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Journal of applied physiology (Bethesda, Md. : 1985)2016; 120(6); 599-607; doi: 10.1152/japplphysiol.00975.2015

Regional heterogeneity in the reactivity of equine small pulmonary blood vessels.

Abstract: Regional differences in large equine pulmonary artery reactivity exist. It is not known if this heterogeneity extends into small vessels. The hypothesis that there is regional heterogeneity in small pulmonary artery and vein reactivity to sympathomimetics (phenylephrine and isoproterenol) and a parasympathomimetic (methacholine) was tested using wire myography on small vessels from caudodorsal (CD) and cranioventral (CV) lung of 12 horses [9 mares, 3 geldings, 8.67 ± 0.81 (age ± SE) yr, of various breeds that had never raced]. To study relaxation, vessels were precontracted with U46619 (10(-6) M). Methacholine mechanism of action was investigated using L-nitroarginine methylester (L-NAME, 100 μM) and indomethacin (10 μM). Phenylephrine did not contract any vessels. Isoproterenol relaxed CD arteries more than CV arteries (maximum relaxation 28.18% and 48.67%; Log IC50 ± SE -7.975 ± 0.1327 and -8.033 ± 0.1635 for CD and CV, respectively, P < 0.0001), but not veins. Methacholine caused contraction of CD arteries (maximum contraction 245.4%, Log EC50 ± SE -6.475 ± 0.3341), and relaxation of CV arteries (maximum relaxation 40.14%, Log IC50 ± SE -6.791 ± 0.1954) and all veins (maximum relaxation 50.62%, Log IC50 ± SE -6.932 ± 0.1986) in a nonregion-dependent manner. L-NAME (n = 8, P < 0.0001) and indomethacin (n = 7, P < 0.0001) inhibited methacholine-induced relaxation of CV arteries, whereas indomethacin augmented CD artery contraction (n = 8, P < 0.0001). Our data demonstrate significant regional heterogeneity in small blood vessel reactivity when comparing the CD to the CV region of the equine lung.
Publication Date: 2016-01-14 PubMed ID: 26769957DOI: 10.1152/japplphysiol.00975.2015Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research primarily investigates the variance in reactivity to certain drugs among small blood vessels in different regions of a horse’s lung. The study specifically compared the responses of small pulmonary vessels in the caudodorsal and cranioventral regions to sympathomimetics and a parasympathomimetic, confirming a significant regional difference in the vessels’ reactivity.

Objective and Methodology of the Study

  • This study wanted to ascertain if regional differences exist in the reactivity of small vessels in a horse’s lung, as previously known for large pulmonary arteries.
  • The researchers tested this by studying the reactivity of small vessels from caudodorsal (CD) and cranioventral (CV) lung areas of twelve horses to certain sympathomimetics (phenylephrine and isoproterenol) and a parasympathomimetic (methacholine).
  • The method employed for this study was wire myography — a technique for measuring the mechanical properties of small blood vessels.
  • For studying relaxation, the vessels were precontracted using U46619, a synthetic analogue of prostaglandin.

Findings of the Study

  • Phenylephrine did not cause any contraction in the vessels.
  • Isoproterenol resulted in more relaxation in CD arteries as compared to CV arteries. However, it did not induce any effect on the veins.
  • In contrast, methacholine caused contraction of CD arteries, but relaxation of CV arteries and all veins.
  • The regional independent effect of methacholine was studied using another two drugs: L-nitroarginine methylester (L-NAME), and indomethacin. Both of them inhibited methacholine-induced relaxation of CV arteries, while indomethacin increased CD artery contraction.

Conclusion of the Study

  • The results show significant heterogeneity in reactivity of small blood vessels across CD and CV regions of the equine lung. This could have implications for understanding lung diseases and developing potential treatment strategies for horses.

Cite This Article

APA
Stack A, Derksen FJ, Williams KJ, Robinson NE, Jackson WF. (2016). Regional heterogeneity in the reactivity of equine small pulmonary blood vessels. J Appl Physiol (1985), 120(6), 599-607. https://doi.org/10.1152/japplphysiol.00975.2015

Publication

ISSN: 1522-1601
NlmUniqueID: 8502536
Country: United States
Language: English
Volume: 120
Issue: 6
Pages: 599-607

Researcher Affiliations

Stack, Alice
  • Department of Large Animal Clinical Sciences, Michigan State University, East Lansing, Michigan; stackalice@gmail.com.
Derksen, Frederik J
  • Department of Large Animal Clinical Sciences, Michigan State University, East Lansing, Michigan;
Williams, Kurt J
  • Department of Pathobiology and Diagnostic Investigation, Michigan State University, East Lansing, Michigan; and.
Robinson, N Edward
  • Department of Large Animal Clinical Sciences, Michigan State University, East Lansing, Michigan;
Jackson, William F
  • Department of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan.

MeSH Terms

  • 15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid / pharmacology
  • Animals
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / physiology
  • Female
  • Horses
  • Indomethacin / pharmacology
  • Isoproterenol / pharmacology
  • Lung / blood supply
  • Male
  • Methacholine Chloride / pharmacology
  • Myography / methods
  • NG-Nitroarginine Methyl Ester / pharmacology
  • Phenylephrine / pharmacology
  • Pulmonary Artery / drug effects
  • Pulmonary Artery / physiology
  • Vasoconstriction / drug effects
  • Vasoconstrictor Agents / pharmacology
  • Vasodilation / drug effects
  • Vasodilation / physiology
  • Veins / drug effects
  • Veins / physiology

Citations

This article has been cited 2 times.
  1. Ceriotti S, Bullone M, Leclere M, Ferrucci F, Lavoie JP. Severe asthma is associated with a remodeling of the pulmonary arteries in horses. PLoS One 2020;15(10):e0239561.
    doi: 10.1371/journal.pone.0239561pubmed: 33091038google scholar: lookup
  2. Poole DC, Erickson HH. Exercise-induced pulmonary hemorrhage: where are we now?. Vet Med (Auckl) 2016;7:133-148.
    doi: 10.2147/VMRR.S120421pubmed: 30050846google scholar: lookup