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Small Decrements in Systemic Glucose Provoke Increases in Hypothalamic Blood Flow Prior to the Release of Counterregulatory Hormones

  1. Kathleen A. Page1,
  2. Jagriti Arora2,
  3. Maolin Qiu2,
  4. Rachna Relwani1,
  5. R. Todd Constable2 and
  6. Robert S. Sherwin1
  1. 1Department of Internal Medicine, Division of Endocrinology, Yale University School of Medicine, New Haven, Connecticut
  2. 2Department of Diagnostic Radiology, Yale University School of Medicine, New Haven, Connecticut
  1. Corresponding author: Kathleen A. Page, kathleen.page{at}yale.edu

Abstract

OBJECTIVE—The hypothalamus is the central brain region responsible for sensing and integrating responses to changes in circulating glucose. The aim of this study was to determine the time sequence relationship between hypothalamic activation and the initiation of the counterregulatory hormonal response to small decrements in systemic glucose.

RESEARCH DESIGN AND METHODS—Nine nondiabetic volunteers underwent two hyperinsulinemic clamp sessions in which pulsed arterial spin labeling was used to measure regional cerebral blood flow (CBF) at euglycemia (∼95 mg/dl) on one occasion and as glucose levels were declining to a nadir of ∼50 mg/dl on another occasion. Plasma glucose and counterregulatory hormones were measured during both study sessions.

RESULTS—CBF to the hypothalamus significantly increased when glucose levels decreased to 77.2 ± 2 mg/dl compared with the euglycemic control session when glucose levels were 95.7 ± 3 mg/dl (P = 0.0009). Hypothalamic perfusion was significantly increased before there was a significant elevation in counterregulatory hormones.

CONCLUSIONS—Our data suggest that the hypothalamus is exquisitely sensitive to small decrements in systemic glucose levels in healthy, nondiabetic subjects and that hypothalamic blood flow, and presumably neuronal activity, precedes the rise in counterregulatory hormones seen during hypoglycemia.

Footnotes

  • Published ahead of print at http://diabetes.diabetesjournals.org on 18 November 2008.

    Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.

    The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

    • Accepted November 11, 2008.
    • Received September 3, 2008.
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This Article

  1. Diabetes February 2009 vol. 58 no. 2 448-452
  1. » Abstract
  2. All Versions of this Article:
    1. db08-1224v1
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