首页> 外文期刊>Developmental psychobiology. >Neonatal alcohol exposure impairs acquisition of eyeblink conditioned responses during discrimination learning and reversal in weanling rats.
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Neonatal alcohol exposure impairs acquisition of eyeblink conditioned responses during discrimination learning and reversal in weanling rats.

机译:新生儿饮酒会削弱在断奶大鼠的识别学习和逆转过程中获得眨眼条件反应的能力。

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摘要

Discrimination and reversal of the classically conditioned eyeblink response depends on cerebellar-brainstem interactions with the hippocampus. Neonatal "binge" exposure to alcohol at doses of 5 g/kg/day or more has been shown to impair single-cue eyeblink conditioning in both weanling and adult rats. The present study exposed neonatal rats to acute alcohol intubations across different developmental periods (postnatal day [PND] 4-9 or PND7-9) and tested them from PND26-31 on discriminative classical eyeblink conditioning and reversal. A high dose of alcohol (5 g/kg/day) dramatically impaired conditioning relative to controls when exposure occurred over PND4-9, but produced mild or no impairments when delivered over PND7-9. These findings support previous claims that developmental exposure period plays a critical role in determining the deleterious effects of alcohol on the developing brain. A lower dose of alcohol (4 g/kg/day) delivered from PND4-9--lower than has previously been shown to affect single-cue eyeblink conditioning--also produced deficits on the discrimination task, suggesting that discrimination learning and acquisition of responding to CS+ during reversal may be especially sensitive behavioral indicators of alcohol-induced brain damage in this rat model.
机译:经典条件眨眼反应的区分和逆转取决于与海马的小脑-脑干相互作用。新生的“暴饮暴食”的酒精暴露量为5 g / kg / day或更高,已表明在断奶和成年大鼠中都会损害单线索眨眼条件。本研究使新生大鼠在不同的发育时期(产后第[PND] 4-9或PND7-9)接受了急性酒精插管,并从PND26-31对他们进行了区分性经典眨眼条件和逆转的测试。当暴露在PND4-9之上时,相对于对照组,高剂量的酒精(5 g / kg /天)会严重损害调理能力,但通过PND7-9传递时则产生轻度或无损害。这些发现支持了以前的观点,即发育暴露期在确定酒精对发育中的大脑的有害作用中起着至关重要的作用。从PND4-9递送的酒精剂量较低(4 g / kg /天)-比以前显示的会影响单提示眨眼条件的酒精剂量低-也会导致歧视任务的不足,这表明歧视的学习和获取逆转期间对CS +的应答可能是该大鼠模型中酒精引起的脑损伤的特别敏感的行为指标。

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