节点文献
钾通道开放剂对抗原诱发大鼠肥大细胞释放组胺的抑制作用
INHIBITION OF ALLERGIC HISTAMINE RELEASE FROM RAT PERITONEAL MAST CELLS BY POTASSIUM CHANNEL OPENERS
【摘要】 本文报道钾通道开放剂米诺地尔(Min)、二氮嗪(Dia)和钙拮抗剂硝苯啶(Nif)对抗原诱发大鼠腹腔肥大细胞(PMC)释放组胺的影响。以卵清蛋白免疫大鼠并触发PMC释放组胺。给大鼠Min200mg/kg灌胃;用含有Dia的孵化液预处理;或用Nif125mg/kg灌胃后,触发剂诱发PMC的组胺释放率与对照组比较均有显著差异(P<0.01)。结果提示,肥大细胞可能存在钾通道,钾通道开放剂可能具有治疗过敏性疾病的前景。
【Abstract】 The effects of potassium channel openers minoxidil (Min), diazoxide (Dia) and calcium antagonist nefedipine (Nif) on allergic histamine release from rat peritoneal mast cells (PMC) were investigated. Male SD rats were sensitized with 50μg of ovalbumin and 10 mg of Al(OH)3 ip.Two weeks later, PMC suspensions were prepared and 10μg/ml ovalbumin added to the suspensions as antigen. The results showed that the percentage of histamine release in control was 42. 7 ±9. 0%. After treatment with Min (200 mg/kg ig), Dia (500μmmol/L in vitro )and Nif (125mg/kg ig ) the percentages of histamine release were 18. 1±9. 7%, 19. 5±3. 6% and 11. 7±4. 7% respectively. In comparison with the control the differences were statistically significant (P<0. 01 ). The results suggest that calcium channels and potassium channels may by involved in the allergic histamine release from rat PMC. Potassium channel openers may be a group of useful agents for the treatment of allergic diseases.
【Key words】 Minoxidil; Diazoxide; Mast cells; Potassium channels/drug eff; Histamine liberation /drug eff; Rats; Hypersensitivity/drug ther;
- 【文献出处】 浙江医科大学学报 , 编辑部邮箱 ,1997年02期
- 【分类号】R96
- 【被引频次】3
- 【下载频次】36