Biological activity of Echinops spinosus on inhibition of paracetamol-induced renal inflammation

Hegazy, Marwa; Emam, Manal A.; Khattab, Hemmat I.; Helal, Nesma M.;

Abstract


This study was designed to evaluate the possible mechanisms through which Echinops spinosus (ES) extract demonstrates nephroprotective effect on the paracetamol acetominophen (N-acetyl-p-aminophenol (APAP)) induced nephrotoxicity in rats. Twenty-four Swiss albino rats were divided into four groups (six rats each). The placebo group was orally administered sterile saline, the APAP group received APAP (200 mg·kg -1 ·day -1 i.p.) daily, the ES group was given ES extract orally (250 mg/kg), and the APAP + ES group received APAP as for the APAP group and administrated the ES extract as for the ES group. Pretreatment of methyl alcohol extract of ES reduced the protein expression of inflammatory parameters including cyclooxygenase-2 and nuclear factor ?B in the kidney. It also reduced the mRNA gene expression of tumor necrosis factor-α and interleukin-1β. The ES extract compensated for deficits in the total antioxidant activity, suppressed lipid peroxidation, and amended the APAP-induced histopathological kidney alterations. Moreover, ES treatment restored the elevated levels of urea nitrogen in the blood and creatinine in the serum by APAP. The ES extract attenuated the APAP-induced elevations in renal nitric oxide levels. We clarified that the ES extract has the potential to defend the kidney from APAP-induced inflammation, and the protection mechanism might be through decreasing oxidative stress and regulating the inflammatory signaling pathway through modulating key signaling inflammatory biomarkers.


Other data

Title Biological activity of Echinops spinosus on inhibition of paracetamol-induced renal inflammation
Authors Hegazy, Marwa ; Emam, Manal A.; Khattab, Hemmat I.; Helal, Nesma M.
Keywords Acetaminophen | Gas chromatography mass-spectrometry | Nephrotoxicity | Oxidative stress | Phytochemicals
Issue Date 1-Jan-2019
Journal Biochemistry and Cell Biology 
ISSN 08298211
DOI 10.1139/bcb-2018-0212
PubMed ID 30933551
Scopus ID 2-s2.0-85063981455

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