期刊文献+

Cav3.2通道在伤害性感受中的作用

The nociception role of Cav3.2 calcium channel
原文传递
导出
摘要 背景疼痛是危害人类健康,影响人类生存质量的重要因素,但目前可用于临床治疗的手段尚不能满足患者的无痛要求,且存在不同程度的副作用,其主要原因之一是目前对疼痛的产生机制尚未完全明了。最近的研究表明,T型钙通道Cav3.2亚型在疼痛信号转导中起重要作用。目的综述T型钙通道Cav3.2亚型在痛觉传导中的作用。内容阐述位于背根神经节(dorsalrootganglion,DRG)的T型钙通道参与传递生理性疼痛(疼痛感知)和病理性疼痛(神经病理性疼痛)伤害性刺激信号。趋向T型钙离子通道可调控疼痛伤害性刺激信号转导,并可作为可能的疼痛治疗靶点。 Background Some of the earliest detailed descriptions of biophysical properties of low voltage-activated or transient (T) type Calcium channels were done using in vitro preparation of primary sensory or dorsal root ganglion (DRG) neurons that are known for their functional role in processing pain signals. However, in spite of these early discoveries, T-type calcium channels were not implicated in sensory transmission in general and pain processing (nociception) in particular until recently. Objective To summarize the important role of peripheral T-type Calcium channels in boosting nociceptive transmission. Content T-type calcium channels in peripheral sensory neurons play important role under physiological conditions (e.g. acute noeiceptive pain ) and to pain processing under pathological conditions. Trend peripheral T-type Calcium channels in nociception and the value of these channels as cellular targets for potential drug developments.
作者 苏昊 徐世元
出处 《国际麻醉学与复苏杂志》 CAS 2015年第10期941-944,共4页 International Journal of Anesthesiology and Resuscitation
关键词 离子通道 T型钙通道 伤害性刺激 T-type calcium channel Dorsal root ganglion Nociception
  • 相关文献

参考文献19

  • 1尹晴,屠伟峰,陶元祥,马亚平,康旭.钙通道阻滞剂的镇痛作用及其机制研究进展[J].国际麻醉学与复苏杂志,2013,34(8):748-751. 被引量:3
  • 2Park.YG. Park HY. Lee CJ. et al, Ca (V)3.1 is a tremor rhythm pacemaker in the inferior olive [J]. Proc Natl Acad Sci USA. 2010. 107(23): 10731-10736.
  • 3Todorovic SM. Jevtovic - Todorovic V. Neuropathic pain: role for presynaptic T -type channels in nociceptive signaling [J]. Pflugers Arch. 2013. 465(7): 921-927.
  • 4Todorovic SM. Jevtovic -Todorovic V. T -type voltage-gated calcium channels as targets for the development of novel pain therapies [J]. Br J Pharmacol , 2011. 163(3): 484495.
  • 5Ku WH. Schneider SP. Multiple T -type Ca2+ current subtypes in electrophysiologically characterized hamster dorsal hom neurons: possible role in spinal sensory integration [J]. J Neurophysiol, 2011. 106(5): 2486-2498.
  • 6Francois A. Kerckhove N. Meleine M. et al. State-dependent properties of a new T-type calcium channel blocker enhance Ca(V) 3.2 selectivity and supportanalgesic effects [J]. Pain. 2013. 154 (2): 283-293.
  • 7林思芳,谭宏宇,叶铁虎,马士平,王晓良.氯胺酮对大鼠海马神经元低电压激活钙电流的抑制作用[J].国际麻醉学与复苏杂志,2013,34(2):99-102. 被引量:2
  • 8Bogeski I. Kappl R. Kummerow C. et al. Redox regulation of calcium ion channels: chemical and physiological aspects [J]. Cell Calcium. 2011. 50(5): 407423.
  • 9Todorovic SM. Jevtovic -Todorovic V. Redox regulation of neuronal voltage -gated calcium channels [J]. Antioxid Redox Signal. 2014. 21 (6): 880-89l.
  • 10Perez - Reyes E. Lee JH. Ins and outs of T -channel structure function[J]. Pflugers Arch. 2014. 466(4): 627-633.

二级参考文献33

  • 1Markman JD, Dworkin RH. Ion channel targets and treatment efficacy in neuropathic pain. J Pain, 2006, 7( 1Suppl): $38-$47.
  • 2Winquist ILl, Pan JQ, Gribkoff VK. Use-dependent blockade of Cav2.2 voltage-gated calcium channels for neuropathic pain. Biochemical Pharmacology, 2005, 70(4): 489-499.
  • 3Hashizume K. Diagnosis and treatment of chronic pain by pain clinicians. Brain Nerve, 2012, 64(11): 1315-1322.
  • 4Shao PP, Ye F, Chakravarty PK, et al. Aminopipefidine sulfonamide Ca (v)2.2 channel inhibitors for the treatment of chronic pain. J Med Chem, 2012, 55(22): 9847-9855.
  • 5Matthews EA, Bee LA, Stephens GJ, et al. The Car2. 3 calcium channel antagonist SNX-482 reduces dorsal horn neuronal responses in a rat model of chronic neuropathic pain. European Journal of Neuroscience, 2007, 25(12) : 3561-3569.
  • 6Abbadie C, Mcmanus OB, Sun SY, et al. Analgesic effects of a substituted N-triazole oxindole (TROX-1), a state-dependent, voltage-gated calcium channel 2 blocker. J Pharmacol Exp Ther, 2010, 334(2): 545-555.
  • 7Ahier C, Dale CS, Kisilevsky AE, et al. Differential role of N-type calcium channel splice isoforms in pain. J Neurosci, 2007, 27 (24) : 6363-6373.
  • 8Tyagarajan S, Chakravarty PK, Park M, et al. A potent and selective indole N-type calcium channel (Cav2. 2) blocker for thetreatment of pain. Bioorganic & Medicinal Chemistry Letters, 2010, 21(2): 869-873.
  • 9Klimis H, Adams DJ, Callaghan B, et al. A novel mechanism of inhibition of high-voltage activated calcium channels by alpha- conotoxins contributes to relief of nerve injury-induced neuropathic pain. Pain, 2011, 152(2): 259-266.
  • 10Schroeder CI, Doering C J, Zamponi GW, et al. N-type calcium channel blockers: novel therapeutics for the treatment of pain. Med Chem, 2006, 2(5): 535-543.

共引文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部