4.4 Article

Opioid-like adverse effects of tianeptine in male rats and mice

期刊

PSYCHOPHARMACOLOGY
卷 239, 期 7, 页码 2187-2199

出版社

SPRINGER
DOI: 10.1007/s00213-022-06093-w

关键词

Tianeptine; Abuse potential assessment; Intracranial self-stimulation; Locomotion; Gastrointestinal motility; Respiratory depression; Whole-body plethysmography

资金

  1. National Institute on Drug Abuse [P30DA033934]
  2. National Institute of Justice, Office of Justice Programs, US Department of Justice [2019R2-CX-0046]

向作者/读者索取更多资源

The study found that tianeptine has a lower abuse potential compared to commonly abused opioids in rats, as it exhibits resistance to tolerance and dependence. However, tianeptine does produce acute adverse effects similar to opioid agonists, including motor impairment, constipation, and respiratory depression.
Rationale Tianeptine is a mu-opioid receptor (MOR) agonist with increasing reports of abuse in human populations. Preclinical data regarding the abuse potential and other opioid-like adverse effects of tianeptine at supratherapeutic doses are sparse. Objectives The present study evaluated tianeptine in a rat model of abuse potential assessment and in mouse models of motor, gastrointestinal, and respiratory adverse effects. Methods Abuse potential was assessed in adult male Sprague-Dawley rats using an intracranial self-stimulation (ICSS) procedure to determine effects of acute and repeated tianeptine on responding for electrical brain stimulation. Male ICR mice were used to determine the effects of tianeptine in assays of locomotor behavior and gastrointestinal motility. Male Swiss-Webster mice were monitored for respiratory changes using whole-body plethysmography. Results In rats, acute tianeptine produced weak and delayed evidence for abuse-related ICSS facilitation at an intermediate dose (10 mg/kg, IP) and pronounced, naltrexone-preventable ICSS depression at a higher dose (32 mg/kg, IP). Repeated 7-day tianeptine (10 and 32 mg/kg/day, IP) produced no increase in abuse-related ICSS facilitation, only modest tolerance to ICSS depression, and no evidence of physical dependence. In mice, tianeptine produced dose-dependent, naltrexone-preventable locomotor activation. Tianeptine (100 mg/kg, SC) also significantly inhibited gastrointestinal motility and produced naloxone-reversible respiratory depression. Conclusions Tianeptine presents as a MOR agonist with resistance to tolerance and dependence in our ICSS assay in rats, and it has lower abuse potential by this metric than many commonly abused opioids. Nonetheless, tianeptine produces MOR agonist-like acute adverse effects that include motor impairment, constipation, and respiratory depression.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据