Interaction of cholecystokinin and diazepam: effects on brain monoamines.

abstract：:We have studied the effects of neurotensin (NT) on the release of [3H]dopamine ([3H]DA) evoked by terminal depolarization with either K+, veratridine or 4-aminopyridine (4-AP). NT (1-1000 nM) induced a net potentiation (up to 170%) of the K+ (25 mM)-evoked release of [3H]DA. The capacity of NT to potentiate the effect...

journal_title：Fundamental & clinical pharmacology

authors： Boireau A,Miquet JM,Olivier V

更新日期：1993-01-01 00:00:00

abstract：:Several recent reports have described the antiarrhythmic effects of a single high oral dose of amiodarone but clinical electrophysiologic effects have not been reported. The present study was performed to assess electrophysiologic effects in 12 patients. After baseline electrophysiologic studies (EPS) patients were ad...

journal_title：Fundamental & clinical pharmacology

authors： Deharo JC,Durand A,Macaluso G,Malaterre H,Le Tallec L,Panagides D,Bory M,Djiane P

更新日期：1997-01-01 00:00:00

abstract：:A new quinoline containing selenium, 4-phenylselenyl-7-chloroquinoline (4-PSQ), was described and synthetized by our research group. Recently, we demonstrated the potential antinociceptive and anti-inflammatory of 4-PSQ. For this reason, the first objective of this study was to expand our previous findings by investig...

journal_title：Fundamental & clinical pharmacology

authors： Silva VDG,Reis AS,Pinz MP,da Fonseca CAR,Duarte LFB,Roehrs JA,Alves D,Luchese C,Wilhelm EA

更新日期：2017-10-01 00:00:00

abstract：:Viral infections remain a major cause of economic loss with an unmet need for novel therapeutic agents. Ivermectin is a putative antiviral compound; the proposed mechanism is the inhibition of nuclear translocation of viral proteins, facilitated by mammalian host importins, a necessary process for propagation of infec...

journal_title：Fundamental & clinical pharmacology

authors： Kinobe RT,Owens L

更新日期：2021-01-11 00:00:00

abstract：:The action of ouabain, a cell membrane Na+, K+-ATPase blocker, on contractions induced by manganese ions (Mn2+) in Ca2+-free, isotonic solutions with varying concentrations of K+ in the external medium were investigated in order to evaluate the underlying role of external Na+ in Mn2+-induced contractions in isolated t...

journal_title：Fundamental & clinical pharmacology

authors： Nasu T,Takahashi K

更新日期：2005-06-01 00:00:00

abstract：:Chelerythrine, a potent inhibitor of protein kinase C (PKC), was evaluated for its effect on inositol phosphate (IP) metabolism in newborn rat cardiomyocytes in culture. In a first step, we evaluated the effect of chelerythrine on IP accumulation in basal conditions. For a 10(-4) M dose, 5-phosphatase activity (which ...

journal_title：Fundamental & clinical pharmacology

authors： Le Corvoisier P,Lacotte J,Laplace M,Crozatier B

更新日期：2002-02-01 00:00:00

abstract：:Lithium causes erectile dysfunction in patients but its mechanism is yet unknown. The aim of our study was to verify the effect of acute lithium administration on the nonadrenergic noncholinergic (NANC)- and endothelium-mediated relaxation of guinea pig isolated corpus cavernosum. Although lithium (0.5, 1, and 5mm) ha...

journal_title：Fundamental & clinical pharmacology

authors： Ghasemi M,Farrokhi-Khajeh-Pasha Y,Ostovaneh MR,Dehpour AR

更新日期：2011-04-01 00:00:00

abstract：:The off-label and unlicensed use of drugs to treat children is a common practice that occurs either in hospital or in the community. This derives from the fact that research for establishing drug efficacy and safety in children has not been carried out due to ethical problems, logistical difficulties, financial and le...

journal_title：Fundamental & clinical pharmacology

authors： Cuzzolin L,Zaccaron A,Fanos V

更新日期：2003-02-01 00:00:00

abstract：:The aim of this review is to comment the results described in the literature concerning the possible pharmacodynamic mechanisms involved in the improvement of quality of life of angiotensin converting enzyme inhibitors that is just a working hypothesis. These drugs, widely used in the treatment of hypertension, preven...

journal_title：Fundamental & clinical pharmacology

authors： Govantes C,Marín J

更新日期：1996-01-01 00:00:00

abstract：:A meta-analysis was performed on the results of clinical trials of buflomedil in intermittent claudication. The analysis used results from 744 patients enrolled in ten studies, conducted at 42 centers in seven countries. All studies were randomized, double-blind, placebo-controlled trials which measured improvement in...

journal_title：Fundamental & clinical pharmacology

authors： Walker GA,Mac Hannaford JC

更新日期：1995-01-01 00:00:00

abstract：:Overdose cardiac effects of imipramine are due to fast Na channel blockade and are clinically reversed by administration of sodium lactate which induces alkalosis (about pH 7.50) and hypernatremia (about 8 mM). The mechanisms of this beneficial effect of Na lactate were explored in vitro on guinea-pig ventricular myoc...

