The purpose of this application is to test a new model for the physiology of energy homeostasis. We hypothesize that hormones that circulate at concentrations proportional to body fat content, such as insulin and leptin, reduce food intake and body weight by acting upon discrete hypothalamic signaling systems referred to as central effector pathways. The combined actions of insulin and leptin in the hypothalamus are proposed in turn to potentiate the response of brainstem to afferent, meal-satiety signals such as cholecystokinin (CCK) that lead to the termination of single meals. Though this mechanism, the amount of consumed during individual meals is proposed to decrease when hypothalamic leptin (or insulin) signaling is increased, leading to weight loss. Conversely, the effect of a sustained energy deficit to deplete body fat stores is hypothesized to reduce hypothalamic leptin signaling and thereby increase meal size, since animals become relatively insensitive to signals that terminate the meal. The first major objective of this application is to clarify the interactions between insulin and leptin in the control of food intake and hypothalamic neuropeptide gene expression. This will be accomplished by 1) determining if brain responsiveness to insulin can be restored in leptin-deficient ob/ob mice by infusing leptin systemically at a low dose, and 2) by determining if the effect of leptin to lower circulating insulin levels limits its ability to reduce food intake. The second major objective is to investigate the effect of leptin on the satiety and brainstem response to CCK. Studies will investigate 1) if reduced CCK responsiveness induced by fasting or genetic leptin deficiency is reversed by site or both; and 3) if central effector peptides that are regulated by leptin act in the hypothalamus to modulate the brainstem and feeding responses to CCK. By improving our understanding of the integration of long and short-term regulators of energy intake, these studies will help to identify sites for therapeutic intervention in the treatment of obesity and other weight disorders.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK012829-33
Application #
6380363
Study Section
Metabolism Study Section (MET)
Program Officer
Smith, Philip F
Project Start
1975-12-01
Project End
2004-04-30
Budget Start
2001-05-01
Budget End
2002-04-30
Support Year
33
Fiscal Year
2001
Total Cost
$294,655
Indirect Cost
Name
University of Washington
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
Williams, Diana L; Schwartz, Michael W; Bastian, L Scot et al. (2008) Immunocytochemistry and laser capture microdissection for real-time quantitative PCR identify hindbrain neurons activated by interaction between leptin and cholecystokinin. J Histochem Cytochem 56:285-93
Wisse, Brent E; Ogimoto, Kayoko; Morton, Gregory J et al. (2007) Central interleukin-1 (IL1) signaling is required for pharmacological, but not physiological, effects of leptin on energy balance. Brain Res 1144:101-6
Wisse, Brent E; Kim, Francis; Schwartz, Michael W (2007) Physiology. An integrative view of obesity. Science 318:928-9
Wisse, Brent E; Ogimoto, Kayoko; Tang, Jingjing et al. (2007) Evidence that lipopolysaccharide-induced anorexia depends upon central, rather than peripheral, inflammatory signals. Endocrinology 148:5230-7
Wisse, Brent E; Ogimoto, Kayoko; Schwartz, Michael W (2006) Role of hypothalamic interleukin-1beta (IL-1beta) in regulation of energy homeostasis by melanocortins. Peptides 27:265-73
Pardini, Aaron W; Nguyen, Hong T; Figlewicz, Dianne P et al. (2006) Distribution of insulin receptor substrate-2 in brain areas involved in energy homeostasis. Brain Res 1112:169-78
Mundinger, Thomas O; Cummings, David E; Taborsky Jr, Gerald J (2006) Direct stimulation of ghrelin secretion by sympathetic nerves. Endocrinology 147:2893-901
Gelling, Richard W; Morton, Gregory J; Morrison, Christopher D et al. (2006) Insulin action in the brain contributes to glucose lowering during insulin treatment of diabetes. Cell Metab 3:67-73
Trevaskis, James; Walder, Ken; Foletta, Victoria et al. (2005) Src homology 3-domain growth factor receptor-bound 2-like (endophilin) interacting protein 1, a novel neuronal protein that regulates energy balance. Endocrinology 146:3757-64
Porte Jr, Daniel; Baskin, Denis G; Schwartz, Michael W (2005) Insulin signaling in the central nervous system: a critical role in metabolic homeostasis and disease from C. elegans to humans. Diabetes 54:1264-76

Showing the most recent 10 out of 146 publications