for reasons other than any licit use; (c) to treat pain without affecting mood as an opioid analgesic in absence of a ot3ß4 nicotinic receptor antagonist would; (d) in absence of pain, to decrease the tendency of a human to self-administer an opioid agonist analgesic; (e) to allow a muscle relaxant, an anti-seizure medication, an anxiolytic drug or a hypnotic drug to be administered such that the respective muscle

relaxing, anti-seizure, anxiolytic or hypnotic effects are realized while the emotional feeling of pleasure is dissociated, at least partially, from the muscle relaxing, anti-seizure, anxiolytic or hypnotic effects; (f) to enable certain local anesthetics to be administered while decreasing the likelihood that the local anesthetic would be over-self administered to obtain pleasure beyond the relief of pain due to direct local anesthetic action on pain transmission impulses; (g) to enable tertrahydrocannibal ("THC") and its derivatives to be administered for treatment of anorexia, nausea, glaucoma or neuropathic pain while decreasing the likelihood that the THC-like drug would be over-self administered to obtain pleasure beyond the relief of anorexia, nausea, pain or glaucoma associated with intended prescribed therapeutic regimens; (h) to treat repetitive compulsive behavior such as self-mutilation, over- eating or pathological self-administration of certain drugs such as nicotine or ethanol; (i) to treat obesity by administration of a drug that dissociates, at least partially, eating from the emotional feeling of pleasure; and (j) to treat other pathological behavioral or psychiatric maladies involving an imbalance of central nervous system dopamine homeostasis.

Further objects advantages of the present invention will become apparent from a consideration of the ensuing description and figures.

Drawing Figures FIGURE 1 demonstrates striatal dopamine increases with use of the opioid agonist morphine.

FIGURE 2 demonstrates that areas of the brain other than those regions related to mesolimbic pleasure, reward and wanting are central to modulating pain mediated by opioid receptors in the brain.

FIGURE 3 demonstrates that neurotransmitters other than dopamine are effective in transmission of pain mediated by opioid receptors in the spinal cord.

Description of the Invention The present invention consists of an amount of an opioid agonist analgesic effective to produce a positive physiologic response for any licit use of the opioid analgesic, and an amount of an oc3ß4 ("alpha-three-beta-four") nicotinic receptor antagonist effective to inhibit, antagonize, prevent or diminish dopaminergic effects within the area of the brain responsible for pleasure, reward or wanting, in the same pharmaceutical composition, and a suitable carrier therefore.

In one embodiment of the invention, the x3 ß4 nicotinic receptor antagonist is 18-methoxycoronaridine (hereafter,"18-MC"). However, any number of suitable a3p4 nicotinic receptor antagonists may be used. Other such suitable antagonists include mecamylamine, dextromethorphan and dextrophan.

In light of the present invention, the development of other ot3 ß4 nicotinic receptor antagonists may occur that may also be suitable for the invention. The method by which one may test a drug for a, 3 (34 nicotinic receptor antagonism is previously described in the scientific literature and would be known to one skilled in that art. A list of possible candidates for being an α3ß4 nicotinic receptor antagonist in addition to the stated known α3ß4 nicotinic receptor antagonists include: 18-hydroxycoronaridine; 18-hydroxyvoacangine; 18- hydroxyconopharyngine; 16-ethoxycarbonyl-18-hydroxyibogamine ; 16- ethoxycarbonyl-18-hydroxyibogaine; 16-ethoxycarbonyl-18-hydroxyibogaline; 16-hydroxymethyl-18-hydroxyibogamine; 16-hydroxymethyl-18- hydroxyibogaine; 16-hydroxymethyl-18-hydroxyibogaline; 18- methoxyvoacangine; 18-methoxyconopharyngine; 16-ethoxycarbonyl-18- methoxyibogamine ; 16-ethoxycarbonyl-18-methoxyibogaine ; 16- ethoxycarbonyl-18-methoxyibogaline ; 16-hydroxymethyl-18-methoxyibogamine ; 16-hydroxymethyl-18-methoxyibogaine; 16-hydroxymethyl-18-

