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冷却诱导的支气管收缩:离子泵和离子载体系统的作用。

Cooling-induced bronchoconstriction: the role of ion-pumps and ion-carrier systems.

作者信息

Mustafa S M, Pilcher C W, Williams K I

机构信息

Department of Pharmacology and Toxicology, Faculty of Medicine, Safat, Kuwait.

出版信息

Pharmacol Res. 1999 Feb;39(2):125-36. doi: 10.1006/phrs.1998.0412.

Abstract

The mechanism of cold-induced bronchoconstriction is poorly understood. Our previous results show that cooling-induced contractions (CIC) do not involve activation of cell surface receptor systems nor innervation nor Ca2+ uptake. However, the results show that CIC is mainly dependent on intracellular Ca2+ [32]. Isolated tracheal strips and bronchiolar segments were suspended in organ baths containing Krebs' solution for isometric tension recording. Tissue responses during stepwise cooling from 37 to 5 degrees C were examined. Cooling ovine tracheal strips and bronchiolar ring segments to 20 degrees C caused a rapid contraction which decreased slowly until it reached the basal level in approximately 30 min. There is a significant inhibition of 45Ca2+ efflux at 20 degrees C to those incubated at 37 degrees C. This prompted this study whose aim was to determine the role of ion-pump and ion-carrier systems on cooling mechanisms. Inhibition of the Na+/K+ pump with ouabain (10 micrometer) evoked contraction in tracheal and bronchiolar preparations. When cooling was superimposed on this contraction the cooling-induced contractions were reduced in the bronchiolar segments. In the tracheal strips, at temperatures down to 15 degrees C ouabain converted the contractions to a relaxation, but further cooling to 10 and 5 degrees C resulted in contractions that were similar to control at 5 degrees C. Staurosporine, a protein kinase inhibitor (1 micrometer) enhanced CIC in trachea and bronchiole. Vanadate, a Ca2+-ATPase pump inhibitor (1 mm) potentiated CIC in the two preparations. Trifluoperazine and W-7, calmodulin antagonists (10 and 100 micrometer) enhanced CIC in tracheal preparations but not in the bronchiolar segments. Thapsigargin and cyclopiazonic acid (CPA), inhibitors of sarcoplasmic reticulum (SR) Ca2+-ATPase pump (1 and 10 micrometer) potentiated CIC in tracheal but not in bronchiolar preparations. Amiloride, Na+/H+ and Na+/Ca2+ exchange system inhibitor (1 mm) abolished CIC in both trachea and bronchiole. These results show a strong relationship between cooling and the activity of ion transport systems and indicate that CIC is due to inhibition of calcium removal mechanisms as a result of inhibition of these ion-pump and ion carrier systems.

摘要

冷诱导支气管收缩的机制目前尚不清楚。我们之前的研究结果表明,冷却诱导的收缩(CIC)并不涉及细胞表面受体系统的激活、神经支配或钙离子摄取。然而,结果表明CIC主要依赖于细胞内钙离子[32]。将分离的气管条和细支气管段悬挂于含有 Krebs 溶液的器官浴槽中,用于等长张力记录。检测从37℃逐步冷却至5℃过程中的组织反应。将绵羊气管条和细支气管环段冷却至20℃会引起快速收缩,该收缩会缓慢下降,直到大约30分钟后达到基础水平。与在37℃孵育的情况相比,在20℃时45Ca2+外流受到显著抑制。这促使了本研究的开展,其目的是确定离子泵和离子载体系统在冷却机制中的作用。用哇巴因(10微摩尔)抑制Na+/K+泵会在气管和细支气管制剂中引起收缩。当在此收缩基础上叠加冷却时,细支气管段的冷却诱导收缩会减弱。在气管条中,温度降至15℃时,哇巴因使收缩转变为舒张,但进一步冷却至10℃和5℃时,会导致类似于5℃时对照的收缩。星形孢菌素,一种蛋白激酶抑制剂(1微摩尔)可增强气管和细支气管中的CIC。钒酸盐,一种Ca2+-ATP酶泵抑制剂(1毫摩尔)可增强两种制剂中的CIC。三氟拉嗪和W-7,钙调蛋白拮抗剂(10和100微摩尔)可增强气管制剂中的CIC,但在细支气管段中无此作用。毒胡萝卜素和环匹阿尼酸(CPA),肌浆网(SR)Ca2+-ATP酶泵抑制剂(1和10微摩尔)可增强气管制剂中的CIC,但在细支气管制剂中无此作用。氨氯地平,Na+/H+和Na+/Ca2+交换系统抑制剂(1毫摩尔)可消除气管和细支气管中的CIC。这些结果表明冷却与离子转运系统的活性之间存在密切关系,并表明CIC是由于这些离子泵和离子载体系统受到抑制,导致钙清除机制受到抑制所致。

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