Smith T K, Ward S M, Zhang L, Buxton I L, Gerthoffer W T, Sanders K M, Keef K D
Department of Physiology, University of Nevada, Reno 89557.
Am J Physiol. 1993 Apr;264(4 Pt 1):G708-17. doi: 10.1152/ajpgi.1993.264.4.G708.
The effects of beta-adrenergic receptor stimulation on the electrical and mechanical activity of canine colonic circular muscles were compared with forskolin (Fsk), a known stimulator of adenylate cyclase. The actions of isoproterenol (Iso) were mediated by beta 2-receptors. Iso and Fsk increased intracellular adenosine 3',5'-cyclic monophosphate (cAMP) levels in both the presence and absence of acetylcholine (ACh), whereas ACh (0.3 microM) alone reduced cAMP levels. These agents caused inhibition of spontaneous and ACh-induced contractions. Inhibition was associated with a reduction in the amplitude and duration of electrical slow waves recorded near the submucosal border. Near the myenteric border, Iso and Fsk hyperpolarized the membrane by up to 30 mV and changed the pattern of electrical rhythmicity. These effects were mimicked by 8-bromo-cAMP (1-3 mM). Contractile inhibition with Fsk and Iso was associated with a decrease in the amplitude and duration of Ca2+ transients measured with fura-2 fluorescence. cAMP (10-300 microM) reduced the Ca2+ sensitivity of the contractile apparatus in muscles permeabilized with staphylococcal alpha-toxin. The actions of Iso appear linked to cAMP. We hypothesize that cAMP produces relaxation both by modulation of membrane ionic channels with a consequent decline in the entry of Ca2+ as well as through a decrease in the sensitivity of the contractile apparatus to Ca2+.
将β-肾上腺素能受体刺激对犬结肠环行肌电活动和机械活动的影响与已知的腺苷酸环化酶刺激剂福斯可林(Fsk)进行了比较。异丙肾上腺素(Iso)的作用由β2受体介导。无论有无乙酰胆碱(ACh),Iso和Fsk均能提高细胞内3',5'-环磷酸腺苷(cAMP)水平,而单独使用ACh(0.3 microM)则会降低cAMP水平。这些药物可抑制自发性和ACh诱导的收缩。抑制作用与黏膜下边界附近记录的电慢波振幅和持续时间的降低有关。在肌间边界附近,Iso和Fsk使膜超极化高达30 mV,并改变电节律模式。这些效应可被8-溴-cAMP(1-3 mM)模拟。Fsk和Iso引起的收缩抑制与用fura-2荧光测量的Ca2+瞬变振幅和持续时间的降低有关。cAMP(10-300 microM)降低了用葡萄球菌α毒素通透的肌肉中收缩装置对Ca2+的敏感性。Iso的作用似乎与cAMP有关。我们推测,cAMP通过调节膜离子通道从而减少Ca2+内流以及降低收缩装置对Ca2+的敏感性来产生舒张作用。