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躯体性和心理性应激对大鼠血浆皮质酮变化的影响 被引量:40

THE PLASMA CORTICOSTERONE IN RATS DURING PHYSICAL AND PSYCHOLOGICAL STRESS
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摘要 本实验以血浆皮质酮分泌量为大鼠应激反应指标。实验分三阶段进行:Ⅰ期.适应(第1~7天),在此期所有动物对环境及实验盒适应性训练。Ⅱ期.心理性应激的形成(第8~14天).随机分三组进行:对照(C)组仅给不规则光;规则光(R)组给光后再于尾部施电刺激,光与电刺激间隔恒定;不规则光(Ⅰ)组给光和电刺激,但两者间隔随机。C、R、I三组所接受的光刺激量相等,R、I组所接受的电刺激量相等。Ⅲ期.心理性应激的记忆(第15天).此期各组电刺激均撤除,余同第Ⅱ期。结果显示,在Ⅱ期末及Ⅲ期,R、I组血浆皮质酮均明显高于C组,I组高于R组。 The plasma corticosterone level of rats was determined and used as acriterion for magnitude of stress response in this model. The rats wererandomly divided into three groups: C, control group; R, regular lightgroup; Ⅰ, irregular light group.The experiment was successively carried out in three stages:Ⅰ. adaptation (7 days); Ⅱ. development of stress(7 days);and Ⅲ. psychological induction of stress (0-24 hrs). Stage Ⅰ: all animalswere adapted to the cage and other environmental cues. Stage Ⅱ. in groupR electric shocks were applied to the tail regularly with a fixed intervalafter the lights were given. In group I the same amount of light and ele-ctric shocks were irregularly applied. In group C only irregular light wasgiven. Stage Ⅲ. all tail shocks were omitted and the same protocol oflights were used in different groups. The results showed that the plasmacorticosterone levels in the R and I groups were significantly higher thanthose in the C group (p<0.01.StageⅡ: R,24.9+\-5.8; Ⅰ,34.9+\-2.0;C,11.7+\-1.7. Stage Ⅲ. R,24.1+\-3.3; Ⅰ, 33.9+\-2.5; C,13.1+\-5.0. In every group n was 9 and the unit was ug/dl.), there was a signi-ficant difference between stress responses of R and I groups, both at stageⅡ and Ⅲ (P<0.05).
出处 《心理学报》 CSSCI CSCD 北大核心 1991年第4期418-425,共8页 Acta Psychologica Sinica
基金 全军医药卫生科研基金
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参考文献4

  • 1杨俊,林葆城,王成海,宋朝佑,朱鹤年.心理性应激对人体血压、心率、呼吸及血浆、脑脊液中精氨酸加压素免疫活性物质含量的影响[J]心理学报,1989(02).
  • 2陈宜张,王春安,袁文俊,邢宝仁,陈治棠,严进.损毁下丘脑不同脑区对折断腿骨所致血浆皮质酮变化的影响[J]第二军医大学学报,1987(01).
  • 3汤慈美,林文娟,孙丽华.痛信号对痛反应阈和脑内去甲肾上腺素与5-羟色胺含量的影响[J]科学通报,1980(08).
  • 4T. Onaka,K. Yagi,M. Hamamura. Vasopressin secretion: suppression after light and tone stimuli previously paired with footshocks in rats[J] 1988,Experimental Brain Research(2):291~297

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