Curcumin mitigates acrylamide‐induced ovarian antioxidant disruption and apoptosis in female Balb/c mice: A comprehensive study on gene and protein expressions

Author:

Alaee Sanaz12,Khodabandeh Zahra2,Dara Mahintaj2,Hosseini Elham34ORCID,Sharma Mona5

Affiliation:

1. Department of Reproductive Biology, School of Advanced Medical Sciences and Technologies Shiraz University of Medical Sciences Shiraz Iran

2. Stem Cells Technology Research Center Shiraz University of Medical Sciences Shiraz Iran

3. Department of Obstetrics and Gynecology, Mousavi Hospital, School of Medicine Zanjan University of Medical Sciences Zanjan Iran

4. Zanjan Metabolic Diseases Research Center Zanjan University of Medical Sciences Zanjan Iran

5. Department of Reproductive Biology AIIMS New Delhi India

Abstract

AbstractCurcumin is known for its antioxidant properties. This study aimed to investigate the impact of curcumin on acrylamide (ACR)‐induced alterations in the first‐line antioxidant defense of ovarian tissue. Female Balb/c mice were divided into control, ACR (50 mg/kg), ACR/CUR100 (received Acr + curcumin100 mg/kg), and ACR/CUR200 (Acr + curcumin 200 mg/kg) groups, and received oral treatments for 35 days. Evaluation of antioxidant enzyme expression (Sod, Cat, Gpx genes), pro‐apoptotic gene expressions (Bax, Caspase 3), and anti‐apoptotic gene expression (Bcl2l1) at mRNA and protein levels was done. Percentage of apoptotic cells using Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay was performed. The model group (ACR) showed decreased mRNA expression of Sod, Cat, and Gpx genes compared with the control group. Treatment with two different doses of curcumin (CUR100 and CUR200) significantly increased Sod, Cat, and Gpx gene expression, with CUR200 demonstrating significant recovery. SOD, CAT, and GPX protein levels were similar to mRNA expression trends, significantly increased with curcumin administration. Acrylamide exposure significantly increased Bax and Caspase 3 expression and decreased Bcl2l1 gene expression leading to a notable rise in apoptosis in ACR group as compared to the control group. Conversely, curcumin administration, significantly reduced Bax and Caspase 3 expressions, with an increase in Bcl2l1expression, though not statistically significant. TUNEL assay revealed a substantial decrease in apoptosis in curcumin‐received groups. In our study, ACR exposure adversely affected ovarian antioxidant defense thereby leading to increased pro‐apoptotic markers. Notably, curcumin treatment effectively mitigated these effects, restored antioxidant potential, and reduced acrylamide‐induced toxicity in female mouse ovaries.

Funder

Shiraz University of Medical Sciences

Publisher

Wiley

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