PMID- 18617608 OWN - NLM STAT- MEDLINE DCOM- 20090106 LR - 20211020 IS - 0013-7227 (Print) IS - 1945-7170 (Electronic) IS - 0013-7227 (Linking) VI - 149 IP - 11 DP - 2008 Nov TI - Nonclassical mechanisms of progesterone action in the brain: I. Protein kinase C activation in the hypothalamus of female rats. PG - 5509-17 LID - 10.1210/en.2008-0712 [doi] AB - The modulation of gene regulation by progesterone (P) and its classical intracellular regulation by progestin receptors in the brain, resulting in alterations in physiology and behavior has been well studied. The mechanisms mediating the short latency effects of P are less well understood. Recent studies have revealed rapid nonclassical signaling action of P involving the activation of intracellular signaling pathways. We explored the involvement of protein kinase C (PKC) in P-induced rapid signaling in the ventromedial nucleus of the hypothalamus (VMN) and preoptic area (POA) of the rat brain. Both the Ca2+-independent (basal) PKC activity representing the activation of PKC by the in vivo treatments and the Ca+2-dependent (total) PKC activity assayed in the presence of exogenous cofactors in vitro were determined. A comparison of the two activities demonstrated the strength and temporal status of PKC regulation by steroid hormones in vivo. P treatment resulted in a rapid increase in basal PKC activity in the VMN but not the POA. Estradiol benzoate priming augmented P-initiated increase in PKC basal activity in both the VMN and POA. These increases were inhibited by intracerebroventricular administration of a PKC inhibitor administered 30 min prior to P. The total PKC activity remained unchanged demonstrating maximal PKC activation within 30 min in the VMN. In contrast, P regulation in the POA significantly attenuated total PKC activity +/- estradiol benzoate priming. These rapid changes in P-initiated PKC activity were not due to changes in PKC protein levels or phosphorylation status. FAU - Balasubramanian, Bhuvana AU - Balasubramanian B AD - Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, USA. FAU - Portillo, Wendy AU - Portillo W FAU - Reyna, Andrea AU - Reyna A FAU - Chen, Jian Zhong AU - Chen JZ FAU - Moore, Anthony N AU - Moore AN FAU - Dash, Pramod K AU - Dash PK FAU - Mani, Shaila K AU - Mani SK LA - eng GR - R01 NS049160/NS/NINDS NIH HHS/United States GR - NS053588/NS/NINDS NIH HHS/United States GR - MH072933/MH/NIMH NIH HHS/United States GR - R01 NS053588/NS/NINDS NIH HHS/United States GR - MH-63954/MH/NIMH NIH HHS/United States GR - R01 MH072933/MH/NIMH NIH HHS/United States GR - NS049160/NS/NINDS NIH HHS/United States GR - R01 MH063954/MH/NIMH NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural DEP - 20080710 PL - United States TA - Endocrinology JT - Endocrinology JID - 0375040 RN - 0 (Indoles) RN - 0 (Maleimides) RN - 0 (Protein Kinase Inhibitors) RN - 4G7DS2Q64Y (Progesterone) RN - EC 2.7.11.11 (Cyclic AMP-Dependent Protein Kinases) RN - EC 2.7.11.13 (Protein Kinase C) RN - EC 2.7.11.17 (Calcium-Calmodulin-Dependent Protein Kinase Type 2) RN - L79H6N0V6C (bisindolylmaleimide I) RN - SY7Q814VUP (Calcium) SB - IM MH - Animals MH - Brain/*drug effects/physiology MH - Calcium/metabolism/pharmacology MH - Calcium-Calmodulin-Dependent Protein Kinase Type 2/metabolism MH - Cerebral Cortex/drug effects/enzymology/metabolism MH - Cyclic AMP-Dependent Protein Kinases/metabolism MH - Enzyme Activation/drug effects MH - Female MH - Hypothalamus/*drug effects/enzymology/metabolism MH - Indoles/pharmacology MH - Maleimides/pharmacology MH - Ovariectomy MH - Phosphorylation/drug effects MH - Preoptic Area/drug effects/enzymology MH - Progesterone/*pharmacology MH - Protein Kinase C/antagonists & inhibitors/*metabolism/physiology MH - Protein Kinase Inhibitors/pharmacology MH - Rats MH - Rats, Sprague-Dawley MH - Signal Transduction/drug effects PMC - PMC2584599 EDAT- 2008/07/12 09:00 MHDA- 2009/01/07 09:00 PMCR- 2009/11/01 CRDT- 2008/07/12 09:00 PHST- 2008/07/12 09:00 [pubmed] PHST- 2009/01/07 09:00 [medline] PHST- 2008/07/12 09:00 [entrez] PHST- 2009/11/01 00:00 [pmc-release] AID - en.2008-0712 [pii] AID - 4348 [pii] AID - 10.1210/en.2008-0712 [doi] PST - ppublish SO - Endocrinology. 2008 Nov;149(11):5509-17. doi: 10.1210/en.2008-0712. Epub 2008 Jul 10.