ALCOHOL
酒精
ISSN: 0741-8329
自引率: 6.4%
发文量: 115
被引量: 2959
影响因子: 2.555
通过率: 暂无数据
出版周期: 双月刊
审稿周期: 暂无数据
审稿费用: 0
版面费用: 暂无数据
年文章数: 115
国人发稿量: 16

投稿须知/期刊简介:

Alcohol will publish original reports in English of new and systematic studies in the various fields of alcohol research. All aspects of alcohol's biological action will be covered, including anatomy, biochemistry, cell biology, physiology, pharmacology, toxicology, behavior, social anthropology, and clinical problems. Of immense value to both practitioners and basic scientists, Alcohol is the major international journal devoted solely to biomedical research on alcohol and alcoholism. Appearing nine times per year, the journal is dedicated to excellence and in-depth reporting of the burgeoning literature on alcoholism as a disease state. Topics include, but are not limited to, biomedical factors in the etiology of alcoholism; biomedical factors in the pathologic effects of uncontrolled drinking; biological and biochemical markers in the identification of alcoholism; new drugs and chemotherapeutic strategies in the treatment of uncontrolled drinking; alcohol withdrawal; and psychological and biological problems associated with fetal alcohol syndrome. Alcohol features original research articles, review articles, theoretical articles, brief communications, and rapid communications. Brief communications should describe a new method, technique, or apparatus or present the results of experiments that can be reported briefly with a minimal number of figures and tables. Rapid communications should be original and of high quality and should not exceed four printed pages in length. A limited number of pertinent literature reviews and theoretical articles, results of symposia, abstracts and/or proceedings of meetings, and more comprehensive studies may also be published as special issues of or supplements to the journal. All special issues and supplements are subject to our standard peer-review procedure and final approval by the Editors.

期刊描述简介:

Alcohol will publish original reports in English of new and systematic studies in the various fields of alcohol research. All aspects of alcohol's biological action will be covered, including anatomy, biochemistry, cell biology, physiology, pharmacology, toxicology, behavior, social anthropology, and clinical problems. Of immense value to both practitioners and basic scientists, Alcohol is the major international journal devoted solely to biomedical research on alcohol and alcoholism. Appearing nine times per year, the journal is dedicated to excellence and in-depth reporting of the burgeoning literature on alcoholism as a disease state. Topics include, but are not limited to, biomedical factors in the etiology of alcoholism; biomedical factors in the pathologic effects of uncontrolled drinking; biological and biochemical markers in the identification of alcoholism; new drugs and chemotherapeutic strategies in the treatment of uncontrolled drinking; alcohol withdrawal; and psychological and biological problems associated with fetal alcohol syndrome. Alcohol features original research articles, review articles, theoretical articles, brief communications, and rapid communications. Brief communications should describe a new method, technique, or apparatus or present the results of experiments that can be reported briefly with a minimal number of figures and tables. Rapid communications should be original and of high quality and should not exceed four printed pages in length. A limited number of pertinent literature reviews and theoretical articles, results of symposia, abstracts and/or proceedings of meetings, and more comprehensive studies may also be published as special issues of or supplements to the journal. All special issues and supplements are subject to our standard peer-review procedure and final approval by the Editors.

最新论文
  • Time-course concentration of ethanol, acetaldehyde and acetate in rat brain dialysate following alcohol self-administration.

    The unclear mechanisms of ethanol metabolism in the brain highlight the need for a deeper understanding of its metabolic pathways. This study used in vivo microdialysis to simultaneously sample ethanol and its metabolites, acetaldehyde and acetate, in the rat striatum following self-administration of ethanol, emphasizing the natural oral exposure route. To enhance the self-administration, rats underwent two-bottle-choice and limited access training. Dialysate samples, collected every 10 minutes for 2.5 hours, were analyzed using gas chromatography with flame ionization detection (GC-FID). The measured time courses of dialysate concentrations of ethanol, acetaldehyde, and acetate provided insights into dynamics of ethanol metabolism. Notably, in a subject with low ethanol consumption (0.29 g/kg), the concentration of acetaldehyde remained below the limit of detection throughout the experiment. However, the acetate concentration was clearly increased after ethanol consumption in this subject and was comparable to that of other rats with higher ethanol consumption. Compared with focusing only on peak values in the time-courses of concentrations of ethanol and its metabolites, calculating areas under curves provided better models of the relationships between ethanol intake and individual ethanol metabolites, as indicated by the r-square values for the linear regressions. This approach of using the area under the curve accounts for both the amplitude and duration of the concentration profiles, reducing the impact of variations in individual drinking patterns. In vivo microdialysis enables concurrent sampling of brain metabolites during oral ethanol administration, contributing insights into metabolite dynamics. To our knowledge, this paper is the first to report measurement of all three analytes in the brain following self-administration of ethanol. Future studies will explore regional variations and dynamics post-ethanol dependence, further advancing our understanding of ethanol metabolism in the brain.

