2017
Prenylated flavonoid morusin protects against TNBS-induced colitis in rats
VOCHYANOVA, Z; Marie ČULENOVÁ; Dominik ROTREKL; V SMEKAL; P FICTUM et al.Základní údaje
Originální název
Prenylated flavonoid morusin protects against TNBS-induced colitis in rats
Autoři
VOCHYANOVA, Z; Marie ČULENOVÁ; Dominik ROTREKL; V SMEKAL; P FICTUM; Pavel SUCHÝ; Jan GAJDZIOK; Karel ŠMEJKAL a J HOSEK
Vydání
Plos one, San Francisco, Public Library of Science, 2017, 1932-6203
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 2.766
Označené pro přenos do RIV
Ne
Organizační jednotka
Farmaceutická fakulta
UT WoS
EID Scopus
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 26. 2. 2021 07:56, Mgr. Hana Hurtová
Anotace
V originále
Morusin is a prenylated flavonoid isolated from the root bark of Morus alba. Many studies have shown the ability of flavonoids to act as anti-inflammatory agents. The aim of this study was to evaluate the effect of morusin on experimentally colitis induced by 2,4,6-trinitroben-zensulfonic acid in Wistar rats and to compare it with sulfasalazine, a drug conventionally used in the treatment of inflammatory bowel disease. Morusin was administered by gavage at doses of 12.5, 25, or 50 mg/kg/day for five days. The colonic tissue was evaluated macroscopically, histologically, and by performing immunodetection and zymographic analysis to determine the levels of antioxidant enzymes [superoxide dismutase (SOD) and catalase (CAT)], interleukin (IL)-1 beta, and transforming growth factor (TGF)-beta 1 and the activities of matrix metalloproteinases (MMP) 2 and 9. The tissue damage scores were significantly reduced with increasing dose of morusin, however efficacy was not demonstrated at the highest dose. At the dose of 12.5 mg/kg, morusin exerted therapeutic effectivity similar to that of sulfasalazine (50 mg/kg). This was associated with significant reduction of TGF-beta 1 levels and MMP2 and MMP9 activities, and slight reduction of IL-1 beta. Our results suggest that morusin possesses therapeutic potential for the treatment of chronic inflammatory diseases.