Gano Anny, Vore Andrew S, Geraci Daniella, Varlinskaya Elena I, Deak Terrence
Developmental Exposure Alcohol Research Center (DEARC), Behavioral Neuroscience Program, Department of Psychology, Binghamton University, Binghamton, NY 13902-6000, United States of America.
Pharmacol Biochem Behav. 2025 May;250:173998. doi: 10.1016/j.pbb.2025.173998. Epub 2025 Mar 17.
Loss of motivated behavior, or apathy, is a key feature across multiple affective disorders, and is assessed via operant effort-based decision-making (EBDM). The mechanisms of amotivation have been connected to pro-inflammatory signaling which can directly impact dopamine signaling. Chronic alcohol exposure is associated with altered immune signaling and impaired goal-directed behavior, so the present studies assessed the impact of adolescent intermittent ethanol (AIE) on EBDM in adulthood across sex. Adolescent male and female (N = 32/n = 8 per group) Sprague-Dawley rats were exposed to ethanol (4 g/kg) intragastrically on a 3 days on/2 days off schedule during postnatal days ~30-50 or given vehicle, and allowed to age into adulthood (P80+). All rats were then trained on the operant EBDM concurrent FR5/chow task, after which we tested the impact of sex and AIE history on responding 1) during breakpoint challenge raising the FR requirement in a log pattern, 2) 90 min after immune challenge (2 μg/kg IL-1β), 3) 18 h after 3.5 g/kg intraperitoneal ethanol challenge (hangover), and 4) immediately after a 30-min restraint stress challenge. Immune challenge disrupted motivated behavior without affecting appetite. No effects of AIE emerged and sex differences were evident throughout all challenges. Females responded less for pellets yet persisted responding until a higher breakpoint. This work indicates that AIE does not alter baseline or evoked EBDM as can be measured with this approach. Testing across aging and using other modalities should be performed to continue examining the effects of chronic alcohol on apathy.
动机行为丧失,即冷漠,是多种情感障碍的关键特征,可通过基于操作性努力的决策(EBDM)进行评估。无动机的机制与促炎信号传导有关,促炎信号传导可直接影响多巴胺信号传导。长期饮酒与免疫信号改变和目标导向行为受损有关,因此本研究评估了青春期间歇性乙醇(AIE)对成年期不同性别的EBDM的影响。在出生后约30 - 50天,将青春期雄性和雌性(每组N = 32/n = 8)Sprague-Dawley大鼠按3天饮酒/2天不饮酒的时间表灌胃给予乙醇(4 g/kg)或给予溶剂对照,然后使其成长至成年期(P80+)。然后所有大鼠接受操作性EBDM并发FR5/食物任务训练,之后我们测试了性别和AIE史对以下反应的影响:1)在断点挑战期间以对数模式提高FR要求时;2)免疫挑战(2 μg/kg IL-1β)后90分钟;3)3.5 g/kg腹腔注射乙醇挑战(宿醉)后18小时;4)30分钟束缚应激挑战后立即测试。免疫挑战扰乱了动机行为,但不影响食欲。未发现AIE有影响,并且在所有挑战中性别差异均很明显。雌性对食丸的反应较少,但会持续反应直到更高的断点。这项工作表明,AIE不会改变用这种方法测量的基线或诱发的EBDM。应进行跨年龄测试并使用其他方式继续研究慢性酒精对冷漠的影响。