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Neuroprotective effects of rosmarinic acid on ciguatoxin in primary human neurons

机译:迷迭香酸对人原代神经元雪茄毒素的神经保护作用

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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.
机译:Ciguatoxin(CTX)是由微藻类(鞭毛)Gambierdiscus spp。产生的一种有毒化合物,并通过海洋食物链进行了生物积累和生物转化,从而导致神经功能缺损。为了确定CTX介导的人类神经元细胞毒性的机制,我们测量了细胞外乳酸脱氢酶(LDH)活性,烟酰胺腺嘌呤二核苷酸(NAD +)的细胞内水平和139位丝氨酸的H2AX磷酸化,作为人类神经元原代培养物中DNA损伤的一种量度用Pacific(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活性随时间和剂量而增加,同时在5-200 nM的浓度范围内伴随细胞内NAD +水平的下降和DNA损伤的增加。我们还显示,用迷迭香酸(RA)(Heliotropium foertherianum(Boraginaceae)的活性成分)进行预处理和后处理可以减弱CTX介导的神经毒性。这些结果进一步突出了RA在治疗CTX诱导的神经功能缺损中的潜力。

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