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在曾暴露于安非他命的大鼠的伏隔核核心中,运动敏化由 ghrelin 和 D1 多巴胺受体激动剂表达。

Locomotor sensitization is expressed by ghrelin and D1 dopamine receptor agonist in the nucleus accumbens core in amphetamine pre-exposed rat.

机构信息

Department of Physiology, Brain Korea 21 Plus Project for Medical Science, Brain Research Institute, Yonsei University College of Medicine, Seoul, South Korea.

出版信息

Addict Biol. 2018 May;23(3):849-856. doi: 10.1111/adb.12533. Epub 2017 Jun 21.

Abstract

Ghrelin modulates mesolimbic dopaminergic pathways in the brain in addition to its role in feeding. We investigated what roles ghrelin in the nucleus accumbens (NAcc) core may play in mediating locomotor activating effects of amphetamine (AMPH). First, when rats were administered with AMPH (1 mg/kg, i.p.) following a bilateral microinjection of ghrelin (0.1 or 0.5 μg/side) into the NAcc core, their locomotor activity was significantly enhanced, while these effects were blocked by co-microinjection of ghrelin receptor antagonist (0.5 μg/side) into this site. Second, we pre-exposed rats to saline or amphetamine (1 mg/kg, i.p.) every 2 to 3 days for a total of four times. After 2 weeks of drug-free withdrawal period, we examined the effect of saline, ghrelin (0.5 μg/side), D1 dopamine receptor agonist, SKF81297 (0.5 μg/side) or ghrelin (0.5 μg/side) + SKF81297 (0.5 μg/side) directly microinjected into the NAcc core on locomotor activity. When we measured rats' locomotor activity for 1 hour immediately following microinjections, only ghrelin + SKF81297 produces sensitized locomotor activity, while all others have no effects. These results suggest that ghrelin may have a distinct role in the NAcc core to provoke the sensitized locomotor activity induced by psychomotor stimulants, and further, it may produce these effects by interaction with D1 dopamine receptors.

摘要

除了在进食中发挥作用外,Ghrelin 还可以调节大脑中的中脑边缘多巴胺能通路。我们研究了 Ghrelin 在伏隔核核心(NAcc)中的作用可能在介导安非他命(AMPH)的运动激活作用中发挥的作用。首先,当大鼠在 NAcc 核心双侧微量注射 Ghrelin(0.1 或 0.5μg/侧)后给予 AMPH(1mg/kg,ip)时,其运动活性显著增强,而这些作用被该部位共微量注射 Ghrelin 受体拮抗剂(0.5μg/侧)所阻断。其次,我们每隔 2-3 天给大鼠预先暴露于盐水或安非他命(1mg/kg,ip),总共 4 次。在 2 周的无药物戒断期后,我们检查了盐水、Ghrelin(0.5μg/侧)、D1 多巴胺受体激动剂 SKF81297(0.5μg/侧)或 Ghrelin(0.5μg/侧)+SKF81297(0.5μg/侧)直接微量注射到 NAcc 核心对运动活性的影响。当我们在微注射后立即测量大鼠 1 小时的运动活性时,只有 Ghrelin+SKF81297 产生了敏化的运动活性,而其他所有物质都没有影响。这些结果表明,Ghrelin 可能在 NAcc 核心中具有独特的作用,以引发精神兴奋剂引起的敏化运动活性,而且它可能通过与 D1 多巴胺受体的相互作用产生这些作用。

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