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首页> 外文期刊>Aquatic Toxicology >Non invasive high resolution in vivo imaging of alpha-naphthylisothiocyanate (ANIT) induced hepatobiliary toxicity in STII medaka
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Non invasive high resolution in vivo imaging of alpha-naphthylisothiocyanate (ANIT) induced hepatobiliary toxicity in STII medaka

机译:α-萘基异硫氰酸酯(ANIT)诱导的青high STII肝胆毒性的无创高分辨率体内成像

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摘要

A novel transparent stock of medaka (Oryzias latipes; STII), homozygous recessive for all four pigments (iridophores, xanthophores, leucophores, melanophores), permits transcutaneous, high resolution (<1mum) imaging of internal organs and tissues in living individuals. We applied this model to in vivo investigation of alpha -naphthylisothiocyanate (ANIT) induced hepatobiliary toxicity. Distinct phenotypic responses to ANIT involving all aspects of intrahepatic biliary passageways (IHBPs), particularly bile preductular epithelial cells (BPDECs), associated with transitional passageways between canaliculi and bile ductules, were observed. Alterations included: attenuation/dilation of bile canaliculi, bile preductular lesions, hydropic vacuolation of hepatocytes and BPDECs, mild BPDEC hypertrophy, and biliary epithelial cell (BEC) hyperplasia. Ex vivo histological, immunohistochemical, and ultrastructural studies were employed to aid in interpretation of, and verify, in vivo findings. 3D reconstructions from in vivo investigations provided quantitative morphometric and volumetric evaluation of ANIT exposed and untreated livers. The findings presented show for the first time in vivo evaluation of toxicity in the STII medaka hepatobiliary system, and, in conjunction with prior in vivo work characterizing normalcy, advance our comparative understanding of this lower vertebrate hepatobiliary system and its response to toxic insult.
机译:一种新颖的透明花of(Oryzias latipes; STII),对所有四种颜料(虹膜,黄原体,隐色体,黑素体)纯合隐性,可对活体个体的内部器官和组织进行透皮高分辨率(<1um)成像。我们将此模型应用于体内α-萘基异硫氰酸酯(ANIT)诱导的肝胆毒性的研究。观察到对ANIT的明显表型反应,涉及肝内胆道(IHBP)的各个方面,特别是胆小管上皮上皮细胞(BPDECs),其与小管和胆管之间的过渡通道有关。改变包括:胆小管的衰减/扩张,胆管前病变,肝细胞和BPDEC的水泡空泡,轻度BPDEC肥大和胆道上皮细胞(BEC)增生。进行了体外组织学,免疫组织化学和超微结构研究,以帮助解释和验证体内发现。来自体内研究的3D重建提供了对ANIT暴露和未治疗的肝脏的定量形态和体积评估。提出的发现首次显示了对STII medaka肝胆系统的毒性的体内评估,并结合表征正常性的先前体内工作,提高了我们对该低等脊椎动物肝胆系统及其对毒性损伤的反应的比较理解。

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