Investigating the potential role of swertiamarin on insulin resistant and non-insulin resistant granulosa cells of poly cystic ovarian syndrome patients

• Published in: Journal of ovarian research Vol. 16; no. 1; pp. 55 - 11
• Main Authors: Belani, Muskaan A, Shah, Preeti, Banker, Manish, Gupta, Sarita S
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 18.03.2023; BioMed Central; BMC
• Subjects: 17β-Estradiol; AKT protein; Androgens; Cytochrome P-450; Dehydrogenases; Diabetes; Diabetes therapy; Enzymatic activity; Enzymes; Fat metabolism; Fatty acids; Female; Fertility; Fertility drugs; Gene expression; Granulosa cells; Granulosa Cells - metabolism; Hormones; Humans; Infertility; Insulin; Insulin - pharmacology; Insulin Resistance; Insulin-like growth factors; Menstruation; Metformin; Metformin - pharmacology; Metformin - therapeutic use; Ovaries; Physiological aspects; Polycystic ovary syndrome; Polycystic Ovary Syndrome - metabolism; Progesterone; Protein kinase C; Proteins; Secretions; Stein-Leventhal syndrome; Steroidogenesis; Steroids; Womens health
• ISSN: 1757-2215; 1757-2215
• DOI: 10.1186/s13048-023-01126-0

Conventional drugs have limitations due to prevalence of contraindications in PCOS patients. To explore the potential effects of swertiamarin, on abrupted insulin and steroidogenic signaling in human luteinized granulosa cells from PCOS patients with or without insulin resistance. hLGCs from 8 controls and 16 PCOS patients were classified for insulin resistance based on down regulation of protein expression of insulin receptor-β (INSR- β) as shown in our previous paper. Cells were grouped as control, PCOS-IR and PCOS-NIR, treated with swertiamarin (66 µM) and metformin (1 mM). Expression of key molecules involved in insulin signaling, fat metabolism, IGF system and steroidogenesis were compared between groups. Swertiamarin significantly (P < 0.05) reversed the expression of INSR-β, PI(3)K, p-Akt, PKC-ζ, PPARγ, (P < 0.01) IRS (Ser 307) and IGF system in PCOS-IR group and was equally potent to metformin. In the same group, candidate genes viz SREBP1c, FAS, ACC-1 and CPT-1 were down regulated by swertiamarin (P < 0.001) and metformin (P < 0.001). Significant upregulation was demonstrated in expression of StAR, CYP19A1, 17β-HSD and 3β-HSD when treated with swertiamarin (P < 0.01) and metformin (P < 0.01) in PCOS-IR followed by increase in 17β-HSD and 3β-HSD enzyme activity along with estradiol and progesterone secretions. However, swertiamarin did not reveal any effect on PCOS-NIR group as compared to metformin that significantly (P < 0.01) reversed all the parameters related to steroidogenesis and down regulated basal expression of insulin signaling genes. Swertiamarin, presents itself as a potential fertility drug in hLGCs from PCOS-IR patients.