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Title: Antagonistic effects of a covalently dimerized insulin derivative on insulin receptors in 3T3-L1 adipocytes

Journal Article · · Proceedings of the National Academy of Sciences of the United States of America; (USA)
;  [1]; ;  [2]
  1. Institut fuer Pharmakologie and Toxikologie der Universitaet Goettingen (Germany, F.R.)
  2. Deutsches Wollforschungsinstitut, Aachen (Germany, F.R.)

In the present study the authors describe the antagonistic effects of the covalently dimerized insulin derivative B29,B29{prime}-suberoyl-insulin on insulin receptors in 3T3-L1 mouse cells. In differentiated 3T3-L1 adipocytes, the derivative fully inhibits binding of {sup 125}I-labeled insulin to its receptor with about the same affinity as unlabeled insulin. In contrast, the dimerized derivative only partially (approximately 20%) mimics insulin's effects on glucose transport and DNA synthesis in the absence of insulin. In the presence of insulin, the agent competitively inhibits insulin-stimulated DNA synthesis (({sup 3}H)thymidine incorporation into total DNA), glucose transport activity (2-deoxyglucose uptake rate), and insulin receptor tyrosine kinase activity. In rat adipocytes, in contrast, the dimerized derivative stimulates glucose transport (initial 3-O-methylglucose as well as 2-deoxyglucose uptake rates) to the same extent as insulin does, and it fails to inhibit the effect of insulin. The data indicate that the dimerized insulin derivative B29,B29{prime}-suberoyl-insulin is an insulin receptor antagonist (partial agonist) which retains a moderate intrinsic activity. The effects of this agent reveal a striking difference in insulin receptor-mediated stimulation of glucose transport between 3T3-L1 fatty fibroblasts and the mature rat adipocyte.

OSTI ID:
6718510
Journal Information:
Proceedings of the National Academy of Sciences of the United States of America; (USA), Vol. 87:3; ISSN 0027-8424
Country of Publication:
United States
Language:
English