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作 者:马骥[1] hotmail.com 张汝忠[1] hotmail.com 杨海春[1] hotmail.com 顾勇[1] hotmail.com 周江华[1] hotmail.com 林善锬[1] hotmail.com
机构地区:[1]上海医科大学华山医院肾脏科,emailjima3200040
出 处:《中华肾脏病杂志》2000年第2期93-97,共5页Chinese Journal of Nephrology
基 金:国家自然科学基金!39470335
摘 要:目的 探讨T型钙通道在实验性糖尿病肾病中的作用。方法 采用单侧肾切除的糖尿病大鼠模型,分别每日灌胃给予T型钙通道阻滞剂米地尔(Mib),L型钙通道阻滞剂氨氯地平,血管紧张素转换酶抑制剂西拉普利及Mib与Cil合用(M+C),共4周,并使各药物处理组血压相近(每组n=6 ̄8)。结果 Mib Cil和M+C治疗组较末治疗的糖尿病(DM)组尿白蛋白量明显减少(MibL:7.69±1.87,Cil:5.Objective To investigate the role of T-type calcium channel in streptozotocin(STZ)induced early diabetic nephropathy. Methods Uninephrectomized, STh (65 mg/kg) -induced diabetic male SD rats were used. In order to reach the same reduction of blood pressure, 30 mg/kg mibefradil [Mib,T-type calcium channel blocker), 30 mg/kg amlodipine (Aml, L-type calcium channel blocker), 10 mg/kg cilazapril (Cil, angiotensin converting enzyme inhibitor), 25 mg/kg Mib and 8 mg/kg Cil(M + C) were delivered daily by gavage from the next day of the intreduction to diabetes and totally for 4 weeks,respectively (n = 6 ~ 8 for each group). Results Compared with the untreated uninephrectomized diabetic group (DM), Mib, Cil and M + C treated rats presented substantially less urinary albumin excretion [Mib:7. 69±1. 87, Cil: 5. 53±1. 45, M + C: 3. 87±10. 88 vs. DM: 17. 67±4. 90, (μg/24 h); P <0. 05,respectively], and lower creatinine clearance rate (Ccr) than DM rats. Pathohistological study revealed that,there were less glomerular matrix, larninin and type Ⅳ collagen in Cil and M + C groups compared with the DM. Meanwhile, the glomerular deposition of laminin and type Ⅳ collagen in Mib treated rats were also remarkably less than those of DM, but still significantly greater than the M + C poup. No apparent impact on albuminuria, glomerular matrix accumulation and collagen Ⅳ deposition in Aml treated diabetic kidney were detected. However, in Aml group it still showed significantly lowered proteinuria, Ccr and less laminin volume. M + C treaed rats had least renal changes in terms of glomerular matrix and type Ⅳ collagen deposition among the diabetic rats. Conclusion T-type calcium channel blockage can reduce albuminuria and renal extrecellular matrix accumulation in experimental diabetic rat, and additional benefit can be achieved by combination with ACE inhibitor, suggesting the different role of T-type calcium channel in pmgression of diabetic nephropathy from that of angiotensin and L-type calcium channel, the mechanism of
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