Stirrat A, Nelli S, Dowell F J, Martin W
Division of Neuroscience and Biomedical Systems, Institute of Biomedical and Life Sciences, University of Glasgow, Glasgow, Scotland, UK.
Br J Pharmacol. 2008 Mar;153(6):1162-8. doi: 10.1038/sj.bjp.0707499. Epub 2007 Oct 8.
We previously reported that ascorbate inhibits flow- and agonist-induced, EDHF-mediated vasodilatation in the bovine ciliary circulation. This study examined whether ascorbate had similar actions in the rat mesenteric vasculature.
The effects of ascorbate were examined both in rat second order mesenteric arterial rings suspended in a static wire myograph and the rat mesentery perfused at different rates of flow.
Ascorbate (50 microM) had no effect on U46619-induced tone or acetylcholine-induced, EDHF-mediated vasodilatation in either rings of mesenteric artery or the perfused mesentery at rates of flow below 10 ml min(-1). At higher rates of flow, ascorbate produced two distinct effects in the rat mesentery: a rapid and maintained enhancement of vasoconstrictor tone and a slow (max at 3 h) inhibition of acetylcholine-induced, EDHF-mediated vasodilatation. The enhancement of vasoconstrictor tone appeared to be due to inhibition of flow-induced EDHF-like activity, since it was endothelium-dependent, but could be elicited during blockade of nitric oxide synthase and cyclooxygenase. Despite this, the classical inhibitors of EDHF, apamin and charybdotoxin, failed to affect the ascorbate-induced enhancement of tone, although they inhibited acetylcholine-induced vasodilatation.
Ascorbate inhibits both flow- and agonist-induced EDHF in the rat mesentery. The strikingly different timecourses of these two effects, together with their differential sensitivity to apamin and charybdotoxin, suggest that the flow- and agonist-induced EDHFs in the rat mesenteric vasculature may either be different entities or operate by different mechanisms.
我们之前报道过,抗坏血酸可抑制牛睫状体循环中血流及激动剂诱导的、内皮衍生超极化因子(EDHF)介导的血管舒张。本研究检测抗坏血酸在大鼠肠系膜血管系统中是否有类似作用。
在置于静态线肌张力测定仪中的大鼠二级肠系膜动脉环以及以不同流速灌注的大鼠肠系膜中检测抗坏血酸的作用。
在流速低于10 ml·min⁻¹时,抗坏血酸(50 μM)对U46619诱导的张力或乙酰胆碱诱导的、EDHF介导的肠系膜动脉环或灌注肠系膜中的血管舒张均无影响。在较高流速时,抗坏血酸在大鼠肠系膜中产生两种不同效应:血管收缩张力迅速且持续增强,以及对乙酰胆碱诱导的、EDHF介导的血管舒张的缓慢抑制(3小时达最大值)。血管收缩张力的增强似乎是由于对血流诱导的EDHF样活性的抑制,因为它依赖于内皮,但在一氧化氮合酶和环氧化酶被阻断时也可引发。尽管如此,EDHF的经典抑制剂蜂毒明肽和大蝎毒素虽能抑制乙酰胆碱诱导的血管舒张,但却未能影响抗坏血酸诱导的张力增强。
抗坏血酸抑制大鼠肠系膜中血流及激动剂诱导的EDHF。这两种效应显著不同的时间进程,以及它们对蜂毒明肽和大蝎毒素的不同敏感性,表明大鼠肠系膜血管系统中血流及激动剂诱导的EDHF可能是不同的实体,或者通过不同的机制起作用。