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Hypothalamus Lateral area

Divalent mercury in rats has been reported to poorly penetrate the blood-brain barrier [23], However, there is an impairment of the blood-brain barrier within hours after mercury treatment [24, 25], By means of autoradiographic techniques, it was demonstrated [26] that after a single intravenous injection of labelled mercuric chloride, large portions of the radioactive mercury were detected in the cerebellar grey matter, area postrema, hypothalamus and areas near the lateral ventricle of mice. [Pg.192]

The result of this anatomical characteristic of endothelial cells in the CNS is an increased resistance to water-soluble and ionized drugs entering the brain, and cerebrospinal fluid (CSF), from capillary blood. However, in a few areas of the brain the barrier is absent. These areas include the lateral nuclei of the hypothalamus, the area postrema of the fourth ventricle, the pineal body, and the posterior lobe of the hypophysis. Highly lipophilic compounds can cross the barrier. Tranquilizers such as diazepam and its analogs are known to gain access rapidly to the CSF with a half-life (tm) entry time of less than 1 minute. [Pg.39]

Preoptic region and hypothalamus Lateral preoptic area Medial preoptic area Medial preoptic nucleus Magnocellular preoptic nucleus Suprachiasmatic nucleus Supraoptic nucleus Anterior hypothalamic area Lateral hypothalamic area Periventricular nucleus Paraventricular hypothalamic nucleus Arcuate nucleus Dorsal hypothalamic area Ventromedial hypothalamic nucleus Dorsomedial hypothalamic nucleus Compact part Tuber cinereum Posterior hypothalamic area Premammillary nucleus Supramammillary nucleus Medial mammillary nucleus Lateral mammillary nucleus... [Pg.208]

In the mammalian brain orexins are almost exclusively expressed in a small group of neurons located in the lateral hypothalamus (LH) andperifornical area (PEA)... [Pg.909]

Methippara, M., Alam, Md. N., Szymusiak, R McGinty, D. (2003). Preoptic area warming inhibits wake-active neurons in the perifornical lateral hypothalamus. [Pg.20]

Narcolepsy, a sleep disorder characterized by excessive daytime sleepiness and cataplexy, may be caused by the lack of hypocretin mRNA and peptides in humans (Peyron et al., 2000) or a disruption of the hypocretin receptor 2 or its ligand in dogs and mice (Lin et al., 1999 Chemelli et al., 1999). Hypocretin-containing neurons are located exclusively in the dorsomedial, lateral, and perifornical hypothalamic areas (Peyron et al., 1998). Two hypocretin sequences, Hcrt-1 (orexin-A) and Hcrt-2 (orexin-B), are generated from a single preprohypocretin (De Lecea et al., 1998 Peyron et al, 1998 Sakurai et al, 1998). Axons from these neurons are found in the hypothalamus, locus coeruleus (LC), raphe nuclei, tuberomamillary nucleus, midline thalamus, all levels of spinal cord, sympathetic and parasympathetic centers, and many other brain regions... [Pg.95]

The neural structures involved in the promotion of the waking (W) state are located in the (1) brainstem [dorsal raphe nucleus (DRN), median raphe nucleus (MRN), locus coeruleus (LC), laterodorsal and pedunculopontine tegmental nuclei (LDT/PPT), and medial-pontine reticular formation (mPRF)] (2) hypothalamus [tuberomammillary nucleus (TMN) and lateral hypothalamus (LH)[ (3) basal forebrain (BFB) (medial septal area, nucleus basalis of Meynert) and (4) midbrain ventral tegmental area (VTA) and substantia nigra pars compacta (SNc) (Pace-Schott Hobson, 2002 Jones, 2003). The following neurotransmitters function to promote W (1) acetylcholine (ACh LDT/PPT, BFB) (2) noradrenaline (NA LC) (3) serotonin (5-HT DRN, MRN) (4) histamine (HA TMN) (5) glutamate (GLU mPRF, BFB, thalamus) (6) orexin (OX LH) and (7) dopamine (DA VTA, SNc) (Zoltoski et al, 1999 Monti, 2004). [Pg.244]

Hypothalamus medial and lateral preoptic areas anterior, lateral, and posterior hypothalamic areas dorsomedial and ventromedial nuclei tuberomammillary nucleus medial and lateral preoptic areas, lateral hypothalamic area, dorsomedial nucleus, complex of mammillary bodies... [Pg.249]

Figure 10.2 The suprachiasmatic nuclei (SCN) and other possible diencephalic targets for melatonin in sleep regulation. See text for details. VLPO, ventrolateral preoptic area DMH, dorsomedial hypothalamus LHA, lateral hypothalamic area. Figure 10.2 The suprachiasmatic nuclei (SCN) and other possible diencephalic targets for melatonin in sleep regulation. See text for details. VLPO, ventrolateral preoptic area DMH, dorsomedial hypothalamus LHA, lateral hypothalamic area.
Figure 11.2 Increases in wakefulness after intracerebroventricular (ICV) or intrahypothalamic administration of ghrelin, neuropeptide Y (NPY), and orexin-A in the first hour of the light period in rats. LH, lateral hypothalamus MPA, medial preoptic area PVN, paraventricular nucleus asterisks denote significant differences from baseline. Orexin data are extracted from Vogel et at, J. Neuroscience Methods, 2002, 118 89-96. Figure 11.2 Increases in wakefulness after intracerebroventricular (ICV) or intrahypothalamic administration of ghrelin, neuropeptide Y (NPY), and orexin-A in the first hour of the light period in rats. LH, lateral hypothalamus MPA, medial preoptic area PVN, paraventricular nucleus asterisks denote significant differences from baseline. Orexin data are extracted from Vogel et at, J. Neuroscience Methods, 2002, 118 89-96.
The central adrenergic system. It is only recently that immunohistochemical methods have been developed to show that adrenaline-containing cells occur in the brain. Some of these cells are located in the lateral tegmental area, while others are found in the dorsal medulla. Axons from these cells innervate the hypothalamus, the locus coeruleus and the dorsal motor nucleus of the vagus nerve. While the precise function of adrenergic system within the brain is uncertain, it may be surmized that adrenaline could play a role in endocrine regulation and in the central control of blood pressure. There is evidence that the concentration of this amine in cerebrospinal fluid... [Pg.69]

The mRNA coding for 5-HT6 receptor has been localized in the rat brain by Northern blot, PCR, and in situ hybridization (206,207,213,214) (see also Fig. 10) and the protein by immunohistochemistry (213). The first and more detailed description on the localization of mRNA coding for 5-HT6 receptor was published by Ward and co-workers (215), reporting that the main rat brain regions where this receptor is expressed is the pyramidal layer of the olfactory tubercle, islands of Calleja, nucleus accumbens, striatum, hippocampus, and piriform cortex. At moderate levels, it is expressed in other cortical areas, the olfactory bulb, some nuclei of the hypothalamus and amygdale, the habenula, and the cerebellum. No mRNA expression is found in the raphe nucleus. These results were confirmed later (204). [Pg.345]


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Hypothalamus

Lateral area

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