Department of Physiology, Chungbuk National University College of Medicine, Cheongju 361-763, Korea.
Korean J Physiol Pharmacol. 2008 Apr;12(2):59-64. doi: 10.4196/kjpp.2008.12.2.59. Epub 2008 Apr 30.
In our previous study, we found that spermine and putrescine inhibited spontaneous and acetylcholine (ACh)-induced contractions of guinea-pig stomach via inhibition of L-type voltage-dependent calcium current (VDCC(L)). In this study, we also studied the effect of spermidine on mechanical contractions and calcium channel current (I(Ba)), and then compared its effects to those by spermine and putrescine. Spermidine inhibited spontaneous contraction of the gastric smooth muscle in a concentration-dependent manner (IC(50)=1.1+/-0.11 mM). Relationship between inhibition of contraction and calcium current by spermidine was studied using 50 mM high K(+)-induced contraction: Spermidine (5 mM) significantly reduced high K(+) (50 mM)-induced contraction to 37+/-4.7% of the control (p<0.05), and inhibitory effect of spermidine on I(Ba) was also observed at a wide range of test potential in current/voltage (I/V) relationship. Pre- and post-application of spermidine (5 mM) also significantly inhibited carbachol (CCh) and ACh-induced initial and phasic contractions. Finally, caffeine (10 mM)-induced contraction which is activated by Ca(2+)-induced Ca(2+) release (CICR),' was also inhibited by pretreatment of spermidine (5 mM). These findings suggest that spermidine inhibits spontaneous and CCh-induced contraction via inhibition of VDCC(L) and Ca(2+) releasing mechanism in guinea-pig stomach.
在我们之前的研究中,我们发现精胺和腐胺通过抑制 L 型电压依赖性钙电流 (VDCC(L)) 抑制了豚鼠胃的自发性和乙酰胆碱 (ACh) 诱导的收缩。在本研究中,我们还研究了精脒对机械收缩和钙通道电流 (I(Ba)) 的影响,然后将其与精胺和腐胺的作用进行了比较。精脒呈浓度依赖性抑制胃平滑肌的自发性收缩(IC(50)=1.1+/-0.11 mM)。使用 50 mM 高 K(+) 诱导的收缩研究了精脒对收缩和钙电流的抑制作用关系:精脒(5 mM)显著降低高 K(+)(50 mM)诱导的收缩至对照的 37+/-4.7%(p<0.05),并且在电流/电压 (I/V) 关系中的广泛测试电位下也观察到了精脒对 I(Ba) 的抑制作用。精脒(5 mM)的预应用和后应用也显著抑制了 carbachol (CCh) 和 ACh 诱导的初始和相性收缩。最后,咖啡因 (10 mM) 诱导的收缩是通过 Ca(2+) 诱导的 Ca(2+) 释放 (CICR) 激活的,用精脒(5 mM)预处理也抑制了这种收缩。这些发现表明,精脒通过抑制豚鼠胃中的 VDCC(L) 和 Ca(2+) 释放机制抑制自发性和 CCh 诱导的收缩。