β_lactam antibiotics against drug addiction: A novel therapeutic option

Author:

Esmaili‐Shahzade‐Ali‐Akbari Peyman1ORCID,Ghaderi Amir1ORCID,Hosseini Seyyed Mohammad Mehdi2,Nejat Fatemeh3,Saeedi‐Mofrad Maryam4,Karimi‐Houyeh Motahareh4,Ghattan Alireza4,Etemadi Amirreza4,Rasoulian Elham5,Khezri Arina6

Affiliation:

1. Department of Addiction Studies, School of Medicine Kashan University of Medical Sciences Kashan Iran

2. Department of Internal Medicine, Faculty of Medicine Azad Ardabil University of Medical Sciences Ardabil Iran

3. Department of Biology and Health Sciences Meredith College Raleigh North Carolina USA

4. Student Research Committee Kashan University of Medical Sciences Kashan Iran

5. Department of Medical‐Surgical Nursing, School of Nursing Midwifery Shahid Beheshti University of Medical Sciences Tehran Iran

6. Department of Anesthesia, School of Allied Medicine Tehran University of Medical Sciences Tehran Iran

Abstract

AbstractDrug addiction as a problem for the health of the individual and the society is the result of a complex process in which there is an interaction between brain nuclei and neurotransmitters (such as glutamate). β‐lactam antibiotics, due to their enhancing properties on the glutamate transporter glutamate transporter‐1, can affect and counteract the addictive mechanisms of drugs through the regulation of extracellular glutamate. Since glutamate is a key neurotransmitter in the development of drug addiction, it seems that β‐lactams can be considered as a promising treatment for addiction. However, more research in this field is necessary to identify other mechanisms involved in their effectiveness. This article is a review of the studies conducted on the effect of β‐lactam administration in preventing the development of drug addiction, as well as their possible cellular and molecular mechanisms. This review suggests the clinical use of β‐lactam antibiotics that have weak antimicrobial properties (such as clavulanic acid) in the treatment of drug dependence.

Publisher

Wiley

Subject

Drug Discovery

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