• 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

与海湾战争部署相关的地塞米松诱导的皮质醇抑制增强。

Enhanced cortisol suppression to dexamethasone associated with Gulf War deployment.

作者信息

Golier Julia A, Schmeidler James, Legge Juliana, Yehuda Rachel

机构信息

Department of Psychiatry, James J Peters VA Medical Center, 130 West Kingsbridge Road, Bronx, NY 10468, USA.

出版信息

Psychoneuroendocrinology. 2006 Nov;31(10):1181-9. doi: 10.1016/j.psyneuen.2006.08.005. Epub 2006 Oct 16.

DOI:10.1016/j.psyneuen.2006.08.005
PMID:17049422
Abstract

OBJECTIVE

To examine whether PTSD or post-deployment health symptoms in veterans of the first Gulf War (Operation Desert Shield/Storm) are associated with enhanced suppression of the pituitary-adrenal axis to low-dose dexamethasone (DEX).

METHOD

Plasma cortisol and lymphocyte glucocorticoid receptor (GR) number were measured at 08:00 h on two consecutive days, before and after administration of 0.5mg of DEX at 23:00 h in 42 male Gulf War veterans (14 without psychiatric illness, 16 with PTSD only, and 12 with both PTSD and MDD) and 12 healthy male veterans not deployed to the Gulf War or another war zone.

RESULTS

In the absence of group differences in basal cortisol levels or GR number, Gulf War veterans without psychiatric illness and Gulf War veterans with PTSD only had significantly greater cortisol suppression to DEX than non-deployed veterans and Gulf War veterans with both PTSD and MDD. Gulf War deployment was associated with significantly greater cortisol suppression to DEX controlling for weight, smoking status, PTSD, and MDD; PTSD was not associated with response to DEX. Among Gulf War veterans musculoskeletal symptoms were significantly associated with cortisol suppression and those who reported taking anti-nerve gas pills (i.e., pyridostigmine bromide) during the war had significantly greater DEX-induced cortisol suppression than those who did not.

CONCLUSIONS

The data demonstrate that alterations in neuroendocrine function are associated with deployment to the Gulf War and post-deployment musculoskeletal symptoms, but not PTSD. Additional studies are needed to examine the relationship of enhanced glucocorticoid responsivity to deployment exposures and chronic unexplained medical symptoms in Gulf War veterans.

摘要

目的

研究第一次海湾战争(沙漠盾牌/风暴行动)退伍军人的创伤后应激障碍(PTSD)或部署后健康症状是否与垂体-肾上腺轴对低剂量地塞米松(DEX)的抑制增强有关。

方法

在42名男性海湾战争退伍军人(14名无精神疾病、16名仅有PTSD、12名同时患有PTSD和重度抑郁障碍[MDD])以及12名未被部署到海湾战争或其他战区的健康男性退伍军人中,于连续两天的08:00测量血浆皮质醇和淋巴细胞糖皮质激素受体(GR)数量,在23:00给予0.5mg DEX之前和之后进行测量。

结果

在基础皮质醇水平或GR数量无组间差异的情况下,无精神疾病的海湾战争退伍军人和仅有PTSD的海湾战争退伍军人对DEX的皮质醇抑制作用明显大于未部署的退伍军人以及同时患有PTSD和MDD的海湾战争退伍军人。控制体重、吸烟状况、PTSD和MDD后,海湾战争部署与对DEX的皮质醇抑制作用明显增强有关;PTSD与对DEX的反应无关。在海湾战争退伍军人中,肌肉骨骼症状与皮质醇抑制作用显著相关,且那些报告在战争期间服用抗神经毒气药丸(即溴化吡啶斯的明)的人比未服用者的DEX诱导的皮质醇抑制作用明显更大。

结论

数据表明神经内分泌功能的改变与部署到海湾战争及部署后肌肉骨骼症状有关,但与PTSD无关。需要进一步研究来探讨糖皮质激素反应性增强与海湾战争退伍军人的部署暴露及慢性不明原因医学症状之间的关系。

