DYNORPHIN-(1-13) SUPPRESSES HEROIN WITHDRAWAL SYMPTOMS IN 6 ADDICTS

Similar documents
Opioids Research to Practice

Episode Five Debriefing: Teacher Guide

Buprenorphine pharmacology

Substitution Therapy for Opioid Use Disorder The Role of Suboxone

3/26/14. Opiates PSY B396 ALCOHOL, ALCOHOLISM, & DRUG ABUSE. Early History Cont d. Early History. Opiate Use in the 19th century. Technology Advances

Opioids Research to Practice

PAIN & ANALGESIA. often accompanied by clinical depression. fibromyalgia, chronic fatigue, etc. COX 1, COX 2, and COX 3 (a variant of COX 1)

Opioids Research to Practice

Prevention of Development of Tolerance and Dependence to Opiate in Mice by BR-16A (Mentat) A Herbal Psychotropic Preparation

Medication-Assisted Treatment (MAT) Overview

THE OPIUM POPPY OPIOID PHARMACOLOGY 2/18/16. PCTH 300/305 Andrew Horne, PhD MEDC 309. Papaver somniferum. Poppy Seeds Opiates

Unit II Problem 7 Pharmacology: Substance Abuse, Dependence and Addiction

How serious is the opiate problem in Fairfield County?

Long term pharmacotherapy for Alcohol Dependence: Anti Craving agents

Charles P. O Brien, MD, PhD University of Pennsylvania No financial conflicts, patents, speakers bureaus

Drugs Used In Management Of Pain. Dr. Aliah Alshanwani

Analgesia for Patients with Substance Abuse Disorders. Lisa Jennings CN November 2015

Methadone Maintenance 101

Opioids- Indica-ons, Equivalence, Dependence and Withdrawal Methadone Maintenance (OST) Paul Glue

An overview of Medication Assisted Treatment (MAT) and acute pain management on MAT

Abuse Potential of Morphine/ Dextromethorphan Combinations

Opioid Agonists. Natural derivatives of opium poppy - Opium - Morphine - Codeine

WR Fentanyl Symposium. Opioids, Overdose, and Fentanyls

LONG TERM PHARMACOTHERAPY OF OPIOID DEPENDENCE

Pain and its Treatments. Our Goals: Understand: What is pain and what causes it? 2. What are different types of pain? 3. How do opioid drugs work?

Buprenorphine: An Introduction. Sharon Stancliff, MD Harm Reduction Coalition September 2008

Implementing Buprenorphine Treatment in Opioid Treatment Programs Webinar 2, October 3, 2018

SHARED CARE GUIDELINE FOR THE MANAGEMENT OF PATIENTS ON NALTREXONE FOR OPIOID DEPENDENCE

Medication Assisted Treatment. MAT Opioid dependence/addiction Opioid treatment programs OTP Regulation of OTP Office Based Treatment

Opioids Research to Practice

THE STATE OF MEDICINE IN ADDICTION RECOVERY

3/15/2018. Pain. Pain. Opioid Analgesics Addiction. Pain

Opioid use in older adults Is it a good idea? Regional Geriatric Rounds April 26, 2013

Opioid dependence: Detoxification

Are codeine and dihydrocodeine the same

Opioids. October 29, Addiction Medicine Review Course CSAM, Newport Beach, CA

Receptor Sites and Drug Design

Kurt Haspert, MS, CRNP University of Maryland Baltimore Washington Medical Center

Pain management. Coleman Palliative Care Conference: February 2016 Josh Baru MD Stacie Levine MD

Medications in the Treatment of Opioid Use Disorder: Methadone and Buprenorphine What Really Are They?

Session 7: Opioids and Club Drugs 7-1

Opioids Research to Practice

Opioid dependence and buprenorphine treatment

Clinical Guidelines and Procedures for the Use of Naltrexone in the Management of Opioid Dependence Abbreviated Version

Pharmacotherapy for Substance Use Disorders

Opioid Step Policy. Description. Section: Prescription Drugs Effective Date: April 1, 2018

What Is Heroin? Examples of Opioids. What Science Says about Opioid Use Disorder and Its Treatment 6/27/2016

Medication for Addiction Treatment (MAT)

GOALS AND OBJECTIVES

Buprenorphine as a Treatment Option for Opioid Use Disorder

The prolong DOMINANT elimination. ROUTE of administration in heroin abuse is intravenous (IV)

Slide 1. Slide 2. Slide 3. Opioid (Narcotic) Analgesics and Antagonists. Lesson 6.1. Lesson 6.1. Opioid (Narcotic) Analgesics and Antagonists

Methadone Treatment. in federal prison

Medication-Assisted Treatment. What Is It and Why Do We Use It?

