Characterization of Gut Microbiota in Rats and Rhesus Monkeys After Methamphetamine Self-administration

Li He1, Jia-Hui Zhou2, Huan Li1

  • 1Department of Psychiatry and National Clinical Research Center for Mental Disorders, The Second Xiangya Hospital of Central South University, Changsha, 410011, Hunan, China.

PubMed

Insights

Methamphetamine (MA) alters gut microbiota (GM) in rats and rhesus monkeys. Lactobacillus genus changes correlate with MA uptake, suggesting it as a potential therapeutic target for preventing MA abuse.

Area of Science:

  • Microbiology and Neuroscience
  • Addiction Research
  • Animal Models of Drug Abuse

Background:

  • Methamphetamine (MA) is a globally significant drug of abuse.
  • The precise mechanisms underlying MA addiction are not fully understood.
  • Gut microbiota (GM) has been implicated in influencing addictive behaviors, but species-specific changes during MA addiction require further investigation.

Purpose of the Study:

  • To investigate the dynamic changes in gut microbiota composition during MA self-administration acquisition.
  • To compare GM alterations in two distinct mammalian models: rhesus monkeys and rats.
  • To explore the association between GM shifts and MA intake.

Main Methods:

  • Establishment of MA self-administration models in male Sprague-Dawley rats and male rhesus monkeys.
  • Collection of fecal samples pre- and post-MA self-administration training.
  • 16S rRNA sequencing for comprehensive gut microbiota analysis.

Main Results:

  • Gut microbiota alterations were more pronounced in rats compared to rhesus monkeys.
  • The genus Clostridia_vadinBB60_group showed a significant decrease post-MA self-administration in both species.
  • Changes in Lactobacillus abundance were negatively correlated with total MA uptake in rats and showed a similar trend in rhesus monkeys.

Conclusions:

  • Methamphetamine self-administration induces significant gut microbiota alterations in both rats and rhesus monkeys.
  • The genus Lactobacillus may serve as a conserved therapeutic target for mitigating MA uptake across species.
  • Further research into the gut-brain axis in MA addiction is warranted.

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