磺胺吡啶
磺胺吡啶
药代动力学
益生菌
药物代谢
药理学
药品
化学
内科学
新陈代谢
溃疡性结肠炎
生物
生物化学
医学
细菌
遗传学
疾病
有机化学
作者
Hee Ji Lee,Hu Zhang,David A. Orlovich,J. Paul Fawcett
出处
期刊:Xenobiotica
[Taylor & Francis]
日期:2012-02-21
卷期号:42 (8): 791-797
被引量:42
标识
DOI:10.3109/00498254.2012.660508
摘要
Probiotics are live microorganisms claimed to exert beneficial effects on the host. This study investigated their effect on the metabolism and pharmacokinetics of sulfasalazine (SSZ), a drug whose efficacy depends on metabolism by azoreductase (AR) in the gut microbiota to sulfapyridine (SP) and 5-acetylsalicylic acid (5-ASA). The probiotic strains Lactobacillus acidophilus L10, Bifidobacterium lactis B94 and Streptococcus salivarius K12 possessed AR activity and a corresponding ability to metabolize SSZ. Treatment of male Wistar rats (n = 5) with oral 2 g doses of a mixture of the three probiotics (total dose 1.8 × 10⁹ cfu) every 12 h for 3 days resulted in a significant increase (p < 0.05) in AR activity in ex vivo colon contents with a corresponding increase in SSZ metabolism. Similar probiotic treatment of male Wistar rats (n = 8) followed by an oral 100 mg/kg dose of SSZ produced high plasma levels of SP, but pharmacokinetic parameters of SSZ and SP were not significantly different from control rats given SSZ. These results indicate that probiotic strains possess AR activity and can metabolize SSZ. Treatment with probiotics increases AR activity in the gut microbiota but has no effect on plasma levels of SSZ and SP following a subsequent oral dose of SSZ.
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