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从莲(Nelumbo nucifera Gaertn)中分离并鉴定出一种三苄基异喹啉生物碱,一种新型潜在的平滑肌松弛剂。

Isolation and identification of a tribenzylisoquinoline alkaloid from Nelumbo nucifera Gaertn, a novel potential smooth muscle relaxant.

作者信息

Yang Guang-Ming, Sun Jie, Pan Yang, Zhang Jun-Li, Xiao Min, Zhu Min-Sheng

机构信息

School of Pharmacy, Nanjing University of Chinese Medicine, 138 Xianlin Avenue, Qixia District, Nanjing 210023, China.

Model Animal Research Center and MOE Key Laboratory of Animal Models of Disease, Nanjing University, 12 Xuefu Road, Pukou District, Nanjing 210061, China.

出版信息

Fitoterapia. 2018 Jan;124:58-65. doi: 10.1016/j.fitote.2017.10.020. Epub 2017 Nov 3.

DOI:10.1016/j.fitote.2017.10.020
PMID:29108933
Abstract

A new skeleton benzylisoquinoline (BI) named neoliensinine (1) was isolated from embryos of lotus seed (Nelumbo nucifera Gaertn.), a traditional Chinese herb. The tribenzylisoquinoline (TBI) structure of 1 was confirmed by interpreting spectroscopic data of UV, IR, MS, 1D and 2D NMR. The stereo-configurations of the new compound, together with two known bisbenzylisoquinolines (BBI), neferine and isoliensinine were established by analyzing H NMR and C NMR spectra. The relaxation of 1, neferine, isoliensinine and liensinine in isolated mesenteric vascular smooth muscle (VSM) was evaluated. All the four BIs could efficiently inhibit MVSM contraction induced by 124mM KCl, with IC values of 2.407μM (1), 1.169μM (neferine), 3.504μM (isoliensinine) and 3.583μM (liensinine), respectively, suggesting that they were all potential relaxants for abnormal smooth muscle contractions. Interestingly, VSM treated by the three BBIs could re-contract when being stimulated by KCl after the drugs were removed, while VSM dealt with the TBI couldn't. It indicated that 1 has much high affinity with the molecular targets on relaxation of VSM contraction, which may relate to the unique skeleton with three BI groups.

摘要

从传统中药莲子(Nelumbo nucifera Gaertn.)的胚中分离出一种新的骨架苄基异喹啉(BI),命名为新莲心碱(1)。通过对紫外、红外、质谱、一维和二维核磁共振光谱数据的解析,确定了1的三苄基异喹啉(TBI)结构。通过分析氢核磁共振和碳核磁共振光谱,确定了新化合物以及两种已知的双苄基异喹啉(BBI)——莲心碱和异莲心碱的立体构型。评估了1、莲心碱、异莲心碱和莲心宁碱对离体肠系膜血管平滑肌(VSM)的舒张作用。这四种BIs均能有效抑制124mM氯化钾诱导的MVSM收缩,其IC值分别为2.407μM(1)、1.169μM(莲心碱)、3.504μM(异莲心碱)和3.583μM(莲心宁碱),表明它们都是异常平滑肌收缩的潜在舒张剂。有趣的是,用三种BBI处理过的VSM在去除药物后受到氯化钾刺激时会再次收缩,而用TBI处理过的VSM则不会。这表明1与VSM收缩舒张的分子靶点具有很高的亲和力,这可能与具有三个BI基团的独特骨架有关。

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