AJP - Endo Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Endocrinol Metab 272: E86-E93, 1997;
0193-1849/97 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Farrag, H. M.
Right arrow Articles by Cowett, R. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Farrag, H. M.
Right arrow Articles by Cowett, R. M.

AJP - Endocrinology and Metabolism, Vol 272, Issue 1 E86-E93, Copyright © 1997 by American Physiological Society


ARTICLES

Persistent glucose production and greater peripheral sensitivity to insulin in the neonate vs. the adult

H. M. Farrag, L. M. Nawrath, J. E. Healey, E. J. Dorcus, R. E. Rapoza, W. Oh and R. M. Cowett
Department of Pediatrics, Brown University School of Medicine, Providence, Rhode Island, USA.

Insulin resistance has been reported to partially explain the clinical appearance of neonatal hyperglycemia. To determine the relative resistance to insulin of glucose production vs. glucose utilization, the euglycemic hyperinsulinemic clamp technique was employed for the first time in the human neonate and was combined with stable isotopic determination of glucose production and glucose utilization. The basal rates of glucose production and glucose utilization were determined, after which each neonate was clamped at his or her own euglycemic glucose concentration while receiving regular human insulin at one rate of 0.2, 0.5, 1.0, 2.0, or 4.0 mU. kg-1.min-1. Persistent glucose production (> or = 1 mg.kg-1.min-1) during the clamp was recorded for all groups. A significant increase in the glucose infusion rate (P < 0.001) and in percent glucose utilization (P < 0.01) occurred in the 2.0 and 4.0 mU.kg-1.min-1 insulin groups. Metabolic clearance rate of insulin was significantly greater in the neonate compared with the adult at the 2.0 mU.kg-1.min-1 insulin infusion rate (P = 0.036). Our results indicate that, in contrast to the adult, the neonate has persistent glucose production (P = 0.001) and greater peripheral sensitivity to insulin (P = 0.015).


This article has been cited by other articles:


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
K. L. Gatford, M. J. De Blasio, P. Thavaneswaran, J. S. Robinson, I. C. McMillen, and J. A. Owens
Postnatal ontogeny of glucose homeostasis and insulin action in sheep
Am J Physiol Endocrinol Metab, June 1, 2004; 286(6): E1050 - E1059.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
N. L. Gelardi, R. E. Rapoza, J. F. Renzulli, and R. M. Cowett
Insulin resistance and glucose transporter expression during the euglycemic hyperinsulinemic clamp in the lamb
Am J Physiol Endocrinol Metab, December 1, 1999; 277(6): E1142 - E1149.
[Abstract] [Full Text] [PDF]


Home page
PediatricsHome page
W. W. Hay, J. MD, A. Lucas, W. C. Heird, E. Ziegler, E. Levin, G. D. Grave, C. S. Catz, and S. J. Yaffe
Workshop Summary: Nutrition of the Extremely Low Birth Weight Infant
Pediatrics, December 1, 1999; 104(6): 1360 - 1368.
[Full Text]


Home page
Pediatr. Rev.Home page
A. H. Hemachandra and R. M. Cowett
Neonatal Hyperglycemia
Pediatr. Rev., July 1, 1999; 20(7): 16e - 24.
[Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online