Suppr超能文献

氧张力对猪冠状动脉阻力小动脉血流诱导性血管舒张的影响。

Effects of oxygen tension on flow-induced vasodilation in porcine coronary resistance arterioles.

作者信息

Jimenez A H, Tanner M A, Caldwell W M, Myers P R

机构信息

Dalton Cardiovascular Research Center, University of Missouri, Columbia 65211, USA.

出版信息

Microvasc Res. 1996 May;51(3):365-77. doi: 10.1006/mvre.1996.0033.

Abstract

Vascular tone has been shown to be importantly influenced by flow-induced release of endothelium-derived vasodilators. The purpose of the present study was to test the hypothesis that in porcine coronary resistance-size arterioles, flow-induced vasodilation is sensitive to oxygen tension. Arterioles (55-150 mu m) were studied in vitro under conditions of constant intraluminal pressure to dynamically measure arteriolar diameter in response to changes in flow or, alternatively, in response to bradykinin under three conditions: hyperoxia (pO(2) 400 mm Hg), normoxia (pO(2) 160 mm Hg), and hypoxia (p0(2) 40 mm Hg). Under conditions of constant pressure and no flow, hypoxia alone resulted in vasodilation that was blocked by the nitric oxide synthase inhibitor omega-nitro-L-arginine methyl ester (L-NAME). Hypoxia did not alter the vasodilator response to bradykinin when compared to the vasodilator response to bradykinin during normoxia. During hyperoxia, flow-induced vasodilation was significantly reduced by either indomethacin, or L-NAME. Indomethacin and L-NAME combined completely abolished flow-induced vasodilation under conditions of hyperoxia. Under conditions of normoxia and hypoxia, indomethacin or L-NAME alone only partially blocked flow-induced vasodilation. No further inhibition was observed when indomethacin and L-NAME were combined. Glybenclamide failed to alter flow-induced vasodilation either alone or in combination with indomethacin and L-NAME. The results suggest that the mechanisms responsible for flow-induced vasodilation in coronary arterioles are complex and are different depending upon the oxygen tension. During hyperoxia, vasodilation is due to the combined actions of prostanoids and nitric oxide, while under conditions of normoxia and hypoxia, flow-induced vasodilation is the result of not only prostanoids and nitric oxide, but of another as of yet unidentified oxygen-sensitive endogenous vasodilator.

摘要

血管张力已被证明受到血流诱导的内皮衍生血管舒张剂释放的重要影响。本研究的目的是检验以下假设:在猪冠状动脉阻力大小的小动脉中,血流诱导的血管舒张对氧张力敏感。在恒定管腔内压力条件下,对小动脉(55 - 150μm)进行体外研究,以动态测量小动脉直径对血流变化的响应,或者在三种条件下对缓激肽的响应:高氧(pO₂ 400 mmHg)、常氧(pO₂ 160 mmHg)和低氧(pO₂ 40 mmHg)。在恒定压力且无血流的条件下,单独低氧导致血管舒张,该舒张被一氧化氮合酶抑制剂ω-硝基-L-精氨酸甲酯(L-NAME)阻断。与常氧期间缓激肽引起的血管舒张反应相比,低氧并未改变对缓激肽的血管舒张反应。在高氧期间,吲哚美辛或L-NAME均可显著降低血流诱导的血管舒张。在高氧条件下,吲哚美辛和L-NAME联合使用完全消除了血流诱导的血管舒张。在常氧和低氧条件下,单独使用吲哚美辛或L-NAME仅部分阻断血流诱导的血管舒张。当吲哚美辛和L-NAME联合使用时,未观察到进一步的抑制作用。格列本脲单独使用或与吲哚美辛和L-NAME联合使用均未能改变血流诱导的血管舒张。结果表明,冠状动脉小动脉中血流诱导血管舒张的机制很复杂,并且根据氧张力的不同而不同。在高氧期间,血管舒张是由于前列腺素和一氧化氮的联合作用,而在常氧和低氧条件下,血流诱导的血管舒张不仅是前列腺素和一氧化氮的结果,而且是另一种尚未确定的氧敏感内源性血管舒张剂的结果。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验