The aim of this study was to investigate the effects of nomegestrol acetate (NOMAc) on the central nervous system by analyzing the neurosteroid allopregnanolone and the opioid beta-endorphin (β-endorphin). 104 Wistar female rats were used in this study; one group of fertile and one group of ovariectomized rats were used as control. The others were ovariectomized and they underwent a 2-week oral treatment of NOMAc (0.05, 0.1, 0.2, 0.5, 1 mg/kg/day), alone or with 0.05 mg/kg/day of estradiol valerate (E2V). Allopregnanolone and β-endorphin were assessed in different brain areas and in circulation. Ovariectomy decreased allopregnanolone anywhere except in the adrenal gland and E2V reversed the effects of ovariectomy. 0.5 and 1 mg/kg/day of NOMAc increased allopregnanolone levels in hippocampus. Combined administration of 1 mg/kg/day of NOMAc plus E2V induced a further increase of allopregnanolone levels in hippocampus, hypothalamus, and anterior pituitary. NOMAc (1 mg/kg/day) decreased the adrenal content of allopregnanolone, both by itself and associated with E2V. NOMAc increased hippocampal and hypothalamic content of β-endorphin at the highest doses, and it increased positively E2V action, at 1 mg/kg/day, also in anterior pituitary and plasma. These findings reinforce the clinical data regarding the capability of NOMAc to modulate the pathways involved in mood and behaviour. In fact, due to the NOMAc action on hippocampus, hypothalamus, and anterior pituitary, our results highlight the selectivity of NOMAc on part of the limbic system and the anterior pituitary, regarding both allopregnanolone and β-endorphin. © 2008 Elsevier Ltd. All rights reserved.

Lenzi, E., Pluchino, N., Begliuomini, S., Ninni, F., Freschi, L., Centofanti, M., et al. (2008). Effects of nomegestrol acetate administration on central and peripheral beta-endorphin and allopregnanolone in ovx rats. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 110(1), 67-75 [10.1016/j.jsbmb.2008.02.002].

Effects of nomegestrol acetate administration on central and peripheral beta-endorphin and allopregnanolone in ovx rats

LUISI S.;
2008

Abstract

The aim of this study was to investigate the effects of nomegestrol acetate (NOMAc) on the central nervous system by analyzing the neurosteroid allopregnanolone and the opioid beta-endorphin (β-endorphin). 104 Wistar female rats were used in this study; one group of fertile and one group of ovariectomized rats were used as control. The others were ovariectomized and they underwent a 2-week oral treatment of NOMAc (0.05, 0.1, 0.2, 0.5, 1 mg/kg/day), alone or with 0.05 mg/kg/day of estradiol valerate (E2V). Allopregnanolone and β-endorphin were assessed in different brain areas and in circulation. Ovariectomy decreased allopregnanolone anywhere except in the adrenal gland and E2V reversed the effects of ovariectomy. 0.5 and 1 mg/kg/day of NOMAc increased allopregnanolone levels in hippocampus. Combined administration of 1 mg/kg/day of NOMAc plus E2V induced a further increase of allopregnanolone levels in hippocampus, hypothalamus, and anterior pituitary. NOMAc (1 mg/kg/day) decreased the adrenal content of allopregnanolone, both by itself and associated with E2V. NOMAc increased hippocampal and hypothalamic content of β-endorphin at the highest doses, and it increased positively E2V action, at 1 mg/kg/day, also in anterior pituitary and plasma. These findings reinforce the clinical data regarding the capability of NOMAc to modulate the pathways involved in mood and behaviour. In fact, due to the NOMAc action on hippocampus, hypothalamus, and anterior pituitary, our results highlight the selectivity of NOMAc on part of the limbic system and the anterior pituitary, regarding both allopregnanolone and β-endorphin. © 2008 Elsevier Ltd. All rights reserved.
Lenzi, E., Pluchino, N., Begliuomini, S., Ninni, F., Freschi, L., Centofanti, M., et al. (2008). Effects of nomegestrol acetate administration on central and peripheral beta-endorphin and allopregnanolone in ovx rats. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 110(1), 67-75 [10.1016/j.jsbmb.2008.02.002].
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11365/18613
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