The ameliorative effect of cerium oxide nanoparticles on chlorpyrifos induced hepatotoxicity in a rat model: Biochemical, molecular and immunohistochemical study

ElsevierVolume 81, January 2024, 127346Journal of Trace Elements in Medicine and BiologyAuthor links open overlay panel, , , , Highlights•

Chronic exposure to Chlorpyrifos (CPF) induced hepatotoxicity in rats.

CPF induced up-regulation of inflammatory markers and apoptotic markers.

Cerium oxide nanoparticles (CeO2NPs) could alleviate CPF- induced hepatoxicity.

CeO2NPs cause down-regulation of anti-oxidative (SOD, CAT and NFE2L2) markers.

CeO2NPs cause down-regulation of anti-apoptotic (Bcl 2 & Gadd45) markers.

AbstractBackground

Chlorpyrifos (CPF) is a widely used insecticide that causes toxicity to living organisms through the production of free radicals. Cerium oxide nanoparticles (CeO2NPs) are a new antioxidant agent that has proved therapeutic effects. We evaluated the effect of CeO2NPs on CPF hepatotoxicity.

Methods

Forty rats were randomized into four groups. Group I: rats received 1 ml corn oil by gastric tube once daily and 0.5 ml PBS by intra-peritoneal injection twice a week for 4 weeks. Group II: received CeO2NPs 0.5 mg/kg in PBS by i.p. injection, twice weekly for four weeks. Group III: were treated with oral administration of CPF 13.5 mg/kg in corn oil daily for 4 weeks. Group IV: received CPF as in group III, then each animal received CeO2NPs twice weekly for four weeks as in group II. Twenty-four hours after the last dose, rats were anesthetized and sera were collected for liver enzymes assessment. Afterwards, rats were sacrificed, livers were excised, the right lobe of each liver was fixed for immunohistochemical studies, and the left lobe was homogenized for oxidative profile assessment and molecular analysis.

Results

CPF group showed significant increase in liver transaminases, disturbance of the oxidative profile with up-regulation of BAX expression and down-regulation in the Bcl-2, Gadd45 and NFE2L2. CPF caused severe histopathological liver damage as well as significant increase in anti-Caspase 3 and TNF immunostaining. The CeO2NPs treated group revealed significant improvement of all previous parameters.

Conclusion

CeO2NPs could alleviate CPF hepatoxicity through decreasing expression of the inflammatory and apoptotic proteins and increasing the activity of antioxidant enzymes.

AbbreviationsCeO2NPs

Cerium oxide nanoparticles

Gadd45

Growth arrest and DNA damage-inducible gene

NFE2L2

Nuclear factor erythroid derived 2-like2

Nrf2

The nuclear factor erythroid 2-related factor 2

Keywords

Chlorpyrifos

CeO2NPs

Hepatotoxicity

Oxidative stress

Apoptosis

View Abstract

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