Compositions, Methods and Uses of a Teneurin C-Terminal Associated Peptide-1 (TCAP-1) for Treating Opioid Addiction

Abstract

The present matter relates to compositions comprising a Teneurin C-terminal Associated Peptide-1 (TCAP-1), or a pharmaceutically acceptable salt or ester thereof or a pharmaceutical composition comprising same and methods and uses of same for preventing and/or treating opioid addiction.

Claims

1. A method for preventing and/or treating opioid addiction in a subject in need thereof comprising administering to the subject a therapeutically effective amount of a teneurin c-terminal associated peptide-1 (a TCAP-1 peptide), or a pharmaceutically acceptable salt or ester thereof or a pharmaceutical composition comprising same, wherein the amino acid sequence of said TCAP-1 peptide consists essentially of: (i) an amino acid sequence having at least 95% identity to an amino acid sequence selected from the group consisting of SEQ ID NOs: 1, 2 or 3; optionally wherein: (a) the carboxy terminal end of said peptide is amidated or comprises an amidation signal sequence; and/or (b) when the amino terminal amino acid of said peptide is a glutamine, the glutamine is in the form of pyroglutamic acid.

2. The method of claim 1 wherein the glutamine is in the form of pyroglutamic acid.

3. The method of claim 1 wherein the TCAP-1 peptide consists of any one of SEQ. ID. NOs: 1, 2 or 3 which is optionally amidated at the carboxy terminal and wherein the glutamine is optionally a pyroglutamic acid at the amino terminal.

4. The method of claim 3 wherein the TCAP-1 is amidated at the carboxy terminal.

5. The method of claim 4 wherein the glutamine at the amino terminal is a pyroglutamic acid.

6. The method of claim 4 wherein the TCAP-1 is SEQ. ID. NO. 1.

7. The method of claim 4 wherein the TCAP-1 is SEQ. ID. NO. 2.

8. The method of claim 1 wherein the subject is a human.

9. The method of claim 1 wherein the opioid is selected from: natural, synthetic or semi-synthetic opioids.

10. The method of claim 8 wherein the opioid is selected from one or more of the group: morphine, fentanyl, heroin, opium, oxycodone, hydrocodone, Codeine, and Methadone.

11. A therapeutically effective amount of a teneurin c-terminal associated peptide-1 (TCAP-1 peptide), or a pharmaceutically acceptable salt or ester thereof or a pharmaceutical composition comprising same for preventing and/or treating opioid addiction in a subject in need thereof wherein the amino acid sequence of said TCAP-1 peptide consists essentially of: (i) an amino acid sequence having at least 95% identity to an amino acid sequence selected from the group consisting of SEQ ID NOs: 1, 2 or 3; optionally wherein: (a) the carboxy terminal end of said peptide is amidated or comprises an amidation signal sequence; and/or (b) when the amino terminal amino acid of said peptide is a glutamine the glutamine is in the form of pyroglutamic acid.

12. The therapeutically effective amount of a teneurin c-terminal associated peptide-1 (TCAP-1 peptide) of claim 11 wherein the glutamine is in the form of pyroglutamic acid.

13. The therapeutically effective amount of a teneurin c-terminal associated peptide-1 (TCAP-1 peptide) of claim 11 wherein the TCAP-1 peptide consists of any one of SEQ. ID. NOs: 1, 2 or 3 which is optionally amidated at the carboxy terminal and wherein the glutamine is optionally a pyroglutamic acid at the amino terminal.

14. The therapeutically effective amount of a teneurin c-terminal associated peptide-1 (TCAP-1 peptide) of claim 13 wherein the TCAP-1 is amidated at the carboxy terminal.

15. The therapeutically effective amount of a teneurin c-terminal associated peptide-1 (TCAP-1 peptide) of claim 14 wherein the glutamine at the amino terminal is a pyroglutamic acid.

16. The therapeutically effective amount of a teneurin c-terminal associated peptide-1 (TCAP-1 peptide) of claim 14 wherein the TCAP-1 is SEQ. ID. NO. 1.

17. The therapeutically effective amount of a teneurin c-terminal associated peptide-1 (TCAP-1 peptide) of claim 14 wherein the TCAP-1 is SEQ. ID. NO. 2.

18. The therapeutically effective amount of a teneurin c-terminal associated peptide-1 (TCAP-1 peptide) of claim 11 wherein the subject is a human.

