Contractile effect of trimethylamine and trimethylamine‐ n‐oxide on isolated human umbilical arteries

Abstract Background The aim of this study is to investigate the effect of trimethylamine (TMA) and trimethylamine‐ n‐oxide (TMAO) on the contractility of human umbilical artery and the possible mechanisms involved. Methods Vasoactive responses to TMA and TMAO on human umbilical artery rings were measured in isolated organ baths. Cumulative dose–response curves for TMA and TMAO were obtained before and after incubation with atropine, yohimbine, prazosin, indomethacin, verapamil, and Ca+2‐free Krebs–Henselite solution. Results Administration of cumulative TMA and TMAO resulted in dose‐dependent contraction at concentrations ranging from 10 to 100 mM on human umbilical artery rings. TMA‐induced contractions were more potent than TMAO‐induced contractions (TMA: −logEC50 = 1.00 ± 0.02, TMAO: −logEC50 = 0.57 ± 0.02). Contraction responses to TMA were significantly lower in the presence of verapamil and in the absence of external Ca+2( p < 0.001, p < 0.05, respectively). Conclusion Our results showed that TMA and TMAO caused vasoconstriction in isolated human umbilical artery rings. Our findings also indicated that TMA but not TMAO‐induced vasoconstriction was partially dependent on extracellular Ca2+ and calcium influx through L‐type Ca2+ channels. Our results suggest that TMA and TMAO may have the potential to contribute to cardiovascular diseases through their direct effect on vascular contractility in human arteries..

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:49

Enthalten in:

Journal of Obstetrics and Gynaecology Research - 49(2023), 7, Seite 1736-1742

Beteiligte Personen:

Ongun, Mert C. [VerfasserIn]
Orgul, Gokcen [VerfasserIn]
Celik, Cetin [VerfasserIn]
Bariskaner, Hulagu [VerfasserIn]

Anmerkungen:

© 2023 Japan Society of Obstetrics and Gynecology

Umfang:

7

doi:

10.1111/jog.15656

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

WLY016230345