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  • Narcolepsy/*physiopathology  (2)
  • Benzodiazepines/pharmacology/*therapeutic use  (1)
  • 1
    Publication Date: 1991-05-31
    Description: Narcolepsy is a neurological disorder characterized by sleepiness and episodes of cataplexy. Cataplexy is an abrupt loss of muscle tone, most often triggered by sudden, strong emotions. A subset of cells in the medial medulla of the narcoleptic dog discharged at high rates only in cataplexy and rapid eye movement (REM) sleep. These cells were noncholinergic and were localized to ventromedial and caudal portions of the nucleus magnocellularis. The localization and discharge pattern of these cells indicate that cataplexy results from a triggering in waking of the neurons responsible for the suppression of muscle tone in REM sleep. However, most medullary cells were inactive during cataplexy but were active during REM sleep. These data demonstrate that cataplexy is a distinct behavioral state, differing from other sleep and waking states in its pattern of brainstem neuronal activity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Siegel, J M -- Nienhuis, R -- Fahringer, H M -- Paul, R -- Shiromani, P -- Dement, W C -- Mignot, E -- Chiu, C -- HL41370/HL/NHLBI NIH HHS/ -- NS14610/NS/NINDS NIH HHS/ -- NS23724/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1991 May 31;252(5010):1315-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Neurobiology Research, Veterans Affairs Medical Center, Sepulveda, CA 91343.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/1925546" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Catalepsy/pathology/*physiopathology ; Choline O-Acetyltransferase/analysis ; Dogs ; Electroencephalography ; Electromyography ; Electrophysiology ; Medulla Oblongata/*pathology/physiopathology ; Narcolepsy/*physiopathology ; Neurons/*physiology ; Sleep, REM/physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 1983-05-06
    Description: Concentrations of biogenic amine metabolites in discrete brain areas differed significantly between dogs with genetically transmitted narcolepsy and age- and breed-matched controls. Dopamine and 3,4-dihydroxyphenylacetic acid were consistently elevated in the brains of narcoleptic animals, while homovanillic acid was not. Narcoleptic animals consistently exhibited lower utilization of dopamine and higher intraneuronal degradation of dopamine but no uniform decrease in serotonin utilization. Hence neuropathology appears to be associated with genetically transmitted canine narcolepsy. The data indicate a nonglobal depression of dopamine utilization or turnover or both.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mefford, I N -- Baker, T L -- Boehme, R -- Foutz, A S -- Ciaranello, R D -- Barchas, J D -- Dement, W C -- MH 05804/MH/NIMH NIH HHS/ -- MH 23861/MH/NIMH NIH HHS/ -- NS 13211/NS/NINDS NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1983 May 6;220(4597):629-32.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6188216" target="_blank"〉PubMed〈/a〉
    Keywords: 3,4-Dihydroxyphenylacetic Acid/analysis ; Animals ; *Brain Chemistry ; *Disease Models, Animal ; Dogs ; Dopamine/analysis ; Epinephrine/analysis ; Homovanillic Acid/analysis ; Humans ; Hydroxyindoleacetic Acid/analysis ; Narcolepsy/*physiopathology ; Norepinephrine/analysis ; Serotonin/analysis ; Sleep, REM/physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 1984-06-15
    Description: Normal sleepers underwent sleep recordings and daytime tests of sleep tendency, performance, and mood while being shifted 180 degrees in their sleep-wake schedule. After two baseline 24-hour periods, subjects postponed sleep until noon. For the next three 24-hour periods, they were in bed from 1200 to 2000 and received triazolam, flurazepam, or placebo at bedtime in parallel groups. Placebo subjects showed significant sleep loss after the shift. Active medication reversed this sleep loss. Despite good sleep, flurazepam subjects appeared most impaired of the three groups on objective assessments of waking function; triazolam subjects were least impaired.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Seidel, W F -- Roth, T -- Roehrs, T -- Zorick, F -- Dement, W C -- NIMH 05804/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1984 Jun 15;224(4654):1262-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6729454" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Arousal/drug effects ; Benzodiazepines/pharmacology/*therapeutic use ; Emotions/drug effects ; Female ; Flurazepam/pharmacology/therapeutic use ; Humans ; Male ; Sleep/drug effects ; Sleep Wake Disorders/*drug therapy ; Triazolam/pharmacology/therapeutic use
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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