19. The therapeutically effective amount of a teneurin c-terminal associated peptide-1 (TCAP-1 peptide) of claim 11 wherein the opioid is selected from the group consisting of: natural, synthetic or semi-synthetic opioids.

20. The therapeutically effective amount of a teneurin c-terminal associated peptide-1 (TCAP-1 peptide) of claim 19 wherein the opioid is selected from one or more of the group: morphine, fentanyl, heroin, opium, oxycodone, hydrocodone, Codeine, and Methadone.

21-22. (canceled)

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0018] In order that the subject matter may be readily understood, embodiments are illustrated by way of examples in the accompanying drawings, in which:

[0019] FIG. 1 is the TCAP-1 SEQ. ID. Nos. 1-3 for mouse, human and G. gallus, respectively.

[0020] FIG. 2 is a schematic illustration of the study design of Example 1 for the mouse Saelens drug-precipitated withdrawal study where TCAP-1 was administered pre-morphine.

[0021] FIG. 3 is a table illustrating the results of Example 1 showing that TCAP-1 blunts opioid withdrawal stress response in a dose dependent manner.

[0022] FIG. 4 is a bar graph illustrating the results of FIG. 3 that TCAP-1 blunts opioid withdrawal stress response in a dose dependent manner.

[0023] FIG. 5 is a schematic illustration of the saelens test in mice single dose TCAP-1 post-morphine as described in Example 2.

[0024] FIG. 6 is a table illustrating the results of Example 2.

[0025] FIG. 7 is a bar graph illustrating the results of FIG. 6.

[0026] FIG. 8A is a schematic illustration of the study design of Example 3.

[0027] FIG. 8B is a bar graph showing the results of the precipitated withdrawal test in mice of Example 3, specifically #jumps/20 minutes in mice versus vehicle used (saline, morphine alone, CRH antagonist (CP154,526) and TCAP-1.

[0028] FIG. 9A is a bar graph showing results of Saelens precipitated withdrawal test in mice of Example 3 of Group Mean (#jumps/20 minutes) versus noted vehicle (saline, CP154,526 (5, 20, and 50 mg/kg) and TCAP-1 250 nmole/kg) in a dose response study.

[0029] FIG. 9B is a bar group of plasma corticosterone levels in mice using the Saelens precipitated withdrawal model of Example 3 in the dose response study, showing Group mean ng/ml of plasma corticosterone versus vehicle (saline, CP154,526 (5,20, and 50 mg/kg) and TCAP-1 250 nmole/kg).

[0030] FIG. 10 is a schematic illustration of the study design of Example 4.

[0031] FIG. 11 is a bar graph illustrating the Saelens precipitated withdrawal test in mouse of Example 4 showing #jumps/t-5-20 minutes versus vehicle (no treatment (F>N), TCAP-1 250 nmole/kg and 500 nmole/kg in fentanyl treated mice.

DETAILED DESCRIPTION

[0032] Teneurin C-terminal associated peptides (TCAPs 1-4) are four paralogous bioactive peptides located at the distal extracellular end of each teneurin transmembrane protein. First described by Lovejoy et al and described in U.S. Pat. No. 8,088,889, which is herein incorporated by reference. TCAP-1 can be independently (and synthetically) transcribed and has biological actions distinct from the teneurins, demonstrating functional independence from its proprotein. It has a unique mechanism of action. ADGRL (Latrophilin), an adhesion G protein coupled receptor (GPCR), has recently been identified as part of the ligand-receptor complex that binds the teneurin/TCAP system. Previously elucidated in neurons, the teneurin/TCAP-ADGRL complex is associated with glucose metabolism; however, it is not well understood in other tissues.

[0033] Opioid addiction has been linked with CRH driven behaviours, such as jumping, grooming, and inhibition of appetite.

Definitions

[0034] “Preventing” as used herein in reference to preventing opioid addiction or onset means in the context of administering a TCAP-1 to a patient who is or will be or may be receiving opioids to minimize risk of developing an addiction to opioids and includes preventing or minimizing risk of relapse or recidivism.

[0035] “Stressor” or “Traumatic Event” as used herein means an event or events that precipitates the use of or an addiction to an opioid, e.g., any event that may be painful, e.g. surgery, injury, physiological or hormonal (e.g. fibroids, menses) or behavioural (e.g. a scare, remembering stress events).