相似文献

1
Enhanced cortisol suppression to dexamethasone associated with Gulf War deployment.与海湾战争部署相关的地塞米松诱导的皮质醇抑制增强。
Psychoneuroendocrinology. 2006 Nov;31(10):1181-9. doi: 10.1016/j.psyneuen.2006.08.005. Epub 2006 Oct 16.
2
Pituitary response to metyrapone in Gulf War veterans: relationship to deployment, PTSD and unexplained health symptoms.海湾战争退伍军人垂体对甲吡酮的反应:与部署、创伤后应激障碍及不明健康症状的关系
Psychoneuroendocrinology. 2009 Oct;34(9):1338-45. doi: 10.1016/j.psyneuen.2009.04.004. Epub 2009 May 14.
3
The ACTH response to dexamethasone in Persian Gulf War veterans.海湾战争退伍军人中促肾上腺皮质激素对地塞米松的反应。
Ann N Y Acad Sci. 2006 Jul;1071:448-53. doi: 10.1196/annals.1364.040.
4
Twenty-four hour plasma cortisol and adrenocorticotropic hormone in Gulf War veterans: relationships to posttraumatic stress disorder and health symptoms.海湾战争退伍军人的24小时血浆皮质醇和促肾上腺皮质激素:与创伤后应激障碍和健康症状的关系。
Biol Psychiatry. 2007 Nov 15;62(10):1175-8. doi: 10.1016/j.biopsych.2007.04.027. Epub 2007 Jul 5.
5
Neuroendocrine response to CRF stimulation in veterans with and without PTSD in consideration of war zone era.考虑到战区时代,创伤后应激障碍(PTSD)患者和非 PTSD 患者退伍军人的 CRF 刺激的神经内分泌反应。
Psychoneuroendocrinology. 2012 Mar;37(3):350-7. doi: 10.1016/j.psyneuen.2011.07.004. Epub 2011 Aug 2.
6
Differences in the response to the combined DEX-CRH test between PTSD patients with and without co-morbid depressive disorder.患有和未患有共病抑郁障碍的创伤后应激障碍患者对联合地塞米松-促肾上腺皮质激素释放激素试验反应的差异。
Psychoneuroendocrinology. 2008 Apr;33(3):313-20. doi: 10.1016/j.psyneuen.2007.11.016. Epub 2008 Jan 22.
7
Glucocorticoid receptor polymorphisms and post-traumatic stress disorder.糖皮质激素受体基因多态性与创伤后应激障碍
Psychoneuroendocrinology. 2005 Apr;30(3):297-306. doi: 10.1016/j.psyneuen.2004.08.006.
8
Enhanced cortisol suppression in response to dexamethasone administration in traumatized veterans with and without posttraumatic stress disorder.在有和没有创伤后应激障碍的创伤退伍军人中,给予地塞米松后皮质醇抑制作用增强。
Psychoneuroendocrinology. 2007 Apr;32(3):215-26. doi: 10.1016/j.psyneuen.2006.12.009. Epub 2007 Feb 12.
9
Hypocortisolism and increased glucocorticoid sensitivity of pro-Inflammatory cytokine production in Bosnian war refugees with posttraumatic stress disorder.波斯尼亚战争难民创伤后应激障碍患者的皮质醇减退及促炎细胞因子产生的糖皮质激素敏感性增加
Biol Psychiatry. 2004 Apr 1;55(7):745-51. doi: 10.1016/j.biopsych.2003.11.018.
10
[The Gulf War Syndrome twenty years on].二十年后的海湾战争综合征
Encephale. 2013 Oct;39(5):332-8. doi: 10.1016/j.encep.2012.11.003. Epub 2013 Jan 23.

引用本文的文献

1
Exposing the latent phenotype of Gulf War Illness: examination of the mechanistic mediators of cognitive dysfunction.揭示海湾战争综合征的潜在表型:认知功能障碍的机制中介因素研究。
Front Immunol. 2024 Jun 11;15:1403574. doi: 10.3389/fimmu.2024.1403574. eCollection 2024.
2
Basal forebrain cholinergic systems as circuits through which traumatic stress disrupts emotional memory regulation.基底前脑胆碱能系统作为创伤应激破坏情绪记忆调节的回路。
Neurosci Biobehav Rev. 2024 Apr;159:105569. doi: 10.1016/j.neubiorev.2024.105569. Epub 2024 Feb 1.
3
Modeling Neuroimmune Interactions in Human Subjects and Animal Models to Predict Subtype-Specific Multidrug Treatments for Gulf War Illness.
在人类受试者和动物模型中模拟神经免疫相互作用,以预测海湾战争病的亚型特异性多药物治疗。
Int J Mol Sci. 2021 Aug 9;22(16):8546. doi: 10.3390/ijms22168546.
4
Is PTSD-Phenotype Associated with HPA-Axis Sensitivity? Feedback Inhibition and Other Modulating Factors of Glucocorticoid Signaling Dynamics.创伤后应激障碍表型是否与 HPA 轴敏感性相关?糖皮质激素信号转导动力学的反馈抑制和其他调节因素。
Int J Mol Sci. 2021 Jun 3;22(11):6050. doi: 10.3390/ijms22116050.
5
Acetylcholinesterase inhibitor exposures as an initiating factor in the development of Gulf War Illness, a chronic neuroimmune disorder in deployed veterans.乙酰胆碱酯酶抑制剂暴露可作为海湾战争疾病(一种在部署的退伍军人中发生的慢性神经免疫疾病)发展的起始因素。
Neuropharmacology. 2020 Jul;171:108073. doi: 10.1016/j.neuropharm.2020.108073. Epub 2020 Apr 2.
6
Progression of intervention-focused research for Gulf War illness.干预聚焦型海湾战争疾病研究进展。
Mil Med Res. 2019 Oct 18;6(1):31. doi: 10.1186/s40779-019-0221-x.
7
Altered Pituitary Gland Structure and Function in Posttraumatic Stress Disorder.创伤后应激障碍中垂体结构和功能的改变
J Endocr Soc. 2017 Apr 13;1(6):577-587. doi: 10.1210/js.2017-00069. eCollection 2017 Jun 1.
8
Recent research on Gulf War illness and other health problems in veterans of the 1991 Gulf War: Effects of toxicant exposures during deployment.近期关于1991年海湾战争退伍军人的海湾战争综合症及其他健康问题的研究:部署期间接触有毒物质的影响。
Cortex. 2016 Jan;74:449-75. doi: 10.1016/j.cortex.2015.08.022. Epub 2015 Sep 25.
9
Butyrylcholinesterase genotype and enzyme activity in relation to Gulf War illness: preliminary evidence of gene-exposure interaction from a case-control study of 1991 Gulf War veterans.丁酰胆碱酯酶基因型和酶活性与海湾战争综合征的关系:来自1991年海湾战争退伍军人病例对照研究的基因-暴露相互作用的初步证据。
Environ Health. 2015 Jan 9;14:4. doi: 10.1186/1476-069X-14-4.
10
Reduced peripheral expression of the glucocorticoid receptor α isoform in individuals with posttraumatic stress disorder: a cumulative effect of trauma burden.创伤后应激障碍个体外周糖皮质激素受体 α 亚型表达减少:创伤负担的累积效应。
PLoS One. 2014 Jan 21;9(1):e86333. doi: 10.1371/journal.pone.0086333. eCollection 2014.