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噻虫嗪和皂石对虹鳟鱼生理反应的影响:神经网络介导的方法。

Physiological response of thiamethoxam and ulexite in rainbow trout: A neural network-mediated approach.

机构信息

Department of Sea Food Processing, Faculty of Fisheries, Atatürk University, Erzurum, Türkiye.

Department of Aquaculture, Faculty of Fisheries, Atatürk University, Erzurum, Türkiye.

出版信息

Comp Biochem Physiol C Toxicol Pharmacol. 2024 Jan;275:109760. doi: 10.1016/j.cbpc.2023.109760. Epub 2023 Oct 11.

Abstract

Fish, which are in constant contact with water, serve as an important ecological indicator of aquatic environment health. Therefore, in this study, in the name of neural degeneration, thiamethoxam (TMX) insecticide in the cerebral tissue of Oncorhynchus mykiss; neurotoxic endpoints such as biomarkers of oxidative stress, DNA damage and the status of antioxidant enzymes have been identified. Antioxidant enzyme (CAT, SOD, GPx, GSH) activities were significantly inhibited by TMX administration, and MDA and MPO values increased as a result of the stimulation of ROS (p < 0.05). It was interpreted that ulexite (UX) added to the medium was effective in favor of antioxidants and tried to prevent MDA and MPO levels. It was determined that Nrf-2, one of the inflammation parameters, was inhibited as a result of TMX application, and the supplementation of UX to the medium created merits similar to the no treatment group. In the 48th and 96th hour analyses of cerebral tissue, it was determined that IL-6 and TNF-α values were induced in TMX applied groups and UX tried to inhibit this situation. It was commented that TMX induced DNA damage and apoptosis at 48th-96th h, whereas UX suppressed this situation. The results provide possible in vivo evidence that UX supplements can reduce TMX-mediated oxidative stress and brain damage in O. mykiss brain tissue.

摘要

鱼类与水持续接触,是水生环境健康的重要生态指标。因此,在本研究中,以神经退行性病变为名,研究噻虫嗪(TMX)杀虫剂在虹鳟脑组织中的作用;鉴定了氧化应激、DNA 损伤和抗氧化酶状态等神经毒性终点的生物标志物。TMX 给药显著抑制了抗氧化酶(CAT、SOD、GPx、GSH)的活性,ROS 刺激导致 MDA 和 MPO 值增加(p<0.05)。解释说,向培养基中添加沸石(UX)有利于抗氧化剂,并试图防止 MDA 和 MPO 水平升高。结果表明,由于 TMX 的应用,炎症参数之一的 Nrf-2 受到抑制,而向培养基中添加 UX 创造了类似于未处理组的优点。在脑组织的第 48 小时和第 96 小时分析中,确定 TMX 应用组中诱导了 IL-6 和 TNF-α 值,而 UX 试图抑制这种情况。评论说,TMX 在第 48 小时至第 96 小时诱导了 DNA 损伤和细胞凋亡,而 UX 抑制了这种情况。结果提供了可能的体内证据,表明 UX 补充剂可以减少 TMX 介导的氧化应激和 O. mykiss 脑组织损伤。

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