[0036] “Therapeutically Effective Amount” as used herein when applied to dose or amount refers to that quantity of a compound or pharmaceutical composition that is sufficient to result in a desired activity upon administration to a living animal body. It is understood that a therapeutic amount may vary depending on a number of factors, including but not limited to gender, weight, body mass or body surface area, severity of a condition, age (e.g., child, teen, adult, or senior).

“Treating” or “treatment” as used herein in the context of opioid addiction means alleviating or controlling or managing the symptoms of opioid addiction and/or withdrawal and not necessarily “curing” or “curing permanently” opioid addiction but can also include same.

DESCRIPTION

[0037] Opioid addiction is a major unmet medical need. Current treatments for opioid addiction are suboptimal with regard to efficacy, side effects, or both. Corticotrophin releasing hormone (CRH), a hypothalamic neuropeptide, plays a central role in mental and behavioral responses to environmental stress. CRH is overproduced in opioid withdrawal patients, and they seem to be more sensitive to the actions of CRH.

[0038] Although TCAP and teneurins have been largely studied in the brain and shown to have normalizing effects on stressed or high and low anxiety animals (See U.S. Pat. No. 8,088,889, which is herein incorporated by reference). The TCAP, portion of teneurin proteins, blocks CRH activities through a separate receptor called latrophilin and synthesized TCAP given to rodents reverses stress-induced behavioral dysfunction, including anxiety and depression. It has better relief of illness in current responders and greater efficacy in current non-responders with fewer side effects, e.g. less sedation, less harmful pharmacology and less dependency.

[0039] TCAP-1 calms anxious behavior without sedation or evidence of dependency. As an intervention in drug addiction, in one aspect TCAP-1 can be used to reduce drug seeking behavior. In another aspect, it could be used without interfering with reward circuitry to depress mood. The pharmacological benefits of TCAP-1 administration persist for significant periods after one dose, reflecting its ability to restore long-term balance to brain function. It appears to counteract CRH effects.

[0040] Prior to the present invention, no studies were previously done in an opioid addiction model/protocol which is a separate and distinct addiction. Therefore, the inventors examined the specific role of TCAP-1 in such a model. As illustrated herein it has been shown that a TCAP-1 peptide could be used to treat and/or prevent opioid addiction and that it counteracts CRH effects and is more effective than a CRH antagonist.

[0041] Teneurin C-Terminal Associated Peptide-1 (TCAP-1)

[0042] TCAP-1 as used herein is a peptide that consists of a sequence found at the c-terminal of Teneurin M-1 peptide, more particularly described below (and collectively referred herein as “a TCAP-1 peptide”). There is considerable cross-species homology.

[0043] In some embodiments the TCAP-1 peptide (“TCAP-1”) is a 41-mer peptide selected from SEQ. ID. NOs 1 to 3 (see also FIG. 1). In some embodiments it is an amidated peptide, (such as a C-terminal amidated peptide and/or having an amidation signal sequence, such as GRR), in some other embodiments the TCAP has a pyroglutamic acid at the N-terminal. In other embodiments, it has both a pyroglutamic acid at the N-terminal and is amidated at the C-terminal.

[0044] In other embodiments it is a human TCAP-1. In some embodiments it is a 41 mer c-terminal amidated peptide consisting of the following sequence:

TABLE-US-00001 Amidated Human TCAP-1 (41 mer) Gln* Gln Leu Leu Ser Thr Gly Arg Val Gln Gly Tyr Asp Gly Tyr Phe Val Leu Ser Val Glu Gln Tyr Leu Glu Leu Ser Asp Ser Ala Asn Asn Ile His Phe Met Arg Gln Ser Glu Ile - NH.sub.2
* In some embodiments the N-terminal glutamic acid may be a pyroglutamic acid.

[0045] In some other embodiments, the peptide used is a salt, ester, solvate, polymorph or enantiomer of SEQ. ID. NOs. 1 to 3, preferably SEQ. ID. NO. 1, or any amidated or pyroglutamic acid or amidated and pyroglutamic acid form of SEQ. ID. NOs. 1 to 3.

[0046] In some other embodiments, conservative substitutions or modifications can be made to the peptide sequence which does not affect its structure or function and thus could be used for the present invention, such as various species homologs. For instance, those present in species homologs, such as the mouse, human or G. gallus TCAP-1 sequences (SEQ. ID. NOs. 1 3) where the fifth amino acid may be selected from: Gly, Asn or Ser. In some embodiments, the peptide has 95% identity to SEQ. ID. NOs. 1, 2, or 3. There is a high degree of homology amongst species, for instance the mouse TCAP-1 (Mus musculus) has the same sequence as the rat TCAP-1 (Rattus norvegicus), while the human TCAP-1 and that of the long-tailed Macaque (Macaca fascicularis) are the same.

