Effects of standard diets from different sources on growth and some organ parameters of rats


Keywords:
Diet growth performance internal organ open formula wistar
B. GENC
M. SALMAN
Ş. TÜTÜNCÜ
M. ERMIŞ
H. MURUZ
Abstract

This study aims to determine the effects of open and closed formulated standard diets supplied from different sources on growth performance and internal organ development of laboratory rats. Five-week-old 32 Wistar rats were used. A special control group diet was produced in accordance with the criteria determined by the National Research Council (NRC) (1995). Three different most preferred commercial open and closed-formula diets produced by international and local companies were used as trial groups’ diets. The experiment was carried out for 12 weeks. Weekly feed consumption, body weight change, internal organ weight, intestinal organ weigths and lengths, intestinal villi heigth and crypt depth were measured in groups. The body weight values of the control group and the first group fed with open-formula diet were found at the highest level (P <0.05). The control group diet had a positive effect on small intestine villi heigth and crypt depth (P <0.05). The nutrient contents and energy values of the diets of experimental groups were determined as different from the commercial firm notifications. As a result of the research, it is concluded that the diets prepared with open-formula give more reliable results in the growth performance and development of internal organs of Wistar rats.

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Andreoli MF, Stoker C, Rossetti MF, Lazzarino GP, Luque EH, Ramos JG (2016) Dietary withdrawal of phytoestrogens resulted in higher gene expression of 3-beta-HSD and ARO but lower 5-alpha-R-1 in male rats. Nutrition research 36: 1004-1012.
AOAC (2012) Official methods of analysis 19th ed. Association of official analytical of official chemicals, Washington, DC, USA.
Bailey SA, Zidell RH, Perry RW (2004) Relationships between organ weight and body/brain weight in the rat: what is the best analytical endpoint? Toxicol Pathol 32: 448-466.
Barszcz M, Tusino A, Taciak M, Lukowicz JP, Molenda M, Morawski A (2014): Effect of the composition and autoclave sterilizationof diets for laboratory animals on pellet hardness and growth performance of mice. Ann Anim Sci 14 (2): 315-328.
Barnard DE, Lewis SM, Teter BB, Thigpen JE (2009) Open- and Closed-Formula Laboratory Animal Diets and Their Importance to Research. J Am Assoc Lab Anım 48: 709-713.
Bellinger L, Langley-Evans SC (2005) Fetal programming of appetite by exposure to a maternal low-protein diet in the rat. Clin Sci 109: 413-420.
Belobrajdic DP, McIntosh GH, Owens JA (2014) A High-Whey-Protein Diet Reduces Body Weight Gain and Alters Insulin Sensitivity Relative to Red Meat in Wistar Rats. J Nutr 134: 1454-1458.
Bielohuby M, Bodendorf K, Brandstetter H, Bidlingmaier M, Kienzle E (2010): Predicting metabolisable energy in commercial rat diets:physiological fuel values may be misleading. Br J Nutr 103(10):1525-33.
Bowen J, Noakes M, Clifton PM (2006a) Energy intake, ghrelin, and cholecystokinin after different carbohydrate and protein preloads in overweight men. J Clin Endocrinol Metab 91: 1477-83.
Bowen J, Noakes M, Clifton PM (2006b) Appetite regulatory hormone responses to various dietary proteins differ by body mass index status despite similar reductions in ad libitum energy intake. J Clin Endocrinol Metab 91: 2913-19.
Crossmon G (1937) A modification of Mallory’s connective tissue stain with a discussion of the principles involved. Anat Rec 69:33-38.
Faith R, Hessler JR (2006) Housing and environment, In: Suckow MA, Weisbroth SH, Franklin CL, editors. The laboratory rat. Academic Press San Diego: pp 303-337.
Faipoux R, Tom´e D, Gougis S, Darcel N, Fromentin G (2008) Proteins activate satiety-related neuronal pathways in the brainstem and hypothalamus of rats. J Nutr 38:1172-78.
Garlick PJ, McNurlan MA, Ballmer PE (1991) Influence of dietary protein intake on whole-body protein turnover in humans. Diabetes Care 14:1189-98.
Genç B (2017) Laboratuvar Hayvanı Diyetleri ve Hayvan Besleme Bilimindeki Yeri. Lalahan Hay Araşt Enst Derg 57: 105-111.
Idoko AS, Oladiji AT, Ilouno E (2015) Growth Performance of Rats Maintained On Citrullus colocynthis Seed Coat-based Diet. IOSR-JBB (1) 4: 09-14.
