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环氧化酶抑制对离子导入 1-和 2-肾上腺素能受体激动剂引起的男性和女性手指血管反应的影响。

Effects of cyclooxygenase inhibition on vascular responses evoked in fingers of men and women by iontophoresis of 1- and 2-adrenoceptor agonists.

机构信息

School of Clinical and Experimental Medicine, College of Medical and Dental Sciences, University of Birmingham, Birmingham B15 2TT, UK.

出版信息

J Physiol. 2011 Sep 15;589(Pt 18):4555-64. doi: 10.1113/jphysiol.2011.215020. Epub 2011 Aug 1.

Abstract

In 10 men and nine women aged 20-23 years, we aimed to establish whether endogenous prostanoids synthesised by cyclooxygenase (COX) affect responses evoked in the finger by α(1)- or α(2)-adrenoceptor agonists. Cutaneous red cell flux (cRCF) was recorded in dorsal finger during iontophoresis of phenylephrine (PE) or clonidine (0.5 mm, seven 0.1 mA pulses followed by one 0.2 mA pulse: 30 s each at 60 s intervals) before and after the COX inhibitor aspirin (600 mg p.o.). In men, PE evoked a biphasic mean increase/decrease in cRCF before but a monophasic mean decrease in cRCF of 30-40% after aspirin (P < 0.05). In women in the low oestrogen (E(2)) phase of the menstrual cycle, PE evoked a decrease in cRCF (30-40%; P < 0.05) that was unchanged by aspirin, whereas in the high E(2) phase, PE evoked no change before but a graded decrease in cRCF (30-40%; P < 0.05) after aspirin. Clonidine evoked a decrease in cRCF (∼30%; P < 0.05) in men before, but not after, aspirin. Clonidine evoked both increases and decreases in cRCF before and after aspirin in women in the low and high E(2) phases (P > 0.05). We propose that finger vasoconstriction evoked by extraluminal α(1)-adrenoceptor stimulation is blunted by vasodilator COX products in young men and overcome by their action in women in the high, but not low E(2), phase of the menstrual cycle. By contrast, α(2)-adrenoceptor stimulation evokes finger vasoconstriction that is mediated by vasoconstrictor COX products in young men, but evokes no consistent response in women in the low or high E(2) phases of the menstrual cycle.

摘要

在 10 名 20-23 岁的男性和 9 名女性中,我们旨在确定内源性前列腺素是否由环氧化酶(COX)合成,影响手指对 α(1)-或 α(2)-肾上腺素受体激动剂的反应。在使用苯肾上腺素(PE)或可乐定(0.5mm,七个 0.1mA 脉冲,随后一个 0.2mA 脉冲:每个脉冲 30s,间隔 60s)进行离子电渗后,在手指背侧记录表皮红细胞通量(cRCF)。在男性中,PE 在前阿司匹林(600mg 口服)后诱发 cRCF 的双相平均增加/减少,但阿司匹林后 cRCF 的单相平均减少 30-40%(P<0.05)。在月经周期低雌激素(E(2))阶段的女性中,PE 诱发 cRCF 减少(30-40%;P<0.05),阿司匹林无变化,而在高 E(2)阶段,PE 在前无变化,但阿司匹林后 cRCF 逐渐减少(30-40%;P<0.05)。在男性中,可乐定诱发 cRCF 减少(约 30%;P<0.05),但阿司匹林后无变化。在低和高 E(2)阶段的女性中,可乐定在阿司匹林前后均可诱发 cRCF 的增加和减少(P>0.05)。我们提出,外腔 α(1)-肾上腺素受体刺激引起的手指血管收缩被年轻男性中的血管扩张 COX 产物减弱,并在月经周期高 E(2)阶段而不是低 E(2)阶段的女性中被其作用克服。相比之下,α(2)-肾上腺素受体刺激引起的手指血管收缩是由年轻男性中的血管收缩 COX 产物介导的,但在月经周期低或高 E(2)阶段的女性中没有引起一致的反应。

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