scholarly journals The link between inflammation, bugs, the intestine and the brain in alcohol dependence

2017 ◽  
Vol 7 (2) ◽  
pp. e1048-e1048 ◽  
Author(s):  
S Leclercq ◽  
P de Timary ◽  
N M Delzenne ◽  
P Stärkel
Keyword(s):  
1991 ◽  
Vol 45 (1) ◽  
pp. 27-35 ◽  
Author(s):  
Akira Kato ◽  
Motohiro Tsuji ◽  
Michihiko Nakamura ◽  
Teruo Nakajima

Author(s):  
Anna Shlіakhova ◽  
Elena Veselovska ◽  
Olga Berchenko ◽  
Anna Titkova ◽  
Elena Prikhodko

Introduction. Disturbances of the molecular nitrosergic mechanisms of brain activity regulation underlie the reduction of brain protective functions under alcohol dependence. However, development of pathogenetically substantiated approaches to the correction of nitrogen oxide (NO) imbalance in the structures of the limbico-neocortical system of the brain (LNCSB) remains insufficient. Objective. To study the effect of intranasal sodium nitroprusside (SNP) administration on anxiety, electrical activity of the LNCSB and NO content in the hippocampus, hypothalamus and septum + nucleus аccumbens of rats with alcohol dependence. Materials and methods. The studies were carried out on 50 nonlinear white adult male rats in a chronic experiment in 3 groups: intact rats; rats with alcohol dependence; rats with alcohol dependence and intranasal SNP administration. The model of alcohol dependence was created by voluntary alcohol intake at a dose of 1.25 g/kg body weight of rat for 35 days. SNP was administered intranasal at a dose of 8 μg/kg body weight of the animal. The level of anxiety was determined by means of neuroethological tests: multi-parameter comprehensive assessment of anxiety, «open field» and «tail suspension test». The electrical activity of LNCSB was registered by the stereotactic introduction of electrodes. The concentration of NO was investigated in the hippocampus, hypothalamus, septum + nucleus аccumbens Results. Intranasal administration of SNP to rats with alcohol dependence led to suppression of convulsive and paroxysmal activity, caused by alcoholization and withdrawal of alcohol, on the electroencephalogram of the structures of the LNCSB and increased the absolute power of biopotentials of the delta and theta ranges on the spectrogram of the hippocampus. Reduction of anxiety was found in rats with a high baseline level of anxiety accompanied by recovery of NO level, which was depleted by chronic alcoholization, in the hypothalamus and hippocampus. Conclusions. Intranasal administration of SNP as a NO donor causes anxiolytic effects in the state of alcohol withdrawal depending on the baseline level of anxiety: in rats with the high baseline level of anxiety – reduces this level; in rats with the low baseline level – restrains it at the level of anxiety after alcohol intake. Intranasal administration of SNP to the rats with alcohol withdrawal causes positive changes in the electroencephalogram of the LNCSB, which are manifested in suppression of convulsive and paroxysmal activity and enhancement of brain biopotentials in alpha and delta ranges on spectrogram of hippocampus with sustaining this effect for whole day. Intranasal administration of SNP is a source of short-term supply of NO to brain cells, which leads to the restoration of NO levels in the hypothalamus, hippocampus, septum and nucleus accumbens – structures that are involved in the regulation of emotional motivational behavior. Key words. limbic-neocortical system of the brain, model of alcohol dependence, anxiety, nitric oxide, sodium nitroprusside


Author(s):  
Anna Powell ◽  
Mark Tommerdahl ◽  
Yasir Abbasi ◽  
Harry Sumnall ◽  
Catharine Montgomery

2011 ◽  
Vol 16 (3) ◽  
pp. 499-509 ◽  
Author(s):  
Malik Mumtaz Taqi ◽  
Igor Bazov ◽  
Hiroyuki Watanabe ◽  
Donna Sheedy ◽  
Clive Harper ◽  
...  
Keyword(s):  

The results of studying the dynamics of clinical and psychopathological manifestations, cognitive disorders, brain electrogenesis in patients with alcohol dependence under the influence of therapy according to the treatment standards (I group) and using the drug "Cereglia" in complex correction (II group) are shown in the work. As a result of treatment revealed positive dynamics of psychopathological symptoms relief in both groups was revealed; in patients II group improving electrogenesis brain manifested a decrease of irritatie, regress polymorphic paroxysmal activity, the representation of slow-wave complexes, normalization of the ratio of alpha- and beta-rhythms, the emergence of regional differences and the reactions of absorption on the functional load clinically manifested by increase of functional activity of the brain and improving cognitive function (improving ability to work and steadfastness of focus, logic of judgments, the correctness and validity of generalizations, processes of semantic memorization, the ability to highlight the main meaning of the perceived material, the ability to analyze, understand and put into words the information received), before the performance standards, the test execution time was significantly shorter in group II patients than in group I patients (p<0.05) and was closer to the test execution time in the control group. It was found that the dynamics of cognitive functions under the influence of treatment is a marker of the degree of manifestations of encephalopathy and evaluation of the effectiveness of therapy with the use of the drug "Cereglia".


