Search results for "Ethanol intake"

showing 7 items of 7 documents

Resilience to social defeat-induced increased in ethanol intake: neuroinflammation response

2022

El estrés social es el principal factor de riesgo de las conductas adictivas. El fenotipo susceptible al estrés se ha convertido en la última década en un objetivo de estudio para la aplicación de tratamientos eficaces que mejoren la resiliencia al estrés. La promoción del afrontamiento activo mediante intervenciones farmacológicas y ambientales positivas está científicamente validada en el tratamiento de las adicciones. Sin embargo, estas intervenciones para promover la resiliencia durante la adolescencia como medida preventiva de experiencias estresantes intensas durante la edad adulta no han sido ampliamente estudiadas. Por ello, el objetivo principal de la presente Tesis Doctoral fue de…

ethanol intakesocial stress:PSICOLOGÍA [UNESCO]UNESCO::PSICOLOGÍAresilienceneuroinflammation
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Modulation of alcohol consumption using an operant self-administration paradigm: effects of a new dopamine aminoacidic conjugate, Phenylalanine-β(3,4…

2014

Rewarding and reinforcing properties of alcohol have been shown to be mediated by activation of the mesolimbic dopaminergic system. Experimental evidences suggest that mesolimbic dopamine system is hypofunctional in addicted brain; further, reduced dopaminergic activity outlasts somatic signs of withdrawal and may drive craving and relapse. Boosting strategy on dopaminergic neurons could represent a valid therapy. Effects of pharmacological manipulation of brain Dopaminergic receptors by a new dopamine conjugate, Phenylalanine-β(3,4dihydroxyphenyl)-etilamide (DA-Phen), on operant behaviour and on both acute and prolonged withdrawal symptoms during ethanol abstinence have been evaluated. Mal…

operant conditioning taskSettore BIO/14 - Farmacologiadopamine derivatives.ethanol intake reduction
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Does ethanol intake interfere with the evaluation of glycated hemoglobins?

1989

Ethanol and/or its metabolites interfere with the chromatographic assay of glycated hemoglobins. Fasting plasma glucose, blood ethanol, HbA(1), HbA(1c), HbA(1a+b), MCV and GGT were determined in 22 control subjects; 22 alcoholics, 22 diabetic patients and 22 alcoholic diabetic patients. Fasting plasma glucose and all hemoglobin fractions were lower in alcoholic subjects and, except for HbA(1a+b), higher in diabetic patients and in alcoholic diabetic patients. HbA(1), and HbA(1c) correlated well with plasma glucose but not with blood ethanol, MCV and GGT. Glycated hemoglobin was not found to be a useful marker for alcohol abuse. With the chromatographic method we used, the evaluation of glyc…

Blood GlucoseMalemedicine.medical_specialtyAlcohol DrinkingEndocrinology Diabetes and MetabolismAlcohol abusechemistry.chemical_compoundEndocrinologyInternal medicineDiabetes mellitusInternal MedicinemedicineDiabetes MellitusHumansGlycated HemoglobinEthanolEthanolbusiness.industryGeneral MedicineFastingMiddle Agedmedicine.diseaseControl subjectsAlcoholismEndocrinologyDiabetes Mellitus Type 1chemistryDiabetes Mellitus Type 2Metabolic control analysisFemaleGlycated hemoglobinHemoglobinEthanol intakebusinessActa diabetologica latina
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Binge-Like, Naloxone-Sensitive, Voluntary Ethanol Intake at Adolescence Is Greater Than at Adulthood, but Does Not Exacerbate Subsequent Two-Bottle C…

2020

The present study assessed the effects of ethanol exposure during adolescence or adulthood. We exposed Wistar rats, males or females, to self-administered 8–10% (v/v) ethanol (BINGE group) during the first 2 h of the dark cycle, three times a week (Monday, Wednesday, and Friday) during postnatal days (PDs) 32–54 or 72–94 (adolescent and adults, respectively). During this period, controls were only handled, and a third (IP) condition was given ethanol intraperitoneal administrations, three times a week (Monday, Wednesday, and Friday), at doses that matched those self-administered by the BINGE group. The rats were tested for ethanol intake and preference in a two-bottle (24 h long) choice tes…

