نتایج جستجو برای: ht1 receptor antagonists

تعداد نتایج: 615397  

Journal: :International Journal of Molecular Sciences 2018

The activity of dopamine (DA)-containing neurons in the ventral tegmental area (VTA) is a key mechanism in mesolimbic reward processing that has modulatory effects on different diencephalic structures like hippocampus (HIP), and receives inhibitory feedback and excitatory feed forward control. In addition, within the hippocampus, DA receptors are mostly located in the dorsal part (CA1) and dopa...

Journal: :Biological & pharmaceutical bulletin 2013
Takuji Machida Kenji Iizuka Masahiko Hirafuji

5-hydroxytryptamine (5-HT) in the bloodstream is largely contained in platelets and circulates throughout the entire vascular system. 5-HT released from activated platelets dramatically changes the function of vascular smooth muscle cells (VSMCs) and endothelial cells (ECs). In VSMCs, 5-HT induces proliferation and migration via 5-HT2A receptors. These effects are further enhanced by vasoactive...

Journal: :international journal of epidemiologic research 2015
ali momeni mitra momeni masoud amiri

background and aims: diabetic nephropathy (dn) is the most common cause of end-stage renal failure which could increase the risk of cardiovascular disease and morbidity and mortality in patients. the aim of this study was to investigate new modalities for treatment of diabetic nephropathy. methods:this study was a mini-review research to investigate drugs that are used for dn treatment. results...

Journal: :The Journal of General Physiology 1990
J Yang

Ionic currents induced by 5-hydroxytryptamine (5-HT) in cultured neuroblastoma N18 cells were studied using whole-cell voltage clamp. The response was blocked by 1-10 nM 5-HT3 receptor-specific antagonists MDL 7222 or ICS 205-930, but not by 1 microM 5-HT1/5-HT2 receptor antagonist spiperone or 5-HT2 receptor-specific antagonist ketanserin. These 5-HT3 receptors seem to be ligand-gated channels...

2015
David Horgan Helen Dimitriou

Objective: To explore psychiatrists’ opinions on the effectiveness and side-effects of current pharmacological antidepressant treatments in Australia. Method: A postal survey was sent to all consultant psychiatrists in Australia. Results: A total of 412 psychiatrists replied. The mean remission rate for depression reported by the sample was 54%. Following a partial but inadequate response to an...

1999
A. LEONARDI

Several novel N-arylpiperazine derivatives were synthesized and tested for their 1) affinity and functional activity on 5-hydroxytryptamine1A (5-HT1A) receptors in vitro; 2) activity in models predictive of antagonism at somatodendritic and postsynaptic 5-HT1A receptors; and 3) effects on the micturition reflex in anesthetized and conscious rats. These studies also included 1-(2-methoxyphenyl)-...

Journal: :Journal of neurophysiology 1999
K K Fitzgerald D H Sanes

The lateral superior olive (LSO) is a primary site of binaural convergence that responds selectively to changes in interaural level difference (ILD) by integrating ipsilateral excitatory and contralateral inhibitory inputs. The circuit matures during the first three postnatal weeks, undergoing several structural and functional changes that are influenced by afferent activity. Therefore modulati...

Journal: :British journal of pharmacology 1999
P De Vries E W Willems J P Heiligers C M Villalón P R Saxena

1. It has previously been shown that the antimigraine drug sumatriptan constricts porcine carotid arteriovenous anastomoses via 5-HT1-like receptors, identical to 5-H1B/1D receptors. The recent availability of silent antagonists selective for the 5-HT1B (SB224289) and 5-HT1D (BRL15572) receptor led us to further analyse the nature of receptors involved. 2. In pentobarbitone-anaesthetized, bilat...

Journal: :journal of the iranian chemical research 0
nader saemian radioisotope section / nuclear science research school, nuclear science and technology research institute, tehran, p.o. box: 11365-3486, iran kameh esmailli radioisotope section / nuclear science research school, nuclear science and technology research institute, tehran, p.o. box: 11365-3486, iran gholamhossein shirvani radioisotope section / nuclear science research school, nuclear science and technology research institute, tehran, p.o. box: 11365-3486, iran mohsen javaheri radioisotope section / nuclear science research school, nuclear science and technology research institute, tehran, p.o. box: 11365-3486, iran omid khalili arjomandi radioisotope section / nuclear science research school, nuclear science and technology research institute, tehran, p.o. box: 11365-3486, iran

four amidine nr2b-selective nmda receptor antagonists, n-( 2-methoxy benzyl) -3-phenyl-acrylamidine, n-[diduterio(2-methoxyphenyl) methyl]-3-phenyl-acrylamidine, n-benzyl-3-phenyl-acryl amidine and n-[diduterio(phenyl)methyl]-3-phenyl-acrylamidine, all fourlabeled with carbon-14 in the 1-position, have been synthesized as part of 5-step sequence fromba14co3.

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