INCREASES IN MATURE BRAIN-DERIVED NEUROTROPHIC FACTOR PROTEIN IN THE FRONTAL CORTEX AND BASAL FOREBRAIN DURING CHRONIC SLEEP RESTRICTION IN RATS: POSSIBLE ROLE IN INITIATING ALLOSTATIC ADAPTATION

被引:19
作者
Wallingford, J. K. [1 ]
Deurveilher, S. [1 ]
Currie, R. W. [1 ]
Fawcett, J. P. [2 ,3 ]
Semba, K. [1 ,4 ,5 ]
机构
[1] Dalhousie Univ, Dept Med Neurosci, Halifax, NS B3H 4R2, Canada
[2] Dalhousie Univ, Dept Pharmacol, Halifax, NS B3H 4R2, Canada
[3] Dalhousie Univ, Dept Surg, Halifax, NS B3H 4R2, Canada
[4] Dalhousie Univ, Dept Psychol & Neurosci, Halifax, NS B3H 4R2, Canada
[5] Dalhousie Univ, Dept Psychiat, Halifax, NS B3H 4R2, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
sleep deprivation; Western blot; basal forebrain; frontal cortex; hippocampus; allostasis; GENE-EXPRESSION; MESSENGER-RNA; METABOLIC CONSEQUENCES; DEPRIVATION; BDNF; WAKEFULNESS; HIPPOCAMPUS; HOMEOSTASIS; STRESS; INTENSITY;
D O I
10.1016/j.neuroscience.2014.06.067
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Chronic sleep restriction (CSR) has various negative consequences on cognitive performance and health. Using a rat model of CSR that uses alternating cycles of 3 h of sleep deprivation (using slowly rotating activity wheels) and 1 h of sleep opportunity continuously for 4 days ('3/1' protocol), we previously observed not only homeostatic but also allostatic (adaptive) sleep responses to CSR. In particular, non-rapid eye movement sleep (NREMS) electroencephalogram (EEG) delta power, an index of sleep intensity, increased initially and then declined gradually during CSR, with no rebound during a 2-day recovery period. To study underlying mechanisms of these allostatic responses, we examined the levels of brain-derived neurotrophic factor (BDNF), which is known to regulate NREMS EEG delta activity, during the same CSR protocol. Mature BDNF protein levels were measured in the frontal cortex and basal forebrain, two brain regions involved in sleep and EEG regulation, and the hippocampus, using Western blot analysis. Adult male Wistar rats were housed in motorized activity wheels, and underwent the 3/1 CSR protocol for 27 h, for 99 h, or for 99 h followed by 24 h of recovery. Additional rats were housed in either locked wheels (locked wheel controls [LWCs]) or unlocked wheels that rats could rotate freely (wheel-running controls [WRCs]). BDNF levels did not differ between WRC and LWC groups. BDNF levels were increased, compared to the control levels, in all three brain regions after 27 h, and were increased less strongly after 99 h, of CSR. After 24 h of recovery, BDNF levels were at the control levels. This time course of BDNF levels parallels the previously reported changes in NREMS delta power during the same CSR protocol. Changes in BDNF protein levels in the cortex and basal forebrain may be part of the molecular mechanisms underlying allostatic sleep responses to CSR. (C) 2014 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:174 / 183
页数:10
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