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荜澄茄精油成分对 Novikoff 肝癌细胞活力和通过 Cx43 缝隙连接通讯的影响。

The effect of nutmeg essential oil constituents on Novikoff hepatoma cell viability and communication through Cx43 gap junctions.

机构信息

Institute of Cardiology, Lithuanian University of Health Sciences, Kaunas LT-50162, Lithuania.

Department of Drug Technology and Social Pharmacy, Lithuanian University of Health Sciences, Kaunas LT 50162, Lithuania; Institute of Pharmaceutical Technologies, Lithuanian University of Health Sciences, Kaunas LT-50162, Lithuania.

出版信息

Biomed Pharmacother. 2021 Mar;135:111229. doi: 10.1016/j.biopha.2021.111229. Epub 2021 Feb 1.

Abstract

Essential oils from plants are a potential source of molecules having anti-inflammatory, anticancer, cardiotropic, and other activities. However, most of these effects lack mechanistic explanations and structure-activity relationship testing. In the present study, we: 1) identified the nutmeg essential oil (NEO) composition; 2) using molecular docking, we determined the putative regulatory binding sites on the connexin 43 (Cx43) that is responsible for gap junction-dependent intercellular communication (GJIC) in the majority of tissues; 3) examined the effect of NEO and its three constituents - sabinene, α-pinene, and α-copaene - on GJ conductance and gating in Novikoff cells expressing endogenous Cx43; and 4) verified whether NEO effects on GJIC correlated with its action on Novikoff cell viability, proliferation, and colony formation capability. Our results revealed NEO and its constituents as potent and efficient Cx43 GJ inhibitors acting by slow gating mechanism. In addition, NEO reduced Novikoff hepatoma cell viability, proliferation, and colony formation capability; however, this was achieved at higher doses and was unrelated to its effects on GJIC.

摘要

植物精油是具有抗炎、抗癌、心脏保护等活性的分子的潜在来源。然而,这些作用大多数缺乏机制解释和构效关系测试。在本研究中,我们:1)鉴定肉豆蔻精油(NEO)的组成;2)通过分子对接,确定负责大多数组织中间隙连接依赖性细胞间通讯(GJIC)的连接蛋白 43(Cx43)上的假定调节结合位点;3)检测 NEO 及其三种成分 - 柠檬烯、α-蒎烯和α-古巴烯 - 对表达内源性 Cx43 的 Novikoff 细胞 GJ 电导和门控的影响;4)验证 NEO 对 GJIC 的作用是否与其对 Novikoff 肝癌细胞活力、增殖和集落形成能力的作用相关。我们的结果表明,NEO 及其成分是有效的 Cx43 GJ 抑制剂,作用机制为缓慢门控机制。此外,NEO 降低了 Novikoff 肝癌细胞活力、增殖和集落形成能力;然而,这是在更高剂量下实现的,与 GJIC 无关。

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