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Enhanced fear extinction through infralimbic perineuronal net digestion: The modulatory role of adolescent alcohol exposure 通过边缘下神经周围网络消化增强恐惧消除:青少年酒精暴露的调节作用。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-12-20 DOI: 10.1016/j.alcohol.2024.12.006
J. Daniel Obray , Adam R. Denton , Jayda Carroll-Deaton , Kristin Marquardt , L. Judson Chandler , Michael D. Scofield
Perineuronal nets (PNNs) are specialized components of the extracellular matrix that play a critical role in learning and memory. In a Pavlovian fear conditioning paradigm, degradation of PNNs affects the formation and storage of fear memories. This study examined the impact of adolescent intermittent ethanol (AIE) exposure by vapor inhalation on the expression of PNNs in the adult rat prelimbic (PrL) and infralimbic (IfL) subregions of the medial prefrontal cortex. Results indicated that following AIE, the total number of PNN positive cells in the PrL cortex increased in layer II/III but did not change in layer V. Conversely, in the IfL cortex, the number of PNN positive cells decreased in layer V, with no change in layer II/III. In addition, the intensity of PNN staining was significantly altered by AIE exposure, which narrowed the distribution of signal intensity, reducing the number of high and low intensity PNNs. Given these changes in PNNs, the next experiment assessed the effects of AIE and PNN digestion on extinction of a conditioned fear memory. In Air control rats, digestion of PNNs by bilateral infusion of Chondroitinase ABC (ChABC) into the IfL cortex enhanced fear extinction and reduced contextual fear renewal. In contrast, both fear extinction learning and contextual fear renewal remained unchanged following PNN digestion in AIE exposed rats. These results highlight the sensitivity of prefrontal PNNs to adolescent alcohol exposure and suggest that ChABC-induced plasticity is reduced in the IfL cortex following AIE exposure.
神经周围网络(PNNs)是细胞外基质的特殊组成部分,在学习和记忆中起关键作用。在巴甫洛夫恐惧条件反射范式中,pnn的退化影响恐惧记忆的形成和储存。本研究探讨了青春期间歇性乙醇(AIE)暴露对成年大鼠内侧前额叶皮层边缘前区(PrL)和边缘下区(IfL) PNNs表达的影响。结果表明,AIE后,PrL皮层中PNN阳性细胞总数在第II/III层增加,但在第V层没有变化。相反,在IfL皮层中,PNN阳性细胞总数在第V层减少,第II/III层没有变化。此外,AIE暴露显著改变PNN染色强度,使信号强度分布变窄,高、低强度PNN数量减少。考虑到PNN的这些变化,下一个实验评估了AIE和PNN消化对条件恐惧记忆消退的影响。在空气对照大鼠中,通过双侧向IfL皮层输注ChABC(软骨素酶ABC)来消化pnn可增强恐惧消退并减少情境恐惧更新。相比之下,AIE暴露大鼠的PNN消化后,恐惧消退学习和情境恐惧更新保持不变。这些结果强调了前额叶PNNs对青少年酒精暴露的敏感性,并表明在AIE暴露后,chabc诱导的IfL皮质可塑性降低。
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引用次数: 0
7. Alcohol consumption affects MSC differentiation capacity in orthopaedic trauma patients 7. 饮酒影响骨科创伤患者骨髓间充质干细胞分化能力
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-12-01 DOI: 10.1016/j.alcohol.2024.10.010
A.B. Boyd, E.L. Murdoch, J.J. Callaci
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引用次数: 0
32. Alcohol-induced tissue injury at the gut-liver-brain axis is more severe in diabetic mice 32. 酒精引起的肠-肝-脑轴组织损伤在糖尿病小鼠中更为严重
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-12-01 DOI: 10.1016/j.alcohol.2024.10.035
N. Shashikanth , L. Basa , R. Rajenthiran, C. Nguyen, P. Raju, S.C. Lee, C. Shekhar, F. Giorgianni, R.K. Rao
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引用次数: 0
12. Role of Foxp3+ regulatory T cells in chronic ethanol consumption and sepsis pathogenesis 12. Foxp3+调节性T细胞在慢性乙醇消耗和脓毒症发病中的作用
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-12-01 DOI: 10.1016/j.alcohol.2024.10.015
M.B. Gutierrez, C.M. Coopersmith, M.L. Ford
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引用次数: 0
20. Myeloid TLR4 deficient mice are not protected from alcohol-mediated liver injury and inflammation: contribution of hepatocytes and neutrophils 20.。髓系TLR4缺陷小鼠不受酒精介导的肝损伤和炎症的保护:肝细胞和中性粒细胞的贡献
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-12-01 DOI: 10.1016/j.alcohol.2024.10.023
A. Mandal, A. Ratna, J. Thanikasalam, E. Kurt-Jones, P. Mandrekar
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引用次数: 0
2. Ethanol exposure impairs LC3-associated phagocytosis via IL-1β-ATG16L1 pathway in macrophages 2. 乙醇暴露通过IL-1β-ATG16L1途径损害巨噬细胞lc3相关吞噬
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-12-01 DOI: 10.1016/j.alcohol.2024.10.005
A. Ahuja, B. Pant, E. Cross, D. Shrestha, S. Abraham, R. Scheraga, V. Vachharajani
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引用次数: 0
36. mRNA profile of mouse large intestine epithelial cells after DSS colitis and ethanol exposure 36. DSS结肠炎和乙醇暴露后小鼠大肠上皮细胞mRNA谱
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-12-01 DOI: 10.1016/j.alcohol.2024.10.039
M.M. Tschann , A.R. Cannon , M.N. Xi , M.A. Choudhry
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引用次数: 0
11. Inhibition of c-Fos mitigates alcohol-induced miR144 in lung fibroblasts 11. 抑制c-Fos可减轻肺成纤维细胞中酒精诱导的miR144
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-12-01 DOI: 10.1016/j.alcohol.2024.10.014
J. Guo, X. Fan, D. Guidot, V. Sueblinvong
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引用次数: 0
24. Alcohol administration and fecal microbiota transplantation alter the gut microbiome and metabolome in a murine model of Multiple Sclerosis 24. 在多发性硬化症小鼠模型中,酒精管理和粪便微生物群移植改变了肠道微生物群和代谢组
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-12-01 DOI: 10.1016/j.alcohol.2024.10.027
A.S.P. Nuncio , A.C. Neville , B. Caslin , C. Maguire , O. Brady , S. Shah , E. Idnani , K.A. Kinney , L.J. Noble-Haeusslein , R.A. Josephs , P. Misztal , E. Melamed
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引用次数: 0
40. Utilization of lipidomics to evaluate the lipid profile of trauma patients with detectable blood alcohol levels on admission 40. 利用脂质组学评估入院时可检测血液酒精水平的创伤患者的脂质谱
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-12-01 DOI: 10.1016/j.alcohol.2024.10.043
D. Vitharana, A.R. Masoud, O. Jackson-Weaver, J. Dennis, A. Mansouri, J. Adamec, P. Molina, A. Smith
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引用次数: 0
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Alcohol
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