Relative bioavailability of humate-manganese complex for broilers fed a corn-soya bean meal diet

J Anim Physiol Anim Nutr (Berl). 2019 Jan;103(1):108-115. doi: 10.1111/jpn.13009. Epub 2018 Oct 23.

Abstract

The experiment was conducted to investigate the bioavailability of manganese (Mn) from humate-Mn complex relative to Mn sulphate for the starter broilers fed a conventional corn-soya bean meal diet. A total of 560 1-day-old Arbor Acres male broiler chicks were randomly allotted to one of eight replicate cages (10 chicks per cage) for each of seven treatments in a completely randomized design involving a 2 × 3 factorial arrangement of treatments with two Mn sources (humate-Mn and Mn sulphate) and three levels of added Mn (60, 120 or 180 mg Mn/kg) plus a Mn-unsupplemented control diet containing 27.23 mg Mn/kg by analysis. At 14 days of age, the blood, liver, heart and tibia were collected for Mn analyses, and the activity and mRNA abundance of heart manganese superoxide dismutase (MnSOD). The results showed that humate-Mn supplementation decreased feed intake from day 1 to day 14, whereas it did not influence (p > 0.20) body weight at day 14 as compared to Mn sulphate. The Mn source did not influence Mn concentration in the liver, heart and tibia, and the activity and mRNA abundance of heart MnSOD, while humate-Mn decreased plasma Mn as compared to Mn sulphate. The Mn concentration in the plasma and heart, and the activity and mRNA abundance of heart MnSOD increased linearly as dietary Mn concentration increased. Based on slope ratios from multiple linear regressions of Mn concentrations in the plasma and heart, and the activity and mRNA abundance of heart MnSOD on daily intake amount of dietary analysed Mn, the bioavailability of humate-Mn complex relative to Mn sulphate (100%) was 82.8, 90.4, 82.8 and 81.9 respectively. These results indicated that the Mn from humate-Mn complex was just as bioavailable as the Mn from Mn sulphate for the starter broilers (day 1-14).

Keywords: Mn concentration; MnSOD; bioavailability; broiler; gene expression; humate-manganese.

Publication types

  • Clinical Trial, Veterinary

MeSH terms

  • Animal Feed / analysis
  • Animal Nutritional Physiological Phenomena
  • Animals
  • Biological Availability
  • Chickens / metabolism*
  • Diet / veterinary
  • Gene Expression Regulation, Enzymologic / drug effects
  • Glycine max*
  • Humic Substances*
  • Male
  • Manganese / administration & dosage
  • Manganese / pharmacokinetics*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Random Allocation
  • Superoxide Dismutase / metabolism
  • Zea mays*

Substances

  • Humic Substances
  • RNA, Messenger
  • Manganese
  • Superoxide Dismutase