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在补充钠和耗尽钠的大鼠舔食 NaCl 溶液过程中,多巴胺 D1 样和 D2 样受体可能在行为激活和“效价”奖赏评估中发挥作用。

Possible role of dopamine D1-like and D2-like receptors in behavioural activation and "contingent" reward evaluation in sodium-replete and sodium-depleted rats licking for NaCl solutions.

机构信息

Dipartimento di Scienze del Farmaco, Università di Sassari, Sassari, Italy.

出版信息

Pharmacol Biochem Behav. 2012 Mar;101(1):99-106. doi: 10.1016/j.pbb.2011.12.004. Epub 2011 Dec 14.

Abstract

Based on the different effects of the dopamine D1-like and D2-like receptor antagonists SCH 23390 and raclopride on the measures of licking microstructure in rats, we suggested that the level of activation of reward-associated responses depends on dopamine D1-like receptor stimulation, and is updated, or "reboosted", on the basis of a dopamine D2-like receptor-mediated reward evaluation. To further test this hypothesis, we examined the effects of the dopamine D2-like receptor antagonist raclopride (0, 25, 125, 250μg/kg) and of the dopamine D1-like receptor antagonist SCH 23390 (0, 10, 20 and 40μg/kg) on the microstructure of licking for two different NaCl solutions (0.9% and 2.7%) in rats in sodium-replete status and in the sodium-depleted status induced by the diuretic drug furosemide. Rats were exposed to each solution for 180 seconds after the first lick. Both in sodium-replete and in sodium-depleted status, SCH 23390 produced a decrease of burst number, a measure of behavioural activation, without affecting their size, a measure of reward evaluation. Raclopride reduced burst number but appeared also to exert some effects on burst size. Sodium depletion resulted in an increased intake for both NaCl solutions due to an increase in burst number and size, and in a reduced sensitivity to the effect of raclopride on lick number. These results are not in contrast with the proposed hypothesis and are consistent with previous evidence suggesting a role for dopamine D2-like receptors in the increased NaCl appetite induced by sodium depletion.

摘要

基于多巴胺 D1 样和 D2 样受体拮抗剂 SCH 23390 和 raclopride 对大鼠舔舐微观结构测量的不同影响,我们认为与奖励相关反应的激活水平取决于多巴胺 D1 样受体的刺激,并基于多巴胺 D2 样受体介导的奖励评估进行更新或“重新增强”。为了进一步检验这一假设,我们检查了多巴胺 D2 样受体拮抗剂 raclopride(0、25、125、250μg/kg)和多巴胺 D1 样受体拮抗剂 SCH 23390(0、10、20 和 40μg/kg)对舔舐两种不同 NaCl 溶液(0.9%和 2.7%)微观结构的影响,这些溶液在呋塞米诱导的钠充足状态和钠耗竭状态下的大鼠中使用。大鼠在第一次舔舐后,暴露于每种溶液 180 秒。在钠充足和钠耗竭状态下,SCH 23390 均降低了爆发次数(行为激活的测量),而不影响其大小(奖励评估的测量)。Raclopride 降低了爆发次数,但似乎也对爆发大小产生了一些影响。钠耗竭导致两种 NaCl 溶液的摄入量增加,原因是爆发次数和大小增加,以及对 raclopride 对舔食次数影响的敏感性降低。这些结果与提出的假设并不矛盾,并且与先前的证据一致,即多巴胺 D2 样受体在钠耗竭诱导的 NaCl 食欲增加中起作用。

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