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European journal of pharmacology2014; 740; 66-71; doi: 10.1016/j.ejphar.2014.06.016

Equine digital veins are more sensitive to superoxide anions than digital arteries.

Abstract: This work was designed to investigate (i) the effect of superoxide dismutase (SOD) inhibition on endothelial function and (ii) the free radical-induced endothelial dysfunction in equine digital veins (EDVs) and equine digital arteries (EDAs) isolated from healthy horses. EDV and EDA rings were suspended in a 5 ml organ bath containing Krebs solution. After a 60 min equilibration period, EDV and EDA rings were contracted with phenylephrine. Then, cumulative concentration-response curves (CCRCs) to acetylcholine were performed. In both EDVs and EDAs, acetylcholine (1 nM to 10 µM) produced concentration-dependent relaxation. We investigated the influence of SOD inhibition by diethyldithiocarbamate (DETC; 100 µM), a CuZnSOD inhibitor, on EDAs and EDVs relaxant responses to acetylcholine. Acetylcholine -mediated relaxation was impaired by DETC only in EDVs. SOD activity assayed by a xanthine-xanthine oxidase method was higher in EDAs compared with EDVs (P<0.05). CCRCs to acetylcholine established in the presence of pyrogallol (30 µM) or homocysteine (20 µM), two superoxide anions generating systems showed that in both EDVs and EDAs, the acetylcholine-mediated relaxation was significantly impaired by pyrogallol and homocysteine. This impairment was more pronounced in EDVs than in EDAs. Moreover, the pyrogallol-induced impairment of acetylcholine-mediated relaxation was potentiated by DETC to a greater extent in EDVs. We concluded that due to the lower activity of SOD, EDVs are more sensitive to superoxide anions than EDAs. So, any alteration of superoxide anions metabolism is likely to have a more important impact on venous rather than arterial relaxation.
Publication Date: 2014-07-08 PubMed ID: 25014758DOI: 10.1016/j.ejphar.2014.06.016Google Scholar: Lookup
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  • Journal Article

Summary

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The research investigates how superoxide dismutase (SOD), a critical antioxidant enzyme, affects the function of blood vessels in horses’ hooves. The authors find that veins are more susceptible to damage from reactive oxygen species than arteries due to lower SOD activity.

Research Objectives and Methodology

  • The study sought to explore the effect of inhibiting superoxide dismutase (SOD) on endothelial function. These are the cells lining the interior of blood vessels, which play a role in vascular relaxation and contraction.
  • The authors tested for oxidative-stress-induced endothelial dysfunction in both equine digital veins (EDVs) and equine digital arteries (EDAs), using tissues sourced from healthy horses. Oxidative stress is a harmful condition resulting from an imbalance between the production of reactive oxygen species (free radicals) and antioxidant defenses.
  • After suspending the EDV and EDA tissues in a 5 ml organ bath filled with Krebs solution (an artificial fluid mimicking the body’s internal environment), the researchers initiated contraction using a drug called phenylephrine. This was followed by application of acetylcholine, a substance that causes vessel relaxation, to generate concentration-response curves.

Investigating the Role of SOD and Free Radicals

  • The impact of inhibiting SOD activity was assessed using diethyldithiocarbamate (DETC), a recognized inhibitor of SOD. Acetylcholine-induced relaxation was found to be significantly affected only in the veins, not the arteries.
  • The SOD activity was higher in arteries than in veins when evaluated using the xanthine-xanthine oxidase method, indicating a stronger defense against oxidative stress in arteries.
  • The concentrations of acetylcholine needed to produce a response, derived from two superoxide anion-generating systems (pyrogallol and homocysteine), illustrated that both EDVs and EDAs were adversely affected. The effect, however, was significantly more pronounced in the veins, further pointing to their higher susceptibility to superoxide-induced oxidative stress.

Conclusions

  • The study concludes that equine digital veins are hypothesize to be more sensitive to damage from superoxide anions due to lower SOD activity than arteries.
  • A marked impact on venous, rather than arterial, relaxation is anticipated if alterations occur in the metabolism of superoxide anions. Such vascular dysfunction could potentially impact the health and performance of horses, emphasizing the need for further investigation into this aspect of equine health.

Cite This Article

APA
Lapo RA, Gogny M, Chatagnon G, Lalanne V, Harfoush K, Assane M, Desfontis JC, Mallem MY. (2014). Equine digital veins are more sensitive to superoxide anions than digital arteries. Eur J Pharmacol, 740, 66-71. https://doi.org/10.1016/j.ejphar.2014.06.016

Publication

ISSN: 1879-0712
NlmUniqueID: 1254354
Country: Netherlands
Language: English
Volume: 740
Pages: 66-71
PII: S0014-2999(14)00458-0

Researcher Affiliations

Lapo, Rock Allister
  • Ecole Inter-états des Sciences et Médecine Vétérinaires BP 5077 Dakar, Senegal.
Gogny, Marc
  • LUNAM Université, Oniris, UPSP 5304 de Physiopathologie Animale et Pharmacologie Fonctionnelle, Atlanpole La Chantrerie, BP 40706, Nantes F-44307, France.
Chatagnon, Gérard
  • LUNAM Université, Oniris, Unité de Sécurité Sanitaire des Biotechnologies de la Reproduction, Atlanpole La Chantrerie, BP 40706, Nantes, F-44307, France.
Lalanne, Valérie
  • LUNAM Université, Oniris, UPSP 5304 de Physiopathologie Animale et Pharmacologie Fonctionnelle, Atlanpole La Chantrerie, BP 40706, Nantes F-44307, France.
Harfoush, Khaled
  • LUNAM Université, Oniris, UPSP 5304 de Physiopathologie Animale et Pharmacologie Fonctionnelle, Atlanpole La Chantrerie, BP 40706, Nantes F-44307, France.
Assane, Moussa
  • Ecole Inter-états des Sciences et Médecine Vétérinaires BP 5077 Dakar, Senegal.
Desfontis, Jean-Claude
  • LUNAM Université, Oniris, UPSP 5304 de Physiopathologie Animale et Pharmacologie Fonctionnelle, Atlanpole La Chantrerie, BP 40706, Nantes F-44307, France.
Mallem, Mohamed Yassine
  • LUNAM Université, Oniris, UPSP 5304 de Physiopathologie Animale et Pharmacologie Fonctionnelle, Atlanpole La Chantrerie, BP 40706, Nantes F-44307, France. Electronic address: yassine.mallem@oniris-nantes.fr.

MeSH Terms

  • Acetylcholine / pharmacology
  • Animals
  • Arteries / physiology
  • Ditiocarb / pharmacology
  • Forelimb
  • Horses
  • In Vitro Techniques
  • Phenylephrine / pharmacology
  • Superoxides / antagonists & inhibitors
  • Superoxides / metabolism
  • Vasoconstrictor Agents / pharmacology
  • Vasodilation / drug effects
  • Vasodilator Agents / pharmacology
  • Veins / physiology

Citations

This article has been cited 1 times.
  1. Chen H, Zhu H, Yang J, Zhu Y, Mei J, Shen H, Liang K, Zhang X. Role of Programmed Cell Death 4 (PDCD4)-Mediated Akt Signaling Pathway in Vascular Endothelial Cell Injury Caused by Lower-Extremity Ischemia-Reperfusion in Rats. Med Sci Monit 2019 Jun 29;25:4811-4818.
    doi: 10.12659/MSM.914035pubmed: 31253757google scholar: lookup