2001
DOI: 10.1016/s0024-3205(00)01010-9
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The effect of ketamine hydrochloride anesthesia on basal and N-methyl-D,L-aspartate induced plasma prolactin secretion in the adult male rhesus monkey

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Cited by 9 publications
(23 citation statements)
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“…Our results with the anesthetics ketamine and isoflurane are very similar to those of previous studies, showing an initial rise in prolactin levels followed by a gradual decline (Reber et al 1998;Puri et al 1981;Rizvi et al 2001;Hergovich et al 2001). Prior studies suggest that isoflurane may produce a larger prolactin response than ketamine, though the data are from different species and sex.…”
Section: Anesthetic Effects On Prolactinsupporting
confidence: 88%
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“…Our results with the anesthetics ketamine and isoflurane are very similar to those of previous studies, showing an initial rise in prolactin levels followed by a gradual decline (Reber et al 1998;Puri et al 1981;Rizvi et al 2001;Hergovich et al 2001). Prior studies suggest that isoflurane may produce a larger prolactin response than ketamine, though the data are from different species and sex.…”
Section: Anesthetic Effects On Prolactinsupporting
confidence: 88%
“…Prior studies suggest that isoflurane may produce a larger prolactin response than ketamine, though the data are from different species and sex. Isoflurane in human females has shown a 9 to 12-fold increase in prolactin (Reber et al 1998;Marana et al 2003), while ketamine produced a 2-to 4-fold increase in male macaques after a single injection (Puri et al 1981;Rizvi et al 2001). A study in adult baboon females found no significant difference in PRL release between constant-rate i.v.…”
Section: Anesthetic Effects On Prolactinmentioning
confidence: 99%
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“…Os aminoácidos excitatórios como glutamato e aspartato, agindo predominantemente com receptores N-metil-D-aspartato (NMDA), estão envolvidos na regulação central da secreção de vários hormônios pituitários anteriores inclusive prolactina (PRL), considerando que a ketamina, um anestésico extensamente usado, foi indicado para antagonizar uma variedade de receptores NMDA mediados por estes aminoácidos excitatórios (RIZVI et al, 2000).…”
Section: Sistema Nervoso Central (Snc)unclassified