The endothelin receptor antagonist macitentan ameliorates endothelin-mediated vasoconstriction and promotes the survival of retinal ganglion cells in rats.

endothelins glaucoma macitentan neuroprotection vasoconstriction

Journal

Frontiers in ophthalmology
ISSN: 2674-0826
Titre abrégé: Front Ophthalmol (Lausanne)
Pays: Switzerland
ID NLM: 9918419176106676

Informations de publication

Date de publication:
2023
Historique:
medline: 1 1 2023
pubmed: 1 1 2023
entrez: 11 3 2024
Statut: ppublish

Résumé

Glaucoma is a chronic and progressive eye disease, commonly associated with elevated intraocular pressure (IOP) and characterized by optic nerve degeneration, cupping of the optic disc, and loss of retinal ganglion cells (RGCs). The pathological changes in glaucoma are triggered by multiple mechanisms and both mechanical effects and vascular factors are thought to contribute to the etiology of glaucoma. Various studies have shown that endothelin-1 (ET-1), a vasoactive peptide, acting through its G protein coupled receptors, ET

Identifiants

pubmed: 38464735
doi: 10.3389/fopht.2023.1185755
pmc: PMC10921982
pii:
doi:

Types de publication

Journal Article

Langues

eng

Déclaration de conflit d'intérêts

Conflict of interest The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The authors RK and DS declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

Auteurs

Bindu Kodati (B)

Department of Pharmacology and Neuroscience, University of North Texas Health Science Center, Fort Worth, TX, United States.
North Texas Eye Research Institute, University of North Texas Health Science Center, Fort Worth, TX, United States.

Wei Zhang (W)

Department of Pharmacology and Neuroscience, University of North Texas Health Science Center, Fort Worth, TX, United States.
North Texas Eye Research Institute, University of North Texas Health Science Center, Fort Worth, TX, United States.

Shaoqing He (S)

Department of Pathology, Children's Health at Dallas, Dallas, TX, United States.

Jennifer H Pham (JH)

Department of Pharmacology and Neuroscience, University of North Texas Health Science Center, Fort Worth, TX, United States.
North Texas Eye Research Institute, University of North Texas Health Science Center, Fort Worth, TX, United States.

Kallen J Beall (KJ)

Department of General Surgery, Honor Health, Phoenix, AZ, United States.

Zoe E Swanger (ZE)

Texas College of Osteopathic Medicine, University of North Texas Health Science Center, Fort Worth, TX, United States.

Vignesh R Krishnamoorthy (VR)

Department of Cell and Molecular Pharmacology, Loyola University, Maywood, IL, United States.

Payton E Harris (PE)

Department of Graduate Medical Education, Medical City, Fort Worth, TX, United States.

Trent Hall (T)

Williams College, Williamstown, MA, United States.

Ashley V Tran (AV)

School of Natural Sciences and Mathematics, The University of Texas at Dallas, Richardson, TX, United States.

Renuka M Chaphalkar (RM)

Department of Ophthalmology, School of Medicine, University of California, San Francisco, CA, United States.

Sai H Chavala (SH)

Department of Surgery, Burnett School of Medicine at Texas Christian University (TCU), Fort Worth, TX, United States.

Dorota L Stankowska (DL)

Department of Pharmacology and Neuroscience, University of North Texas Health Science Center, Fort Worth, TX, United States.
North Texas Eye Research Institute, University of North Texas Health Science Center, Fort Worth, TX, United States.

Raghu R Krishnamoorthy (RR)

Department of Pharmacology and Neuroscience, University of North Texas Health Science Center, Fort Worth, TX, United States.
North Texas Eye Research Institute, University of North Texas Health Science Center, Fort Worth, TX, United States.

Classifications MeSH