Protective effect of chrysin, a flavonoid, on the genotoxic activity of carboplatin in mice.
Basit L JanAjaz AhmadAltaf KhanMuneeb U RehmanKhalid M AlkharfyPublished in: Drug and chemical toxicology (2021)
Carboplatin is amongst the most commonly used anticancer drugs for the management of several human malignancies. However, it has displayed genotoxic properties against normal cells. Evaluation of natural products for their protective effects against chemotherapeutic drug induced toxicity has been growing in recent years. A naturally occurring flavonoid, chrysin, has strong antioxidant abilities and protects against DNA impairment. This study used multiple assays to evaluate the levels of damage to DNA in normal cells and to examine any possible protective role of chrysin against such damage. Male BALB/c mice were administered chrysin orally in two doses of 20 and 40 mg/kg for 10 consecutive days and then a single injection of carboplatin [90 mg/kg body weight (b.w.)] was administered intraperitoneally to induce carboplatin toxicity. 24 h after the carboplatin injection, mice were sacrificed. DNA damage was evaluated using several genotoxicity tests (8-Hydroxydeoxy-guanosine marker, comet assay, micronucleus test, and chromosomal aberration assay) to identify diverse types of damage to the DNA. The results suggest that pretreatment with chrysin significantly decreased the level of DNA damage caused by carboplatin probably due to its potent antioxidant traits. Therefore, chrysin can be considered to be developed as a chemoprotective agent against chemotherapy associated side-effects.
Keyphrases
- oxidative stress
- induced apoptosis
- dna damage
- phase ii study
- drug induced
- circulating tumor
- liver injury
- body weight
- phase iii
- high throughput
- high fat diet induced
- locally advanced
- single molecule
- cell cycle arrest
- cell free
- endothelial cells
- open label
- anti inflammatory
- dna repair
- type diabetes
- wild type
- gene expression
- cell death
- copy number
- pi k akt
- adipose tissue
- oxide nanoparticles