1998
DOI: 10.1016/s0006-8993(97)01357-7
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GABA receptor mediated suppression of defensive rage behavior elicited from the medial hypothalamus of the cat: role of the lateral hypothalamus

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Cited by 44 publications
(19 citation statements)
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“…In humans, activation of the medial hypothalamus was observed during exposure to a traumatic painful stimulus that elicited an intense emotional experience (Hsieh et al, 1996). For all these species, vocalizations are part of their defensive reaction to imminent threat (Fernandez De Molina and Hunsperger, 1962;Jürgens, 1979;Blanchard et al, 1986Blanchard et al, , 2001, and consistent with the present findings bicuculline and muscimol administered into the medial hypothalamus facilitates and suppresses defensive responding, respectively (Silveira and Graeff, 1992;Roeling et al, 1993;Silveira et al, 1995;Strzelczuk and Romaniuk, 1995;Cheu and Siegel, 1998;Zagrodzka et al, 2000). As exposure to a noxious stimulus is the prototypical imminent threat to an individual it is not surprising that noxious stimulation would engage neural circuits that govern execution of innate defensive responses.…”
Section: Discussionsupporting
confidence: 87%
See 1 more Smart Citation
“…In humans, activation of the medial hypothalamus was observed during exposure to a traumatic painful stimulus that elicited an intense emotional experience (Hsieh et al, 1996). For all these species, vocalizations are part of their defensive reaction to imminent threat (Fernandez De Molina and Hunsperger, 1962;Jürgens, 1979;Blanchard et al, 1986Blanchard et al, , 2001, and consistent with the present findings bicuculline and muscimol administered into the medial hypothalamus facilitates and suppresses defensive responding, respectively (Silveira and Graeff, 1992;Roeling et al, 1993;Silveira et al, 1995;Strzelczuk and Romaniuk, 1995;Cheu and Siegel, 1998;Zagrodzka et al, 2000). As exposure to a noxious stimulus is the prototypical imminent threat to an individual it is not surprising that noxious stimulation would engage neural circuits that govern execution of innate defensive responses.…”
Section: Discussionsupporting
confidence: 87%
“…The dmVMH along with other interconnected medial hypothalamic nuclei (dorsal premammillary nucleus and anteriomedial hypothalamus-medial preoptic area) constitute a hypothalamic behavioral control system that governs the execution of innate defensive responses to environmental threats (Petrovich et al, 2001;Canteras, 2002). These hypothalamic nuclei exhibit c-Fos activation following exposure to either noxious or non-noxious threatening stimuli (Bullitt, 1990;Sandner, et al, 1993;Canteras et al, 1997;Liu et al, 1998;Rodella et al, 1998;Beckett et al, 1999;Dielenberg, et al, 2001;Parry et al, 2002), and inactivation or damage of these sites blocks naturally occurring defensive behaviors (Canteras et al, 1997;Cheu and Siegel, 1998;Markham et al, 2004). Stimulation of these medial hypothalamic nuclei elicits defensive responding in rats, cats and monkeys (Fernandez de Molina and Hunsperger, 1962;Lipp and Hunsperger, 1978;Milani and Graeff, 1987), and in humans generates reports of fear, anxiety and horror (Ervin et al, 1969;Heath, 1975;Iacono and Nashold, 1982;Tasker, 1982).…”
Section: Discussionmentioning
confidence: 99%
“…However, activation of the 5-HT 2 receptor in the midbrain PAG potentiates defensive rage behavior [56]. The interesting deduction from the aforementioned findings is the differential effects of these two serotonin subtypes upon defensive behavior, specific to the PAG or neurons in the medial hypothalamus associated with the expression of defense in rats, mice [57], cat [58] and during spontaneous defensive or attack response behavior in humans [48].…”
Section: Discussionmentioning
confidence: 95%
“…Increasing GABA activity in rats suppressed shock-induced defensive aggression (Rodgers et al 1982) and mouse-killing (Delini-Stula and Vassout 1978;Bolin et al 1982;Molina et al 1986). Similarly, in cats, the hypothalamically evoked defensive ''rage'' reaction was decreased by treatment with the GABA agonist muscimol (Cheu and Siegel 1998). The above studies on GABA all relied on pharmacological treatment.…”
Section: Discussionmentioning
confidence: 99%