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环氧化酶产物介导了内皮素 -1 在人体中诱导的皮肤血管舒张。

Cyclooxygenase products mediate the cutaneous vasodilation induced by endothelin-1 in humans.

作者信息

Di Maria G U, Bellofiore S, Puglisi S, Novo S, Ricciardolo F L, Mistretta A

机构信息

Institute of Respiratory Disease, University of Catania, Italy.

出版信息

Regul Pept. 1993 Sep 22;47(3):233-8. doi: 10.1016/0167-0115(93)90390-t.

Abstract

Intradermal injection of endothelin-1 (ET-1) causes vasoconstriction (pallor) at the injection site, surrounded by a larger area of vasodilation (flare) in humans. Some of the vasomotor responses to ET-1 are thought to be mediated by prostaglandins. In the present study, we investigated the involvement of cyclooxygenase-derived products of arachidonic acid metabolism on the cutaneous vasomotor responses to ET-1. Ten normal subjects (25-44 years) were studied after treatment with either indomethacin (50 mg t.i.d.) or placebo according to a double blind cross-over design. Five doses of ET-1 (5 x 10(-5) to 5 x 10(-1) pmol) were injected intradermally 2 h after the last dose of indomethacin or placebo. Pallor and flare areas measured by planimetry 15 min after the injection were analyzed to evaluate cutaneous vasomotor responses to ET-1. ET-1 induced dose-dependent pallor and flare responses that were significant at the dose of 5 x 10(-3) pmol or greater. Indomethacin did not affect the ET-1-induced pallor but significantly shifted to the right the flare dose-response curve to ET-1. The inhibition of the flare response to 5 x 10(-1) pmol ET-1 was 58.9 +/- 8.5%. These results indicate that the cutaneous vasodilation induced by intradermal injection of ET-1 is mediated by the release of vasodilating cyclooxygenase products.

摘要

皮内注射内皮素-1(ET-1)会在注射部位引起血管收缩(皮肤苍白),在人体中其周围会出现更大面积的血管扩张(红晕)。一些对ET-1的血管运动反应被认为是由前列腺素介导的。在本研究中,我们调查了花生四烯酸代谢的环氧化酶衍生产物在皮肤对ET-1的血管运动反应中的作用。按照双盲交叉设计,对10名正常受试者(25 - 44岁)在给予吲哚美辛(50毫克,每日三次)或安慰剂治疗后进行研究。在最后一剂吲哚美辛或安慰剂给药2小时后,皮内注射5个剂量的ET-1(5×10⁻⁵至5×10⁻¹皮摩尔)。注射后15分钟通过面积测量法测量皮肤苍白和红晕面积,以评估皮肤对ET-1的血管运动反应。ET-1诱导剂量依赖性的皮肤苍白和红晕反应,在5×10⁻³皮摩尔或更高剂量时具有统计学意义。吲哚美辛不影响ET-1诱导的皮肤苍白,但使ET-1的红晕剂量反应曲线显著右移。对5×10⁻¹皮摩尔ET-1的红晕反应抑制率为58.9±8.5%。这些结果表明,皮内注射ET-1诱导的皮肤血管扩张是由血管舒张性环氧化酶产物的释放介导的。

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