Lipids in Health and Disease | |
Hypolipidemic effects of lactic acid bacteria fermented cereal in rats | |
Anthony Alaba Bakare3  Stella Uche Eriobu3  Omokaro Ogherebe3  Kazeem Ayoola Disu3  James Oluwafemi Ita3  Catherine Lohi Ebohon3  Linda Adugo Okafor3  Morenike Omitola3  Falilat Yetunde Fetuga3  Oluwanifemi Olokodana3  Oluwaseyi Ogunnowo3  Tinuola Gbemi Apelehin3  Temitope Adeola Jentegbe3  Deborah Tolulope Ogunfowokan3  Adeboye Olufemi Osibogun3  Esther Bunmi Babatope3  Oluwasetemi Daropale3  Ahmeed Adekola Shorinola3  Adeyemi Adeola Ogunnowo3  Tosin Oluyinka Oladunjoye3  Tope Adebusola Adesanmi3  Ibrahim Akorede Adegbola3  Martin Oluseye Kolawole3  Rahman Abiodun Olalere3  Olugbenga Obajimi Adebawo1  Oladipo Ademuyiwa2  Muinat Moronke Adeyanju3  Immaculata Oyeyemi Banjoko3  | |
[1] Department of Biochemistry, Ben Carson School of Medicine, Babcock University, Ilishan-Remo, Nigeria;Department of Biochemistry, University of Agriculture, Abeokuta, Nigeria;Department of Biochemistry, Olabisi Onabanjo University, Ikenne-Remo, Nigeria | |
关键词: Fermentation; Cereals; Probiotics; Lactic acid bacteria; Dyslipidemia; | |
Others : 1160118 DOI : 10.1186/1476-511X-11-170 |
|
received in 2012-04-16, accepted in 2012-11-28, 发布年份 2012 | |
【 摘 要 】
Background
The objectives of the present study were to investigate the efficacy of the mixed culture of Lactobacillus acidophilus (DSM 20242), Bifidobacterium bifidum (DSM 20082) and Lactobacillus helveticus (CK60) in the fermentation of maize and the evaluation of the effect of the fermented meal on the lipid profile of rats.
Methods
Rats were randomly assigned to 3 groups and each group placed on a Diet A (high fat diet into which a maize meal fermented with a mixed culture of Lb acidophilus (DSM 20242), B bifidum (DSM 20082) and Lb helveticus (CK 60) was incorporated), B (unfermented high fat diet) or C (commercial rat chow) respectively after the first group of 7 rats randomly selected were sacrificed to obtain the baseline data. Thereafter 7 rats each from the experimental and control groups were sacrificed weekly for 4 weeks and the plasma, erythrocytes, lipoproteins and organs of the rats were assessed for cholesterol, triglyceride and phospholipids.
Results
Our results revealed that the mixed culture of Lb acidophilus (DSM 20242), B bifidum (DSM 20082) and Lb helveticus (CK 60) were able to grow and ferment maize meal into ‘ogi’ of acceptable flavour. In addition to plasma and hepatic hypercholesterolemia and hypertriglyceridemia, phospholipidosis in plasma, as well as cholesterogenesis, triglyceride constipation and phospholipidosis in extra-hepatic tissues characterized the consumption of unfermented hyperlipidemic diets. However, feeding the animals with the fermented maize diet reversed the dyslipidemia.
Conclusion
The findings of this study indicate that consumption of mixed culture lactic acid bacteria (Lb acidophilus (DSM 20242), Bifidobacterium bifidum (DSM 20082) and Lb helveticus (CK 60) fermented food results in the inhibition of fat absorption. It also inhibits the activity of HMG CoA reductase. This inhibition may be by feedback inhibition or repression of the transcription of the gene encoding the enzyme via activation of the sterol regulatory element binding protein (SREBP) transcription factor. It is also possible that consumption of fermented food enhances conversion of cholesterol to bile acids by activating cholesterol-7α-hydroxylase.
【 授权许可】
2012 Banjoko et al.; licensee BioMed Central Ltd.
【 预 览 】
Files | Size | Format | View |
---|---|---|---|
20150410094138765.pdf | 898KB | download | |
Figure 11. | 26KB | Image | download |
Figure 10. | 90KB | Image | download |
Figure 9. | 99KB | Image | download |
Figure 8. | 101KB | Image | download |
Figure 7. | 103KB | Image | download |
Figure 6. | 97KB | Image | download |
Figure 5. | 105KB | Image | download |
Figure 4. | 100KB | Image | download |
Figure 3. | 35KB | Image | download |
Figure 2. | 96KB | Image | download |
Figure 1. | 78KB | Image | download |
【 图 表 】
Figure 1.
