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口服和注射间苯二酚黄对某些肝脏和肠道生化参数的影响。

Effect of oral and parenteral administration of metanil yellow on some hepatic and intestinal biochemical parameters.

作者信息

Ramchandani S, Das M, Joshi A, Khanna S K

机构信息

Dyes & Food Adulterant Toxicology Laboratory, Industrial Toxicology Research Centre, Mahatma Gandhi Marg, Lucknow, India.

出版信息

J Appl Toxicol. 1997 Jan-Feb;17(1):85-91. doi: 10.1002/(sici)1099-1263(199701)17:1<85::aid-jat394>3.0.co;2-k.

Abstract

Metanil yellow, a non-permitted colour for food commodities, is used in the leather, paper and textile industries. In this paper the effect of oral and parenteral administration of Metanil yellow on hepatic and intestinal biochemical parameters was investigated. Oral administration of Metanil yellow (430 mg kg-1 body wt.) for 7 days caused significant depletion of hepatic and intestinal glutathione levels (33-52%) with a concomitant increase in lipid peroxidation (49-121%). Metanil yellow treatment for 7 days also led to a significant increase in cytochrome P-450 (P-450)-dependent aryl hydrocarbon hydroxylase (AHH) activity (99-223%) in the liver and intestine. Cytosolic glutathione-S-transferase (GST) (32-136%) and quinone reductase (QR) (20-92%) activities were also found to be substantially induced in hepatic and intestinal tissues following oral treatment of Metanil yellow. It is interesting to note that oral treatment of Metanil yellow showed a greater response in cytosolic enzymes of hepatic tissue as compared to intestine. Single parenteral administration of Metanil yellow (80 mg kg-1 body wt.) caused significant induction of P-450 and its dependent monooxygenases. Even after 5 days of single parenteral administration of Metanil yellow, hepatic AHH activity showed an elevation of 48% while other monooxygenases were marginally increased. Cytosolic GST and QR showed respective peak inductions of 92% and 60% after 2 and 3 days of parenteral administration of Metanil yellow, which levels off after the 5th day. It can be concluded that Metanil yellow acts as an inducer of a specific form of microsomal P-450 and cytosolic GST and QR, which may involve a cytosolic Ah receptor.

摘要

金莲黄是一种食品中禁用的色素,用于皮革、纸张和纺织工业。本文研究了经口和非经口给予金莲黄对肝脏和肠道生化参数的影响。经口给予金莲黄(430毫克/千克体重)7天,导致肝脏和肠道谷胱甘肽水平显著降低(33%-52%),同时脂质过氧化增加(49%-121%)。给予金莲黄7天还导致肝脏和肠道中细胞色素P-450(P-450)依赖性芳烃羟化酶(AHH)活性显著增加(99%-223%)。经口给予金莲黄后,肝脏和肠道组织中的胞质谷胱甘肽-S-转移酶(GST)(32%-136%)和醌还原酶(QR)(20%-92%)活性也被显著诱导。有趣的是,与肠道相比,经口给予金莲黄对肝脏组织胞质酶的反应更大。单次非经口给予金莲黄(80毫克/千克体重)可显著诱导P-450及其依赖性单加氧酶。即使在单次非经口给予金莲黄5天后,肝脏AHH活性仍升高了48%,而其他单加氧酶略有增加。经非经口给予金莲黄2天和3天后,胞质GST和QR分别出现92%和60%的峰值诱导,在第5天后趋于平稳。可以得出结论,金莲黄可作为微粒体P-450以及胞质GST和QR特定形式的诱导剂,这可能涉及胞质芳烃受体。

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