Bonev A D, Nelson M T
Department of Pharmacology, University of Vermont, Colchester 05446-2500.
Am J Physiol. 1993 Dec;265(6 Pt 1):C1723-8. doi: 10.1152/ajpcell.1993.265.6.C1723.
We explored the possibility that muscarinic receptor stimulation can inhibit ATP-sensitive K+ (KATP) channels in smooth muscle cells from guinea pig urinary bladder. Whole cell K+ currents were measured in smooth muscle cells isolated from the detrusor muscle of the guinea pig bladder. Stimulation of muscarinic receptors by carbachol (CCh; 10 microM) inhibited KATP currents by 60.7%. Guanosine 5'-O-(2-thiodiphosphate) in the pipette (internal) solution prevented the CCh-induced inhibition of KATP currents. Activators of protein kinase C (PKC), a diacylglycerol analogue, and phorbol 12-myristate 13-acetate inhibited KATP currents by 63.5 and 73.9%, respectively. Blockers of PKC (bisindolylmaleimide GF-109203X and calphostin C) greatly reduced CCh inhibition of KATP currents. We propose that muscarinic receptor stimulation inhibits KATP channels in smooth muscle cells from urinary bladder through activation of PKC.
我们探究了毒蕈碱受体刺激能否抑制豚鼠膀胱平滑肌细胞中ATP敏感性钾通道(KATP通道)的可能性。在从豚鼠膀胱逼尿肌分离出的平滑肌细胞中测量全细胞钾电流。用卡巴胆碱(CCh;10微摩尔)刺激毒蕈碱受体可使KATP电流抑制60.7%。移液管(内部)溶液中的5'-O-(2-硫代二磷酸)鸟苷可防止CCh诱导的KATP电流抑制。蛋白激酶C(PKC)的激活剂、二酰基甘油类似物和佛波醇12-肉豆蔻酸酯13-乙酸盐分别使KATP电流抑制63.5%和73.9%。PKC阻滞剂(双吲哚马来酰亚胺GF-109203X和钙磷蛋白C)大大降低了CCh对KATP电流的抑制作用。我们提出,毒蕈碱受体刺激通过激活PKC来抑制膀胱平滑肌细胞中的KATP通道。