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单萜类化合物圆叶当归醇诱导的TRPM8通道激活是肠系膜动脉舒张的基础。

TRPM8 Channel Activation Induced by Monoterpenoid Rotundifolone Underlies Mesenteric Artery Relaxation.

作者信息

Silva Darizy Flavia, de Almeida Monica Moura, Chaves Cinthia Guedes, Braz Ana Letícia, Gomes Maria Aparecida, Pinho-da-Silva Leidiane, Pesquero Jorge Luiz, Andrade Viviane Aguiar, Leite Maria de Fátima, de Albuquerque José George Ferreira, Araujo Islania Giselia Albuquerque, Nunes Xirley Pereira, Barbosa-Filho José Maria, Cruz Jader dos Santos, Correia Nadja de Azevedo, de Medeiros Isac Almeida

机构信息

Departamento de Bio-regulação, Universidade Federal da Bahia (UFBA), Salvador, Bahia, Brazil, 40110-902.

Departamento de Ciências Farmacêuticas, Universidade Federal da Paraíba (UFPB), João Pessoa, Paraíba, Brazil, 58059-900.

出版信息

PLoS One. 2015 Nov 23;10(11):e0143171. doi: 10.1371/journal.pone.0143171. eCollection 2015.

Abstract

In this study, our aims were to investigate transient receptor potential melastatin-8 channels (TRPM8) involvement in rotundifolone induced relaxation in the mesenteric artery and to increase the understanding of the role of these thermosensitive TRP channels in vascular tissue. Thus, message and protein levels of TRPM8 were measured by semi-quantitative PCR and western blotting in superior mesenteric arteries from 12 week-old Spague-Dawley (SD) rats. Isometric tension recordings evaluated the relaxant response in mesenteric rings were also performed. Additionally, the intracellular Ca2+ changes in mesenteric artery myocytes were measured using confocal microscopy. Using PCR and western blotting, both TRPM8 channel mRNA and protein expression was measured in SD rat mesenteric artery. Rotundifolone and menthol induced relaxation in the isolated superior mesenteric artery from SD rats and improved the relaxant response induced by cool temperatures. Also, this monoterpene induced an increase in transient intracellular Ca2+. These responses were significantly attenuated by pretreatment with capsazepine or BCTC, both TRPM8 channels blockers. The response induced by rotundifolone was not significantly attenuated by ruthenium red, a non-selective TRP channels blocker, or following capsaicin-mediated desensitization of TRPV1. Our findings suggest that rotundifolone induces relaxation by activating TRPM8 channels in rat superior mesenteric artery, more selectively than menthol, the classic TRPM8 agonist, and TRPM8 channels participates in vasodilatory pathways in isolated rat mesenteric arteries.

摘要

在本研究中,我们的目的是研究瞬时受体电位香草酸亚型8通道(TRPM8)在圆叶当归酚诱导的肠系膜动脉舒张中的作用,并增进对这些热敏性瞬时受体电位(TRP)通道在血管组织中作用的理解。因此,我们通过半定量PCR和蛋白质印迹法检测了12周龄Spague-Dawley(SD)大鼠肠系膜上动脉中TRPM8的信使核糖核酸(mRNA)和蛋白质水平。还进行了等长张力记录以评估肠系膜血管环的舒张反应。此外,使用共聚焦显微镜测量了肠系膜动脉肌细胞内的钙离子(Ca2+)变化。利用PCR和蛋白质印迹法,我们检测了SD大鼠肠系膜动脉中TRPM8通道的mRNA和蛋白质表达。圆叶当归酚和薄荷醇可诱导SD大鼠离体肠系膜上动脉舒张,并增强低温诱导的舒张反应。此外,这种单萜类化合物可引起细胞内钙离子的瞬时增加。用TRPM8通道阻滞剂辣椒素受体拮抗剂或BCTC预处理可显著减弱这些反应。圆叶当归酚诱导的反应并未被非选择性TRP通道阻滞剂钌红或辣椒素介导的瞬时受体电位香草酸亚型1(TRPV1)脱敏所显著减弱。我们的研究结果表明,圆叶当归酚通过激活大鼠肠系膜上动脉中的TRPM8通道诱导舒张,比经典的TRPM8激动剂薄荷醇更具选择性,并且TRPM8通道参与了离体大鼠肠系膜动脉的血管舒张途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0dd/4657920/dd26e398b24e/pone.0143171.g001.jpg

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