[0047] In some other embodiments, the TCAP-1 peptide comprises any one of SEQ. ID. NOs. 4-9 or a salt, ester, solvate, polymorph or enantiomer of thereof, or any amidated or pyroglutamic acid, or amidated and pyroglutamic acid form thereof.

[0048] Opioids

[0049] Opiates are alkaloids originally derived from the poppy plant. People use this type of drug for both recreational and medicinal purposes. There are opiates that come from the natural opium plant, while some manufacture opiates to have the same chemical structure as the natural ones, e.g. synthetic or semi-synthetic opioids. Furthermore, opiates include a wide range from prescription painkillers such as fentanyl and morphine, to illegal drugs like heroin.

[0050] Natural opioids come from natural sources such as the opium plant. While some labs completely manufacture opioid drugs, natural ones come directly from the poppy seed. Although some think natural opiates are less risky than synthetic ones, they are still very addictive and can cause respiratory depression that leads to an overdose.

[0051] Synthetic opiates act on the same areas of the brain as natural ones and produce many of the same effects. They are entirely human-made with chemicals not found in the poppy plant, morphine or opium. Thus, the chemicals used in these synthetic drugs vary.

[0052] Semi-synthetic opiates are a blend of natural and man-made sources developed.

[0053] Examples of opioids include but are not limited to: Opium, Heroin, Oxycodone (e.g., Oxycontin, Roxicodone, Xtampza ER, and Oxaydo), Hydrocodone (e.g., Vicodin, Lorcet, Lortab), Codeine, Morphine (MS Contin, Oramorph SR, Avinza, and Arymo ER), Hydromorphone (Dilaudid and Exalgo), Fentanyl (Actiq, Fentora, Duragesic, Subsys, Abstral, and Lazanda), Methadone (Dolophine and Methadose), Meperidine (Demerol); Opioid analgesic: Tramadol (ConZip, Ultram, and Ryzolt); Carfentanil.

[0054] Opioid Withdrawal Symptoms

[0055] Withdrawal symptoms range from mild to severe. Indeed, symptoms can vary based on the length of time taking a particular drug, dosage, which specific drug, method of use, medical conditions, the presence of emotional issues, and biological and environmental factors. In general, opiate withdrawal usually starts within 6 to 12 hours for short-acting opiates, and within 30 hours for longer-acting ones. Symptoms may include but are not limited to: muscle aches, trouble falling and staying asleep, yawning, anxiety, runny nose, sweating, rapid heart rate, hypertension, nausea and vomiting, and diarrhea.

[0056] There are well known accepted animal models and tests that have been developed and used to screen for opiate withdrawal effects, such as analgesic responses to opiates and other agents. The mouse jumping test—a simple screening method to estimate the physical dependence capacity of analgesics. (See for example, Saelens J K, Granat F R, Sawyer W K, The mouse jumping test—a simple screening method to estimate the physical dependence capacity of analgesics. Arch Int Pharmacodyn Ther. 1971. April; 190(2):213-8; Rainer Spanagel, PhD*, Animal models of addiction, Dialogues Clin. Neurosci. 2017 September; 19(3):247-258; Wendy J Lynch, Katherine L Nicholson, Mario E Dance, Richard W Morgan, Patricia L Foley, Animal Models of Substance Abuse and Addiction: Implications for Science, Animal Welfare, and Society, Comp Med. 2010 June; 60(3): 177-188, all of which are herein incorporated by reference.)

[0057] Pharmaceutical Compositions

[0058] The present invention contemplates the administration of a pharmaceutical composition comprising a TCAP-1 peptide as described herein (including an amidated and/or pyroglutamic acid form of TCAP-1 or a peptide with 95% identity to SEQ. ID. NOs. 1-3 as shown in FIG. 1) and a pharmaceutically acceptable carrier.

