Ogata M, Iizuka Y, Murata R, Hikichi N
Department of Pharmaceutics, Tohoku College of Pharmacy, Sendai, Japan.
Biol Pharm Bull. 1996 Dec;19(12):1586-90. doi: 10.1248/bpb.19.1586.
We studied the effect of diabetes on the pharmacokinetics of cyclosporin A (CyA) after intravenous and oral administration of CyA using the plasma and lymph of streptozotocin (STZ)-induced diabetic rat. There were no significant differences in the systemic and lymphatic availabilities after intravenous administration of CyA in diabetic rats compared with those of the controls. On the other hand, systemic and lymphatic availabilities after oral administration of CyA were significantly different in diabetic rats compared to those in the controls. These results suggest that the pharmacokinetics of CyA, particularly absorption, were altered in diabetic rats. Gastrointestinal transit in diabetic rats was also studied. The gastric emptying rate in diabetic rats was enhanced compared with that of the controls, but small intestinal transit was reduced in diabetic rats, suggesting that a change in gastrointestinal transit in diabetic rats may influence the absorption of CyA. The increased absorption of CyA from the digestive tract of diabetic rats altered not only the systemic availability but also the lymphatic availability, suggesting that altered systemic availability may cause adverse effects and that altered lymphatic availability may influence the immunosuppressive effects.
我们使用链脲佐菌素(STZ)诱导的糖尿病大鼠的血浆和淋巴,研究了糖尿病对静脉注射和口服环孢素A(CyA)后其药代动力学的影响。与对照组相比,糖尿病大鼠静脉注射CyA后的全身和淋巴利用率没有显著差异。另一方面,糖尿病大鼠口服CyA后的全身和淋巴利用率与对照组相比有显著差异。这些结果表明,糖尿病大鼠中CyA的药代动力学,尤其是吸收,发生了改变。我们还研究了糖尿病大鼠的胃肠转运情况。与对照组相比,糖尿病大鼠的胃排空率提高,但小肠转运减少,这表明糖尿病大鼠胃肠转运的变化可能会影响CyA的吸收。糖尿病大鼠消化道中CyA吸收的增加不仅改变了全身利用率,也改变了淋巴利用率,这表明全身利用率的改变可能会导致不良反应,而淋巴利用率的改变可能会影响免疫抑制作用。