Zobrazeno 1 - 10
of 218
pro vyhledávání: '"J. Fialip"'
Autor:
Frédéric Libert, Anne-Sophie Wattiez, Loiodice S, Christine Courteix, Alain Eschalier, A.-M. Privat, J. Fialip
Publikováno v:
British Journal of Pharmacology. 163:792-803
BACKGROUND AND PURPOSE Antidepressants are one of the recommended treatments for neuropathic pain. However, their analgesic action remains unpredictable, and there are no selection criteria for clinical use. Better knowledge of their mechanism of act
Publikováno v:
Journal of Pharmacy and Pharmacology. 53:1117-1123
A new series of N-substituted dioxo-imidazo[3,4-c]thiazoles have been prepared and evaluated for their analgesic activity. The structures of these new derivatives were confirmed by IR, 1H NMR and 13C NMR spectra, and by elemental analysis. When admin
Publikováno v:
Brain Research. 887:239-249
This work describes a new animal model of neuropathic pain produced by the single intraperitoneal administration of Taxol (32 mg/kg) to male Sprague-Dawley rats. During the course of the experiment, the clinical status of the rats remained satisfacto
Publikováno v:
Pharmacy and Pharmacology Communications. 6:387-396
A new series of 4,6-diaryl pyridazin-3-ones substituted on the nitrogen atom in the 2-position have been prepared and evaluated for their analgesic activity in the phenylbenzo-quinone-induced abdominal constriction test. Most of the eighteen compound
Publikováno v:
Pharmacology Biochemistry and Behavior. 60:519-525
The aim of this study was to examine the role of dopamine neurotransmission in the effects of morphine in the learned helplessness paradigm in rats, a generally recognized model of depression. In this model, rats first exposed to inescapable shocks (
Publikováno v:
Pharmaceutical Biology. 36:280-286
Sedative activity of Juglans regia L. (Juglandaceae) chloroform extract and of one of its isolated constituents was evaluated in mice. Dry chloroform extract and juglone, orally administered at 6.5 mg/kg and 0.125 mg/kg, respectively, induced marked
Publikováno v:
Life Sciences. 59:PL133-PL139
The antinociceptive effect of racemic tetrahydropapaveroline (THP), of its two R(+)- and S(-) enantiomers, of 1-2-dehydro-THP and of 1-carboxy-THP was assessed using different pain tests in mice. None of these drugs possessed a significant activity i
Publikováno v:
General Pharmacology: The Vascular System. 27:215-219
The purposes of the present study were as follows: 1. 1. After an acute intraperitoneal (IP) administration of amitriptyline (AMI) to male Sprague-Dawley rats we found that: (i) its absorbtion rate is rapid; (ii) its elimination half-life is much sho
Publikováno v:
Psychopharmacology. 123:71-78
The aim of this study was to investigate the possible involvement of the mu-opioid system on the learned-helplessness paradigm, an experimental model of depression, in rats. In this test, rats were first exposed to inescapable foot-shocks (IS); 48 h
Publikováno v:
Fundamental & Clinical Pharmacology. 8:525-531
Kinetics of amitriptyline (AMI), its demethylated metabolites nortriptyline (NOR) and demethylnortriptyline (DM-NOR), and its hydroxylated metabolites, the E and Z isomers or 10-hydroxy-amitriptyline (E- and Z-10-OH-AMI) and of 10-hydroxynortriptylin