Transglutaminase 2 Inhibitor LDN 27219 Age-Dependently Lowers Blood Pressure and Improves Endothelium-Dependent Vasodilation in Resistance Arteries.
Age Factors
Animals
Blood Pressure
/ drug effects
Endothelium, Vascular
/ physiology
GTP-Binding Proteins
/ antagonists & inhibitors
Large-Conductance Calcium-Activated Potassium Channels
/ physiology
Male
Myocytes, Smooth Muscle
/ drug effects
Nitric Oxide
/ physiology
Protein Conformation
Protein Glutamine gamma Glutamyltransferase 2
Rats
Rats, Wistar
Transglutaminases
/ antagonists & inhibitors
Vascular Resistance
Vasodilation
/ drug effects
aging
blood pressure
fibrosis
nitric oxide
potassium channels
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
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