• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

应激诱导的酒精摄入的性别差异:以杏仁核和炎症通路为重点的临床前研究综述。

Sex differences in stress-induced alcohol intake: a review of preclinical studies focused on amygdala and inflammatory pathways.

机构信息

Department of Psychiatry, Yale University, 34 Park Street, 3Rd Floor Research, New Haven, CT, 06508, USA.

Yale Interdepartmental Neuroscience Program, New Haven, CT, USA.

出版信息

Psychopharmacology (Berl). 2022 Jul;239(7):2041-2061. doi: 10.1007/s00213-022-06120-w. Epub 2022 Mar 31.

DOI:10.1007/s00213-022-06120-w
PMID:35359158
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9704113/
Abstract

Clinical studies suggest that women are more likely than men to relapse to alcohol drinking in response to stress; however, the mechanisms underlying this sex difference are not well understood. A number of preclinical behavioral models have been used to study stress-induced alcohol intake. Here, we review paradigms used to study effects of stress on alcohol intake in rodents, focusing on findings relevant to sex differences. To date, studies of sex differences in stress-induced alcohol drinking have been somewhat limited; however, there is evidence that amygdala-centered circuits contribute to effects of stress on alcohol seeking. In addition, we present an overview of inflammatory pathways leading to microglial activation that may contribute to alcohol-dependent behaviors. We propose that sex differences in neuronal function and inflammatory signaling in circuits centered on the amygdala are involved in sex-dependent effects on stress-induced alcohol seeking and suggest that this is an important area for future studies.

摘要

临床研究表明,女性在应对压力时比男性更有可能重新开始饮酒;然而,这种性别差异的机制尚不清楚。许多临床前行为模型被用于研究应激诱导的酒精摄入。在这里,我们回顾了用于研究应激对啮齿动物饮酒影响的范式,重点关注与性别差异相关的发现。迄今为止,应激诱导饮酒的性别差异研究有些有限;然而,有证据表明,杏仁核为中心的回路有助于应激对酒精寻求的影响。此外,我们还概述了导致小胶质细胞激活的炎症途径,这可能与酒精依赖行为有关。我们提出,杏仁核为中心的回路中神经元功能和炎症信号的性别差异参与了应激诱导的酒精寻求的性别依赖性影响,并表明这是未来研究的一个重要领域。

相似文献

1
Sex differences in stress-induced alcohol intake: a review of preclinical studies focused on amygdala and inflammatory pathways.应激诱导的酒精摄入的性别差异:以杏仁核和炎症通路为重点的临床前研究综述。
Psychopharmacology (Berl). 2022 Jul;239(7):2041-2061. doi: 10.1007/s00213-022-06120-w. Epub 2022 Mar 31.
2
Role of microglia in stress-induced alcohol intake in female and male mice.小胶质细胞在应激诱导的雌性和雄性小鼠酒精摄入中的作用。
bioRxiv. 2024 Jun 6:2024.06.05.597614. doi: 10.1101/2024.06.05.597614.
3
Amygdala 14-3-3ζ as a novel modulator of escalating alcohol intake in mice.杏仁核 14-3-3ζ 作为一种新型调节因子,可促进小鼠酒精摄入量增加。
PLoS One. 2012;7(5):e37999. doi: 10.1371/journal.pone.0037999. Epub 2012 May 22.
4
Traumatic stress reactivity promotes excessive alcohol drinking and alters the balance of prefrontal cortex-amygdala activity.创伤后应激反应会促进过度饮酒,并改变前额叶皮层-杏仁核活动的平衡。
Transl Psychiatry. 2013 Aug 27;3(8):e296. doi: 10.1038/tp.2013.70.
5
Sex-specific plasticity in CRF regulation of inhibitory control in central amygdala CRF1 neurons after chronic voluntary alcohol drinking.慢性自愿性饮酒后,中央杏仁核 CRF1 神经元中 CRF 调节抑制控制的性别特异性可塑性。
Addict Biol. 2022 Jan;27(1):e13067. doi: 10.1111/adb.13067. Epub 2021 Jun 2.
6
The Endocrine System and Alcohol Drinking in Females.女性的内分泌系统与饮酒行为。
Alcohol Res. 2020 Jul 23;40(2):02. doi: 10.35946/arcr.v40.2.02. eCollection 2020.
7
Repetitive binge-like consumption based on the Drinking-in-the-Dark model alters the microglial population in the mouse hippocampus.基于暗时饮酒模型的重复性 binge-like 消费会改变小鼠海马体中的小胶质细胞群体。
J Integr Neurosci. 2021 Dec 30;20(4):933-943. doi: 10.31083/j.jin2004094.
8
Genome-wide transcriptomics of the amygdala reveals similar oligodendrocyte-related responses to acute and chronic alcohol drinking in female mice.杏仁核的全基因组转录组学研究揭示了雌性小鼠急性和慢性酒精摄入后相似的少突胶质细胞相关反应。
Transl Psychiatry. 2022 Nov 12;12(1):476. doi: 10.1038/s41398-022-02231-2.
9
Neurobiology of relapse to alcohol in rats.大鼠酒精复吸的神经生物学
Pharmacol Ther. 2002 Apr-May;94(1-2):137-56. doi: 10.1016/s0163-7258(02)00200-0.
10
Differential expression of μ-opioid receptors in the nucleus accumbens, amygdala and VTA depends on liking for alcohol, chronic alcohol intake and estradiol treatment.伏隔核、杏仁核和 VTA 中 μ 阿片受体的差异表达取决于对酒精的喜好、慢性酒精摄入和雌二醇处理。
Behav Brain Res. 2020 Jan 27;378:112255. doi: 10.1016/j.bbr.2019.112255. Epub 2019 Sep 21.

