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
AUTHORS (6)
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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