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大脑皮层中Arc和Zif268 mRNA的肾上腺素能受体相互依赖性调节

Interdependent adrenergic receptor regulation of Arc and Zif268 mRNA in cerebral cortex.

作者信息

Essali Norah, Sanders Jeff

机构信息

College of Medicine, Texila American University, Georgetown, Guyana.

Department of Pharmacology and Experimental Neuroscience, 985800 Nebraska Medical Center, Omaha, NE 68198-5800, USA.

出版信息

Neurosci Lett. 2016 Jan 26;612:38-42. doi: 10.1016/j.neulet.2015.12.002. Epub 2015 Dec 3.

Abstract

Norepinephrine is a neurotransmitter that signals by stimulating the α1, α2 and β adrenergic receptor (AR). We determined the role of these receptors in regulating the immediate early genes, Activity Regulated Cytoskeleton Associated Protein (Arc) and Zif268 in the rat cerebral cortex. RX821002, an α2-AR antagonist, produced Arc and Zif268 elevations across cortical layers. Next we examined the effects of delivering RX821002 with an α1-AR antagonist, prazosin, and a β-AR antagonist, propranolol. RX821002 given with a prazosin and propranolol cocktail, or with each of these antagonists individually, decreased Arc and Zif268 to saline-treated control levels in most cortical layers. Arc and Zif268 levels were also similar to saline-treated control levels when rats were given a prazosin and propranolol cocktail alone, or when each of these antagonists were delivered individually. Taken together, these data reveal that α2-AR uniquely exert a tonic inibitory regulation of both Arc and Zif268 compared to α1 and β-AR. However, the ability of RX821002 to increase Arc and Zif268 is interdependent with α1 and β-AR signaling.

摘要

去甲肾上腺素是一种神经递质,通过刺激α1、α2和β肾上腺素能受体(AR)来传递信号。我们确定了这些受体在调节大鼠大脑皮层即刻早期基因、活性调节细胞骨架相关蛋白(Arc)和Zif268中的作用。α2-AR拮抗剂RX821002使整个皮层各层的Arc和Zif268水平升高。接下来,我们研究了将RX821002与α1-AR拮抗剂哌唑嗪和β-AR拮抗剂普萘洛尔联合使用的效果。将RX821002与哌唑嗪和普萘洛尔的混合物一起给药,或者分别与这两种拮抗剂单独给药,在大多数皮层层中,Arc和Zif268水平降低至生理盐水处理的对照水平。当大鼠单独给予哌唑嗪和普萘洛尔混合物,或者单独给予这两种拮抗剂中的任何一种时,Arc和Zif268水平也与生理盐水处理的对照水平相似。综上所述,这些数据表明,与α1和β-AR相比,α2-AR对Arc和Zif268具有独特的紧张性抑制调节作用。然而,RX821002增加Arc和Zif268的能力与α1和β-AR信号传导相互依赖。

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