Ottesen B
Acta Physiol Scand. 1981 Oct;113(2):193-9. doi: 10.1111/j.1748-1716.1981.tb06882.x.
The effect of vasoactive intestinal polypeptide (VIP) on uterine smooth muscle electrical and mechanical activity in non-pregnant estradiol-treated rabbits was investigated using in vivo and in vitro methods. The studies were performed on spontaneous, oxytocin-, carbachol-, and prostaglandin-42 alpha-induced activity. VIP had a dose-related inhibitory effect on both myoelectrical and mechanical activity. The concentration needed for 50% inhibition (ID50) was 2 x 10(-10) mol VIP . 1(-1) (in vivo), an 6 x 10(-8) mol VIP . 1(-1) (in vitro). This inhibition was unaffected by the presence of atropine (10(-5) mol . 1(-1)), propranolol (10(-5)), phentolamine (10(-5)), naloxone (10(-5)), apamin (10(-5)), and tetrodotoxin (10(-5)). These findings indicate that VIP may act via a specific receptor on the smooth muscle and supports the hypothesis that VIP may be a neurotransmitter involved in the local nervous control of uterine smooth muscle activity.
采用体内和体外方法,研究了血管活性肠肽(VIP)对未孕雌二醇处理家兔子宫平滑肌电活动和机械活动的影响。研究针对自发活动、催产素、卡巴胆碱和前列腺素 - 42α诱导的活动进行。VIP对肌电活动和机械活动均有剂量相关的抑制作用。50%抑制所需浓度(ID50)在体内为2×10(-10)mol VIP·1(-1),在体外为6×10(-8)mol VIP·1(-1)。这种抑制不受阿托品(10(-5)mol·1(-1))、普萘洛尔(10(-5))、酚妥拉明(10(-5))、纳洛酮(10(-5))、蜂毒明肽(10(-5))和河豚毒素(10(-5))的影响。这些发现表明,VIP可能通过平滑肌上的特定受体起作用,并支持VIP可能是参与子宫平滑肌活动局部神经控制的神经递质这一假说。