methoxyibogaline; 18-benzyloxycoronaridine ; 18-benzyloxyvoacangine; 18- benzyloxyconopharyngine; 16-ethoxycarbonyl-18-benzyloxyibogamine ; 16- ethoxycarbonyl-18-benzyloxyibogaine ; 16-ethoxycarbonyl-18- benzyloxyibogaine; 18-hydroxycoronaridine laurate; 18-hydroxyvoacangine laurate; 16-ethoxycarbonyl-18-hydroxyibogamine laurate; 16-ethoxycarbonyl-18- hydroxyibogaine laurate; 16-ethoxycarbonyl-18-hydroxyibogaline laurate; 18- hydroxycoronaridine acetate; 18-hydroxycoronaridine citrate; 18- hydroxycoronaridinetartrate ; 18-hydroxyvoacangine acetate ; 18- hydroxyvoacangine citrate; 18-hydroxyvoacangine tartrate; 18- hydroxyconopharyngine acetate; 18-hydroxyconopharyngine citrate; 18- hydroxyconopharyngine tartrate; 16-ethoxycarbonyl-18-hydroxyibogamine acetate ; 16-ethoxycarbonyl-18-hydroxyibogamine citrate; 16-ethoxycarbonyl-18- hydroxyibogamine tartrate; 16-ethoxycarbonyl-18-hydroxyibogaine acetate; 16- ethoxycarbonyl-18-hydroxyibogaine citrate; 16-ethoxycarbonyl-18- hydroxyibogaine tartrate; 16-ethoxycarbonyl-18-hydroxyibogaline acetate; 16- ethoxycarbonyl-18-hydroxyibogaline citrate; 16-ethoxycarbonyl-18- hydroxyibogaline tartrate; 18-hydroxycoronaridine methoxyethoxymethyl ether; 18-hydroxyvoacangine-methoxyethoxy-methyl ether; 18- hydroxyconopharyngine-methoxy-ethoxy-methyl ether; 16-ethoxycarbonyl-18- hydroxyibogamine-methoxy-ethoxy-methyl ether; 16-ethoxycarbonyl-18- hydroxyibogaine-methoxy-ethoxy-methyl ether; 16-ethoxycarbonyl-18- hydroxyibogaline-methoxy-ethoxy-methyl ether; and pharmaceutically acceptable acids, bases and salts thereof. As used herein, pharmacologically acceptable acids, bases and salts are those acids, bases and salts that are non-toxic for use in human subjects. Toxicity is measured by those means established by those skilled in the art and may include local toxicity in a composition for local use, or systemic toxicity for systemic use, respectively. These compounds are listed for illustrative purposes only, and are not intended to be all encompassing of every a3 (34 nicotinic receptor antagonist that can be used within the context of the present invention, and are in no way intended to limit the scope of the present invention. For instance, harmaline, ibogaine or its congeners, derivatives or

metabolites, and other iboga alkaloids and their derivatives may prove suitable as a3 (34-antagonists for the present invention.

Suitable opioid agonists for the invention include: alfenanil; allylprodine; alphaprodine; anileridine ; fentanyl; sufentanil ; carfentanil; lofentanil; cyclazocine; morphine; benzylmorphine; desomorphine; normorphine; dextromoramide; benzitramide; clonitazene; codeine; dihydrocodeine; levorphanol; oxycodone; oxycodone; propoxyphene; meperidine; methadone; normethadone; meptazinol; nicomorphine; LAAM; pentazocine, cyclozine, remifentanil, heroin, morphine-6-glucuronide ("M6G"); nalbuphine; buprenorphine; butorphanol; meptazinol; dezocine; diampromide; pethidine; hydromorphone; diamorphine; dihydromorphine; dimenoxadol; piritramide; nicomorphine; tilidine; tramadol; opium; beta-endorphin; met-enkaphalin; DAGO; delta-enkephalin; dynorphin A; SKF-10,047 ; peptide F; BAM12P ; Leu- enkephalin; N-alpha-acetylmethadone ; dihydromorphine; etorphine; oxymorphone; and pharmaceutically acceptable acids, bases and salts thereof.

The term"opioid agonist"here is meant to mean any drug, molecule or compound that binds to and activates an opioid receptor. As an example, the mu- agonist and kappa antagonist buprenorphine, which is generally referred to as either a"partial opioid agonist"or a"mixed opioid agonist/antagonist, "is defined in this paragraph as an opioid agonist because it meets the definition of any drug, molecule or compound that binds to and activates an opioid receptor. These opioid drugs are listed for illustrative purposes only, and are not intended to be all encompassing of every opioid agonist analgesic that can be used within the context of the present invention, and are in no way intended to limit the scope of the present invention.

Factors to be taken into consideration in formulating or compounding the present invention are the elimination half-lives, volumes of distribution, affinity for target receptors, relative bioavailabilities with different routes of administration, pKa (H+ dissociation constant or constants), and metabolism of the component drug compounds, etc. Also important are potential toxic effects

of the component drug compounds. Taking these factors into consideration, and in light of the present invention, those skilled in the art will be able to formulate the invention based on the usual and routine laboratory and clinical testing that must be done on all drug products developed in the United States. For example, ibogaine has been shown to cause tremors in human and animal subjects alike, and at certain doses has been shown to be neurotoxic, especially on Purkinje nerve cells. 18-MC has been shown to be devoid of these undesirable characteristics. Therefore, it would be logical and consistent with the present invention to combine 18-MC in a single composition with an opioid agonist analgesic preferably over combining ibogaine with the opioid agonist. Such routine trials will confirm the optimal oc3ß4 antagonist/opioid agonist combination. For example, the percent"first pass metabolism"of 18-MC may be determined, and this will aid in determining the optimal amount of 18-MC in an orally administered embodiment of the invention as compared to an embodiment intended for parenteral use where the alimentary track is initially bypassed.

By way of example only, a typical course of events of bringing a drug to human use is first to test in the drug in animals such as rats. For a variety of reasons, a drug in development may be administered in a form that is most convenient for experimental methods in animals that is not the intended end use for humans. One such example is to inject a drug into the peritoneal space. Such intraperitoneal access is used, for example, in dialysis for treatment of kidney failure. It is used in rat experiments as a means of systemic administration because of relative ease of administration in these animals. Eventually, a conversion must be calculated, based on laboratory and clinical testing typical of all drug development in the United States, to develop an optimal dose for the route of administration that will eventually be used in a human, whether it is by enteral or parenteral route. These methods are established and well known to those skilled in the art.

EXAMPLE 1 : Morphine and 18-MC are combined with a suitable pharmacological carrier in a single pharmaceutical composition.

EXAMPLE 2: Oxycodone and 18-MC are combined with a suitable pharmacological carrier in a single pharmaceutical composition.