OPIOID USE DISORDER AND THE PSYCHIATRIC EMERGENCY ROOM THE VA CT MODEL

Methadone Treatment. in federal prison

The science of the mind: investigating mental health Treating addiction

Fentanyls and Naloxone. Opioids, Overdose, and Naloxone

OPIATES AND ADDICTION MEDICATIONS. Dr. Carroll W. Thornburg, D.O Chief Medical Officer in Primary Care and Addiction Services

9/13/2017. Buprenorphine Treatment (Suboxone) Disclosures. We ve Got a Big Opioid Problem. Selahattin Kurter, MD Spectrum Healthcare

DISCLAIMER: ECHO Nevada emphasizes patient privacy and asks participants to not share ANY Protected Health Information during ECHO clinics.

Karam Darwish. Dr. Munir. Munir Gharaibeh

SW OREGON OPIOID SUMMIT. Medication Assisted Recovery for Opioid Use Disorder. Gregory S. Brigham, Ph.D. Adapt / SouthRiver CHC / Compass

Prescription Opioid Addiction

Dr M H Mosaddegh Pharm D, PhD

SUBOXONE Film, SUBOXONE Tablets, and SUBUTEX Tablets. Risk Evaluation and Mitigation Strategy (REMS) Program

Anabolic Androgenic Steroids and the Brain

Substance Use Disorders

The available evidence in the field of treatment of opiate: The experience of developing the WHO clinical guidelines

Substance Use Disorders (SUDs) and Medication Assisted Treatment (MAT) for Opiates

Medication Assisted Treatment:

Serious Mental Illness and Opioid Use Disorder

Perinatal, Neonatal, Pediatric Conference

The Patient with an Addiction

Outpatient Treatment, Psychiatric and Substance Use Disorders, Rehabilitation

Topics of today s training

Optimizing Suboxone in Opioid Addicts

SUBOXONE TREATMENT PROGRAM

John Murphy DO, MS Lynx Healthcare

Opioids. Sergio Hernandez, MD

Module II Opioids 101 Opiate Opioid

Dr Alistair Dunn. General Practitioner Whangarei

Grand Rapids Police Department

A prisoners guide to buprenorphine

Analgesia is a labeled indication for all of the approved drugs I will be discussing.

Biological Psychology. Unit Two AH Mr. Cline Marshall High School Psychology

PALLIATIVE CARE PRESCRIBING FOR PATIENTS WHO ARE SUBSTANCE MISUSERS

biologically active heptadecapeptide (endorphin/[leu]enkephalin/neuropeptide/opioid peptide)

OST. Pharmacology & Therapeutics. Leo O. Lanoie, MD, MPH, FCFP, CCSAM, ABAM, MRO

Opioid Dependence and Its Treatment. Laura F. McNicholas, M.D., Ph.D. CMJC VAMC, Philadelphia University of Pennsylvania, Dept of Psychiatry

Opioid Dependence and Buprenorphine Management

Vivitrol Drug Court and Medication Assisted Treatment

The Rising Tide of Prescription Opioid Use Disorders and Current Treatment Options

VOLUME C. Pharmacological Treatment for Drug Use Disorders Drug Treatment for Special Populations

EDUCATIONAL COMMENTARY METHADONE

Proposed Revision to Med (i)

DERBYSHIRE JOINT AREA PRESCRIBING COMMITTEE SHARED CARE AGREEMENT

Chronic Pain, Opioids, & Addiction: Assessing and Managing Risk

Alcoholism has been demonstrated to have a genetic component, especially among men.

niap Terms and Definitions

Transcription:

DYNORPHIN-(1-13) SUPPRESSES HEROIN WITHDRAWAL SYMPTOMS IN 6 ADDICTS H.L. WEN (Neurosurgical Unit, Kwong Wah Hospital, Tung Wah Group of Hospitals, Kowloon, Hong Kong) P. Y. C. WEN (79 Hurlingham Court, Ranelagh Gardens, London, SW6 3Ur, England) ABSTRACT Six cases heroin abusers, during withdrawal, were given iv normal saline and dynorphin-(1-13), respectively. After saline a slight placebo effect was noticed. When dynorphin-(1-13) given iv, withdrawal scores were lowered significantly. This result suggests that dynorphin-(1-13) can suppress withdrawal syndrome. The side effects due to dynorphin-(1-13) were very minimal. KEY WORDS dynorphin; heroin; withdrawal symptoms; patients. Recently the porcine pituitary peptide, dynorphin, was purified and found to have potent opiate-like agonist properties in the guinea pig ileum and mouse vas deferens bioassay(1). The sequence of the first 13 amino acids in this peptide has been determined and an abbreviated peptide dynorphin-(1-13) containing leuenkephalin at its N-terminal end, followed by the C-terminal extension-arg-arg- Ile-Arg-Pro-Lys-Leu-Lys-OH has been synthesized. (2). This synthetic product was confirmed to be potent by the guinea pig ileum assay but was rather weak in the mouse tail-flick testr(3). The reason for its weak activity in vivo may attribute to rapid degradation by amino-peptidase and carboxypeptidase(4). Although dynorphin-(1-13) is of low activity in vivo, it can inhibit both morphine and B-endorphin induced analgesia. However, unlike narloxone, it does not precipitate jumping in dependent animals but can effectively suppress spontaneous with- drawal jumping(s). In view of the above finding, we thought it would be appropriate to investigate whether dynorphin-(1-13) could attenuate the withdrawal syndrome of heroin abusers. This paper reports our preliminary findings on the use of dynorphin-(1-13) to relieve the withdrawal syndrome of 6 heroin addicts. MATERIALS & METHODS The patients were 6 male volunteer heroin abusers with long standing history. Informed consent was obtained. Their age ranged from 22 to 55 years, with the 87

