Results 261 to 270 of about 40,021 (309)
Some of the next articles are maybe not open access.

Analgesic effects of serotonin and receptor-selective serotonin agonists in the rat spinal cord

General Pharmacology: The Vascular System, 1991
1. Serotonin (5-HT) and selective 5-HT receptor agonists were administered intrathecally (i.t.) in rats, and the antinociceptive efficacy of these agents was assessed on the tail-flick and hot plate tests. 2. The 5-HT receptor agonists examined in this study included the 5-HT1A agonist 8-hydroxy-N,N-dipropyl-2-aminotetralin (8-OH-DPAT), the 5-HT1B ...
T, Crisp   +5 more
openaire   +2 more sources

Subsensitivity of serotonin and substance P receptors involved in nociception after repeated administration of a serotonin receptor agonist

Journal of Neural Transmission, 1989
The antinociceptive effects of subcutaneous 5-methoxy-N,N-dimethyltryptamine (5-MeODMT) and 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) and the responses to intrathecal (i.th.) serotonin (5-HT) and substance P (SP) were examined in mice after repeated administration of 5-MeODMT (3 mg/kg every 30 min for 4 hours).
P K, Eide, K, Hole
openaire   +2 more sources

Serotonin 1B receptor stimulation reduces D1 receptor agonist-induced dyskinesia

NeuroReport, 2009
Dopamine replacement therapy for the treatment of Parkinson's disease leads to deleterious abnormal involuntary movements (AIMs), known as L-3,4-dihydroxyphenylalanine (L-DOPA)-induced dyskinesia, which parallels enhanced striatal dopamine D1 receptor-mediated signaling. Recent evidence suggests stimulation of striatal serotonin (5-HT) 1B receptors may
Karen L Eskow, Jaunarajs   +6 more
openaire   +2 more sources

Definition of a Pharmacophore for Partial Agonists of Serotonin 5-HT3 Receptors

Journal of Chemical Information and Computer Sciences, 1999
A definition of a partial agonists serotonin 5-HT3 pharmacophore was carried out by considering a three-dimensional model which correlates the chemical structures of series of piperazinopyrrolothienopyrazines, piperazinopyridopyrrolopyrazines, piperazinopyrroloquinolaxines, piperazinopyridopyrroloquinoxalines, aminoalkyloximinopyrroloindoles ...
Cyril Daveu   +5 more
openaire   +2 more sources

SEROTONIN 5-HT2C RECEPTOR AGONISTS: POTENTIAL FOR THE TREATMENT OF OBESITY

Molecular Interventions, 2005
Obesity continues to be a burgeoning health problem worldwide. Before their removal from the market, fenfluramine and the more active enantiomer dexfenfluramine were considered to be among the most effective of weight loss agents. Much of the weight loss produced by fenfluramine was attributed to the direct activation of serotonin 5-HT(2C) receptors in
openaire   +2 more sources

The Serotonin 5-HT4 Receptor. 1. Design of a New Class of Agonists and Receptor Map of the Agonist Recognition Site

Journal of Medicinal Chemistry, 1995
The design and synthesis of a new class of potent and selective 5-HT4 receptor agonists containing an indole nucleus linked to a carbazimidamide are presented. A conformational study of the 5-HT4 receptor agonists serotonin and zacopride led to the identification of an initial pharmacophore and to the definition of a three-dimensional map of the 5-HT4 ...
K H, Buchheit   +7 more
openaire   +2 more sources

Serotonin and Human Myoclonus

Archives of Neurology, 1994
This is a critical review of the serotonin hypothesis of myoclonus for the purpose of identifying new pharmacologic therapies. The literature on myoclonus and serotonin neuropharmacology reveals evidence for serotonergic abnormalities in some human myoclonic disorders, new serotonin receptor subtypes and data on their molecular structure and function ...
openaire   +2 more sources

Clozapine is a partial agonist at cloned, human serotonin 5-HT1A receptors

Neuropharmacology, 1996
Clozapine exhibited 10-fold higher affinity than haloperidol for human 5-HT1A receptors expressed in Chinese Hamster Ovary cells (CHO-h5-HT1A) (Kis = 160 and 1910 nM respectively). Whereas haloperidol did not alter the basal binding of [35S]GTP gama S to CHO-h5HT1A membranes, clozapine stimulated it with an EC50 of 2320 nM and an efficacy of 49 ...
A, Newman-Tancredi   +3 more
openaire   +2 more sources

The Effect of Quipazine, A Serotonin Receptor Agonist, on Serum Corticosterone Concentration in Rats

Endocrine Research Communications, 1978
Quipazine, a serotonin receptor agonist, increased serum corticosterone within 30 min after its i.p. injection (at 10 mg/kg) into rats; the effect persisted at 1 and 2 hrs, but not at 4 hrs. Elevation of serum corticosterone did not occur with a 1.25 mg/kg dose of quipazine but was dose-related over a 2.5-20 mg/kg dose range.
R W, Fuller, H D, Snoddy, J A, Clemens
openaire   +2 more sources

Headache, Raynaud’s syndrome and serotonin receptor agonists in systemic lupus erythematosus

Lupus, 2006
There are potential concerns regarding serotonin receptor agonists in SLE patients with migraine, particularly patients with concomitant Raynaud’s syndrome. We estimated the prevalence of lupusrelated headache and Raynaud’s syndrome in the Montreal General Hospital SLE clinic cohort and evaluated the relationship between these two variables in ...
S, Bernatsky   +3 more
openaire   +2 more sources

Home - About - Disclaimer - Privacy