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咖啡因引起大鼠主动脉平滑肌收缩和舒张的机制。

Mechanisms of caffeine-induced contraction and relaxation of rat aortic smooth muscle.

作者信息

Watanabe C, Yamamoto H, Hirano K, Kobayashi S, Kanaide H

机构信息

Division of Molecular Cardiology, Research Institute of Angiocardiology, Kyushu University, Fukuoka, Japan.

出版信息

J Physiol. 1992 Oct;456:193-213. doi: 10.1113/jphysiol.1992.sp019333.

Abstract
  1. Using front-surface fluorimetry and Fura-2, we determined the effects of caffeine on cytosolic calcium concentration ([Ca2+]i) and on tension of strips of the rat thoracic aorta. We also determined the effects of caffeine on 45Ca2+ influx into the strips. The objective was to elucidate the mechanism of contraction and relaxation in vascular smooth muscle, as induced by caffeine. 2. In normal physiological salt solution (PSS), caffeine induced a transient tension development, while it induced a biphasic change in [Ca2+]i. The initial transient peak in [Ca2+]i which coincided with tension development was followed by a sustained increase. Thus, changes in tension did not follow changes in [Ca2+]i. In Ca(2+)-free PSS, both the caffeine-induced contraction and the increase in [Ca2+]i were transient. It was suggested that in both the presence and absence of extracellular Ca2+, the transient increase in [Ca2+]i was due to the release of Ca2+ from the intracellular store. Although the sustained increase in [Ca2+]i depended on extracellular Ca2+, it was not affected by diltiazem, a Ca2+ antagonist. 3. Caffeine inhibited the increase in [Ca2+]i and tension development during 118 mM-K+ depolarization, in a concentration-dependent manner. The extent of reduction in tension (relaxation) was greater than that expected from the reduction in [Ca2+]i based on the [Ca2+]i-tension relationship observed with K+ depolarization. Pretreatment of the strips with ryanodine did not alter the inhibitory effects of caffeine. 4. Caffeine inhibited the increased [Ca2+]i and developed tension during stimulation by 10(-5) M-noradrenaline, in a concentration-dependent manner. 5. Dibutyryl cAMP (10(-4) M) inhibited both high K(+)-induced and noradrenaline-induced tension development. Inhibition of an increase in [Ca2+]i in relation to the inhibition of tension during noradrenaline stimulation was much greater than that in 118 mM-K+ depolarization. 6. Although caffeine per se had no effect on 45Ca2+ influx in the strips in normal PSS, caffeine did inhibit the increase in 45Ca2+ influx stimulated by 118 mM-K+ or by 10(-5) M-noradrenaline, to a similar extent and with similar IC50 values. 7. The characteristic features of the effects of caffeine on vascular smooth muscle, i.e. the transient nature of contraction and the relaxation of precontracted strips could be explained as follows: caffeine is able to reduce [Ca2+]i after releasing Ca2+ from intracellular stores; however, this may play a minor role. Independent of the [Ca2+]i reduction, the second messenger, cAMP, might directly influence the [Ca2+]i-tension relationship, and if so, would play a major role.
摘要
  1. 我们使用表面荧光法和Fura-2,测定了咖啡因对大鼠胸主动脉条带胞质钙浓度([Ca2+]i)和张力的影响。我们还测定了咖啡因对45Ca2+流入条带的影响。目的是阐明咖啡因诱导的血管平滑肌收缩和舒张机制。2. 在正常生理盐溶液(PSS)中,咖啡因诱导短暂的张力发展,同时它诱导[Ca2+]i出现双相变化。与张力发展同时出现的[Ca2+]i初始短暂峰值之后是持续升高。因此,张力变化并不跟随[Ca2+]i变化。在无钙PSS中,咖啡因诱导的收缩和[Ca2+]i升高都是短暂的。提示在细胞外钙存在和不存在的情况下,[Ca2+]i的短暂升高都是由于细胞内钙库释放钙所致。虽然[Ca2+]i的持续升高依赖于细胞外钙,但它不受钙拮抗剂地尔硫䓬的影响。3. 咖啡因以浓度依赖的方式抑制118 mM-K+去极化期间[Ca2+]i的升高和张力发展。张力降低(舒张)的程度大于根据K+去极化时观察到的[Ca2+]i-张力关系由[Ca2+]i降低所预期的程度。用ryanodine预处理条带并没有改变咖啡因的抑制作用。4. 咖啡因以浓度依赖的方式抑制10(-5) M去甲肾上腺素刺激期间[Ca2+]i的升高和张力发展。5. 二丁酰cAMP(10(-4) M)抑制高钾诱导的和去甲肾上腺素诱导的张力发展。去甲肾上腺素刺激期间,与张力抑制相关的[Ca2+]i升高的抑制作用比118 mM-K+去极化时大得多。6. 虽然咖啡因本身对正常PSS中条带的45Ca2+流入没有影响,但咖啡因确实抑制118 mM-K+或10(-5) M去甲肾上腺素刺激引起的45Ca2+流入增加,程度相似且IC50值相似。7. 咖啡因对血管平滑肌作用的特征,即收缩的短暂性和预收缩条带的舒张,可以如下解释:咖啡因能够在从细胞内钙库释放钙后降低[Ca2+]i;然而,这可能起次要作用。与[Ca2+]i降低无关,第二信使cAMP可能直接影响[Ca2+]i-张力关系,如果是这样,将起主要作用。

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