Are Histamine H3 Antagonists the Definitive Treatment for Acute Methamphetamine Intoxication?

Author:

Kitanaka Nobue1,Kitanaka, Junichi1ORCID,Hall F. Scott2,Tanaka, Koh-ichi3,Tomita Kazuo4,Igarashi Kento5,Nishiyama Nobuyoshi3,Sato Tomoaki4,Uhl George R.56

Affiliation:

1. Department of Pharmacology, Hyogo College of Medicine, Hyogo 663-8501, Japan

2. Department of Pharmacology and Experimental Therapeutics, College of Pharmacy and Pharmaceutical Sciences, University of Toledo, Toledo, Ohio 43614, USA

3. Division of Pharmacology, Department of Pharmacy, School of Pharmacy, Hyogo University of Health Sciences, Hyogo 650-8530, Japan

4. Department of Applied Pharmacology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima 890-8544, Japan

5. Neurology and Research Services, New Mexico VA Healthcare System, Albuquerque, New Mexico 87108, USA

6. Departments of Neurology, Neuroscience, Molecular Genetics and Microbiology, University of New Mexico, Albuquerque, New Mexico 87131, USA

Abstract

Background: Methamphetamine (METH) is classified as a Schedule II stimulant drug under the United Nations Convention on Psychotropic Substances of 1971. METH and other amphetamine analogues (AMPHs) are powerful addictive drugs. Treatments are needed to treat the symptoms of METH addiction, chronic METH use, and acute METH overdose. No effective treatment for METH abuse has been established because alterations of brain functions under the excessive intake of abused drug intake are largely irreversible due in part to brain damage that occurs in the course of chronic METH use. Objective: Modulation of brain histamine neurotransmission is involved in several neuropsychiatric disorders, including substance use disorders. This review discusses the possible mechanisms underlying the therapeutic effects of histamine H3 receptor antagonists on symptoms of methamphetamine abuse. Conclusion: Treatment of mice with centrally acting histamine H3 receptor antagonists increases hypothalamic histamine contents and reduces high-dose METH effects while potentiating lowdose effects via histamine H1 receptors that bind released histamine. On the basis of experimental evidence, it is hypothesized that histamine H3 receptors may be an effective target for the treatment METH use disorder or other adverse effects of chronic METH use.

Funder

Japan Society for the Promotion of Science KAKENHI

Publisher

Bentham Science Publishers Ltd.

Subject

Psychiatry and Mental health

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