نتایج جستجو برای: zolpidem

تعداد نتایج: 964  

2016
Tom P Freeman Rebecca A Pope Matthew B Wall James Bisby Maartje Luijten Chandni Hindocha Will Lawn Claire Mokrysz Abigail Moss Michael A P Bloomfield Celia J A Morgan David J Nutt H Valerie Curran

Objective: Efforts to promote the cessation of harmful alcohol use are hindered by the affective and physiological components of alcohol withdrawal (AW), which can include life-threatening seizures. Although previous studies of AW and relapse have highlighted the critical importance of the N-methyl-D-aspartate receptor (NMDAR) subunit GluN2B and the detrimental role of stress, little is known a...

Journal: :Addiction 2003
G Hajak W E Müller H U Wittchen D Pittrow W Kirch

AIMS The non-benzodiazepine hypnotics zolpidem and zopiclone, which are indicated for short-term treatment of insomnia, were considered originally by physicians as almost devoid of abuse and dependence potential. Several recent publications, however, have suggested that both agents carry a significant risk of abuse. To substantiate and re-evaluate this situation, the world literature was review...

Journal: :Annales de Toxicologie Analytique 2008

2007
Sue Wilson David Nutt

insomnia has a major impact on health, performance, economic productivity and quality of life. it is important to assess patients with sleep disturbance comprehensively and distinguish insomnia from other conditions, such as excessive daytime sleepiness and parasomnias. once a diagnosis of insomnia is established, behavioural treatments should be tried initially. prescription of short-term medi...

2014
Khaldun M. Al Azzam Lee Kam Yit Bahruddin Saad Hassan Shaibah

The aim of the current study was to develop a simple, precise, and accurate capillary zone electrophoresis method for the determination of zolpidem tartrate in tablet dosage form. Separation was conducted in normal polarity mode at 25°C, 22 kV, using hydrodynamic injection for 10 s. Separation was achieved using a background electrolyte of 20 mM disodium hydrogen phosphate adjusted with phospho...

Journal: :Cerebral cortex 2008
Afia B Ali Alex M Thomson

Previous studies indicated that one class of dendrite-preferring hippocampal interneurones inhibits pyramidal cells via alpha 5 gamma-aminobutyric acid (GABA(A)) receptors whereas parvalbumin- and CCK-containing basket cells act via alpha1 and alpha2/3 GABA(A) receptors, respectively. This study asked whether there is selective insertion of different alpha subunit-containing GABA(A) receptors a...

2012
James FM Myers Lula Rosso Ben J Watson Sue J Wilson Nicola J Kalk Nicoletta Clementi David J Brooks David J Nutt Federico E Turkheimer Anne R Lingford-Hughes

This positron emission tomography (PET) study aimed to further define selectivity of [(11)C]Ro15-4513 binding to the GABARα5 relative to the GABARα1 benzodiazepine receptor subtype. The impact of zolpidem, a GABARα1-selective agonist, on [(11)C]Ro15-4513, which shows selectivity for GABARα5, and the nonselective benzodiazepine ligand [(11)C]flumazenil binding was assessed in humans. Compartment...

Journal: :Zeitschrift fur Naturforschung. C, Journal of biosciences 1997
M Alvarez de Sotomayor M D Herrera C Perez-Guerrero E Marhuenda

Zolpidem is an imidazopyridine sedative-hypnotic which interacts with central benzodiazepine-receptors. To examine its effects on uterine smooth muscle we have compared with those obtained by diltiazem, papaverine and diazepam on different experimental models. The IC50 values obtained indicate similar behaviour of zolpidem and diazepam. They showed more active against the spontaneous contractio...

Journal: :International clinical psychopharmacology 1999
C R Soldatos D G Dikeos A Whitehead

Differences in development of tolerance and occurrence of rebound insomnia have been well established between rapidly and slowly eliminated benzodiazepine hypnotics. Based on meta-analytic methodology, this study assesses whether there are such differences among the rapidly eliminated benzodiazepine and benzodiazepine-like hypnotics (brotizolam, midazolam, triazolam, zolpidem and zopiclone). Al...

Journal: :The Journal of pharmacology and experimental therapeutics 1997
D M Edgar W F Seidel K W Gee N C Lan G Field H Xia J E Hawkinson S Wieland R B Carter P L Wood

An endogenous neuroactive steroid, pregnanolone, and an orally available synthetic analog, CCD-3693, were administered to rats at the middle of their circadian activity phase (6 hr after lights off). Electroencephalogram-defined sleep-wake states, locomotor activity and body temperature were concurrently measured 30 hr before and after treatment. Identical procedures were used to test triazolam...

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