Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8536844 | Pharmacology & Therapeutics | 2018 | 76 Pages |
Abstract
Patients who suffer from alcohol use disorders (AUDs) usually go through various socio-behavioral and pathophysiological changes that take place in the brain and other organs. Recently, consumption of unhealthy food and excess alcohol along with a sedentary lifestyle has become a norm in both developed and developing countries. Despite the beneficial effects of moderate alcohol consumption, chronic and/or excessive alcohol intake is reported to negatively affect the brain, liver and other organs, resulting in cell death, organ damage/failure and death. The most effective therapy for alcoholism and alcohol related comorbidities is alcohol abstinence, however, chronic alcoholic patients cannot stop drinking alcohol. Therefore, targeted therapies are urgently needed to treat such populations. Patients who suffer from alcoholism and/or alcohol abuse experience harmful effects and changes that occur in the brain and other organs. Upon stopping alcohol consumption, alcoholic patients experience acute withdrawal symptoms followed by a protracted abstinence syndrome resulting in the risk of relapse to heavy drinking. For the past few decades, several drugs have been available for the treatment of AUDs. These drugs include medications to reduce or stop severe alcohol withdrawal symptoms during alcohol detoxification as well as recovery medications to reduce alcohol craving and support abstinence. However, there is no drug that completely antagonizes the adverse effects of excessive amounts of alcohol. This review summarizes the drugs which are available and approved by the FDA and their mechanisms of action as well as the medications that are under various phases of preclinical and clinical trials. In addition, the repurposing of the FDA approved drugs, such as anticonvulsants, antipsychotics, antidepressants and other medications, to prevent alcoholism and treat AUDs and their potential target mechanisms are summarized.
Keywords
CPPPFCMORCRHCTAPCCOTRCDRBLANACCIEAWSPDEMDDTACPPARnAChRAMPAHDDBPDICVCB1intracerebroventricularNMDAN-methyl-d-aspartateVTAOXRAVPDSM-IVNTXFLX5-HT2AVGCC5-HT7CRF1ARISNRIRCTCYP3A4MSPMASQCYP2D6WGCNAFDAOCDSACTHHigh Alcohol Drinkingbasolateral amygdalaBDNFPACsAudAripiprazolechronic intermittent ethanolpost-traumatic stress disorderPTSDMajor depressive disorderAlcohol use disorderborderline personality disorderattention deficit hyperactivity disorderAddictionAlcoholAlcoholismNeurotransmittersConditioned taste aversionADHDWeighted gene co-expression network analysisconditioned place preferencePositron emission tomographyCASAHADDORDiDFood and Drug AdministrationAlcohol withdrawal syndromecytochrome P450 2D6cytochrome P450 3A4brain derived neurotrophic factorPhosphodiesteraseFluoxetineprefrontal cortexbrain circuitrypoison control centerHamilton Depression Rating Scaleobsessive compulsive drinking scaleSSRIcravingHPAventral tegmental areaNaltrexoneProgressive ratioNucleus accumbenscorticotropin releasing hormonevareniclinearginine vasopressinKORvoltage gated calcium channelPETRandomized Clinical TrialVARGABAnicotinic acetylcholine receptororexin receptorkappa opioid receptorMu opioid receptoroxytocin receptordelta opioid receptorcannabinoid receptor-1Ghrelin receptor
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Authors
Mohammed Akbar, Mark Egli, Young-Eun Cho, Byoung-Joon Song, Antonio Noronha,