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Edible oil adulterants, argemone oil and butter yellow, as aetiological factors for gall bladder cancer

机译:食用油掺杂物,精油和黄油黄是胆囊癌的病因

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摘要

Carcinogenic potential of argemone oil (AO) and butter yellow (BY), the adulterants encountered in edible oil, in gall bladder of Swiss albino mice was undertaken to investigate the potential aetiological factors of gall bladder carcinoma (GBC) in the Indo-Gangetic basin. Twice weekly intraperitoneal (ip) administration of AO (5 ml/kg body wt) and BY (25 mg/kg body wt) to Swiss albino male and female mice for 30 and 60 days indicated that females were more vulnerable to these adulterants in terms of responses to inflammatory markers. Subsequent experiments with dietary exposure of AO (1%) and BY (0.06%) for 6 months in female mice showed symptoms related to cachexia, jaundice and anaemia. High levels of total cholesterol, low density lipoprotein (LDL), TG, bilirubin and low level of high density lipoprotein (HDL) as well as gallstone formation was shown by AO exposure only, leading to the development of adenocarcinoma. BY exposure resulted in adenoma and hyperplasia without stone formation. The cyclooxygenase (COX-2) overexpression was found to be related to prostaglandin E2 (PGE2) production in AO treated mice but not in BY exposed animals, thereby indicating a differential pathway specific carcinogenicity. PGE2 stimulates the secretion of secreted mucins (MUC5AC), which is involved in stone formation following AO exposure. Enhanced secretion of membrane bound mucins (MUC4) in BY and AO exposed mice resulted in the activation of ErbB2 and downstream signalling such as p-AKT, p-ERK and p-JNK, which ultimately affects the target proteins, p53 and p21 leading to adenoma and adenocarcinoma, respectively. The study suggests that AO and BY are responsible for producing GBC in mice along with stone formation in the AO exposed animals.
机译:研究了瑞士白化病小鼠胆囊中食用油中所掺入的掺假物精油(AO)和黄油黄(BY)的致癌潜力,以研究印度恒河盆地胆囊癌(GBC)的潜在病因。 。每周两次对瑞士的白化病雄性和雌性小鼠进行腹膜内(ip)AO(5 ml / kg体重)和BY(25 mg / kg体重)腹腔注射30天和60天,这表明雌性更容易受到这些掺假的影响对炎症标志物的反应随后在雌性小鼠中进行AO(1%)和BY(0.06%)饮食暴露6个月的实验,显示出与恶病质,黄疸和贫血相关的症状。仅通过AO暴露即可显示高水平的总胆固醇,低密度脂蛋白(LDL),TG,胆红素和低水平的高密度脂蛋白(HDL)以及胆结石的形成,从而导致腺癌的发展。 BY暴露导致腺瘤和增生,没有结石形成。发现环氧合酶(COX-2)的过表达与AO处理的小鼠中前列腺素E2(PGE2)的产生有关,而与BY暴露的动物无关,因此表明差异途径的特异性致癌性。 PGE2刺激分泌的粘蛋白(MUC5AC)的分泌,粘蛋白的分泌与AO暴露后结石形成有关。暴露于BY和AO的小鼠中的膜结合粘蛋白(MUC4)分泌增强,导致ErbB2的激活以及下游信号传导(例如p-AKT,p-ERK和p-JNK),最终影响目标蛋白p53和p21,从而导致腺瘤和腺癌。研究表明,AO和BY负责在小鼠中产生GBC以及AO暴露动物中的结石形成。

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