Department of Physiology, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, 807-8555, Japan.
Orthopaedic Surgery, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, 807-8555, Japan.
Sci Rep. 2017 Nov 16;7(1):15728. doi: 10.1038/s41598-017-16049-2.
Various studies contributed to discover novel mechanisms of central arginine vasopressin (AVP) system responsible for the behaviour albeit endogenous vasopressin activation. We established a novel transgenic rat line which expresses both human muscarinic acetylcholine receptors (hM3Dq), of which ligand is clozapine-N-oxide (CNO), and mCherry fluorescence specifically in AVP neurons. The mCherry neurons that indicate the expression of the hM3Dq gene were observed in the suprachiasmatic (SCN), supraoptic (SON), and paraventricular nuclei (PVN). hM3Dq-mCherry fluorescence was localized mainly in the membrane of the neurons. The mCherry neurons were co-localized with AVP-like immunoreactive (LI) neurons, but not with oxytocin-LI neurons. The induction of Fos, which is the indicator for neuronal activity, was observed in approximately 90% of the AVP-LI neurons in the SON and PVN 90 min after intraperitoneal (i.p.) administration of CNO. Plasma AVP was significantly increased and food intake, water intake, and urine volume were significantly attenuated after i.p. administration of CNO. Although the detailed mechanism has unveiled, we demonstrated, for the first time, that activation of endogenous AVP neurons decreased food intake. This novel transgenic rat line may provide a revolutionary insight into the neuronal mechanism regarding central AVP system responsible for various kind of behaviours.
各种研究有助于发现中枢精氨酸加压素 (AVP) 系统的新机制,这些机制负责行为,尽管内源性加压素被激活。我们建立了一种新型的转基因大鼠品系,该品系特异性地在 AVP 神经元中表达人毒蕈碱型乙酰胆碱受体 (hM3Dq),其配体是氯氮平-N-氧化物 (CNO) 和 mCherry 荧光。指示 hM3Dq 基因表达的 mCherry 神经元可见于视交叉上核 (SCN)、视上核 (SON) 和室旁核 (PVN)。hM3Dq-mCherry 荧光主要定位于神经元的膜上。mCherry 神经元与 AVP 样免疫反应性 (LI) 神经元共定位,但与催产素-LI 神经元不共定位。Fos 的诱导,作为神经元活性的指标,在 CNO 腹腔内给药 90 分钟后,SON 和 PVN 中的大约 90%的 AVP-LI 神经元中观察到。腹腔内给予 CNO 后,血浆 AVP 显著增加,摄食量、饮水量和尿量显著减少。虽然详细的机制尚未揭示,但我们首次证明,激活内源性 AVP 神经元会减少食物摄入。这种新型的转基因大鼠品系可能为中枢 AVP 系统负责各种行为的神经元机制提供了革命性的见解。