Departments of Pharmacology of the School of Medicine of Ribeirão Preto, University of São Paulo, 14049-900 Ribeirão Preto, São Paulo, Brazil.
Department of Natural Active Principles and Toxicology, School of Pharmaceutical Sciences, UNESP - São Paulo State University, Araraquara 14800-903, Brazil.
Prog Neuropsychopharmacol Biol Psychiatry. 2019 Mar 2;90:16-27. doi: 10.1016/j.pnpbp.2018.11.001. Epub 2018 Nov 3.
We investigated the involvement of nitrergic neurotransmission within the paraventricular nucleus of the hypothalamus (PVN) in modulation of local neuronal activation, autonomic and neuroendocrine responses and behavioral consequences of acute restraint stress in rats. Bilateral microinjections of the selective neuronal nitric oxide (NO) synthase (nNOS) inhibitor N-Propyl-L-arginine (NPLA) or the NO scavenger carboxy-PTIO into the PVN reduced arterial pressure and heart rate increases, as well as the fall in cutaneous tail temperature induced by restraint stress. PVN injection of either NPLA or carboxy-PTIO also inhibited restraint-induced increases in anxiety-related behaviors in the elevated plus-maze 24 h later. Local microinjection of NPLA or carboxy-PTIO into the PVN reduced the number of c-fos-immunoreactive neurons in the dorsal parvocellular, ventromedial, medial parvocellular and lateral magnocelllular portions of the PVN in animals subjected to restraint stress. However, neither NPLA nor carboxy-PTIO into the PVN affected restraint-induced increases in plasma corticosterone concentration. The present results indicate that PVN nitrergic neurotransmission acting via nNOS activation has a facilitatory influence on autonomic responses to acute restraint and the delayed emotional consequences of restraint stress. Our results also provide evidence of a prominent role of local nitrergic neurotransmission in PVN neuronal activation during stress.
我们研究了下丘脑室旁核(PVN)内的氮能神经传递在调节急性束缚应激大鼠局部神经元激活、自主和神经内分泌反应以及行为后果中的作用。双侧微注射选择性神经元一氧化氮合酶(nNOS)抑制剂 N-丙基-L-精氨酸(NPLA)或 NO 清除剂羧基-PTIO 到 PVN 可降低动脉血压和心率的增加,以及束缚应激引起的皮肤尾温下降。24 小时后,PVN 注射 NPLA 或羧基-PTIO 也抑制了束缚应激引起的高架十字迷宫中焦虑相关行为的增加。局部微注射 NPLA 或羧基-PTIO 到 PVN 可减少束缚应激大鼠 PVN 背侧小细胞、腹内侧、中间小细胞和外侧大细胞部分的 c-fos 免疫反应神经元的数量。然而,PVN 内注射 NPLA 或羧基-PTIO 均不影响束缚应激引起的血浆皮质酮浓度升高。本研究结果表明,PVN 氮能神经传递通过 nNOS 激活对急性束缚的自主反应和束缚应激的延迟情绪后果具有促进作用。我们的结果还提供了证据,表明局部氮能神经传递在应激期间 PVN 神经元激活中起重要作用。