[0059] The phrase “pharmaceutically acceptable”, as used in connection with compositions of the invention, refers to molecular entities and other ingredients of such compositions that are physiologically tolerable and do not typically produce untoward reactions when administered to a mammal (e.g., human). Preferably, as used herein, the term “pharmaceutically acceptable” means approved by a regulatory agency of the Federal or a state government or listed in the U.S. Pharmacopeia (USP), National Formulary (NF), or other generally recognized pharmacopeia for use in mammals, and more particularly in humans. Active Pharmaceutical Ingredients (APIs) of the present invention may be in the form of pharmaceutically acceptable salts. “Pharmaceutically acceptable salts” refers to those salts which possess the biological effectiveness and properties of the parent compound and which are not biologically or otherwise undesirable.

[0060] The pharmaceutical compositions of the present invention may comprise one or more excipients. Excipients which may be used include carriers, surface active agents (surfactants), thickening (viscosity) agents, emulsifying agents, binding agents, dispersion or suspension agents, buffering agents, penetration-enhancing agents, solubilizers, colorants, sweeteners, flavoring agents, coatings, disintegrating agents, lubricants, preservatives, isotonic agents, and combinations thereof. The selection and use of suitable excipients is taught in Gennaro, ed., Remington: The Science and Practice of Pharmacy, 20th Ed. (Lippincott Williams & Wilkins 2003), the disclosure of which is incorporated herein by reference.

[0061] The term “carrier” applied to pharmaceutical compositions of the invention refers to a diluent, excipient, or vehicle with which an active compound is administered. Such pharmaceutical carriers can be liquids, such as water, saline solutions, aqueous dextrose solutions, aqueous glycerol solutions, and lipids and oils, including those of petroleum, animal, vegetable or synthetic origin. Suitable pharmaceutical carriers are described in “Remington's Pharmaceutical Sciences” by E. W. Martin, 18.sup.th Edition.

[0062] In some embodiments, the dosage form is a subcutaneous dosage form. This differs from direct administration to the brain, amygdala, or Intracerebroventricular (“ICV”). Subcutaneous administration has many advantages over direct administration to the brain.

[0063] In some embodiments as in the composition used in the Examples, the composition dissolves an amidated and/or pyroglutamic acid form of TCAP in a saline solution and is subcutaneously administered into animals (not ICV or amygdala). This formulation has advantages over prior forms for delivery, i.e., ICV or amygdala, in that it does not require additional sedatives, or the like for administration. In other embodiments, the formulation is an oral (buccal or sublingual) or nasal formulation.

[0064] The compositions may, if desired, be presented in a pack or dispenser device which may contain one or more unit dosage forms containing the active ingredient(s). The pack may, for example, comprise metal or plastic foil, such as a blister pack. Compositions of the invention formulated in a compatible pharmaceutical carrier may also be prepared, placed in an appropriate container, and labeled for treatment of an indicated condition.

[0065] In some embodiments, TCAP-1 and the pharmaceutical compositions of the invention are used to prevent or treat opioid addiction in an animal, in some embodiments mammals, including but not limited to humans, dogs, cats, horses, sheep, cattle.

Methods and Uses

[0066] In some embodiments, a TCAP-1 peptide as described herein and the pharmaceutical compositions comprising same can prevent and/or treat opioid addiction, and/or assist to minimize withdrawal symptoms of opioid addiction. In some embodiments it can be used or administered to a patient before e.g., an anticipated use of opioids, such as for instance surgery, injury and/or during or after a traumatic event. In some embodiments, the traumatic event is selected from the group consisting of: a medical procedure such as surgery, cramping, including but not limited to associated with fibroids or menses, back or joint pain, injury, or inflammation, or other event.

[0067] In some embodiments the TCAP-1 peptide and pharmaceutical compositions comprising same of the present invention can be used in methods for treating and/or preventing opioid addiction or associated withdrawal symptoms by administering an effective amount of a TCAP-1 peptide to a patient in need thereof, before, during or after a traumatic event or stressor or anticipated traumatic event or stressor where opioid use and ceasing of such use is anticipated. For instance, when a person undergoes surgery, opioids to control the pain may be prescribed for a set period of time. A TCAP-1 peptide may be used to assist a patient when said prescription ends to reduce addiction or risk of addiction and assist in transitioning the patient off opioid use.

[0068] In some other embodiments, a TCAP-1 peptide can be used in a opioid addiction treatment and/or prevention protocol.

[0069] The present invention is described in the following Examples, which are set forth to aid in the understanding of the invention, and should not be construed to limit in any way the scope of the invention as defined in the claims which follow thereafter.

Examples

[0070] The following examples illustrate the role of TCAP-1 in preventing and treating opioid addiction.

