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Shatavarin-IV rescues the Di (2-ethylhexyl) phthalate (DEHP) induced oxidative stress in rat granulosa cells in vitro.
- Source :
-
Reproductive toxicology (Elmsford, N.Y.) [Reprod Toxicol] 2024 Dec; Vol. 130, pp. 108737. Date of Electronic Publication: 2024 Oct 26. - Publication Year :
- 2024
-
Abstract
- Studies provide notable evidence that oxidative stress (OS) mediated reactive oxygen species (ROS) disturb reproductive health. We have shown in our previous publication that exposure of Di-(2-ethylhexyl) phthalate (DEHP), induces OS mediated ROS generation which inhibits steroid synthesis. In the present study, we demonstrated the ameliorative/protective effects of one of the steroidal saponins, i.e., Shatavarin-IV, isolated from the roots of Asparagus racemosus against DEHP induced OS in rat granulosa cells. Granulosa cells were exposed with DEHP alone (400 μM), Shatavarin-IV alone (8 μg/ml), and a combination of DEHP + Shatavarin-IV (400 μM + 8 μg/ml) in vitro for 24 hrs. Intracellular ROS, OS/hypoxia, mitochondrial membrane potential, steroid-responsive genes expression were analyzed. The results revealed that the effective dose of DEHP (400 µg) significantly increased OS compared to the control by increasing ROS levels, mitochondrial membrane potential, and β-galactosidase activity with a higher level of apoptotic genes (Bax, Caspase-3) expression at mRNA level. Further, DEHP significantly (p < 0.05) reduced mRNA expression of steroidogenic responsive genes (StAR, CYP17A1, and CYP19A1) in granulosa cells treated with above combination compared to control. Interestingly, co-treatment of DEHP + Shatavarin-IV significantly suppressed the DEHP induced OS, ROS, β-galactosidase levels and enhanced steroidogeneic and apoptotic gene expression activities, which suggests that Shatavarin-IV rescued DEHP-induced changes that may useful for the prevention of DEHP- induced reproductive toxicity.<br />Competing Interests: Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Pawan K. Dubey reports administrative support, equipment, drugs, or supplies, and statistical analysis were provided by Banaras Hindu University. Pawan K. Dubey reports a relationship with Banaras Hindu University that includes: employment. Pawan K. Dubey has patent pending to Assignee. NA<br /> (Copyright © 2024 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Female
Saponins pharmacology
Rats, Sprague-Dawley
Cells, Cultured
Plasticizers toxicity
Rats
Aromatase genetics
Aromatase metabolism
Caspase 3 metabolism
Caspase 3 genetics
Phosphoproteins metabolism
Phosphoproteins genetics
Apoptosis drug effects
Antioxidants pharmacology
Cell Survival drug effects
Steroid 17-alpha-Hydroxylase
Diethylhexyl Phthalate toxicity
Granulosa Cells drug effects
Granulosa Cells metabolism
Oxidative Stress drug effects
Reactive Oxygen Species metabolism
Membrane Potential, Mitochondrial drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1873-1708
- Volume :
- 130
- Database :
- MEDLINE
- Journal :
- Reproductive toxicology (Elmsford, N.Y.)
- Publication Type :
- Academic Journal
- Accession number :
- 39490591
- Full Text :
- https://doi.org/10.1016/j.reprotox.2024.108737