Yun Sujin, Wennerholm Michelle, Shelton Jonathan E, Bonaventure Pascal, Letavic Michael A, Shireman Brock T, Lovenberg Timothy W, Dugovic Christine
Department of Neuroscience, Janssen Research and Development, L.L.C.San Diego, CA, USA.
Front Behav Neurosci. 2017 May 8;11:83. doi: 10.3389/fnbeh.2017.00083. eCollection 2017.
Orexins peptides exert a prominent role in arousal-related processes including stress responding, by activating orexin-1 (OX1R) and orexin-2 (OX2R) receptors located widely throughout the brain. Stress or orexin administration stimulates hyperarousal, adrenocorticotropic hormone (ACTH) and corticosterone release, and selective OX1R blockade can attenuate several stress-induced behavioral and cardiovascular responses but not the hypothalamic-pituitary-adrenal (HPA) axis activation. As opposed to OX1R, OX2R are preferentially expressed in the paraventricular hypothalamic nucleus which is involved in the HPA axis regulation. In the present study, we investigated the effects of a psychological stress elicited by cage exchange (CE) on ACTH release in two murine models (genetic and pharmacological) of selective OX2R inhibition. CE-induced stress produced a significant increase in ACTH serum levels. Mice lacking the OX2R exhibited a blunted stress response. Stress-induced ACTH release was absent in mice pre-treated with the selective OX2R antagonist JNJ-42847922 (30 mg/kg po), whereas pre-treatment with the dual OX1/2R antagonist SB-649868 (30 mg/kg po) only partially attenuated the increase of ACTH. To assess whether the intrinsic and distinct sleep-promoting properties of each antagonist could account for the differential stress response, a separate group of mice implanted with electrodes for standard sleep recording were orally dosed with JNJ-42847922 or SB-649868 during the light phase. While both compounds reduced the latency to non-rapid eye movement (NREM) sleep without affecting its duration, a prevalent REM-sleep promoting effect was observed only in mice treated with the dual OX1/2R antagonist. These data indicate that in a psychological stress model, genetic or pharmacological inhibition of OX2R markedly attenuated stress-induced ACTH secretion, as a separately mediated effect from the NREM sleep induction of OX2R antagonism.
食欲素肽通过激活广泛分布于大脑中的食欲素-1(OX1R)和食欲素-2(OX2R)受体,在包括应激反应在内的与觉醒相关的过程中发挥重要作用。应激或给予食欲素会刺激过度觉醒、促肾上腺皮质激素(ACTH)和皮质酮释放,选择性阻断OX1R可减弱几种应激诱导的行为和心血管反应,但不会减弱下丘脑-垂体-肾上腺(HPA)轴的激活。与OX1R不同,OX2R在下丘脑室旁核中优先表达,该核参与HPA轴调节。在本研究中,我们在选择性OX2R抑制的两种小鼠模型(基因模型和药理模型)中,研究了笼舍交换(CE)引发的心理应激对ACTH释放的影响。CE诱导的应激使ACTH血清水平显著升高。缺乏OX2R的小鼠应激反应减弱。用选择性OX2R拮抗剂JNJ-42847922(30mg/kg口服)预处理的小鼠中,应激诱导的ACTH释放消失,而用双OX1/2R拮抗剂SB-649868(30mg/kg口服)预处理仅部分减弱了ACTH的升高。为了评估每种拮抗剂固有的和独特的促睡眠特性是否可以解释不同的应激反应,另一组植入电极用于标准睡眠记录的小鼠在光照期口服给予JNJ-42847922或SB-649868。虽然两种化合物都缩短了非快速眼动(NREM)睡眠的潜伏期且不影响其持续时间,但仅在用双OXl/2R拮抗剂处理的小鼠中观察到普遍的快速眼动睡眠促进作用。这些数据表明,在心理应激模型中,OX2R的基因或药理抑制显著减弱了应激诱导的ACTH分泌,这是与OX2R拮抗作用诱导NREM睡眠的独立介导效应。