Oral administration of hesperidin a citrus flavonone in rats counteracts the oxidative stress the inflammatory cytokine production and the hepatotoxicity induced by the ingestion of 2 3 7 8 tetrachlorodibenzo p dioxin TCDD
Yükleniyor...
Dosyalar
Tarih
2013
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Eur.Cytokine Netw
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
The objective of the current study was to investigate the protective effects of hesperidin against oxidative
stress, altered cytokines levels and histological changes in rats induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin
(TCDD). Rats were divided randomly into four equal groups (Control, TCDD, hesperidin and TCDD+hesperidin).
TCDD and hesperidin were given by gavage, dissolved in corn oil at doses of 2 /kg/week and 50 mg/kg/day respectively.
The blood and tissue samples were taken from all rats on the 60th day, to be analyzed for the determination of
oxidative stress, histological changes and cytokine levels. The results indicated that hesperidin prevented oxidative
damage caused by TCDD via decrease lipid peroxidation and increased antioxidant defense systems. It also reversed
the histological damage induced by TCDD. Although, TCDD led to a significant increase in TNF- and IL-1 levels,
hesperidin treatment was able to normalize these values in rats. In conclusion, it was shown that TCDD caused
adverse effects as regards cytokine levels, histological alterations and oxidative stress in rats. However, hesperidin
treatment mitigated these toxic effects. These results suggest that hesperidin could play a protective role against
TCDD toxicity.
Açıklama
Anahtar Kelimeler
TCDD, Hesperidin, Cytokine, Oxidative stress, Histological alterations
Kaynak
Eur.Cytokine Netw
WoS Q Değeri
Scopus Q Değeri
Cilt
24
Sayı
2
Künye
Bentli, R. Çiftçi, O. Çetin, A. Ünlü, M. Başak, N. Çay, M. (2013). Oral administration of hesperidin a citrus flavonone in rats counteracts the oxidative stress the inflammatory cytokine production and the hepatotoxicity induced by the ingestion of 2 3 7 8 tetrachlorodibenzo p dioxin TCDD . Eur.Cytokine Netw, 24 -2, 91-96.
