Saxena Vaishnavi, Bakhasha Jumman, Arya Neeti, Singh Rashmi, Singh Raveena, Khan Rubina, Singh Ritu, Trivedi Sunil P, Kumar Manoj, Yadav Kamlesh K, Trivedi Abha
Toxicogenomics Laboratory, Department of Animal Science, M. J. P. Rohilkhand University, Bareilly, 243006, India.
Department of Zoology, Lucknow University, Lucknow, 226007, India.
Fish Physiol Biochem. 2025 Feb;51(1):26. doi: 10.1007/s10695-024-01434-2. Epub 2024 Dec 15.
Cadmium pollution is a major environmental issue threatening aquatic ecosystems and the health of aquatic organisms. Our study examines cadmium toxicity at different levels, highlighting pyroptotic cell death in the freshwater fish Channa punctatus (spotted snakehead). For this purpose, 90 well-acclimatized fish were categorized into three groups: one control and two treatment groups, i.e., T1 and T2, which were exposed to two sub-lethal concentrations of cadmium chloride (Cdcl), i.e., 1.18 mg/L (one-tenth of 96-h lethal concentration [LC]) and 2.36 mg/L (one-fifth of 96-h LC), respectively, for a duration of 7, 14, and 21 days. Post-completion of experimental periods, various assessments were carried out. Reactive oxygen species levels significantly increased, indicating enhanced oxidative stress, along with elevated activities of superoxide dismutase and catalase (P < 0.05). In contrast, reduced glutathione levels decreased in a dose- and duration-dependent manner (P < 0.05). Additionally, lipid peroxidation increased markedly, and liver biomarkers, including serum glutamic oxaloacetic transaminase, serum glutamic pyruvic transaminase, alkaline phosphatase, and lactate dehydrogenase, were significantly elevated (P < 0.05) in a time- and concentration-dependent pattern. Histopathological investigations of liver revealed pronounced deformities that were dose-dependent, with higher concentrations of cadmium causing more severe damage. Subsequently, prolonged cadmium exposure led to pyroptosis in the hepatocytes, characterized by the elevated expression of nucleotide-binding domain, leucine-rich-containing family, pyrin domain-containing-3; caspase-1, interleukin-1β, interleukin-18; apoptosis-associated speck-like protein containing a CARD; and Gasdermin E. These results highlighted the significant impact of cadmium on C. punctatus, underscoring its importance as a key bio-indicator for aquatic pollution. The study emphasizes the urgent need to monitor and regulate cadmium levels to protect aquatic life and maintain ecological balance.
镉污染是威胁水生生态系统和水生生物健康的一个主要环境问题。我们的研究考察了不同水平的镉毒性,突出了淡水鱼斑鳢(Channa punctatus)中的细胞焦亡。为此,将90条适应性良好的鱼分为三组:一组为对照组,两组为处理组,即T1和T2,分别暴露于两种亚致死浓度的氯化镉(Cdcl),即1.18毫克/升(96小时致死浓度[LC]的十分之一)和2.36毫克/升(96小时LC的五分之一),持续7天、14天和21天。实验期结束后,进行了各种评估。活性氧水平显著升高,表明氧化应激增强,同时超氧化物歧化酶和过氧化氢酶的活性也升高(P < 0.05)。相比之下,还原型谷胱甘肽水平呈剂量和时间依赖性下降(P < 0.05)。此外,脂质过氧化显著增加,包括血清谷草转氨酶、血清谷丙转氨酶、碱性磷酸酶和乳酸脱氢酶在内的肝脏生物标志物在时间和浓度依赖性模式下显著升高(P < 0.05)。肝脏的组织病理学研究显示出明显的畸形,且呈剂量依赖性,镉浓度越高,损伤越严重。随后,长时间暴露于镉导致肝细胞发生细胞焦亡,其特征为含核苷酸结合寡聚化结构域、富含亮氨酸重复序列家族、含pyrin结构域蛋白3(NLRP3)、半胱天冬酶-1(caspase-1)、白细胞介素-1β(IL-1β)、白细胞介素-18(IL-18)、含CARD结构域的凋亡相关斑点样蛋白(ASC)和Gasdermin E(GSDME)的表达升高。这些结果突出了镉对斑鳢的重大影响,强调了其作为水污染关键生物指示物的重要性。该研究强调迫切需要监测和调控镉水平,以保护水生生物并维持生态平衡。