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Ca2+ current expression in pituitary melanotrophs of neonatal rats and its regulation by D2 dopamine receptors.
Author(s) -
Gomora J C,
Avila G,
Cota G
Publication year - 1996
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.1996.sp021344
Subject(s) - medicine , endocrinology , dopaminergic , dopamine , dopamine receptor d2 , sulpiride , dopamine receptor , biology , chemistry , neuroscience
1. We have examined the voltage‐dependent Ca2+ channel activity of rat melanotrophs during the early postnatal period. The cells were dissociated from pituitary intermediate lobes, kept in culture for 5‐24 h and then subjected to whole‐cell patch‐clamp experiments. 2. Like their adult counterparts, neonatal melanotrophs were able to generate Na+ currents, K+ currents and Ca2+ currents in response to membrane depolarization. Ca2+ currents were carried by both low‐ and high‐threshold Ca2+ channels. 3. High‐threshold Ca2+ current density decreased sharply between postnatal day 4 (P4) and P12. This period coincides with the onset of dopaminergic innervation within the intermediate lobe. Accordingly, the developmental decrease in Ca2+ current density was largely reversed by chronic in vivo treatment with sulpiride, a dopamine D2 receptor antagonist. 4. Prolonging the time in culture from 5 h to 8 days did not significantly alter the Ca2+ channel activity of P3 melanotrophs, whereas the high‐threshold Ca2+ current in previously innervated (P14) melanotrophs stayed small for the first 24 h and then increased 3‐fold during the subsequent 4‐5 days. This increase required RNA and protein synthesis and was prevented by adding D2 agonists to the culture medium. 5. These results provide evidence for a postnatal suppression of high‐threshold Ca2+ current expression in pituitary melanotrophs mediated by presynaptic dopamine neurons through D2 dopamine receptors.

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