Saida K, Van Breemen C
J Gen Physiol. 1984 Aug;84(2):307-18. doi: 10.1085/jgp.84.2.307.
We examined the effects of cyclic AMP (cAMP) on the intracellular Ca2+ release in both the intact and skinned arterial smooth muscle. The amount of Ca2+ in the sarcoplasmic reticulum (SR) was estimated indirectly by caffeine-induced contraction of the skinned preparation and directly by caffeine-stimulated 45Ca efflux from the previously labeled skinned preparation. The norepinephrine-induced release contraction was markedly enhanced by dibutyryl cAMP (dbcAMP) and reduced by propranolol. The stimulatory effect of dbcAMP was best observed when the muscle was exposed to 10(-5) M dbcAMP and 2 X 10(-6) M norepinephrine was used to induce the release contraction. 10(-5) M cAMP had no effect on the Ca2+-induced contraction or on the pCa-tension relationship in the skinned preparation. This concentration of cAMP increased Ca2+ uptake into the SR of the skinned preparation when the Ca2+ in the SR was first depleted. 10(-5) M cAMP stimulated Ca2+-induced Ca2+ release from the SR after optimal Ca2+ accumulation by the SR. The results indicate that the stimulatory effect of cAMP on the norepinephrine-induced release contraction could be due to enhancement of the Ca2+-induced Ca2+ release from the SR in arterial smooth muscle.
我们研究了环磷酸腺苷(cAMP)对完整和去皮动脉平滑肌细胞内Ca2+释放的影响。通过咖啡因诱导去皮制剂收缩间接估计肌浆网(SR)中的Ca2+量,并通过咖啡因刺激先前标记的去皮制剂中45Ca流出直接估计。去甲肾上腺素诱导的释放收缩被二丁酰cAMP(dbcAMP)显著增强,并被普萘洛尔减弱。当肌肉暴露于10(-5)M dbcAMP且使用2×10(-6)M去甲肾上腺素诱导释放收缩时,观察到dbcAMP的刺激作用最佳。10(-5)M cAMP对去皮制剂中Ca2+诱导的收缩或pCa-张力关系没有影响。当SR中的Ca2+首先耗尽时,该浓度的cAMP增加了去皮制剂中Ca2+摄取到SR中。在SR最佳积累Ca2+后,10(-5)M cAMP刺激了SR中Ca2+诱导的Ca2+释放。结果表明,cAMP对去甲肾上腺素诱导的释放收缩的刺激作用可能是由于增强了动脉平滑肌中SR的Ca2+诱导的Ca2+释放。