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靶向兴奋性谷氨酸受体治疗吗啡耐受性:一篇叙述性综述。

Targeting Excitatory Glutamate Receptors for Morphine Tolerance: A Narrative Review.

作者信息

Huang Min, Luo Limin, Wang Wenying, Xu Hao, Chen Moxi, Ma Xiaqing, Xu Tao

机构信息

Department of Anesthesiology, Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Department of Anesthesiology, First Affiliated Hospital of Nanjing Medical University, Nanjing, China.

出版信息

CNS Neurosci Ther. 2025 Jun;31(6):e70468. doi: 10.1111/cns.70468.

Abstract

BACKGROUND

Opioids remain a primary treatment for moderate-to-severe chronic pain, but prolonged use frequently induces analgesic tolerance. Excitatory glutamate receptors, ubiquitous in the central and peripheral nervous systems, are pivotal in physiological and pathological processes and are now recognized as significant contributors to opioid tolerance development.

METHODS

We comprehensively analyzed experimental data from our team's intensive investigations over the past 10 years, alongside relevant peer-reviewed studies on glutamate receptor mechanisms in opioid tolerance.

RESULTS

Excitatory glutamate receptors (including NMDA, AMPA, and metabotropic subtypes) fundamentally regulate neuroadaptations underlying morphine tolerance. Our work and others' demonstrate their involvement in synaptic plasticity, neuroinflammation, and downstream signaling pathways that drive tolerance.

CONCLUSIONS

Targeting excitatory glutamate receptors presents a promising therapeutic strategy for mitigating opioid tolerance. Future research should prioritize elucidating receptor-specific mechanisms, peripheral-central nervous system crosstalk, and translating preclinical findings into clinically viable.

摘要

背景

阿片类药物仍然是中重度慢性疼痛的主要治疗方法,但长期使用常常会导致镇痛耐受性。兴奋性谷氨酸受体在中枢和外周神经系统中普遍存在,在生理和病理过程中起关键作用,现在被认为是阿片类药物耐受性发展的重要因素。

方法

我们全面分析了我们团队在过去10年深入研究的实验数据,以及关于阿片类药物耐受性中谷氨酸受体机制的相关同行评审研究。

结果

兴奋性谷氨酸受体(包括NMDA、AMPA和代谢型亚型)从根本上调节吗啡耐受性背后的神经适应性。我们的工作及其他人的研究表明,它们参与了驱动耐受性的突触可塑性、神经炎症和下游信号通路。

结论

靶向兴奋性谷氨酸受体为减轻阿片类药物耐受性提供了一种有前景的治疗策略。未来的研究应优先阐明受体特异性机制、外周-中枢神经系统的相互作用,并将临床前研究结果转化为临床可行的方法。

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