Early laminar events involving endothelial activation in horses with black walnut– induced laminitis

John P. Loftus Department of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA 01003

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Samuel J. Black Department of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA 01003

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Amanda Pettigrew Department of Veterinary Clinical Sciences, College of Veterinary Medicine, The Ohio State University, Columbus, OH 43210

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Eric J. Abrahamsen Department of Veterinary Clinical Sciences, College of Veterinary Medicine, The Ohio State University, Columbus, OH 43210

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James K. Belknap Department of Veterinary Clinical Sciences, College of Veterinary Medicine, The Ohio State University, Columbus, OH 43210

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Abstract

Objective—To determine proinflammatory gene expression, endothelial adhesion molecule gene expression, and matrix metalloproteinase (MMP) concentrations in laminar specimens at 1.5 hours after administration of black walnut extract (BWE) and to compare these values with later time points.

Animals—25 horses.

Procedures—After nasogastric administration of BWE, anesthesia was induced at 1.5 hours in early time point (ETP) horses (n = 5), between 3 and 4 hours in developmental time point horses (5), and between 9 and 10 hours in acute onset of lameness time point horses (5). Anesthesia was induced at 3 and 10 hours after nasogastric administration of water in 2 groups of control horses (3-hour control group, n = 5; 10-hour control group, 5). Real-time quantitative PCR assay was performed on laminar specimens from control and ETP horses for cyclooxygenase (COX)-1, COX-2, interleukin (IL)-1β, tumor necrosis factor-α, IL-6, IL-8, IL-10, MMP-2, and MMP-9 gene expression; and on laminar specimens from all groups for endothelial adhesion molecules, intercellular adhesion molecule (ICAM)-1, and E-selectin gene expression. Leukocyte emigration was assessed via CD13 immunohistochemistry, and gelatinase accumulation was determined by gelatin zymography.

Results—Laminar concentrations of IL-1β, IL-6, IL-8, COX-2, ICAM-1, and E-selectin mRNA were significantly increased in ETP horses, compared with control horses. Concentrations of IL-1β, IL-8, ICAM-1, and E-selectin mRNA peaked at 1.5 hours. In ETP horses, leukocyte emigration was present in 3 of 5 horses and pro–MMP-9 was detected in 2 of 5 horses.

Conclusions and Clinical Relevance—Results indicated that endothelial activation and laminar inflammation are early events in laminitis; MMP accumulation likely is a downstream event.

Abstract

Objective—To determine proinflammatory gene expression, endothelial adhesion molecule gene expression, and matrix metalloproteinase (MMP) concentrations in laminar specimens at 1.5 hours after administration of black walnut extract (BWE) and to compare these values with later time points.

Animals—25 horses.

Procedures—After nasogastric administration of BWE, anesthesia was induced at 1.5 hours in early time point (ETP) horses (n = 5), between 3 and 4 hours in developmental time point horses (5), and between 9 and 10 hours in acute onset of lameness time point horses (5). Anesthesia was induced at 3 and 10 hours after nasogastric administration of water in 2 groups of control horses (3-hour control group, n = 5; 10-hour control group, 5). Real-time quantitative PCR assay was performed on laminar specimens from control and ETP horses for cyclooxygenase (COX)-1, COX-2, interleukin (IL)-1β, tumor necrosis factor-α, IL-6, IL-8, IL-10, MMP-2, and MMP-9 gene expression; and on laminar specimens from all groups for endothelial adhesion molecules, intercellular adhesion molecule (ICAM)-1, and E-selectin gene expression. Leukocyte emigration was assessed via CD13 immunohistochemistry, and gelatinase accumulation was determined by gelatin zymography.

Results—Laminar concentrations of IL-1β, IL-6, IL-8, COX-2, ICAM-1, and E-selectin mRNA were significantly increased in ETP horses, compared with control horses. Concentrations of IL-1β, IL-8, ICAM-1, and E-selectin mRNA peaked at 1.5 hours. In ETP horses, leukocyte emigration was present in 3 of 5 horses and pro–MMP-9 was detected in 2 of 5 horses.

Conclusions and Clinical Relevance—Results indicated that endothelial activation and laminar inflammation are early events in laminitis; MMP accumulation likely is a downstream event.