Cognitive NeuroscienceWistarPoison controlBinge drinkingPhysiologyAlcohollcsh:RC321-57103 medical and health scienceschemistry.chemical_compound//purl.org/becyt/ford/3.3 [https]Behavioral Neuroscience0302 clinical medicineNaloxoneInjury preventionmedicinelcsh:Neurosciences. Biological psychiatry. NeuropsychiatryOriginal Research030304 developmental biology0303 health sciencesbinge exposureEthanolnaloxonebusiness.industryNeuropsychology and Physiological PsychologychemistryTurnover//purl.org/becyt/ford/3 [https]adolescenceethanolEthanol intakebusiness030217 neurology & neurosurgeryNeurosciencemedicine.drugFrontiers in Behavioral Neuroscience
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Pharmacology of Acamprosate: An Overview

2003

In the last years important advances have been made in the development of drugs for the treatment of alcohol addiction. Acamprosate (calcium bis‐acetylhomotaurine) is one of the better established drugs in this field on the European market. This review focuses first on the pharmacokinetics of acamprosate. The published data and the recent advances in our knowledge on the mechanisms involved in the intestinal absorption and elimination of this drug are summarized. The importance of pharmacokinetics for the proper clinical use of acamprosate is highlighted. The anti‐relapse as well as the well‐known effects of acamprosate on ethanol intake are discussed. The recent experiments in animal model…

DrugTaurineAcamprosatemedia_common.quotation_subjectBiological AvailabilityPharmacologyReceptors N-Methyl-D-AspartateArticleIntestinal absorptionmedicineAnimalsHumansEuropean marketmedia_commonPharmacologyAlcohol addictionAlcohol dependenceAlcoholismNeuropsychology and Physiological PsychologyAcamprosateIntestinal AbsorptionEthanol intakePsychologyAlcohol Deterrentsmedicine.drugBiological availability
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P-77D-PENICILLAMINE, A POTENTIAL ETHANOL ANTI-RELAPSE DRUG, DOES NOT REDUCE THE VOLUNTARY ETHANOL INTAKE IN LONG-TERM EXPERIENCED RATS

2015

Experimental evidence has demonstrated that the reinforcing effects of ethanol crucially depend on the brain formation of acetaldehyde (ACD). Rationally supported by this basis, we previously evaluated a novel strategy to prevent relapse in alcoholism based on chemical ACD inactivation using D-Penicillamine (DP). Under our experimental …

DrugEthanolbusiness.industrymedia_common.quotation_subjectPenicillamineAcetaldehydeGeneral MedicinePharmacologychemistry.chemical_compoundchemistryBiochemistrymedicineEthanol intakebusinessmedicine.drugmedia_commonAlcohol and Alcoholism
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Binge ethanol drinking during adolescence modifies cocaine responses in mice

2016

Binge ethanol drinking is an emerging pattern of excessive consumption among adolescents and young adults. Repeated ethanol intoxication has negative consequences during critical periods of brain development. Therefore, binge ethanol intake represents a vulnerability factor that promotes subsequent manifestations of neuropsychiatric disorders. In this study, we investigated the effects of oral binge ethanol intake during adolescence on the subsequent effects of cocaine in C57BL/6 mice. Firstly, we evaluated the oral ethanol intake of two binge ethanol procedures with different ethanol concentrations (20% v/v versus 30%, v/v). The highest ethanol intake was found in mice exposed to the lowe…

Malemedicine.medical_specialtyAlcohol DrinkingBinge drinkingSelf AdministrationBehavioural sensitizationBinge DrinkingMice03 medical and health scienceschemistry.chemical_compound0302 clinical medicineCocaineInternal medicinemedicineBinge ethanolAnimalsPharmacology (medical)Young adultPharmacologyEthanolBehavior AnimalEthanolbusiness.industryAge Factors3. Good health030227 psychiatryMice Inbred C57BLPsychiatry and Mental healthEndocrinologychemistryEthanol intakeEthanol intoxicationSelf-administrationbusinessLocomotion030217 neurology & neurosurgeryJournal of Psychopharmacology
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