Thermo-TRP通道参与化疗药物诱导的外周疼痛

Q4 Biochemistry, Genetics and Molecular Biology
M. K. Yıldırım
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引用次数: 0

摘要

越来越多的证据表明,细胞内游离钙([Ca2+]i)浓度的紊乱在外周疼痛的病理生理学中起着重要作用。Ca2+通过不同的通道通过细胞膜,如化学通道和电压门控通道。除了众所周知的阳离子通道外,最近还发现了一些通道,即瞬时受体电位(TRP)家族。至少,哺乳动物细胞中的11个TRP通道已被鉴定为热敏TRP(thermo-TRP)通道(Uchida等人,2017)。两个TRP通道(TRPV1和TRPV2)被高温激活。五个TRP通道(TRPV1-4和TRPM2)被不同的热温度激活,尽管TRP通道中的两个通道(TRPA1和TRPM8)分别被低温和低温激活(Naziroglu和Braidy,2017)。众所周知,[Ca2+]i浓度的增加而细胞内Mg2+水平的降低诱导一氧化氮合酶(NOS)的激活。通过NOS的催化活性,一氧化氮在神经元中合成。反过来,它通过产生兴奋性氨基酸和P物质来诱导疼痛(Medvedeva等人,2008)。最近的研究结果表明,化疗药物(即顺铂、奥沙利铂和紫杉醇)通过激活热TRP通道(如TRPA1、TRPV1和TRPM8)诱导线粒体氧化应激,尽管抗氧化剂通过抑制实验动物中的TRP通道来诱导对疼痛诱导的保护作用(Materazzi等人,2012)。在口头陈述中,我讨论了化疗药物通过调节TRP通道对外周疼痛的新作用。我得出的结论是,化疗药物会引起TRP通道激活和氧化应激,这可能导致外周疼痛的病理学。TRP通道激活与化疗药物之间的确切关系似乎仍有待确定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Involvement of Thermo TRP channels on chemothrepeutic agents-induced peripheral pain
Accumulating evidences have indicated that  disturbances in intracellular free calcium ([Ca2+]i)  concentration play an important role in the  pathophysiology of peripheral pain. Ca2+ passes cell  membrane via different channels such as chemical and  voltage gated channels. Apart from the well-known  cation channels, there is recently discovered channels  namely transient receptor potential (TRP) family. At  least, 11 TRP channels in mammalian cells have been  identified as thermosensitive TRP (thermo-TRP)  channels (Uchida et al. 2017). Two TRP channels  (TRPV1 and TRPV2) are activated by high  temperatures. Five TRP channels (TRPV1-4 and  TRPM2) are activated by different heat temperatures,  although two of TRP channels (TRPA1 and TRPM8)  are activated by cold and cool temperatures,  respectively (Naziroglu and Braidy, 2017). It is well  known that increase of [Ca2+]i concentration but  decrease of intracellular Mg2+ levels induces activation  of nitric oxide synthase (NOS) enzyme. By catalytic  activity of NOS, nitric oxide synthetizes in neurons. In  turn, it induces pain through production of excitatory  amino acids and substance P (Medvedeva et al. 2008).  Results of recent studies indicated involvement of  chemothrepeutic agents (i.e. cisplatin, oxaliplatin and  paclitaxel)-induced mitochondrial oxidative stress  through activation of Thermo TRP channels such as  TRPA1, TRPV1 and TRPM8, although antioxidants  induced protective action on the pain induction through  inhibition of the TRP channels in the experimental  animals (Materazzi et al. 2012). In the oral presentation,  I discussed novel effects of chemotherapeutic agents on  the peripheral pain by the regulation of TRP channels.  I concluded that the chemotherapeutic agents  cause TRP channel activation and oxidative stress,  which may lead to the pathology of peripheral pain. It seems to that the exact relationship between TRP  channel activation and chemotherapeutic agents still  remain to be determined.
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来源期刊
Journal of Cellular Neuroscience and Oxidative Stress
Journal of Cellular Neuroscience and Oxidative Stress Biochemistry, Genetics and Molecular Biology-Biophysics
CiteScore
1.10
自引率
0.00%
发文量
8
期刊介绍: Journal of Cellular Neuroscience and Oxidative Stress isan online journal that publishes original research articles, reviews and short reviews on themolecular basisofbiophysical,physiological and pharmacological processes thatregulate cellular function, and the control or alteration of these processesby theaction of receptors, neurotransmitters, second messengers, cation, anions,drugsor disease. Areas of particular interest are four topics. They are; 1. Ion Channels (Na+-K+Channels, Cl– channels, Ca2+channels, ADP-Ribose and metabolism of NAD+,Patch-Clamp applications) 2. Oxidative Stress (Antioxidant vitamins, antioxidant enzymes, metabolism of nitric oxide, oxidative stress, biophysics, biochemistry and physiology of free oxygen radicals) 3. Interaction Between Oxidative Stress and Ion Channels in Neuroscience (Effects of the oxidative stress on the activation of the voltage sensitive cation channels, effect of ADP-Ribose and NAD+ on activation of the cation channels which are sensitive to voltage, effect of the oxidative stress on activation of the TRP channels in neurodegenerative diseases such Parkinson’s and Alzheimer’s diseases) 4. Gene and Oxidative Stress (Gene abnormalities. Interaction between gene and free radicals. Gene anomalies and iron. Role of radiation and cancer on gene polymorphism)
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