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Microglial alterations induced by psychoactive drugs: A possible mechanism in substance use disorder?
Clarissa Catale1, Silvia Bussone2, Luisa Lo Iacono3
1Department of Psychology, University of Rome "La Sapienza", Via dei Marsi, 78, 00185 Rome, Italy.
Abstract:
Recently, the xenobiotic hypothesis has implicated the immune system in targeting substances of abuse as foreign molecules and stimulating inflammatory responses. Microglial cells are the resident immune cells of the central nervous system and function in homeostatic surveillance. Microglial changes that are induced by exposure to substances of abuse appear to mediate in part the establishment of addiction and the persistence of drug-mediated biological and behavioral changes. In this context, interest in the study of drug-microglia interactions has increased recently. This review summarizes the most recent preclinical rodent and clinical studies on the interaction between microglia and various classes of drugs of abuse, such as ethanol, psychostimulants, and opioids. The principal biological mechanisms of the communication between substances of abuse and microglia will be described to consider putative mechanisms of the establishment of drug addiction and future potential targets for treating substance use disorder.
Insights
The immune system, specifically microglial cells in the brain, plays a key role in addiction by responding to drugs of abuse. Understanding these drug-microglia interactions may reveal new treatments for substance use disorder.
Area of Science:
- Neuroimmunology
- Neuropharmacology
- Addiction Science
Background:
- The xenobiotic hypothesis suggests the immune system targets drugs of abuse, causing inflammation.
- Microglial cells, the brain's immune cells, are altered by substance exposure.
- These microglial changes are linked to addiction establishment and persistence.
Purpose of the Study:
- To review recent preclinical and clinical studies on drug-microglia interactions.
- To describe biological mechanisms linking drugs of abuse and microglia.
- To identify potential therapeutic targets for substance use disorder.
Main Methods:
- Review of preclinical rodent studies.
- Analysis of clinical studies.
- Examination of biological communication mechanisms.
Main Results:
- Substances of abuse, including ethanol, psychostimulants, and opioids, interact with microglia.
- These interactions contribute to the neurobiological underpinnings of addiction.
- Microglial activation is a key factor in drug-mediated changes.
Conclusions:
- Microglia are central players in the neurobiology of addiction.
- Understanding drug-microglia communication is crucial for developing novel treatments.
- Targeting microglial pathways offers potential for treating substance use disorder.
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