Araştırma Makalesi
BibTex RIS Kaynak Göster
Yıl 2024, , 227 - 232, 26.03.2024
https://doi.org/10.55262/fabadeczacilik.1429111

Öz

Proje Numarası

7655.

Kaynakça

  • Jaworska, K., Bielinska, K., Gawrys-Kopczynska, M., & Ufnal, M. (2019). TMA (trimethylamine), but not its oxide TMAO (trimethylamine-oxide), exerts haemodynamic effects: implications for interpretation of cardiovascular actions of gut microbiome. Cardiovasc Res, 115(14), 1948-1949. doi:10.1093/cvr/cvz231

The Inhibitory Effect of Trimethylamine (TMA), an Intestinal Bacterial Metabolite, on Endothelial Vasorelaxation in Rat Mesenteric Artery

Yıl 2024, , 227 - 232, 26.03.2024
https://doi.org/10.55262/fabadeczacilik.1429111

Öz

The effect of the gut microbiota metabolite trimethylamine-(TMA) in isolated vessels is unknown yet. Previously TMAO, the hepatic oxidation product of TMA, at 3 mM has been shown to inhibit endothelium-dependent vasorelaxations of isolated arteries only after 24-hour-interactions. In this study, the effects of TMA (at 1 mM) on endothelium-dependent relaxations with acute (1 or 4 hours) and longer (24 hours) incubation periods were evaluated in superior mesenteric arteries of rat. Acute exposure to TMA of 1 hour significantly inhibited acetylcholine-stimulated endothelium-derived hyperpolarizing (EDH) type relaxations, and this inhibition gradually intensified as the incubation period was prolonged to 4, and 24 hours. The area under the curves (AUCs) of the relaxation-response curves after 1 and 24 hours of TMA incubation were found significantly different compared to each other, whereas similar AUC values were obtained after 4, and 24 hours of incubations. Contractile responses to phenylephrine, and nitric oxide (NO)-mediated relaxations of acetylcholine were similar in arteries before and after pretreatment with TMA for 24 hours. These data indicate that TMA selectively inhibits EDH-type relaxations in rat isolated mesenteric arteries. Although the inhibitory effect of TMA intensifies over time, it appears to be more pronounced during acute incubation periods. The findings strengthen the evidence that TMA is a more toxic metabolite on vascular tone than TMAO.

Etik Beyan

The ethical approval was obtained by local ethics committee of Hacettepe University (No: 2018-45).

Destekleyen Kurum

Hacettepe Scientific Research Projects Coordination Unit

Proje Numarası

7655.

Kaynakça

  • Jaworska, K., Bielinska, K., Gawrys-Kopczynska, M., & Ufnal, M. (2019). TMA (trimethylamine), but not its oxide TMAO (trimethylamine-oxide), exerts haemodynamic effects: implications for interpretation of cardiovascular actions of gut microbiome. Cardiovasc Res, 115(14), 1948-1949. doi:10.1093/cvr/cvz231
Toplam 1 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Temel Farmakoloji
Bölüm Araştırma Makalesi
Yazarlar

Melike Hacer Özkan 0000-0003-3395-3847

Proje Numarası 7655.
Yayımlanma Tarihi 26 Mart 2024
Gönderilme Tarihi 31 Ocak 2024
Kabul Tarihi 26 Şubat 2024
Yayımlandığı Sayı Yıl 2024

Kaynak Göster

APA Özkan, M. H. (2024). The Inhibitory Effect of Trimethylamine (TMA), an Intestinal Bacterial Metabolite, on Endothelial Vasorelaxation in Rat Mesenteric Artery. Fabad Eczacılık Bilimler Dergisi, 49(1), 227-232. https://doi.org/10.55262/fabadeczacilik.1429111