    被引量:- 发表:1970

  • Operant ethanol self-administration behaviors do not predict sex differences in continuous access home cage drinking.

    Understanding sex differences in disease prevalence is critical to public health, particularly in the context of alcohol use disorder (AUD). The goal of this study was to understand sex differences in ethanol drinking behavior and define the precise conditions under which sex differences emerge. Consistent with prior work, C57BL/6J females drank more than males under continuous access two-bottle choice conditions. However, using ethanol self-administration - where an operant response results in access to an ethanol sipper for a fixed time period - we found no sex differences in operant response rates or ethanol consumption (volume per body weight consumed, as well as lick behavior). This remained true across a wide range of parameters including acquisition, when the ethanol sipper access period was manipulated, and when the concentration of the ethanol available was scaled. The only sex differences observed were in total ethanol consumption, which was explained by differences in body weight between males and females, rather than by sex differences in motivation to drink. Using dimensionality reduction approaches, we found that drinking behavior in the operant context did not cluster by sex, but rather clustered by high and low drinking phenotypes. Interestingly, these high and low drinking phenotypes in the operant context showed no correlation with those same categorizations in the home cage context within the same animals. These data underscore the complexity of sex differences in ethanol consumption, highlighting the important role that drinking conditions/context plays in the expression of these differences.

    被引量:- 发表:1970

  • Impact of social vulnerability index on patients with alcohol-related liver disease.

    Alcohol related liver disease (ALD) affects diverse communities with individual and social characteristics that can impact outcomes. The social vulnerability index (SVI) assigns a score between 0 and 1, where higher scores represent an increased risk of social vulnerability. We sought to assess the impact of SVI on outcomes of patients hospitalized with ALD with access to social support services. Hospitalizations for ALD at our institution between March and August 2019 were reviewed. All patients were assigned an SVI score based on their residential census tract. Per our standard practice, patients were screened by care coordinators to identify needs for rehabilitation counseling, and care coordination after discharge. Demographics, hepatic decompensation, critical care needs, readmission, and mortality were compared. Among 73 patients admitted for alcoholic hepatitis, 32 had a low SVI and 42 had a high SVI. African American patients were more likely to have a higher SVI (35% vs 0%, p=<0.001). No significant difference in outcomes based on SVI was noted. There were 393 patients admitted for alcoholic cirrhosis including 166 with a low SVI and 227 with a high SVI. Patients that were African American (23.6% vs 5.5%, p=<0.001) or disabled (41.4% vs 29.5%, p = 0.008) had a higher SVI. No significant difference in outcomes based on SVI was noted. Most patients admitted for ALD had a high SVI; however, SVI did not impact hospitalization outcomes.

    被引量:- 发表:1970

  • A novel alcohol+nicotine co-use self-administration procedure reveals sex differences and differential alteration of mesocorticolimbic TLR- and cholinergic-related neuroimmune gene expression in rats.

    被引量:- 发表:1970

  • The effects of moderate prenatal alcohol exposure on performance in hippocampal-sensitive spatial memory and anxiety tasks by adult male and female rat offspring.

    Moderate prenatal alcohol exposure (mPAE) results in structural alterations to the hippocampus. Previous studies have reported impairments in hippocampal-sensitive tasks, but have not compared performance between male and female animals. In the present study, performance in hippocampal-sensitive spatial memory and anxiety behavior tests were compared across adult male and female saccharin (SACC) control mPAE Long-Evans rat offspring. Two tests of spatial memory were conducted that were aimed at assessing memory for recently acquired spatial information: A delayed spatial alternation task using an M-shaped maze and a delayed match-to-place task in the Morris water task. In both tasks, rats in SACC and mPAE groups showed similar learning and retention of a spatial location even after a 2-h interval between encoding and retention. A separate group of adult male and female SACC and mPAE rat offspring were tested for anxiety-like behaviors in the elevated plus-maze paradigm. In this test, both male and female mPAE rats exhibited a significantly greater amount of time and a greater number of head dips in the open arms, while locomotion and open arm entries did not differ between groups. The results suggest that mPAE produces a reduction in anxiety-like behaviors in both male and female rats in the elevated plus-maze.

    被引量:- 发表:1970

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