Local Lactate Perfusion of the Ventromedial Hypothalamus Suppresses Hypoglycemic Counterregulation
- 1Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut
- 2Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut
- 3Howard Hughes Medical Institute, New Haven, Connecticut
Abstract
We have previously reported that a glucosensor integrating hormonal responses to hypoglycemia is located in the ventromedial hypothalamus (VMH) and that local VMH glucose perfusion blocks counterregulatory hormone responses. To determine whether the by-product of glucose metabolism, lactate, can function within the VMH as an alternative for glucose, we delivered lactate locally to the VMH, during systemic hypoglycemia. For this purpose, we combined bilateral VMH microdialysis perfusion (metabolically active l-lactate or its nonmetabolizable d-isomer) with a euglycemic-hypoglycemic clamp in conscious chronically catheterized Sprague-Dawley rats. Local VMH perfusion with l-lactate decreased counterregulatory hormone responses to hypoglycemia by 80–85% as compared with the nonmetabolizable d-lactate control. Moreover, hormonal suppression with l-lactate was accompanied by an approximate fourfold increase in the amount of exogenous glucose infused to maintain a stable hypoglycemic plateau (P < 0.05). In conclusion, the glucose-sensing mechanism in the VMH responds to lactate and, thus, is not specific for glucose. This implies that the VMH may act as a fuel sensor rather than as a glucose sensor.
Footnotes
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Address correspondence and reprint requests to Robert S. Sherwin Yale University School of Medicine, Department of Internal Medicine, P.O. Box 208020, New Haven, CT 06520-8020. E-mail: robert.sherwin{at}yale.edu.
Received for publication 12 September 2002 and accepted in revised form 17 December 2002.
ECF, extracellular fluid solution; VMH, ventromedial hypothalamus.
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