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Topic:Oxidative Stress

Oxidative stress in horses refers to an imbalance between the production of reactive oxygen species (ROS) and the ability of the horse's body to detoxify these reactive intermediates or repair the resulting damage. It can occur as a result of various physiological and environmental factors, such as exercise, illness, or exposure to toxins. Oxidative stress can lead to cellular damage, affecting lipids, proteins, and DNA. In horses, it is studied in the context of its potential impact on performance, health, and disease progression. This page compiles peer-reviewed research studies and scholarly articles that explore the mechanisms, effects, and management of oxidative stress in equine health.
Mammalian erythrocyte glutathione reductase: kinetic constants and saturation with cofactor.
American journal of veterinary research    October 1, 1975   Volume 36, Issue 10 1511-1513 
Harvey JW, Kaneko JJ.Glutathione reductase (GR) was studied in erythrocytes of horses, cats, dogs, and man. Glutathione reductase activity was measured in hemolysates with and without preincubation of hemolysates with flavinadenine dinucleotide. The percentage saturation of GR apoenzyme with cofactor (flavin-adenine dinucleotide) was lower in cats and dogs than in horses or man. The greatest amount of inactive apoenzyme was in feline erythrocytes. Total GR activity listed in order by species is cat greater than man greater than dog greater than horse. Kinetic constants for oxidized glutathione and reduced nicotina...
Digitoxin metabolism by rat liver microsomes.
Biochemical pharmacology    September 1, 1975   Volume 24, Issue 17 1639-1641 doi: 10.1016/0006-291x(75)90200-4
Schmoldt A, Benthe HF, Haberland G, Jallon JM, Risler Y, Iwatsubo M, Karuzina II, Bachmanova GI, Kuznetsova GP, Izotov MV, Archakov AI, Kröger H....It has been found that NADPH-dependent hydroxylation of dimethylaniline, aniline, p- and o-nitroanisol and lipid peroxidation is inhibited by the tyrosine-copper (II) complex (low molecular weight analog of superoxide dismutase), which is indicative of a possibility of superoxide radicals formation in these reactions. The inhibition of the above-mentioned reactions with Tyr2-Cu2+ is less pronounced or absent, if cumole hydroperoxide is used as cosubstrate instead of NADPH. Differences in the Tyr2-Cu2+ complex effects on the cumule hydroperoxide-dependent xenobiotics hydroxylation and lipid per...
Photooxidation of horse and sperm-whale myoglobin sensitized by the heme group.
Photochemistry and photobiology    October 1, 1974   Volume 20, Issue 4 357-369 doi: 10.1111/j.1751-1097.1974.tb06588.x
Folin M, Gennari G, Jori G.The irradiation of horse and sperm-whale Fe” or Fez’ myoglobins with visible light showed that axial ligands that render the heme diamagnetic (e.g. 02, CO or CN-) endow the hemoproteins with a marked photosensitivity. In contrast, high-spin myoglobins are unaffected by visible light. These findings appear to be of general validity for all hemo-proteins and are in agreement with the involvment of the triplet state of the heme as the reactive intermediate. In all cases, the overall photoprocess occurs within a very narrow spatial range, leading to specific modification of these photoox...
A cupro-zinc protein with superoxide dismutase activity from horse liver. Isolation and properties.
Comparative biochemistry and physiology. B, Comparative biochemistry    April 15, 1974   Volume 47, Issue 4 767-777 doi: 10.1016/0305-0491(74)90022-4
Albergoni V, Cassini A.No abstract available
An examination of the oxidation of aldehydes by horse liver alcohol dehydrogenase.
The Journal of biological chemistry    November 10, 1972   Volume 247, Issue 21 7106-7107 
Hinson JA, Neal RA.No abstract available
The autoxidation of horse hemoglobin: the effect of glutathione.
Biochimica et biophysica acta    June 26, 1972   Volume 273, Issue 1 30-39 doi: 10.1016/0304-4165(72)90188-2
Rifkind JM.The reduced glutathione in the erythrocyte was found to inhibit the autoxidation of purified horse hemoglobin. It was observed that much higher concentrations of oxidized glutathione also stabilize hemoglobin. The stabilization by oxidized glutathione most likely involves the formation of a mixed disulfide with the reactive β-93 sulfhydryl groups on the hemoglobin. A similar effect is also observed with N-ethyl- maleimide and HgCl2 which also react with the sulfhydryl groups. The apparent stabilization by reduced glutathione is partially due to the reduction of ferrihemoglobin formed by autox...
The transport of oxidized glutathione from the erythrocytes of various species in the presence of chromate.
The Biochemical journal    October 1, 1969   Volume 114, Issue 4 833-837 doi: 10.1042/bj1140833
Srivastava SK, Beutler E.1. Erythrocytes from normal and glucose 6-phosphate dehydrogenase-deficient humans were subjected to hydrogen peroxide diffusion to oxidize the GSH. Studies were carried out in the presence and absence of chromate to inhibit glutathione reductase and with or without the addition of glucose. 2. The GSH content of erythrocytes from other species was oxidized by subjecting them to hydrogen peroxide diffusion in the presence of chromate and glucose. 3. Chromate (1.3mm) inhibited glutathione reductase by about 80%, whereas glucose 6-phosphate dehydrogenase, 6-phosphogluconate dehydrogenase, hexokin...
[Oxidation of Horse Oxyhemoglobin by Sodium Nitrite].
Seikagaku. The Journal of Japanese Biochemical Society    January 1, 1965   Volume 37 14-20 
KAKIZAKI T, SATO M, TSURUTA H, HASEGAWA H.No abstract available
Hydrogen Transfer Between Reduced Diphosphopyridine Nucleotide Dehydrogenase and the Respiratory Chain. II. An Initial Lag in the Oxidation of Reduced Diphosphopyridine Nucleotide.
The Journal of biological chemistry    June 1, 1964   Volume 239 2049-2054 
MINAKAMI S, SCHINDLER FJ, ESTABROOK RW.No abstract available
L-carnitine added to post-thawed semen acts as an antioxidant and a stimulator of equine sperm metabolism.
   March 18, 2026  
The objective of this study was to enhance the in vitro sperm quality and in vivo fertility of frozen-thawed equine semen by the addition of l-carnitine (LC) to post-thawed semen. Different concentrations of LC were added to thawed samples to obtain four treatments control and 0.5, 1 and 2 mM LC. In the in vitro experiments, sperm motility and kinematics, membrane integrity and intracellular calcium ion concentration ([Ca ] ) were investigated, and the antioxidant bioactivity of LC was assessed by measuring hydrogen peroxide and nitrite concentrations (NO ). The fertility rate was assessed v...
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