Shin H Y, Lee E H, Shin T Y, Kim H M
College of Pharmacy, Wonkwang University, Iksan, South Korea.
Pharmacol Res. 1997 Aug;36(2):141-6. doi: 10.1006/phrs.1997.0218.
We investigated the effect of cytochalasin D on anaphylaxis. Cytochalasin D dose-dependently inhibited systemic anaphylaxis induced by compound 48/80 in rats. Especially, cytochalasin D inhibited compound 48/80-induced systemic anaphylaxis 100% with a dose of 1 microg g-1 body weight (BW). Cytochalasin D significantly inhibited serum histamine levels induced by compound 48/80. Cytochalasin D (10(-1) microg g-1 BW) also inhibited local anaphylaxis activated by anti-dinitrophenyl (DNP) IgE to 79.6+/-1.8%. Cytochalasin D dose-dependently inhibited histamine release from the rat peritoneal mast cells activated by compound 48/80 or anti-DNP IgE. The level of cAMP in rat peritoneal mast cells, when cytochalasin D was added, transiently and significantly increased about fourfold compared with that of basal cells. Our studies provide evidence that cytochalasin D will be beneficial in the treatment of anaphylaxis.
我们研究了细胞松弛素D对过敏反应的影响。细胞松弛素D对化合物48/80诱导的大鼠全身性过敏反应具有剂量依赖性抑制作用。特别是,细胞松弛素D以1微克/克体重(BW)的剂量可100%抑制化合物48/80诱导的全身性过敏反应。细胞松弛素D显著抑制化合物48/80诱导的血清组胺水平。细胞松弛素D(10⁻¹微克/克体重)也将抗二硝基苯基(DNP)IgE激活的局部过敏反应抑制至79.6±1.8%。细胞松弛素D对化合物48/80或抗DNP IgE激活的大鼠腹腔肥大细胞组胺释放具有剂量依赖性抑制作用。添加细胞松弛素D时,大鼠腹腔肥大细胞中的环磷酸腺苷(cAMP)水平与基础细胞相比瞬时且显著增加约四倍。我们的研究提供了证据表明细胞松弛素D在过敏反应治疗中将会有益。