THE BULLETIN OF THE HONG KONG MEDICAL ASSOCIATION VOL. 35, 1983 X+-SD = 32.3 +- 11.4 years. The duration of addiction varied from 5 to 14 years, that was 9.7+3.0 years. The amount of money spent per day per person was from HK$80 to HK$300, which was HK$143.3+-90.7. A packet of no. 3 heroin costs between HK$50 to HK$100 (net 0.15 to 0.3 g). All of the subjects started taking heroin by inhalation and then slowly changed to iv injection afterwards. Two patients injected themselves t.i.d., the rest q.i.d. All of them had received previous treatment in the rehabilitation centres in Hong Kong but relapsed. Three of them were on methadone maintenance in addition to their heroin intake. After admission to the hospital, complete physical examination was carried out. Urine was examined to establish that the patients were on drug(s). Prior to admission to the hospital, all the patients invariably had taken heroin and as a result showed no sign of abstinence. After admission, no medication was given, except only when patient could not sleep, then one tablet (2 mg) of flunitrazepam (Rohypnol) was given. The patients were usually admitted to the hospital at noon on the day prior to the investigation. Upon admission, they were taught to mark a scale indicating the severity of the withdrawal syndrome according to a modified scoring procedure(6). Scoring was also done parallelly by the nurses (observers) on duty when the investigation was carried out. The following morning the patients were observed for symptoms and signs of withdrawal. When it was established that they had a high withdrawal syndrome (score of 75 or more), 2 ml of normal saline (NS) were injected iv over an interval of 2 min and withdrawal symptoms were scored in every 15 min for 1 h. At the end of this period, dynorphin-(1-13) (Peninsula Labs, Belmont, CA) was given iv at 125 ug/kg in 2 ml NS. Scoring of withdrawal was carried out every 15 min for a period up to 1 h after the iv. Side effects due to the iv of dynorphin-(1-13) were also monitored continuously by doctors on duty. The patients, the nurses and the doctor who gave the iv had no knowledge on the nature of the solutions. Withdrawal scores were analysed using the Student s t-test. RESULT After admission to the hospital (seetable 1) it was found that the scores for the withdrawal syndrome of the patients were mild. There was no difference in the patients and nurses (observers) rating. When the patients had a full blown withdrawal syndrome, usually in the following day, the scores were double those of admissions (i.e, before NS). After the administration of normal saline (NS) withdrawal scores were generally lowered, suggesting that there may be a mild placebo effect. However, by the t-test, the reduction of scores was not significant. After the iv of dynorphin-(1-13), the average score recorded by the patients was lowered by 30% compared with that obtained before NS. Scoring carried out by the nurses produced similar results. In view of these findings dynorphin-(1-13) is likely to be active in suppressing withdrawal in human. It is also our experience that dynorphin-(1-13) not only suppresses withdrawal syndrome but its duration of 88