Contributor Notes

Dr. Abrahamsen's present address is Ocala Equine Hospital, 10855 NW US Hwy 27, Ocala, FL 34482.

Address correspondence to Dr. Belknap.
  • 1.

    Allen D Jr, Clark ES, Moore JN, et al. Evaluation of equine digital Starling forces and hemodynamics during early laminitis. Am J Vet Res 1990;51:19301934.

    • Search Google Scholar
    • Export Citation
  • 2.

    Eaton SA, Allen D, Eades SC, et al. Digital Starling forces and hemodynamics during early laminitis induced by an aqueous extract of black walnut (Juglans nigra) in horses. Am J Vet Res 1995;56:13381344.

    • Search Google Scholar
    • Export Citation
  • 3.

    Adair HS III, Goble D, Schmichammer JL, et al. Laminar microvascular flow, measured by means of laser Doppler flowmetry, during the prodromal stages of black walnut-induced laminitis in horses. Am J Vet Res 2000;61:862868.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 4.

    Waguespack RW, Cochran A, Belknap JK. Expression of the cyclooxygenase isoforms in the prodromal stage of black walnutinduced laminitis in horses. Am J Vet Res 2004;65:17241729.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 5.

    Waguespack RW, Kemppainen RJ, Cochran A, et al. Increased expression of MAIL, a cytokine-associated nuclear protein, in the prodromal stage of black walnut-induced laminitis. Equine Vet J 2004;36:285291.

    • Search Google Scholar
    • Export Citation
  • 6.

    Black SJ, Lunn DP, Yin C, et al. Leukocyte emigration in the early stages of laminitis. Vet Immunol Immunopathol 2006;109:161166.

  • 7.

    Belknap JK, Giguere S, Pettigrew A, et al. Lamellar proinflammatory cytokine expression patterns at the developmental stage and at the onset of lameness: innate vs. adaptive immune response. Equine Vet J 2006;39:4247.

    • Search Google Scholar
    • Export Citation
  • 8.

    Blikslager AT, Yin C, Cochran AM, et al. Cyclooxygenase expression in the early stages of equine laminitis: a cytological study. J Vet Intern Med 2005;20:11911196.

    • Search Google Scholar
    • Export Citation
  • 9.

    Fontaine GL, Belknap JK, Allen D, et al. Expression of interleukin-1 beta in the digital laminae of horses in the prodromal stage of experimentally induced laminitis. Am J Vet Res 2001;62:714720.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 10.

    Katwa LC, Johnson PJ, Ganjam VK, et al. Activation of extracellular matrix metalloproteinases in equine laminitis. Equine Vet J 1999;31:243247.

    • Search Google Scholar
    • Export Citation
  • 11.

    Pollitt CC, Kyaw-Tanner M, French KR, et al. Equine laminitis, in Proceedings. 49th Annu Conv Am Assoc Equine Pract 2003;49:103115.

  • 12.

    Kyaw-Tanner M, Pollitt CC. Equine laminitis: increased transcription of matrix metalloproteinase-2 (MMP-2) occurs during the developmental phase. Equine Vet J 2004;36:221225.

    • Search Google Scholar
    • Export Citation
  • 13.

    Mungall BA, Pollitt CC. Zymographic analysis of equine laminitis. Histochem Cell Biol 1999;112:467472.

  • 14.

    Hurley DJ, Parks RJ, Reber AJ, et al. Dynamic changes in circulating leukocytes during the induction of equine laminitis with BWE. Vet Immunol Immunopathol 2006;110:195296.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 15.

    Loftus JP, Belknap JK, Black SJ. Matrix metalloproteinase-9 in laminae of BWE treated horses correlates with neutrophil abundance. Vet Immunol Immunopathol 2006;113:267276.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 16.

    Galey FD, Whiteley HE, Goetz TE, et al. Black walnut (Juglans nigra) toxicosis: a model for equine laminitis. J Comp Pathol 1991;104:313326.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 17.

    Garton NJ, Gilleron M, Brando T, et al. A novel lipoarabinomannan from the equine pathogen Rhodococcus equi. Structure and effect on macrophage cytokine production. J Biol Chem 2002;277:3172231733.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 18.

