Abstract
These studies tested the hypothesis that estradiol facilitates norepinephrine (NE) neurotransmission by modulating alpha 2- adrenoceptor-mediated inhibition of NE release. KCl-induced overflow of 3H from superfused slices preloaded with 3H-NE was Ca2+ dependent. Hypothalamic slices from estradiol-treated rats exposed to a single KCl pulse (S1) had modestly (20%) but significantly elevated NE release when compared to slices from ovariectomized (OVX) rats. Blockade of alpha 2-adrenoceptors by pretreatment with the imidazoline antagonists idazoxan (IDA) and RX821002 (RX) markedly facilitated NE release during S1 in hypothalamic slices from OVX rats; this facilitation was attenuated or absent in slices from estradiol-treated rats. In additional studies slices were stimulated twice, 24 min apart (S1 and S2), for 3 min with 20 mM KCl. In the absence of drug, the amount of 3H- NE released during S2 was always less than the amount released during S1 (i.e., S2:S1 approximately 0.6), regardless of whether slices were from OVX or estradiol-treated females. When 10 microM IDA was applied after S1 and 15 min prior to S2, the S2: S1 ratio increased to 1.8 +/- 0.1 in hypothalamic slices from OVX animals. In contrast, the S2:S1 ratio rose only to 1.1 +/- 0.2 in slices from estradiol-treated animals. RX applied before S2 markedly increased the S2:S1 ratio in both hypothalamic and preoptic area slices from OVX rats but failed to increase the S2:S1 ratio in slices from estradiol-treated rats. Interestingly, the modest effects of alkaloid alpha 2-antagonists such as yohimbine and rauwolscine on NE release in hypothalamic and preoptic area slices were not modified by estradiol.(ABSTRACT TRUNCATED AT 250 WORDS)
