Liu Guangyang, Shen Xiaoyun, Li Yuanfeng
School of Life Science and Engineering, Southwest University of Science and Technology, No. 59, Middle Section of Qinglong Avenue, Fucheng District, 621010, Mianyang, China.
School of Life Sciences, Liaocheng University, No. 1, Hunan Road, 252000, Liaocheng, China.
Toxicol Res (Camb). 2024 Oct 7;13(5):tfae162. doi: 10.1093/toxres/tfae162. eCollection 2024 Oct.
Food safety is closely related to environmental pollution. It is worth noting that the long-term accumulation of Cd, a toxic heavy metal, in animals may pose a threat to human health through food chain. Previous studies have found that Cd exposure may cause liver metabolic disorders of black goats, but the mechanism of its impact on liver proteome of goats has not been widely studied. Therefore, in this study, ten male goats (Nubian black goat × native black goat) were exposed to Cd via drinking water containing CdCl2 (20 mg Cd·kg - 1·BW) for 30 days (five male goats per group). Blood physiology and liver antioxidant indices in black goats were determined and differentially expressed proteins (DEPs) in the livers of Cd-exposed goats were profiled by using TMT-labelled proteomics. It was found that plasma Hb and RBC levels as well as PCV values were decreased, liver SOD, GSH-Px, T-AOC and CAT levels were decreased, and MDA level was increased in Cd-treated goats, and 630 DEPs (up 326, down 304) in the livers of Cd-treated goats. Proteomics analysis revealed that Cd exposure affected glutathione metabolism and drug metabolism-cytochrome P450. We identified GP×2, GSTM3, and TBXAS1 as potential protein markers of early Cd toxicity in goats. This study provided theoretical basis for early diagnosis of Cd poisoning in goats.
食品安全与环境污染密切相关。值得注意的是,有毒重金属镉在动物体内的长期积累可能通过食物链对人类健康构成威胁。以往研究发现,镉暴露可能导致黑山羊肝脏代谢紊乱,但其对山羊肝脏蛋白质组的影响机制尚未得到广泛研究。因此,本研究中,10只雄性山羊(努比亚黑山羊×本地黑山羊)通过饮用含CdCl2(20 mg Cd·kg-1·BW)的水暴露于镉中30天(每组5只雄性山羊)。测定了黑山羊的血液生理指标和肝脏抗氧化指标,并采用TMT标记蛋白质组学对镉暴露山羊肝脏中的差异表达蛋白(DEP)进行了分析。结果发现,镉处理山羊的血浆血红蛋白和红细胞水平以及红细胞压积值降低,肝脏超氧化物歧化酶、谷胱甘肽过氧化物酶、总抗氧化能力和过氧化氢酶水平降低,丙二醛水平升高,镉处理山羊肝脏中有630个差异表达蛋白(上调326个,下调304个)。蛋白质组学分析表明,镉暴露影响了谷胱甘肽代谢和药物代谢-细胞色素P450。我们确定GP×2、GSTM3和TBXAS1为山羊早期镉毒性的潜在蛋白质标志物。本研究为山羊镉中毒的早期诊断提供了理论依据。