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Rho激酶与疼痛及其抑制剂的临床应用 被引量:5

Rho kinase and pain and clinical application of its inhibitors
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摘要 小分子GTP结合蛋白Rho及其下游Rho激酶对细胞的收缩、迁移、增殖、黏附和凋亡等活动具有重要的调控作用。该文通过阐述Rho/Rho激酶信号通路在疼痛的产生和持续过程中的作用及其抑制剂在临床研究中的使用案例,探讨Rho/Rho激酶作为镇痛药物的作用靶点的可能性。大量的实验和临床研究表明,Rho/Rho激酶通过其介导的细胞信号传导系统参与神经性疼痛、炎症性疼痛、糖尿病性周围神经疼痛、脑血管痉挛、血管痉挛性心绞痛及骨癌痛等,因此,Rho/Rho激酶可作为防治疼痛的潜在药物作用靶点,为临床上预防和治疗疼痛提供新的思路和策略。 Small GTP binding protein Rho and its downstream Rho-kinase pathway play an important role in the various cellular functions, including contraction, migration, proliferation, adhe-sion and apoptosis, etc. This article reviews the role of Rho/Rho-kinase pathway in the pain generation and development and clinical application of Rho/Rho-kinase inhibitors. It discusses the feasibility of Rho/Rho-kinase as a target for analgesics. Ac-cumulating experimental and clinical evidences indicate that Rho/Rho-kinase pathway is involved in the neuropathic pain, inflammatory pain, diabetic painful neuropathy, cerebral vaso-spasm, vasospastic angina and cancer pain, etc. Therefore, Rho/Rho-kinase is a potential drug target of the pain, and it provides new therapeutic treatments and strategies for pain in clinic.
出处 《中国药理学通报》 CAS CSCD 北大核心 2014年第4期448-451,共4页 Chinese Pharmacological Bulletin
基金 国家自然科学基金面上项目(No 81173031 81202511)
关键词 RHO蛋白 RHO激酶 疼痛 抑制剂 药物靶点 镇痛 Rho Rho-kinase pain inhibitor drug target analgesia
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  • 1余惠旻,彭求贤,刘塔斯,杨大坚,陈新滋.反左金丸水提物对人胃癌细胞SGC-7901凋亡及bcl-2、bax基因表达的影响[J].中国实验方剂学杂志,2008,14(11):28-31. 被引量:8
  • 2朱雪琦,刘清泉,姚咏明.脓毒症动物模型制备方法的研究进展[J].中国危重病急救医学,2006,18(2):114-116. 被引量:30
  • 3Clark J, Sharp F. Bilirubin oxidation products (BOXes) and their role in cerebral vasospasm after subarachnoid hemor- rhage. J Cereb Blood Flow Metabol, 2006, 26 ( 10 ) : 1223-1233.
  • 4Wurster WL, Pyne-Geithman GJ, Peat IR, et al. Bilirubin oxidation products (BOXes) : synthesis, stability and chemi- cal characteristics. Acta Neurochir Suppl,2008, 104:43-50.
  • 5Lyons MA, Shukla R, Zhang K, et al. Increase of metabolic activity and disruption of normal contractile protein distribution by bilirubin oxidation products in vascular smooth-muscle ceils. J Neurosurg, 2004, 100(3) : 505-511.
  • 6Frykholm P, Andersson JL, Langstrom B, et al. Haemodynam- ic and metabolic disturbances in the acute stage of subarachnoid haemorrhage demonstrated by PET. Acta Neurol Scand,.2004,109(1): 25-32.
  • 7Pyne-Geithman G J, Nair SG, Caudell DN, et al. PKC and Rho in vascular smooth muscle: Activation by BOXes and SAH CSF. Front Biosci, 2008,13: 1526-1534.
  • 8Massett MP, Ungvari Z, Csiszar A, et al. Different roles of PKC and MAP kinases in arteriolar constrictions to pressure and agonists. Am J Physiol Heart Circ Physiol, 2002, 283 (6) :2282-2287.
  • 9ho K, Shimomura E, Iwanage T, et al. Essential role of Rho kinase in the Ca2+ sensitization of prostaglandin f2a-induced contraction of rabbit aortae. J Physiol, 2003 , 546 ( 3 ) : 823 -836.
  • 10Hou S, Xu R, Clark JF, et al. Bilirubin oxidation end prod- ucts directly alter K channels important in the regulation of vascular tone. J Cereb Blood Flow Metab, 2011, 31(1) : 102-112.

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