    Vandesompele J, De Preter K, Pattyn F, et al. Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol 2002;3:111.

    • Search Google Scholar
    • Export Citation
  • 19.

    Hood DM. The pathophysiology of chronic laminitis. Vet Clin North Am Equine Pract 1999;15:481494.

  • 20.

    Eades SC, Holm AM, Moore RM. A review of the pathophysiology and treatment of acute laminitis: pathophysiologic and therapeutic implications of endothelin-1, in Proceedings. 48th Annu Conv Am Assoc Equine Pract 2002;48:353361.

    • Search Google Scholar
    • Export Citation
  • 21.

    Pollitt CC, Davies CT. Equine laminitis: its development coincides with increased sublamellar blood flow. Equine Vet J Suppl 1998;125132.

    • Search Google Scholar
    • Export Citation
  • 22.

    Belknap JK, Black SJ. Review of the pathophysiology of the developmental stages of equine laminitis, in Proceedings. 51st Annu Conv Am Assoc Equine Pract 2005;51:383388.

    • Search Google Scholar
    • Export Citation
  • 23.

    Boontham P, Chandran P, Rowlands B, et al. Surgical sepsis: dysregulation of immune function and therapeutic implications. Surgeon 2003;1:187206.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 24.

    Bhatia M, Moochhala S. Role of inflammatory mediators in the pathophysiology of acute respiratory distress syndrome. J Pathol 2004;202:145156.

  • 25.

    Motoyama M, Yamazaki S, Eto-Kimura A, et al. Positive and negative regulation of nuclear factor-kappaB-mediated transcription by IkappaB-zeta, an inducible nuclear protein. J Biol Chem 2005;280:74447451.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 26.

    Kim HY, Rikihisa Y. Expression of interleukin-1beta, tumor necrosis factor alpha, and interleukin-6 in human peripheral blood leukocytes exposed to human granulocytic ehrlichiosis agent or recombinant major surface protein P44. Infect Immun 2000;68:33943402.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 27.

    Walzog B, Weinmann P, Jeblonski F, et al. A role for beta(2) integrins (CD11/CD18) in the regulation of cytokine gene expression of polymorphonuclear neutrophils during the inflammatory response. FASEB J 1999;13:18551865.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 28.

    Hadjiminas DJ, McMasters KM, Peyton JC, et al. Tissue tumor necrosis factor mRNA expression following cecal ligation and puncture or intraperitoneal injection of endotoxin. J Surg Res 1994;56:549555.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 29.

    Laszik Z, Nadasdy T, Johnson LD, et al. Renal interleukin-1 expression during endotoxemia and gram-negative septicemia in conscious rats. Circ Shock 1994;43:115121.

    • Search Google Scholar
    • Export Citation
  • 30.

    Tsai BM, Wang M, Pitcher JM, et al. Disparate IL-1beta and iNOS gene expression in the aorta and pulmonary artery after endotoxemia. Surg Infect (Larchmt) 2006;7:2127.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 31.

    Middleton J, Patterson AM, Gardner L, et al. Leukocyte extravasation: chemokine transport and presentation by the endothelium. Blood 2002;100:38533860.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 32.

    Kaplanski G, Farnarier C, Kaplanski S, et al. Interleukin-1 induces interleukin-8 secretion from endothelial cells by a juxtacrine mechanism. Blood 1994;84:42424248.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 33.

    van Griensven M, Probst C, Muller K, et al. Leukocyte-endothelial interactions via ICAM-1 are detrimental in polymicrobial sepsis. Shock 2006;25:254259.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 34.

    Cohen J. The immunopathogenesis of sepsis. Nature 2002;420:885891.

  • 35.

    Stearns ME, Wang M, Hu Y, et al. Interleukin 10 blocks matrix metalloproteinase-2 and membrane type 1-matrix metalloproteinase synthesis in primary human prostate tumor lines. Clin Cancer Res 2003;9:11911199.

    • Search Google Scholar
    • Export Citation
  • 36.

    Fortunato SJ, Menon R, Lombardi SJ, et al. Interleukin-10 inhibition of gelatinases in fetal membranes: therapeutic implications in preterm premature rupture of membranes. Obstet Gynecol 2001;98:284288.

    • Search Google Scholar
    • Export Citation

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