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一种瞬时受体电位阳离子通道 V3 的膳食激动剂可引起内皮依赖性血管舒张。

A dietary agonist of transient receptor potential cation channel V3 elicits endothelium-dependent vasodilation.

机构信息

Department of Biomedical Sciences, Colorado State University, Fort Collins, CO 80523-1680, USA.

出版信息

Mol Pharmacol. 2010 Apr;77(4):612-20. doi: 10.1124/mol.109.060715. Epub 2010 Jan 19.

Abstract

The Mediterranean diet may be responsible for lower cardiovascular disease rates in Southern versus Northern European countries. Oregano is used abundantly in Mediterranean cooking, but potential cardiovascular benefits have not been investigated. Carvacrol, present in oregano, activates the transient receptor potential (TRP) cation channels TRPA1 and TRPV3. We hypothesized that chemosensing of this dietary molecule by TRP channels in the endothelium promotes arterial relaxation. TRPA1 and TRPV3 were detected in the endothelium of intact arteries. Carvacrol causes concentration-dependent increases in the intracellular [Ca(2+)] of native cerebral artery endothelial cells and is more potent (EC(50) = 34 microM) than the TRPA1 agonist allyl isothiocyanate (EC(50) = 400 microM) or the TRPV3 agonist eugenol (EC(50) = 2.3 mM). Carvacrol also activates TRPV3-like cation currents in cerebral artery endothelial cells. Carvacrol elicits vasodilation of intact cerebral arteries (EC(50) = 4.1 microM) that is accompanied by smooth muscle hyperpolarization and a decrease in the intracellular [Ca(2+)] of arterial myocytes. Endothelium disruption inhibits carvacrol-induced vasodilation, but block of nitric-oxide synthase and cyclooxygenase activity does not alter the response. Vasodilation in response to carvacrol is inhibited when blockers of Ca(2+)-activated K(+) channels are present in the lumen or when the inwardly rectifying K(+) channel blocker BaCl(2) is present in the superfusion bath. Carvacrol-induced dilation is not diminished by a TRPA1 antagonist but is inhibited by the TRPV blocker ruthenium red. Our findings show that oregano can relax arteries by activating TRPV3 channels in the endothelium. This effect may account for some of the cardioprotective effects of the Mediterranean diet.

摘要

地中海饮食可能是导致南欧与北欧国家心血管疾病发病率较低的原因之一。牛至在地中海烹饪中大量使用,但尚未研究其潜在的心血管益处。存在于牛至中的香芹酚激活瞬时受体电位 (TRP) 阳离子通道 TRPA1 和 TRPV3。我们假设,这种膳食分子通过内皮细胞中的 TRP 通道进行化学感应可促进动脉舒张。TRPA1 和 TRPV3 存在于完整动脉的内皮细胞中。香芹酚引起内源性大脑动脉内皮细胞的细胞内 [Ca(2+)]浓度依赖性增加,其作用比 TRPA1 激动剂丙烯基异硫氰酸酯(EC(50)=400μM)或 TRPV3 激动剂丁香酚(EC(50)=2.3mM)更强。香芹酚还激活大脑动脉内皮细胞中的 TRPV3 样阳离子电流。香芹酚引起完整大脑动脉的血管舒张(EC(50)=4.1μM),同时伴有平滑肌超极化和动脉平滑肌细胞内 [Ca(2+)]的减少。内皮细胞破坏抑制香芹酚引起的血管舒张,但一氧化氮合酶和环氧化酶活性的阻断不会改变反应。当腔内存在 Ca(2+)-激活的 K(+) 通道阻断剂或当存在内向整流 K(+) 通道阻断剂 BaCl(2)时,香芹酚引起的血管舒张被抑制。存在于腔内的 Ca(2+)-激活的 K(+) 通道阻断剂或当存在内向整流 K(+) 通道阻断剂 BaCl(2)时,香芹酚引起的血管舒张被抑制。存在于腔内的 Ca(2+)-激活的 K(+) 通道阻断剂或当存在内向整流 K(+) 通道阻断剂 BaCl(2)时,香芹酚引起的血管舒张被抑制。存在于腔内的 Ca(2+)-激活的 K(+) 通道阻断剂或当存在内向整流 K(+) 通道阻断剂 BaCl(2)时,香芹酚引起的血管舒张被抑制。香芹酚诱导的扩张不受 TRPA1 拮抗剂的影响,但受 TRPV 阻断剂钌红的抑制。我们的发现表明,牛至可以通过激活内皮细胞中的 TRPV3 通道来舒张动脉。这种作用可能是地中海饮食的一些心脏保护作用的原因之一。

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