2014
DOI: 10.1186/1472-6882-14-457
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Immunohistochemical and molecular study on the protective effect of curcumin against hepatic toxicity induced by paracetamol in Wistar rats

Abstract: BackgroundAn overdose of paracetamol is a frequent reason for liver and renal toxicity and possible death and curcumin has hepatoprotective properties against liver damage. The exact mechanism of such protection is not clear. Therefore, this study was conducted to examine the molecular levels of the protective effect of curcumin on paracetamol overdose induced hepatic toxicity in rats.MethodsMale Wistar rats were allocated into 4 groups. Control group, administered corn oil; curcumin group, administered curcum… Show more

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Cited by 62 publications
(44 citation statements)
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“…Subsequently, blood samples were taken from the medial canthus of the eye. Total RNA was extracted from the thymus as previously discussed (22). For leukocyte RNA extraction, 1 ml QIAzol was added to 350 ml total blood collected in tubes containing an anticoagulant.…”
Section: Serum Cytokine and Immunoglobulin (Ig) Assaysmentioning
confidence: 99%
“…Subsequently, blood samples were taken from the medial canthus of the eye. Total RNA was extracted from the thymus as previously discussed (22). For leukocyte RNA extraction, 1 ml QIAzol was added to 350 ml total blood collected in tubes containing an anticoagulant.…”
Section: Serum Cytokine and Immunoglobulin (Ig) Assaysmentioning
confidence: 99%
“…Thereafter, 5-lm thick sections were prepared and then stained with hematoxylin and eosin (HE) for histopathological examination (Suvarna et al 2013). Another group of embedded paraffin sections was also prepared for immunodetection of CD4 and CD8 (T-and B-lymphocytes marker, respectively)-positive cells using an avidin-biotin-peroxidase (ABC) method of Soliman et al (2014) and Mohamed et al (2015). In brief, the sections were deparaffinized and treated with 3% H 2 O 2 for 10 min to inactivate endogenous peroxidases.…”
Section: Histopathological and Immunohistochemical Investigationmentioning
confidence: 99%
“…Fixed tissues were processed routinely including washing, dehydration, clearing, paraffin embedding, casting, sectioning to 5 μm sections for using in hematoxylin and eosin staining (Soliman et al 2014). For immunohistochemistry, tissue sections of pancreas were deparaffinized then treated with 3% H 2 O 2 for 10 min to inactivate peroxidases, heated in 10 mM citrate buffer at 121°C for 30 min for antigen retrieval, blocked in 5% normal serum for 20 min, and incubated with a primary polyclonal anti-insulin (dilution, 1:100 in PBS; sc-9168, Santa Cruz Biotechnology) antibody overnight at 4°C.…”
Section: Pancreatic Histolopathology and Immunohistochemistrymentioning
confidence: 99%