Blockade of MK-801-Induced Heat Shock Protein 72/73 in Rat Brain by Antipsychotic and Monoaminergic Agents Targeting D2, 5-HT1A, 5-HT2A and 1-Adrenergic Receptors

Publisher： Bentham Science Publishers

E-ISSN： 1996-3181|13|1|104-111

ISSN： 1871-5273

Source： CNS & Neurological Disorders - Drug Targets (Formerly Current Drug Targets - CNS & Neurological Disorders), Vol.13, Iss.1, 2014-02, pp. : 104-111

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Limited participation of 5-HT 1A and 5-HT 2A/2C receptors in the clozapine-induced Fos-protein expression in rat forebrain regions

By Sebens J.B.   Kuipers S.D.   Koch T.   Ter Horst G.J.   Korf J.  

European Journal of Pharmacology, Vol. 408, Iss. 1, 2000-11 ,pp. : 11-17

Elsevier

Access to resources Recommend Favorite

Dual Ligands Targeting Dopamine D2 and Serotonin 5-HT1A Receptors as New Antipsychotical or Anti-Parkinsonian Agents

By  

Current Medicinal Chemistry, Vol. 21, Iss. 4, 2014-02 ,pp. : 437-457

Bentham Science Publishers

Access to resources Recommend Favorite

1 -Adrenergic and 5-HT 2 -Serotonergic Effects of Some -Alkoxy- -phenylethylamines on Isolated Rat Thoracic Aorta - pharmacological evaluation at D 1 dopamine receptors

By Torres M.A.   Rezende C.   Cassels B.K.  

General Pharmacology, Vol. 31, Iss. 1, 1998-07 ,pp. : 51-54

Elsevier

Access to resources Recommend Favorite

Alprazolam potentiates the antiaversive effect induced by the activation of 5-HT1A and 5-HT2A receptors in the rat dorsal periaqueductal gray

By Bortoli Valquíria   Nogueira Regina   Zangrossi Hélio  

Psychopharmacology, Vol. 198, Iss. 3, 2008-06 ,pp. : 341-349

Springer Publishing Company

Access to resources Recommend Favorite

Effects of Fluvoxamine and Fluoxetine on 5-HT1A and 5-HT2A Receptors in Mouse Brain

By Hirano Kazufumi   Yamada Shizuo   Kimura Ryohei  

Pharmacology Communications, Vol. 12, Iss. 4, 2002-10 ,pp. : 215-221

Taylor & Francis Ltd

Access to resources Recommend Favorite