Butakov S S, Ignatov Iu D
Eksp Klin Farmakol. 1996 Mar-Apr;59(2):9-11.
Analgesic effect of calcitonin administered in doses of 1, 3, and 5 U/100 g was studied in rats. Intrathecal administration of calcitonin (0.015 U) results in higher increase in analgesic effect compared to intraventricular injection. Intramuscular (1, 3, and 5 U/100 g) and intraventricular (0.1 U) injection of parathormone exert no analgesic effect, whereas intrathecal injection in a dose of 0.1 U resulted in statistically significant analgesia. High correlation was found for nociception and calcium level in blood. Nifedipine and isoptin (1, 5, and 10 mg/kg) were shown to reduce significantly the analgesic effect of calcitonin. On the membrane of the isolated neuron of mollusk calcitonin (10(-9) - 10(-7) M) increased and in a concentration of 10(-6) M decreased JCa. Inhibiting effect of isoptin on JCa was found for combined action of calcitonin and isoptin on the neuron membrane.
研究了以1、3和5 U/100 g剂量给予大鼠降钙素的镇痛效果。与脑室内注射相比,鞘内注射降钙素(0.015 U)导致镇痛效果有更高的提升。肌肉注射(1、3和5 U/100 g)和脑室内注射(0.1 U)甲状旁腺激素没有镇痛作用,而0.1 U剂量的鞘内注射产生了统计学上显著的镇痛效果。发现伤害感受与血液中钙水平高度相关。硝苯地平和异搏定(1、5和10 mg/kg)显示可显著降低降钙素的镇痛效果。在软体动物的分离神经元膜上,降钙素(10(-9)-10(-7) M)使JCa增加,而在10(-6) M浓度时使JCa降低。发现异搏定对JCa有抑制作用,这是降钙素和异搏定对神经元膜联合作用的结果。