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Oxidative stress and postmortem meat quality in crossbred lambs.
Herrera, Nicolas J; Bland, Nicolas A; Ribeiro, Felipe A; Henriott, Morgan L; Hofferber, Eric M; Meier, Jakob; Petersen, Jessica L; Iverson, Nicole M; Calkins, Chris R.
Affiliation
  • Herrera NJ; Department of Animal Science, University of Nebraska-Lincoln, Lincoln, NE 68583-0908, USA.
  • Bland NA; Department of Animal Science, University of Nebraska-Lincoln, Lincoln, NE 68583-0908, USA.
  • Ribeiro FA; Department of Animal Science, University of Nebraska-Lincoln, Lincoln, NE 68583-0908, USA.
  • Henriott ML; Department of Animal Science, University of Nebraska-Lincoln, Lincoln, NE 68583-0908, USA.
  • Hofferber EM; Department of Biological Systems Engineering, University of Nebraska-Lincoln, Lincoln, NE 68503-0908, USA.
  • Meier J; Department of Biological Systems Engineering, University of Nebraska-Lincoln, Lincoln, NE 68503-0908, USA.
  • Petersen JL; Department of Animal Science, University of Nebraska-Lincoln, Lincoln, NE 68583-0908, USA.
  • Iverson NM; Department of Biological Systems Engineering, University of Nebraska-Lincoln, Lincoln, NE 68503-0908, USA.
  • Calkins CR; Department of Animal Science, University of Nebraska-Lincoln, Lincoln, NE 68583-0908, USA.
J Anim Sci ; 99(7)2021 Jul 01.
Article in En | MEDLINE | ID: mdl-33991192
ABSTRACT
The objective of this study was to evaluate effects of different levels of lipopolysaccharide (LPS)-mediated oxidative stress on fresh meat quality. Crossbred lambs (n = 29) were blocked by weight and fed a standard finishing ration for the duration of the study. Lambs were individually housed and treatment groups were administered one of three intravenous injections every 72 h across a three-injection (9-day) cycle saline control (control), 50 ng LPS/kg body weight (BW) (LPS50), or 100 ng LPS/kg BW (LPS100). Rectal temperatures were measured to indicate inflammatory response. Lambs were harvested at the Loeffel Meat Laboratory and 80 mg of pre-rigor Longissimus lumborum were collected in control and LPS100 treatments within 30 min postmortem for RNA analysis. Wholesale loins were split and randomly assigned 1 or 14 d of wet aging. Chops were fabricated after aging and placed under retail display (RD) for 0 or 7 d. Animal was the experimental unit. LPS-treated lambs had increased (P < 0.05) rectal temperatures at 1, 2, 4, and 24 h post-injection. Transcriptomics revealed significant (Praw < 0.05) upregulation in RNA pathways related to generation of oxidative stress in LPS100 compared with control. A trend was found for tenderness (Warner-Bratzler shear force, WBSF; P = 0.10), chops from LPS50 having lower shear force compared with control at 1 d postmortem. Muscle from LPS50 treatment lambs exhibited greater troponin T degradation (P = 0.02) compared with all treatments at 1 d. Aging decreased WBSF (P < 0.0001), increased sarcoplasmic calcium concentration (P < 0.0001), pH (P < 0.0001), and proteolysis (P < 0.0001) across treatments. Following aging, chops increased discoloration as RD increased (P < 0.0001), with control chops aged 14 d being the most discolored. Chops from lambs given LPS had higher (P < 0.05) a* values compared with control at 14 d of aging. The L* values were greater (P < 0.05) in LPS100 compared with both LPS50 and control. Aging tended (P = 0.0608) to increase lipid oxidation during RD across either aging period. No significant differences (P > 0.05) in sarcomere length, proximate composition, fatty acid composition, or isoprostane content were found. These results suggest that defined upregulation of oxidative stress has no detriment on fresh meat color, but may alter biological pathways responsible for muscle stress response, apoptosis, and enzymatic processes, resulting in changes in tenderness early postmortem.
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Full text: 1 Database: MEDLINE Main subject: Sheep, Domestic / Meat Limits: Animals Language: En Year: 2021 Type: Article

Full text: 1 Database: MEDLINE Main subject: Sheep, Domestic / Meat Limits: Animals Language: En Year: 2021 Type: Article