Antibiotics promote abdominal fat accumulation in broilers

Anim Sci J. 2020 Jan-Dec;91(1):e13326. doi: 10.1111/asj.13326.

Abstract

Antibiotics stimulate the growth of animals but result in drug residues and bacterial resistance. In this study, the negative effect of antibiotics on abdominal fat deposition was evaluated in broilers. The results showed that adding both chlortetracycline (50 g/1,000 kg) and tylosin (50 g/1,000 kg) significantly increased abdominal fat weight, abdominal fat percentage (p < .05), and triglyceride and cholesterol levels (p < .05) in blood. Also, both products synchronously stimulated intestinal absorption and synthesis of liver fat. The expression levels of the peroxisome proliferator-activated receptor γ (PPARγ), diacylgycerol acyltransferase 2 (DGAT2), lipoprotein lipase (LPL), and fatty acid-binding protein (FABP4) genes in abdominal fat tissue significantly increased (p < .05 or 0.01) when antibiotics were added to the feed. However, no significant difference was found in expression of the fatty acid synthesis (FAS) or acetyl CoA carboxylase (ACC) genes. Further in vitro study results revealed that antibiotics had no effect on fat content or the related gene expression levels in preadipocytes. In summary, the antibiotics induced fat deposition in adipose tissues by activating extracellular absorption of fatty acids from intestinal absorption and synthesis of liver fat. However, it shows no direct regulation by adipose tissue.

Keywords: abdominal fat deposition; antibiotic; broiler; gene expression; regulatory mechanism.

MeSH terms

  • Abdominal Fat / metabolism*
  • Adipose Tissue / metabolism
  • Animals
  • Anti-Bacterial Agents / adverse effects
  • Anti-Bacterial Agents / pharmacology*
  • Chickens / growth & development*
  • Chickens / metabolism*
  • Chlortetracycline / adverse effects
  • Chlortetracycline / pharmacology*
  • Cholesterol / blood
  • Diacylglycerol O-Acyltransferase / metabolism
  • Fatty Acid-Binding Proteins / genetics
  • Fatty Acid-Binding Proteins / metabolism
  • Gene Expression
  • Intestinal Absorption
  • Lipoprotein Lipase / genetics
  • Lipoprotein Lipase / metabolism
  • PPAR gamma / genetics
  • PPAR gamma / metabolism
  • Triglycerides / blood
  • Tylosin / adverse effects
  • Tylosin / pharmacology*

Substances

  • Anti-Bacterial Agents
  • Fatty Acid-Binding Proteins
  • PPAR gamma
  • Triglycerides
  • Cholesterol
  • Diacylglycerol O-Acyltransferase
  • Lipoprotein Lipase
  • Chlortetracycline
  • Tylosin