[0071] Materials and Methods

[0072] TCAP-1 Composition

[0073] Amidated human TCAP-1 (SEQ. ID. NO. 1) was suspended in 0.9% saline. [10 nmol/Kg, Ambiopharm] for subcutaneous injection in the interscapular region.

[0074] Amidated human TCAP-1 peptide used in the composition was synthesized on an automated peptide synthesizer, Model Novayn Crystal (NovaBiochem) on PEG-PS resin using continuous flow Fmoc chemistry (Calbiochem-NovabiochemGroup). Eight times excess diisopropyl ethyl amine (Sigma-Aldrich) and four times excess Fmoc-amino acid activated with HATU (0-(7-azabenzotriazol)-1-3, 3-tetramethyluronium hexfluorophosphate; Applied Biosystems) at a 1:1 (mol/mol) ratio were used during the coupling reaction. The reaction time was 1 h. A solution of 20% piperidine (Sigma-Aldrich) in N, N-dimethylformide (DMF; Caledon Laboratories) was used for the deprotection step in the synthesis cycle. The DMF was purified in-house and used fresh each time as a solvent for the synthesis. The cleavage/deprotection of the final peptide was carried out with trifluoroacetic acid (TFA), thioanisole, 1, 2 ethandithiol, m-cresole, triisopropylsilane, and bromotrimethyl silane (Sigma-Aldrich) at a ratio of 0:10:5:1:1:5. Finally, it was desalted on a Sephadex G-10 column using aqueous 0.1% TFA solution and lyophilized.

[0075] In some experiments mTCAP was also used and prepared similarly to hTCAP-1 as above.

Animals

[0076] All animal studies were performed in the United States and followed the requirements set out in applicable laws, including the Animal Health and Welfare Act and regulations and approved by the Institutional Animal Care and Use Committee of Neosome Life Sciences, Lexington Mass. USA.

[0077] Male mice Swiss Webster mice from Charles River Laboratory (18 22 g). All procedures were approved by Neosome Life Sciences IACUC and in accordance with applicable laws and guidelines regarding use of animals.

Statistics

[0078] Tests were used to assess statistical significances. Student's t-test and ANOVAs were used unless specifically stated otherwise. Statistics were denoted by *p<0.05, **p<0.01, ***p<0.001, ****p<0.0001.

Clinical Trials in an Opioid Addiction Model

Example 1: Saelens Drug-Precipitated Withdrawal in the Mouse TCAP-1 Pre-Morphine

[0079] Protocol

[0080] A schematic of the protocol can be seen in FIG. 2.

[0081] Mice were administered saline (Groups 1, 2 and 8) or TCAP-1 (Groups 2 7) solution daily subcutaneously for three days at 10 a.m. each day.

[0082] On day four the mice were administered saline (Groups 1 and 8) or 32 mg/kg of morphine by intraperitoneal injection (I.P.) (Groups 2 7) at 9, 10, 11 a.m. and 1 and 3 p.m.

[0083] On day five, the mice were administered saline (Groups 1), 32 mg/kg of morphine by intraperitoneal injection (I.P.) (Groups 2 7) or MK-801 (Group 8) at 9 and 11 a.m.

[0084] Two hours after the 11 a.m. injection (at 1 p.m.), naloxone 10 mg/kg I.P was injected and the mice were observed over 20 minutes and number of jumps recorded.

[0085] Naloxone is a non-selective and competitive opioid receptor antagonist. It works by reversing the depression of the central nervous system and respiratory system caused by opioids. It is a medication used to block the effects of opioids, especially in overdose. Administration to opioid-dependent individuals may cause symptoms of opioid withdrawal, including restlessness agitation, nausea, vomiting, a fast heart rate, and sweating. It induces withdrawal.

[0086] MK-801 is a non-competitive antagonist of N-Methyl D aspartate receptor, a glutamate receptor which is an excitatory neurotransmitter.

