首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Effects of ampicillin on cystine/glutamate antiporter and glutamate transporter 1 isoforms as well as ethanol drinking in male P rats
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Effects of ampicillin on cystine/glutamate antiporter and glutamate transporter 1 isoforms as well as ethanol drinking in male P rats

机译:氨苄青霉素对雄性胱氨酸/谷氨酸抗糖浆和谷氨酸转运蛋白的影响及雄性P大鼠乙醇饮用

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Evidence demonstrated that glial cells, mainly astrocytes, regulate glutamate uptake through several glutamate transporters. Among these glutamate transporters, glutamate transporter 1 (GLT-1; its human homolog is excitatory amino acid transporter-2) is responsible for the majority of glutamate uptake. Cystine-glutamate antiporter (xCT) is another glial protein critical in regulating glutamate transmission. Several studies from our laboratory demonstrated that attenuation of ethanol intkae was associated in part with upregulation of xCT and GLT-1 expression suggesting the important role of these transporters in the treatment of ethanol dependence. We found recently that beta-lactam antibiotic, ampicillin, upregulated GLT-1 expression in the prefrontal cortex (PFC) and nucleus accumbens (NAc) and consequently reduced ethanol intake in alcohol-preferring (P) rats. In this study, we investigated the effects of ampicillin on the expression of xCT and GLT-1 isoforms (GLT-1 a and GLT-1 b) as well as on GLAST expression. We found that ampicillin reduced ethanol intake as compared to the saline (control)-treated group. In addition, we found that ampicillin induced upregulation of xCT, GLT-1a, and GLT-1b expression in both the PFC and NAc, but had no effect on GLAST expression. Our findings provide significant role of ampicillin on upregulating xCT and GLT-1 isoforms expression, might be suggested as possible targets for the attenuation of ethanol consumption.
机译:证据表明,胶质细胞主要是星形胶质细胞,调节谷氨酸摄取通过几种谷氨酸转运蛋白。在这些谷氨酸转运蛋白中,谷氨酸转运蛋白1(glt-1;其人同源物是兴奋性氨基酸转运蛋白-2)负责大多数谷氨酸摄取。胱氨酸 - 谷氨酸altiPorter(XCT)是调节谷氨酸透射率关键的另一种胶质蛋白。我们实验室的几项研究表明,乙醇Intkae的衰减部分与XCT和GLT-1表达的上调有关,表达这些转运蛋白在治疗乙醇依赖中的重要作用。我们最近发现β-内酰胺抗生素,氨苄青霉素,上额叶皮质(PFC)和核常规(NAc)中的上调的Glt-1表达,并因此降低了醇偏好(P)大鼠的乙醇摄入量。在这项研究中,我们研究了氨苄青霉素对XCT和GLT-1同种型(GLT-1A和GLT-1b)表达的影响以及Glast表达。与盐水(对照) - 治疗组相比,我们发现氨苄青霉素降低了乙醇摄入量。此外,我们发现氨苄青霉素在PFC和NAC中诱导XCT,GLT-1A和GLT-1B表达的上调,但对PLAST表达没有影响。我们的发现提供了氨苄青霉素对上调XCT和Glt-1同种型表达的显着作用,可能表明可以作为升高乙醇消耗的靶标。

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