This project's objective is to identify the role of enteroglucagon as a humoral mediator of intestinal adaptation. The intestine has long been known to exhibit two distinct types of adaptation. First, intestinal mucosal mass increases, and hence absorption of all nutrients increases, under many conditions associated with increased energy needs leading to hyperphagia. Second, specific intestinal transporters are up- or down-regulated by changes in dietary levels or body stores of their substrates. Strongly suggestive but not conclusive evidence makes it likely that enteroglucagon is a (the?) humoral mediator of the former response, and may also contribute to the latter response in the case of dietary carbohydrate effects on intestinal glucose transporters. Hence this project will test enteroglucagon's role in adaptation by means of in vivo studies in rats, employing critical tests that could not be carried out until recently because of lack of knowledge of endogenous enteroglucagon forms, their limited availability for in-vivo testing, and inadequate assays. One approach will be to test the effects of chronic infusions of two enteroglucagon peptides, oxyntomodulin and GLP-1 7-36 amide, on mucosal growth and on intestinal nutrient uptake. The other approach will be to test the effect of immunoneutralizing enteroglucagon on both types of adaptation in two rat models that this laboratory developed. One of the models produces a several-fold increase in mucosal mass, the other a two-fold increase in glucose transporter activity. The health relatedness of this project derives from the role of intestinal adaptation in important clinical conditions, such as diabetes, short bowel syndrome, pregnancy, lactation, and exercise.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK042973-02
Application #
3244206
Study Section
General Medicine A Subcommittee 2 (GMA)
Project Start
1990-09-01
Project End
1993-08-31
Budget Start
1991-09-01
Budget End
1992-08-31
Support Year
2
Fiscal Year
1991
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
Schools of Medicine
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Secor, Stephen M (2008) Digestive physiology of the Burmese python: broad regulation of integrated performance. J Exp Biol 211:3767-74
Collie, N L; Zhu, Z; Jordan, S et al. (1997) Oxyntomodulin stimulates intestinal glucose uptake in rats. Gastroenterology 112:1961-70
Jackson, S; Diamond, J (1995) Ontogenetic development of gut function, growth, and metabolism in a wild bird, the Red Jungle Fowl. Am J Physiol 269:R1163-73
Secor, S M; Diamond, J (1995) Adaptive responses to feeding in Burmese pythons: pay before pumping. J Exp Biol 198:1313-25
Secor, S M; Stein, E D; Diamond, J (1994) Rapid upregulation of snake intestine in response to feeding: a new model of intestinal adaptation. Am J Physiol 266:G695-705
Collie, N L; Walsh, J H; Wong, H C et al. (1994) Purification and sequence of rat oxyntomodulin. Proc Natl Acad Sci U S A 91:9362-6
Diamond, J; Hammond, K (1992) The matches, achieved by natural selection, between biological capacities and their natural loads. Experientia 48:551-7