羟基化苯并[a]蒽诱导斑点小鳞鱼肝脏细胞凋亡相关基因的表达。

IF 3.9 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES Toxics Pub Date : 2024-12-18 DOI:10.3390/toxics12120915
Muhammad Ahya Rafiuddin, Hajime Matsubara, Kaito Hatano, Masato Honda, Kenji Toyota, Kouhei Kuroda, Keito Tsunoda, Yukihiro Furusawa, Yoshiaki Tabuchi, Tetsushi Hirano, Akihiro Sakatoku, Chun-Sang Hong, Ajai K Srivastav, Thumronk Amornsakun, Nobuaki Shimizu, Mohamed I Zanaty, Tatsuo Harumi, Kohei Yamauchi, Tamás Müller, Ning Tang, Atsuhiko Hattori, Kazuichi Hayakawa, Nobuo Suzuki
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引用次数: 0

摘要

已知多环芳烃(PAHs)对鱼类有毒性作用。在这项研究中,我们研究了苯[a]蒽(BaA),一种多环芳烃,对鱼肝脏代谢的影响。在10天的时间内,对点状小刺鱼(Girella punctata)腹腔注射BaA (10 ng/g体重)4次。BaA显著降低已知骨代谢相关的血浆因子,如钙和无机磷。此外,血浆中已知的肝脏代谢相关因子水平显著降低,包括铁离子、总胆汁酸、总胆红素、游离胆红素、天冬氨酸转氨酶和碱性磷酸酶。有趣的是,BaA的单羟基化代谢物,如3羟基苯[a]蒽(3- ohbaa),在注射BaA的啃食鱼的胆汁中被检测到。这种羟基化形式的BaA是在其自由形式中发现的,而不是与葡萄糖醛酸或硫酸结合。由于缺乏蚕食鱼的全基因组序列数据,我们通过从头RNA测序分离了两个蚕食鱼特异性凋亡相关因子(TNF受体超家族成员1A: tnfrsf1a和TNF超家族成员10:tnfsf10)。在肝组织培养中,3-OHBaA (10-6 M)显著上调肝脏中tnfrsf1a和tnfsf10的表达。这些结果提供了第一个证据,证明3-OHBaA代谢物对硬骨鱼的肝脏有毒性作用。
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Hydroxylated-Benz[a]anthracenes Induce Two Apoptosis-Related Gene Expressions in the Liver of the Nibbler Fish Girella punctata.

Polycyclic aromatic hydrocarbons (PAHs) are known to have toxic effects on fish. In this study, we examined the effects of benz[a]anthracene (BaA), a type of PAH, on fish liver metabolism. Nibbler fish (Girella punctata) were intraperitoneally injected with BaA (10 ng/g body weight) four times over a 10-day period. BaA significantly decreased known bone metabolism-related plasma factors such as calcium and inorganic phosphorus. Moreover, significant reductions were observed in the plasma levels of known liver metabolism-related factors, including ferrous ions, total bile acids, total bilirubin, free bilirubin, aspartate aminotransferase, and alkaline phosphatase. Interestingly, mono-hydroxylated metabolites of BaA, such as 3 hydroxylbenz[a]anthracene (3-OHBaA), were detected in the bile of BaA-injected nibbler fish. This hydroxylated form of BaA was found in its free form, rather than conjugated with glucuronic acid or sulfuric acid. Due to the lack of whole-genome sequence data for the nibbler fish, two nibbler fish-specific apoptosis-related factors (TNF receptor superfamily member 1A: tnfrsf1a and TNF superfamily member 10: tnfsf10) were isolated by De novo RNA sequencing. In a liver tissue culture, 3-OHBaA (10-6 M) significantly upregulated the expression of tnfrsf1a and tnfsf10 in the liver. These results provide the first evidence that 3-OHBaA metabolites exhibit toxic effects on the liver in teleost.

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来源期刊
Toxics
Toxics Chemical Engineering-Chemical Health and Safety
CiteScore
4.50
自引率
10.90%
发文量
681
审稿时长
6 weeks
期刊介绍: Toxics (ISSN 2305-6304) is an international, peer-reviewed, open access journal which provides an advanced forum for studies related to all aspects of toxic chemicals and materials. It publishes reviews, regular research papers, and short communications. Our aim is to encourage scientists to publish their experimental and theoretical results in detail. There is, therefore, no restriction on the maximum length of the papers, although authors should write their papers in a clear and concise way. The full experimental details must be provided so that the results can be reproduced. Electronic files or software regarding the full details of calculations and experimental procedure can be deposited as supplementary material, if it is not possible to publish them along with the text.
期刊最新文献
RETRACTED: Di Paola et al. Environmental Risk Assessment of Dexamethasone Sodium Phosphate and Tocilizumab Mixture in Zebrafish Early Life Stage (Danio rerio). Toxics 2022, 10, 279. RETRACTED: Paola et al. Environmental Impact of Pharmaceutical Pollutants: Synergistic Toxicity of Ivermectin and Cypermethrin. Toxics 2022, 10, 388. RETRACTED: Di Paola et al. Combined Effects of Potassium Perchlorate and a Neonicotinoid on Zebrafish Larvae (Danio rerio). Toxics 2022, 10, 203. Human Activity as a Growing Threat to Marine Ecosystems: Plastic and Temperature Effects on the Sponge Sarcotragus spinosulus. Subchronic Exposure to Low-Dose Chlorfenapyr and Emamectin Benzoate Disrupts Kidney Metabolism in Rats.
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