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Glucagon- and insulin degradation by hemolysate of human erythrocytes.

作者信息

Hildebrandt W, Kohnert K D, Blech W

机构信息

Institute of Biochemistry, Martin-Luther University Halle-Wittenberg, GDR.

出版信息

Biomed Biochim Acta. 1987;46(7):557-63.

PMID:3322271
Abstract

Hemolysates of human erythrocytes contain a highly specific insulin- and glucagon-degrading activity which is comparable to the so-called insulin- and glucagon-degrading proteinase (IGP, EC 3.4.23.5) found in other tissues. Glucagon degradation is inhibited by its cleavage products. Insulin, proinsulin and also cleavage products of insulin are effective inhibitors of glucagon degradation. The isolated insulin A- and B-chains are also capable of inhibiting the splitting of glucagon, but a higher concentrations. On the other hand, glucagon influences insulin degradation. Naturally occurring substances within commercially available human serum albumin have remarkable inhibitory effects on the glucagon degradation.

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