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长期使用安非他命导致组织中谷氨酸和谷氨酰胺能神经递质调质牛磺酸和犬尿氨酸水平的破坏。

Long-term disruption of tissue levels of glutamate and glutamatergic neurotransmission neuromodulators, taurine and kynurenic acid induced by amphetamine.

机构信息

Department of Experimental and Clinical Neuroscience, Institute of Psychiatry and Neurology, 9 Sobieskiego St, Warsaw, 02-957, Poland.

Department of Experimental and Clinical Pharmacology, Centre for Preclinical Research and Technology, Medical University of Warsaw, 1B Banacha St, Warsaw, 02-097, Poland.

出版信息

Psychopharmacology (Berl). 2024 Jul;241(7):1387-1398. doi: 10.1007/s00213-024-06570-4. Epub 2024 Mar 14.

Abstract

RATIONALE

Chronic amphetamine (AMPH) use leading to addiction results in adaptive changes within the central nervous system that persist well beyond the drug's elimination from the body and can precipitate relapse. Notably, alterations in glutamatergic neurotransmission play a crucial role in drug-associated behaviours.

OBJECTIVES

This study aimed to identify changes induced by amphetamine in glutamate levels and the neuromodulators of glutamatergic neurotransmission (taurine and kynurenic acid) observable after 14 and 28 days of abstinence in key brain regions implicated in addiction: the cortex (Cx), nucleus accumbens (Acb), and dorsolateral striatum (CPu-L).

METHODS

The rats were administered 12 doses of amphetamine (AMPH) intraperitoneally (i.p.) at 1.5 mg/kg. The behavioural response was evaluated through ultrasonic vocalizations (USV). High-performance liquid chromatography (HPLC) was used to measure the levels of glutamate, taurine, and kynurenic acid in the Cx, Acb, and CPu-L after 14 and 28 days of abstinence.

RESULTS

AMPH administration led to sensitisation towards AMPH's rewarding effects, as evidenced by changes in USV. There was a noticeable decrease in kynurenic acid levels and an increase in both taurine and glutamate in the CPu-L, along with an increase in glutamate levels in the Cx, 28 days following the final AMPH injection.

CONCLUSIONS

The most significant changes in the tissue levels of glutamate, taurine, and kynurenic acid were seen in the CPu-L 28 days after the last dose of AMPH. The emergence of these changes exclusively after 28 days suggests that the processes initiated by AMPH use and subsequent abstinence take time to become apparent and may be enduring. This could contribute to the incubation of craving and the risk of relapse. Developing pharmacological strategies to counteract the reduction in kynurenic acid induced by psychostimulants may provide new avenues for therapy development.

摘要

背景

慢性安非他命(AMPH)滥用导致成瘾,会导致中枢神经系统发生适应性变化,这些变化在药物从体内消除后仍会持续很长时间,并可能引发复发。值得注意的是,谷氨酸能神经传递的改变在与药物相关的行为中起着至关重要的作用。

目的

本研究旨在确定在关键的成瘾相关脑区(皮质(Cx)、伏隔核(Acb)和背外侧纹状体(CPu-L))中,在停药 14 天和 28 天后,安非他命引起的谷氨酸水平以及谷氨酸能神经传递的神经调节剂(牛磺酸和犬尿氨酸)的变化。

方法

大鼠腹腔内(i.p.)给予 12 次安非他命(AMPH)(1.5mg/kg)。通过超声发声(USV)评估行为反应。高效液相色谱法(HPLC)用于测量停药 14 天和 28 天后 Cx、Acb 和 CPu-L 中谷氨酸、牛磺酸和犬尿氨酸的水平。

结果

AMPH 给药导致 AMPH 奖赏效应的敏感化,这表现为 USV 的变化。CPu-L 中的犬尿氨酸水平明显降低,牛磺酸和谷氨酸水平均升高,而 Cx 中的谷氨酸水平在最后一次 AMPH 注射后 28 天升高。

结论

在最后一次 AMPH 剂量后 28 天,CPu-L 中的谷氨酸、牛磺酸和犬尿氨酸的组织水平发生了最显著的变化。这些变化仅在 28 天后出现,表明由 AMPH 使用和随后的禁欲引起的过程需要时间才能显现出来,并且可能是持久的。这可能导致渴望的潜伏期和复发的风险增加。开发对抗精神兴奋剂引起的犬尿氨酸减少的药理学策略可能为治疗开发提供新途径。

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