Results 281 to 290 of about 746,801 (362)
Some of the next articles are maybe not open access.
Journal of Neurochemistry, 1981
D. Kilpatrick, R. Slepetis, N. Kirshner
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D. Kilpatrick, R. Slepetis, N. Kirshner
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Comparative behavioral and neurochemical activities of cholinergic antagonists in rats.
Journal of Pharmacology and Experimental Therapeutics, 1993The comparative behavioral and neurochemical activities of the muscarinic cholinergic antagonists scopolamine, trihexyphenidyl and pirenzepine, and the nicotinic cholinergic antagonist mecamylamine were evaluated in rats. The three muscarinic antagonists,
F. Bymaster +3 more
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Effects of nicotine on fixed-interval behavior and their modification by cholinergic antagonists.
Journal of Pharmacology and Experimental Therapeutics, 1970The effects of nicotine were studied on operant responding maintained in rats by a fixed-interval 88-second schedule of water reinforcement. Nicotine was administered immediately prior to the experimental session in doses of 0.05 to 0.4 mg/kg s.c.
M. Stitzer, J. Morrison, E. Domino
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Functional sudomotor responses to cholinergic agonists and antagonists in the mouse.
Journal of the Autonomic Nervous System, 1995J. Vilches, X. Navarro, E. Verdú
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[Effects of cholinergic antagonists in stress].
Patologicheskaia fiziologiia i eksperimental'naia terapiia, 2007Effects of methacine, hexamethonium and their combinations with neostigmine on activity of B-lymphocytes in various phases of immune response and development of stress ulcers induced in animals were studied. The drugs were found to modulate B-lymphocyte activity for 28 days and longer.
G I, Nezhinskaia +2 more
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Journal of Pharmacology and Experimental Therapeutics, 1972
Morphine-HCl (50 mg/kg s.c.) produced a fall in the rectal tenmperature of rats maintained in an ambient temperature of 20°C. The administratioin of p -chlorophenylalanine ( p -CPA, 320 mg/kg i.p.) 48 hours before the morphine injection prevented the ...
T. Oka, M. Nozaki, E. Hosoya
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Morphine-HCl (50 mg/kg s.c.) produced a fall in the rectal tenmperature of rats maintained in an ambient temperature of 20°C. The administratioin of p -chlorophenylalanine ( p -CPA, 320 mg/kg i.p.) 48 hours before the morphine injection prevented the ...
T. Oka, M. Nozaki, E. Hosoya
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Novel alkoxy-oxazolyl-tetrahydropyridine muscarinic cholinergic receptor antagonists
Psychopharmacology, 1995The purpose of the present studies was to compare a novel series of alkoxy-oxazolyl-tetrahydropyridines (A-OXTPs) as muscarinic receptor antagonists. The affinity of these compounds for muscarinic receptors was determined by inhibition of [3H]pirenzepine to M1 receptors in hippocampus, [3H]QNB to M2 receptors in brainstem, and [3H]oxotremorine-M to ...
H E, Shannon +4 more
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Aryldiazonium Salts as Antagonists at Cholinergic Muscarinic Receptors
Canadian Journal of Physiology and Pharmacology, 1974A series of aryldiazonium salts were synthesized and tested for inhibitory activity on the longitudinal muscle of the guinea pig ileum. The most potent member of the series, benzenediazonium fluoborate (BDF) (at 10−4 M with incubation for 5 min), produced a dose ratio of 600 for acetylcholine (Ach), 58 for cis-2-methyl-4-trimethylammonium methyl-1,3 ...
D H, Ross, D J, Triggle
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Journal of Pharmacology and Experimental Therapeutics, 1988
A number of cholinergic muscarinic (M) agonists and antagonists were studied for their ability to enhance tritiated acetylcholine ([3H]ACh) release from electrically field-stimulated rat hippocampal slices.
R. Pohorecki, R. Head, E. F. Domino
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A number of cholinergic muscarinic (M) agonists and antagonists were studied for their ability to enhance tritiated acetylcholine ([3H]ACh) release from electrically field-stimulated rat hippocampal slices.
R. Pohorecki, R. Head, E. F. Domino
semanticscholar +1 more source

