Docosahexaenoic acid (22:6n3)-induced relaxation of the rat aorta.

Docosahexaenoic acid (22:6n3)-induced relaxation of the rat aorta.
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二十二碳六烯酸 (22:6n3) 诱导大鼠主动脉舒张。

DOI:
10.1016/0014-2999(90)90644-l
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发表时间:
1990
影响因子:
5
通讯作者:
N. Salem
N. Salem
中科院分区:
医学2区
文献类型:
--
作者:
M. Engler;J. Karanian;N. Salem

文献摘要

被引文献

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饮食中摄入含有二十碳五烯酸和二十二碳六烯酸的鱼和鱼油补充剂,与心血管系统的有利变化有关,如降低血压。因此,我们观察了二十二碳六烯酸(22:6n3)对大鼠主动脉平滑肌等长张力的影响。在非预收缩的血管中,22:6N3可引起浓度依赖的(1-127μM)松弛(6-30%)。浓度依赖的二十二碳六烯酸(1-44μM)可逆转苯肾上腺素(7-43%)和U44069(8-52%)引起的大鼠主动脉环收缩。这些结果表明,22:6N3对大鼠主动脉的松弛作用是浓度依赖的,而不是收缩激动剂所特有的。
Dietary consumption of fish and fish oil supplements, containing eicosapentaenoic acid and docosahexaenoic acid, has been associated with favorable alterations in the cardiovascular system, such as, a reduction in blood pressure. Therefore, the effects of docosahexaenoic acid (22:6n3) on isometric tension of rat aortic smooth muscle were investigated. A concentration-dependent (1–127 μM) relaxation (6–30%) was induced by 22:6n3 in non-precontracted vessels. Docosaehexaenoic acid, concentration dependently (1–44 μM) reversed contractions of rat aortic rings induced by phenylephrine (7–43%) and by U44069 (8–52%). These results indicate that the relaxant effects produced by 22 : 6n3 in the rat aorta are concentration-dependent and not specific to the contractile agonist.