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硝米特在大鼠体内的代谢。II. 硝基还原位点。

Metabolism of nitromide in the rat. II. Sites of nitro-reduction.

作者信息

Facchini V, Griffiths L A

出版信息

Xenobiotica. 1980 Apr;10(4):299-305. doi: 10.3109/00498258009033758.

DOI:10.3109/00498258009033758
PMID:7415211
Abstract
  1. Nitromide (3,5-dinitrobenzamide) is reduced to monoamino- and diamino-metabolites in vitro on anaerobic incubation with rat intestinal microflora. This conversion is suppressed by the antibiotics neomycin, tetracycline and bacitracin. 2. Nitromide is also in part reduced to monoamino but not diamino metabolites when incubated aerobically with homogenates of rat liver. 3. Pretreatment of rats with the antibiotics did not decrease their ability to form monoamino metabolites from nitromide, although formation of diamino metabolites was suppressed. 4. An antibiotic regime shown to suppress the methaemoglobinaemia resulting from the administration of nitrobenzene did not significantly reduce the methaemoglobinaemia resulting from the administration of nitromide.
摘要
  1. 硝唑酰胺(3,5 - 二硝基苯甲酰胺)在体外与大鼠肠道微生物群进行厌氧培养时会被还原为单氨基和二氨基代谢产物。这种转化受到抗生素新霉素、四环素和杆菌肽的抑制。2. 硝唑酰胺在与大鼠肝脏匀浆进行需氧培养时,也有部分会被还原为单氨基而非二氨基代谢产物。3. 用抗生素对大鼠进行预处理,虽会抑制二氨基代谢产物的形成,但不会降低它们从硝唑酰胺形成单氨基代谢产物的能力。4. 已证明能抑制因给予硝基苯导致的高铁血红蛋白血症的抗生素方案,对因给予硝唑酰胺导致的高铁血红蛋白血症并无显著降低作用。

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