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Mediodorsal nucleus

Benjamin RM, Jackson JC, Golden GT, West CH. 1982. Sources of olfactory inputs to opossum mediodorsal nucleus identified by horseradish peroxidase and autoradiographic methods. J Comp Neurol 207 358-368. [Pg.184]

Pirot S, Jay TM, Glowinski J, Thierry A-M (1994) Anatomical and electrophysiological evidence for an excitatory amino acid pathway from the thalamic mediodorsal nucleus to the prefrontal cortex in the rat. Eur J Neurosci 6 1225-1234. [Pg.40]

Anterodorsal nucleus Anteroventral nucleus Anteromedial nucleus Mediodorsal nucleus Laterodorsal nucleus Lateroposterior nucleus Ventrolateral nucleus Ventroposterolateral nucleus Ventroposteromedial nucleus Thalamic gustatory nucleus Posterior nuclear group Gelatinosus (or submedius) nucleus Centrolateral nucleus Centromedial nucleus Paracentral nucleus... [Pg.207]

Mogenson GJ, Ciriello J, Garland J, Wu M (1987) Ventral pallidum projections to mediodorsal nucleus of the thalamus an anatomical and electrophysiological investigation in the rat. Brain Res., 404, 221-230. [Pg.464]

Benjamin, R.M. and Jackson, J.C, (1974) Unit discharges in the mediodorsal nucleus of the squirrel monkey evoked by electrical stimulation of the olfactory bulb. Brain Res., 75, 181-192... [Pg.557]

Ferreira, A., Dahlof, L. G., and Hansen, S. (1987). Olfactory mechanisms in the control of maternal aggression, appetite, and fearfulness effects of lesions to olfactory receptors, mediodorsal thalamic nucleus, and insular prefrontal cortex. Behavioral Neuroscience 101, 709-717. [Pg.459]

Dopamine receptors include at least 4 subtypes which are concentrated in the striatum where D1 and D2 are evenly distributed and D3 is concentrated in the limbic portion, nucleus accumbens (Herroelen et al., 1994). D2 but not D1 receptors also occur throughout the cerebral cortex particularly temporal lobe, and D3 receptors are also present in lower densities in hippocampus and amygdala. D3 receptors are localised in several thalamic nuclei including the lateral geniculate, mediodorsal and anteroventral. [Pg.12]

Pakkenberg B. 1990. Pronounced reduction of total neuron number in mediodorsal thalamic nucleus and nucleus accumbens in schizophrenics. Arch Gen Psychiatry 47 1023-1028. [Pg.309]

Groenewegen HJ (1988) Organization of the afferent connections of the mediodorsal thalamic nucleus in the rat, related to the mediodorsal-prefrontal topography. Neuroscience 27 379-431. [Pg.96]

Melchitzky DS, Lewis DA (2001) Dopamine transporter-immunoreactive axons in the mediodorsal thalamic nucleus of the macaque monkey. Neuroscience 703 1033-1042. [Pg.101]

Fig. 3. Schematic illustration of proposed dopamine pathways in the human forebrain originating from the dorsal tier (DT) and ventral tier (VT) mesencephalic cell populations. A, anterior thalamus BF, basal forebrain BL, basolateral amygdala Ce, central amygdala DS, dorsal striatum (includes the caudate nucleus and putamen) Ec, entorhinal cortex F, frontal cortex Hipp, hippocampus MD, mediodorsal thalamus O, occipital cortex P, parietal cortex T, temporal cortex VS, ventral striatum. Fig. 3. Schematic illustration of proposed dopamine pathways in the human forebrain originating from the dorsal tier (DT) and ventral tier (VT) mesencephalic cell populations. A, anterior thalamus BF, basal forebrain BL, basolateral amygdala Ce, central amygdala DS, dorsal striatum (includes the caudate nucleus and putamen) Ec, entorhinal cortex F, frontal cortex Hipp, hippocampus MD, mediodorsal thalamus O, occipital cortex P, parietal cortex T, temporal cortex VS, ventral striatum.
Fig. 8. Anatomical organization of the dopamine D2 mRNA in the adult human brain (whole hemisphere horizontal images) at a dorsal (A) and ventral (B) level. The D2 mRNA is predominantly expressed in the striatum, mesencephalon (SN), hypothalamus. Adapted from Hurd et al. (2001). A, anterior thalamus Cb, cerebellum Cl, claustrum CN, caudate nucleus CNt, tail of caudate nucleus Cun, cuneus F, frontal lobe hipp, hippocampus hyp, hypothalaus I, insular cortex MD, mediodorsal thalamus mPFC, medial prefrontal cortex mm, medial mammillary nucleus NAc, nucleus accumbens O, occipital lobe Phg, parahippocampal gyrus Pu, putamen Pul, pulvinar SN, substantia nigra T, temporal lobe. Fig. 8. Anatomical organization of the dopamine D2 mRNA in the adult human brain (whole hemisphere horizontal images) at a dorsal (A) and ventral (B) level. The D2 mRNA is predominantly expressed in the striatum, mesencephalon (SN), hypothalamus. Adapted from Hurd et al. (2001). A, anterior thalamus Cb, cerebellum Cl, claustrum CN, caudate nucleus CNt, tail of caudate nucleus Cun, cuneus F, frontal lobe hipp, hippocampus hyp, hypothalaus I, insular cortex MD, mediodorsal thalamus mPFC, medial prefrontal cortex mm, medial mammillary nucleus NAc, nucleus accumbens O, occipital lobe Phg, parahippocampal gyrus Pu, putamen Pul, pulvinar SN, substantia nigra T, temporal lobe.
Russchen FT, Amaral DG, Price JL (1987) The afferent input to the magnocellular division of the mediodorsal thalamic nucleus in the monkey, Macaca fascicularis. J Comp Neurol 256 175-210. [Pg.569]

MCPO magnocellular preoptic nucleus 18-25, 85, 93-95 MD mediodorsal thalamic nucleus 25-27, 35, 79, 81, 103-105, 109 MDC mediodorsal thalamic nucleus, central part 29-33, 106-108 MdD medullary reticular nucleus, dorsal part 74-78, 82-83, 91-95 MDL mediodorsal thalamic nucleus, lateral part 28-34, 81, 105-110 MDM mediodorsal thalamic nucleus, medial part 28-34, 80,106-108 MDPL mediodorsal thalamic nucleus, paralaminar part 30... [Pg.494]

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