Behavioral and biochemical effects of alcohol withdrawal in female C3H/HeNRj and C57BL/6JRj mice

被引:3
作者
Tonetto, Simone [1 ,2 ,3 ]
Weikop, Pia [4 ]
Brudek, Tomasz [2 ,5 ]
Thomsen, Morgane [1 ,2 ,3 ]
机构
[1] Univ Hosp Copenhagen, Psychiat Ctr Copenhagen, Lab Neuropsychiat, Copenhagen, Denmark
[2] Univ Hosp Copenhagen, Bispebjerg Frederiksberg Hosp, Copenhagen Ctr Translat Res, Copenhagen, Denmark
[3] Univ Copenhagen, Fac Hlth & Med Sci, Dept Neurosci, Copenhagen, Denmark
[4] Univ Copenhagen, Ctr Translat Neuromed, Copenhagen, Denmark
[5] Univ Hosp Copenhagen, Bispebjerg Frederiksberg Hosp, Res Lab Stereol & Neurosci, Copenhagen, Denmark
基金
美国国家卫生研究院;
关键词
alcohol withdrawal; mouse strains; behavioral tests; HPLC; neuroinflammation; CHRONIC INTERMITTENT ETHANOL; INDUCED NEUROINFLAMMATION; ULTRASONIC VOCALIZATIONS; NEGATIVE AFFECT; SEX-DIFFERENCES; EXPOSURE; DRINKING; NOREPINEPHRINE; RECEPTORS; STRESS;
D O I
10.3389/fnbeh.2023.1143720
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
BackgroundAlcohol use disorder (AUD) is a major problem of our society and is often characterized and worsened by relapse. Prolonged alcohol exposure leads to numerous biochemical alterations that, upon cessation of alcohol intake, cause an array of immediate and lasting withdrawal symptoms. Acute withdrawal and neuroinflammation can be harmful in themselves, and lasting withdrawal symptoms contribute to relapse. Here, we conducted an initial feasibility study assessing several behavioral and neurochemical factors in female C3H/HeNRj (C3H) and C57BL/6JRj (B6) mice to determine which strain showed the clearest alcohol withdrawal symptoms during long-term abstinence and neurochemical alterations following re-exposure. MethodsFemale C3H and B6 mice (n = 12 per group/strain) were intermittently exposed to alcohol-containing or control liquid diets for 3 weeks. Acute and prolonged withdrawal symptoms were assessed over a period of 3 weeks using a battery of behavioral test, comprised of alcohol self-administration, anhedonia, hyperalgesia, anxiety-like and depressive-like disturbances. Brain inflammation was measured by multiplex cytokine assay. Monoamine levels in the hippocampus and striatum, as well as exploratory analyses of cations levels in the cerebellum, were assessed by High-Performance Liquid Chromatography (HPLC). ResultsBoth C3H and B6 alcohol-exposed mice displayed decreased saccharin intake or preference and higher stress levels assessed by ultrasonic vocalizations (USVs) recordings. B6 but not C3H alcohol-exposed mice also exhibited a slower decline of alcohol oral self-administration (OSA), hyperalgesia, elevated brain TNF-alpha and elevated serotonin turnover. ConclusionOur findings highlight the suitability of the B6 strain to study the behavioral and neurochemical alterations caused by alcohol withdrawal and the potential efficacy of experimental treatments, not only in early detoxification, but also in prolonged abstinence. The feasibility of these assays is important because long-lasting withdrawal symptoms are often the main cause of relapse in alcohol-dependent patients.
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页数:18
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共 66 条
[51]   Sex differences in the association between impulsivity and driving under the influence of alcohol in young adults: The specific role of sensation seeking [J].
Navas, Juan F. ;
Martin-Perez, Cristina ;
Petrova, Dafina ;
Verdejo-Garcia, Antonio ;
Cano, Marta ;
Sagripanti-Mazuquin, Omar ;
Perandres-Gomez, Ana ;
Lopez-Martin, Angela ;
Cordovilla-Guardia, Sergio ;
Megias, Alberto ;
Perales, Jose C. ;
Vilar-Lopez, Raquel .
ACCIDENT ANALYSIS AND PREVENTION, 2019, 124 :174-179
[52]   Cytokines and chemokines as biomarkers of ethanol-induced neuroinflammation and anxiety-related behavior: Role of TLR4 and TLR2 [J].
Pascual, Maria ;
Balino, Pablo ;
Aragon, Carlos M. G. ;
Guerri, Consuelo .
NEUROPHARMACOLOGY, 2015, 89 :352-359
[53]   Changes in plasma noradrenaline and serotonin levels and craving during alcohol withdrawal [J].
Patkar, AA ;
Gopalakrishnan, R ;
Naik, PC ;
Murray, HW ;
Vergare, MJ ;
Marsden, CA .
ALCOHOL AND ALCOHOLISM, 2003, 38 (03) :224-231
[54]   High-throughput behavioral phenotyping in the expanded panel of BXD recombinant inbred strains [J].
Philip, V. M. ;
Duvvuru, S. ;
Gomero, B. ;
Ansah, T. A. ;
Blaha, C. D. ;
Cook, M. N. ;
Hamre, K. M. ;
Lariviere, W. R. ;
Matthews, D. B. ;
Mittleman, G. ;
Goldowitz, D. ;
Chesler, E. J. .
GENES BRAIN AND BEHAVIOR, 2010, 9 (02) :129-159
[55]   Deficit in brain reward function and acute and protracted anxiety-like behavior after discontinuation of a chronic alcohol liquid diet in rats [J].
Rylkova, Daria ;
Shah, Hina P. ;
Small, Elysia ;
Bruijnzeel, Adrie W. .
PSYCHOPHARMACOLOGY, 2009, 203 (03) :629-640
[56]   BEHAVIORAL AND PHARMACOLOGICAL CHARACTERIZATION OF THE ELEVATED ZERO-MAZE AS AN ANIMAL-MODEL OF ANXIETY [J].
SHEPHERD, JK ;
GREWAL, SS ;
FLETCHER, A ;
BILL, DJ ;
DOURISH, CT .
PSYCHOPHARMACOLOGY, 1994, 116 (01) :56-64
[57]   THE EFFECT OF ALCOHOL CONSUMPTION ON MATERNAL AND CORD BLOOD ELECTROLYTE AND TRACE ELEMENT LEVELS [J].
Skalny, Anatoly V. ;
Berezkina, Elena S. ;
Kiyaeva, Elena V. ;
Alidzhanova, Inara E. ;
Grabeklis, Andrew R. ;
Tinkov, Alexey A. .
ACTA SCIENTIARUM POLONORUM-TECHNOLOGIA ALIMENTARIA, 2016, 15 (04) :439-445
[58]   Increased Responding for Alcohol and Resistance to Aversion in Female Mice [J].
Sneddon, Elizabeth A. ;
Ramsey, Olivia R. ;
Thomas, Annemarie ;
Radke, Anna K. .
ALCOHOL-CLINICAL AND EXPERIMENTAL RESEARCH, 2020, 44 (07) :1400-1409
[59]   Measuring behavior in mice with chronic stress depression paradigm [J].
Strekalova, Tatyana ;
Steinbusch, Harry W. M. .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2010, 34 (02) :348-361
[60]   Severe Hypomagnesaemia Causing Reversible Cerebellopathy [J].
te Riele, M. G. E. ;
Verrips, A. .
CEREBELLUM, 2014, 13 (05) :659-662