SELECTIVE CECAL BACTERIAL CHANGES MEDIATE THE ADVERSE EFFECTS ASSOCIATED WITH HIGH PALMOLEIN OR HIGH STARCH DIETS: PROPHYLACTIC ROLE OF FLAX OIL

Authors

  • Annapurna V. V. Microbiology and Immunology Division
  • Hemalatha R. Microbiology and Immunology Division
  • Raviteja A. CMR College of Pharmacy, Affiliated to Jawaharlal Nehru Technological University, Hyderabad 501401, India
  • Ramaraju Avs. Department of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research, Hyderabad 500037, India
  • Narendra Babu K. Microbiology and Immunology Division
  • Thirupathaiah Y. Microbiology and Immunology Division
  • Shujauddin Mohd. Microbiology and Immunology Division
  • Harishankar N. National Centre for Laboratory Animal Sciences
  • Balakrishna N. Statistics Division, National Institute of Nutrition, Jamai-Osmania, Hyderabad 500007, India

Keywords:

Palmolein, Starch, Flax oil, Calorie intake, Cecal bacteria, Immune function, Body composition, Lipid profile, Omega 3 fatty acids

Abstract

Objective: Studies on the dynamics of gut bacteria in relation to metabolic adverse effects induced by high palmolein or high starch diets and in relation to health benefits of uncommon foods are lacking. Our aim was to assess under controlled conditions, the impact of vegetable based palmitic acid rich, high fat diet or a high starch diet on various metabolic parameters in relation to selective gut bacterial alterations in rats and also to see the effect of flaxseed oil supplementation on these parameters.

Methods: Wistar Rats were fed for 4 mo either a control diet(CT) or a 30% high fat diet (HF) or HF diet with flax oil supplemented at two different doses (HFF1 and HFF2) or a 78% high starch diet (HC) after which they were sacrificed and analyzed for selective cecal bacteria, hematology, immune function and body composition.

Results: High palmolein diet fed rats showed a decrease in colony forming units of lactobacillus, enterococci, streptococci bacteria and an increase in enterobacteriaceae in the cecum unlike HC fed rats. While high palmolein diet was found to impair immunity and increase inflammation, high starch diet affected body composition and lipid profile. Supplementing the flax seed oil ameliorated most of the adverse effects of high palmolein diet.

Conclusions: Independent of energy intakes both high palmolein and high starch intakes have differential adverse effects. It can be envisaged that the adverse effects of feeding palmolein are mediated through immune impairment and inflammatory response, which in turn are associated with altered gut bacteria profile; and flax oil was found to have a prophylactic role in controlling these adverse effects. This study emphasizes the need to evaluate immunological as well as bacterial profile while assessing the safety of dietary fats in addition to traditional methods.

 

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References

Patrice D Cani, Rodrigo Bibiloni, Claude Knauf, Aure lie Waget, Audrey M Neyrinck, Nathalie M Delzenne, et al. Changes in gut microbiota control metabolic endotoxemia-inducedinflammation in high-fat diet–induced obesity and diabetes in mice. Diabetes 2008;57:1470–81.

Kerstin Stemmer, Diego Perez-Tilve, Gayathri Ananthakrishnan, Anja Bort, Randy J Seeley, Matthias H Tschop, et al. High-fat-diet-induced obesity causes an inflammatory and tumor-promoting microenvironment in the rat kidney. Dis Models Mech 2012;5:627-35.

Mohan V, Radhika G, Vijayalakshmi P, Sudha V. Can the diabetes/cardiovascular disease epidemic in India be explained, at least in part, by excess refined grain (rice) intake? Indian J Med Res 2010;131:369-72.

Wolever TMS, Mehling C. Long term effect of varying the source or amount of dietary carbohydrate on postprandial plasma glucose, insulin, triacylglycerol and free fatty acid concentrations in subjects with impaired glucose tolerance. Am J Clin Nutr 2003;77:612-21.

Wilkes, Jason J, Arend Bonen, Rhonda C. Bell. A modified high-fat diet induces insulin resistance in rat skeletal muscle but not adipocytes. Am J Physiol (Endocrinol Metab) 1998;275:E679–86.

Antoni Zamora. Fats, oils, fatty acids, triglycerides. Fatty acid composition of somecommon edible fats and oils; 2013. Available form: URL: http://www.scientificpsychic. com/ fitness/fattyacids1.html. [Last accessed on 25 Aug 2015].

Leonard H Storlien, Arthur B Jenkins, Donald J Chisholm, Wendy S Pascoe, Sue Khouri, Edward W Kraegen. Influence of dietary fat composition on development of insulin resistance in rats: relationship to muscle triglyceride and omega-3 fatty acids in muscle phospholipid. Diabetes 1991;40:280-9.

Simopoulos AP. Omega-3 fatty acidsin inflammation and autoimmune diseases. J Am Coll Nutr 2002;21:495-505.

Guide for the Care and Use of Laboratory Animals: NIH Publication; 1985.

Azita Hekmatdoost, Mohammad M Feizabadi, Abolghasem Djazayery, Abbas Mirshafiey, Mohammad R Eshraghian, et al. The effect of dietary oils on cecalmicroflora in experimental colitis in mice. Indian J Gastroenterol 2008;27:186-9.

