Ameliorative effect of sesame oil on experimentally induced polycystic ovary syndrome: A cross‐link between XBP‐1/PPAR‐1, regulatory proteins for lipogenesis/steroids

Author:

Elshamy Amira Mostafa1ORCID,Shatat Doaa2,AbuoHashish Norhan Ahmed3,Safa Mohamed Abd Elmotaal4,Elgharbawy Nashwa4,Ibrahim Hoda Ali1,Barhoma Ramez Abd Elmoneim5,Eltabaa Eman Fawzy5,Ahmed Ahmed S.67,Shalaby Amany Mohamed8,Alabiad Mohamed Ali9,Alorini Mohammed10,Ibrahim Rowida Raafat1ORCID

Affiliation:

1. Department of Medical Biochemistry & Molecular Biology, Faculty of Medicine Tanta University Tanta Egypt

2. Department of Gynecology and Obstetrics, Faculty of Medicine Tanta University Tanta Egypt

3. Department of Pharmacology, Faculty of Medicine Tanta University Tanta Egypt

4. Department of Internal medicine, Faculty of Medicine Tanta University Tanta Egypt

5. Department of Physiology, Faculty of Medicine Tanta University Tanta Egypt

6. Department of Anatomy & Embryology, Faculty of Medicine Tanta University Tanta Egypt

7. Department of Biomedical sciences, Faculty of Medicine Gulf Medical University Ajman United Arab Emirates

8. Department of Histology and Cell Biology, Faculty of Medicine Tanta University Tanta Egypt

9. Department of Pathology, Faculty of Medicine Zagazig University Zagazig Egypt

10. Department of Basic Medical Sciences, Unaizah College of Medicine and Medical Sciences Qassim University Unaizah Saudi Arabia

Abstract

AbstractPolycystic ovary syndrome (PCOS) is a mixed endocrine/metabolic/reproductive disorder in women of reproductive age. Sesame oil (SO) contains sesame lignans & vitamin E with broad‐spectrum antioxidant and anti‐inflammatory effects. This study investigates the ameliorative effect of SO on experimentally induced PCOS and elucidates the possible molecular mechanisms with a deeper focus on the different signaling pathways involved. The study was carried out on 28 nonpregnant female Wister albino rats that were divided into four equal groups; Group I (control group) received oral 0.5% wt/vol carboxymethyl cellulose daily. Group II (SO group): orally administered SO (2 mL/kg body wt./day) for 21 days. Group III (PCOS group) received letrozole daily, 1 mg/kg, for 21 days. Group IV (PCOS + SO group): concomitantly administered letrozole and SO for 21 days. The serum hormonal and metabolic panel and the homogenate ATF‐1, StAR, MAPK, PKA, and PI3K levels of the ovarian tissue were calorimetrically evaluated. However, endoplasmic reticulum (ER) stress was evaluated by ovarian XBP1 and PPAR‐γ messenger RNA expression level using the qRT‐PCR technique. Ovarian COX‐2 was detected immunohistochemically. The results suggest that SO‐treated PCOS rats showed a significantly improved hormonal, metabolic panel, inflammatory, and ER stress status with concomitant decreases in ATF‐1, StAR, MAPK, PKA, and PI3K in ovarian rats compared to the correspondent values in PCOS without treatment.ConclusionsThe protective effects of SO against PCOS are triggered by ameliorating regulatory proteins of ER stress, lipogenesis, and steroidogenesis through the PI3K/PKA and MAPK/ERK2 signaling cascades.Significance StatementPolycystic ovary syndrome (PCOS) is the most common mixed endocrine‐metabolic dysfunction among women within the reproductive period, with an estimated prevalence of 5%–26% worldwide. Doctors traditionally recommend metformin for PCOS patients. However, metformin is known to be associated with significant adverse effects and contraindications. This work aimed at shedding light on the ameliorative effect of sesame oil (SO), natural polyunsaturated fatty acids‐rich oil, on the induced PCOS model. SO proved to have a marvelous effect on the metabolic and endocrine derangements in the PCOS rat model. We hoped to provide a valuable alternative treatment for PCOS patients to avoid the side effects of metformin and to help PCOS patients for whom metformin is contraindicated.

Publisher

Wiley

Subject

Cell Biology,Clinical Biochemistry,General Medicine,Biochemistry

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