DYNORPHIN-(1-13) SUPPRESSES HEROIN WITHDRAWAL SYMPTOMS IN 6 ADDICTS action is much longer than that of p-endorphin (unpublished data), DALA(7) and DAMME(8). Right after iv dynorphin-(1-13), the patients usually feel moie relaxed. In order to determine the potency of dynorphin-(1-13), patients wereasked to state the amount of money they spent on heroin which would given the equivalent potency of the iv dynorphin. They would say that it was about half the amount of the money they spent per day. After 20-25 min, the response was increased to the equivalent of the whole amount of heroin intake per day. These results suggest that the patients wre satisfied with dynorphin-(1-13) even though there was no feeling of euphoria. 45 min after iv dynorphin-(1-13), minor symptoms and signs of withdrawal began to reappear, if not counteracted, a full blown picture occurred after 3 1/2-4 h. The side effects (Table 2) observable after iv dynorphin-(1-13) were only noted when the patients were questioned. Otherwise, they showed no complaint at all. The feeling of warmth and flushings of the body, especially over the face were seen in 5/6 patients. This lasted 10 min and then other side effects were noted. These side effects were similar to those of B-endorphin, DALA and DAMME but much milder. No catatonia was noticed and none of the patients complained about severe formication of the extremities and the lower part of the back. Only 2 patients complained of precordial formication. DISCUSSION It has been observed previously that dynorphin-(1-13) could inhibit morphine or B-endorphin induced analgesia despite of not having appreciable analgesic activity itself. It showed no inhibitory effect on D-ala2-D-leu5-enkephalin or D-Ala2, MePhe4, Met-(0)5-ol-enkephalin induced analgesia in naive animal. However, it did effectively block the spontaneous withdrawal jumping in morphine dependent animals(5). Our finding on the suppression of the withdrawal syndrome after iv dynorphin-(1-13) on heroin abusers supported the finding(5) of suppression of the withdrawal jumping on morphine dependent animals. The question is, how dynorphin-(1-13), when itself is not an analgesic, is able to attenuate the withdrawal syndrome of heroin abusers. Dynorphin-(1-13) when given toanimals up to 100 times that of morphinesulphate on a molar basis resulted in no development of dependence (9). In heroin addiction both the level of p-endorphin and dynorphin are probably suppressed. After dynorphin administration, an enhancement of p-endorphin content around the opiate receptor sites may be induced. As this process continues the level of p-endorphin in the opiate receptors is brought back to its normal state thus attenuating the withdrawal syndrome. When dynorphin-(1-13) is administered, its action on withdrawal is immediate. This implies that it probably can penetrate the blood brain barrier very rapidly since it is known that this peptide has a very short half-life in vivo. The side effects of dynorphin-(1-13) were very minimal and the only complaint that the patients had, which occured on 2 occasions, was the precordial formica- 89

THE BULLETIN OF THE HONG KONG MEDICAL ASSOCIATION VOL. 35, 1983 tion. Why was it limited only to the precordial region requires further investigation. In contrast, when B-endorphin, DALA and DAMME were administered the formication were all over the body, mainly in the extremities, especially in the lower pat-t of the body. Catatonia was present after p-endorphin(10) and DALA(7) injection, but not in DAMME(8) or dynorphin-(1-13). Based on our observations, it would be reasonable if a long acting dynorphin-(1-13) could be synthesized and used for detoxification of opiate addiction or even for the treatment of chronic pain, when applied in. conjunction with minute amount of opiates. Even with its present structure, dynorphin-(1-13) could enhance the action of morphine as already reported(5). It is our conclusion that dynorphin-(1-13) does alleviate the withdrawal syndrome of heroin abusers and the side effects are inconsequential. ACKNOWLEDGEMENTS We wish to thank the staff of the Neurosurgical Unit, Kwong Wah Hospital, Tung Wah Group of Hospitals, Kowloon, Hong Kong, where this investigation was carried out. References 1 Lowney LI, Gentleman SB, Goldstein A. Life Sci 1979 June 18; vol 24:2377 2 Goldstein A, Tachibana S, Lowney LI, Hunkapiller M, Hood L. Proc Natl Acad Sci USA 1979 76(12):6666 3 Friedman HJ, Jen MF, Chang JK, Lee NM, Loh HH. Eur J Pharmacol 1981 69:357 4 5 Herman BH, Leslie F, Goldstein A. Life Sci 1980 Sept 8; voi 27:883 Tulunay FC, Jen MF, Chang JK, Loh HH, Lee NM. J Pharmacol Exp Therap 1981 219(2): 296 6 Kolb L, Hemmelsbach CK. Am J Psychiat 1936 94:759 7 Wen HL. Mod Med Asia 1980 16:57 8 Wen HL. 1981 (Unpublished) 9 Lee NM and Loh HH 1981 Personal Communication 10 Bloom F, Segal D, Ling N and Guillemin R. Science 1976 194-630 90

DYNORPHIN-(1-13) SUPPRESSES HEROIN WITHDRAWAL SYMPTOMS IN 6 ADDICTS Table 1. Effect of dynorphin-(1-13) on opiate withdrawal scores in 6 addicts (x+- S.D.) Admission Before NS After NS After Dyn-(l-13) Patient 46+17 81 +9 72*9 56+ 10 Nurse 47* 14 74_+6 65_+8 52_t6** * 0.01 < P < 0.001 ** P > 0.001 compared with before NS Table 2, Side effects after iv dynorphin-(1-13) Symptom Patients Feeling warmth 5 Flushing 5 Dizziness 3 Abdominal pain 3 Feeling cold 2 Sweating 2 Thirsty 2 Tiredness 2 Precordialformication 2 Headache 1 91