Büyükafşar Kansu, Levent Adnan
Department of Pharmacology, Medical Faculty, Mersin University Campus, Yenişehir, Mersin 33169,
Biochem Biophys Res Commun. 2003 Apr 11;303(3):777-81. doi: 10.1016/s0006-291x(03)00422-4.
In this study effects of Rho kinase inhibitors have been examined on the mouse gastric fundal smooth muscle reactivity and neurotransmitter (acetylcholine) release. Two Rho-kinase inhibitors, Y-27632 and fasudil (HA-1077), conspicuously suppressed the contractile responses to carbachol (CCh) and KCl as well as electrical field stimulation (EFS, 40 V, 0.5 ms, and 20 s). pEC(50) value for CCh and EC(50) value for KCl were 6.68+/-0.15 M and 10.4+/-2.8 mM, respectively. EFS induced reproducible contraction (38.3+/-4.75 mN/g tissue) which was almost abolished and potentiated in the presence of atropine (10(-6)M) and eserine (10(-6)M), respectively. The Rho-kinase inhibitors relaxed the fundic strips preconstricted by submaximal concentration of CCh or KCl in a concentration dependent manner. With CCh-elicited contraction, the pEC(50) values of Y-27632 and fasudil were 5.45+/-0.14 and 5.11+/-0.14 M, respectively (p>0.05). However, the pEC(50) values for Y-27632 and fasudil on KCl-induced tone were 6.09+/-0.1 and 5.35+/-0.06 M (p<0.001), respectively. Moreover, [3H]acetylcholine ([3H]ACh) release upon EFS from the gastric fundus was measured and it was found that Y-27632 (10(-4)M) significantly impaired the release. At 3 Hz the radioactivity ratio obtained after and before EFS (S(2)/S(1) ratio) was 0.88+/-0.03 in control but 0.63+/-0.08 in the presence of 10(-4)M Y-27632 (p<0.05). These results suggest that Rho kinase inhibitors can not only relax the gastric fundus but also modulate CCh, cholinergic nerve stimulation, and KCl-induced contraction. Furthermore, Rho/Rho kinase signalling may play a role in the neurotransmitter (ACh) release in the mouse gastric fundus.
在本研究中,已检测了Rho激酶抑制剂对小鼠胃底平滑肌反应性和神经递质(乙酰胆碱)释放的影响。两种Rho激酶抑制剂,Y-27632和法舒地尔(HA-1077),显著抑制了对卡巴胆碱(CCh)、氯化钾(KCl)以及电场刺激(EFS,40V,0.5ms,20s)的收缩反应。CCh的pEC(50)值和KCl的EC(50)值分别为6.68±0.15M和10.4±2.8mM。EFS诱导出可重复的收缩(38.3±4.75mN/g组织),在阿托品(10⁻⁶M)和毒扁豆碱(10⁻⁶M)存在时,该收缩反应分别几乎被消除和增强。Rho激酶抑制剂以浓度依赖性方式松弛由亚最大浓度的CCh或KCl预收缩的胃底条带。对于CCh诱导的收缩,Y-27632和法舒地尔的pEC(50)值分别为5.45±0.14和5.11±0.14M(p>0.05)。然而,Y-27632和法舒地尔对KCl诱导张力的pEC(50)值分别为6.09±0.1和5.35±0.06M(p<0.001)。此外,还测量了胃底在EFS作用下[³H]乙酰胆碱([³H]ACh)的释放,发现Y-27632(10⁻⁴M)显著损害了释放。在3Hz时,EFS前后获得的放射性比值(S₂/S₁比值)在对照中为0.88±0.03,但在存在10⁻⁴M Y-27632时为0.63±0.08(p<0.05)。这些结果表明,Rho激酶抑制剂不仅可以松弛胃底,还可以调节CCh、胆碱能神经刺激以及KCl诱导的收缩。此外,Rho/Rho激酶信号传导可能在小鼠胃底神经递质(ACh)释放中起作用。