大鼠主动脉环β -肾上腺素能血管扩张剂反应的年龄相关性差异。

Maria del Carmen Castillo-Hernandez, Noemi Meraz-Cruz, Gustavo Guevara-Balcazar, Jorge Lopez-Canales, Oscar Lopez-Canales, Norma Galindo, Carlos Castillo-Henkel
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引用次数: 0

摘要

血管扩张剂对β -肾上腺素能药物反应的年龄依赖性变化机制尚不清楚。本研究的目的是比较3周龄和3个月龄雄性Wistar大鼠对异丙肾上腺素(一种非选择性β -肾上腺素能受体激动剂)和苯肾上腺素或KCl预收缩主动脉环的反应。研究了两个年龄组对异丙肾上腺素反应的机制和β -肾上腺素能受体亚型。内皮切除、KCl (40 mM)预收缩、四乙基铵或N(omega)-硝基- l -精氨酸甲酯预处理均可抑制老年大鼠主动脉环对异丙肾上腺素的血管舒张反应。当TEA和L-NAME同时给药时,抑制是完全的。在两个年龄组中,对异丙肾上腺素的反应不受β -肾上腺素能拮抗剂CGP20712A的影响,但被ICI 118551 (β -肾上腺素能拮抗剂)和SR 59230A(非选择性β -肾上腺素能拮抗剂)显著抑制,这种抑制在老年大鼠中更为明显。与年轻大鼠不同,老年大鼠对异丙肾上腺素的反应部分依赖于内皮一氧化氮和K+通道。在两个年龄组中,β 2-和β 3-,但不涉及β 1-肾上腺素能受体。β 2和β 3肾上腺素能受体的相对参与程度可能随着年龄的变化而变化,并解释了对异丙肾上腺素反应的差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Age-related differences in the beta-adrenergic vasodilator response in rat aortic rings.

Mechanisms underlying age-dependent changes in vasodilator responses to beta-adrenergic drugs are poorly understood. The aim of the current study was to compare responses to isoproterenol (a non-selective beta-adrenergic receptor agonist) in phenylephrine or KCl precontracted aortic rings from 3 week and 3 month old male Wistar rats. Both the mechanism and the subtype of beta-adrenergic receptor underlying the response to isoproterenol in the both age groups were examined. Endothelial removal, pre-contraction with KCl (40 mM), pre-treatment with tetraethylammonium or with N(omega)-Nitro-L-arginine methyl ester inhibited the vasodilator response to isoproterenol only in aortic rings from older rats. The inhibition was total when TEA and L-NAME were administered together. In both age groups the response to isoproterenol was unaffected by the beta1-adrenergic antagonist CGP20712A, but was significantly inhibited by ICI 118551 (a beta2-adrenergic-antagonist) and to a greater extent by SR 59230A (a non-selective beta 3-adrenergic antagonist), the inhibition being more evident in the older rats. Unlike younger rats, in older animals the response to isoproterenol was partially dependent on endothelial nitric oxide and on K+ channels. In both age groups, beta2- and beta3-, but not beta1-adrenergic receptors were involved. The degree of relative participation of beta2 and beta3 adrenergic receptors may change with age and explain the differences in response to isoproterenol.

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