Hypericum perforatum L. Nanoemulsion Mitigates Cisplatin-Induced Chemobrain via Reducing Neurobehavioral Alterations, Oxidative Stress, Neuroinflammation, and Apoptosis in Adult Rats.
Heba Muhammed Ali KhalilHanan M A El HenafyIslam A KhalilAlaa F BakrMohamed Ibrahim Mohamed FahmyNancy S YounisRiham Adel El-ShiekhPublished in: Toxics (2023)
Cisplatin (Cis) is a potent chemotherapeutic agent; however, it is linked with oxidative stress, inflammation, and apoptosis, which may harmfully affect the brain. Hypericum perforatum L. (HP L.) is a strong medicinal plant, but its hydrophobic polyphenolic compounds limit its activity. Therefore, our study aimed to investigate the neuroprotective action of HP L. and its nanoemulsion (NE) against Cis-induced neurotoxicity. The prepared HP.NE was subjected to characterization. The droplet size distribution, surface charge, and morphology were evaluated. In addition, an in vitro dissolution study was conducted. Compared to Cis-intoxicated rats, HP L. and HP.NE-treated rats displayed improved motor activity and spatial working memory. They also showed an increase in their antioxidant defense system and a reduction in the levels of pro-inflammatory cytokines in the brain. Moreover, they showed an increase in the expression levels of the PON-3 and GPX genes, which are associated with a reduction in the brain levels of COX-2 and TP-53. These findings were confirmed by reducing the immunohistochemical expression of nuclear factor kappa (NF-ƘB) and enhanced Ki-67 levels. In conclusion, HP L. is a promising herb and could be used as an adjuvant candidate to ameliorate chemotherapeutic-induced neurotoxicity. Moreover, HP.NE has superior activity in lessening Cis-induced oxidative stress, inflammation, and apoptosis in brain tissue.
Keyphrases
- oxidative stress
- diabetic rats
- nuclear factor
- working memory
- cerebral ischemia
- resting state
- white matter
- ischemia reperfusion injury
- dna damage
- toll like receptor
- induced apoptosis
- poor prognosis
- endoplasmic reticulum stress
- functional connectivity
- high glucose
- cell death
- lps induced
- cell cycle arrest
- gene expression
- subarachnoid hemorrhage
- early stage
- anti inflammatory
- genome wide
- lipopolysaccharide induced
- squamous cell carcinoma
- cell proliferation
- heat shock
- drug induced
- traumatic brain injury
- inflammatory response
- binding protein
- single cell
- long non coding rna
- brain injury
- heat stress
- pi k akt
- locally advanced
- childhood cancer