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猫肺血管床中对乙酰胆碱的张力依赖性反应。

Tone-dependent responses to acetylcholine in the feline pulmonary vascular bed.

作者信息

Hyman A L, Kadowitz P J

机构信息

Department of Surgery, School of Medicine, Tulane University, New Orleans, Louisiana 70112.

出版信息

J Appl Physiol (1985). 1988 May;64(5):2002-9. doi: 10.1152/jappl.1988.64.5.2002.

Abstract

The effects of an increase in base-line tone on pulmonary vascular responses to acetylcholine were investigated in the pulmonary vascular bed of the intact-chest cat. Under conditions of controlled blood flow and constant left atrial pressure, intralobar injections of acetylcholine under low-tone base-line conditions increased lobar arterial pressure in a dose-related manner. When tone was increased moderately by alveolar hypoxia, acetylcholine elicited dose-dependent decreases in lobar arterial pressure, and at the highest dose studied, acetylcholine produced a biphasic response. When tone was raised to a high steady level with the prostaglandin analogue, U46619, acetylcholine elicited marked dose-related decreases in lobar arterial pressure. Atropine blocked both vasoconstrictor responses at low tone and vasodilator responses at high tone, whereas meclofenamate and BW 755C had no effect on responses to acetylcholine at low or high tone. The vasoconstrictor response at low tone was blocked by pirenzepine (20 and 50 micrograms/kg iv) but not gallamine (10 mg/kg iv). The vasodilator response at high tone was not blocked by pirenzepine (50 micrograms/kg iv) or gallamine or pancuronium (10 mg/kg iv). The present data support the concept that pulmonary vascular responses to acetylcholine are tone dependent and suggest that the vasoconstrictor response under low-tone conditions is mediated by a high-affinity muscarinic (M1)-type receptor. These data also suggest that vasodilator responses under high-tone conditions are mediated by muscarinic receptors that are neither M1 nor M2 low-affinity muscarinic-type receptor and that responses to acetylcholine are not dependent on the release of cyclooxygenase or lipoxygenase products.

摘要

在完整胸腔猫的肺血管床中,研究了基线张力增加对肺血管对乙酰胆碱反应的影响。在控制血流和恒定左心房压力的条件下,在低张力基线条件下叶内注射乙酰胆碱,叶动脉压呈剂量依赖性升高。当通过肺泡低氧适度增加张力时,乙酰胆碱引起叶动脉压剂量依赖性降低,并且在研究的最高剂量下,乙酰胆碱产生双相反应。当用前列腺素类似物U46619将张力提高到高稳定水平时,乙酰胆碱引起叶动脉压明显的剂量依赖性降低。阿托品阻断低张力时的血管收缩反应和高张力时的血管舒张反应,而甲氯芬那酸和BW 755C对低张力或高张力时对乙酰胆碱的反应无影响。低张力时的血管收缩反应被哌仑西平(静脉注射20和50微克/千克)阻断,但未被加拉明(静脉注射10毫克/千克)阻断。高张力时的血管舒张反应未被哌仑西平(静脉注射50微克/千克)、加拉明或泮库溴铵(静脉注射10毫克/千克)阻断。目前的数据支持肺血管对乙酰胆碱的反应依赖于张力的概念,并表明低张力条件下的血管收缩反应由高亲和力毒蕈碱(M1)型受体介导。这些数据还表明,高张力条件下的血管舒张反应由既不是M1也不是M2低亲和力毒蕈碱型受体的毒蕈碱受体介导,并且对乙酰胆碱的反应不依赖于环氧化酶或脂氧化酶产物的释放。

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