Relative ability of aqueous humor from dogs with and without primary angle-closure glaucoma and ADAMTS10 open-angle glaucoma to catalyze or inhibit collagenolysis.

canine extracellular matrix glaucoma matrix metalloproteinases (MMP) tissue inhibitors of metalloproteinases (TIMP)

Journal

Veterinary ophthalmology
ISSN: 1463-5224
Titre abrégé: Vet Ophthalmol
Pays: England
ID NLM: 100887377

Informations de publication

Date de publication:
01 Sep 2023
Historique:
revised: 23 07 2023
received: 21 06 2023
accepted: 16 08 2023
medline: 2 9 2023
pubmed: 2 9 2023
entrez: 1 9 2023
Statut: aheadofprint

Résumé

The objective of the study was to compare the ability of aqueous humor (AH) from dogs with primary angle-closure glaucoma (CPACG), companion dogs without overt evidence of CPACG, and Beagles with and without ADAMTS10 open-angle glaucoma (ADAMTS10-OAG) to catalyze or inhibit collagenolysis. Seventeen normal pet dogs, 27 dogs with CPACG, 19 Beagles with ADAMTS10-OAG, and 4 unaffected Beagles. A fluorescein-based substrate degradation assay was used to assess AH proteolytic capacity. Samples were then assayed using the same substrate degradation assay, with recombinant activated matrix metalloproteinase-2 (MMP-2) added to measure protease inhibition effects. For the protease activity assay, relative fluorescence (RF) for AH from normal pet dogs was 13.28 ± 2.25% of control collagenase while RF for AH from dogs with CPACG was 17.47 ± 4.67%; RF was 8.57 ± 1.72% for ADAMTS10-OAG Beagles and 7.99 ± 1.15% for unaffected Beagles. For the MMP-2 inhibition assay, RF for AH from normal dogs was 34.96 ± 15.04% compared to MMP-2 controls, while RF from dogs with CPACG was 16.69 ± 7.95%; RF was 85.85 ± 13.23% for Beagles with ADAMTS10-OAG and 94.51 ± 8.36% for unaffected Beagles. Significant differences were found between dogs with CPACG and both normal pet dogs and dogs with ADAMTS10-OAG and between normal pet dogs and both groups of Beagles. AH from dogs with CPACG is significantly more able to catalyze proteolysis and inhibit MMP-2 than AH from normal dogs or dogs with ADAMTS10-OAG. Results suggest that pathogenesis may differ between CPACG and ADAMTS10-OAG.

Identifiants

pubmed: 37658474
doi: 10.1111/vop.13143
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NEI NIH HHS
ID : R01 EY032478
Pays : United States
Organisme : NIH HHS
ID : R01-EY032478
Pays : United States
Organisme : NIH HHS
ID : R01-EY025752
Pays : United States

Informations de copyright

© 2023 American College of Veterinary Ophthalmologists.

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Auteurs

Stephanie A Pumphrey (SA)

Department of Clinical Sciences, Cummings School of Veterinary Medicine at Tufts University, North Grafton, Massachusetts, USA.

Christine D Harman (CD)

Michigan State University Veterinary Medical Center, East Lansing, Michigan, USA.

Amanda L Anderson (AL)

Michigan State University Veterinary Medical Center, East Lansing, Michigan, USA.

Benjamin Sweigart (B)

Biostatistics, Epidemiology, and Research Design (BERD) Center, Tufts Medical Center, Boston, Massachusetts, USA.

András M Komáromy (AM)

Michigan State University Veterinary Medical Center, East Lansing, Michigan, USA.

Classifications MeSH