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豚鼠肠系膜动静脉血管中激肽和神经激肽受体的特性研究。

Characterization of receptors for kinins and neurokinins in the arterial and venous mesenteric vasculatures of the guinea-pig.

作者信息

Berthiaume N, Claing A, Regoli D, Warner T D, D'Orléans-Juste P

机构信息

Department of Pharmacology, Medical School, Université de Sherbrooke, Québec, Canada.

出版信息

Br J Pharmacol. 1995 Aug;115(7):1319-25. doi: 10.1111/j.1476-5381.1995.tb15043.x.

Abstract
  1. In the present work, we have studied the microvascular reactivity of the arterial and venous mesenteric beds of the guinea-pig to bradykinin, neurokinins and other agents. 2. The vasoactive properties of three selective agonists for neurokinin receptors, namely [Sar9, Met (O2)11]SP (NK1), [beta-Ala8]NKA(4-10) (NK2) and [MePhe7]NKB (NK3), were evaluated on precontracted arterial and venous mesenteric vasculatures of the guinea-pig. The NK1-selective agonist, [Sar9,Met(O2)11]SP (1 to 1000 pmol), induced an endothelium-dependent and N omega-nitro-L-arginine methyl ester (L-NAME)-sensitive relaxation of the arterial vasculature precontracted with methoxamine, whereas the NK2 and NK3-selective agonists were virtually inactive at high doses (1000 pmol). 3. The three selective neurokinin receptor agonists were inactive in the non-precontracted arterial and venous mesenteric vasculatures as well as in the precontracted venous mesenteric vasculature. 4. Bradykinin (0.1 to 100 pmol) induced a marked dose- and endothelium-dependent vasodilatation of the precontracted arterial and venous vasculatures. ED50 values were 5.5 pmol on the arterial side and 1.9 pmol on the venous side. In contrast, desArg9-bradykinin was inactive at doses up to 1000 pmol. Furthermore, on the arterial and venous sides, a higher dose of bradykinin (1000 pmol), induced a biphasic effect, a transient constriction followed by a marked and sustained vasodilatation. The vasodilator effects of bradykinin were abolished by Hoe 140 (0.1 microM) and CHAPS, markedly reduced by L-NAME and were unaffected by [Leu8]desArg9-bradykinin (0.1 microM) on both sides of the mesenteric vasculature. Hoe 140 also abolished the arterial vasoconstrictions induced by high doses of bradykinin. 5. Noradrenaline, angiotensin II and endothelin-1 produced contractions on both sides of the mesenteric circulation, while acetylcholine (arterial side) and sodium nitroprusside (arterial and venous sides) caused vasodilatation.6. Our study supports the view that NK1 receptors responsible for vasodilatation are present solely in the endothelium of the arterial mesenteric vasculature of the guinea-pig. On the other hand, bradykinin(0.1 to 100 pmol) exerts predominantly vasodilator effects on both sides of the mesenteric vasculature via selective activation of B2 receptors located on the endothelium. The same receptor type located on the smooth muscle appears to be responsible for the arterial and venous constriction with high doses of bradykinin.
摘要
  1. 在本研究中,我们研究了豚鼠肠系膜动脉和静脉床对缓激肽、神经激肽及其他药物的微血管反应性。2. 对三种神经激肽受体选择性激动剂,即[Sar9, Met (O2)11]SP (NK1)、[β - Ala8]NKA(4 - 10) (NK2) 和 [MePhe7]NKB (NK3) 的血管活性特性,在豚鼠预先收缩的肠系膜动脉和静脉血管系统上进行了评估。NK1 选择性激动剂[Sar9,Met(O2)11]SP(1至1000皮摩尔),可诱导用甲氧明预先收缩的动脉血管系统产生内皮依赖性且对Nω - 硝基 - L - 精氨酸甲酯(L - NAME)敏感的舒张,而NK2和NK3选择性激动剂在高剂量(1000皮摩尔)时几乎无活性。3. 这三种选择性神经激肽受体激动剂在未预先收缩的肠系膜动脉和静脉血管系统以及预先收缩的肠系膜静脉血管系统中均无活性。4. 缓激肽(0.1至100皮摩尔)可诱导预先收缩的动脉和静脉血管系统产生明显的剂量依赖性和内皮依赖性血管舒张。动脉侧的ED50值为5.5皮摩尔,静脉侧为1.9皮摩尔。相比之下,去精氨酸9 - 缓激肽在高达1000皮摩尔的剂量下无活性。此外,在动脉侧和静脉侧,较高剂量的缓激肽(1000皮摩尔)会产生双相效应,先是短暂收缩,随后是明显且持续的血管舒张。缓激肽的血管舒张作用可被Hoe 140(0.1微摩尔)和CHAPS消除,被L - NAME显著降低,且在肠系膜血管系统两侧均不受[Leu8]去精氨酸9 - 缓激肽(0.1微摩尔)影响。Hoe 140也消除了高剂量缓激肽诱导的动脉血管收缩。5. 去甲肾上腺素、血管紧张素II和内皮素 - 1在肠系膜循环两侧均引起收缩,而乙酰胆碱(动脉侧)和硝普钠(动脉侧和静脉侧)引起血管舒张。6. 我们的研究支持这样一种观点,即负责血管舒张的NK1受体仅存在于豚鼠肠系膜动脉血管的内皮中。另一方面,缓激肽(0.1至100皮摩尔)通过选择性激活位于内皮上的B2受体,在肠系膜血管系统两侧主要发挥血管舒张作用。位于平滑肌上的相同受体类型似乎是高剂量缓激肽引起动脉和静脉收缩的原因。

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