引用本文的文献

1
Relationship between biological sex and the endocrine stress response following a binge-like dose of alcohol.暴饮剂量酒精后生物性别与内分泌应激反应之间的关系。
Alcohol Clin Exp Res (Hoboken). 2025 Aug 1. doi: 10.1111/acer.70094.
2
Binge alcohol and the neuroendocrinology of the aging female.酗酒与衰老女性的神经内分泌学
Front Neuroendocrinol. 2025 Jul;78:101201. doi: 10.1016/j.yfrne.2025.101201. Epub 2025 Jun 4.
3
Prenatal methadone exposure produces functional and molecular alterations in the basolateral amygdala and decreased voluntary ethanol intake in female, but not male offspring.

本文引用的文献

1
Oxytocin Attenuates the Stress-Induced Reinstatement of Alcohol-Seeking in Male Rats: Role of the Central Amygdala.催产素减轻雄性大鼠应激诱导的觅酒行为恢复:中央杏仁核的作用
Biomedicines. 2021 Dec 15;9(12):1919. doi: 10.3390/biomedicines9121919.
2
Social isolation-related depression accelerates ethanol intake via microglia-derived neuroinflammation.社交隔离相关的抑郁通过小胶质细胞衍生的神经炎症加速乙醇摄入。
Sci Adv. 2021 Nov 5;7(45):eabj3400. doi: 10.1126/sciadv.abj3400.
3
Uncovering microglial pathways driving sex-specific neurobiological effects in stress and depression.
产前接触美沙酮会导致雌性后代基底外侧杏仁核出现功能和分子改变,并减少其自愿乙醇摄入量,但对雄性后代无此影响。
Front Behav Neurosci. 2025 Apr 15;19:1570951. doi: 10.3389/fnbeh.2025.1570951. eCollection 2025.
4
Epidemiology characteristics of the drinking patterns and alcohol consumption among adults in Hainan Province, China.中国海南省成年人饮酒模式与酒精消费的流行病学特征
Front Public Health. 2025 Mar 17;13:1490439. doi: 10.3389/fpubh.2025.1490439. eCollection 2025.
5
Sex differences in the microglial response to stress and chronic alcohol exposure in mice.小鼠小胶质细胞对应激和慢性酒精暴露的性别差异。
Biol Sex Differ. 2025 Mar 4;16(1):19. doi: 10.1186/s13293-025-00701-y.
6
Alcohol Consumption and Autoimmune Diseases.饮酒与自身免疫性疾病
Int J Mol Sci. 2025 Jan 20;26(2):845. doi: 10.3390/ijms26020845.
7
Ethanol's impact on the brain: a neurobiological perspective on the mechanisms of memory impairment.乙醇对大脑的影响:记忆损伤机制的神经生物学观点。
Mol Biol Rep. 2024 Jun 25;51(1):782. doi: 10.1007/s11033-024-09748-3.
8
Subjective stress and any drinking during alcohol treatment: Disentangling within and between person autoregressive effects.酒精治疗期间的主观压力与饮酒情况:剖析个体内和个体间的自回归效应。
Neurobiol Stress. 2023 Dec 16;29:100602. doi: 10.1016/j.ynstr.2023.100602. eCollection 2024 Mar.
9
Nicotinic regulation of microglia: potential contributions to addiction.烟碱对小胶质细胞的调节:对成瘾的潜在贡献。
