Plasma |
RPM for 28 d prepartum and 60 d postpartum |
Improvements in plasma biomarkers indicating reduced oxidative stress and inflammation and enhanced liver function. Increased neutrophil phagocytosis and oxidative burst. |
Batistel et al. (2018)
|
Plasma |
Abomasal infusion of Glu for first 21 d postpartum |
Infusions of Gln increased the abundance of CD4 T-cells on day 4 postpartum and increased the abundance of monocytes. |
Doepel et al. (2006)
|
Mammary gland |
RPM for 28 d prepartum and 60 d postpartum |
Methionine supply upregulated expression of genes involved in antioxidant metabolism and increased activation of NFE2L2. |
Han et al. (2018)
|
Plasma |
Intravenous infusions of Gln for 5 d post-calving |
Glutamine infusion decreased plasma haptoglobin and increased LPS-binding protein and SAA. |
Jafari et al. (2006)
|
Subcutaneous adipose |
RPM for 28 d prepartum and 60 d postpartum |
Enhanced Met supply increased mRNA and protein abundance of enzymes related to GSH metabolism. |
Liang et al. (2019a)
|
PMNL |
Incubation with Met and/or choline |
Supplemental Met coupled with adequate choline enhanced gene expression of pathogen recognition mechanisms. Methionine ameliorated the increased inflammation and oxidative stress observed when cells were incubated without choline. |
Lopreiato et al. (2019)
|
Plasma and milk |
Protected Gln for 21 d postpartum |
Increased total blood protein and albumin, decreased plasma aspartate aminotransferase, and milk somatic cell count. |
Nemati et al. (2018)
|
Whole blood |
RPM for 21 d prepartum and 30 d postpartum |
Increased whole blood neutrophil phagocytosis on day 21 postpartum with supplemental Met. |
Osorio et al. (2013a) |
Liver |
RPM for 21 d prepartum and 30 d postpartum |
Methionine supply altered flux through 1-carbon metabolism via changes in mRNA to support antioxidant and Met synthesis. |
Osorio et al. (2014a)
|
Liver and plasma |
RPM for 21 d prepartum and 30 d postpartum |
Methionine increased liver GSH and decreased concentrations of plasma biomarkers of inflammation. |
Osorio et al. (2014b)
|
Plasma |
RPM for 28 d during mid-lactation |
Increased proliferative ability of peripheral blood T lymphocytes with supplemental Met. |
Soder and Holden (1999)
|
Plasma |
RPM for 21 d prepartum and postpartum |
Increased antioxidant capacity of plasma and CD4+/CD8+ T lymphocyte ratio with Met supply. |
Sun et al. (2016)
|
Whole blood |
RPM for 21 d prepartum and 30 d postpartum |
Methionine damped the hyper-response of IL-1β during an LPS challenge through improvements in oxidative stress. |
Vailati-Riboni et al. (2017)
|
Plasma |
Jugular infusion of Arg and LPS in mid-lactation cows |
Arginine alleviated LPS-triggered inflammation by decreasing IL-6, inducible NOS, and LPS-binding protein |
Zhao et al. (2018a)
|
Serum |
Jugular infusion of Arg and LPS in mid-lactation cows |
Infusion of Arg promoted antioxidant mechanisms during LPS-triggered inflammation by increasing total antioxidant capacity and GSH peroxidase activity and decreasing malondialdehyde. |
Zhao et al. (2018b)
|
Liver and plasma |
RPM for 21 d prepartum and 30 d postpartum |
Increased hepatic GSH and improved plasma biomarkers of liver function and inflammation with Met. Neutrophil phagocytosis capacity and oxidative burst were also increased with Met. |
Zhou et al. (2016a)
|
Liver |
RPM for 21 d prepartum and 30 d postpartum |
Enhanced Met supply increased mRNA expression of genes associated with PC and antioxidant synthesis. |
Zhou et al. (2017b)
|
PMNL |
RPM for 21 d prepartum and 30 d postpartum |
Decreased expression of genes related to inflammation and oxidative stress. |
Zhou et al. (2018b)
|