Graefe Steven B., Rahimi Nader, Mohiuddin Shamim S.
Creighton University School of Medicine
Boston University Medical Campus, Boston, MA
Substance P (SP) is an 11-amino acid-long neuropeptide expressed by the central nervous system (CNS), the peripheral nervous system, and immune cells. SP is a member of the tachykinin (TAC) family of neuropeptides encoded by the TAC1 gene. SP elicits its activity via interacting with the G protein-coupled neurokinin receptors (NKRs), including NK1R, NK2R, and NK3R. NKRs are expressed on the surface of various cell types, including the blood vessels and lymphatics endothelial cells, immune cells, fibroblasts, and neurons. Activation of NKRs stimulates inositol trisphosphate/diacylglycerol (IP3/DAG) and cyclic adenosine monophosphate (cAMP) second messenger in a cell context-dependent manner. Activation of NKRs mediates complex neuronal signaling pathways linked to sensations and emotional responses. Emerging evidence suggests that substance P plays other vital roles in inflammation, wound healing, and angiogenesis. Agents that inhibit substance P activity are currently being investigated as potential drugs for pain relief and other clinical conditions.
P物质(SP)是一种由中枢神经系统(CNS)、外周神经系统和免疫细胞表达的11个氨基酸长的神经肽。SP是由TAC1基因编码的速激肽(TAC)神经肽家族的成员。SP通过与G蛋白偶联神经激肽受体(NKRs)相互作用来发挥其活性,包括NK1R、NK2R和NK3R。NKRs在包括血管和淋巴管内皮细胞、免疫细胞、成纤维细胞和神经元在内的各种细胞类型表面表达。NKRs的激活以细胞背景依赖的方式刺激肌醇三磷酸/二酰甘油(IP3/DAG)和环磷酸腺苷(cAMP)第二信使。NKRs的激活介导与感觉和情绪反应相关的复杂神经元信号通路。新出现的证据表明,P物质在炎症、伤口愈合和血管生成中发挥其他重要作用。目前正在研究抑制P物质活性的药物作为缓解疼痛和其他临床病症的潜在药物。