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1 ntrast to the classical role ascribed to the 5-HT1 receptors.
2 tryptamine (5-CT), a nonselective agonist of 5-HT1 receptors.
3 lay neurons to 5-carboxytryptamine (5-CT), a 5-HT1 receptor agonist that preferentially activates the
4 ylserotonin (100 microg kg-1, i.a.), and the 5-HT1 receptor agonist, 5-carboxamidotryptamine (100 mic
5 re elevated but then returned to normal by a 5-HT1 receptor agonist, sumatriptan.
6 e investigated the inhibitory effects of six 5-HT1 receptor agonists in this model: 3-(1,2,5,6-tetrah
7 ylation in response to serotonin, SSRIs, and 5-HT1 receptor agonists.
8 ced melatonin suppression was blocked by the 5-HT(1) receptor antagonist, methiothepin, but not by th
9                                              5-HT1 receptor antagonists have been discovered with goo
10 ght involve inhibition of MAP kinases, since 5-HT1 receptors can increase mitogen-activated protein (
11                       Instead, activation of 5-HT1 receptors caused a slow and remarkably prolonged i
12 gs indicate that preferential stimulation of 5-HT1 receptors, expressed on thin fiber muscle afferent
13 mobility of the extracellular surface in the 5-HT(1) receptor family and manipulate the architecture
14       We find that several serotonin type-1 (5-HT1) receptor genes are expressed in retinal ganglion
15 tter in bulbospinal descending pathways, and 5-HT(1) receptors have been shown to inhibit synaptic tr
16 emonstrate that activation of the endogenous 5-HT1 receptor is coupled to calcium signaling pathways
17  we show that agonist-mediated activation of 5-HT1 receptors leads to enhanced and ectopic axonal reg
18 c interneurons and direct inhibition via the 5-HT1 receptors on MCs.
19 stablish the existence of triptan-sensitive (5-HT1) receptors on postsynaptic central trigeminal neur
20 ells during regeneration and that inhibiting 5-HT1 receptors or components of the 5-HT pathway select
21                                 We show that 5-HT1 receptor signaling is dispensable during ON develo
22   This may largely be due to activation of a 5-HT1 receptor subtype and not to desensitization.
23 SSOFRAs with improved selectivity over other 5-HT(1) receptor subtypes.
24 s for further understanding the roles of the 5-HT1 receptor subtypes and providing new approaches for
25 brane environment these four closely related 5-HT1 receptor subtypes exhibit different G protein coup