Behavioural brain research · 2025
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.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Salgado-Rohner Carlos José, Bendaña-Córdoba Fernando René, Hernandes Paloma Molina, Acunha Renata Moreira, Biagioni Audrey Franceschi, Medeiros Priscila, de Freitas Renato Leonardo, Coimbra Norberto Cysne
Аннотация
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.