Strict glycemic control reduces the occurrence of microvascular complications of diabetes at the cost of a three-fold increase in the frequency of severe hypoglycemia. Euglycemic levels are restored by hormonal and neural counter-regulatory mechanisms at the expense of enhance rates of substrate mobilization and rates of glucose production. Our studies have demonstrates that insulin-induced hypoglycemia is also associated with enhanced rates of whole body proteolysis and amino acid oxidation, as well as a significant enhancement in gut protein breakdown. This response, in its majority, is controlled by CNS glucopenia. Our studies suggest that sites responsible for controlling protein and amino acid metabolism during hypoglycemia are most likely located in the hind brain. The general hypothesis of the present proposal is that the """"""""CNS-Gut"""""""" axis plays a pivotal role in mobilization of amino acids and proteins during the catabolic response to stress. The studies designed will be performed in the chronically catheterized conscious dog and will investigate the contribution of forebrain and hindbrain neuroglucopenia to triggering the proteolytic responses. In addition, the studies proposed will use surgical and pharmacological interventions to investigate the involvement of direct extrinsic innervation of the """"""""gut"""""""" as well as sympathetic, parasympathetic and serotoninergic contribution to modulation the proteolytic responses. The associated hormonal and glucoregulatory responses as well as the contribution of the gut-derived amino acids to enhanced rates of hepatic gluconeogenic amino acid utilization will be assessed using a combination of isotopic and AV difference techniques. Complimentary studies in a rodent model of hypoglycemia to be performed in the final stages of this proposal will be aimed at defining the contribution of specific brain region glucopenia to the proteolytic responses to hypoglycemia. Furthermore, they will determine the specific neurotransmitter alterations that are associated with hypoglycemia. The results from these studies responses to hypoglycemia. These findings will contribute to the understanding of CNS modulation of the peripheral protein and amino acid alterations that are an integral part of the metabolic response to stress.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
7R01DK042562-09
Application #
6342451
Study Section
Metabolism Study Section (MET)
Program Officer
Jones, Teresa L Z
Project Start
1992-01-01
Project End
2002-12-31
Budget Start
2000-10-01
Budget End
2000-12-31
Support Year
9
Fiscal Year
2000
Total Cost
$208,084
Indirect Cost
Name
Sinai Hospital of Baltimore
Department
Type
DUNS #
074920364
City
Baltimore
State
MD
Country
United States
Zip Code
21215
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Cersosimo, E; Molina, P E; Abumrad, N N (1997) Renal glucose production during insulin-induced hypoglycemia. Diabetes 46:643-6
Cersosimo, E; Ajmal, M; Naukam, R J et al. (1997) Role of the kidney in plasma glucose regulation during hyperglycemia. Am J Physiol 272:E756-61
Molina, P E; Williams, P; Abumrad, N N (1997) Histaminergic contribution to the metabolic effects of neuroglucopenia. Am J Physiol 272:R1918-24
Bundz, S; Molina, P E; Lang, C H et al. (1995) Endogenous opiates do not modulate LPS-induced alterations in carbohydrate metabolism. Shock 4:397-402
Molina, P E; Jabbour, K; Williams, P et al. (1994) Effect of acute ethanol intoxication on glucoregulation during prolonged insulin-induced hypoglycemia. Am J Physiol 267:R1280-7
Flakoll, P J; Borel, M J; Wentzel, L S et al. (1994) The role of glucagon in the control of protein and amino acid metabolism in vivo. Metabolism 43:1509-16
Yousef, K A; Tepper, P G; Molina, P E et al. (1994) Differential control of glucoregulatory hormone response and glucose metabolism by NMDA and kainate. Brain Res 634:131-40
Petit, F; Jarrous, A; Dickinson, R D et al. (1994) Contribution of central and peripheral adrenergic stimulation to IL-1 alpha-mediated glucoregulation. Am J Physiol 267:E49-56
Molina, P E; Tepper, P G; Yousef, K A et al. (1994) Central NMDA enhances hepatic glucose output and non-insulin-mediated glucose uptake by a nonadrenergic mechanism. Brain Res 634:41-8

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