Heymans Institute of Pharmacology, Ghent University, Ghent, 9000, Belgium.
Naunyn Schmiedebergs Arch Pharmacol. 2013 Aug;386(8):671-84. doi: 10.1007/s00210-013-0855-2. Epub 2013 Apr 3.
Our objective was to investigate the role of phosphodiesterase (PDE)3 and PDE4 and cGMP in the control of cAMP metabolism and of phosphorylation of troponin I (TnI) and phospholamban (PLB) when 5-HT4 receptors are activated in pig left atrium. Electrically paced porcine left atrial muscles, mounted in organ baths, received stimulators of particulate guanylyl cyclase (pGC) or soluble guanylyl cyclase (sGC) and/or specific PDE inhibitors followed by 5-HT or the 5-HT4 receptor agonist prucalopride. Muscles were freeze-clamped at different moments of exposure to measure phosphorylation of the cAMP/protein kinase A targets TnI and PLB by immunoblotting and cAMP levels by enzyme immunoassay. Corresponding with the functional results, 5-HT only transiently increased cAMP content, but caused a less quickly declining phosphorylation of PLB and did not significantly change TnI phosphorylation. Under combined PDE3 and PDE4 inhibition, the 5-HT-induced increase in cAMP levels and PLB phosphorylation was enhanced and sustained, and TnI phosphorylation was now also increased. Responses to prucalopride per se and the influence thereupon of PDE3 and PDE4 inhibition were similar except that responses were generally smaller. Stimulation of pGC together with PDE4 inhibition increased 5-HT-induced PLB phosphorylation compared to 5-HT alone, consistent with functional responses. sGC stimulation hastened the fade of inotropic responses to 5-HT, while cAMP levels were not altered. PDE3 and PDE4 control the cAMP response to 5-HT4 receptor activation, causing a dampening of downstream signalling. Stimulation of pGC is able to enhance inotropic responses to 5-HT by increasing cAMP levels, while sGC stimulation decreases contraction to 5-HT cAMP independently.
我们的目的是研究磷酸二酯酶 (PDE)3 和 PDE4 以及 cGMP 在控制 cAMP 代谢和肌钙蛋白 I (TnI) 和磷蛋白 (PLB) 磷酸化中的作用,当 5-HT4 受体在猪左心房被激活时。在器官浴中安装的电起搏猪左心房肌肉,接受颗粒鸟苷酸环化酶 (pGC) 或可溶性鸟苷酸环化酶 (sGC) 的刺激剂,以及/或特定的 PDE 抑制剂,然后接受 5-HT 或 5-HT4 受体激动剂普拉克索。肌肉在暴露于不同时间点时进行冷冻夹闭,以通过免疫印迹测量 cAMP/蛋白激酶 A 靶标 TnI 和 PLB 的磷酸化,并通过酶免疫测定测量 cAMP 水平。与功能结果相对应,5-HT 仅短暂增加 cAMP 含量,但导致 PLB 的磷酸化下降速度较慢,并且没有显著改变 TnI 磷酸化。在联合 PDE3 和 PDE4 抑制下,5-HT 诱导的 cAMP 水平和 PLB 磷酸化增加并持续,并且 TnI 磷酸化现在也增加。普拉克索本身的反应及其对 PDE3 和 PDE4 抑制的影响相似,只是反应通常较小。与单独使用 5-HT 相比,pGC 刺激加上 PDE4 抑制增加了 5-HT 诱导的 PLB 磷酸化,这与功能反应一致。sGC 刺激加速了对 5-HT 的变力反应消退,而 cAMP 水平没有改变。PDE3 和 PDE4 控制 5-HT4 受体激活引起的 cAMP 反应,导致下游信号转导减弱。pGC 刺激能够通过增加 cAMP 水平增强对 5-HT 的变力反应,而 sGC 刺激独立于 cAMP 降低对 5-HT 的收缩作用。