EXAMPLE 3: Oxycodone is combined with dextromethorphan and 18-MC with a suitable pharmacological carrier as a single pharmaceutical composition.

EXAMPLE 4: Hydrocodone is combined with mecamylamine and dextromethorphan with a suitable pharmacological carrier as a single pharmaceutical composition.

EXAMPLE 5: Oxycodone is combined with nalmefene and 18-MC with a suitable pharmacological carrier as a single pharmaceutical composition.

EXAMPLE 6: Oxycodone is combined with dextromethorphan, mecamylamine and nalmefene with a suitable pharmacological carrier as a single pharmaceutical composition.

Combining multiple a3p4 antagonists in a single pharmaceutical composition is not arbitrary or random. It has been shown that dextromethorphan, which is also a NMDA receptor antagonist, when administered in combination with 18-MC, yields effects involving the"wanting center"of the brain to a greater extent than can be attributed to the simple additive effects of dextromethorphan and 18-MC on the wanting center. Therefore, there appears to be a synergistic effect when 18-MC and dextromethorphan are administered together. Nalmefene, in ultra low doses may potentiate the analgesic effect of the combined opioid agonist analgesic, allowing lower

doses of the opioid to be administered for a given dose to produce a certain analgesic effect. Thus, an opioid is administered at lesser dose for any licit use, while at the same time not producing a psychological wanting of the opioid for other than any licit use in this example.

The present invention also encompasses the combined administration in a single composition of an opioid agonist analgesic, a a3 ß4 nicotinic receptor antagonist, and an NMDA receptor antagonist. Here, NMDA receptor is meant to mean N-methyl-D- aspartate receptor that binds glycine or phenylcyclidine. There may be beneficial effects attributed to blocking the NMDA receptor that complement the beneficial effects of blocking the a3p4 receptor, when administered together with an opioid agonist analgesic. Such beneficial effects are explained separately in the prior art.

EXAMPLE 7: Hydrocodone is combined in a single pharmaceutical composition with a a3ß4 nicotinic receptor antagonist and a non-opioid analgesic such as a non-steroidal anti- inflammatory drug ("NSAID") such as aspirin, ibuprofen, naproxen, etc. , or with acetaminophen (Tylenol@), with a suitable pharmacological carrier. Other NSAID's that may be used consistent with the present invention include, but are not limited to diclofenac, benoxaprofen, flurbiprofen, fenoprofen, flubufen, ketoprofen, ketorolac, indoprofen, piroprofen, carprofen, oxaprozin, pramoprofen, muroprofen, trioxaprofen, suprofen, aminoprofen, tiaprofenic acid, indomethacin, sulindac, tolmentin, zomepirac, tiopinac, acemetacin, fentiazac, clinanac, oxpinac, piroxicam.

EXAMPLE 8: A pharmaceutical preparation formulated for nasal administration such that active drugs are systemically absorbed via the nasal cavity mucus membranes containing butorphanol and a suitable a3p4 nicotinic receptor antagonist. The more preferred a3p4 nicotinic receptor antagonist is one that with or without permeation enhancers is better suited for absorption across the nasal mucosa. This, in light of the present invention, is easily determined by those skilled in the art based on the chemical properties of the

particular a3 ß4 nicotinic receptor antagonist, and which is confirmed by routine laboratory and clinical testing.

EXAMPLE 9: A pharmaceutical preparation formulated for sublingual administration containing buprenorphine as the opioid agonist analgesic, naloxone as an opioid antagonist, and a suitable oc3ß4 nicotinic receptor antagonist. Here, the active ingredients for any licit use are buprenorphine and the a3 ß4 nicotinic receptor antagonist, where naloxone is usually poorly absorbed by the sublingual route of administration. The more preferred a3p4 nicotinic receptor antagonist is one that with or without permeation enhancers is better suited for absorption under the human tongue.

This, in light of the present invention, is easily determined by those skilled in the art based on the chemical properties of the particular a3p4 nicotinic receptor antagonist, and which is confirmed by routine laboratory and clinical testing. Such chemical properties may include pH of the sublingual preparation, the lipid solubility of the active drug, the ionic charge of the {x3 ß4 nicotinic receptor antagonist, and other properties that are well described in prior art and well known to those skilled in the art.

EXAMPLE 10 : A sustained release preparation of opioid agonist analgesic formulated for prolonged systemic administration by any of a known variety of means including microencasulation, inclusion within an erodable matrix, as part of a hydrogel composition, entrapment by a polymer or mixture of polymers, organic linkage as part of a degradable polymer-drug formulation, etc. , containing morphine, a suitable a3ß4 nicotinic receptor antagonist, and a suitable carrier thereof.

EXAMPLE 11: A transdermal apparatus for delivering fentanyl, similar in general concept to the Duragesic# patch (Jannsen Pharmaceuticals), except that which contains a suitable a3p4 nicotinic receptor antagonist. The more preferred a3p4 nicotinic receptor antagonist is one that with or without permeation enhancers is better suited for absorption through the

human skin. This, in light of the present invention, is easily determined by those skilled in the art based on the chemical properties of the particular a3p4 nicotinic receptor antagonist, and which is confirmed by routine laboratory and clinical testing. Such chemical properties may include pH of the ingredients of the transdermal apparatus that are delivered to the surface of the skin, the lipid solubility of the active drug, the ionic charge of the a3p4 nicotinic receptor antagonist, and other properties that are well described in prior art and well known to those skilled in the art.

