Department of Environmental Sciences, Graduate School of Natural and Applied Sciences, Gazi University, Ankara, Turkey.
Department of Biology, Faculty of Science and Letters, Aksaray University, 68100, Ankara, Turkey.
Ecotoxicology. 2022 Oct;31(8):1217-1230. doi: 10.1007/s10646-022-02579-7. Epub 2022 Sep 5.
Highly persistent perfluorooctane sulfonate (PFOS) is an industrial fluorinated organic chemical with significant bioaccumulation and biomagnification properties. The purpose of this study was to determine the toxic effects of sublethal PFOS on the aquatic invertebrate organism, narrow-clawed crayfish [Astacus leptodactylus Eschscholtz, 1823]. The 96 h LC value was determined as 48.81 mg/L (34.19-63.68 mg/L) with probit analysis. The sublethal experimental design was formed into four groups solvent control (DMSO, dimethyl sulphoxide), non-treated control group, and 1/10 (5 mg/L) and 1/100 (0.5 mg/L) of 96 h LC of PFOS, and crayfish were exposed for 48 h, 7 d, and 21 d under laboratory conditions. Total haemocyte counts (THCs) decreased, while the haemolymph total antioxidant status (TAS) values increased (p < 0.05) after exposure to 0.5 and 5 mg/L PFOS for 48 h, 7 d, and 21 d. Haemolymph total oxidative stress (TOS) levels significantly increased at 5 mg/L PFOS concentration (p < 0.05). Catalase (CAT) activities increased at both concentrations after 48 h and 7 d and then returned to control levels after 21 d; whereas superoxide dismutase (SOD) and glutathione peroxidase (GPX) activities did not change in muscle tissue (p > 0.05). GPX and CAT activities decreased, but SOD activity increased in hepatopancreas tissue (p < 0.05). SOD activity at both concentrations and CAT activity at 5 mg/L PFOS exposure decreased in gill tissue, while GPX activity increased at both concentrations of 48 h and 7 d and returned to control values on day 21 of exposure. Histopathological alterations were detected in hepatopancreas and gill tissues. Lamellar deformations, epithelial hyperplasia, and haemocytic infiltrations were observed in the gill tissues, whereas tubular degeneration, tubule loss, necrosis, and lesions in the hepatopancreas tissues were the major recorded alterations. As a result, the sublethal concentrations of PFOS have toxic effects on crayfish and histologically cause tissue damage. Our findings also support a better understanding of the early toxicological effects of PFOS in freshwater ecosystems. Also, it could be concluded that A. leptodactylus is a reliable model for examining histopathological alterations and differences in enzyme activities together with the haemolymph findings in toxicology studies amid aquatic species.
高持久性全氟辛烷磺酸 (PFOS) 是一种具有重要生物蓄积性和生物放大性的工业含氟有机化学品。本研究的目的是确定亚致死浓度 PFOS 对水生无脊椎动物小龙虾(Astacus leptodactylus Eschscholtz,1823)的毒性影响。通过概率分析确定 96 小时 LC 值为 48.81mg/L(34.19-63.68mg/L)。亚致死实验设计分为四组:溶剂对照组(DMSO,二甲基亚砜)、未处理对照组、以及 1/10(5mg/L)和 1/100(0.5mg/L)的 96 小时 LC 的 PFOS,小龙虾在实验室条件下暴露 48 小时、7 天和 21 天。暴露于 0.5 和 5mg/L PFOS 48 小时、7 天和 21 天后,总血淋巴计数(THC)下降,而血淋巴总抗氧化状态(TAS)值升高(p<0.05)。5mg/L PFOS 浓度下血淋巴总氧化应激(TOS)水平显著升高(p<0.05)。CAT 活性在 48 小时和 7 天后均在两个浓度下升高,然后在 21 天后恢复到对照水平;而肌肉组织中的 SOD 和 GPX 活性没有变化(p>0.05)。肝胰腺组织中 GPX 和 CAT 活性下降,SOD 活性增加(p<0.05)。鳃组织中 SOD 活性在两个浓度下和 CAT 活性在 5mg/L PFOS 暴露下降低,而 GPX 活性在 48 小时和 7 天的两个浓度下增加,并在暴露第 21 天恢复到对照值。在肝胰腺和鳃组织中检测到组织病理学改变。在鳃组织中观察到板层变形、上皮增生和血淋巴细胞浸润,而在肝胰腺组织中主要观察到管状退化、管腔丧失、坏死和病变。因此,亚致死浓度的 PFOS 对小龙虾具有毒性作用,并在组织学上造成组织损伤。我们的研究结果还支持对淡水生态系统中 PFOS 的早期毒理学效应有更好的理解。此外,可以得出结论,A. leptodactylus 是一种可靠的模型,可用于检查水生物种毒理学研究中的组织病理学改变和酶活性差异以及血淋巴发现。