نتایج جستجو برای: gaba a

تعداد نتایج: 13435664  

Journal: :research in molecular medicine 0
shokoufe nikpour moghaddam department of biochemistry, school of biology, islamic azad university of falavarjan durdi qujeq department of biochemistry and biophysics, faculty of medicine, babol university of medical sciences, babol, iran ali asghar rastegari efahani department of biophysics, school of biology, islamic azad university of falavarjan shaghayeq nikpour moghaddam department of microbiology, school of biology, islamic azad university of tonekabon

background: there are some reports in the literature showing that hypothalamus synthesizes and secretes amino acid neurotransmitters. according to several studies, elevated serum levels of gamma-amino butyric acid (gaba), a potent inhibitory neurotransmitter, have recently been implicated in the pathogenesis of neural diseases. the purpose of this research was to estimate the effects of curcumi...

Journal: :Nuclear medicine and biology 2004
Markus Mitterhauser Wolfgang Wadsak Leila Wabnegger Leonhard-Key Mien Stefan Tögel Oliver Langer Werner Sieghart Helmut Viernstein Kurt Kletter Robert Dudczak

[(11)C]Flumazenil, a highly selective benzodiazepine antagonist is the most extensively used GABA(A) ligand for PET so far. To overcome half life disadvantages of (11)C a [(18)F]-labeled flumazenil derivative, 2'-[(18)F]fluoroflumazenil (FFMZ) was developed and biologically evaluated with respect to the GABA(A) receptor. Organ with the highest uptake was the pituitary gland. Brain uptake was hi...

Journal: :Organic & biomolecular chemistry 2015
Vladimir A Maslivetc Marina Rubina Michael Rubin

A one-pot synthesis of various GABA amides has been demostrated, employing the nucleophilic addition of primary and secondary amines across the double bond of cyclopropene-3-carboxamides, followed by ring-opening of the resulting donor-acceptor cyclopropanes and subsequent in situ reduction of enamine (imine) intermediates.

Journal: :Neuropsychobiology 2005
Peter Zwanzger Cornelius Schule Daniela Eser Thomas C Baghai Frank Padberg Robin Ella Hans-Jürgen Moller Rainer Rupprecht Norbert Kathmann

BACKGROUND Saccadic eye velocity (SEV) has been shown to be a reliable neurophysiological tool for the assessment of gamma-aminobutyric acid GABA(A) receptor sensitivity. Administration of benzodiazepines targeting the GABA(A) receptor decreases SEV in healthy volunteers. Tiagabine is a new antiepileptic drug which acts via selective blockade of GABA reuptake. Therefore, we examined the effects...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2003
Jian Wang ShuHong Liu Ursula Haditsch WeiHong Tu Kimberley Cochrane Gholamreza Ahmadian Linda Tran Jadine Paw YuTian Wang Isabelle Mansuy Michael M Salter You Ming Lu

Long-term depression (LTD) is an activity-dependent weakening of synaptic efficacy at individual inhibitory synapses, a possible cellular model of learning and memory. Here, we show that the induction of LTD of inhibitory transmission recruits activated calcineurin (CaN) to dephosphorylate type-A GABA receptor (GABA(A)Rs) via the direct binding of CaN catalytic domain to the second intracellula...

Alijan Ahmadi Ahangar, Durdi Qujeq, Mohsen Hosinian,

Changes in extra and intracellular neurotransmitter amino acids concentration in the early stage of acute cerebral ischemia have been reported. In this the study, serum level of gamma aminobutyric acid (GABA) and L-Arginine in acute ischemic stroke patients was assessed. 60 patients with acute ischemic stroke and sixthy healthy volunteers as a control group were assessed. Serum GABA was measure...

Journal: :Advances in pharmacology 2015
Jane R Hanrahan Mary Chebib Graham A R Johnston

In this overview, we highlight some recent advances in the interaction of natural and synthetic flavonoids with ionotropic GABA receptors. Examples of positive, negative, and neutralizing allosteric modulators as well as allosteric agonists are given. Flavonoids appear to act via multiple binding sites on GABA receptors. Unraveling these active sites remains a major task.

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2005
Neil J Ingham David McAlpine

We investigated the role of GABAergic inhibition on the responses of inferior colliculus (IC) neurons sensitive to interaural time differences (ITDs) in anesthetized guinea pigs. Responses to static and dynamic ITDs were obtained before, during, and after recovery from ionotophoretic application of GABA, or antagonists to the GABA(A) receptor gabazine and bicuculline. For most neurons, a linear...

Journal: :international journal of molecular and cellular medicine 0
mohsen hosinian student research committee, babol university of medical sciences, babol, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی بابل (babol university of medical sciences) durdi qujeq cellular and molecular biology research center (cmbrc), health reasearch institute, babol university of medical sciences, babol, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی بابل (babol university of medical sciences) alijan ahmadi ahangar mobility impairment research center, babol university of medical sciences, babol, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی بابل (babol university of medical sciences)

changes in extra and intracellular neurotransmitter amino acids concentration in the early stage of acute cerebral ischemia have been reported. in this the study, serum level of gamma aminobutyric acid (gaba) and l-arginine in acute ischemic stroke patients was assessed. 60 patients with acute ischemic stroke and sixthy healthy volunteers as a control group were assessed. serum gaba was measure...

Journal: :Behavioral neuroscience 2008
Shirley Zhang Jacquelyn Cranney

The current study examined the effects of systemic administration of a GABA agonist [midazolam (MDZ)] and a GABA antagonist (bicuculline) on fear responding after brief CS exposure, a procedure thought to involve memory reconsolidation. Using a contextual fear-conditioning paradigm, rats were initially given two context-shock training trials, followed 24 hrs later by a 90-s context exposure (re...

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