首页> 外文期刊>Behavioural Brain Research: An International Journal >Removal of short-term isolation stress differentially influences prepulse inhibition in APO-SUS and APO-UNSUS rats.
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Removal of short-term isolation stress differentially influences prepulse inhibition in APO-SUS and APO-UNSUS rats.

机译:短期隔离应力的消除差异性地影响APO-SUS和APO-UNSUS大鼠的预脉冲抑制。

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EPIDEMIOLOGICAL STUDIES HAVE REPORTED THAT THE RISK OF DEVELOPING SCHIZOPHRENIA INCREASES WITH THE NUMBER OF GENES ONE SHARES WITH PATIENTS SUFFERING FROM SCHIZOPHRENIA [GOTTESMAN SCHIZOPHRENIA GENESIS, NEW YORK: Freeman; 1991]. In addition, stressful life events are known to increase the risk of developing schizophrenia [Schizophr Res 30 (1998) 251] resulting in the stress hypothesis of schizophrenia. Remarkably, stress increases the release of dopamine and noradrenaline in the nucleus accumbens [Brain Res 554 (1991) 217], which links the stress hypothesis with the known dopamine hypothesis of schizophrenia. Additionally an increased dopamine transmission in the nucleus accumbens (Nacc) is known to disturb prepulse inhibition (ppi) [Pharmacol Biochem Behav 49 (1994) 155], a phenomenon observed in, among others, schizophrenics [Arch Gen Psychiatry 47 (1990) 181].Some years ago we have genetically selected two rat-lines which are marked by a high (APO-SUS) and by a low (APO-UNSUS) apomorphine susceptibility. Similar to schizophrenics the APO-SUS rat-line shows a reduced ppi [J Neurosci 15 (1995) 7604]. However, these data were obtained after a period of mild stress, namely a 24-h period of social isolation. Mild stress changes the line specific differences of APO-SUS and APO-UNSUS rats. The stress pushes the APO-SUS rat in the direction of an APO-UNSUS and vice versa, especially as far as it concerns the dopamine and noradrenaline activity in the nucleus accumbens [Cools AR, van-den Bos R, Ellenbroek BA, Gaiting function of noradrenaline in the ventral striatum: its role in behavioural responses to environmental and pharmacological challenges. In: Willner P, Scheel-Kruger J, editors. The mesolimbic dopamine system: from motivation to action. New York: Wiley; 1991 [Chapter 6]; Cools AR, Rots NY, De-Kloet ER, Apomorphine-susceptible and apomorphine-unsusceptible Wistar rats: a new tool in the search for the function of striatum in switching behavioural strategies. In: Pea G (Ed.), The basal ganglia IV, New York: Plenum Press; 1994; Brain Res Bull 24 (1990) 49; Behav Neurosci 108 (1994) 1107]. Therefore, in the present paper we investigated the ppi response in non-stressed, i.e. non-isolated APO-SUS and APO-UNSUS rats. In agreement with this hypothesis, we found that removal of the stress led to an increase of ppi in the APO-SUS, but a decrease in the APO-UNSUS.These data clearly shows that the ppi is stress-dependent in APO-SUS and APO-UNSUS rats. It is suggested that the differential stress-induced change in the dopaminergic and the noradrenergic system influences the reaction of APO-SUS and APO-UNSUS rats on ppi.
机译:流行病学研究表明,患精神分裂症的人患基因分裂症的风险增加,因为患有精神分裂症的患者一股基因的份额增加。[GOTTESMAN SCHIZOPHRENIA GENESIS,纽约:弗里曼; 1991]。另外,已知应激性生活事件会增加发生精神分裂症的风险[Schizophr Res 30(1998)251],导致精神分裂症的应激假设。显着地,压力增加伏隔核中多巴胺和去甲肾上腺素的释放[Brain Res 554(1991)217],这将压力假说与已知的精神分裂症多巴胺假说联系起来。另外,已知伏隔核(Nacc)中多巴胺传递的增加会干扰脉冲前抑制(ppi)[Pharmacol Biochem Behav 49(1994)155],这种现象在精神分裂症患者中观察到[Arch Gen Psychiatry 47(1990)181]。 ]。几年前,我们从基因上选择了两种大鼠品系,其特征是高(APO-SUS)和低(APO-UNSUS)的阿扑吗啡敏感性。与精神分裂症相似,APO-SUS大鼠系显示降低的ppi [J Neurosci 15(1995)7604]。但是,这些数据是在经过轻度压力(即社交孤立24小时)后获得的。轻度压力会改变APO-SUS和APO-UNSUS大鼠的线特异性差异。应力将APO-SUS大鼠推向APO-UNSUS方向,反之亦然,特别是涉及伏伏核中的多巴胺和去甲肾上腺素活性时[应力AR,van-den Bos R,Ellenbroek BA,步态功能肾上腺素在腹侧纹状体中的作用:其在对环境和药理学挑战的行为反应中的作用。在:Willner P,Scheel-Kruger J,编辑中。中脑边缘的多巴胺系统:从动机到行动。纽约:威利; 1991年[第6章];冷却AR,Rots NY,De-Kloet ER,对阿扑吗啡敏感和对阿扑吗啡不敏感的Wistar大鼠:一种寻找纹状体在改变行为策略中功能的新工具。于:Pea G(Ed。),基底神经节IV,纽约:全体会议出版社; 1994年; Brain Res Bull 24(1990)49; Behav Neurosci 108(1994)1107]。因此,在本文中,我们研究了非应激即非分离的APO-SUS和APO-UNSUS大鼠的ppi反应。与此假设相符,我们发现消除压力导致APO-SUS中ppi升高,但导致APO-UNSUS降低。这些数据清楚地表明,ppo在APO-SUS和APO-UNSUS大鼠。提示在多巴胺能和去甲肾上腺素能系统中,不同的应激诱导的变化会影响APO-SUS和APO-UNSUS大鼠对ppi的反应。

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