Compan Valérie, Zhou Mingming, Grailhe Régis, Gazzara Russell A, Martin Renee, Gingrich Jay, Dumuis Aline, Brunner Daniela, Bockaert Joël, Hen René
Unité Propre de Recherche Centre National de la Recherche Scientifique 2580, Génomique fonctionnelle, Montpellier 34094, France.
J Neurosci. 2004 Jan 14;24(2):412-9. doi: 10.1523/JNEUROSCI.2806-03.2004.
To study the functions of 5-HT4 receptors, a null mutation was engineered in the corresponding gene. 5-HT4 receptor knock-out mice displayed normal feeding and motor behaviors in baseline conditions but abnormal feeding and locomotor behavior in response to stress and novelty. Specifically, stress-induced hypophagia and novelty-induced exploratory activity were attenuated in the knock-out mice. In addition, pentylenetetrazol-induced convulsive responses were enhanced in the knock-out mice, suggesting an increase in neuronal network excitability. These results provide the first example of a genetic deficit that disrupts the ability of stress to reduce feeding and body weight and suggest that 5-HT4 receptors may be involved in stress-induced anorexia and seizure susceptibility.
为了研究5-羟色胺4(5-HT4)受体的功能,研究人员对相应基因进行了无效突变。5-HT4受体基因敲除小鼠在基线条件下表现出正常的进食和运动行为,但在面对压力和新异刺激时,其进食和运动行为出现异常。具体而言,基因敲除小鼠的应激诱导性摄食减少和新异刺激诱导的探索活动减弱。此外,基因敲除小鼠对戊四氮诱导的惊厥反应增强,提示神经网络兴奋性增加。这些结果首次证明了一种基因缺陷会破坏应激降低进食量和体重的能力,并表明5-HT4受体可能参与应激诱导的厌食症和癫痫易感性。