Brain dopamine and serotonin metabolism and eating behavior of rats under space restrictin stress
空间限制应激下大鼠脑内多巴胺和血清素代谢及饮食行为
基本信息
- 批准号:06670969
- 负责人:
- 金额:$ 1.28万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for General Scientific Research (C)
- 财政年份:1994
- 资助国家:日本
- 起止时间:1994 至 1995
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Dopamine and serotonin metabolism in the rat brain (prefrontal cortex, nucleus accumbens, ventrolateral striatum, hypothalamus) were studied using in vivo microdialysis during rebound hyperphagia, (A) followed by 22 hour food deprivation, (B) induced by a time restricted feeding schedule, and (C) under the space restriction as a psychological stress. When female Wister rats were set free from the time restricted feeding schedule, daily food intake significantly increased. This rebound hyperphagia was further enhanced by adding a space restriction stress. Dopamine metabolism increased in the prefrontal cortex and nucleus accumbens of all groups, especially C group, of rats. Whereas dopamine metabolism in the striatum increased only in C group. In the hypothalamus, basal levels of dopamine was low and undetectable. Serotonin metabolism in the prefrontal cortex, increased in B group and further increased in C group. Whereas basal levels of serotonin was very low in nucleus accumbens, ventrolateral striatum, and hypothalamus, there was no significant difference among the 3 groups. These results suggest that eating behavior itself may be related to dopamine metabolism in prefrontal cortex and nucleus accumbens, and serotonin metabolism in prefrontal cortex, and rebound hyperphagia may be related serotonin metabolism in prefrontal cortex, and enhanced rebound hyperphagia under the space restriction stress may be related dopamine metabolism in prefrontal cortex and striatum, and serotonin metabolism in prefrontal cortex.
采用体内微透析的方法研究了反跳性贪食(A) 22小时食物剥夺、(B)限时进食、(C)空间限制心理应激下大鼠大脑(前额叶皮质、伏隔核、腹外侧纹状体、下丘脑)多巴胺和血清素代谢。当雌性Wister大鼠不受时间限制喂养时,日摄食量显著增加。通过增加空间限制应力,这种反跳性贪食进一步增强。各组大鼠前额叶皮层和伏隔核多巴胺代谢增加,其中以C组明显。而纹状体多巴胺代谢仅在C组增加。在下丘脑,多巴胺的基础水平很低,无法检测到。前额叶皮层血清素代谢,B组升高,C组进一步升高。虽然伏隔核、腹外侧纹状体和下丘脑的血清素基础水平很低,但3组间无显著差异。上述结果提示,进食行为本身可能与前额皮质和伏隔核多巴胺代谢、前额皮质5 -羟色胺代谢有关,反跳性贪食可能与前额皮质5 -羟色胺代谢有关,空间限制应激下反跳性贪食增强可能与前额皮质和纹状体多巴胺代谢、前额皮质5 -羟色胺代谢有关。
项目成果
期刊论文数量(38)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Inoue,K: "Effects of flavoxamine on food in take during rebound hyperphagia induced by restricted scheduled feeding of rats" J,Neurochem. 65. S,173 (1995)
Inoue,K:“黄沙明对大鼠限制性定时喂养引起的食欲亢进反弹期间摄入食物的影响”J,Neurochem。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Fujisaki, Yasutoshi: "Effects of space restriction on feeding behavior and dopamine metabolism in the nucleus accumbens during rebound hyperphagia of rats" Bulletin of the Japanese Neurochemical Society. 34. 66-67 (1995)
Fujisaki,Yasutoshi:“空间限制对大鼠进食过多反弹期间伏隔核中摄食行为和多巴胺代谢的影响”日本神经化学学会通报。
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- 影响因子:0
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Fujisaki, Yasutoshi: "Effects of space restriction on feeding behavior and dopamine metabolism in the prefrontal cortex of rats during rebound hyperphagia induced by time restricted feeding schedule" Bulletin of the Japanese Neurochemical Society. 33. 406
Fujisaki,Yasutoshi:“时间限制喂养计划引起的反弹性食欲亢进期间,空间限制对喂养行为和大鼠前额皮质多巴胺代谢的影响”日本神经化学学会通报。
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- 影响因子:0
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INOUE,KOKI: "Effects of fluvoxamine on food intake during rebound hyperphagia induced by restricted scheduled feeding of rats" J.Neurochemistry. 65. S173 (1995)
INOUE, KOKI:“氟伏沙明对大鼠限制性定时喂养诱导的食欲亢进期间食物摄入的影响”J.Neurochemistry。
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- 发表时间:
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- 影响因子:0
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藤嵜泰利: "ラット時間制限給餌によるrebound hyperphagiaに閉所ストレスを加えた時の摂餌行動と側坐核ドパンミン" 神経化学. 34. 66-67 (1995)
Yasutoshi Fujisaki:“当幽闭恐怖应激添加到大鼠限时进食引起的反弹性食欲亢进时,进食行为和伏隔核多巴明”《神经化学》34. 66-67 (1995)。
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- 影响因子:0
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{{ truncateString('KIRIIKE Nobuo', 18)}}的其他基金
Effects of maternal separation on high carbohydrate contained food consumption in rebound hyperphagia and neurotransmitter
母体分离对食量反弹和神经递质中高碳水化合物食物消耗的影响
- 批准号:
14570940 - 财政年份:2002
- 资助金额:
$ 1.28万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
ANALYSIS OF RAT'S BEHAVIOR BY VIDEO AND BRAIN DOPAMIN METABOLISM DURING HYPERPHAGIA INDUCED BY SCHEDULED FEEDING
通过视频分析大鼠在定时喂食引起的暴食期间的行为和脑多巴胺代谢
- 批准号:
11670961 - 财政年份:1999
- 资助金额:
$ 1.28万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
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