1989
DOI: 10.1016/0306-4522(89)90106-1
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N-methyl-d-aspartate receptors in the cortex and hippocampus of baboon (Papio anubis andPapio papio)

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Cited by 25 publications
(7 citation statements)
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“…area 24). In contrast to these differences in regional patterns between New World and Old World monkeys and man, the laminar distribution of LGlutamate and NMDA receptors is identical in all primate species analysed to date, with the highest densities being found in the supragranular layers (Geddes et al 1989;Jansen et al 1989;Young et al 1990;Zilles et al 1991;present observations). Since the putative glutamatergic thalamocortical and corticocortical fibres terminate preferentially in the supragranular layers (Streit 1984;Jones 1986), a matching laminar distribution between receptors and the respective excitatory transmitter is found.…”
Section: Discussionmentioning
confidence: 67%
See 1 more Smart Citation
“…area 24). In contrast to these differences in regional patterns between New World and Old World monkeys and man, the laminar distribution of LGlutamate and NMDA receptors is identical in all primate species analysed to date, with the highest densities being found in the supragranular layers (Geddes et al 1989;Jansen et al 1989;Young et al 1990;Zilles et al 1991;present observations). Since the putative glutamatergic thalamocortical and corticocortical fibres terminate preferentially in the supragranular layers (Streit 1984;Jones 1986), a matching laminar distribution between receptors and the respective excitatory transmitter is found.…”
Section: Discussionmentioning
confidence: 67%
“…Detailed studies of its connections (Barbas and Mesulam 1981;Porrino and Goldman-Rakic 1982;Arikuni et al 1983Arikuni et al , 1988Bugbee and Goldman-Rakic 1983;Arnsten and Goldman-Rakic 1984;Goldman-Rakic and Porrino 1985;Goldman-Rakic 1987, 1991a;Huerta et al 1987;Barbas 1988;Giguere and Goldman-Rakic 1988;Selemon and Goldman-Rakic 1988) and cyto-and myeloarcbitecture (Preuss and Goldman-Rakic 1991b) have been carried out. Information on the distribution of neurotransmitters or presynaptic marker enzymes in various primate species is also available (Lehmann et al 1984;Lewis et al 1986;Berger et al 1988;Everitt et al 1988;Gaspar et al 1989;Lewis and Morrison 1989;Lewis 1991), and has been matched by data on the distribution of specific neurotransmitter receptors (Hoyer et al 1986a, b;Pazos et al 1987a, b;Mash et al, 1988;Geddes et al 1989;Janssen et al 1989;Goldman-Rakic et al 1990;Young et al 1990;Yates et al 1991;Zilles 1991).…”
Section: Introductionmentioning
confidence: 99%
“…In the absence of occipital lobe ictal or IEDs, it is unclear why the occipital CBF would be increased, but positive occipital CBF correlations with ketamine dose in the PS baboons suggest a particular susceptibility to ketamine. As NMDA-receptors are less concentrated in the visual cortices of the baboon, the CBF changes may be mitigated by neurotransmitters other than glutamate (Geddes et al, 1989; Ticku et al, 1992). If occipital GABA concentrations are decreased in the photosensitive baboon as they are in patients with juvenile myoclonic epilepsy, which is associated with a high prevalence of photosensitivity (Petroff et al, 2001), CBF increases may reflect decreased regional inhibition of a global excitatory effect of ketamine.…”
Section: Discussionmentioning
confidence: 99%
“…Radioligand binding studies have shown that NMDA receptors are distributed preferentially in the superficial layers (Monaghan and Cotman, 1985;Geddes et al, 1989), where neurons are known to send collaterals on to their neighboring cells. Thus, the function of NMDA receptors may be to subserve these polysynaptic pathways.…”
Section: Roles Of Nmda and Non-nmda Receptorsmentioning
confidence: 99%