journal_title：Fundamental & clinical pharmacology

authors： Adamantidis MM,Adnet-Bonte C,Adnet P,Durocher A,Dupuis BA

更新日期：1992-01-01 00:00:00

abstract：:Oxidized low density lipoprotein (ox-LDL) and lectin-like oxidized low density lipoprotein receptor-1 (LOX-1) have been implicated in the development of atherosclerosis. This study was designed to investigate the expression regulation of LOX-1 by ox-LDL and the potential underlying mechanisms in cultured rat vascular ...

journal_title：Fundamental & clinical pharmacology

authors： Sun Y,Chen X

更新日期：2011-10-01 00:00:00

abstract：:The aim of the present study was the investigation of pretreatment effects with clonidine (0.06 mg/kg, intraperitoneal [i.p.]), lithium (1 mEq, i.p.) or quinine (0.5 mg/kg, i.p.) on the activities of various drugs acting on noradrenergic and/or serotonergic systems in the mouse tail suspension test. Drugs used in the ...

journal_title：Fundamental & clinical pharmacology

authors： Redrobe JP,Bourin M

更新日期：1997-01-01 00:00:00

abstract：:The aim of phase I studies per se is to explore the tolerance of new compounds which have demonstrated a certain level of activity in animals at sufficiently low non-toxic doses. In most cases, these studies are conducted in 2 steps in a limited number of healthy male volunteers: a single rising dose study followed by...

journal_title：Fundamental & clinical pharmacology

authors： Thiercelin JF

更新日期：1990-01-01 00:00:00

abstract：:We determined the pharmacological and the antiemetic properties of SR 49059, a selective nonpeptide V(1a) receptor antagonist, on cisplatin-induced emesis in the piglet. Firstly, we clearly demonstrate that SR 49059 is a potent V(1a) receptor antagonist in vitro and in vivo in the piglet. In binding studies, [3H]-SR 4...

journal_title：Fundamental & clinical pharmacology

authors： Grélot L,Girod V,Dapzol J,Maffrand JP,Serradeil-Le Gal C

更新日期：2001-06-01 00:00:00

abstract：:Stepwise multiple regression analyses were applied to 44 atazanavir pharmacokinetic profiles from 44 HIV-1 infected patients concomitantly treated with raltegravir with the goal of identifying limited sampling strategies for the prediction of drug AUC(0-12) . Atazanavir trough-based equations failed to reliably predic...

journal_title：Fundamental & clinical pharmacology

authors： Cattaneo D,Ripamonti D,Baldelli S,Cozzi V,Fucile S,Clementi E

更新日期：2013-04-01 00:00:00

abstract：:Cyclo-oxygenase (COX) has been reported to play a significant role in neurodegeneration and other brain-related disorders. Recent studies have reported that COX plays a significant role in the pathophysiology of brain-related disorders and COX-2 inhibitors could be useful drug therapy in neurodegenerative disorders. T...

journal_title：Fundamental & clinical pharmacology

authors： Dhir A,Naidu PS,Kulkarni SK

更新日期：2006-06-01 00:00:00

abstract：:Clonidine (CL) and Rilmenidine (RI) are among the most frequently prescribed centrally- acting antihypertensives. Here we compared CL and RI effects on psychogenic cardiovascular reactivity to sonant, luminous, motosensory, and vibrotactile stimuli during neurogenic hypertension. The femoral artery and vein of Wistar ...

journal_title：Fundamental & clinical pharmacology

authors： Mendonça MM,Costa AN,Moraes GCA,Martins GM,Almeida AF,Rincon GCN,Siqueira JPR,Padilha DM,Moya MI,Ferreira-Neto ML,Gomes RM,Pedrino GR,Fontes MAP,Colombari E,Crestani CC,Fajemiroye JO,Xavier CH

更新日期：2021-01-19 00:00:00

abstract：:The effects of Ketotifen and disodium cromoglycate were investigated on human and rabbit platelet activation. Ketotifen inhibited dose-dependently human and rabbit platelet aggregation. The paf-acether pathway was the most markedly influenced by Ketotifen in human and rabbit platelets (IC50 = 38.8 +/- 7.7 microM and 7...

journal_title：Fundamental & clinical pharmacology

authors： Devillier P,Arnoux B,Lalau Keraly C,Landes A,Marsac J,Benveniste J

更新日期：1990-01-01 00:00:00

abstract：:Anxiety following heart failure (HF) and/or myocardial infarction (MI) can impede recovery and constitute a major risk factor for further cardiac events. The present study was aimed to evaluate anxiety following doxorubicin (DOX)-induced cardiomyopathy, a rodent model for HF, in mice. Furthermore, the study investigat...

