伊索弗拉恩减弱了老鼠微血管中cAMP介导的血管扩张
K W Park1, H B Dai, E Lowenstein
1Department of Anesthesia and Critical Care, Beth Israel Hospital, Harvard Medical School, Boston, MA 02215, USA.
Circulation
|November 1, 1995
概括
吸入麻醉剂异氨酸降低了β-上腺素和循环腺单酸盐 (cAMP) 介导的血管扩张. 血管放松的这种损害发生在腺酸环酶激活的下游.
科学领域:
- 心血管生理学心血管生理学
- 麻醉学 麻醉学
- 药理学 药理学是指药理学的学科.
背景情况:
- 吸入麻醉剂如异氨酸可以影响血管功能.
- 已知循环氨酸单酸盐 (cGMP) 介导的内皮依赖血管扩张被异氨酸减弱.
研究的目的:
- 为了研究异氨酸对β-上腺素和循环腺单酸盐 (cAMP) 介导的血管扩张的影响.
- 确定异黄素对cAMP依赖放松的抑制作用的特定部位.
主要方法:
- 使用来自Wistar老鼠的隔离压力冠状动脉.
- 血管预先收缩,并为各种血管扩展剂生成度-反应曲线,在有或没有2%的异.
- 这些药物包括异二醇,化,福斯科林,8-Br-cAMP和RO20-1724.
主要成果:
- 异氨酸显著减弱了对所有测试剂的放松反应.
- 贝塔上腺和cAMP介导的血管扩张被isoflurane减少.
- 尽管具有正常的固酶活性,但仍观察到抑制作用.
结论:
- 伊索弗劳兰会影响cAMP介导的血管扩张.
- 损伤的机制位于腺酸环酶激活的下游.
- 异氨酸不会增强cAMP化酶的活性,从而导致这种衰减.
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