The anti-inflammatory effect of dimethyl trisulfide in experimental acute pancreatitis

Various organosulfur compounds, such as dimethyl trisulfide (DMTS), display anti-inflammatory properties. We aimed to examine the effects of DMTS on acute pancreatitis (AP) and its mechanism of action in both in vivo and in vitro studies. AP was induced in FVB/n mice or Wistar rats by caerulein, eth...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Orján Erik Márk
Kormányos Eszter Sára
Fűr Gabriella
Dombi Ágnes
Bálint Emese Réka
Balla Zsolt
Balog Beáta Adél
Dágó Ágnes
Totonji Ahmad
Bátai István Zoárd
Jurányi Eszter Petra
Ditrói Tamás
Al-omari Ammar
Pozsgai Gábor
Kormos Viktória
Nagy Péter
Pintér Erika
Rakonczay Zoltán
Kiss Lóránd
Dokumentumtípus: Cikk
Megjelent: 2023
Sorozat:SCIENTIFIC REPORTS 13 No. 1
Tárgyszavak:
doi:10.1038/s41598-023-43692-9

mtmt:34183455
Online Access:http://publicatio.bibl.u-szeged.hu/28471
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520 3 |a Various organosulfur compounds, such as dimethyl trisulfide (DMTS), display anti-inflammatory properties. We aimed to examine the effects of DMTS on acute pancreatitis (AP) and its mechanism of action in both in vivo and in vitro studies. AP was induced in FVB/n mice or Wistar rats by caerulein, ethanol-palmitoleic acid, or L-ornithine-HCl. DMTS treatments were administered subcutaneously. AP severity was assessed by pancreatic histological scoring, pancreatic water content, and myeloperoxidase activity measurements. The behaviour of animals was followed. Pancreatic heat shock protein 72 (HSP72) expression, sulfide, and protein persulfidation were measured. In vitro acinar viability, intracellular Ca 2+ concentration, and reactive oxygen species production were determined. DMTS dose-dependently decreased the severity of AP. It declined the pancreatic infiltration of leukocytes and cellular damage in mice. DMTS upregulated the HSP72 expression during AP and elevated serum sulfide and low molecular weight persulfide levels. DMTS exhibited cytoprotection against hydrogen peroxide and AP-inducing agents. It has antioxidant properties and modulates physiological but not pathophysiological Ca 2+ signalling. Generally, DMTS ameliorated AP severity and protected pancreatic acinar cells. Our findings indicate that DMTS is a sulfur donor with anti-inflammatory and antioxidant effects, and organosulfur compounds require further investigation into this potentially lethal disease. 
650 4 |a Klinikai orvostan 
700 0 1 |a Kormányos Eszter Sára  |e aut 
700 0 1 |a Fűr Gabriella  |e aut 
700 0 1 |a Dombi Ágnes  |e aut 
700 0 1 |a Bálint Emese Réka  |e aut 
700 0 1 |a Balla Zsolt  |e aut 
700 0 1 |a Balog Beáta Adél  |e aut 
700 0 1 |a Dágó Ágnes  |e aut 
700 0 1 |a Totonji Ahmad  |e aut 
700 0 1 |a Bátai István Zoárd  |e aut 
700 0 1 |a Jurányi Eszter Petra  |e aut 
700 0 1 |a Ditrói Tamás  |e aut 
700 0 2 |a Al-omari Ammar  |e aut 
700 0 2 |a Pozsgai Gábor  |e aut 
700 0 2 |a Kormos Viktória  |e aut 
700 0 2 |a Nagy Péter  |e aut 
700 0 2 |a Pintér Erika  |e aut 
700 0 2 |a Rakonczay Zoltán  |e aut 
700 0 2 |a Kiss Lóránd  |e aut 
856 4 0 |u http://publicatio.bibl.u-szeged.hu/28471/1/2023-OrjanE-DMTS_AP.pdf  |z Dokumentum-elérés