EXAMPLE 12: A pharmaceutical composition consisting essentially of the components of DextroMorphTM (Algos Pharmaceuticals, now Endo Pharmaceuticals) except that a suitable a3p4 nicotinic receptor antagonist is included as an additional component.

Here, dextromethorphan is included as an NMDA receptor antagonist for the purposes of decreasing tolerance built to morphine and to allow a less amount of morphine to cause a given analgesic effect. Dextromethorphan as an NMDA receptor antagonist does not decrease the wanting of, the euphoric effect of, or the rewarding effect of morphine on the pleasure reward center of the brain by the mechanism described in the present invention involving the indirect dopamine decreasing affect of blocking a3 ? 4 nicotinic receptor from acetylcholine. Other NMDA receptor antagonists such as MK-801, dextorphan or d-methadone may also be used.

It should be pointed out that many compounds, molecules or drugs that work by attaching to a known receptor, may act at more than one kind of receptor. For instance, a given oc3ß4 nicotinic receptor antagonist may also block a4 (32 nicotinic receptors or NMDA receptors, but to a different extent, and with different affinities than it attaches to a a3p4 nicotinic receptor. The term"a3 (34 nicotinic receptor antagonist"is used herein to define any drug that attaches to and blocks a (x3p4 nicotinic receptor such that acetylcholine or other activating neurotransmitter is impeded from binding to and activating the a3p4 nicotinic receptor. The present patent may therefore include other receptor blockers except those that are duplicative of the present invention by way of inherency in the prior art. For example, dextromethorphan is both an a3p4 nicotinic

receptor blocker as well as a NMDA receptor blocker. Where the present patent cannot claim dextromethorphan and opioid agonist as a composition due to inherency of a prior art patent (in compositions where the opioid agonist is similar in structure to morphine- see below), the present patent claims the use of dextromethorphan to decrease wanting of the opioid agonist that is distinct from its use of decreasing tolerance to, or for increasing the relative potency of, the opioid agonist which is claimed in prior art to be due to dextromethorphan's NMDA receptor blocking ability.

If the NMDA receptor antagonist is dextromethorphan (e. g. DextroMorph), and the (x3p4 nicotinic receptor antagonist here is 18-MC or mecamylamine, this will result in a decrease wanting for the morphine to an effect much greater than could possibly be effected by dextromethorphan without 18-MC or mecamylamine, respectively.

DextroMorphTM is purported to treat opioid tolerance and to decrease the amount of morphine needed for a given analgesic effect, and is not purported to decrease the wanting, of morphine. In fact, dextromethorphan as a NMDA receptor antagonist is thought to be effective in preventing tolerance and enhancing analgesia only with opioids similar in structure to morphine, and has been shown not to have such significant effects with opioid agonist analgesics of dissimilar structures. However, in the present invention, when dextromethorphan is considered as an a3 (34 nicotinic receptor antagonist, it is expected that the effects of dextromethorphan would be similar on acetylcholine blockade at the (x3p4 nicotinic receptor antagonist regardless of the chemical structure of the opioid agonist analgesic. Therefore, one cannot correctly argue that an opioid agonist with a chemical structure not similar to morphine, when combined with dextromethorphan for decreasing the wanting of the opioid agonist analgesic that is dissimilar to morphine, is inherent in an invention that broadly claims the combination of any opioid agonist analgesic and dextromethorphan as an NMDA receptor antagonist for the purpose of decreasing tolerance to, and decreasing the amount necessary for, the (dissimilar) opioid agonist analgesic. In this example being described, the a3p4 nicotinic receptor antagonist is added as an additional component to the NMDA receptor antagonist dextromethorphan.

EXAMPLE 13: A pharmaceutical composition consisting essentially of the components of OxyTrexrM (Pan Theraeutics, Inc.), except that a suitable ot3ß4 nicotinic receptor antagonist is included as an additional component. Here, naltrexone is combined with oxycodone in a single pharmaceutical composition. The naltrexone, an opioid antagonist, is included so to act on opioid receptors such that at very low doses of naltrexone it potentiates, or at least does not antagonize, the effects at opioid receptors of the opioid agonist analgesic oxycodone, but at higher dose of naltrexone will effective block opioid receptors such that the opioid agonist effect of the oxycodone will be effectively antagonized. Neither of the active drugs of OxyTrex acts on nicotinic receptors to antagonize binding of acetylcholine at the receptor, which indirectly results in decreased dopaminergic effects within the pleasure-reward center of the brain.

EXAMPLE 14: A pharmaceutical composition consisting essentially of the components of MorVivaTM (Pain Therapeutics, Inc.), except that a suitable a3 (34 nicotinic receptor antagonist is included as an additional component. Here, naltrexone is combined with morphine in a single pharmaceutical composition. The naltrexone, an opioid antagonist, is included so to act on opioid receptors such that at very low doses of naltrexone it potentiates, or at least does not antagonize, the effects at opioid receptors of the opioid agonist analgesic oxycodone, and the naltrexone also purportedly prevents the build up of tolerance to the morphine. Neither of the active drugs of MorViva acts on nicotinic receptors to antagonize binding of acetylcholine at the receptor, which indirectly results in decreased dopaminergic effects within the pleasure-reward center of the brain.

