Research Topics
Species | Maciej GasiorSummaryAffiliation: National Institutes of Health Country: USA Publications
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Detail Information
Publications
Neuroprotective and disease-modifying effects of the ketogenic dietMaciej Gasior
Epilepsy Research Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892 3702, USA
Behav Pharmacol 17:431-9. 2006....
Chlormethiazole potentiates the discriminative stimulus effects of methamphetamine in ratsMaciej Gasior
Epilepsy Research Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, 10 Center Drive, MSC 1408, Building 10, Room 5N250, Bethesda, MD 20892 1408, USA
Eur J Pharmacol 494:183-9. 2004..e., benzodiazepines and barbiturates), suggesting the involvement of non-GABAergic mechanisms in the effects produced by chlormethiazole...
Pharmacological modulation of GABA(B) receptors affects cocaine-induced seizures in miceMaciej Gasior
Drug Development Group, Behavioral Neuroscience Branch, National Institute on Drug Abuse, National Institutes of Health, 5500 Nathan Shock Drive, Baltimore, MD 21224, USA
Psychopharmacology (Berl) 174:211-9. 2004..Previous data have demonstrated that the convulsant effects of cocaine can be modulated by compounds that increase levels of endogenous gamma-aminobutyric acid (GABA) or that directly stimulate GABA(A) receptors...
Anticonvulsant and proconvulsant actions of 2-deoxy-D-glucoseMaciej Gasior
Epilepsy Research Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA
Epilepsia 51:1385-94. 2010..For comparison, we studied 3-methyl-glucose (3-MG), which like 2-DG accumulates in cells and reduces glucose uptake, but does not inhibit glycolysis...
Attenuation of the stimulant and convulsant effects of cocaine by 17-substituted-3-hydroxy and 3-alkoxy derivatives of dextromethorphanAgustin Zapata
Drug Development Group, National Institute on Drug Abuse Intramural Research Program, National Institutes of Health, 5500 Nathan Shock Drive, Baltimore, MD 21224, USA
Pharmacol Biochem Behav 74:313-23. 2003..These findings point to potentially novel pharmacological strategies for blocking cocaine stimulant and toxic effects...
Effects of cocaine-kindling on the expression of NMDA receptors and glutamate levels in mouse brainRafal M Kaminski
Drug Development Group, Behavioral Neuroscience Branch, National Institute on Drug Abuse, NIH, 5500 Nathan Shock Drive, Baltimore, MD 21224, USA
Neurochem Res 36:146-52. 2011..These data suggest that enhancement of depolarization stimulated glutamate release may be one of the mechanisms underlying the development of increased seizure susceptibility after cocaine kindling...
Caffeine potentiates the discriminative-stimulus effects of nicotine in ratsMaciej Gasior
National Institute on Drug Abuse, Intramural Research Program, National Institutes of Health, Baltimore, MD 21224, USA
Psychopharmacology (Berl) 162:385-95. 2002..Caffeine and nicotine are the main psychoactive ingredients of coffee and tobacco, respectively, with a high frequency of concurrent use in humans...
NAALADase (GCP II) inhibition prevents cocaine-kindled seizuresJeffrey M Witkin
Drug Development Group, Addiction Research Center, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD, USA
Neuropharmacology 43:348-56. 2002..Similarly, acutely-administered 2-PMPA did not block cocaine seizures in fully-kindled mice. NAALADase inhibition thus provides a novel means of attenuating the development of cocaine seizure kindling...
Efficacy of the ketogenic diet in the 6-Hz seizure testAdam L Hartman
Epilepsy Research Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA
Epilepsia 49:334-9. 2008....
The anticonvulsant activity of acetone, the major ketone body in the ketogenic diet, is not dependent on its metabolites acetol, 1,2-propanediol, methylglyoxal, or pyruvic acidMaciej Gasior
Epilepsy Research Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892 3702, USA
Epilepsia 48:793-800. 2007..The anticonvulsant mechanism of acetone is unknown, but it is metabolized to several bioactive substances that could play a role...
