Nuttle L C, Farley J M
Department of Pharmacology and Toxicology, University of Mississippi Medical Center, Jackson, USA.
J Pharmacol Exp Ther. 1996 May;277(2):753-60.
The effects of adenosine 3':5'-cyclic monophosphate (cAMP) on acetylcholine (ACh)-induced oscillations in intracellular calcium concentration ([Ca++]i) and Ca(++)-activated Cl- current (ClCa current) were determined in isolated tracheal smooth muscle cells. Whole-cell current was measured in individual smooth muscle cells with patch clamp methodology. At a holding potential of -80 mV, ACh (0.1 microM) elicits base line-separated oscillations in ClCa current which correlate with oscillations in [Ca++]i. The addition of the beta adrenoceptor agonist isoproterenol (ISO) (10 nM to 1 microM) in the continued presence of ACh caused a concentration-dependent decrease in the frequency of the oscillations in ClCa current with significant reductions in oscillation frequency of 21.4 and 81.5% in the presence of 0.01 and 0.1 microM ISO, respectively (P < .05). This effect was mimicked by both forskolin (FSK) (3 microM) and 3-isobutyl-1-methylxanthine (IBMX) (30 microM). ISO and forskolin also inhibited ACh-induced oscillations in [Ca++]i measured by confocal fluorescence microscopy in non-voltage-clamped cells loaded with the Ca(++)-sensitive dye, fluo3. The inhibition of ACh-induced oscillations in ClCa current by ISO was partially reversed by increasing extracellular Ca++. These data are consistent with previous observations that the frequency of ACh-induced oscillations in [Ca++]i and ClCa current is dependent on the concentration of extracellular Ca++ and the influx of Ca++ through a verapamil-sensitive pathway. Moreover, these results lend support to the hypothesis that beta adrenoceptors inhibit the ACh-induced increase in [Ca++]i through a cAMP-dependent mechanism that inhibits Ca++ influx and in independent of changes in membrane potential.
在分离的气管平滑肌细胞中,测定了3':5'-环磷酸腺苷(cAMP)对乙酰胆碱(ACh)诱导的细胞内钙浓度([Ca++]i)振荡和钙激活氯电流(ClCa电流)的影响。采用膜片钳技术在单个平滑肌细胞中测量全细胞电流。在-80 mV的钳制电位下,ACh(0.1 μM)引发ClCa电流中与[Ca++]i振荡相关的基线分离振荡。在持续存在ACh的情况下添加β肾上腺素能受体激动剂异丙肾上腺素(ISO)(10 nM至1 μM)导致ClCa电流振荡频率呈浓度依赖性降低,在存在0.01和0.1 μM ISO时,振荡频率分别显著降低21.4%和81.5%(P <.05)。这种效应被毛喉素(FSK)(3 μM)和3-异丁基-1-甲基黄嘌呤(IBMX)(30 μM)模拟。ISO和毛喉素还抑制了在加载钙敏感染料fluo3的非电压钳制细胞中通过共聚焦荧光显微镜测量的ACh诱导的[Ca++]i振荡。增加细胞外Ca++可部分逆转ISO对ACh诱导的ClCa电流振荡的抑制作用。这些数据与先前的观察结果一致,即ACh诱导的[Ca++]i和ClCa电流振荡频率取决于细胞外Ca++浓度以及通过维拉帕米敏感途径的Ca++内流。此外,这些结果支持了以下假设:β肾上腺素能受体通过抑制Ca++内流的cAMP依赖性机制抑制ACh诱导的[Ca++]i增加,且与膜电位变化无关。