hdl:10101/npre.2007.1439.1
2 votes

Application of the Sensory Contact Model for Pharmacological Studies under Simulated Clinical Conditions

Natalia N. Kudryavtseva1, Damira F. Avgustinovich1, Natalia P. Bondar1, Michael V. Tenditnik1 & Irina L. Kovalenko1

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  1. Institute of Cytology and Genetics SD RAS

This manuscript is a preprint. A published version is available at:

http://www.ncbi.nlm.nih.gov/pubmed/18473754 (Peer Reviewed) Published as: "An experimental approach for the study of psychotropic drug effects under simulated clinical conditions" in Current Drug Metabolism V.9, N 4, May 2008 p. 352-36
Document Type:
Manuscript
Date:
Received 19 December 2007 07:27 UTC; Posted 19 December 2007
Subjects:
Neuroscience, Pharmacology
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Abstract:

The sensory contact model allows forming different psycho-pathological states (anxious depression, catalepsy, social withdrawal, pathological aggression, cognition disturbances, anhedonia, addictive states etc.) produced by repeated agonistic interactions in male mice and investigating the therapeutic and preventive properties of any drug as well as its efficiency under simulated clinical conditions. This approach can be useful for a better understanding of the drugs’ action in different stages of disease development in individuals. It is suggested that this behavioral approach and pharmacological designs may be applied for the screening of novel psychotropic drugs.

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This document is licensed to the public under the Creative Commons Attribution 3.0 License
How to cite this document:

Kudryavtseva, Natalia, Avgustinovich, Damira, Bondar, Natalia, Tenditnik, Michael, and Kovalenko, Irina. Application of the Sensory Contact Model for Pharmacological Studies under Simulated Clinical Conditions. Available from Nature Precedings <http://hdl.handle.net/10101/npre.2007.1439.1> (2007)

Version info:

Published version:

http://www.ncbi.nlm.nih.gov/pubmed/18473754 (Peer Reviewed) Published as: "An experimental approach for the study of psychotropic drug effects under simulated clinical conditions" in Current Drug Metabolism V.9, N 4, May 2008 p. 352-36

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