EXAMPLE 15: A pharmaceutical composition consisting essentially of the components of OxyContindD (Purdue Pharma, LLP) except that a suitable oc3 (34 nicotinic receptor antagonist is included as an additional component. Here, oxycodone is released in a more prolonged or sustained release formulation for oral administration and enteric absorption. OxyContin when crushed, loses its sustained release characteristics, such

that absorption is fast. This method of crushing OxyContin'tablets has been used illicitly by those seeking euphoric effects rather than analgesia or any licit use, and the crushed tablets are then ingested orally (per os), injected intravenously, or"snorted" (insufflation) through the nares (nostrils) for absorption through nasal mucosa.

Including an effective amount of a ot3 ß4 nicotinic receptor antagonist, as for example 18-MC, would tend to negate the euphoric affects. Thus, a human seeking effects of oxycodone other than for any licit use would be less motivated to crush an"OxyContin@- 18-MC-containing"tablet. This would be of great societal importance.

EXAMPLE 16: A pharmaceutical preparation formulated for intravenous, intramuscular or subcutaneous administration containing meperidine as the active opioid agonist analgesic ingredient, which also contains a suitable amount of a a3p4 nicotinic receptor antagonist to effectively diminish the increase in dopamine in the pleasure-reward center of the brain that is associated with meperidine administration.

EXAMPLE 17: A pharmaceutical composition formulated for oral use consisting essentially of an opioid agonist, wherein an analgesically effective amount of an orally active opioid agonist is combined with an opioid antagonist into an oral dosage form which would require at least a two-step extraction process to be separated from the opioid agonist, the amount of antagonist extracted being sufficient to counteract the opioid agonist effects if extracted together with the opioid agonist and administered parenterally, which also contains a3 (34 nicotinic receptor antagonist, preferably with the oc3 (34 nicotinic receptor antagonist contained within the same extraction compartment as the opioid agonist analgesic.

By more specific example, the opioid agonist analgesic is hydromorphone, the opioid antagonist is nalmefene hydrochloride and the cx3ß4 nicotinic receptor antagonist is 18-MC.

Nalmefene is more preferred as opioid antagonist than naltrexone when combined in a single composition with an opioid agonist analgesic because nalmefene has more simple pharmacokinetics in that naltrexone is metabolized in humans to 6-beta- naltrexol, which is a more potent and longer lasting opioid antagonist than is its parent compound naltrexone. Thus, with naltrexone administration, there will be two circulating effective opioid antagonists with different binding affinities and different termination half-lives, occurring at constantly changing ratios of one to the other (the parent naltrexone, and the metabolite 6-beta-naltrexol). On the other hand, nalmefene has no appreciably active metabolites in humans, therefore opioid blockade due to circulating concentrations of active antagonist is much more easy to predict with nalmefene than with naltrexone.

EXAMPLE 18: A pharmaceutical composition consisting essentially of the components of Lortabe (UCB Pharma, Inc.), except that a suitable a3p4 nicotinic receptor antagonist is included as an additional component.

EXAMPLE 19: A pharmaceutical composition consisting essentially of the components of Vicoprofen' (Knoll Laboratories), except that 18-MC is included as an additional component.

EXAMPLE 20: A pharmaceutical composition consisting essentially of the components of PercoceO (Endo Pharmaceuticals, Inc.), except that mecamylamine is included as an additional component.

EXAMPLE 21 : A pharmaceutical composition consisting essentially of the components of Vicodinm (Knoll Laboratories), except that a suitable a3p4 nicotinic receptor antagonist is included as an additional component.

EXAMPLE 22: The opioid agonist analgesic hydrocodone is included in a pharmaceutical tablet composition with an opioid antagonist where the opioid antagonist is separately encapsulated with a coating that is generally resistant to digestion or degradation by non- traumatic transfer through the alimentary or gastrointestinal track. Here,"non-traumatic" is meant to mean the natural passage through the alimentary system that would not cause a physical crushing of such a small coated particle as is the encapsulated opioid antagonist. When ingested orally, the opioid antagonist is not released from encapsulation, preventing its systemic action on opioid antagonists. However, if the tablet composition is physically crushed by traumatic means prior to ingestion or administration, whether it is by enteral or parenteral administration, the opioid antagonist will be released from encapsulation, thereby making it available for systemic action to antagonize the opioid agonist analgesic included within the tablet composition at opioid receptors. The encapsulation may be accomplished by any of a known number of means described in the prior art, such as by coating with a polymer that is resistant to the digestive process within the gastrointestinal track. Included within the tablet would be a a3 (34 nicotinic receptor antagonist, such as 18-MC. The 18-MC could be contained as an admixture with the hydrocodone, or within the encapsulation with the opioid antagonist, or with both the hydrocodone and within the encapsulation with the opioid antagonist. For completion's sake of this example, the opioid antagonist is naltrexone.

Though many examples are presented herein that embody the present invention, they are for illustrative purposes only and are not intended to limit the scope of the present invention. Further, though the mechanisms of action presented herein are stated in good faith as those postulated to be responsible for the working of the present invention, the invention is not defined solely by the theory of action, but rather also by the composition or compositions taught herein, and therefore it is claimed by letters patent the compositions and methods written below, regardless of any subsequent work that might alter the body of knowledge upon which the postulated mechanisms of action may now rely.

