Conde Kristie, Meza Cecilia, Kelly Martin J, Sinchak Kevin, Wagner Edward J
Graduate College of Biomedical Sciences, Western University of Health Sciences, Pomona, Calif., USA.
Neuroendocrinology. 2016;103(6):787-805. doi: 10.1159/000443765. Epub 2016 Jan 16.
Estradiol rapidly regulates the activity of arcuate nucleus (ARH) proopiomelanocortin (POMC) neurons that project to the medial preoptic nucleus (MPN) to regulate lordosis. Orphanin FQ/nociceptin (OFQ/N) acts via opioid receptor-like (ORL)-1 receptors to inhibit these POMC neurons. Therefore, we tested the hypothesis that estradiol excites POMC neurons by rapidly attenuating inhibitory ORL-1 signaling in these cells. Hypothalamic slices through the ARH were prepared from ovariectomized rats injected with Fluorogold into the MPN. Electrophysiological recordings were generated in ARH neurons held at or near -60 mV, and neuronal phenotype was determined post hoc by immunohistofluorescence. OFQ/N application induced robust outward currents and hyperpolarizations via G protein-gated, inwardly rectifying K+ (GIRK) channels that were attenuated by pretreatment with either 17-β estradiol (E2) or E2 conjugated to bovine serum albumin. This was blocked by the estrogen receptor (ER) antagonist ICI 182,780 and mimicked by the Gq-coupled membrane ER (Gq-mER) ligand STX and the ERα agonist PPT. Inhibiting phosphatidylinositol-3-kinase (PI3K) blocked the estrogenic attenuation of ORL-1/GIRK currents. Antagonizing either phospholipase C (PLC), protein kinase C (PKC), protein kinase A (PKA) or neuronal nitric oxide synthase (nNOS) also abrogated E2 inhibition of ORL-1/GIRK currents, whereas activation of PKC, PKA, protein kinase B (Akt) and nNOS substrate L-arginine all attenuated the OFQ/N response. This was observed in 92 MPN-projecting, POMC-positive ARH neurons. Thus, ORL-1 receptor-mediated inhibition of POMC neurons is rapidly and negatively modulated by E2, an effect which is stereoselective and membrane initiated via Gq-mER and ERα activation that signals through PLC, PKC, PKA, PI3K and nNOS.
雌二醇可迅速调节弓状核(ARH)中阿片促黑素皮质素原(POMC)神经元的活性,这些神经元投射至内侧视前核(MPN)以调节脊柱前凸。孤啡肽/痛敏肽(OFQ/N)通过阿片样受体(ORL)-1受体发挥作用,抑制这些POMC神经元。因此,我们检验了这样一个假说:雌二醇通过迅速减弱这些细胞中抑制性ORL-1信号来兴奋POMC神经元。从向MPN注射了荧光金的去卵巢大鼠制备穿过ARH的下丘脑切片。在保持于-60 mV或接近-60 mV的ARH神经元中进行电生理记录,并且在记录后通过免疫荧光确定神经元表型。应用OFQ/N通过G蛋白门控内向整流钾离子(GIRK)通道诱导出强劲的外向电流和超极化,而用17-β雌二醇(E2)或与牛血清白蛋白偶联的E2预处理可减弱这种作用。这被雌激素受体(ER)拮抗剂ICI 182,780阻断,并被Gq偶联膜雌激素受体(Gq-mER)配体STX和ERα激动剂PPT模拟。抑制磷脂酰肌醇-3-激酶(PI3K)可阻断雌激素对ORL-1/GIRK电流的减弱作用。拮抗磷脂酶C(PLC)、蛋白激酶C(PKC)、蛋白激酶A(PKA)或神经元型一氧化氮合酶(nNOS)也可消除E2对ORL-1/GIRK电流的抑制作用,而激活PKC、PKA、蛋白激酶B(Akt)和nNOS底物L-精氨酸均可减弱OFQ/N反应。在92个投射至MPN的POMC阳性ARH神经元中观察到了这种现象。因此,ORL-1受体介导的对POMC神经元的抑制作用被E2迅速且负向调节,这一效应具有立体选择性,且是通过Gq-mER和ERα激活在细胞膜上起始的,通过PLC、PKC、PKA、PI3K和nNOS进行信号传导。