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芳樟醇对蜗牛Caucasotachea atrolabiata中枢神经元兴奋性的影响。

The effects of linalool on the excitability of central neurons of snail Caucasotachea atrolabiata.

作者信息

Vatanparast Jafar, Bazleh Sara, Janahmadi Mahyar

机构信息

Department of Biology, Shiraz University, Shiraz, Iran.

Department of Biology, Shiraz University, Shiraz, Iran.

出版信息

Comp Biochem Physiol C Toxicol Pharmacol. 2017 Feb;192:33-39. doi: 10.1016/j.cbpc.2016.12.004. Epub 2016 Dec 6.

Abstract

Linalool is a major constituent of the essential oil of several plant species and possesses several biological activities. In this work, we studied the effects of linalool on excitability of central neurons of land snail Caucasotachea atrolabiata and tried to elucidate the underlying mechanisms. The lower concentration of linalool (0.1mM) showed suppressive action on spontaneous activity and pentylenetetrazole-induced epileptiform activity. These effects were associated with elevation of the action potential threshold and reduction of action potential rising phase, supporting the inhibitory action of linalool on Na channels. At this concentration it also prolonged the post stimulus inhibitory period that can take part in its antiepileptic effect and apparently results from increased action potential duration and indirect augmentation of Ca-activated K currents. At higher concentration, however, linalool (0.4mM) increased the neuronal excitability and induced epileptiform activity. The modulatory effects on action potential waveform during preconvulsive period suggest that the recent effect is mainly dependent on the suppression of outward potassium currents underlying repolarization phase and afterhyperpolarization. The linalool-induced epileptiform activity was abolished by Ca2 channel blockers, nifedipine and nickel chloride, and selective inhibitor of protein kinase C, chelerythrine, suggesting that Ca2 inward currents and protein kinase C (PKC) activity are required for linalool-induced epileptiform activity. Our results support the antiepileptic activity of linalool at lower dose, but it shows epileptogenic activity when applied directly on snail neurons at higher dose. Linalool may also be a potential therapeutic agent for activating PKC.

摘要

芳樟醇是几种植物精油的主要成分,具有多种生物活性。在本研究中,我们研究了芳樟醇对陆地蜗牛高加索阿特罗拉比阿塔中枢神经元兴奋性的影响,并试图阐明其潜在机制。较低浓度的芳樟醇(0.1mM)对自发活动和戊四氮诱导的癫痫样活动具有抑制作用。这些作用与动作电位阈值的升高和动作电位上升相的降低有关,支持了芳樟醇对钠通道的抑制作用。在此浓度下,它还延长了刺激后抑制期,这可能参与其抗癫痫作用,并且显然是由于动作电位持续时间增加和钙激活钾电流的间接增强所致。然而,在较高浓度下,芳樟醇(0.4mM)增加了神经元兴奋性并诱导了癫痫样活动。惊厥前期对动作电位波形的调节作用表明,最近的这种作用主要取决于对复极化期和超极化后外向钾电流的抑制。芳樟醇诱导的癫痫样活动被钙通道阻滞剂硝苯地平和氯化镍以及蛋白激酶C的选择性抑制剂白屈菜红碱所消除,这表明芳樟醇诱导的癫痫样活动需要钙内向电流和蛋白激酶C(PKC)活性。我们的结果支持了低剂量芳樟醇的抗癫痫活性,但当以高剂量直接应用于蜗牛神经元时,它表现出致癫痫活性。芳樟醇也可能是一种激活PKC的潜在治疗剂。

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