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利坦色林与绵羊血压及液体调节中的血清素能机制

Ritanserin and serotonergic mechanisms in blood pressure and fluid regulation in sheep.

作者信息

Nelson M, Coghlan J P, Denton D A, Tresham J J, Whitworth J A, Scoggins B A

机构信息

Howard Florey Institute of Experimental Physiology and Medicine, University of Melbourne, Parkville, Victoria, Australia.

出版信息

Clin Exp Pharmacol Physiol. 1987 Jul;14(7):555-63. doi: 10.1111/j.1440-1681.1987.tb01874.x.

Abstract
  1. In previous studies, exogenous serotonin (5-HT), administered intravenously, caused dose-related increases in mean arterial pressure and heart rate in conscious sheep. The 5-HT2 antagonist ketanserin (0.1 mg/kg per h, i.v.) was shown to lower blood pressure in the conscious sheep primarily through antagonism of alpha-adrenoceptors. 2. A newer 5-HT2 antagonist, ritanserin, is a more selective antagonist in vivo, as it attenuated or abolished pressor responses to exogenous 5-HT, but not to phenylephrine. 3. When infused alone, ritanserin (0.1 mg/kg per h, i.v.) failed to produce a decrease in blood pressure, suggesting that 5-HT antagonistic properties are not sufficient by themselves to lower blood pressure. 4. Ritanserin displayed a different metabolic profile to ketanserin, with a markedly decreased water intake. The mechanism of this effect is unresolved, but may imply a permissive role for 5-HT in the modulation of drinking responses in the sheep. 5. Ritanserin did not modify ACTH-induced hypertension in sheep.
摘要
  1. 在先前的研究中,静脉注射外源性血清素(5-羟色胺,5-HT)会使清醒绵羊的平均动脉压和心率呈剂量相关增加。5-HT2拮抗剂酮色林(0.1毫克/千克每小时,静脉注射)已被证明主要通过拮抗α-肾上腺素能受体来降低清醒绵羊的血压。2. 一种更新的5-HT2拮抗剂利坦色林在体内是一种更具选择性的拮抗剂,因为它减弱或消除了对外源性5-HT的升压反应,但对去氧肾上腺素则没有。3. 单独输注时,利坦色林(0.1毫克/千克每小时,静脉注射)未能使血压降低,这表明5-HT拮抗特性本身不足以降低血压。4. 利坦色林与酮色林表现出不同的代谢特征,饮水量显著减少。这种效应的机制尚未明确,但可能意味着5-HT在调节绵羊饮水反应中起允许作用。5. 利坦色林不会改变绵羊中促肾上腺皮质激素诱导的高血压。

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