This article is available to subscribers. Subscribe now. Already have an account? Sign in

Original ArticleFree PreviewArchive

The Effects of Biosynthetic Human Proinsulin on Carbohydrate Metabolism in Non-Insulin-Dependent Diabetes Mellitus

List of authors.
  • Harry S. Glauber, M.D.,
  • Robert R. Henry, M.D.,
  • Penny Wallace, R.N., M.S.N.,
  • Bruce H. Frank, Ph.D.,
  • John A. Galloway, M.D.,
  • Robert M. Cohen, M.D.,
  • and Jerrold M. Olefsky, M.D.

Abstract

We compared the glucose-lowering effect of proinsulin, the precursor molecule of insulin, with that of insulin itself. In patients with non-insulin-dependent diabetes mellitus (NIDDM) in whom proinsulin (0.2 U per kilogram of body weight) was subcutaneously injected at 9 a.m., fasting glucose levels (247±22 mg per deciliter [±SEM]) became normal within six hours and elevated rates of hepatic glucose output were lowered. The response to regular insulin (0.2 U per kilogram) was of similar magnitude but faster. Glucose clearance was stimulated less by proinsulin, reflecting its preferential action in suppressing glucose output. Hypoglycemia occurred in five of nine insulin-treated patients, but in only one of nine proinsulin-treated patients.

After proinsulin injection at bedtime (30.5±4 U), serum proinsulin concentrations reached a peak by five hours and declined gradually thereafter. Fasting hepatic glucose output became normal, and euglycemia was sustained without overnight hypoglycemia. Proinsulin reduced plasma glucose more effectively than an equal unit dosage of NPH insulin, but since higher doses of NPH insulin were not used, no conclusions could be drawn about the relative desirability of these preparations for clinical use.

We conclude that (1) subcutaneously injected proinsulin has prolonged pharmacokinetics in plasma and can normalize plasma glucose in NIDDM characterized by severe hyperglycemia; (2) as compared with the hypoglycemic effects of regular insulin, those of proinsulin are mostly due to suppression of hepatic glucose output, with little stimulation of glucose disposal and less hypoglycemia; and (3) proinsulin may have a role in the treatment of NIDDM. (N Engl J Med 1987; 316:443–9.)

Funding and Disclosures

Supported by funds from the Medical Research Service of the Veterans Administration, by grants (AM-33649, AM-13941, and AM-20595) from the National Institutes of Arthritis, Metabolism, and Digestive Diseases, by a grant (RR-0827) from the Clinical Research Center Branch of the National Institutes of Health, and by a research grant from Eli Lilly and Company. During the course of these studies, Dr. Henry was the recipient of a fellowship from the Medical Research Council of Canada.

We are indebted to Trina Morrison, Richard Thorn, Pamela Elliott, and Paul Rue for technical assistance in performing these studies, to Cleon Tate and Elizabeth Martinez for assistance in preparing the manuscript, to the nurses of the UCSD Clinical Research Center and San Diego VAH Special Diagnostic and Treatment Unit for caring for our patients, and to G. Paul Shragg, CLINFO system manager.

Author Affiliations

From the Department of Medicine, University of California, San Diego, and the Veterans Administration Medical Center, San Diego; the Department of Medicine, University of Chicago, Chicago; and Eli Lilly and Company, Indianapolis. Address reprint requests to Dr. Olefsky at the University of California, San Diego, Department of Medicine — M-023E, La Jolla, CA 92093.

Print Subscriber? Activate your online access.