Alpha 1- noradrenergic receptor signalling in the dorsal raphe nucleus is critical for panic -like behaviour and defensive antinociception elicited by GABAergic disinhibition in dorsomedial, lateral and dorsal premammillary hypothalamic nuclei

IF 2.3 3区 心理学 Q2 BEHAVIORAL SCIENCES
Carlos José Salgado-Rohner , Fernando René Bendaña-Córdoba , Paloma Molina Hernandes , Renata Moreira Acunha , Audrey Franceschi Biagioni , Priscila Medeiros , Renato Leonardo de Freitas , Norberto Cysne Coimbra
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引用次数: 0

Abstract

Hypothalamic nuclei are essential for the organisation of fear-induced defensive behaviours oriented to safe places, followed by unconditioned fear-induced antinociception, whereas midbrain tectum structures are associated with non-oriented escape responses. This study aimed to investigate the involvement of the noradrenergic system in both defensive behaviour and fear-induced antinociception. Wistar rats were pre-treated with microinjections of either physiological saline (0.2 µL) or the alpha1-noradrenergic selective antagonist WB4101 (5.0 µg/0.2 µL) into the dorsal raphe nucleus (DRN). After ten minutes, animals received a second microinjection of either physiological saline or bicuculline methiodide (40 ng/200 nL) into one of the following hypothalamic nuclei: dorsomedial (DMH), lateral (LH), or dorsal premammillary (PMd). Fear-induced behaviours were recorded in a circular open-field arena, and nociceptive thresholds were assessed using the tail-flick test for up to 60 min. Microinjections of WB4101 into the DRN resulted in a significant reduction in the frequency and duration of alertness, flat back approach, defensive immobility, and escape behaviours evoked by disinhibition of gamma-aminobutyric acid type A (GABAA) receptors in the hypothalamic nuclei. Furthermore, a significant reduction in defensive antinociception was observed from 0 to 30 min following the end of hypothalamically orchestrated escape behaviours. These findings suggest that alpha1-noradrenergic receptors in the DRN modulate both defensive behaviour and unconditioned fear-induced antinociception elicited by impaired GABAergic neurotransmission in the hypothalamus.
中隔背核α 1-去甲肾上腺素能受体信号在下丘脑核gaba能解除抑制引起的惊恐发作样防御行为和防御性抗感觉中起关键作用。
下丘脑核对于组织恐惧诱发的防御性行为至关重要,这些行为以安全的地方为导向,随后是无条件的恐惧诱发的抗感觉,而中脑顶盖结构与非定向的逃避反应有关。本研究旨在探讨去甲肾上腺素能系统在防御行为和恐惧诱导的抗感觉中的作用。将生理盐水(0.2µL)或α - 1-去甲肾上腺素能选择性拮抗剂WB4101(5.0µg/0.2µL)微注射至中缝背核(DRN),对Wistar大鼠进行预处理。10分钟后,将生理盐水或双丘碱(40ng/ 200nl)微量注射到下丘脑内侧背核(DMH)、外侧核(LH)或乳头前背核(PMd)。在一个圆形的露天场地中记录恐惧诱发的行为,并使用长达60分钟的甩尾测试评估伤害阈值。向DRN中微量注射WB4101导致下丘脑核γ -氨基丁酸a型(GABAA)受体去抑制引起的警觉性、平背接近、防御性不动和逃避行为的频率和持续时间显著减少。此外,在下丘脑精心策划的逃避行为结束后的0到30分钟内,观察到防御性抗感觉的显著减少。这些发现表明DRN中的α - 1-去甲肾上腺素能受体调节由下丘脑gaba能神经传递受损引起的防御行为和无条件恐惧诱导的抗感觉。
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来源期刊
Behavioural Brain Research
Behavioural Brain Research 医学-行为科学
CiteScore
5.60
自引率
0.00%
发文量
383
审稿时长
61 days
期刊介绍: Behavioural Brain Research is an international, interdisciplinary journal dedicated to the publication of articles in the field of behavioural neuroscience, broadly defined. Contributions from the entire range of disciplines that comprise the neurosciences, behavioural sciences or cognitive sciences are appropriate, as long as the goal is to delineate the neural mechanisms underlying behaviour. Thus, studies may range from neurophysiological, neuroanatomical, neurochemical or neuropharmacological analysis of brain-behaviour relations, including the use of molecular genetic or behavioural genetic approaches, to studies that involve the use of brain imaging techniques, to neuroethological studies. Reports of original research, of major methodological advances, or of novel conceptual approaches are all encouraged. The journal will also consider critical reviews on selected topics.
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