Seredynski Aurore L, Balthazart Jacques, Ball Gregory F, Cornil Charlotte A
Groupe Interdisciplinaire de Génoprotéomique Appliquée Neurosciences, Research Group in Behavioral Neuroendocrinology, University of Liège, 4000 Liège, Belgium, and.
Department of Psychology, University of Maryland, College Park, Maryland 20742-7201.
J Neurosci. 2015 Sep 23;35(38):13110-23. doi: 10.1523/JNEUROSCI.2056-15.2015.
In addition to the transcriptional activity of their liganded nuclear receptors, estrogens, such as estradiol (E2), modulate cell functions, and consequently physiology and behavior, within minutes through membrane-initiated events. The membrane-associated receptors (mERs) underlying the acute effects of estrogens on behavior have mostly been documented in females where active estrogens are thought to be of ovarian origin. We determined here, by acute intracerebroventricular injections of specific agonists and antagonists, the type(s) of mERs that modulate rapid effects of brain-derived estrogens on sexual motivation in male Japanese quail. Brain aromatase blockade acutely inhibited sexual motivation. Diarylpropionitrile (DPN), an estrogen receptor β (ERβ)-specific agonist, and to a lesser extent 17α-estradiol, possibly acting through ER-X, prevented this effect. In contrast, drugs targeting ERα (PPT and MPP), GPR30 (G1 and G15), and the Gq-mER (STX) did not affect sexual motivation. The mGluR1a antagonist LY367385 significantly inhibited sexual motivation but mGluR2/3 and mGluR5 antagonists were ineffective. LY367385 also blocked the behavioral restoration induced by E2 or DPN, providing functional evidence that ERβ interacts with metabotropic glutamate receptor 1a (mGluR1a) signaling to acutely regulate male sexual motivation. Together these results show that ERβ plays a key role in sexual behavior regulation and the recently uncovered cooperation between mERs and mGluRs is functional in males where it mediates the acute effects of estrogens produced centrally in response to social stimuli. The presence of an ER-mGluR interaction in birds suggests that this mechanism emerged relatively early in vertebrate history and is well conserved. Significance statement: The membrane-associated receptors underlying the acute effects of estrogens on behavior have mostly been documented in females, where active estrogens are thought to be of ovarian origin. Using acute intracerebroventricular injections of specific agonists and antagonists following blockade of brain aromatase, we show here that brain-derived estrogens acutely facilitate male sexual motivation through the activation of estrogen receptor β interacting with the metabotropic glutamate receptor 1a. This behavioral effect occurring within minutes provides a mechanistic explanation of how an estrogen receptor not intrinsically coupled to intracellular effectors can signal from the membrane to govern behavior in a very rapid fashion. It suggests that different subtypes of estrogen receptors could regulate the motivation versus performance aspects of behavior.
除了其配体结合核受体的转录活性外,雌激素(如雌二醇(E2))还能在数分钟内通过膜起始事件调节细胞功能,进而影响生理和行为。雌激素对行为产生急性影响的膜相关受体(mERs)大多在雌性动物中得到证实,其中活性雌激素被认为来源于卵巢。我们在此通过向脑室内急性注射特定的激动剂和拮抗剂,确定了调节脑源性雌激素对雄性日本鹌鹑性动机快速影响的mERs类型。脑芳香化酶阻断可急性抑制性动机。雌激素受体β(ERβ)特异性激动剂二芳基丙腈(DPN)以及在较小程度上可能通过ER-X起作用的17α-雌二醇可预防这种效应。相比之下,靶向ERα(PPT和MPP)、GPR30(G1和G15)以及Gq-mER(STX)的药物不影响性动机。代谢型谷氨酸受体1a拮抗剂LY367385显著抑制性动机,但代谢型谷氨酸受体2/3和代谢型谷氨酸受体5拮抗剂无效。LY367385还阻断了E2或DPN诱导的行为恢复,提供了功能证据,表明ERβ与代谢型谷氨酸受体1a(mGluR1a)信号相互作用以急性调节雄性性动机。这些结果共同表明,ERβ在性行为调节中起关键作用,并且最近发现的mERs和mGluRs之间的合作在雄性动物中具有功能,它介导了中枢产生的雌激素对社会刺激的急性反应。鸟类中存在ER-mGluR相互作用表明这种机制在脊椎动物进化史上出现得相对较早且保守性良好。重要性声明:雌激素对行为产生急性影响的膜相关受体大多在雌性动物中得到证实,其中活性雌激素被认为来源于卵巢。在阻断脑芳香化酶后,通过向脑室内急性注射特定的激动剂和拮抗剂,我们在此表明脑源性雌激素通过激活与代谢型谷氨酸受体1a相互作用的雌激素受体β来急性促进雄性性动机。这种在数分钟内发生的行为效应为一种并非固有地与细胞内效应器偶联的雌激素受体如何从膜发出信号以非常快速地控制行为提供了机制解释。这表明雌激素受体的不同亚型可能调节行为的动机与表现方面。