Protective Effects of Apamin on Acetaminophen-Induced Hepatotoxicity in Mice.
Hyo-Jeong JangJaechan LeemGyun-Moo KimPublished in: Current issues in molecular biology (2023)
Acetaminophen (APAP) overdose can cause severe liver damage, but therapeutic options are limited. Apamin is a natural peptide present in bee venom and has antioxidant and anti-inflammatory properties. Accumulating evidence suggests that apamin has favorable actions in rodent models of inflammatory disorders. Here, we examined the effect of apamin on APAP-evoked hepatotoxicity. Intraperitoneal administration of apamin (0.1 mg/kg) alleviated histological abnormalities and reduced serum levels of liver enzymes in mice injected with APAP. Apamin inhibited oxidative stress through an increase in the amount of glutathione and activation of the antioxidant system. Apamin also attenuated apoptosis with inhibition of caspase-3 activation. Moreover, apamin reduced serum and hepatic levels of cytokines in APAP-injected mice. These effects were accompanied by suppression of NF-κB activation. Furthermore, apamin inhibited chemokine expression and inflammatory cell infiltration. Our results suggest that apamin dampens APAP-evoked hepatotoxicity through inhibiting oxidative stress, apoptosis, and inflammation.
Keyphrases
- oxidative stress
- diabetic rats
- induced apoptosis
- drug induced
- dna damage
- liver injury
- anti inflammatory
- cell death
- signaling pathway
- high fat diet induced
- single cell
- mesenchymal stem cells
- stem cells
- type diabetes
- early onset
- cell cycle arrest
- bone marrow
- heat shock protein
- pi k akt
- immune response
- heat stress
- long non coding rna