Probiotics and the BSH-related cholesterol lowering mechanism: a Jekyll and Hyde scenario

被引:96
作者
Choi, Sy-Bing [1 ]
Lew, Lee-Ching [1 ]
Yeo, Siok-Koon [2 ]
Parvathy, Seema Nair [3 ]
Liong, Min-Tze [1 ]
机构
[1] Univ Sains Malaysia, Sch Ind Technol, Usm 11800, Penang, Malaysia
[2] Taylors Univ, Sch Biosci, Selangor, Malaysia
[3] Sree Buddha Coll Engn, Dept Biotechnol & Biochem Engn, Pandalam, Kerala, India
关键词
Bile salt hydrolase; cholesterol; controversies; deconjugation; probiotic; BILE-SALT HYDROLASE; FARNESOID-X-RECEPTOR; NUCLEAR HORMONE-RECEPTORS; LACTIC-ACID BACTERIA; BIFIDOBACTERIUM-LONGUM; LACTOBACILLUS-ACIDOPHILUS; GENE-EXPRESSION; SMALL-INTESTINE; COLON-CANCER; METABOLISM;
D O I
10.3109/07388551.2014.889077
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Probiotic microorganisms have been documented over the past two decades to play a role in cholesterol-lowering properties via various clinical trials. Several mechanisms have also been proposed and the ability of these microorganisms to deconjugate bile via production of bile salt hydrolase (BSH) has been widely associated with their cholesterol lowering potentials in prevention of hypercholesterolemia. Deconjugated bile salts are more hydrophobic than their conjugated counterparts, thus are less reabsorbed through the intestines resulting in higher excretion into the feces. Replacement of new bile salts from cholesterol as a precursor subsequently leads to decreased serum cholesterol levels. However, some controversies have risen attributed to the activities of deconjugated bile acids that repress the synthesis of bile acids from cholesterol. Deconjugated bile acids have higher binding affinity towards some orphan nuclear receptors namely the farsenoid X receptor (FXR), leading to a suppressed transcription of the enzyme cholesterol 7-alpha hydroxylase (7AH), which is responsible in bile acid synthesis from cholesterol. This notion was further corroborated by our current docking data, which indicated that deconjugated bile acids have higher propensities to bind with the FXR receptor as compared to conjugated bile acids. Bile acids-activated FXR also induces transcription of the IBABP gene, leading to enhanced recycling of bile acids from the intestine back to the liver, which subsequently reduces the need for new bile formation from cholesterol. Possible detrimental effects due to increased deconjugation of bile salts such as malabsorption of lipids, colon carcinogenesis, gallstones formation and altered gut microbial populations, which contribute to other varying gut diseases, were also included in this review. Our current findings and review substantiate the need to look beyond BSH deconjugation as a single factor/mechanism in strain selection for hypercholesterolemia, and/or as a sole mean to justify a cholesterol-lowering property of probiotic strains.
引用
收藏
页码:392 / 401
页数:10
相关论文
共 55 条
[1]  
[Anonymous], 2001, HUM VIT MIN REQ
[2]   The interaction between bacteria and bile [J].
Begley, M ;
Gahan, CGM ;
Hill, C .
FEMS MICROBIOLOGY REVIEWS, 2005, 29 (04) :625-651
[3]   Bile acids as carcinogens in human gastrointestinal cancers [J].
Bernstein, H ;
Bernstein, C ;
Payne, CM ;
Dvorakova, K ;
Garewal, H .
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 2005, 589 (01) :47-65
[4]   INTERRELATIONSHIPS OF BILE-ACID AND PHOSPHOLIPID FATTY-ACID SPECIES WITH CHOLESTEROL SATURATION OF DUODENAL BILE IN HEALTH AND GALLSTONE DISEASE [J].
BERR, F ;
SCHREIBER, E ;
FRICK, U .
HEPATOLOGY, 1992, 16 (01) :71-81
[5]  
Bhagavan NV, 2002, PROTEN AMINO ACID ME, V4th
[6]   Bile acid deconjugation by Lactobacilli and its effects in patients with a short small bowel [J].
Bongaerts, GPA ;
Severijnen, RSVM ;
Tangerman, A ;
Verrips, A ;
Tolboom, JJM .
JOURNAL OF GASTROENTEROLOGY, 2000, 35 (11) :801-804
[7]   The farnesoid X receptor FXRα/NR1H4 acquired ligand specificity for bile salts late in vertebrate evolution [J].
Cai, Shi-Ying ;
Xiong, Liangshi ;
Wray, Charles G. ;
Ballatori, Nazzareno ;
Boyer, James L. .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2007, 293 (03) :R1400-R1409
[8]   Bile acid regulation of gene expression: Roles of nuclear hormone receptors [J].
Chiang, JYL .
ENDOCRINE REVIEWS, 2002, 23 (04) :443-463
[9]   Oxidative DNA damage: mechanisms, mutation, and disease [J].
Cooke, MS ;
Evans, MD ;
Dizdaroglu, M ;
Lunec, J .
FASEB JOURNAL, 2003, 17 (10) :1195-1214
[10]   Bile salt hydrolase activity of three strains of Lactobacillus acidophilus [J].
Corzo, G ;
Gilliland, SE .
JOURNAL OF DAIRY SCIENCE, 1999, 82 (03) :472-480