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猫肺中对儿茶酚胺和组胺的血管快速耐受性的逆转

Reversal of vascular tachyphylaxis to catecholamines and histamine in the feline lung.

作者信息

Cutaia M, Friedrich P, Porcelli R J

机构信息

Veterans Administration Medical Center, Northport, New York 11768.

出版信息

Am Rev Respir Dis. 1988 Jun;137(6):1336-42. doi: 10.1164/ajrccm/137.6.1336.

Abstract

The pulmonary vascular responses to histamine, epinephrine, and norepinephrine demonstrate tachyphylaxis following repetitive exposure in the isolated blood-perfused cat lung. In the present study, we tested the hypothesis that this phenomenon was related to a change in the balance of antagonistic receptor activity. The protocol consisted of 5 consecutive dose-response maneuvers (DR I to V) to 1 amine in each animal separated by 1 h. Once the loss of the initial vasoconstrictor activity had occurred (DR I to IV), the animal was given a receptor blocking agent, either the beta blocker propranolol or the H2 blocker cimetidine, prior to a final dose-response maneuver (DR V). The dose-response relationships were analyzed in terms of 3 parameters: maximum response, slope, and ED50. All the experiments with norepinephrine (n = 6), epinephrine (n = 10), and histamine (n = 25) demonstrated a progressive loss of vasopressor activity as shown by reductions in the maximum response and slope between DR I to IV. In addition, histamine demonstrated a significant increase in ED50 from DR I to IV, which suggested a loss of sensitivity. The loss of vasoconstrictor activity to histamine and the catecholamines was restored by the administration of propranolol prior to DR V. In contrast, cimetidine did not restore the initial vasopressor activity of histamine. The loss of reactivity to histamine was not secondary to changes in circulating catecholamine levels, because the plasma catecholamine levels before DR I and immediately following DR V in a subset of animals (n = 5) were within the reported normal range for this species.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在离体血液灌注的猫肺中,重复暴露后,肺血管对组胺、肾上腺素和去甲肾上腺素的反应显示出快速耐受性。在本研究中,我们检验了这一现象与拮抗受体活性平衡变化有关的假说。实验方案包括对每只动物依次给予5次连续的剂量-反应操作(DR I至V),每次操作间隔1小时,每次针对1种胺类物质。一旦初始血管收缩活性丧失(DR I至IV),在进行最后一次剂量-反应操作(DR V)之前,给动物注射一种受体阻断剂,即β受体阻滞剂普萘洛尔或H2受体阻滞剂西咪替丁。从最大反应、斜率和半数有效剂量(ED50)这3个参数分析剂量-反应关系。所有用去甲肾上腺素(n = 6)、肾上腺素(n = 10)和组胺(n = 25)进行的实验均显示,血管升压活性逐渐丧失,表现为DR I至IV之间最大反应和斜率降低。此外,组胺从DR I至IV的ED50显著增加,这表明敏感性丧失。在DR V之前给予普萘洛尔可恢复对组胺和儿茶酚胺的血管收缩活性丧失。相反,西咪替丁未能恢复组胺最初的血管升压活性。对组胺反应性的丧失并非继发于循环儿茶酚胺水平的变化,因为一部分动物(n = 5)在DR I之前和DR V之后立即测定的血浆儿茶酚胺水平在该物种报道的正常范围内。(摘要截选至250字)

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