The more preferred oc3ß4 nicotinic receptor antagonists for the present invention are those that are most selective for the a3p4 nicotinic receptor, so as to not cause unwanted other effects by binding to and either activating or blocking other receptors. In this respect, 18-MC is predicted to have a much wider therapeutic window than ibogaine, for example, which blocks not only oc3 ß4 nicotinic receptors but NMDA and sigma-2 receptors, and sodium channels and the 5-HT transporter as well. Also, because the essence of the present invention is the simultaneous administration of both an opioid agonist analgesic and an (x3ß4 nicotinic receptor antagonist, the present invention cannot possibly be considered without taking into account what effects the a3p4 nicotinic receptor antagonist may have on opioid receptors. For example, it has been demonstrated that both ibogaine and 18-MC have similar affinities as one another for kappa opioid receptors. When determining the ideal a3p4 nicotinic receptor antagonist for the present invention, one would preferably select an a3p4 nicotinic receptor antagonist that did not block mu opioid receptors so as to allow maximum analgesia in the presence of decreased wanting of the drug. Because stereochemistry of a3 (34 nicotinic receptor antagonists has been shown to influence affinities at mu and delta receptors (Bioorganic & Medicinal Chemistry Letters 10 (2000) 473-476, p. 474-third paragraph), the present invention cannot be reasonably considered"without regard to the stereochemistry. "In fact, one would expect the (-) -enantiomer of 18-MC to be the more preferred stereoisomer of 18-MC for the present invention because (-)-18- methoxycoronaridine has a 10-fold lesser affinity to bind (and presumably block) mu opioid receptor than does the (+)-enantiomer.

EXAMPLE 23: An amount of 18-methoxycoronaridine to effect approximately a 20 micromolar (tir) concentration of 18-methoxycoronaridine at a3p4 nicotinic receptors in the pleasure-reward center of the brain when administered parenterally, combined within the same pharmaceutical composition as 100 milligrams (mg) of meperidine, with a suitable pharmaceutical carrier to deliver both drugs parenterally. When calculating the optimal ratio of 18-MC to meperidine, the ICso of the component drugs should be taken into

consideration, where the ICso of 18-MC at α3ß4 nicotinic receptors is approximately 0.75 µM.

EXAMPLE 24: An amount of 18-methoxycoronaridine to effect approximately a 20 micromolar (, uM) concentration of 18-methoxycoronaridine at (x3p4 nicotinic receptors in the pleasure-reward center of the brain when administered orally (per os or"p. o."), combined within the same pharmaceutical composition as 60 mg of oxycodone, with a suitable pharmaceutical carrier to deliver both drugs via the gastrointestinal tract. Such a pharmaceutical composition may consist essentially of the components of OxyContin° (Purdue Pharma, LLP), except that a suitable a3p4 nicotinic receptor antagonist is included as an additional component to effect a 20 micromolar (, uM) concentration of 18-methoxycoronaridine at a3p4 nicotinic receptors in the pleasure-reward center of the brain. When calculating the optimal ratio of 18-MC to oxycodone, the IC50 of the component drugs should be taken into consideration, where the ICSO of 18-MC at a3, ß4 nicotinic receptors is approximately 0. 75 µM.

EXAMPLE 25: 18-MC and codeine are contained within a common pharmaceutical composition including a suitable carrier thereof in a ratio of 18-MC to codeine of approximately 1.5 : 1 to 2 : 1.

EXAMPLE 26: Dextromethorphan, 18-MC and oxycodone are contained within a common pharmaceutical composition including a suitable carrier thereof in a ratio of approximately 5: 1: 0.21 (i. e. , approximately five to approximately one to approximately 21 one-hundredths), respectively.

In addition to allowing an opioid to be administered to a human effective to relieve pain while simultaneously not allowing for the typical increase in dopamine in regions of the brain that would effect wanting of an opioid or euphoria in a single

pharmaceutical composition, the present invention also applies to non-opioid medications that are commonly over used by self-administration due to increases in dopamine in the pleasure-reward center of the brain. Such other non-opioid medications include muscle relaxants such as benzodiazepines, anti-seizure medications such as barbiturates and benzodiazepines and anxiolytic drugs such as benzodiazepines. Thus, an effective amount of a oc3 (34 nicotinic receptor antagonist is included within the same pharmaceutical composition as a muscle relaxant, an anti-seizure medication or an anxiolytic drug. Further, the local anesthetic cocaine is often preferred by otolaryngologists because of its pain deadening and vasoconstricting properties. Cocaine was very popularly used during nasal surgery by otolaryngologists (a. k. a. ENT physicians), but has more recently come into disfavor for prescribing to patients for fear that they would use the cocaine to effect pleasure or euphoria rather than for therapeutic pain relief. Such misuse of cocaine could make physicians legally liable for illicit use of cocaine, and would also tend for the cocaine to be used more than necessary, consuming more cocaine than therapeutically necessary and further increasing healthcare spending.

Further, cocaine diversion is possible as a patient could sell cocaine prescribed for therapeutic use to that patient, to another patient that does not need pain relief or nasal vasoconstriction, but seeks to use the cocaine solely for is effect of increasing dopamine in the pleasure-reward center of the brain. Therefore, by combining an effective amount of a3 (34 nicotinic receptor antagonist in the same pharmaceutical composition as cocaine, the local effects of cocaine as a local anesthetic and vasoconstrictor would remain intact while the increase in dopamine in the pleasure-reward center of the brain usually associated with intranasal absorption of cocaine would be significantly diminished. Illicit diversion may also be applied to the aforementioned muscle relaxants, anti-seizure medications and anxiolytic drugs, which the present invention would tend to negate.

