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血管紧张素 II AT₁ 受体参与了安非他命在双注射方案中引起的神经元激活。

Angiotensin II AT₁ receptors are involved in neuronal activation induced by amphetamine in a two-injection protocol.

机构信息

Departamento de Farmacología, Facultad de Ciencias Químicas Universidad Nacional de Córdoba, Instituto de Farmacología Experimental Córdoba (IFEC-CONICET), 5000 Córdoba, Argentina.

出版信息

Biomed Res Int. 2013;2013:534817. doi: 10.1155/2013/534817. Epub 2013 Sep 8.

DOI:10.1155/2013/534817
PMID:24089683
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3780567/
Abstract

It was already found that Ang II AT₁ receptors are involved in the neuroadaptative changes induced by a single exposure to amphetamine, and such changes are related to the development of behavioral and neurochemical sensitization. The induction of the immediately early gene c-fos has been used to define brain activated areas by amphetamine. Our aim was to evaluate the participation of AT₁ receptors in the neuronal activation induced by amphetamine sensitization. The study examined the c-fos expression in mesocorticolimbic areas induced by amphetamine challenge (0.5 mg/kg i.p) in animals pretreated with candesartan, a selective AT₁ receptor blocker (3 mg/kg p.o × 5 days), and amphetamine (5 mg/kg i.p) 3 weeks before the challenge. Increased c-fos immunoreactivity was found in response to the amphetamine challenge in the dorsomedial caudate-putamen and nucleus accumbens, and both responses were blunted by the AT₁ receptor blocker pretreatment. In the infralimbic prefrontal cortex, increased c-fos immunoreactivity was found in response to amphetamine and saline challenge, and both were prevented by the AT₁ receptor blocker. No differences were found neither in ventral tegmental area nor prelimbic cortex between groups. Our results indicate an important role for brain Ang II in the behavioral and neuronal sensitization induced by amphetamine.

摘要

已经发现,血管紧张素 II AT₁ 受体参与了单次接触安非他命引起的神经适应性变化,而这种变化与行为和神经化学敏化的发展有关。即刻早期基因 c-fos 的诱导已被用于通过安非他命定义大脑激活区域。我们的目的是评估 AT₁ 受体在安非他命敏化引起的神经元激活中的参与。该研究检查了预先用坎地沙坦(一种选择性 AT₁ 受体阻滞剂,3mg/kg po×5 天)预处理的动物在安非他命(0.5mg/kg ip)挑战时中脑边缘皮质区的 c-fos 表达,安非他命(5mg/kg ip)在挑战前 3 周。在背侧纹状体和伏隔核中,安非他命挑战引起 c-fos 免疫反应性增加,而这两种反应均被 AT₁ 受体阻滞剂预处理所减弱。在边缘下前额皮质中,安非他命和盐水挑战均引起 c-fos 免疫反应性增加,而这两种反应均被 AT₁ 受体阻滞剂所阻止。在腹侧被盖区和前扣带回皮层中,各组之间均未发现差异。我们的结果表明,脑内血管紧张素 II 在安非他命引起的行为和神经元敏化中起着重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46da/3780567/3ff10ec1647f/BMRI2013-534817.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46da/3780567/43987621c361/BMRI2013-534817.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46da/3780567/dec6d7f0e6bf/BMRI2013-534817.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46da/3780567/f37f8c8a56f8/BMRI2013-534817.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46da/3780567/3ff10ec1647f/BMRI2013-534817.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46da/3780567/43987621c361/BMRI2013-534817.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46da/3780567/dec6d7f0e6bf/BMRI2013-534817.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46da/3780567/f37f8c8a56f8/BMRI2013-534817.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46da/3780567/3ff10ec1647f/BMRI2013-534817.004.jpg

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