Pinho G L L, Moura da Rosa C, Yunes J S, Luquet C M, Bianchini A, Monserrat J M
Departamento de Ciências Fisiológicas, Fundação Universidade Federal do Rio Grande, R. Eng Alfredo Huch 475, Rio Grande 96201-900, Brazil.
Comp Biochem Physiol C Toxicol Pharmacol. 2003 Aug;135(4):459-68. doi: 10.1016/s1532-0456(03)00147-9.
Microcystins are toxins produced by cyanobacteria, being toxic to aquatic fauna. It was evaluated alternative mechanisms of microcystins toxicity, including oxidative stress and histopathology in the hepatopancreas of the estuarine crab Chasmagnathus granulatus (Decapoda, Grapsidae). Microcystins was administered to crabs (MIC group) over 1 week, whereas the control (CTR group) received the saline from cyanobacteria culture medium. At day 7, catalase activity was higher in the MIC than in the CTR group, although a decrease of activity was verified in both groups with respect to time 0. Glutathione-S-transferase activity augmented in MIC with respect to CTR, suggesting a higher conjugation rate of the toxins with glutathione. No differences were detected in the superoxide dismutase activity. Lipid peroxidation remained stable in both groups. Histopathological analyses showed that the number of B cells decreased significantly in the CTR as a possible effect of starvation, while no significant change was observed in the MIC group. The hepatopancreas from the MIC group exhibited some necrotic tubules and melanin-like deposits. Overall, results showed that some enzymes of the antioxidant defense system were activated after microcystins exposure, this response being able to maintain lipid peroxidation levels, but insufficient to completely prevent histological damage.
微囊藻毒素是蓝藻产生的毒素,对水生动物有毒。研究评估了微囊藻毒素毒性的其他机制,包括对河口蟹颗粒巨螯蟹(十足目,方蟹科)肝胰腺的氧化应激和组织病理学影响。微囊藻毒素在1周内给予螃蟹(MIC组),而对照组(CTR组)接受来自蓝藻培养基的盐水。在第7天,MIC组的过氧化氢酶活性高于CTR组,尽管两组相对于0时刻的活性均有所下降。与CTR组相比,MIC组的谷胱甘肽 - S - 转移酶活性增强,表明毒素与谷胱甘肽的结合率更高。超氧化物歧化酶活性在两组中未检测到差异。两组的脂质过氧化均保持稳定。组织病理学分析表明,CTR组中B细胞数量显著减少,可能是饥饿的影响,而MIC组未观察到显著变化。MIC组的肝胰腺表现出一些坏死小管和类黑色素沉积。总体而言,结果表明微囊藻毒素暴露后抗氧化防御系统的一些酶被激活,这种反应能够维持脂质过氧化水平,但不足以完全防止组织学损伤。