Benzodiazepines that may be included in a common pharmaceutical composition with an a3ß4 nicotinic receptor antagonist within the context of the present invention include, but are not limited to, alprazolam (Xanax@), clonazepam (Klonopin@), diazepam (Valium°), chlordiazepoxide (Librium@), estazolam (ProSomrM), lorazepam (Ativan°), oxazepam (Serax@), prazepam (CentrexTM), clorazepate (TranxeneTM), triazolam

(Halcion#), temazepam (Restoril@), flurazepam (almane#), midazolam (Versed@), Quazepam (DoralTM), mitrazepam, lormetazolam, loprazolam, clobazam, flunitrazepam (Rohypnol#) and brotizolam.

Barbiturates that may be included in a common pharmaceutical composition with a a3p4 nicotinic receptor antagonist consistent with the present invention include, but are not limited to, butabarbital, butalbital, pentobarbital and secobarbital.

Hypnotic drugs, generally used as an aid for insomnia or sleep disturbance of the central nervous system, that may be included in a common pharmaceutical composition with a cc3p4 nicotinic receptor antagonist consistent with the present invention include, but are not limited to, chloral hydrate, ethchiorvynol, meprobamate, zolpidem (Ambien@) and zaleplon (Sonata@).

Pijnenberg and van Rossum (JPharm Pharmacol 1973 ; 25 : 1003) teach that dopamine injected into the nucleus accumbens increases motor activity, similar to amphetamines, while intrastriatal dopamine injections do not increase motor activity.

This is of particular significance because a3 ß4 nicotinic receptors are hypothesized not to directly involve mesolimbic dopamine pathways (i. e. , the nucleus accumbans), but rather decrease dopamine in the pleasure-reward center of the brain through indirect communications involving the habenulointerpeduncular pathway (see Glick et al, European Journal of Pharmacology 438 (2202), page 104). In other words, amphetamines work directly on the mesolimbic area of the brain to affect pleasure and reward by increasing dopamine, while α3ß4 nicotinic receptor antagonists work indirectly through habenulointerpeduncular pathways to decrease dopamine.

Thus, by selectively blocking a, 3 (34 nicotinic receptors with an α3ß4 nicotinic receptor antagonist like 18-MC, dopamine can be decreased in the pleasure-reward center of the brain while at the same time allowing for amphetamine-like effects such as related to locomotion. Therefore, therapeutic effects of amphetamines such as those related to locomotion can be realized by administering an amphetamine, while

simultaneously administering an effective amount of a3 (34 nicotinic receptor antagonist that tends to reduce the subjective feeling of pleasure apart from the increase in locomotion. In the present invention, a common pharmaceutical composition containing an amphetamine and a a3 (34 nicotinic receptor antagonist (in a suitable carrier) can be administered such that effects that are therapeutic of an amphetamine apart from producing mere pleasure can be separated or dissociated from the pleasure-like effects of the amphetamine.

Amphetamines are unique central nervous system stimulants with many useful therapeutic properties that unfortunately, because of potential pleasure producing effects, tend to be self-administered in amounts in excess of prescribed therapeutic dosing regimens. This characteristic of amphetamines greatly limits their utility in common medical practice. Therefore, there is a great societal need to formulate pharmaceutical compositions of amphetamine-like medications that will not be over administered.

Amphetamines or central nervous stimulant medications that may be included in a common pharmaceutical composition with a (x3p4 nicotinic receptor antagonist consistent with the present invention include, but are not limited to, methylphenidate, dextroamphetamine and pemoline. Other examples are given below. Important medical uses of amphetamines and other central nervous stimulants include decreasing appetite for weight loss (obesity treatment), treatment of narcolepsy (a disorder including inability to stay awake), treatment of attention deficit disorder, among other medical maladies.

THC is the major active chemical component of marijuana. Marijuana has use as a legitimate medication to relieve nausea, stimulate appetite in anorexic patients and to alleviate increased intraocular pressure in the eyeball that is associated with glaucoma.

A pharmaceutical composition, dronabinol (Marinol) is commercially available in the United States, but it is classified as a"Scheduled"narcotic drug that is heavily regulated.

Increased scrutiny of physicians that prescribe either"medical marijuana"or dronabinol has resulted in a hesitance by physicians to prescribe these medications despite well- documented efficacy for the conditions described above. This is due, in part, to the pleasure producing effects associated with THC-like drugs that are separate and apart

from their therapeutic uses. A newer drug in development, code-named"CT-3"is described as a"chirally pure, patented synthetic carboxylic derivative of tetrahydrocannabinol (THC-7C) " (see http ://www. atlan. com/press2002/05-02- 2002. hymn. It is reportedly currently being tested as a treatment for neuropathic pain by its developers. It is likely that CT-3 will be associated with pleasure in addition to its therapeutic analgesic effect due its close chemical resemblance to other cannabonoids.

Cannibinoids are known to increase dopamine concentrations in the pleasure-reward center of the brain. Included among 66 (other) cannibinoids that have been identified in herbal marijuana are delta-9-tetrahydrocannabinol, delta-8-tetrahydrocannabinol, cannabichromene, cannabicyclol, cannabidiol, cannabielsoin, cannabigerol, cannabinidiol, cannabinol, cannabitrol and their various derivatives. Therefore, there is a great societal need to formulate pharmaceutical compositions of THC-like medications that will not be over administered due to pleasurable effects derived from action in the pleasure-reward center of the brain. THC-like drugs, or cannabinoids, may be included in a common pharmaceutical composition with a oc3ß4 nicotinic receptor antagonist consistent with the present invention to meet this societal need.