Figure 2.
Figure 3.
Figure 4.
Figure 5.
Figure 6.
Figure 7.
Figure 8.
Figure 9.
Figure 10.
Figure 11.
【 参考文献 】
- [1]Reid G, Jass J, Sebulsky MT, McCormick JK: Potential uses of probiotics in clinical practice. Clin Microbiol Rev 2003, 16:658-672.
- [2]Basu S, Chatterjee M, Ganguly S, Chandra PK: Efficacy of Lactobacillus rhamnosus GG in acute watery diarrhoea of Indian children: a randomised controlled trial. Paed Child Health 2007, 43:837-842.
- [3]Fernandes CF, Shahani KM: Anticarcinogenic and immunological properties of dietary lactobacilli. J Food Prot 1990, 53:704-710.
- [4]Gill HS, Rutherfurd KJ, Cross ML, Gopal PK: Enhancement of immunity in the elderly by dietary supplementation with the probiotic Bifidobacterium lactis HN019. Am J Clin Nutr 2001, 74:833-839.
- [5]Park YH, Kim JG, Shin YW, Kim HS, Kim YJ, Chun T, Kim SH, Whang KY: Effects of Lactobacillus acidophilus 43121 and a mixture of Lactobacillus casei and Bifidobacterium longum on the serum cholesterol level and fecal sterol excretion in hypercholesterolemia-induced pigs. Biosci Biotechnol Biochem 2008, 72:595-600.
- [6]Lee DK, Jang S, Baek EH, Kim MJ, Lee KS, Shin HS, Chung MJ, Kim JE, Lee KO, Ha NJ: Lactic acid bacteria affect serum cholesterol levels, harmful fecal enzyme activity, and fecal water content. Lipids Health Dis 2009, 8:21. BioMed Central Full Text
- [7]Law MR, Wald NJ, Wu T, Hackshaw A, Bailey A: Systematic underestimation of association between serum cholesterol concentration and ischaemic heart disease in observational studies: data from the BUPA study. Bri Med J 1994, 308(6925):363-366.
- [8]Ross R: The pathogenesis of atherosclerosis: a perspective for 1990s. Nature 1993, 362:801-809.
- [9]Oxman T, Shapira M, Klein R, Avazov N, Rabinowitz B: Oral administration of Lactobacillus induces cardioprotection. J Altern Complement Med 2001, 7(4):345-354.
- [10]Ataie-Jafari A, Larijani B, Alavi Majd H, Tahbaz F: Cholesterol-lowering effect of probiotic yogurt in comparison with ordinary yogurt in mildly to moderately hypercholeserolemic subjects. Annals Nutr Metab 2009, 54:22-27.
- [11]Liong MT: Probiotics: A critical review of their potential role as anti-hypertensives, immune modulators, hypocholesterolemics, and perimenopausal treatments. Nutr Rev 2007, 65:316-328.
- [12]Heon PY, Kim JG, Shin YW, Kim SH, Whang KY: Effect of a dietary inclusion of Lactobacillus acidophilus ATCC43121 on cholesterol metabolism. J Microbiol Biotech 2007, 17(4):655-662.
- [13]De Smet I, Van Hoorde L, De Saeyer N, Vande Woestyne M, Verstraete W: In vitro study of bile salt hydrolase (BSH) activity of BSH isogenic Lactobacillus plantarum 80 strains and estimation of cholesterol lowering through enhanced BSH activity. Microb Ecol Health D 1994, 7:315-329.
- [14]De Smet I, De Boever P, Versteaete W: Cholesterol lowering in pigs through enhanced bacterial bile salt hydrolase activity. Brit J Nutr 1998, 79:185-194.
- [15]Liong MT, Shah NP: Bile salt deconjugation ability, bile salt hydrolase activity and cholesterol coprecipitation ability of lactobacilli strains. Internat Dairy J 2005, 15:391-398.
- [16]du Toit M, Franz CMAP, Dicks LMT, Schillinger U, Haberer P, Warlies B, Ahrens F, Holzapfel WH: Characterisation and selection of probiotic lactobacilli for a preliminary minipig feeding trial and their effect on serum cholesterol levels, faeces pH and faeces moisture content. Int J Food Microbiol 1998, 40:93-104.
