(Q44883665)

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Preferential 5-HT1A autoreceptor occupancy by pindolol is attenuated in depressed patients: effect of treatment or an endophenotype of depression?

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Europe PubMed Central

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7 December 2017

Preferential 5-HT1A autoreceptor occupancy by pindolol is attenuated in depressed patients: effect of treatment or an endophenotype of depression? (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

1 reference

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3

1 reference

Europe PubMed Central

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7 December 2017

Eugenii A. Rabiner

1

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Eugenii A Rabiner

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Europe PubMed Central

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7 December 2017

object named as

Philip J Cowen

4

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Zubin Bhagwagar

2

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7 December 2017

Paul M Grasby

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7 December 2017

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1 September 2004

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7 December 2017

Neuropsychopharmacology

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7 December 2017

29

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7 December 2017

9

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Europe PubMed Central

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7 December 2017

1688-1698

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

https://scigraph.springernature.com/pub.10.1038/sj.npp.1300472

0 references

Differential effects of clomipramine given locally or systemically on extracellular 5-hydroxytryptamine in raphe nuclei and frontal cortex. An in vivo brain microdialysis study.

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Positron emission tomographic analysis of dose-dependent NAD-299 binding to 5-hydroxytryptamine-1A receptors in the human brain

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How does pindolol improve antidepressant action?

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Acceleration of the effect of selected antidepressant drugs in major depression by 5-HT1A antagonists.

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Pindolol--the pharmacology of a partial agonist

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Electrophysiological and neurochemical evidence that pindolol has agonist properties at the 5-HT1A autoreceptor in vivo

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Antagonist properties of (-)-pindolol and WAY 100635 at somatodendritic and postsynaptic 5-HT1A receptors in the rat brain.

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PET imaging of serotonin 1A receptor binding in depression

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[3H]Alnespirone: a novel specific radioligand of 5-HT1A receptors in the rat brain

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Clinical pharmacology of the new beta-adrenergic blocking drugs. Part 6. A comparison of pindolol and propranolol in treatment of patients with angina pectoris. The role of intrinsic sympathomimetic activity

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Parametric imaging of ligand-receptor binding in PET using a simplified reference region model.

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Tracer kinetic modeling of the 5-HT1A receptor ligand [carbonyl-11C]WAY-100635 for PET.

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Regulation of 5-HT1A receptor function in brain following agonist or antidepressant administration

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Serotonin 5-HT1A autoreceptor blockade potentiates the ability of the 5-HT reuptake inhibitor citalopram to increase nerve terminal output of 5-HT in vivo: a microdialysis study.

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Is pindolol a mixed agonist-antagonist at central serotonin (5-HT) receptors?

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Mixed agonist/antagonist properties of NAN-190 at 5-HT1A receptors: behavioural and in vivo brain microdialysis studies.

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Citalopram's ability to increase the extracellular concentrations of serotonin in the dorsal raphe prevents the drug's effect in the frontal cortex.

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Administration of 8-hydroxy-2-(Di-n-propylamino)tetralin in raphe nuclei dorsalis and medianus reduces serotonin synthesis in the rat brain: differences in potency and regional sensitivity

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Differential effects of stress on presynaptic and postsynaptic 5-hydroxytryptamine-1A receptors in the rat brain: an in vitro electrophysiological study

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Differential occupancy of somatodendritic and postsynaptic 5HT(1A) receptors by pindolol: a dose-occupancy study with [11C]WAY 100635 and positron emission tomography in humans

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Effects of ipsapirone on plasma cortisol and body temperature in major depression

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Serotonin receptors in the human brain--III. Autoradiographic mapping of serotonin-1 receptors

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Pindolol augmentation of selective serotonin reuptake inhibitors: PET evidence that the dose used in clinical trials is too low.

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beta-blocker binding to human 5-HT(1A) receptors in vivo and in vitro: implications for antidepressant therapy

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A database of [(11)C]WAY-100635 binding to 5-HT(1A) receptors in normal male volunteers: normative data and relationship to methodological, demographic, physiological, and behavioral variables

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5-Hydroxytryptamine1A receptor occupancy by novel full antagonist 2-[4-[4-(7-chloro-2,3-dihydro-1,4-benzdioxyn-5-yl)-1-piperazinyl]butyl]-1,2-benzisothiazol-3-(2H)-one-1,1-dioxide: a[11C][O-methyl-3H]-N-(2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl)-N

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Effect of pindolol on the function of pre- and postsynaptic 5-HT1A receptors: in vivo microdialysis and electrophysiological studies in the rat brain.

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5-HT1 agonists reduce 5-hydroxytryptamine release in rat hippocampus in vivo as determined by brain microdialysis.

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Electrophysiological responses of serotoninergic dorsal raphe neurons to 5-HT1A and 5-HT1B agonists

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Responses of hippocampal pyramidal cells to putative serotonin 5-HT1A and 5-HT1B agonists: a comparative study with dorsal raphe neurons

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Cellular localization of the 5-HT1A receptor in primate brain neurons and glial cells

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Treatment of acute glomerular nephritis

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1 reference

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1 reference

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5-HT(1A) agonist potential of pindolol: electrophysiologic studies in the dorsal raphe nucleus and hippocampus

1 reference

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Quantitative autoradiography of multiple 5-HT1 receptor subtypes in the brain of control or 5,7-dihydroxytryptamine-treated rats

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7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.NPP.1300472

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

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