Possible Ameliorative Effects of the Royal Jelly on Hepatotoxicity and Oxidative Stress Induced by Molybdenum Nanoparticles and/or Cadmium Chloride in Male Rats.
Reham Z HamzaRasha A Al-EisaNahla S El-ShenawyPublished in: Biology (2022)
The present study aimed to investigate the effect of the royal jelly (RJ) on hepatotoxicity induced by molybdenum nanoparticles (MoO 3 -NPs), cadmium chloride (CdCl 2 ), or their combination in male rats at biochemical, inflammation, immune response, histological, and ultrastructural levels. The physicochemical properties of MoO 3 -NPs have been characterized, as well as their ultrastructural organization. A rat experimental model was employed to assess the liver toxicity of MoO 3 -NPs, even in combination with CdCl 2 . Different cellular studies indicate divergent mechanisms, from increased reactive oxygen species production to antioxidative damage and cytoprotective activity. Seventy male rats were allocated to groups: (i) control; (ii) MoO 3 -NPs (500 mg/kg); (iii) CdCl 2 (6.5 mg/kg); (iv) RJ (85 mg/kg diluted in saline); (v) MoO 3 -NPs followed by RJ (30 min after the MoO 3 -NPs dose); (vi) CdCl 2 followed by RJ; and (vii) a combination of MoO 3 -NPs and CdCl 2 , followed by RJ, for a total of 30 successive days. Hepatic functions, lipid profile, inflammation marker (CRP), antioxidant biomarkers (SOD, CAT, GPx, and MDA), and genotoxicity were examined. Histological changes, an immunological marker for caspase-3, and transmission electron microscope variations in the liver were also investigated to indicate liver status. The results showed that RJ alleviated the hepatotoxicity of MoO 3 -NPs and/or CdCl 2 by improving all hepatic vitality markers. In conclusion, the RJ was more potent and effective as an antioxidant over the oxidative damage induced by the combination of MoO 3 -NPs and CdCl 2 .
Keyphrases
- oxidative stress
- oxide nanoparticles
- immune response
- induced apoptosis
- reactive oxygen species
- dna damage
- diabetic rats
- anti inflammatory
- ischemia reperfusion injury
- heavy metals
- signaling pathway
- dendritic cells
- cell death
- cell proliferation
- umbilical cord
- inflammatory response
- toll like receptor
- heat shock
- mesenchymal stem cells
- electron microscopy