Abstract

Simple SummaryThe lower survival rate and diminished overall growth and performance of low birth weight piglets is an economic and ethical issue in pig production. Adapted nutrition can help to compensate growth retardation, in particular, if nutrients in milk are not sufficient for newborn piglets. This study investigated the effects of oral glutamine supplementation during the first days after birth on skeletal muscle morphology of piglets with low or normal birth weight. The results indicated that glutamine supplementation changed the intramuscular amino acid concentration in the short term and influenced the muscle fiber size and abundance of myosin heavy chain isoforms within longissimus and semitendinosus muscle in neonatal piglets. Furthermore, differences in muscle fiber size and intramuscular lipid deposition were observed between low and normal birth weight piglets that disappeared in older piglets, independent of supplementation. The results indicated a delayed muscle development in low birth weight piglets. This delay can partly be compensated during growth by adequate nutrition.Adapted nutrition can improve the growth of low birth weight (LBW) piglets. Since maternal milk is thought to provide insufficient glutamine (Gln) for LBW piglets, the current study investigated the influence of Gln supplementation during the early suckling period on development and lipid deposition in skeletal muscle. The weight differences between LBW and normal birth weight (NBW) littermates persisted from birth to slaughter (p < 0.001). However, intramuscular Gln and Ala concentrations were altered in piglets according to the supplementation (p < 0.01). There were larger muscle fibers (p = 0.048) in Gln-supplemented piglets. Capillarization or nuclei number per muscle fiber was not influenced by birth weight (BiW) or Gln supplementation. Abundance of myosin heavy chain (MYH) isoforms was slightly altered by Gln supplementation. LBW piglets had more lipid droplets than NBW piglets at day 5 of life in both muscles (p < 0.01). The differences decreased with age. Adipocyte development increased with age, but was not influenced by BiW or supplementation. The results indicate that BiW differences were accompanied by differences in lipid deposition and muscle fiber structure, suggesting a delayed development in LBW piglets. Supplementation with Gln may support piglets to overcome those disadvantages.

Highlights

  • The increased demand for pork has led to selection for larger litter sizes in pig production which has resulted in increased variation of piglet birth weight (BiW) within a litter [1]

  • The current study focused on both the effects of BiW on the development of muscle morphology, including muscle fibers, intramuscular lipids, adipocytes and capillarization during the early postnatal period and on their modulation with Gln supplementation

  • There was a trend for more MYH1 protein in low birth weight (LBW) piglets at 12 dpn (p = 0.074)

Read more

Summary

Introduction

The increased demand for pork has led to selection for larger litter sizes in pig production which has resulted in increased variation of piglet birth weight (BiW) within a litter [1]. About 15–20% of piglets in one litter are affected by low birth weight (LBW) or intrauterine growth restriction (IUGR) caused by inadequate maternal nutrition and insufficient placental functions [2,3]. These animals exhibit lower survival rates, slower postnatal growth and faster deposition of body fat in comparison with normal or heavy birth weight piglets [4]. IUGR piglets or LBW piglets have lower muscle growth and increased fat deposition [7], resulting in higher carcass lipid content and diminished meat quality at slaughter [2]. Adapted nutrition can be used to help LBW piglets partially compensate for the associated negative impacts on growth and developmental retardation

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call