- [17]Cheik NC, Rossi EA, Guerra RLF, Tenorio NM, Nascimento CM Od, Viana FP, Manzoni MSJ, Carlos IZ, Da-Silva PL, Vendramini RC, Damaso AR: Effects of a ferment soy product on the adipocyte area reduction and dyslipidemia control in hypercholesterolemic adult male rats. Lipids Health Dis 2008, 7:50. BioMed Central Full Text
- [18]Xiao JZ, Kondo S, Takahashi N, Miyaji K, Oshida K, Hiramatsu A, Iwatsuki K, Kokubo S, Hosona A: Effects of milk products fermented by Bifidobacterium longum on blood lipids in rats and healthy adult male volunteers. J Dairy Sci 2000, 86:2452-2461.
- [19]Rossi EA, Vendramini RC, Carlos IZ, Ueiji IS, Squinzari MM, Silva I Jr, Valdez GF: Effects of a novel fermented soy product on the serum lipids of hyper-cholesterolemic rabbits. Arq Bras Cardiol 2000, 74:213-216.
- [20]Kitawaki R, Nishimura Y, Takagi N, Iwasaki M, Tsuzuki K, Fukuda M: Effects of lactobacillus fermented soymilk and soy yogurt on hepatic lipid accumulation in rats fed on a cholesterol-free diet. Biosci Biotechnol Biochem 2009, 73(7):1484-1488.
- [21]Fukushima M, Nakano M: The effect of a probiotic on fecal and liver lipid classes in rats. Brit J Nutr 1995, 73:701-710.
- [22]Olukoya DK, Ebigwei SI, Adebawo OO, Osiyemi FO: Plasmid profiles and antibiotic susceptibility patterns of Lactobacillus isolated from fermented foods in Nigeria. Food Microbiol 1993, 10:279-285.
- [23]Oyewole OB, Odunfa SA: Characterization and distribution of lactic acid bacteria in cassava fermentation during fufu production. J Appl Bacteriol 1990, 68:145-152.
- [24]Gidez LI, Miller GJ, Burstein M, Slagle S, Eder HA: A separation and quantitation of subclasses of human plasma high density lipoproteins by a simple precipitation procedure. J Lipid Res 1982, 23:1206-1223.
- [25]Folch J, Lees M, Sloane GH: A simple method for the isolation and purification of total lipids from animal tissues. J Biol Chem 1957, 226:497-509.
- [26]Stewart JCM: Colorimetric determination of phospholipids with ammonium ferrothiocyanate. Anal Biochem 1980, 104:10-14.
- [27]Kriketos AD, Furler SM, Gan SK, Poynten AM, Chisholm DJ, Campbell LV: Multiple indexes of lipid availability are independently related to whole body insulin action in healthy humans. J Clin Endocr Met 2003, 88(2):793-798.
- [28]Rao V, Ramakrishnan S: Indirect assessment of hydroxymethylglutaryl-CoA (HMG-CoA) reductase activity in liver tissue. Clin Chem 1975, 21(10):1523-1525.
- [29]Adebawo OO, Ruiz Barba JL, Warner PJ, Oguntimehin GBO: Regulation of aspartokinase in Lactobacillus plantarum. J Appl Microbiol 1997, 82:191-196.
- [30]Ademuyiwa O, Agarwal R, Chandra R, Behari JR: Lead-induced phospholipidosis and cholesterogenesis in rat tissues. Chem Biol Interact 2009, 179:314-320.
- [31]Botham KM, Mayes PA: Metabolism of acylglycerols and sphingolipids. In Harper’s Illustrated Biochemistry. 27th edition. Edited by Murray RK, Granner DK, Rodwell VW. Boston, U.S.A: McGraw Hill; 2006:209-216.
- [32]Mayes PA: Metabolism of lipids. 1. Fatty acids. In Review of Physiological Chemistry. 17th edition. Edited by Harper HA, Rodwell VW, Mayes PA. San Franscisco. Lange; 1979:321-342.
- [33]Reasor MJ, Kacew S: Drug-induced phospholipidosis: are there functional consequences? Exp Biol Med 2001, 226(9):825-830.
- [34]Sawada H, Takami K, Asahi S: A toxicogenomic approach to drug-induced phospholipidosis; analysis of its induction mechanism and establishment of a novel in-vitro screening system. Toxicol Sci 2005, 83:282-292.
- [35]Abe A, Hiraoka M, Shayman JA: A role for lysosomal phospholipase A2 in drug-induced phospholipidosis. Drug Met Lett 2007, 1:49-53.
- [36]Ooi LG, Liong MT: Cholesterol-lowering effects of probiotics and prebiotics: a review of in-vivo and in-vitro findings. Int J Mol Sci 2010, 11:2499-2522.