Substance P, opioid, and catecholamine systems in the mouse central nervous system (CNS). - Wikidata - wikimedia - TriplyDB

Substance P, opioid, and catecholamine systems in the mouse central nervous system (CNS).

Substance P, opioid, and catecholamine systems in the mouse central nervous system (CNS).

http://www.wikidata.org/entity/Q33893991

about

Effects of the NK1 antagonist, aprepitant, on response to oral and intranasal oxycodone in prescription opioid abusers.Action of tachykinins in the rat hippocampus: modulation of inhibitory synaptic transmission.AMPA receptors are modulated by tachykinins in rat cerebellum neurons.

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P2860

Substance P, opioid, and catecholamine systems in the mouse central nervous system (CNS).

http://www.wikidata.org/entity/Q33893991

description

2002 nî lūn-bûn

@nan

2002 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2002 թվականի հունվարին հրատարակված գիտական հոդված

@hy

2002年の論文

@ja

2002年論文

@yue

2002年論文

@zh-hant

2002年論文

@zh-hk

2002年論文

@zh-mo

2002年論文

@zh-tw

2002年论文

@wuu

name

Substance P, opioid, and catecholamine systems in the mouse central nervous system (CNS).

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Substance P, opioid, and catecholamine systems in the mouse central nervous system (CNS).

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type

label

Substance P, opioid, and catecholamine systems in the mouse central nervous system (CNS).

@ast

Substance P, opioid, and catecholamine systems in the mouse central nervous system (CNS).

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prefLabel

Substance P, opioid, and catecholamine systems in the mouse central nervous system (CNS).

@ast

Substance P, opioid, and catecholamine systems in the mouse central nervous system (CNS).

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P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

Substance P, opioid, and catecholamine systems in the mouse central nervous system (CNS).

@en

P2093

Hill RG

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P2860

Disruption of the dopamine beta-hydroxylase gene in mice suggests roles for norepinephrine in motor function, learning, and memory

The NK1 receptor mediates both the hyperalgesia and the resistance to morphine in mice lacking noradrenaline

Restoration of norepinephrine and reversal of phenotypes in mice lacking dopamine beta-hydroxylase

Neuropathic pain: aetiology, symptoms, mechanisms, and management.

Discovery of the antidepressant and anti-emetic efficacy of substance P receptor (NK1) antagonists.

NK1 (substance P) receptor antagonists--why are they not analgesic in humans?

Rofecoxib [Vioxx, MK-0966; 4-(4'-methylsulfonylphenyl)-3-phenyl-2-(5H)-furanone]: a potent and orally active cyclooxygenase-2 inhibitor. Pharmacological and biochemical profiles.

5-hydroxytryptamine (5-HT)1A autoreceptor adaptive changes in substance P (neurokinin 1) receptor knock-out mice mimic antidepressant-induced desensitization.

Potentiated opioid analgesia in norepinephrine transporter knock-out mice.

Effect of intrathecally administered noradrenergic antagonists on nociception in the rat.

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549-551

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scholarly article

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10.1073/PNAS.032663599

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2

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99

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2002-01-01T00:00:00Z

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11805310

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117340

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