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高脂/精制碳水化合物饮食会增强间歇性缺氧大鼠出现空间学习缺陷的易感性。

High fat/refined carbohydrate diet enhances the susceptibility to spatial learning deficits in rats exposed to intermittent hypoxia.

作者信息

Goldbart A D, Row B W, Kheirandish-Gozal L, Cheng Y, Brittian K R, Gozal D

机构信息

Kosair Children's Hospital Research Institute, Department of Pediatrics, University of Louisville, Louisville, KY 40202, USA.

出版信息

Brain Res. 2006 May 23;1090(1):190-6. doi: 10.1016/j.brainres.2006.03.046. Epub 2006 May 3.

Abstract

BACKGROUND

Intermittent hypoxia during sleep (IH), as occurs in sleep disordered breathing (SDB), induces spatial learning deficits associated with regulation of transcription factors associated with learning and memory in the hippocampal CA1 region in rats. high fat refined carbohydrate diet (HF/RC) can induce similar deficits and associated changes in signaling pathways under normoxic conditions.

METHODS

Sprague-Dawley adult male rats were fed either with (HF/RC) or low fat/complex carbohydrate diet (LF/CC) starting at post-natal day 30 for 90 days, and were then exposed for 14 days during light phase (12 h/day) to either normoxia (RA) or IH (21% and 10% O2 alternations every 90 s). Place-training reference memory task deficits were assessed in the Morris water maze. Total and ser-133 phosphorylated CREB were assessed in different brain regions by Western blotting and immunostaining in rats exposed to normoxia or IH and to LF/CC or HF/RC.

RESULTS

Substantial decreases in CREB phosphorylation occurred in CA1 but not in motor cortex following either IH, HF/RC, and HF/RC + IH. Place-training reference memory task deficits were observed in rats exposed to IH and to HF/RC, and to a much greater extent in rats exposed to HF/RC + IH.

CONCLUSIONS

Nutritional factors alter recruitment of transcription factors, possibly via oxidative-related pathways, and modulate the vulnerability of the CA1 region of the hippocampus to the episodic hypoxia that characterizes SDB, thereby enhancing neurocognitive susceptibility in SDB patients.

摘要

背景

睡眠期间的间歇性低氧(IH),如睡眠呼吸障碍(SDB)中所发生的那样,会诱导大鼠海马CA1区与学习和记忆相关的转录因子调节异常,进而导致空间学习缺陷。高脂精制碳水化合物饮食(HF/RC)在常氧条件下可诱导类似的缺陷及信号通路变化。

方法

从出生后第30天开始,对成年雄性Sprague-Dawley大鼠喂食(HF/RC)或低脂/复合碳水化合物饮食(LF/CC),持续90天,然后在光照期(每天12小时)将其暴露于常氧(RA)或IH(每90秒21%和10%的氧气交替)环境中14天。在莫里斯水迷宫中评估位置训练参考记忆任务缺陷。通过蛋白质免疫印迹法和免疫染色法,对暴露于常氧或IH以及LF/CC或HF/RC的大鼠不同脑区的总CREB和丝氨酸133磷酸化CREB进行评估。

结果

在IH、HF/RC以及HF/RC + IH处理后,CA1区CREB磷酸化显著降低,但运动皮层未出现此现象。在暴露于IH和HF/RC的大鼠中观察到位置训练参考记忆任务缺陷,而在暴露于HF/RC + IH的大鼠中缺陷程度更大。

结论

营养因素可能通过氧化相关途径改变转录因子的募集,并调节海马CA1区对SDB特征性间歇性低氧的易感性,从而增加SDB患者的神经认知易感性。

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