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MeBib通过抑制海马体中的BDNF/ERK/CREB信号通路抑制甲基苯丙胺自我给药反应。

MeBib Suppressed Methamphetamine Self-Administration Response via Inhibition of BDNF/ERK/CREB Signal Pathway in the Hippocampus.

作者信息

Kim Buyun, Jha Sonam, Seo Ji Hae, Jeong Chul-Ho, Lee Sooyeun, Lee Sangkil, Seo Young Ho, Park Byoungduck

机构信息

College of Pharmacy, Keimyung University, Daegu 42601, Republic of Korea.

Department of Biochemistry, School of Medicine, Keimyung University, Daegu 42601, Republic of Korea.

出版信息

Biomol Ther (Seoul). 2020 Nov 1;28(6):519-526. doi: 10.4062/biomolther.2020.041.

Abstract

Methamphetamine (MA) is one of the most commonly abused drugs in the world by illegal drug users. Addiction to MA is a serious public health problem and effective therapies do not exist to date. It has also been reported that behavior induced by psychostimulants such as MA is related to histone deacetylase (HDAC). MeBib is an HDAC6 inhibitor derived from a benzimidazole scaffold. Many benzimidazole-containing compounds exhibit a wide range of pharmacological activity. In this study, we investigated whether HDAC6 inhibitor MeBib modulates the behavioral response in MA self-administered rats. Our results demonstrated that the number of active lever presses in MA self-administered rats was reduced by pretreatment with MeBib. In the hippocampus of rats, we also found MA administration promotes GluN2B, an NMDA receptor subunit, expression, which results in sequential activation of ERK/CREB/BDNF pathway, however, MeBib abrogated it. Collectively, we suggest that MeBib prevents the MA seeking response induced by MA administration and therefore, represents a potent candidate as an MA addiction inhibitor.

摘要

甲基苯丙胺(MA)是全球非法吸毒者最常滥用的毒品之一。对MA成瘾是一个严重的公共卫生问题,目前尚无有效的治疗方法。也有报道称,MA等精神兴奋剂诱发的行为与组蛋白脱乙酰酶(HDAC)有关。MeBib是一种源自苯并咪唑支架的HDAC6抑制剂。许多含苯并咪唑的化合物具有广泛的药理活性。在本研究中,我们调查了HDAC6抑制剂MeBib是否能调节MA自身给药大鼠的行为反应。我们的结果表明,用MeBib预处理可减少MA自身给药大鼠的主动压杆次数。在大鼠海马体中,我们还发现给予MA可促进NMDA受体亚基GluN2B的表达,进而导致ERK/CREB/BDNF通路的相继激活,然而,MeBib可消除这种激活。总体而言,我们认为MeBib可预防MA给药诱导的MA寻求反应,因此,它是一种有潜力的MA成瘾抑制剂候选药物。

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