Methanolic Phoenix dactylifera L. Extract Ameliorates Cisplatin-Induced Hepatic Injury in Male Rats.
Heba Nageh Gad El-HakHany Salah MahmoudEman A AhmedHeba M ElnegrisTahany Saleh AldayelHeba M A AbdelrazekMohamed T A SolimanMenna Allah I El-MenyawyPublished in: Nutrients (2022)
This study investigated the ameliorative potential of methanolic date flesh extract (MDFE) against cisplatin-induced hepatic injury. Twenty male rats (weighing 180-200 g) were allocated into four groups: control; date flesh (DF) group (oral 600 mg/kg MDFE for 21 days); Cis group (7.5 mg/kg i.p. at day 16); and date flesh/cisplatin (DF/Cis) group (oral 600 mg/kg MDFE for 21 days and 7.5 mg/kg i.p. at day 16). Hepatic biochemical parameters in sera, and inflammatory and oxidant/antioxidant hepatic biomarkers were estimated. Hepatic histological changes and the immunohistochemistry of cyclooxygenase-2 (COX-2), nuclear factor kappa B (NF-κB), and alpha smooth muscle actin (α-SMA) were assessed. Pretreatment with MDFE decreased Cis-triggered liver biochemical parameters, oxidative stress, inflammatory biomarkers, and histological damage. Moreover, MDFE treatment reduced Cis-induced hepatic NF-κB, COX-2, and α-SMA protein expression. MDFE exerted a hepatoprotective effect when used concomitantly with Cis. Its effect was mediated via its antioxidant and anti-inflammatory ingredients.
Keyphrases
- oxidative stress
- nuclear factor
- anti inflammatory
- diabetic rats
- smooth muscle
- toll like receptor
- induced apoptosis
- ischemia reperfusion injury
- dna damage
- signaling pathway
- risk assessment
- climate change
- immune response
- cell proliferation
- mouse model
- nitric oxide
- high glucose
- endoplasmic reticulum stress
- cell migration
- nitric oxide synthase
- heat stress
- combination therapy
- atomic force microscopy