Any of the aforementioned opioid agonists, amphetamines, benzodiazepines, barbiturates, other hypnotics, local anesthetics and THC-like drugs may be self- administered in doses in excess of prescribed therapeutic doses when administered as the sole active ingredient of a pharmaceutical composition, due to a tendency to produce pleasure as a phenomenon separate from the respective desired therapeutic effect, e. g., analgesia, skeletal muscle relaxation, reduction of anxiety, decreased appetite, appetite stimulation, etc.

Other previously unappreciated uses of a3 (34 nicotinic receptor antagonists consistent with the present invention follow: to treat repetitive compulsive behavior such as self-mutilation, compulsive stealing (kleptomania), compulsive gambling, over- eating or pathological self-administration of certain drugs such as nicotine or ethanol; to treat obesity by administration of a drug that dissociates, at least partially, eating from the emotional feeling of pleasure. These previously unappreciated uses of oc3ß4 nicotinic receptor antagonists that are taught in the present invention can be implemented

by administering a pharmaceutical composition comprising a jazz nicotinic receptor antagonist in a suitable pharmacological carrier in association with the repetitive compulsive behavior, such that dopamine release in inhibited or diminished in the pleasure reward center of the brain during the compulsive behavior. By doing this, pleasure is dissociated from the compulsive behavior, and because no pleasure is derived from it, the human that exhibited the compulsive behavior will tend not to continue to repeat the behavior because no pleasure is associated with it.

Another previously unappreciated uses of α3ß4 nicotinic receptor antagonists that are taught in the present invention can be implemented by administering a pharmaceutical composition comprising a oc3 ß4 nicotinic receptor antagonist in a suitable pharmacological carrier to a patient suffering a psychiatric malady the etiology of which is associated with a preponderance of dopamine availability or action in the brain. Such pathological behavioral or psychiatric maladies involving an imbalance of central nervous system dopamine homeostasis include, but are not necessarily limited to, psychosis, schizophrenia and obsessive compulsive disorder ("OCD"). "Several lines of evidence show that dopamine is implicated in the mediation of some obsessive compulsive behavior... Increased dopaminergic neurotransmission may be responsible for this" (see Essential Psychopharmacology : Neuroscientific and Practical Implications, ISBN 0-521-42620-0, page 219).

Further examples of the present invention are described below. It is understood however, that these examples are for illustrative purposes only and are not intended to limit the scope of the invention or its claims in any way.

EXAMPLE 27: A pharmaceutical composition comprising the components of Cocaine Hydrochloride Topical Solution (Roxanne Laboratories) and an CC3 P4 nicotinic receptor antagonist.

EXAMPLE 28: A pharmaceutical composition comprising the components of Klonopin@ (Roche Labs) and an oc3ß4 nicotinic receptor antagonist in a suitable carrier.

EXAMPLE 29: A pharmaceutical composition comprising the components of Xanax° (Pharmacia & Upjohn) and an 0353ß4 nicotinic receptor antagonist in a suitable carrier. If the prescribed regimen for Xanax# is every eight hours, then the amount of mecamylamine may be 1 to 2 mg per dose, such that 3 to 6 mg of mecamylamine would be administered daily. For instance, 1 mg alprazolam (the active benzodiazepine in anax#) is combined with 1 mg mecamylamine in a suitable pharmacological carrier such that a single tablet containing 1 mg of each drug is administered per os three times per day.

EXAMPLE 30: A pharmaceutical composition comprising the components of Donnatal# (A.H.

Robbins) and an oc3ß4 nicotinic receptor antagonist in a suitable carrier.

EXAMPLE 31 : A pharmaceutical composition comprising the components of Meridia# (Knoll Laboratories) and an a3p4 nicotinic receptor antagonist in a suitable carrier.

EXAMPLE 32: A pharmaceutical composition comprising the components of Nembutal# (Abbott Labs) and an α3ß4 nicotinic receptor antagonist in a suitable carrier.

EXAMPLE 33: A pharmaceutical composition comprising the components of Adipex-Pe (GATE Pharmaceuticals) and an oc3ß4 nicotinic receptor antagonist in a suitable carrier.

EXAMPLE 34: A pharmaceutical composition comprising the components of Marino (Roxane Laboratories) and an α3ß4 nicotinic receptor antagonist in a suitable carrier.

EXAMPLE 35: A pharmaceutical composition comprising the components of Ritalin# or Ritalin- SR@ (Novartis Pharmaceuticals) and an (x3 ß4 nicotinic receptor antagonist in a suitable carrier.

EXAMPLE 36: 18-methoxycoronaridine in a suitable pharmaceutical carrier is administered to an actively engaged alcoholic human.

18-MC is a preferred α3ß4 nicotinic receptor antagonist, though other a3 {34 nicotinic receptor antagonists may be used within the scope of the present invention.

The present invention may be embodied in many other specific forms employing any of the pharmaceutical/bioactive agents mentioned hereinabove such that an ot3 ß4 nicotinic receptor antagonist and a pharmaceutically acceptable carrier provide for inhibiting dopamine release in the pleasure reward center of the human brain either alone or in combination with the types of drugs described hereinabove without departing from the spirit or essential attributes thereof.