Effects of Repetitive Hypoglycemia on Neuroendocrine Response and Brain Tyrosine Hydroxylase Activity in the Rat
被引:12
作者:
Figlewicz, D. P.
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VA Puget Sound Hlth Care Syst, Seattle, WA 98108 USA
Univ Washington, Dept Psychol, Seattle, WA 98195 USAVA Puget Sound Hlth Care Syst, Seattle, WA 98108 USA
Figlewicz, D. P.
[1
,2
]
Van Dijk, G.
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机构:
Univ Groningen, Dept Anim Physiol, NL-9750 AA Haren, NetherlandsVA Puget Sound Hlth Care Syst, Seattle, WA 98108 USA
Van Dijk, G.
[3
]
Wilkinson, C. W.
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机构:
VA Puget Sound Hlth Care Syst, GRECC, Seattle, WA 98195 USA
Univ Washington, Dept Psychiat, Seattle, WA 98195 USAVA Puget Sound Hlth Care Syst, Seattle, WA 98108 USA
Wilkinson, C. W.
[4
,5
]
Gronbeck, P.
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VA Puget Sound Hlth Care Syst, Seattle, WA 98108 USAVA Puget Sound Hlth Care Syst, Seattle, WA 98108 USA
Gronbeck, P.
[1
]
Higgins, M.
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VA Puget Sound Hlth Care Syst, Seattle, WA 98108 USAVA Puget Sound Hlth Care Syst, Seattle, WA 98108 USA
Higgins, M.
[1
]
Zavosh, A.
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机构:
Univ Washington, Dept Psychol, Seattle, WA 98195 USAVA Puget Sound Hlth Care Syst, Seattle, WA 98108 USA
Zavosh, A.
[2
]
机构:
[1] VA Puget Sound Hlth Care Syst, Seattle, WA 98108 USA
[2] Univ Washington, Dept Psychol, Seattle, WA 98195 USA
[3] Univ Groningen, Dept Anim Physiol, NL-9750 AA Haren, Netherlands
[4] VA Puget Sound Hlth Care Syst, GRECC, Seattle, WA 98195 USA
[5] Univ Washington, Dept Psychiat, Seattle, WA 98195 USA
来源:
STRESS-THE INTERNATIONAL JOURNAL ON THE BIOLOGY OF STRESS
|
2002年
/
5卷
/
03期
Hypoglycemia-associated autonomic failure (HAAF) is a syndrome of acute adaptation to a metabolic stressor, in which neuroendocrine responses to repetitive hypoglycemic bouts are blunted. The CNS mechanisms that contribute to HAAF are unknown. In the present study, we modeled HAAF in the rat and measured the activity of tyrosine hydroxylase (TH) as an index of acute noradrenergic activation, to test the hypothesis that noradrenergic activation of the hypothalamus might be impaired. In association with a significant counter-regulatory response to a single bout of hypoglycemia (elevated corticosterone, catecholamines, and glucagon), TH activity was elevated overall in brainstem NE cell body areas and hypothalamus. With multiple hypoglycemic episodes in a 24 h period, the counter-regulatory response was blunted, and hypothalamic TH activity was comparable to that of saline-infused controls. In a similar paradigm, multiple bouts of CNS neuroglucopenia did not blunt the hyperglycemic or corticosterone responses, and were required for elevation of TH activity. This alternate response pattern suggests that insulin-induced hypoglycemia and cerebral neuroglucopenia represent somewhat different metabolic stressors at the CNS.