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乙醛通过多种细胞机制激发外侧缰核神经元。

Acetaldehyde Excitation of Lateral Habenular Neurons via Multiple Cellular Mechanisms.

机构信息

Department of Anesthesiology, Pharmacology and Physiology, & Neuroscience Rutgers, The State University of New Jersey, New Jersey Medical School, Newark, New Jersey, 07103.

Department of Physiology, and Pharmacology, Medical College, Jinan University, Guangzhou, 510632 China.

出版信息

J Neurosci. 2021 Sep 8;41(36):7532-7545. doi: 10.1523/JNEUROSCI.2913-20.2021. Epub 2021 Jul 29.

Abstract

Acetaldehyde (ACD), the first metabolite of ethanol, is implicated in several of ethanol's actions, including the reinforcing and aversive effects. The neuronal mechanisms underlying ACD's aversive effect, however, are poorly understood. The lateral habenula (LHb), a regulator of midbrain monoaminergic centers, is activated by negative valence events. Although the LHb has been linked to the aversive responses of several abused drugs, including ethanol, little is known about ACD. We, therefore, assessed ACD's action on LHb neurons in rats. The results showed that intraperitoneal injection of ACD increased cFos protein expression within the LHb and that intra-LHb infusion of ACD induced conditioned place aversion in male rats. Furthermore, electrophysiological recording in brain slices of male and female rats showed that bath application of ACD facilitated spontaneous firing and glutamatergic transmission. This effect of ACD was potentiated by an aldehyde dehydrogenase (ALDH) inhibitor, disulfiram (DS), but attenuated by the antagonists of dopamine (DA) receptor (DAR) subtype 1 (SCH23390) and subtype 2 (raclopride), and partly abolished by the pretreatment of DA or DA reuptake blocker (GBR12935; GBR). Moreover, application of ACD initiated a depolarizing inward current () and enhanced the hyperpolarizing-activated currents in LHb neurons. Bath application of Rp-cAMPs, a selective cAMP-PKA inhibitor, attenuated ACD-induced potentiation of EPSCs and Finally, bath application of ZD7288, a selective blocker of hyperpolarization-activated cyclic nucleotide-gated channels, attenuated ACD-induced potentiation of firing, EPSCs, and These results show that ACD exerts its aversive property by exciting LHb neurons via multiple cellular mechanisms, and new treatments targeting the LHb may be beneficial for alcoholism. Acetaldehyde (ACD) has been considered aversive peripherally and rewarding centrally. However, whether ACD has a central aversive property is unclear. Here, we report that ACD excites the lateral habenula (LHb), a brain region associated with aversion and negative valence, through multiple cellular and molecular mechanisms. Intra-LHb ACD produces significant conditioned place aversion. These results suggest that ACD's actions on the LHb neurons might contribute to its central aversive property and new treatments targeting the LHb may be beneficial for alcoholism.

摘要

乙醛(ACD)是乙醇的第一代谢物,与乙醇的几种作用有关,包括强化和厌恶作用。然而,ACD 厌恶作用的神经机制知之甚少。外侧缰核(LHb)是中脑单胺能中心的调节剂,对负价事件激活。尽管 LHb 与包括乙醇在内的几种滥用药物的厌恶反应有关,但对 ACD 的了解甚少。因此,我们评估了 ACD 在大鼠 LHb 神经元中的作用。结果表明,腹腔注射 ACD 可增加 LHb 中的 cFos 蛋白表达,并且 LHb 内输注 ACD 可诱导雄性大鼠形成条件性位置厌恶。此外,对雄性和雌性大鼠脑片的电生理记录显示,ACD 孵育可促进自发放电和谷氨酸能传递。这种 ACD 作用被醛脱氢酶(ALDH)抑制剂双硫仑(DS)增强,但被多巴胺(DA)受体(DAR)亚型 1(SCH23390)和亚型 2(raclopride)拮抗剂减弱,并部分被 DA 或 DA 再摄取阻滞剂(GBR12935;GBR)预处理消除。此外,ACD 引发去极化内向电流()并增强 LHb 神经元中的超极化激活电流。cAMP-PKA 选择性抑制剂 Rp-cAMPs 的灌流减弱了 ACD 诱导的 EPSCs 的增强作用。最后,超极化激活环核苷酸门控通道的选择性阻断剂 ZD7288 的灌流减弱了 ACD 诱导的放电、EPSCs 和的增强作用。这些结果表明,ACD 通过多种细胞机制兴奋 LHb 神经元,发挥其厌恶特性,针对 LHb 的新治疗方法可能有益于治疗酒精中毒。乙醛(ACD)在外周被认为是厌恶的,而在中枢则是奖赏的。然而,ACD 是否具有中枢厌恶特性尚不清楚。在这里,我们报告 ACD 通过多种细胞和分子机制兴奋与厌恶和负价相关的外侧缰核(LHb)。LHb 内 ACD 产生显著的条件性位置厌恶。这些结果表明,ACD 对 LHb 神经元的作用可能有助于其中枢厌恶特性,针对 LHb 的新治疗方法可能有益于治疗酒精中毒。

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