Chemogenomics Knowledgebased Polypharmacology Analyses of Drug Abuse Related G-Protein Coupled Receptors and Their Ligands

Drug abuse (DA) and addiction is a complex illness, broadly viewed as a neurobiological impairment with genetic and environmental factors that influence its development and manifestation. Abused substances can disrupt the activity of neurons by interacting with many proteins, particularly G-protein...

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Main Authors: Xiang-Qun eXie (Author), Lirong eWang (Author), haibin eLiu (Author), Qin eOuyang (Author), Cheng eFang (Author), Weiwei eSu (Author)
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Published: Frontiers Media S.A., 2014-02-01T00:00:00Z.
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100 1 0 |a Xiang-Qun eXie  |e author 
700 1 0 |a Lirong eWang  |e author 
700 1 0 |a haibin eLiu  |e author 
700 1 0 |a haibin eLiu  |e author 
700 1 0 |a Qin eOuyang  |e author 
700 1 0 |a Qin eOuyang  |e author 
700 1 0 |a Cheng eFang  |e author 
700 1 0 |a Weiwei eSu  |e author 
245 0 0 |a Chemogenomics Knowledgebased Polypharmacology Analyses of Drug Abuse Related G-Protein Coupled Receptors and Their Ligands 
260 |b Frontiers Media S.A.,   |c 2014-02-01T00:00:00Z. 
500 |a 1663-9812 
500 |a 10.3389/fphar.2014.00003 
520 |a Drug abuse (DA) and addiction is a complex illness, broadly viewed as a neurobiological impairment with genetic and environmental factors that influence its development and manifestation. Abused substances can disrupt the activity of neurons by interacting with many proteins, particularly G-protein coupled receptors (GPCRs). A few medicines that target the central nervous system (CNS) can also modulate DA related proteins, such as GPCRs, which can act in conjunction with the controlled psychoactive substance(s) and increase side effects. To fully explore the molecular interaction networks that underlie DA and to effectively modulate the GPCRs in these networks with small molecules for DA treatment, we built a drug-abuse domain specific chemogenomics knowledgebase (DA-KB) to centralize the reported chemogenomics research information related to DA and CNS disorders in an effort to benefit researchers across a broad range of disciplines. We then focus on the analysis of GPCRs as many of them are closely related with drug abuse. Their distribution in human tissues was also analyzed for the study of side effects caused by abused drugs. We further implement our computational algorithms/tools to explore DA targets, DA mechanisms and pathways involved in polydrug addiction and to explore polypharmacological effects of the GPCR ligands. Finally, the polypharmacology effects of GPCR-targeted medicines for drug abuse treatment were investigated and such effects can be exploited for the development of drugs with polypharmacophore for drug abuse intervention. The chemogenomics database and the analysis tools will help us better understand the mechanism of drugs abuse and facilitate to design new medications for system pharmacotherapy of drug abuse. 
546 |a EN 
690 |a GPCRs 
690 |a Drug abuse 
690 |a Chemogenomics 
690 |a polypharmacology 
690 |a Polydrug addiction 
690 |a Cloud Computation 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Frontiers in Pharmacology, Vol 5 (2014) 
787 0 |n http://journal.frontiersin.org/Journal/10.3389/fphar.2014.00003/full 
787 0 |n https://doaj.org/toc/1663-9812 
856 4 1 |u https://doaj.org/article/aacd64b16bae4a88a90b5a6e74302959  |z Connect to this object online.