Role of macrophage secretions on rat polycystic ovary: its effect on apoptosis

Blotting, Western Nitric Oxide Synthase Type II Apoptosis Nitric Oxide Real-Time Polymerase Chain Reaction PROTAGLANDIN E2 Dinoprostone Immunoenzyme Techniques ANDROGENS 03 medical and health sciences Contraceptive Agents https://purl.org/becyt/ford/1.6 Animals RNA, Messenger MACROPHAGES https://purl.org/becyt/ford/1 Cells, Cultured Cell Proliferation 0303 health sciences Estradiol Macrophages Androstenedione APOPTOSIS Rats Disease Models, Animal Proto-Oncogene Proteins c-bcl-2 POLYCYSTIC OVARY Female Polycystic Ovary Syndrome
DOI: 10.1530/rep-15-0216 Publication Date: 2015-08-12T02:09:50Z
ABSTRACT
Polycystic ovarian syndrome is the most common endocrine disorder among women of reproductive age. Little known about its etiology, although evidence suggests an intrinsic abnormality in which endocrine, metabolic, neural and immune factors would be involved. In this work, effects macrophage (MO) secretion on apoptosis a polycystic ovary rat model (PCO rat) induced by estradiol valerate are studied. Spleen MO secretions were used to stimulate ovaries interstitial granulosa cells from both PCO control rats. Ovarian hormones prostaglandin E2 (PGE2) measured RIA; mRNA levels Bax, Bcl2 NFkB RT-PCR; inducible nitric oxide synthase (iNOS) western blot. The number apoptotic was evaluated TUNEL. ovary, rats increased Bax expressions TUNEL staining theca cells. addition, produced decrease release, iNOS protein level PGE2 content it also increase androstenedione production cells, comparison with secretions. Considering these results knowing that testosterone stimulates tumour necrosis factor-α modifying response increasing androstenedione, reasonable suggest androgens stimulated could turn cytokine MO, thus maintaining vicious cycle ovary.
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