» Articles » PMID: 37466757

Effect of Parenteral Supplementation of Minerals and Vitamins on Oxidative Stress Biomarkers and Hepatic Fatty Acid Metabolism in Dairy Cows During the Transition Period

Overview
Date 2023 Jul 19
PMID 37466757
Authors
Affiliations
Soon will be listed here.
Abstract

In the present work we aimed to study the effects of parenteral vitamin and mineral supplementation on hepatic fatty acid metabolism as well as on the oxidative stress biomarkers in biological samples of transition cows. The supplemented group (SG, n = 11) received a subcutaneous injection of 5 mL of vitamin A palmitate 35 mg/mL, vitamin E acetate 50 mg/mL plus other injection of 5 mL of copper edetate 10 mg/mL, zinc edetate 40 mg/mL, manganese edetate 10 mg/mL, and sodium selenite 5 mg/mL on days - 60, - 30, and 7 (± 3) relative to calving. The control group (CG, n = 11) received two subcutaneous injections of 5 mL of 9 mg/mL sodium chloride at the same times of the SG. Blood, urine, and liver biopsies were sampled 21 (± 3) days before the expected calving date and 7 and 21 (± 3) days after calving. Results revealed that supplemented animals had higher glutation peroxidase (GSH-Px) activity, lower and higher concentration of 3-nitrotyrosine (3-NT) in the liver and plasma, respectively, higher expression of the mitochondrial beta-oxidation enzyme carnitine palmitoyltransferase 1 in the liver, and lower content of hepatic triacylglycerol, mirroring plasma liver function parameters. No differences between groups were found in the superoxide dismutase activity, MDA concentrations, the protein abundance of peroxisomal acyl-CoA oxidase 1, diacylglycerol O-acyltransferase 1, and peroxisome proliferator-activated receptor alpha. These results suggest that the vitamin and mineral supplementation provided to dairy cows had a beneficial effect on GSH-Px activity, hepatic 3-NT concentration, and on the metabolic adaptation during the peripartum period.

Citing Articles

Association between composite dietary antioxidant index and hyperlipidemia: a cross-sectional study from NHANES (2005-2020).

Zhao M, Zhang D, Zhang Q, Lin Y, Cao H Sci Rep. 2024; 14(1):15935.

PMID: 38987566 PMC: 11237065. DOI: 10.1038/s41598-024-66922-0.

References
1.
Li P, Li X, Fu S, Wu C, Wang X, Yu G . Alterations of fatty acid β-oxidation capability in the liver of ketotic cows. J Dairy Sci. 2012; 95(4):1759-66. DOI: 10.3168/jds.2011-4580. View

2.
Angeli E, Rodriguez F, Rey F, Santiago G, Matiller V, Ortega H . Liver fatty acid metabolism associations with reproductive performance of dairy cattle. Anim Reprod Sci. 2019; 208:106104. DOI: 10.1016/j.anireprosci.2019.06.016. View

3.
Weidinger A, Kozlov A . Biological Activities of Reactive Oxygen and Nitrogen Species: Oxidative Stress versus Signal Transduction. Biomolecules. 2015; 5(2):472-84. PMC: 4496681. DOI: 10.3390/biom5020472. View

4.
Gracia-Sancho J, Lavina B, Rodriguez-Vilarrupla A, Garcia-Caldero H, Fernandez M, Bosch J . Increased oxidative stress in cirrhotic rat livers: A potential mechanism contributing to reduced nitric oxide bioavailability. Hepatology. 2008; 47(4):1248-56. DOI: 10.1002/hep.22166. View

5.
Ho E, Galougahi K, Liu C, Bhindi R, Figtree G . Biological markers of oxidative stress: Applications to cardiovascular research and practice. Redox Biol. 2013; 1:483-91. PMC: 3830063. DOI: 10.1016/j.redox.2013.07.006. View