The effect of gut microbiota on drug metabolism

被引:125
作者
Kang, Mi Jeong [1 ]
Kim, Hyung Gyun [2 ]
Kim, Jin Sung [1 ]
Oh, Do Gyeong [1 ]
Um, Yeon Ji [1 ]
Seo, Chae Shin [1 ]
Han, Ji Won [1 ]
Cho, Hyun Ji [1 ]
Kim, Ghee Hwan [1 ]
Jeong, Tae Cheon [1 ]
Jeong, Hye Gwang [2 ]
机构
[1] Yeungnam Univ, Coll Pharm, Kyongsan 712749, South Korea
[2] Chungnam Natl Univ, Coll Pharm, Taejon 305764, South Korea
基金
新加坡国家研究基金会;
关键词
drugs; gut microbiota; metabolism; natural products; INTESTINAL BACTERIAL METABOLISM; GERM-FREE; IN-VITRO; BETA-GLUCURONIDASE; L-DOPA; ANTIALLERGIC ACTIVITIES; ANAEROBIC DEGRADATION; INDUCE APOPTOSIS; INDUCED TOXICITY; GENE-EXPRESSION;
D O I
10.1517/17425255.2013.807798
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Introduction: Numerous drugs and toxicants must be metabolized to an active form. Metabolic activation by host tissues, such as the liver, has been well studied. However, drug and toxicant metabolism by the intestinal microbiota is an unexplored, but essential, field of study in pharmacology and toxicology. The taxonomic diversity and sheer numbers of the intestinal microbiota, and their capacity to metabolize xenobiotics, underscore the importance of this mode of metabolism. Areas covered: Metabolism by the intestinal microbiota has focused on the natural products of glycosides hydrolyzed by intestinal microbiota enzymes, but not by host tissues. Metabolism of synthetic drugs by the intestinal microbiota has been less-intensively investigated. This review provides an overview of xenobiotic metabolism by the intestinal microbiota of both natural products and synthetic drugs. Expert opinion: Metabolism by the intestinal microbiota might result in a different metabolite profile than that produced by host tissues. This could potentially result in either activation or inactivation of the pharmacological and/or toxicological actions of the compound in question. The contribution of the intestinal microbiota to drug metabolism remains relatively unexplored. Therefore, studies of xenobiotic metabolism by the intestinal microbiota need to be included in new drug development as well as classical studies of host tissue metabolism.
引用
收藏
页码:1295 / 1308
页数:14
相关论文
共 115 条
[1]
AKAO T, 1994, BIOL PHARM BULL, V17, P1573
[2]
Balicalin, the predominant flavone glucuronide of scutellariae radix, is absorbed from the rat gastrointestinal tract as the aglycone and restored to its original form [J].
Akao, T ;
Kawabata, K ;
Yanagisawa, E ;
Ishihara, K ;
Mizuhara, Y ;
Wakui, Y ;
Sakashita, Y ;
Kobashi, K .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2000, 52 (12) :1563-1568
[3]
Akao T, 1996, BIOL PHARM BULL, V19, P136
[4]
AKAO T, 1991, BIOCHEM PHARMACOL, V41, P1025
[5]
Drug metabolome of the Simvastatin formed by human intestinal microbiota in vitro [J].
Aura, Anna-Marja ;
Mattila, Ismo ;
Hyotylainen, Tuulia ;
Gopalacharyulu, Peddinti ;
Bounsaythip, Catherine ;
Oresic, Matej ;
Oksman-Caldentey, Kirsi-Marja .
MOLECULAR BIOSYSTEMS, 2011, 7 (02) :437-446
[6]
Metabolism of ginsenoside Re by human intestinal microflora and its estrogenic effect [J].
Bae, EA ;
Shin, JE ;
Kim, DH .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2005, 28 (10) :1903-1908
[7]
Susceptibility of the H2-receptor antagonists cimetidine, famotidine and nizatidine, to metabolism by the gastrointestinal microflora [J].
Basit, AW ;
Newton, JM ;
Lacey, LF .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 237 (1-2) :23-33
[8]
The conduct of in vitro and in vivo drug-drug interaction studies: A Pharmaceutical Research and Manufacturers of America (PhRMA) perspective [J].
Bjornsson, TD ;
Callaghan, JT ;
Einolf, HJ ;
Fischer, V ;
Gan, L ;
Grimm, S ;
Kao, J ;
King, SP ;
Miwa, G ;
Ni, L ;
Kumar, G ;
McLeod, J ;
Obach, RS ;
Roberts, S ;
Roe, A ;
Shah, A ;
Snikeris, F ;
Sullivan, JT ;
Tweedie, D ;
Vega, JM ;
Walsh, J ;
Wrighton, SA .
DRUG METABOLISM AND DISPOSITION, 2003, 31 (07) :815-832
[9]
Metabolism of isoflavones and lignans by the gut microflora: a study in germ-free and human flora associated rats [J].
Bowey, E ;
Adlercreutz, H ;
Rowland, I .
FOOD AND CHEMICAL TOXICOLOGY, 2003, 41 (05) :631-636
[10]
Baicalein induces cancer cell death and proliferation retardation by the inhibition of CDC2 kinase and survivin associated with opposite role of p38 mitogen-activated protein kinase and AKT [J].
Chao, Jui-I ;
Su, Wen-Chi ;
Liu, Huei-Fang .
MOLECULAR CANCER THERAPEUTICS, 2007, 6 (11) :3039-3048