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双黄酮类化合物对昆虫神经元细胞钾电流的毒性和生理作用。

Toxicity and physiological actions of biflavones on potassium current in insect neuronal cells.

机构信息

Key Laboratory of Coarse Cereal Processing of Ministry of Agriculture and Rural Affairs, College of Pharmacy and Biological Engineering, Chengdu University, Chengdu, Sichuan, China; Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, Sichuan, China.

Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, Sichuan, China.

出版信息

Pestic Biochem Physiol. 2021 Jan;171:104735. doi: 10.1016/j.pestbp.2020.104735. Epub 2020 Oct 16.

Abstract

Stellera chamaejasme L. is a Chinese traditional herb. It has a long history and many medicinal usages. Biflavones, one of the main active ingredients in S. chamaejasme's roots, possess excellent insecticidal activities both in vivo and in vitro. However, the mechanism of these compounds and its potential molecular targets on insect cell were still not clear. Here the whole cell patch clamp technique was used to investigate whether biflavones affects voltage-gated potassium channels (Kv) on insect neuronal cells (AW1 and WG2). The results confirmed that both the three biflavones: neochamaejasmin A (NCA), neochamaejasmin B (NCB) and isochamaejasmin A (ICM) can significantly inhibit the A-type potassium current (I) than delayed rectifier potassium current (I) expressed on insect cells. Moreover, ICM stood out as the strongest inhibition activity on I with IC value of 106.75 μM. Multiple results suggest that the inhibition of potassium current was related to the gating modification of biflavones. ICM produced concentration dependent hyperpolarizing shifts in the voltage dependence of channel steady-state activation and inactivation. Maximal shifts of the ICM-induced V, were -15.1 mV for activation and -6.93 mV for inactivation. ICM also prolonged recovery from inactivation of current. Moreover, the biflavones could inhibited AW1 cell survival in both dose- and time-dependent manners with well correlation of K inhibitory activity. Our study showed that biflavones from S. chamaejasme exhibiting significant blocked effects on Kv of AW1 cells and inhibited cell proliferation. These findings may not only show the toxic mechanisms of biflavones on insect cells, but also suggest that Kv channel play an important role in biflavones' mode of action and may be the new targets for designing novel insecticides.

摘要

瑞香狼毒 L. 是一种中国传统草药。它具有悠久的历史和多种药用用途。双黄酮类化合物是瑞香狼毒根的主要活性成分之一,具有良好的体内外杀虫活性。然而,这些化合物的作用机制及其对昆虫细胞的潜在分子靶点尚不清楚。本研究采用全细胞膜片钳技术研究双黄酮类化合物是否影响昆虫神经元细胞 (AW1 和 WG2) 上的电压门控钾通道 (Kv)。结果证实,三种双黄酮类化合物:新瑞香素 A(NCA)、新瑞香素 B(NCB)和异瑞香素 A(ICM)均能显著抑制昆虫细胞表达的 A 型钾电流(I),而非延迟整流钾电流(I)。此外,ICM 对 I 的抑制活性最强,IC 值为 106.75 μM。多项结果表明,钾电流的抑制与双黄酮类化合物的门控修饰有关。ICM 使通道稳态激活和失活的电压依赖性发生浓度依赖性超极化偏移。最大的 ICM 诱导 V 偏移为激活时为-15.1 mV,失活时为-6.93 mV。ICM 还延长了电流的失活恢复。此外,双黄酮类化合物以剂量和时间依赖的方式抑制 AW1 细胞存活,与 K 抑制活性具有良好的相关性。本研究表明,瑞香狼毒中的双黄酮类化合物对 AW1 细胞 Kv 具有显著的阻断作用,并抑制细胞增殖。这些发现不仅表明双黄酮类化合物对昆虫细胞的毒性机制,而且提示 Kv 通道在双黄酮类化合物的作用模式中发挥重要作用,可能成为设计新型杀虫剂的新靶点。

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