J Neural Transm (Vienna). 2024 May;131(5):425-435. doi: 10.1007/s00702-023-02703-9. Epub 2023 Oct 1.
10
Sex-dependent divergence in the effects of GLP-1 agonist exendin-4 on alcohol reinforcement and reinstatement in C57BL/6J mice.性别依赖性差异:GLP-1 激动剂 exendin-4 对 C57BL/6J 小鼠酒精强化和复饮的影响。
Psychopharmacology (Berl). 2023 Jun;240(6):1287-1298. doi: 10.1007/s00213-023-06367-x. Epub 2023 Apr 28.
揭示在应激和抑郁中驱动性别特异性神经生物学效应的小胶质细胞通路。
Brain Behav Immun Health. 2021 Aug 9;16:100320. doi: 10.1016/j.bbih.2021.100320. eCollection 2021 Oct.
4
Increased Toll-like Receptor-MyD88-NFκB-Proinflammatory neuroimmune signaling in the orbitofrontal cortex of humans with alcohol use disorder.酒精使用障碍患者眶额皮质中 Toll 样受体-MyD88-NFκB-促炎神经免疫信号的增加。
Alcohol Clin Exp Res. 2021 Sep;45(9):1747-1761. doi: 10.1111/acer.14669. Epub 2021 Aug 20.
5
A neural substrate of compulsive alcohol use.强迫性饮酒的神经基础。
Sci Adv. 2021 Aug 18;7(34). doi: 10.1126/sciadv.abg9045. Print 2021 Aug.
6
Structural, functional, and behavioral significance of sex and gonadal hormones in the basolateral amygdala: A review of preclinical literature.性和性腺激素在基底外侧杏仁核中的结构、功能和行为意义:临床前文献综述。
Alcohol. 2022 Feb;98:25-41. doi: 10.1016/j.alcohol.2021.08.001. Epub 2021 Aug 6.
7
NOP receptor antagonism attenuates reinstatement of alcohol-seeking through modulation of the mesolimbic circuitry in male and female alcohol-preferring rats.NOP 受体拮抗作用通过调节雄性和雌性酒精偏好大鼠的中脑边缘回路来减弱觅酒行为的复燃。
Neuropsychopharmacology. 2021 Nov;46(12):2121-2131. doi: 10.1038/s41386-021-01096-1. Epub 2021 Jul 20.
8
Sudden cessation of fluoxetine before alcohol drinking reinstatement alters microglial morphology and TLR4/inflammatory neuroadaptation in the rat brain.氟西汀停药前饮酒复饮会改变大鼠大脑小胶质细胞形态和 TLR4/炎症性神经适应。
Brain Struct Funct. 2021 Sep;226(7):2243-2264. doi: 10.1007/s00429-021-02321-9. Epub 2021 Jul 8.
9
Simvastatin mitigates depressive-like behavior in ovariectomized rats: Possible role of NLRP3 inflammasome and estrogen receptors' modulation.辛伐他汀减轻去卵巢大鼠的抑郁样行为:NLRP3 炎性小体和雌激素受体调节的可能作用。
Int Immunopharmacol. 2021 Jun;95:107582. doi: 10.1016/j.intimp.2021.107582. Epub 2021 Mar 25.
10
Synaptic and behavioral effects of chronic stress are linked to dynamic and sex-specific changes in microglia function and astrocyte dystrophy.慢性应激的突触和行为效应与小胶质细胞功能和星形胶质细胞营养不良的动态及性别特异性变化有关。
Neurobiol Stress. 2021 Mar 4;14:100312. doi: 10.1016/j.ynstr.2021.100312. eCollection 2021 May.