2019 ◽  
Author(s):  
Eric Brenner ◽  
Gayatri R. Tiwari ◽  
Yunlong Liu ◽  
Amy Brock ◽  
R. Dayne Mayfield

AbstractBackgroundAlcoholism remains a prevalent health concern throughout the world. Previous studies have identified transcriptomic patterns in the brain associated with alcohol dependence in both humans and animal models. But none of these studies have systematically investigated expression within the unique cell types present in the brain.ResultsWe utilized single nucleus RNA sequencing (snRNA-seq) to examine the transcriptomes of over 16,000 nuclei isolated from prefrontal cortex of alcoholic and control individuals. Each nucleus was assigned to one of seven major cell types by unsupervised clustering. Cell type enrichment patterns varied greatly among neuroinflammatory-related genes, which are known to play roles in alcohol dependence and neurodegeneration. Differential expression analysis identified cell type-specific genes with altered expression in alcoholics. The largest number of differentially expressed genes (DEGs), including both protein-coding and non-coding, were detected in astrocytes, oligodendrocytes, and microglia.ConclusionsTo our knowledge, this is the first single cell transcriptome analysis of alcohol-associated gene expression in any species, and the first such analysis in humans for any addictive substance. These findings greatly advance understanding of transcriptomic changes in the brain of alcohol-dependent individuals.


Author(s):  
Т.М. Рожнова ◽  
В.А. Спицын ◽  
С.В. Макаров ◽  
С.В. Костюк

Аддиктивные расстройства относятся к мультифакториальным заболеваниям с клинической, генетической и нейрофизиологической гетерогенностью и высокой коморбидностью с другими расстройствами психического спектра. Определяющее влияние на фенотипическую дисперсию расстройств поведения зависимого характера принадлежит генотипу. Полиморфные варианты генов нейромедиаторных систем головного мозга, кодирующих белки, участвующие в регуляции эффекторных реакций и метаболизме психоактивных веществ (ПАВ), можно рассматривать как маркёры поведенческих паттернов и индивидуальной предрасположенности к зависимому поведению. Цель исследования - анализ полиморфных вариантов генов DRD2/ANKK1 и SLC6A3 дофаминергической системы головного мозга у больных алкоголизмом. Генотипирование по TaqIA-полиморфизму в локусе ANKK1/DRD2 (rs1800497) и VNTR-полиморфизму в гене SLC6A3 (DAT1) проводили с использованием метода ПЦР. Выявлено статистически достоверное преобладание частоты аллеля ANKK1*A1 и генотипа ANKK1*A1A2 в группе мужчин с наличием аддиктивного расстройства в форме алкогольной зависимости по сравнению с фенотипически здоровыми представителями контрольной группы (p<0,001). Частота аллеля *А2 и генотипа *A2A2 в исследуемой группе статически значимо ниже этого показателя контрольной выборки. Аллель ANKK1*A1 является фактором риска развития алкогольной зависимости (RR=4,69; EF=0,15) с теснотой связи средней степени (j=0,21), а ANKK1*A2 обладает протекторным свойством (RR=0,84; PF=0,79). Полученные данные указывают на возможность использования генотипирования генов дофаминэргической системы головного мозга для оценки индивидуальной предрасположенности к алкогольной зависимости - у носителей *A1 гена DRD2/ANKK1 риск формирования зависимости в 4,69 раза выше гомозигот по варианту *А2. Addictive disorders are multifactorial diseases with clinical, genetic and neurophysiological heterogeneity and high comorbidity with other disorders of the mental spectrum. The decisive influence on the phenotypic dispersion of disorders of behavior of a dependent nature belongs to the genotype. Polymorphic variants of genes of the neurotransmitter systems of the brain that encode proteins involved in the regulation of effector reactions and the metabolism of psychoactive substances can be considered as markers of behavioral patterns and an individual predisposition to dependent behavior. Genotyping by TaqIA polymorphism at the ANKK1/DRD2 locus (rs1800497) and VNTR polymorphism in the SLC6A3 gene (DAT1) was performed using the PCR. A statistically significant predominance of the frequency of the ANKK1*A1 allele and the ANKK1*A1A2 genotype was revealed in the group of men with the presence of addictive disorder in the form of alcohol dependence compared to phenotypically healthy representatives of the control group (p <0.001). The frequency of *A2 and genotype *A2A2 were statistically significantly lower in the study group than in the control. The ANKK1*A1 allele is a risk factor for the development of alcohol dependence (RR=4.69; EF=0.15) with a moderate linkage (j=0.21), and ANKK1*A2 has a protective property (RR=0.84; PF=0.79). The data obtained indicate the possibility of using genotyping of the genes of the dopaminergic system of the brain to assess an individual predisposition to alcohol dependence - in carriers of *A1 of the DRD2/ANKK1 gene, the risk of dependence formation is 4.69 higher than homozygotes in the *A2 variant.


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