Transglutaminase 2 Inhibitor LDN 27219 Age-Dependently Lowers Blood Pressure and Improves Endothelium-Dependent Vasodilation in Resistance Arteries.


Journal

Hypertension (Dallas, Tex. : 1979)
ISSN: 1524-4563
Titre abrégé: Hypertension
Pays: United States
ID NLM: 7906255

Informations de publication

Date de publication:
01 2021
Historique:
pubmed: 1 12 2020
medline: 7 7 2021
entrez: 30 11 2020
Statut: ppublish

Résumé

Transglutaminase 2 (TG2) is an enzyme which in the open conformation exerts transamidase activity, leading to protein cross-linking and fibrosis. In the closed conformation, TG2 participates in transmembrane signaling as a G protein. The unspecific transglutaminase inhibitor cystamine causes vasorelaxation in rat resistance arteries. However, the role of TG2 conformation in vascular function is unknown. We investigated the vascular effects of selective TG2 inhibitors by myography in isolated rat mesenteric and human subcutaneous resistance arteries, patch-clamp studies on vascular smooth muscle cells, and blood pressure measurements in rats and mice. LDN 27219 promoted the closed TG2 conformation and inhibited transamidase activity in mesenteric arteries. In contrast to TG2 inhibitors promoting the open conformation (Z-DON, VA5), LDN 27219 concentration-dependently relaxed rat and resistance human arteries by a mechanism dependent on nitric oxide, large-conductance calcium-activated and voltage-gated potassium channels 7, lowering blood pressure. LDN 27219 also potentiated acetylcholine-induced relaxation by opening potassium channels in the smooth muscle; these effects were abolished by membrane-permeable TG2 inhibitors promoting the open conformation. In isolated arteries from 35- to 40-week-old rats, transamidase activity was increased, and LDN 27219 improved acetylcholine-induced relaxation more than in younger rats. Infusion of LDN 27219 decreased blood pressure more effectively in 35- to 40-week than 12- to 14-week-old anesthetized rats. In summary, pharmacological modulation of TG2 to the closed conformation age-dependently lowers blood pressure and, by opening potassium channels, potentiates endothelium-dependent vasorelaxation. Our findings suggest that promoting the closed conformation of TG2 is a potential strategy to treat age-related vascular dysfunction and lowers blood pressure.

Identifiants

pubmed: 33249864
doi: 10.1161/HYPERTENSIONAHA.120.15352
doi:

Substances chimiques

Large-Conductance Calcium-Activated Potassium Channels 0
Tgm2 protein, rat 0
Nitric Oxide 31C4KY9ESH
Protein Glutamine gamma Glutamyltransferase 2 EC 2.3.2.13
Transglutaminases EC 2.3.2.13
GTP-Binding Proteins EC 3.6.1.-

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

216-227

Auteurs

Estéfano Pinilla (E)

From the Department of Biomedicine, Pulmonary and Cardiovascular Pharmacology, Aarhus University, Denmark (E.P., S.C.-S., J.P.-D., V.M., N.H.B., U.S.).
Departament of Physiology, Faculty of Pharmacy, Complutense University of Madrid, Spain (E.P., L.R.).

Simon Comerma-Steffensen (S)

From the Department of Biomedicine, Pulmonary and Cardiovascular Pharmacology, Aarhus University, Denmark (E.P., S.C.-S., J.P.-D., V.M., N.H.B., U.S.).
Department of Biomedical Sciences, Veterinary Faculty, Central University of Venezuela (S.C.-S.).

Judit Prat-Duran (J)

From the Department of Biomedicine, Pulmonary and Cardiovascular Pharmacology, Aarhus University, Denmark (E.P., S.C.-S., J.P.-D., V.M., N.H.B., U.S.).

Luis Rivera (L)

Departament of Physiology, Faculty of Pharmacy, Complutense University of Madrid, Spain (E.P., L.R.).

Vladimir V Matchkov (VV)

From the Department of Biomedicine, Pulmonary and Cardiovascular Pharmacology, Aarhus University, Denmark (E.P., S.C.-S., J.P.-D., V.M., N.H.B., U.S.).

Niels Henrik Buus (NH)

From the Department of Biomedicine, Pulmonary and Cardiovascular Pharmacology, Aarhus University, Denmark (E.P., S.C.-S., J.P.-D., V.M., N.H.B., U.S.).
Department of Renal Medicine, Aarhus University Hospital, Denmark (N.H.B.).

Ulf Simonsen (U)

From the Department of Biomedicine, Pulmonary and Cardiovascular Pharmacology, Aarhus University, Denmark (E.P., S.C.-S., J.P.-D., V.M., N.H.B., U.S.).

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Classifications MeSH