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35日龄大鼠的潜伏抑制并非“成年”潜伏抑制:对精神分裂症神经发育模型的启示

Latent inhibition in 35-day-old rats is not an "adult" latent inhibition: implications for neurodevelopmental models of schizophrenia.

作者信息

Zuckerman L, Rimmerman N, Weiner I

机构信息

Department of Psychology, Tel Aviv University, 69978, Tel Aviv, Israel.

出版信息

Psychopharmacology (Berl). 2003 Sep;169(3-4):298-307. doi: 10.1007/s00213-003-1460-8. Epub 2003 Jun 24.

Abstract

RATIONALE

Latent inhibition (LI) refers to retarded conditioning to a stimulus as a consequence of its inconsequential preexposure. Amphetamine-induced disruption of LI and its potentiation by antipsychotic drugs (APDs) in the adult rat are well-established models of schizophrenia and antipsychotic drug action, respectively. It is not clear whether LI can be similarly modulated at prepubertal age.

OBJECTIVES

In view of the notion that schizophrenia is a neurodevelopmental disorder whose overt expression depends on postpubertal brain maturational processes, we investigated whether several manipulations known to modulate LI in adult rats, including systemic administration of amphetamine and the atypical APD clozapine, are capable of producing the same effects in prepubertal (35-day-old) rats.

METHODS

LI was measured in a thirst motivated conditioned emotional response (CER) procedure in which rats received 10 or 40 tone preexposures followed by 2 or 5 tone-footshock pairings.

RESULTS

Like in adults, LI was present with 40 preexposures and 2 conditioning trials. In contrast to findings in adults, LI was resistant to disruption by amphetamine at a dose (1 mg/kg) that significantly increased locomotor activity, as well as by reducing the number of preexposures to ten, increasing the number of conditioning trials to five, or changing the context between preexposure and conditioning. Clozapine (5 mg/kg) and the selective 5HT2A antagonist M100907 (0.3 mg/kg) administered in conditioning were without an effect on "persistent" LI with extended conditioning, but were capable of disrupting LI when administered in the preexposure stage, as found in adults.

CONCLUSION

The results point to functionality within brain systems regulating LI acquisition but not those regulating LI expression in periadolescent rats, further suggesting that postpubertal maturation of the latter systems may underlie schizophrenia-mimicking LI disruption reported in adult rats following perinatal manipulations and possibly disrupted LI observed in schizophrenia.

摘要

原理

潜伏抑制(LI)是指由于刺激物的无关紧要的预暴露而导致对其条件作用的延迟。苯丙胺诱导的成年大鼠LI破坏及其被抗精神病药物(APD)增强分别是精神分裂症和抗精神病药物作用的成熟模型。尚不清楚LI在青春期前年龄是否能被类似地调节。

目的

鉴于精神分裂症是一种神经发育障碍,其明显表现取决于青春期后脑成熟过程的观点,我们研究了几种已知能调节成年大鼠LI的操作,包括全身给予苯丙胺和非典型APD氯氮平,是否能在青春期前(35日龄)大鼠中产生相同的效果。

方法

在口渴动机的条件性情绪反应(CER)程序中测量LI,其中大鼠接受10次或40次音调预暴露,然后进行2次或5次音调-足部电击配对。

结果

与成年大鼠一样,40次预暴露和2次条件试验时存在LI。与成年大鼠的研究结果相反,在显著增加运动活动的剂量(1mg/kg)下,苯丙胺对LI无破坏作用,将预暴露次数减少到10次、将条件试验次数增加到5次或改变预暴露和条件试验之间的环境时,苯丙胺对LI也无破坏作用。在条件试验中给予氯氮平(5mg/kg)和选择性5HT2A拮抗剂M100907(0.3mg/kg)对延长条件试验时的“持续性”LI无影响,但如在成年大鼠中发现的那样,在预暴露阶段给予时能够破坏LI。

结论

结果表明,在调节青春期大鼠LI获得的脑系统中存在功能,但调节LI表达的脑系统中不存在功能,这进一步表明,后者系统的青春期后成熟可能是成年大鼠在围产期操作后出现的模仿精神分裂症的LI破坏以及精神分裂症中观察到的可能被破坏的LI的基础。

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