journal_title：Fundamental & clinical pharmacology

authors： Anwar MJ,Pillai KK,Khanam R,Akhtar M,Vohora D

更新日期：2012-06-01 00:00:00

abstract：:The hypothesis of an interaction between trimetazidine and the immunosuppressive effect of cyclosporin A was investigated in two models: a) ex vivo, the lymphoproliferative response of normal human lymphocytes to phytohemagglutinin and a murine monoclonal antibody against the CD3 T-lymphocyte membrane complex; b) in v...

journal_title：Fundamental & clinical pharmacology

authors： Albengres E,Tillement JP,d'Athis P,Salducci D,Chauvet-Monges AM,Crevat A

更新日期：1996-01-01 00:00:00

abstract：:The effects of nifedipine and nicardipine, 2 dihydropyridines (DHP) used in the treatment of cardiovascular disorders, were compared in frog atrial fibers. Rapid photolysis of nifedipine with a single UV flash (1-ms duration) reversed the block, allowing comparison of effects of both drugs on the same preparation, and...

journal_title：Fundamental & clinical pharmacology

authors： Charnet P,Ouadid H,Richard S,Nargeot J

更新日期：1987-01-01 00:00:00

abstract：:Using an isolated non-working rat heart model, this study investigated the mechanisms of pharmacological pre-conditioning (PC) induced by P2Y receptor stimulation with pyridoxal-5'-phosphate (PLP). After 6-hydroxydopamine pretreatment and a 15-min stabilization period, isolated rat hearts were perfused for 25 min then...

journal_title：Fundamental & clinical pharmacology

authors： Millart H,Alouane L,Oszust F,Chevallier S,Robinet A

更新日期：2009-06-01 00:00:00

abstract：:In rat vena cava and aorta preincubated with [3H]noradrenaline the involvement of imidazoline receptors in modulation of [3H]noradrenaline release from sympathetic nerves was investigated. In the vena cava, the guanidine 1,3-di(2-tolyl)guanidine (DTG) inhibited the electrically evoked [3H]noradrenaline release; the in...

journal_title：Fundamental & clinical pharmacology

authors： Molderings GJ,Göthert M

更新日期：1998-01-01 00:00:00

abstract：:The maturation of the N-acetyltransferase-dependent AFMU production from caffeine was studied during infancy. The group of children (N = 14) consisted of 4 premature newborn infants and ten 1-19 month-old infants who received caffeine citrate solution for the treatment and prevention of apnea. Caffeine, AFMU, 1X and 9...

journal_title：Fundamental & clinical pharmacology

authors： Pons G,Rey E,Carrier O,Richard MO,Moran C,Badoual J,Olive G

更新日期：1989-01-01 00:00:00

abstract：:The pharmacokinetics of penticainide, a class Ic antiarrhythmic drug, was studied in 16 healthy adults (eight males and eight females) after a single 300-mg oral dose in fasting conditions and with a standard meal. Penticainide concentrations in plasma and urine were measured by hplc. The pharmacokinetic parameters of...

journal_title：Fundamental & clinical pharmacology

authors： Berdaï D,Demotes-Mainard F,Philip F,Vinçon G,Montels R,Necciari J,Bannwarth B

更新日期：1994-01-01 00:00:00

abstract：:HMG CoA reductase inhibitors (statins) have an established place in the treatment of coronary artery disease. However, their role in the treatment of heart failure (HF), including HF due to coronary artery disease, has been controversial since beneficial as well as possible harmful effects may occur. Several recent st...

journal_title：Fundamental & clinical pharmacology

authors： Gullestad L,Oie E,Ueland T,Yndestad A,Aukrust P

更新日期：2007-11-01 00:00:00

abstract：:Considering the diseases of the stomach and duodenum, peptic ulcer has been the one with a significant clinical impact. The pathophysiology of peptic ulcer has centred on an imbalance between aggressive and protective factors. The discovery of Helicobacter pylori as a cause of peptic ulcer has changed our approach gre...

journal_title：Fundamental & clinical pharmacology

authors： Sivri B

更新日期：2004-02-01 00:00:00

abstract：:The effects of sub-chronic cold stress on the functioning of hippocampal 5-HT1A receptors in old isolated rats and the possible protective effects of Ginkgo biloba extract (EGb 761) were investigated. Cold exposure during five days, produced a significant reduction of the inhibitory effect of 8-hydroxy-2-(di-n-propyla...

journal_title：Fundamental & clinical pharmacology

authors： Bolaños-Jiménez F,Manhães de Castro R,Sarhan H,Prudhomme N,Drieu K,Fillion G

更新日期：1995-01-01 00:00:00

abstract：:Thienopyridines have become the cornerstone of treatment for percutaneous coronary intervention although no survival benefit has ever been shown with clopidogrel despite increasing loading doses. Newly developed P2Y12 inhibitors are more potent, more predictable, and have a faster onset of action than clopidogrel, cha...

journal_title：Fundamental & clinical pharmacology

authors： Collet JP,O'Connor S

更新日期：2012-02-01 00:00:00