Department of Morphology and Pathology, Federal University of São Carlos, SP, Brazil.
Department of Surgery and Anatomy, USP-University of São Paulo, Ribeirão Preto, SP, Brazil.
Cell Biol Int. 2018 Nov;42(11):1575-1583. doi: 10.1002/cbin.11054. Epub 2018 Sep 26.
Ethanol alters motricity, learning, cognition, and cellular metabolism in the cerebellum. The combination of ethanol with caffeine by consuming "energy drinks" is becoming increasingly popular among young people. We analyzed the use of ethanol and caffeine on apoptosis in the cerebellum of UChB rats. The adult rats were divided into three groups (n = 14/group): UChB group: rats fed with 1:10 (v/v) ethanol ad libitum (free choice for water or ethanol) drinking from >1.9 mL of ethanol/kg body weight/day, Control group and UChB/caffeine group (free choice for water or ethanol + caffeine 300 mg/L). The treatments occurred from Day 100 till Day 150, totalizing 50 days of ethanol/caffeine ingestion. Cerebellar sections were subjected to immunohistochemistry and gene expression for Real Time-PCR (RT-PCR) for Caspase-3, XIAP, and insulin-like growth factor 1-receptor (IGF-1R). The results showed a significant increase in the gene expression of Caspase-3 and XIAP in UChB group. On the other hand, the animals of the UChB/caffeine group showed similar results to the Controls. Regarding IGFR-1, there was greater expression in the UChB groups with strong labeling in Purkinje cells. Ethanol produces neuronal and glial neurodegeneration on the cerebellum of UChB rats. The simultaneous ingestion of ethanol and caffeine reversed the ethanol damages acting caffeine with a neuroprotective effect.
乙醇会改变小脑的运动能力、学习能力、认知能力和细胞代谢。年轻人越来越喜欢将乙醇与咖啡因混合在“能量饮料”中一起饮用。我们分析了乙醇和咖啡因对 UChB 大鼠小脑细胞凋亡的影响。成年大鼠被分为三组(每组 n=14):UChB 组:大鼠自由选择水或乙醇,饮用 1:10(v/v)的乙醇(每天超过 1.9 毫升/千克体重);对照组和 UChB/咖啡因组(自由选择水或乙醇+300 毫克/升咖啡因)。从第 100 天到第 150 天,共进行 50 天的乙醇/咖啡因摄入处理。对小脑切片进行免疫组织化学和实时聚合酶链反应(RT-PCR)检测,分析半胱天冬氨酸蛋白酶-3(Caspase-3)、X 连锁凋亡抑制蛋白(XIAP)和胰岛素样生长因子 1 受体(IGF-1R)的基因表达。结果显示,UChB 组 Caspase-3 和 XIAP 的基因表达显著增加。另一方面,UChB/咖啡因组的动物与对照组的结果相似。关于 IGF-1R,UChB 组的表达水平更高,浦肯野细胞的标记较强。乙醇会导致 UChB 大鼠小脑的神经元和神经胶质细胞发生神经退行性病变。同时摄入乙醇和咖啡因可以逆转乙醇的损伤,起到神经保护作用。