info:eu-repo/semantics/article
Oxidative stress and altered steroidogenesis in the ovary by cholinergic stimulation of coeliac ganglion in the first proestrous in rats. Implication of nitric oxide
Fecha
2016-02-29Registro en:
Delsouc, María Belén; Della Vedova, Maria Cecilia; Ramirez, Dario; Anzulovich Miranda, Ana Cecilia; Delgado, Silvia Marcela; et al.; Oxidative stress and altered steroidogenesis in the ovary by cholinergic stimulation of coeliac ganglion in the first proestrous in rats. Implication of nitric oxide; Academic Press Inc Elsevier Science; Nitric Oxide-Biology and Chemistry; 53; 29-2-2016; 45-53
1089-8603
CONICET Digital
CONICET
Autor
Delsouc, María Belén
Della Vedova, Maria Cecilia
Ramirez, Dario
Anzulovich Miranda, Ana Cecilia
Delgado, Silvia Marcela
Casais, Marilina
Resumen
An ex-vivo Coeliac Ganglion-Superior Ovarian Nerve-Ovary (CG-SON-O) system from virgin rats in the first proestrous was used to test whether cholinergic stimulation of CG affects oxidative status and steroidogenesis in the ovary. The CG and the O were placed in separate buffered-compartments, connected by the SON, and the CG was stimulated by acetylcholine (Ach). To test a possible role of nitric oxide (NO) in the ovarian response to cholinergic stimulation of CG, aminoguanidine (AG) - an inhibitor of inducible-NO synthase was added to the O compartment. After 180 min incubation, the oxidative status was assessed in O whereas nitrite and steroidogenesis were assessed at 30, 120 and 180 min. Ach in CG decreased the total antioxidant capacity, but increased NO production and protein carbonization in O. Ach stimulation of CG increased estradiol, but decreased progesterone release in O by reducing the mRNAs related to their synthesis and degradation. The addition of AG to the O compartment caused an opposite effect, which was more pronounced in the presence of Ach in the CG compartment than in its absence. These results show that the stimulation of the extrinsic-cholinergic innervation of the O increases the concentration of NO, causes oxidative stress and modulates steroidogenesis in the first rat proestrous.