Kasaoka S, Tsuboyama-Kasaoka N, Kawahara Y, Inoue S, Tsuji M, Ezaki O, Kato H, Tsuchiya T, Okuda H, Nakajima S (2004) Histidine supplementation suppresses food intake and fat accumulation in rats. Nutrition 20: 991-96.
Keskin H (1975) Gıda Kimyası, İstanbul Üniversitesi Yayınları İstanbul: p 1046.
King IS, Paterson JYF, Peacock MA, Smith MW, Syme G (1983) Effect of diet upon enterocyte differentiation in the rat jejunum. J Physiol 344: 465-481.
Krishnakumari MK, Rajalakshmi D, Sreenivasan V, Ramasundaram CP (1979) Feeding responses of young and adult albino rats (Rattus norvegicus) to a mixed basal diet. Prec Indian Acad Sci 88: 367-375,
Lejeune MPGM, Westerterp KR, Adam TC, Luscombe-Marsh ND, Plantenga MSW (2006) Ghrelin and glucagon-like peptide 1 concentrations, 24-h satiety, and energy and substrate metabolism during a high-protein diet and measured in a respiration chamber. Am J Clin Nutr. 83: 89-94.
Lephart ED, Porter JP, Lund TD, Bu L, Setchell KD, Ramoz G, Crowley WR (2004) Dietary isoflavones alter regulatory behaviors, metabolic hormones and neuroendocrine function in Long-Evans male rats. Nutr Metab 1: 16.
Mc Kay JA, Groom A, Potter C, Coneyworth LJ, Ford D, Mathers JC, Relton CL (2012) Genetic and non-genetic influences during pregnancy on infant global and site specific DNA methylation: role for folate gene variants and vitamin B12. PLoS One 7 (3).
Nagano T, Wu W, Tsumura K, Yonemoto YH, Kamada T, Haruma K (2016) The inhibitory effect of soybean and soybean isoflavone diets on 2, 4-dinitrofluorobenzene-induced contact hypersensitivity in mice. Bıoscı Bıotech Bıoch 80: 991-997.
NRC (1995) Nutrient Requirements of Laboratory Animals, Fourth Revised Edition, National Academies Press Washington D.C. : p 13.
Pelizzon M (2016) Choice of laboratory animal diet influences intestinal health. Lab Animal 45: 238-239.
Pichon L, Potier M, Tome D, Mikogami T, Laplaize B, Martin RC, Fromentin G (2008) High-protein diets containing different milk protein fractions differently influence food intake and adiposity in rat. Br J Nutr 99: 739- 48.
Plantenga MSW, Nieuwenhuizen A, Tom´e D, Soenen S, Westerterp KR (2009) Dietary Protein, Weight Loss, and Weight Maintenance. Annu Rev Nutr 29:21-41.
Ronis MJ, Acevedo HG, Blackburn ML, Cleves MA, Singhal R, Badger TM (2016) Uterine responses to feeding soy protein isolate and treatment with 17β-estradiol differ in ovariectomized female rats. Toxicol Appl Pharm (297): 68-80.
Schaafsma G (2005) The protein digestibility-corrected amino acid score (PDCAAS)-A concept for describing protein quality in foods and food ingredients: A critical review. J AOAC Int 88: 988-994.
Syme G (1982) The effect of protein-deficient isoenergetic diets on the growth of rat jejunal mucosa. Br J Nutr 48: 25-36.
Thigpen JE, Setchell KDR, Saunders HE, Haseman JK, Grant MG, Forsythe DB (2004) Selecting the appropriate rodent diet for endocrine disruptor research and testing studies. ILAR J 45: 401-416.
Thigpen JE, Setchell KRD, Padilla-Banks E, Haseman JK, Saunders HE, Caviness GF, Kissling GE, Grant MG, Forsythe DB (2007) Variations in the phytoestrogen content between different mill dates of the same diet produces significant differences in the time of vaginal opening in CD1 mice and F344 rats but not in CD Sprague-Dawley rats. Environ Health Perspect 115:1717-1726.
Tome D (2004) Protein, amino acids and the control of food intake. Br J Nutr 92: 27-30.
Torre-Villalvazo I, Tovar AR, Ramos-Barragan VE, Cerbon-Cervantes MA, Torres N (2008) Soy protein ameliorates metabolic abnormalities in liver and adipose tissue of rats fed a high fat diet. J Nutr 138:462-468.
Vanhees K, Vonhögen IGC, Van Schooten FJ, Godschalk RWL (2014) You are what you eat, and so are your children: the impact of micronutrients on the epigenetic programming of offspring. Cell Mol Life Sci 71:271-285.
Veldhorst M, Smeets A, Soenen S, Hochstenbach-Waelen A, Hursel R, Diepvens K, Lejeune M, Luscombe-Marsh N, Plantenga MW (2008) Protein-induced satiety: effects and mechanisms of different proteins. Physiol Behav 23: 300-307.
Yalçın (2011) Yem analizleri (8. Bölüm) Yemler yem hijyeni ve teknolojisi. Ed. Ergün A, Tuncer ŞD Ankara. p: 372.
Yürük AA (2014) Sıçanlarda maternal diyetle fruktoz alımının fetüse etkilerinin bazı lipit parametreleri ve lipogenez açısından incelenmesi. Hacettepe Üniversitesi Sağlık Bilimleri Enstitüsü. Ankara: pp 4-80.