[unreadable] DESCRIPTION (provided by applicant): In this project, we propose to continue our investigation of the biochemical mechanism(s) by which insulin resistance is acquired. Our long-term focus has been on the link between nutrient availability and insulin action. In this regard, the leptin plays in the regulation of hepatic and peripheral insulin action. However, the biochemical and neural circuitries mediating these effects remain to be elucidated. Here we wish to test the hypothesis that leptin exerts its rapid effects on hepatic glucose fluxes via 2 major central components: [unreadable] a) STAT3-dependent effects (mostly leading to rapid stimulation of gluconeogenesis and lipid oxidation); [unreadable] b) STAT3-independent effects (mostly leading to rapid inhibition of glycogenolysis and glucose [unreadable] output). [unreadable] Additionally, more prolonged activation of hypothalamic leptin signaling orchestrates the biological response to nutrient excess by limiting feeding behavior, by increasing energy expenditure and lipid oxidation, and by improving insulin action. Based on preliminary results and on this overall objective we wish to pursue the following specific aims: 1. Does leptin acutely regulate hepatic glucose fluxes via activation of STAT3-independent pathways in the hypothalamus? We will examine whether blocking hypothalamic leptin signaling via STAT3-independent pathways alters leptin action on hepatic nutrient fluxes. 2. Does leptin acutely regulate hepatic glucose fluxes via activation of STAT3-dependent pathways in the hypothalamus? We will examine whether rapid 'loss-of-function' within the hypothalamic STAT3 or melanocortin pathways alters leptin action on hepatic nutrient fluxes. 3. Does leptin acutely inhibit hepatic glucose production via STAT3-independent pathways when its activation of hypothalamic STAT3-dependent pathways is prevented? We will examine whether rapid 'loss-of-function' of STAT3-dependent hypothalamic targets of leptin unveils 'insulin-like' leptin actions on hepatic nutrient fluxes. 4. Does leptin regulate energy balance and insulin action via activation of hypothalamic STAT3-dependent and/or STAT3-independent signaling? We will examine whether week-long manipulations of hypothalamic leptin signaling via selective downstream targets regulate feeding behavior, energy metabolism, and insulin sensitivity. 5. How does short-term over-feeding modify the effects of hypothalamic leptin signaling on hepatic glucose fluxes? We will examine whether short-term stimulation of selective components of hypothalamic leptin signaling 'rescues' the action of leptin on hepatic nutrient fluxes in over-fed rats. [unreadable] [unreadable]
|Effective start/end date||8/1/94 → 5/31/10|
- National Institute of Diabetes and Digestive and Kidney Diseases: $451,360.00
- National Institute of Diabetes and Digestive and Kidney Diseases: $455,437.00
- National Institute of Diabetes and Digestive and Kidney Diseases: $451,304.00
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