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The function of a particular neuronal population is in part determined by its neurotransmitter phenotype. We have found that a neuronal-derived septal cell line (SN56), known for its cholinergic properties, also synthesizes and releases luteinizing hormone-releasing hormone. In addition, these cells express the messenger RNAs encoding estrogen and progesterone receptors. The activation of these receptors by their respective ligands cooperatively modulates the depolarization-induced release of luteinizing hormone-releasing hormone in these cells. We have also found that a number of septal neurons in postnatal (1-week-old) mice are immunoreactive to both choline acetyltransferase and luteinizing hormone-releasing hormone. These results indicate that both neurotransmitters, acetylcholine and luteinizing hormone-releasing hormone, may co-exist in septal neurons of the CNS and that they could be modulated by gonadal hormones, and suggest that luteinizing hormone-releasing hormone could be involved in some of the actions of sex steroids on cholinergic neurotransmission.
Progesterone receptor, Cell Line, Choline O-Acetyltransferase, Gonadotropin-Releasing Hormone, Mice, Prosencephalon, Choline acetyltransferase, Estrogen receptor, Animals, Estrogen Receptor beta, RNA, Messenger, Gonadal Steroid Hormones, Neurons, Reverse Transcriptase Polymerase Chain Reaction, SN56 cells, Estrogen Receptor alpha, Septum, Immunohistochemistry, Acetylcholine, Electrophysiology, Animals, Newborn, Receptors, Estrogen, Sex steroids, Receptors, Progesterone
Progesterone receptor, Cell Line, Choline O-Acetyltransferase, Gonadotropin-Releasing Hormone, Mice, Prosencephalon, Choline acetyltransferase, Estrogen receptor, Animals, Estrogen Receptor beta, RNA, Messenger, Gonadal Steroid Hormones, Neurons, Reverse Transcriptase Polymerase Chain Reaction, SN56 cells, Estrogen Receptor alpha, Septum, Immunohistochemistry, Acetylcholine, Electrophysiology, Animals, Newborn, Receptors, Estrogen, Sex steroids, Receptors, Progesterone
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