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靶向 G 蛋白偶联受体缓解神经性疼痛。

Targeting G protein coupled receptors for alleviating neuropathic pain.

机构信息

Division of Neuroscience & Ageing Biology, CSIR-Central Drug Research Institute, Lucknow, UP, India; University Grants Commission, New Delhi, India.

Division of Neuroscience & Ageing Biology, CSIR-Central Drug Research Institute, Lucknow, UP, India; Academy of Scientific and Innovative Research (AcSIR), Gaziabad, India.

出版信息

Prog Mol Biol Transl Sci. 2022;193(1):99-117. doi: 10.1016/bs.pmbts.2022.06.004. Epub 2022 Jul 22.

Abstract

Pain sensation is a normal physiological response to alert and prevent further tissue damage. It involves the perception of external stimuli by somatosensory neurons, then transmission of the message to various other types of neurons present in the spinal cord and brain to generate an appropriate response. Currently available analgesics exhibit very modest efficacy, and that too in only a subset of patients with chronic pain conditions, particularly neuropathic pain. The G protein-coupled receptors (GPCRs) are expressed on presynaptic, postsynaptic terminals, and soma of somatosensory neurons, which binds to various types of ligands to modulate neuronal activity and thus pain sensation in both directions. Fundamentally, neuropathic pain arises due to aberrant neuronal plasticity, which includes the sensitization of peripheral primary afferents (dorsal root ganglia and trigeminal ganglia) and the sensitization of central nociceptive neurons in the spinal cord or trigeminal nucleus or brain stem and cortex. Owing to the expression profiles of GPCRs in somatosensory neurons and other neuroanatomical regions involved in pain processing and transmission, this article shall focus only on four families of GPCRs: 1- Opioid receptors, 2-Cannabinoid receptors, 3-Adenosine receptors, and 4-Chemokine receptors.

摘要

疼痛感觉是一种正常的生理反应,用于警示和防止进一步的组织损伤。它涉及躯体感觉神经元对外界刺激的感知,然后将信息传递到脊髓和大脑中的各种其他类型的神经元,以产生适当的反应。目前可用的镇痛药显示出非常温和的疗效,而且只是在慢性疼痛患者的亚组中,特别是神经性疼痛患者中。G 蛋白偶联受体(GPCRs)在躯体感觉神经元的突触前、突触后末端和胞体上表达,与各种类型的配体结合,以双向调节神经元活动和疼痛感觉。从根本上讲,神经性疼痛是由于异常的神经元可塑性引起的,包括外周初级传入(背根神经节和三叉神经节)的敏化以及脊髓或三叉神经核或脑干和皮质中中枢伤害感受神经元的敏化。由于 GPCRs 在躯体感觉神经元和其他涉及疼痛处理和传递的神经解剖区域中的表达谱,本文将仅关注四类 GPCRs:1-阿片受体,2-大麻素受体,3-腺苷受体,和 4-趋化因子受体。

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