Allopregnanolone-induced modification of presynaptic basal and K<SUP>+</SUP>-induced [<SUP>3</SUP>H]-norepinephrine efflux from rat cortical slices during the estrous cycle
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Date
1998
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Abstract
Superfused frontal slices of cerebral cortex were preloaded with [H-3]-norepinephrine ([H-3]NE). Basal [H-3]NE efflux and Kf-induced [H-3]NE release were studied during the estrous cycle and in the presence of neurosteroids. Basal [H-3]NE efflux showed estrous cycle-related variations, with lowest values found during estrus and diestrus II. Allopregnanolone (10(-9) M) potentiated basal [H-3]NE efflux from the Ist minute of its application; the effect of the steroid was still present after 20 min. This effect was also dependent upon the estrous cycle, since basal [H-3]NE efflux was mainly increased during estrus diestrus I, and to a lesser degree only during proestrus. During diestrus II and after ovariectomy, basal [H-3]NE efflux was no longer affected by the neurosteroid. In the presence of yohimbine (10(-6) M), the effect of allopregnanolone on basal efflux was potentiated only during the first 3 min but vanished thereafter. Allopregnanolone (10(-9) M) potentiated the K+-induced [H-3]NE release during estrus, but pregnenolone (10(-9) M) was ineffective, suggesting specificity of the neurosteroid. Yohimbine (10(-6) M) also potentiated K+-induced [H-3]NE release. When applied simultaneously with allopregnanolone (10(-9) M), a potentiating effect on [H-3]NE release was observed. The present results suggest that allopregnanolone is a neurosteroid able to modulate norepinephrine release in the cerebral cortex in an estrous cycle-dependent manner, and that the effect could involve noradrenergic alpha-2 receptors.
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catecholamines, cerebral cortex, allopregnanolone, neurosteroids, estrous cycle