1987
DOI: 10.1016/0014-4886(87)90282-2
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Hypnotic action of pentobarbital in mice: A possible mechanism

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Cited by 14 publications
(6 citation statements)
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“…10b). Pentobarbital induced sleep by decreasing neural excitability via direct and/or indirect activation of GABA A receptors [26]. Chlorpromazine is known to prolong pentobarbital-induced sleep time through an antagonistic action in dopaminergic, noradrenergic, and serotonin neurons [27].…”
Section: Resultsmentioning
confidence: 99%
“…10b). Pentobarbital induced sleep by decreasing neural excitability via direct and/or indirect activation of GABA A receptors [26]. Chlorpromazine is known to prolong pentobarbital-induced sleep time through an antagonistic action in dopaminergic, noradrenergic, and serotonin neurons [27].…”
Section: Resultsmentioning
confidence: 99%
“…Fatores que interfiram na velocidade de absorção podem apresentar resultados falsopositivos nessa metodologia. Ligante de sítios localizados nos receptores GABAérgicos do tipo A (Chweh, Swinyard, Wolf, 1987;Lancel, 1999), como os benzodiazepínicos, apresentam esse efeito, evidenciado principalmente pelo prolongamento da duração do sono induzido por agentes hipnóticos, o que foi bem observado nos resultados obtidos, quando o diazepam promoveu aumento do tempo de sono induzido por barbitúrico.…”
Section: Discussionunclassified
“…Several studies have implicated noradrenaline or adrenaline in the maintenance of LH pulses after ovariectomy (21)(22)(23)(24); pentobarbitone treatment, at the dose used in the present study, has been shown to decrease the turnover of noradrenaline in the medial basal hypothalamus and preoptic area of ovariectomized rats (6). Other studies have indicated that the GABAergic system may participate in pulse suppression (25)(26)(27); it is well established that barbiturates potentiate the inhibitory effects of GABA (28)(29)(30)(31)(32). Consequently, given the putative involvement of either (nor)adrenergic or GABAergic systems in LH pulse regulation, we may speculate that preventing the hypothermic response to PB reduces the capacity of this drug to inhibit (nor)adrenergic activity or to potentiate GABAergic activity; an attenuation of either of these effects might be sufficient to prevent LH pulse suppression.…”
Section: Discussionmentioning
confidence: 99%