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Long‐term change of glomerular gelatinolytic activity in rats with streptozotocin‐induced diabetes
Author(s) -
Fukudome Keiichi,
Fujimoto Shouichi,
Kinoshita Hiroshi,
Hara Seiichirou,
Hisanaga Shuichi,
Eto Tanenao
Publication year - 2001
Publication title -
nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.752
H-Index - 61
eISSN - 1440-1797
pISSN - 1320-5358
DOI - 10.1046/j.1440-1797.2001.00063.x
Subject(s) - medicine , endocrinology , diabetic nephropathy , glomerular basement membrane , mesangium , diabetes mellitus , zymography , streptozotocin , matrix metalloproteinase , glomerular mesangium , glomerulosclerosis , nephropathy , basement membrane , kidney , glomerulonephritis , proteinuria , pathology
SUMMARY: In diabetic nephropathy, a decrease in the activity of matrix metalloproteinase (MMP) might contribute to the build‐up of extracellular matrix protein in the mesangium and the glomerular basement membrane (GBM). Levels of MMP activity were measured as gelatinolytic activity in glomerular homogenates isolated from rats 1, 4, 12, 24 and 48 weeks after inducing diabetes mellitus (DM) with streptozotocin. The level of glomerular gelatinolytic activity after 1 week in DM rats was significantly increased compared with that in controls (224.8% of control; DM vs. control, 13.58 vs. 6.04 mU/glomerulus; P < 0.05), then decreased by 48 weeks (week 4, 92.8% of control; week 12, 81.9% of control; week 24, 31.8% of control; week 48, 47.3% of control). Glomerular metalloproteinase migrated on gelatin zymography at positions representing molecular weights of approximately 97, 80, 70 and 65 kDa. The intensity of these lytic bands was increased at 1 week but decreased at 24 and 48 weeks. Light microscopy revealed hypercellularity in the mesangial area at 1 week, followed by mild and marked mesangial expansion with GBM thickening at 12 and 48 weeks respectively. These data suggest that the persistent decrease in glomerular gelatinolytic activity during the chronic phase contributes to mesangial expansion and GBM thickening in DM rats. Moreover, the activity may play different roles at the time of onset and during the progression of diabetic nephropathy.