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迷迭香酸对原代人神经元中海藻毒素的神经保护作用。

Neuroprotective effects of rosmarinic acid on ciguatoxin in primary human neurons.

机构信息

Centre for Healthy Brain Ageing, School of Psychiatry, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia,

出版信息

Neurotox Res. 2014 Feb;25(2):226-34. doi: 10.1007/s12640-013-9429-9. Epub 2013 Oct 5.

Abstract

Ciguatoxin (CTX), is a toxic compound produced by microalgae (dinoflagellate) Gambierdiscus spp., and is bio-accumulated and bio-transformed through the marine food chain causing neurological deficits. To determine the mechanism of CTX-mediated cytotoxicity in human neurons, we measured extracellular lactate dehydrogenase (LDH) activity, intracellular levels of nicotinamide adenine dinucleotide (NAD(+)) and H2AX phosphorylation at serine 139 as a measure for DNA damage in primary cultures of human neurons treated with Pacific (P)-CTX-1B and P-CTX-3C. We found these marine toxins can induce a time and dose-dependent increase in extracellular LDH activity, with a concomitant decline in intracellular NAD(+) levels and increased DNA damage at the concentration range of 5-200 nM. We also showed that pre- and post-treatment with rosmarinic acid (RA), the active constituent of the Heliotropium foertherianum (Boraginaceae) can attenuate CTX-mediated neurotoxicity. These results further highlight the potential of RA in the treatment of CTX-induced neurological deficits.

摘要

雪卡毒素(CTX)是由微藻类(甲藻)冈比甲藻属产生的有毒化合物,并通过海洋食物链进行生物积累和生物转化,导致神经功能缺损。为了确定 CTX 介导的人神经元细胞毒性的机制,我们测量了原代培养的人神经元中细胞外乳酸脱氢酶(LDH)活性、烟酰胺腺嘌呤二核苷酸(NAD(+))的细胞内水平以及作为 DNA 损伤标志物的丝氨酸 139 上的 H2AX 磷酸化,这些神经元用太平洋(P)-CTX-1B 和 P-CTX-3C 处理。我们发现这些海洋毒素可以诱导细胞外 LDH 活性的时间和剂量依赖性增加,同时细胞内 NAD(+)水平下降,在 5-200 nM 的浓度范围内增加 DNA 损伤。我们还表明,迷迭香酸(RA),即半日花(紫草科)的活性成分的预处理和后处理可以减轻 CTX 介导的神经毒性。这些结果进一步强调了 RA 在治疗 CTX 诱导的神经功能缺损方面的潜力。

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