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用光遗传学方法研究神经性痛觉过敏的新方法。

New approach for investigating neuropathic allodynia by optogenetics.

机构信息

Department of Life Innovation, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.

出版信息

Pain. 2019 May;160 Suppl 1:S53-S58. doi: 10.1097/j.pain.0000000000001506.

Abstract

Mechanical allodynia is pain caused by normally innocuous mechanical stimuli and is a cardinal and intractable symptom of neuropathic pain. Roles of low-threshold mechanoreceptors (LTMRs), including Aβ fibers, in mechanical allodynia have previously been proposed, but the necessity and sufficiency of LTMRs in allodynia have not been fully determined. Recent technological advances have made it possible to achieve subpopulation-specific ablation, silencing or stimulation, and to dissect and elucidate complex neuronal circuitry. Recent studies using an optogenetic approach have shown that activation of LTMRs, including Aβ fibers that genetically express channelrhodopsin-2, by illuminating blue light to the skin elicit morphine-resistant withdrawal behaviors after nerve damage. Whole-cell recording has revealed that optical Aβ stimulation after nerve injury causes excitation of lamina I dorsal horn neurons, which are normally silent by this stimulation. Moreover, Aβ stimulation after nerve injury results in activation of central amygdaloid neurons and produces aversive behaviors. In summary, these findings indicate that optogenetics is a powerful approach for investigating LTMR-derived pain (resembling mechanical allodynia) with sensory and emotional features after nerve injury and for discovering novel and effective drugs to treat neuropathic pain.

摘要

机械性痛觉过敏是由正常无害的机械刺激引起的疼痛,是神经病理性疼痛的一个主要且棘手的症状。先前已经提出了低阈值机械感受器(LTMRs),包括 Aβ 纤维,在机械性痛觉过敏中的作用,但 LTMRs 在痛觉过敏中的必要性和充分性尚未完全确定。最近的技术进步使得实现亚群特异性消融、沉默或刺激以及剖析和阐明复杂的神经元回路成为可能。最近使用光遗传学方法的研究表明,通过照亮皮肤激活 LTMRs,包括遗传表达通道视紫红质-2 的 Aβ 纤维,在神经损伤后会引起吗啡抵抗的退缩行为。全细胞记录显示,神经损伤后光学 Aβ 刺激会引起 I 层背角神经元的兴奋,而这种刺激通常会使这些神经元沉默。此外,神经损伤后 Aβ 刺激会导致杏仁中央核神经元的激活,并产生厌恶行为。总之,这些发现表明,光遗传学是一种强大的方法,可以研究神经损伤后具有感觉和情感特征的 LTMR 衍生疼痛(类似于机械性痛觉过敏),并发现治疗神经病理性疼痛的新的有效药物。

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