Microbiology Techniques. Quantifying Bacteria by Spread Plate. Available from: URL: http://www2.hendrix.edu/biology/Cell Web/Techniques/microspread. html. [Last accessed 25 Aug 2015].

Harrison GG, Van Itallie. TB Estimation of body composition: 10. A new approach based on electromagnetic principles. Am J Clin Nutr 1982;35:1176-9.

Moriguchi S, Kato M, Sakai K, Yamamoto S, Shimizu E. Decreased mitogen response of splenic lymphocytes in obese Zucker rats is associated with the decreased expression of glucose transporter1 (GLUT-1). Am J Clin Nutr 1998;67:1124-9.

Pawar RS, Jain AP, Kashaw SK. Haematopoietic activity of Asteracanthalongifolia on cyclophosphamide-induced bone marrow suppression. Indian J Pharm Sci 2006;68:337-40.

Laugerette F, Furet JP, Debard C, Daira P, Loizon E, Geloen A, et al. Oil composition of high-fat diet affects metabolic inflammation differently in connection with endotoxin receptors in mice. Am J Physiol: Endocrinol Metab 2013;302:E374-86.

Kirsty Dougal, Gabriel de la Fuente, Patricia A Harris, Susan E Girdwood, Eric Pinloche, Raymond J Geor, et al. Characterisation of the faecal bacterial community in adult and elderly horses fed a high Fibre, high oil or high Starch diet using 454 pyro sequencing. PLoS ONE 2014;9:e87424.

Simin Liu, ScD. Intake of refined carbohydrates and whole grain foods in relation to risk of type 2 diabetes mellitus and coronary heart disease. J Am Coll Nutr 2002;21:298–306.

Atkins, Robert Dr. Atkins' New Diet Revolution, Revised Edition. Evans; 2003.

Takeuchi H, Matsuo T, Tokuyama K, Shimomura Y, Suzuki M. Diet-induced thermogenesis is lower in rats fed a Lard diet than in those fed a high oleic acid safflower oil diet, a safflower oil diet or a linseed oil diet. J Nutr 1995;125:920-5.

Yoshiharu Shimomãoera, Tomohiro Tamãoera, Masashice Suzuki. Less body fat accumulation in rats fed a safflower oil diet than in rats fed a beef tallow diet. J Nutr 1990;120:1291-6.

Srinivasan MR, Satyanarayana MN. Influence of capsaicin, curcumin and ferulic acid in rats fed high fat diets. J Biosci 1987;12:143-52.

Elizabeth J Parks, Ronald M Krauss, Mark P Christiansen, Richard A Neese, Marc K Hellerstein. Effects of a low-fat, high-carbohydrate diet on VLDL-triglyceride assembly, production, and clearance. J Clin Invest 1999;104:1087-96.

Waddelland M, Fallon HJ. The effect of high-carbohydrate diets on liver triglyceride formation in the rat. J Clin Invest 1973;52:2725-31.

Ble-Castillo JL, Aparicio-Trapala MA, Juárez-Rojop IE, Torres-Lopez JE, Mendez JD, et al. Differential effects of high-carbohydrate and high-fat diet composition on metabolic control and insulin resistance in normal rats. J Environ Res Public Health 2012;9:1663-76.

Li H, Lelliott C, HÃ¥kansson P, Ploj K, Tneld A, Verolin-Johansson M. Intestinal, adipose, and liver inflammation in diet-induced obese mice. Metabolism 2008;54:1704-10.

Edem DO. Palm oil: biochemical, physiological, nutritional, haematological and toxicological aspects. a review. Plant Foods Hum Nutr 2002;57:319-41.

Koh Chu-Sing. Comments on draft document: diet, nutrition and the prevention of chronic diseases. Malaysian palm Oil Promotion Council. Available from: URL: http://www.who.int/ dietphysicalactivity/media/en/gsfao_cmo_068.pdf. [Last accessed 25 Aug 2015].

Palm oil (Elaeisguineensis) Natural Standard Professional Monograph; 2013. Available from: URL: http://www. naturalstandard.com. [Last accessed 25 Aug 2015].

Ekine OA, Ironkwe MO, Oruwari BM. The relationships between feeding graded concentration of dietary palm oil and lipid depositions in tissues, body and organ weights of rabbits. Nigerian Veterinary J 2009;29:58-64.

Shen CL, Yeh JK, Rasty J, Li Y, Watkins BA. Protective effect of dietary long-chain n-3 polyunsaturated fatty acids on bone loss in gonad-intact middle-aged male rats. Br J Nutr 2006;95:462-8.

Rafaelbitzur, Hofit Cohen, Yehuda Kamari, Aviv Shaish, Dror Harats. Triglycerides and HDL Cholesterol. Diabetes Care 2009;32:S373-7.

Published

01-11-2015

How to Cite

V., A. V., H. R., R. A., R. Avs., N. B. K., T. Y., S. Mohd., H. N., and B. N. “SELECTIVE CECAL BACTERIAL CHANGES MEDIATE THE ADVERSE EFFECTS ASSOCIATED WITH HIGH PALMOLEIN OR HIGH STARCH DIETS: PROPHYLACTIC ROLE OF FLAX OIL”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 7, no. 11, Nov. 2015, pp. 89-95, https://journals.innovareacademics.in/index.php/ijpps/article/view/8297.

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