Literature DB >> 9476961

A review of alcohol clearance in humans.

W E Lands1.   

Abstract

The level of blood or brain alcohol is considered to influence alcohol ingestion by causing subjective perceptions or neural activations that are reinforcing or rewarding. Alcohol-dependent people may try to maintain some desired tissue level, drinking to replace the millimolar levels that were cleared from the blood by metabolism. The biomedical literature describes many approaches to understanding the role of blood alcohol levels in human physiology and behavior, and this review examines some of the published results. They include the general kinetics of intake and removal of beverage alcohol as well as the characteristics of many different catalysts that can interact with alcohol. Because ingested alcohol creates blood levels that are a 1000-fold greater than those normally experienced during abstinence, ethanol may impose itself as an alternate substrate for the many oxidoreductases that act physiologically on other endogenous alcohols. Many enzymes that can act on millimolar ethanol have been isolated, and their structural genes are sequenced. Unfortunately, the genetic sequence does not indicate the physiological material upon which the translated gene product may act. In a sense, the set of enzymes with catalytic sites occupied by millimolar ethanol during alcohol drinking might constructively be regarded as "orphan gene products" whose physiological role remains to be clarified. This review is designed to indicate some of what is known, what is not known, and what needs to be known to improve the interpretations regarding adaptations to beverage alcohol and the ability of millimolar levels of alcohol to diminish dysphoria. The dysphoria may be influenced by ethanol, by ethanol metabolites, or by altered metabolism of currently unspecified endogenous substrates. A major challenge is to evaluate the multiple alternative variables within a context that stimulates curiosity and encourages quantitative tests of the relative contribution of each variable to the overall physiology of an individual.

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Year:  1998        PMID: 9476961     DOI: 10.1016/s0741-8329(97)00110-9

Source DB:  PubMed          Journal:  Alcohol        ISSN: 0741-8329            Impact factor:   2.405


  24 in total

1.  Ethanol, Zn2+ and insulin interact as progression factors to enhance DNA synthesis synergistically in the presence of Ca2+ and other cell cycle initiators in fibroblasts.

Authors:  J S Huang; Q B She; K S Crilly; Z Kiss
Journal:  Biochem J       Date:  2000-02-15       Impact factor: 3.857

2.  Rare diseases and orphan drugs.

Authors:  J K Aronson
Journal:  Br J Clin Pharmacol       Date:  2006-03       Impact factor: 4.335

Review 3.  Role of variability in explaining ethanol pharmacokinetics: research and forensic applications.

Authors:  Ake Norberg; A Wayne Jones; Robert G Hahn; Johan L Gabrielsson
Journal:  Clin Pharmacokinet       Date:  2003       Impact factor: 6.447

4.  Additive effects of mitochondrion-targeted cytochrome CYP2E1 and alcohol toxicity on cytochrome c oxidase function and stability of respirosome complexes.

Authors:  Seema Bansal; Satish Srinivasan; Sureshkumar Anandasadagopan; Anindya Roy Chowdhury; Venkatesh Selvaraj; Balaraman Kalyanaraman; Joy Joseph; Narayan G Avadhani
Journal:  J Biol Chem       Date:  2012-03-06       Impact factor: 5.157

5.  Ethanol (EtOH)-induced TGF-β1 and reactive oxygen species production are necessary for EtOH-induced alveolar macrophage dysfunction and induction of alternative activation.

Authors:  Sheena D Brown; Lou Ann S Brown
Journal:  Alcohol Clin Exp Res       Date:  2012-05-02       Impact factor: 3.455

6.  Fetal alcohol-related growth restriction from birth through young adulthood and moderating effects of maternal prepregnancy weight.

Authors:  R Colin Carter; Joseph L Jacobson; Robert J Sokol; Malcolm J Avison; Sandra W Jacobson
Journal:  Alcohol Clin Exp Res       Date:  2012-09-26       Impact factor: 3.455

7.  Contribution of NADH increases to ethanol's inhibition of retinol oxidation by human ADH isoforms.

Authors:  Jennifer R Chase; Mark G Poolman; David A Fell
Journal:  Alcohol Clin Exp Res       Date:  2009-01-16       Impact factor: 3.455

8.  Taok2 controls behavioral response to ethanol in mice.

Authors:  D Kapfhamer; S Taylor; M E Zou; J P Lim; V Kharazia; U Heberlein
Journal:  Genes Brain Behav       Date:  2012-08-31       Impact factor: 3.449

9.  A novel and an effective analytical approach for the LC-MS determination of ethyl glucuronide and ethyl sulfate in urine.

Authors:  Donata Favretto; Alessandro Nalesso; Giampietro Frison; Guido Viel; Pietro Traldi; Santo Davide Ferrara
Journal:  Int J Legal Med       Date:  2009-10-27       Impact factor: 2.686

10.  Solution characterization of the extracellular region of CD147 and its interaction with its enzyme ligand cyclophilin A.

Authors:  Jennifer Schlegel; Jasmina S Redzic; Christopher C Porter; Vyacheslav Yurchenko; Michael Bukrinsky; Wladimir Labeikovsky; Geoffrey S Armstrong; Fengli Zhang; Nancy G Isern; James DeGregori; Robert Hodges; Elan Zohar Eisenmesser
Journal:  J Mol Biol       Date:  2009-06-03       Impact factor: 5.469

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