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患有肾小球疾病的肾病大鼠中性蛋白酶的尿排泄情况。

Urinary excretion of neutral proteinases in nephrotic rats with a glomerular disease.

作者信息

Davin J C, Davies M, Foidart J M, Foidart J B, Dechenne C A, Mahieu P R

出版信息

Kidney Int. 1987 Jan;31(1):32-40. doi: 10.1038/ki.1987.5.

DOI:10.1038/ki.1987.5
PMID:3550215
Abstract

A proliferative glomerulonephritis was induced in rats pre-immunized with rabbit IgG by injecting intravenously a sub-nephrotoxic dose of rabbit anti-glomerular basement membrane (GBM) IgG (A rats). Most rats (80%) developed a severe proteinuria (greater than 100 mg/24 hr) within two to five days after the injection of anti-GBM IgG. At the same time, microscopic examination of the kidneys revealed a glomerular infiltration by mononuclear phagocytes and a prominent decrease in the intensity of the colloidal iron reaction in glomeruli. A non-proliferative glomerular disease was induced in another group of rats (B rats) by intraperitoneal administration of aminonucleoside of puromycin. A marked proteinuria (greater than 100 mg/24 hr) occurred after six days in 90% of animals. Histochemical studies then revealed a decrease in staining intensity of glomeruli for polyanion. No glomerular hypercellularity was noted. In normal rats and in non-proteinuric A or B rats, the 24 hour urinary excretion of neutral proteinases ranged from 1.4 to 7.8 units (mean value +/- SEM, 4.69 +/- 0.60, N = 11), that of laminin ranged from 100 to 3,900 ng (mean value +/- SEM, 1,154 +/- 325, N = 10), and that of type IV collagen ranged from 160 to 420 ng (mean value +/- SEM, 306 +/- 26.5 ng, N = 8). In proteinuric rats from groups A (N = 11) and B (N = 9), the 24 hour urinary excretion of neutral proteinases significantly increased (mean values +/- SEM, 38.55 +/- 8.66 U for A rats and 42.17 +/- 7.92 U for B rats) and ran parallely with that of proteins, laminin and type IV collagen.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过静脉注射亚肾毒性剂量的兔抗肾小球基底膜(GBM)IgG,在预先用兔IgG免疫的大鼠中诱发增殖性肾小球肾炎(A组大鼠)。大多数大鼠(80%)在注射抗GBM IgG后的两到五天内出现严重蛋白尿(超过100mg/24小时)。与此同时,肾脏的显微镜检查显示单核吞噬细胞浸润肾小球,并且肾小球中胶体铁反应强度显著降低。通过腹腔注射嘌呤霉素氨基核苷在另一组大鼠(B组大鼠)中诱发非增殖性肾小球疾病。90%的动物在六天后出现明显蛋白尿(超过100mg/24小时)。组织化学研究随后显示肾小球多阴离子染色强度降低。未观察到肾小球细胞增多。在正常大鼠以及无蛋白尿的A组或B组大鼠中,中性蛋白酶的24小时尿排泄量为1.4至7.8单位(平均值±标准误,4.69±0.60,N = 11),层粘连蛋白为100至3900ng(平均值±标准误,1154±325,N = 10),IV型胶原为160至420ng(平均值±标准误,306±26.5ng,N = 8)。在A组(N = 11)和B组(N = 9)的蛋白尿大鼠中,中性蛋白酶的24小时尿排泄量显著增加(A组大鼠平均值±标准误为38.55±8.66U,B组大鼠为42.17±7.92U),并且与蛋白质、层粘连蛋白和IV型胶原的排泄量平行。(摘要截断于250字)

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