Spinal cord injury induced arrest in estrous cycle of rats is ameliorated by S-nitrosoglutathione: novel therapeutic agent to treat amenorrhea
| Autor: | Mushfiquddin Khan, Anandakumar Shunmugavel, Inderjit Singh, Peter Cheng-te Chou |
|---|---|
| Rok vydání: | 2011 |
| Předmět: |
endocrine system
medicine.medical_specialty endocrine system diseases Urology Endocrinology Diabetes and Metabolism Blotting Western Fluorescent Antibody Technique Ovary Estrous Cycle Pharmacology Rats sprague dawley Article S-Nitrosoglutathione Rats Sprague-Dawley chemistry.chemical_compound Endocrinology Internal medicine medicine Animals Estrogen Receptor beta Spinal cord injury Amenorrhea Estrogen receptor beta Spinal Cord Injuries Estrous cycle business.industry NF-kappa B medicine.disease Rats Sprague dawley Psychiatry and Mental health medicine.anatomical_structure Reproductive Medicine chemistry Connexin 43 Female medicine.symptom business hormones hormone substitutes and hormone antagonists |
| Zdroj: | The journal of sexual medicine. 9(1) |
| ISSN: | 1743-6109 |
| Popis: | Amenorrhea following spinal cord injury (SCI) has been well documented. There has been little research on the underlying molecular mechanisms and therapeutics.The purpose of the present study was to investigate the effect of GSNO in ameliorating SCI-induced amenorrhea through affecting the expression of CX43, NFkB, and ERβ protein.SCI was induced in female SD rats at the T9-T10 level. Estrous stage was determined by vaginal smear. GSNO (50 µg/kg body weight) was gavage fed daily. Animals were sacrificed on day 7 and 14 post SCI. Ovaries were fixed for histological and biochemical studies. Expression levels of ERβ, CX-43, and NFkB were analyzed by Western blot and immunofluorescence.GSNO hastens resumption of the estrous cycle following SCI-induced transient arrest.Resumption of estrous cycle was hastened by GSNO. Atretic and degenerating follicles seen in the ovary of SCI rats on day 14 post-SCI were decreased in GSNO treated animals. The increased CX43 expression observed with SCI ovary was decreased by GSNO. ERβ expression decreased significantly on day 7 and 14 post-SCI and was restored with GSNO treatment. Following SCI, NFkB expression was increased in the ovarian follicles and the expression was reduced with GSNO administration. The number of terminal deoxynucleotidyl transferase-mediated biotinylated uridine triphosphate (UTP) nick end labeling positive follicular and luteal cells was increased after SCI. GSNO-treated animals had significantly fewer apoptotic cells in the ovary.SCI-induced amenorrhea is accompanied by an increase in CX43 expression and a decrease in ERβ expression. SCI animals treated with GSNO resumed the estrous cycle significantly earlier. These results indicate a potential therapeutic value for GSNO in treating amenorrhea among SCI patients. |
| Databáze: | OpenAIRE |
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