Oturai P S, Rasch R, Hasselager E, Johansen P B, Yokoyama H, Thomsen M K, Myrup B, Kofoed-Enevoldsen A, Deckert T
Steno Diabetes Center, Gentofte, Denmark.
APMIS. 1996 Apr;104(4):259-64. doi: 10.1111/j.1699-0463.1996.tb00715.x.
The effects of heparin and aminoguanidine on glomerular basement membrane thickening were studied in streptozotocin diabetic Sprague-Dawley rats. A placebo-treated group and a non-diabetic group served as controls. All diabetic rats remained severely hyperglycaemic (23 mmol/l) throughout the 8-month study period. At the end of this time relative kidney weight was significantly increased in diabetic control rats (4.9 +/- 0.5 g/kg b.w.) compared with non-diabetic rats (3.3 +/- 0.3 g/kg). This increase was not affected by the intervention treatments. Glomerular basement membrane thickness increased 32% in diabetic control rats (240 +/- 24 nm) compared with non-diabetic rats (182 +/- 20 nm). This increase was prevented by s.c. treatment with both unfractionated and low molecular weight heparins, while basement membrane thickness was the same in animals treated with oral heparins and aminoguanidine and untreated diabetic rats. Macroscopic malignant kidney tumours were seen in three aminoguanidine-treated rats. In conclusion, subcutaneously administered heparin prevents diabetes-induced glomerular basement membrane thickening.
在链脲佐菌素诱导的糖尿病斯普拉格-道利大鼠中研究了肝素和氨基胍对肾小球基底膜增厚的影响。设立了安慰剂治疗组和非糖尿病组作为对照。在整个8个月的研究期间,所有糖尿病大鼠均保持严重高血糖状态(23 mmol/l)。在此时间段结束时,与非糖尿病大鼠(3.3±0.3 g/kg体重)相比,糖尿病对照大鼠的相对肾重量显著增加(4.9±0.5 g/kg体重)。这种增加不受干预治疗的影响。与非糖尿病大鼠(182±20 nm)相比,糖尿病对照大鼠的肾小球基底膜厚度增加了32%(240±24 nm)。普通肝素和低分子肝素皮下给药均可防止这种增加,而口服肝素和氨基胍治疗的动物与未治疗的糖尿病大鼠的基底膜厚度相同。在三只接受氨基胍治疗的大鼠中发现了肉眼可见的恶性肾肿瘤。总之,皮下注射肝素可预防糖尿病诱导的肾小球基底膜增厚。