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肾小球基底膜非酶糖基化的酶促可逆性。糖尿病肾小球病主要是可逆的吗?

Enzymatic reversibility of nonenzymatic glycosylation of the glomerular basement membrane. Is the diabetic glomerulopathy principally reversible?

作者信息

Lubec G, Vycudilik W, Coradello H, Pollak A

出版信息

Nephron. 1983;33(1):26-8. doi: 10.1159/000182899.

Abstract

Recent investigations point to the nonenzymatic glycosylation as a cause of long-term complications in diabetes mellitus. We describe an enzymatic activity that cleaves glucose from the glomerular basement membrane (GBM), present in lysosomal preparations of diabetic lymphocytes. The GBM, nonenzymatically glycosylated or obtained from rats with diabetes, were incubated with enzyme preparations, separated on Sephadex G-25 and applied for glucose measurement on gas chromatography and mass spectroscopy. The lysosomal preparation of diabetic lymphocytes cleaved from rat GBM, which were nonenzymatically glycosylated 300-500 ng glucose/mg GBM protein, from diabetic rat GBM 300 ng glucose/mg GBM protein. A lysosomal preparation of normal lymphocytes failed to do so, indicating enzyme induction in the diabetic state. Control studies with the glycosylated hemoglobin AIc confirmed this finding and showed the specificity of the enzyme, as alpha-glucosidase and beta-glucosidase failed to cleave the N-glycosidic bond between glucose and the protein. The enzymatic activity can be described formally as a N-l-deoxyfructofuranosyl-glucohydrolase, which could be responsible for a potential reversibility of diabetic GBM changes.

摘要

近期研究指出非酶糖基化是糖尿病长期并发症的一个原因。我们描述了一种能从肾小球基底膜(GBM)上裂解葡萄糖的酶活性,这种活性存在于糖尿病淋巴细胞的溶酶体制剂中。将非酶糖基化的或取自糖尿病大鼠的GBM与酶制剂一起孵育,在葡聚糖G - 25上进行分离,然后应用气相色谱和质谱法测量葡萄糖。糖尿病淋巴细胞的溶酶体制剂能从大鼠GBM上裂解葡萄糖,非酶糖基化的大鼠GBM每毫克GBM蛋白可裂解300 - 500纳克葡萄糖,糖尿病大鼠GBM每毫克GBM蛋白可裂解300纳克葡萄糖。正常淋巴细胞的溶酶体制剂则不能,这表明在糖尿病状态下存在酶的诱导。用糖化血红蛋白AIc进行的对照研究证实了这一发现,并显示了该酶的特异性,因为α - 葡萄糖苷酶和β - 葡萄糖苷酶无法裂解葡萄糖与蛋白质之间的N - 糖苷键。这种酶活性可被正式描述为一种N - l - 脱氧呋喃果糖基 - 葡糖水解酶,它可能与糖尿病GBM变化的潜在可逆性有关。

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