TABLE-US-00002 TABLE 1 Day 4 (9a.m., 10 a.m., 11 a.m., 1 p.m. Mean # Days 1, and 3 p.m.) and Jumps 2, and 3 Day 5 Day 5 over 20 Group (10a.m.) 9 and 11 a.m.) (1 p.m) Minutes 1 n = 9 Saline Saline Saline 1 2 n = 9 Saline Morphine Naloxone 73 32 mg/kg i.p. 10 mg/kg i.p. 3 n = 3 TCAP-1 Morphine Naloxone 47 10 nmole/kg 32 mg/kg i.p. 10 mg/kg i.p. 4 n = 9 TCAP-1 Morphine Naloxone 47 25 nmole/kg 32 mg/kg i.p. 10 mg/kg i.p. 5 n = 9 TCAP-1 Morphine Naloxone 42 50 nmole/kg 32 mg/kg i.p. 10 mg/kg i.p. 6 n = 9 TCAP-1 Morphine Naloxone 32 100 nmole/kg 32 mg/kg i.p. 10 mg/kg i.p. 7 n = 9 TCAP-1 Morphine Naloxone 16 250 nmole/kg 32 mg/kg i.p. 10 mg/kg i.p. 8 n = 4 Saline Saline MK801 0

[0087] Results

[0088] Results are illustrated in Table 1, the table of FIG. 3 and the bar graph of FIG. 4, wherein the mice administered no TCAP-1 and just morphine had the highest jump rate while those administered TCAP-1 showed reduced jump rates in a dose dependent manner.

Example 2: Saelens Precipitated Withdrawal Test Simile Dose TCAP Post—Morphine

[0089] Protocol

[0090] A schematic of the protocol can be seen in FIG. 5.

[0091] 52 Male, Swiss Webster mice from Charles River Laboratory (18 22 g) were divided into four groups.

[0092] On Day-1, all received receive five intraperitoneal injections of Compound 1 (Morphine or Saline) at 9 am, 10 am, 11 am, 1 μm and 3 pm, day 1. Group 1 (n=8) received saline solution, which Groups 2 4 received morphine.

[0093] On day-2, the mice received two intraperitoneal injections (9 am and 11 am) of the saline (Group 1) or morphine (Groups 2 4) solution.

[0094] At the same time of the 11 a.m. injection, mice received subcutaneously saline solution (Groups 1 and 2), TCAP-1 at 250 nmole/kg (Group 3) or TCAP-1 at 500 nmole/kg (Group 4).

[0095] Two hours after the 11 a.m. injections, all mice received an intraperitoneal injection of Naloxone 10 mg/kg) and were immediately placed individually in an observation area and video recorded 20 minutes. The number of jumps (lifting of all feet off the ground) was recorded for 20 minutes. The following table illustrates the study design.

TABLE-US-00003 TABLE 2 Day - 1 9 a.m., and 10 a.m., 11 a.m., 1 p.m. and Day - 2 Day - 2 Day - 2 Group 9 a.m. and 11 a.m 11 a.m. 1 p.m. 1 n = 8 Saline Saline S.C. Naloxone 10 mg/kg i.p. 2 n = 20 Morphine Saline S.C. Naloxone 32 mg/kg i.p. 10 mg/kg i.p. 3 n = 12 TCAP-1 Naloxone 250 nmole/kg S.C. 10 mg kg i.p. 4 n = 12 TCAP-1 Naloxone 500 nmole/kg S.C. 10 mg/kg i.p.

[0096] Mouse TCAP-1 s.c. (10 mg.Math.ml sterile water, ammonium hydroxide stock solution, Morphine 32 mg/kg i.p and Naloxone 10 mg/kg i p.

[0097] Results

[0098] Results are illustrated in FIGS. 6 and 7 where it can be seen that TCAP-1 significantly reduced the number of jumps in Group 4 mice.

Example 3: Saelens Precipitated Withdrawal Test—CRH Antagonist vs. TCAP-1

[0099] Protocol

[0100] Forty-eight (48 Male, Swiss Webster mice from Charles River Laboratoryr (18-22 g) were used in Example 3.

[0101] Protocol A

[0102] As illustrated in FIG. 8A, 32 Male Swiss Webster mice from Charles River Laboratory (18-22 g) were divided into four groups.

[0103] On day 1, all mice received five intraperitoneal injections of Compound 1 (Morphine (3.2 mg/kg) or Saline) at 9 am, 10 am, 11 am, 1 pm and 3 pm. Group 1 (n=8) received saline solution, while Groups 2-4 received morphine.

[0104] On day 2, the mice received two intraperitoneal injections (9 am and 11 am) of the saline (Group 1) or morphine (Groups 2-4) solution.

[0105] On the same day, at 10 a.m and 12 p.m. the mice received subcutaneously injections as follows: saline solution (Group 1), morphine (Group 2), CHR Antagonist CP154,525 20 mg/kg per time point (Group 3), or TCAP-1 at 250 nmole/kg per time point(Group 4).

