1989
DOI: 10.1007/bf00444705
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Comparative anxiogenic, neuroendocrine, and other physiologic effects of m-chlorophenylpiperazine given intravenously or orally to healthy volunteers

Abstract: The serotonin agonist m-chlorophenylpiperazine (m-CPP) had greater anxiogenic and other mood and cognitive effects when administered intravenously (0.1 mg/kg) rather than orally (0.5 mg/kg) to healthy subjects. Nonetheless, similar elevations in peak plasma cortisol and prolactin concentrations were obtained with the two dosage regimens, and temperature elevations were greater after oral m-CPP. Plateau phase plasma concentrations of m-CPP at the times of the maximum neuroendocrine responses to intravenous and … Show more

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Cited by 201 publications
(96 citation statements)
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“…5-HTID, 5-HTzA. 5-HTzc, and 5-HT3 but also to uz-adrenoreceptors and weakly to dopaminergic receptors (Murphy et al 1989). In addition.…”
Section: Use Of Direct Agonistsmentioning
confidence: 90%
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“…5-HTID, 5-HTzA. 5-HTzc, and 5-HT3 but also to uz-adrenoreceptors and weakly to dopaminergic receptors (Murphy et al 1989). In addition.…”
Section: Use Of Direct Agonistsmentioning
confidence: 90%
“…the development of 5-HT agonists such as m-CPP has made possible the exploration of 5-HT receptor function in humans (Mueller et al 1985;Murphy et al 1989). Studies have reported that both oral and intravenous administration of m-CPP lead to signiflcant Increases in PRL.…”
Section: Use Of Direct Agonistsmentioning
confidence: 99%
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“…These effects are probably mediated through postsynaptic 5-HT1A and 5-HT2A/5-HT2C receptors (Meltzer and Maes 1995). mCPP administration increases body temperature (Murphy et al 1989). These effects are probably mediated through 5-HT2 receptors, because stimulation of 5-HT1A receptors in man and rodents causes hypothermia (Gudelsky et al 1986;Lesch et al 1990), whereas stimulation of 5-HT2 receptors induces hyperthermic effects (Gudelsky et al 1986).…”
mentioning
confidence: 99%
“…At 13:00, an intravenous catheter was placed in an antecubital vein for repeated blood sampling. At 14:30, 2 to 4 capsules of either m-CPP (0.4 mg/kg), ipsapirone (0.3 mg/kg), or placebo were administered orally.Behavioral effects were assessed using the Acute Panic Inventory (Dillon et al 1987) and a modified version of the NIMH Self-Rating Scale (Murphy et al 1989) that comprises 24 questions and defines six subscales of behavioral change: anxiety, activation-euphoria, altered self-reality, depressive affect, dysphoria, and functional deficit. Behavioral ratings were completed at 14: 00, 14:30, 15:00, 15:30, 16:00, 16:30, 17:30, and 18:30.…”
mentioning
confidence: 99%