摘要
本文研究Ca2+对VitK3镇痛作用的影响.在小白鼠辐射热甩尾模型上Vitk3(64mg/kg,ip)’:有明显的镇痛作用(P<0.01),这种作用能被CaCI2(1.0X10-7mol,icv)拮抗(P<0.05),被Ca2+络合剂EGTA(5.26×10-7mol /kg, icv)和Ca2+通道阻滞剂维拉帕米25mg/kg,icv)增强(P值接近0.05)。结果提示,细胞内外Ca2+浓度影响VitK3的镇痛作用.
y means of the tail flick test in mice,the offect of Ca+ on analgesic action of vitamin Ks wasStudied. The results showed that each of vitamin K3(64mg/kg,iP).Ca2+ chelating agent EGTA(5. 26X 10-7vmol/kg, icv) and ca2+ channel blocker verapamil (0. 25mg/kg,icv) possessed analgesic action(P<0.01 respectively), that CaCl2 (1. 0 X 10-7mol/kg, icv) reduced the analgesic action of vitamin k3<p0.01), while both EGTA and verapamil did not enhanced the analgesic action of vitamin K3signifcantly. The results suggest that the intracellular and Ca2+ concentration can Producean effect on the analgesic action of vitamin K3.
出处
《苏州医学院学报》
1994年第1期8-9,共2页
Acta Academiae Medicinae Suzhou