首页> 外文期刊>Toxicon: An International Journal Devoted to the Exchange of Knowledge on the Poisons Derived from Animals, Plants and Microorganisms >Multi-xenobiotic-resistance a possible explanation for the insensitivity of bivalves towards cyanobacterial toxins
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Multi-xenobiotic-resistance a possible explanation for the insensitivity of bivalves towards cyanobacterial toxins

机译:多异源抗药性可能是双壳类动物对蓝细菌毒素不敏感的原因

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摘要

Filterfeeders, such as bivalves, are highly affected during toxic cyanobacterial blooms, as they are non-selective and may use the cyanobacteria as main nutrition source. The freshwater mussel Dreissena polymorpha, living in lakes and rivers coexisting with cyanobacteria, was exposed to 100 mug L(-1) microcystin-LR (MC-LR) for up to three days. MC-LR concentration in mussel tissue and surrounding media was quantified by HPLC-PDA during uptake and depuration phase, revealing an immediate, continuous uptake, and release of non-metabolized toxin, and occurrence of reincorporation. The involvement of multi-xenobiotic-resistance protein (P-glycoprotein, P-gp) on the excretion of MC-LR was evidenced by efflux and accumulation version of the Rhodamine Assay as well as on P-gp gene expression. P-gp expression was enhanced after 1 h exposure but no changes were detected after longer (72 h) exposure. P-gp enzyme activity showed a significant increase with exposure time, supporting the hypothesis that P-gp is involved in the excretion of MC-LR. Induction of biotransformation enzyme such as pi-class glutathione S-transferase (piGST) and antioxidant enzyme catalase (CAT) was immediately inhibited and returned to control values only after more than 72 h expose time. Heat shock protein 70 (hsp70) and protein phosphatase 2A (PP2A) gene expression was not changed due to the treatment with cyanobacterial toxin MC-LR.
机译:滤嘴喂食器,例如双壳类,在有毒的蓝细菌繁殖期间受到严重影响,因为它们是非选择性的,并且可能使用蓝细菌作为主要营养来源。生活在与蓝细菌共存的湖泊和河流中的淡水贻贝Dreissena polymorpha,暴露于100杯L(-1)微囊藻毒素-LR(MC-LR)中长达三天。在吸收和纯化阶段,通过HPLC-PDA对贻贝组织和周围介质中的MC-LR浓度进行定量,显示立即,连续吸收和释放未代谢的毒素,并发生再结合。罗丹明分析的外排和积累形式以及P-gp基因表达证明了多异源抗药性蛋白(P-糖蛋白,P-gp)参与MC-LR的排泄。暴露1 h后P-gp表达增强,但长时间(72 h)暴露后未检测到变化。 P-gp酶活性随暴露时间显着增加,支持了P-gp参与MC-LR排泄的假设。 pi类谷胱甘肽S转移酶(piGST)和抗氧化酶过氧化氢酶(CAT)等生物转化酶的诱导被立即抑制,并且仅在暴露时间超过72小时后才恢复到控制值。热休克蛋白70(hsp70)和蛋白磷酸酶2A(PP2A)基因表达没有改变,因为用蓝细菌毒素MC-LR处理。

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