[0106] Two hours after the 11 a.m. injections, at 1 p.m., all mice received an intraperitoneal (“i.p.”) injection of Naloxone 2.5 mg/kg), baseline blood samples were taken and then they were immediately placed individually in an observation area and video recorded 20 minutes. The number of jumps (lifting of all feet off the ground) were recorded for 20 minutes. A second set of blood samples were taken post-jumps (about 30 minutes after the naloxone administration.

[0107] Results

[0108] FIG. 8B illustrates that TCAP-1 was much more effective and at lower dosages in significantly lowering the number of jumps in opioid injected mice and thus more effective in opioid withdrawal and treating opioid addictions.

[0109] Protocol B

[0110] The same protocol as in Protocol A was followed with the exception that on day 2, there were three Group 3 mice (10 per group) which were administered: 5 mg/kg, 20 mg/kg or 50 mg/kg of the CRH antagonist CP154,526.

[0111] Results

[0112] FIGS. 9 A and 9B illustrate that TCAP-1 is more effective in reducing the number of jumps/20 minutes in the mice, and more effective in reducing plasma corticosterone levels in the mice at lower dosage levels. One would need at least 50 mg/kg of CP154,526 to approach TCAP-1 250 nmole/kg effect on corticosterone levels. The figures illustrate that receptors likely reached saturation at 50 mg/kg CP154,526 (See FIG. 9A), but still had an effect (see FIG. 9B).

Example 4: Saelens Precipitated Withdrawal Test Simile Dose TCAP Post Fentanyl

[0113] Protocol

[0114] As illustrated in FIG. 10, fentanyl instead of morphine was used as the opioid.

[0115] 30 Male, Swiss Webster mice from Charles River Laboratory (18 22 g) were divided into three groups (n=10/group).

[0116] On days −2, −1 and day 0, all mice were administered saline (Group 1) or TCAP-1 250 nmol/kg (Groups 2 and 3) at 10 a.m. each day.

[0117] On day 0 an infusion pump was inserted into each mice was administered fentanyl by infusion for a total of 1 mg/kg/day at days 0, 1, and 2. A pump was used to get high levels of fentanyl (which normally clears quickly) in the system and to induce addiction.

[0118] At 12 p.m. on Day 3, Group 3 received a subcutaneous injection of 500 nmol/kg of TCAP-1.

[0119] At 1 p.m. on Day 3, all mice received an intraperitoneal (“i.p.”) injection of Naloxone 2.5 mg/kg), and then they were immediately placed individually in an observation area and video recorded 20 minutes. The number of jumps (lifting of all feet off the ground) were recorded for 20 minutes.

Results

[0120] As illustrated in FIG. 11, TCAP-1 also resulted in lower number of jumps/t 5-20 minutes in a dose dependent manner than control illustrating that TCAP-1 is effective in the treatment of opioid addiction.

[0121] While the foregoing invention has been described in some detail for purposes of clarity and understanding, it will be appreciated by one skilled in the art, from a reading of the disclosure, that various changes in form and detail can be made without departing from the true scope of the invention in the appended claims.

[0122] All publications, patents, and patent applications are herein incorporated by reference in their entirety to the same extent as if each individual publication, patent or patent application was specifically and individually indicated to be incorporated by reference in its entirety.

REFERENCES

[0123] Anroop B. Nair and Shery Jacob, J Basic Clin Pharm. March 2016-May 2016; 7(2): 27-31 Remington's Pharmaceutical Sciences” by E. W. Martin, 18.sup.th Edition. [0124] Gennaro, ed., Remington: The Science and Practice of Pharmacy, 20th Ed. (Lippincott Williams & Wilkins 2003. [0125] Saelens J K, Granat F R, Sawyer W K, The mouse jumping test—a simple screening method to estimate the physical dependence capacity of analgesics. Arch Int Pharmacodyn Ther. 1971. April; 190(2):213-8 [0126] Rainer Spanagel, PhD*, Animal models of addiction, Dialogues Clin. Neurosci. 2017 September; 19(3):247-258 [0127] Wendy J Lynch, Katherine L Nicholson, Mario E Dance, Richard W Morgan, Patricia L Foley, Animal Models of Substance Abuse and Addiction: Implications for Science, Animal Welfare, and Society, Comp Med. 2010 June; 60(3): 177-188.