Freeman G B, Thurmond J B
Physiol Behav. 1986;37(6):933-8.
Administration of chlordiazepoxide (CDP) (5 mg/kg) decreased plasma corticosterone (CS) levels of mice exposed to noise stress and increased CS levels in nonstressed mice (20 and 40 mg/kg). The increase in CS may be related to an observed decrease in locomotor activity. Quipazine (0.5 mg/kg), a serotonergic agonist, failed to alter CS levels in animals without prior drug treatment and attenuated the rise in CS of nonstressed mice. These results contradicted a possible serotonergic facilitatory effect on CS regulation. Administration of apomorphine (0.5 mg/kg) or clonidine (0.1 mg/kg) prevented the significant reduction of CS levels in stressed mice treated with low doses of CDP. Apomorphine, alone, increased CS of nonstressed mice to levels approximating those of vehicle-treated stressed mice. Thus, a norepinephrine inhibitory effect was not evident and possible dopaminergic involvement in CS response regulation was suggested. It seemed likely that the effect of CDP on the hypothalamic-pituitary-adrenal system was dependent upon the endocrine state of the animal. Mice exposed to stress and exhibiting higher levels of CS were affected differently by CDP treatment than their nonstressed counterparts.
给予氯氮卓(CDP)(5毫克/千克)可降低暴露于噪声应激的小鼠的血浆皮质酮(CS)水平,并增加未受应激小鼠(20和40毫克/千克)的CS水平。CS的增加可能与观察到的运动活动减少有关。喹哌嗪(0.5毫克/千克),一种5-羟色胺能激动剂,在未经事先药物治疗的动物中未能改变CS水平,并减弱了未受应激小鼠CS的升高。这些结果与5-羟色胺能对CS调节的可能促进作用相矛盾。给予阿扑吗啡(0.5毫克/千克)或可乐定(0.1毫克/千克)可防止低剂量CDP治疗的应激小鼠CS水平的显著降低。单独使用阿扑吗啡可使未受应激小鼠的CS升高至接近载体处理的应激小鼠的水平。因此,去甲肾上腺素的抑制作用不明显,并提示多巴胺能可能参与CS反应调节。CDP对下丘脑-垂体-肾上腺系统的作用似乎取决于动物的内分泌状态。暴露于应激并表现出较高CS水平的小鼠与未受应激的小鼠相比,CDP治疗对其影响不同。