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糖尿病大鼠血糖正常化可逆转肾小球高滤过和肾肥大。

Reversal of glomerular hyperfiltration and renal hypertrophy by blood glucose normalization in diabetic rats.

作者信息

Stackhouse S, Miller P L, Park S K, Meyer T W

机构信息

Department of Medicine, Stanford University, California.

出版信息

Diabetes. 1990 Aug;39(8):989-95. doi: 10.2337/diab.39.8.989.

Abstract

Two groups of rats with streptozocin-induced diabetes and one group of nondiabetic control rats were studied. Group 1 diabetic rats received daily insulin to maintain blood glucose levels at 300-400 mg/dl for 44 wk. Group 2 diabetic rats received the same insulin regimen for 37 wk and then received an increased dose of insulin to return blood glucose levels close to normal for 7 wk. Group 3 nondiabetic rats were age-matched controls. Glomerular filtration rate (GFR) and kidney weight were elevated in moderately hyperglycemic group 1 rats compared with group 3 rats. Normalization of blood glucose returned both GFR (group 1, 1.83 +/- 0.04 ml/min; group 2, 1.36 +/- 0.05 ml/min; group 3, 1.45 +/- 0.07 ml/min) and kidney weight (group 1, 2.55 +/- 0.06 g; group 2, 1.82 +/- 0.05 g; group 3, 1.72 +/- 0.06 g) to normal in group 2 rats. Despite a sustained increase in GFR, group 1 rats did not exhibit any increase in glomerular volume (group 1, 2.77 +/- 0.09 x 10(6) microns3; group 2, 2.69 +/- 0.09 x 10(6) microns3; group 3, 2.81 +/- 0.7 x 10(6) microns3). Group 1 rats did, however, exhibit a significant increase in glomerular mesangial volume (group 1, 0.31 +/- 0.02 x 10(6) microns3; group 2, 0.28 +/- 0.02 x 10(6) microns3; group 3, 0.21 +/- 0.01 x 10(6) microns3), which was not reversed by normalization of blood glucose in group 2. These findings show that normalization of blood glucose can reverse established glomerular hyperfiltration and renal hypertrophy in moderately hyperglycemic diabetic rats. They further indicate that mesangial expansion is associated with sustained moderate hyperglycemia in this disease model.

摘要

对两组链脲佐菌素诱导的糖尿病大鼠和一组非糖尿病对照大鼠进行了研究。第1组糖尿病大鼠每日接受胰岛素治疗,以将血糖水平维持在300 - 400mg/dl,持续44周。第2组糖尿病大鼠接受相同的胰岛素治疗方案37周,然后接受增加剂量的胰岛素以使血糖水平接近正常水平,持续7周。第3组非糖尿病大鼠为年龄匹配的对照组。与第3组大鼠相比,中度高血糖的第1组大鼠的肾小球滤过率(GFR)和肾脏重量升高。血糖正常化使第2组大鼠的GFR(第1组,1.83±0.04ml/min;第2组,1.36±0.05ml/min;第3组,1.45±0.07ml/min)和肾脏重量(第1组,2.55±0.06g;第2组,1.82±0.05g;第3组,1.72±0.06g)均恢复正常。尽管GFR持续升高,但第1组大鼠的肾小球体积没有任何增加(第1组,2.77±0.09×10(6)立方微米;第2组,2.69±0.09×10(6)立方微米;第3组,2.81±0.7×10(6)立方微米)。然而,第1组大鼠的肾小球系膜体积显著增加(第1组,0.31±0.02×10(6)立方微米;第2组,0.28±0.02×10(6)立方微米;第3组,0.21±0.01×10(6)立方微米),第2组血糖正常化并未使其逆转。这些发现表明,血糖正常化可逆转中度高血糖糖尿病大鼠已建立的肾小球高滤过和肾脏肥大。它们进一步表明,在该疾病模型中,系膜扩张与持续的中度高血糖有关。

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