US EPA, ORD, National Health and Environmental Effects Research Laboratory, Research Triangle Park, NC 27711, USA.
J Appl Toxicol. 2011 Apr;31(3):242-54. doi: 10.1002/jat.1586. Epub 2010 Oct 8.
Cylindrospermopsin (CYN) is a tricyclic alkaloid toxin produced by fresh water cyanobacterial species worldwide. CYN has been responsible for both livestock and human poisoning after oral exposure. This study investigated the toxicity of CYN to pregnant mice exposed during different segments of gestation. The course of recovery and individual responses to the toxin were evaluated. Adverse effects of CYN were monitored up to 7 weeks post-dosing by clinical examination, histopathology, biochemistry and gene expression. Exposure on gestational days (GD) 8-12 induced significantly more lethality than GD13-17 exposure. Periorbital, gastrointestinal and distal tail hemorrhages were seen in both groups. Serum markers indicative of hepatic injury (alanine amino transferase, aspartate amino transferase and sorbitol dehydrogenase) were increased in both groups; markers of renal dysfunction (blood urea nitrogen and creatinine) were elevated in the GD8-12 animals. Histopathology was observed in the liver (centrilobular necrosis) and kidney (interstitial inflammation) in groups exhibiting abnormal serum markers. The expression profiles of genes involved in ribosomal biogenesis, xenobiotic and lipid metabolism, inflammatory response and oxidative stress were altered 24 h after the final dose. One week after dosing, gross, histological and serum parameters had returned to normal, although increased liver/body weight ratio and one instance of gastrointestinal bleeding was found in the GD13-17 group. Gene expression changes persisted up to 2 weeks post-dosing and returned to normal by 4 weeks. Responses of individual animals to CYN exposure indicated highly significant inter-animal variability within the treated groups.
柱孢藻毒素(CYN)是一种三环生物碱毒素,由世界各地的淡水蓝藻物种产生。CYN 曾导致动物和人类在口服暴露后中毒。本研究调查了 CYN 对不同妊娠阶段暴露的怀孕小鼠的毒性。评估了恢复过程和个体对毒素的反应。通过临床检查、组织病理学、生物化学和基因表达监测 CYN 的不良反应,直至给药后 7 周。在 GD13-17 暴露的基础上,GD8-12 暴露导致的致死率显著增加。两组均出现眶周、胃肠道和尾端远端出血。两组血清标志物均升高,表明肝损伤(丙氨酸氨基转移酶、天冬氨酸氨基转移酶和山梨醇脱氢酶);GD8-12 动物的肾功能障碍标志物(血尿素氮和肌酐)升高。在表现出异常血清标志物的组中观察到肝脏(中央小叶坏死)和肾脏(间质炎症)的组织病理学变化。在最后一次给药后 24 小时,参与核糖体生物发生、异生物质和脂质代谢、炎症反应和氧化应激的基因表达谱发生改变。给药后一周,大体、组织学和血清参数恢复正常,但在 GD13-17 组发现肝/体重比增加和一例胃肠道出血。基因表达变化持续至给药后 2 周,并在 4 周时恢复正常。个别动物对 CYN 暴露的反应表明,处理组内动物间存在高度显著的个体间变异性。