REDUCED GLUCOSE EFFECTIVENESS ASSOCIATED WITH REDUCED INSULIN RELEASE- AN ARTIFACT OF THE MINIMAL-MODEL METHOD

Citation
Dt. Finegood et D. Tzur, REDUCED GLUCOSE EFFECTIVENESS ASSOCIATED WITH REDUCED INSULIN RELEASE- AN ARTIFACT OF THE MINIMAL-MODEL METHOD, American journal of physiology: endocrinology and metabolism, 34(3), 1996, pp. 485-495
Citations number
34
Categorie Soggetti
Physiology
ISSN journal
01931849
Volume
34
Issue
3
Year of publication
1996
Pages
485 - 495
Database
ISI
SICI code
0193-1849(1996)34:3<485:RGEAWR>2.0.ZU;2-9
Abstract
Reduced glucose effectiveness associated with reduced insulin release: artifact of the minimal-model method. Am. J. Physiol. 271 (Endocrinol . Metab. 34): E485-E495, 1996.-We previously demonstrated that minimal model-derived estimates of glucose effectiveness (S-G), based on the frequently sampled intravenous glucose tolerance test (S-GFSIGT), were reduced in islet-transplanted or streptozotocin-treated dogs and in p atients with insulin-dependent diabetes mellitus. To ascertain the val idity of our observations, we compared S-GFSIGT With estimates based o n a basal hormone replacement glucose clamp (S-GBRCLAMP) and a basal h ormone replacement glucose tolerance test (S-GBRGTT) in normal control (CNTL, n = 12) and streptozotocin-treated dogs with normal fasting pl asma glucose (STZ-Rx, n = 9). S-GFSIGT was reduced in STZ-Rx compared with CNTL (P < 0.05). However, neither S-GBRCLAMP nor S-GBRGTT was red uced in the STZ-Rx group (P > 0.05). Comparison of protocols for each subject indicated that S-GFSIGT was greater than either S-GBRCLAMP or S-GBRGTT in control (P < 0.002) but not in STZ-Rx dogs (P > 0.1). The relationship of S-GFSIGT to insulin secretory function suggests that o ur previous conclusion that S-GFSIGT was reduced in subjects with limi ted insulin release may be an artifact of the minimal-model method. Ou r results suggest that caution must be exercised in the interpretation of differences in minimal-model estimates of S-G between subject grou ps with significantly different levels of insulin secretory function.