Massive small bowel resection (SBR) is required therapy for multiple medical and surgical conditions. Intestinal adaptation following SBR is an important compensatory response consisting of mucosal hypertrophy and hyperplasia whit increased bowel caliber, length and thickness. This mitogenic response enhances absorptive and digestive capacity. While it is accepted that adaptation after SBR results in increased cellular proliferation, its effect on programmed cell death (apoptosis) has not been fully elucidated. The experiments described in this application will test the hypothesis that enterocyte apoptosis is increased following small bowel resection and that by retarding apoptosis, the adaptive response of the intestine may be augmented. To this hypothesis, three specific aims are proposed. In the first aim, w will test the hypothesis that enterocyte apoptosis increases during adaptation. Rates of apoptosis and proliferation will be quantified in the ileum during adaptation as well as the expression of apoptosis-associated proteins.
The second aim will test the hypothesis that the balance of apoptosis and proliferation is altered during conditions of enhanced (EGF administration) or inhibited (waved-2 mice) adaptation. Rates of apoptosis and proliferation and expression of apoptosis-associated proteins will be measured under these conditions.
The third aim will delineate a mechanism for apoptosis-associated proteins will measured under these condition.
The third aim will delineate a mechanism for apoptosis during adaptation by testing the hypothesis that the expression of specific proteins are required for apoptosis to occur during adaptation. Transgenic and knockout mice will undergo SBR to determine the impact of specific proto-oncogenes involved during apoptosis. The long-term goals of this application will be to enhance our understanding of intestinal adaptation. By augmenting this response, the requirements and associated morbidity with parenteral nutrition will be reduced.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32DK009882-02
Application #
2905182
Study Section
General Medicine A Subcommittee 2 (GMA)
Program Officer
Podskalny, Judith M,
Project Start
1999-09-25
Project End
Budget Start
1999-09-25
Budget End
2000-06-30
Support Year
2
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Cincinnati Children's Hospital Medical Center
Department
Type
DUNS #
071284913
City
Cincinnati
State
OH
Country
United States
Zip Code
45229
Tai, Ningwen; Wong, F Susan; Wen, Li (2015) The role of gut microbiota in the development of type 1, type 2 diabetes mellitus and obesity. Rev Endocr Metab Disord 16:55-65
O'Brien, David P; Nelson, Lindsey A; Kemp, Christopher J et al. (2002) Intestinal permeability and bacterial translocation are uncoupled after small bowel resection. J Pediatr Surg 37:390-4
O'Brien, D P; Nelson, L A; Stern, L E et al. (2001) Epithelial permeability is not increased in rats following small bowel resection. J Surg Res 97:65-70
Stern, L E; Erwin, C R; O'Brien, D P et al. (2001) Serum from mice after small bowel resection enhances intestinal epithelial cell growth. J Pediatr Surg 36:184-9
Stern, L E; Erwin, C R; Falcone, R A et al. (2001) cDNA microarray analysis of adapting bowel after intestinal resection. J Pediatr Surg 36:190-5
Erwin, C R; Falcone Jr, R A; Stern, L E et al. (2000) Analysis of intestinal adaptation gene expression by cDNA expression arrays. JPEN J Parenter Enteral Nutr 24:311-6
Stern, L E; Huang, F; Kemp, C J et al. (2000) Bax is required for increased enterocyte apoptosis after massive small bowel resection. Surgery 128:165-70
Falcone Jr, R A; Stern, L E; Kemp, C J et al. (2000) Intestinal adaptation occurs independent of transforming growth factor-alpha. J Pediatr Surg 35:365-70
Stern, L E; Falcone Jr, R A; Huang, F et al. (2000) Epidermal growth factor alters the bax:bcl-w ratio following massive small bowel resection. J Surg Res 91:38-42
Stern, L E; Falcone Jr, R A; Kemp, C J et al. (2000) Salivary epidermal growth factor and intestinal adaptation in male and female mice. Am J Physiol Gastrointest Liver Physiol 278:G871-7

Showing the most recent 10 out of 13 publications