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Effect of pachymaran on oxidative stress and DNA damage induced by formaldehyde

To further explore the pharmacological effect of pachymaran, this article studied the inhibition of pachymaran on oxidative stress and genetic damage induced by formaldehyde. 40 adult Kunming male mice were randomly divided into four groups with different interventions. One week later, the contents...

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Detalles Bibliográficos
Autores principales: Zhang, Zhijun, Yang, Yuan, Hu, Changjun, Zhang, Zaiqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10576801/
https://www.ncbi.nlm.nih.gov/pubmed/37838763
http://dx.doi.org/10.1038/s41598-023-44788-y
Descripción
Sumario:To further explore the pharmacological effect of pachymaran, this article studied the inhibition of pachymaran on oxidative stress and genetic damage induced by formaldehyde. 40 adult Kunming male mice were randomly divided into four groups with different interventions. One week later, the contents of serum SOD, GR, MDA, DNA–protein crosslink (DPC), 8-hydroxydeoxyguanosine (8-OHDG) and DNA adduct were determined by ELISA. The results showed that there were statistically significant differences in the contents of SOD, GR and MDA among the four groups (P < 0.01). The activity of SOD and GR increased along with the increase of pachymaran dosage (SOD: r(s) = 0.912, P < 0.01; GR: r(s) = 0.857, P < 0.01), while the content of MDA showing a significant negative correlation (r(s) = − 0.893, P < 0.01). There were statistically significant differences in the levels of DPC, 8-OHDG and DNA adduct among the four groups (DPC and DNA adduct: P < 0.01, 8-OHDG: P < 0.05), the concentration decreased along with the increase of pachymaran dosage (DPC: r(s) = − 0.855, P < 0.01; 8-OHDG:r(s) = − 0.412, P < 0.05, DNA adduct: γ(s) = − 0.869, P < 0.01). It can be inferred that pachymaran can inhibit oxidative stress and DNA damage induced by formaldehyde with the dose–effect relationship.