The neuropharmacology of the ketogenic dietAdam L Hartman
John M Freeman Pediatric Epilepsy Center, Johns Hopkins Hospital, Baltimore, Maryland 21287, USA
Pediatr Neurol 36:281-92. 2007....
Protective efficacy of neuroactive steroids against cocaine kindled-seizures in miceRafal M Kaminski
NIDA Addiction Research Center, 5500 Nathan Shock Drive, Baltimore, MD 21224, USA
Eur J Pharmacol 474:217-22. 2003..These findings demonstrate that some neuroactive steroids attenuate convulsant and sensitizing properties of cocaine and add to a growing literature on their potential use in the modulation of effects of drugs of abuse...
Electroencephalographic and convulsant effects of the delta opioid agonist SNC80 in rhesus monkeysIngela Danielsson
Epilepsy Research Section, National Institute of Neurological Disorders and Stroke, NIH, United States; Cyberonics, Houston, TX, USA
Pharmacol Biochem Behav 85:428-34. 2006..These results suggest that IM administration of SNC80 is less potent in producing convulsant effects than in producing other, potentially useful behavioral effects (e.g. antinociception) in rhesus monkeys...
Prolonged attenuation of amygdala-kindled seizure measures in rats by convection-enhanced delivery of the N-type calcium channel antagonists omega-conotoxin GVIA and omega-conotoxin MVIIAMaciej Gasior
Epilepsy Research Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA
J Pharmacol Exp Ther 323:458-68. 2007....
Influence of some convulsant agents on the protective activity of a novel antiepileptic drug, felbamate, against maximal electroshock in miceMariusz Swiader
Department of Pharmacology and Toxicology, Medical University, Jaczewskiego 8, PL 20-090 Lublin, Poland
Pol J Pharmacol 55:649-53. 2003..It may be concluded that GABAergic inhibition and strychnine-insensitive glycine receptor-mediated events may contribute to the anticonvulsant activity of felbamate...
Effects of cocaine under concurrent fixed ratio schedules of food and IV drug availability: a novel choice procedure in monkeysCarol A Paronis
Preclinical Pharmacology Laboratory ADARC, McLean Hospital, 115 Mill Street, Belmont, MA 02478, USA
Psychopharmacology (Berl) 163:283-91. 2002..The relative reinforcing strength of cocaine can be characterized by the distribution of operant behavior during the availability of other reinforcing stimuli...
Evaluation of the reinforcing effects of monoamine reuptake inhibitors under a concurrent schedule of food and i.v. drug delivery in rhesus monkeysMaciej Gasior
McLean Hospital, Harvard Medical School, Belmont, MA 02478, USA
Neuropsychopharmacology 30:758-64. 2005..The absence of reinforcing effects of atomoxetine support the view that, like desipramine, it has no evident abuse potential...
Variables affecting prepulse inhibition of the startle reflex and the response to antipsychotics in DBA/2NCrl miceDorothy G Flood
CNS Biology, Worldwide Discovery Research, Cephalon, Inc, 145 Brandywine Parkway, West Chester, PA 19380, USA
Psychopharmacology (Berl) 195:203-11. 2007..Thus, the DBA/2 mouse is increasingly used for testing of novel antipsychotics in PPI; however, the strain has not been fully characterized for relevant variables affecting compound testing...
The anticonvulsant activity of acetone does not depend upon its metabolitesMaciej Gasior
Epilepsia 49:936-7. 2008
Modification by dopaminergic drugs of choice behavior under concurrent schedules of intravenous saline and food delivery in monkeysMaciej Gasior
Behaviroal Pharmacology Laboratory/Alcohol and Drug Abuse Research Center, McLean Hospital, Belmont, Massachusetts 02478, USA
J Pharmacol Exp Ther 308:249-59. 2004..v. self-administration behavior engendered by priming doses of cocaine may involve actions mediated through both D1 and D2 families of dopamine receptors...
