Abstract

Conjugated linoleic acid was detected in rabbit caecotrophs, due to the presence of microbial lipid activity in rabbit cecum. However, the effect of CLA as a functional food in growing rabbit is not well established. Therefore, this study was conducted to determine the effect of CLA on production, meat quality, and its nutrigenomic effect on edible parts of rabbit carcass including skeletal muscle, liver, and adipose tissue. Therefore, seventy five weaned V-Line male rabbits, 30 days old, were randomly allocated into three dietary treatments receiving either basal control diet, diet supplemented with 0.5% (CLAL), or 1% CLA (CLAH). Total experimental period (63 d) was segmented into 7 days adaptation and 56 days experimental period. Dietary supplementation of CLA did not alter growth performance, however, the fat percentage of longissimus lumborum muscle was decreased, with an increase in protein and polyunsaturated fatty acids (PUFA) percentage. Saturated fatty acids (SFA) and mono unsaturated fatty acids (MUFA) were not increased in CLA treated groups. There was tissue specific sensing of CLA, since subcutaneous adipose tissue gene expression of PPARA was downregulated, however, CPT1A tended to be upregulated in liver of CLAL group only (P = 0.09). In skeletal muscle, FASN and PPARG were upregulated in CLAH group only (P ≤0.01). Marked cytoplasmic vacuolation was noticed in liver of CLAH group without altering hepatocyte structure. Adipocyte size was decreased in CLA fed groups, in a dose dependent manner (P <0.01). Cell proliferation determined by PCNA was lower (P <0.01) in adipose tissue of CLA groups. Our data indicate that dietary supplementation of CLA (c9,t11-CLA and t10,c12- CLA) at a dose of 0.5% in growing rabbit diet produce rabbit meat rich in PUFA and lower fat % without altering growth performance and hepatocyte structure.

Highlights

  • In ruminants, the effect of microbial fermentation on dietary long-chain fatty acids (LCFA), especially biohydrogenation of polyunsaturated LCFA (PUFA), is relatively well known

  • This could explain the presence of traces of c9,t11C18:2 conjugated linoleic acid (CLA) in rabbit meat and adipose tissue [2,4], CLA (c9, t11-CLA) was only detected in neutral and not the polar lipid fraction of rabbit skeletal muscle [4], supplementation of CLA in rabbit feed is needed to study its nutrigenomic properties

  • Rabbits were blocked for body weight (612.8 ± 24.89 g) and completely randomized into three (n = 25/group) isonitrogenous, isocaloric dietary treatments: 1) CON group was fed a basal control diet supplemented with 1% oleic acid (Techno Pharmachem, India), 2) CLAL group was fed a diet supplemented with 0.5% isomer-mix CLA (Lutrell Pure; BASF, Ludwigshafen,Germany; certified to contain equal proportion of c9,t11- and t10,c12-CLA; EFSA, [20, 21] plus 0.5% oleic acid, and 3) CLAH group was fed a diet supplemented with 1% isomer-mix CLA

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Summary

Introduction

The effect of microbial fermentation on dietary long-chain fatty acids (LCFA), especially biohydrogenation of polyunsaturated LCFA (PUFA), is relatively well known. For most non-ruminant herbivores this effect is likely irrelevant, considering that no LCFA present in the hindgut is absorbed; the coprophagy in rabbit let the LCFA that went through the hindgut microbial fermentation to be absorbed, influencing the fatty acid profiling in the body [2,3]. This could explain the presence of traces of c9,t11C18:2 conjugated linoleic acid (CLA) in rabbit meat and adipose tissue [2,4], CLA (c9, t11-CLA) was only detected in neutral and not the polar lipid fraction of rabbit skeletal muscle [4], supplementation of CLA in rabbit feed is needed to study its nutrigenomic properties. In non-ruminant animals, dietary supplementation of CLA affected growth performance, fatty acid profile, and meat quality [7,8,9]

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