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Patterns of mortality and causes of death in polytrauma patients--has anything changed?多发伤患者的死亡率和死亡原因模式——有变化吗?
Injury. 2009 Sep;40(9):907-11. doi: 10.1016/j.injury.2009.05.006. Epub 2009 Jun 21.
2
Autonomic innervation and regulation of the immune system (1987-2007).自主神经对免疫系统的支配与调节(1987 - 2007年)
Brain Behav Immun. 2007 Aug;21(6):736-45. doi: 10.1016/j.bbi.2007.03.008. Epub 2007 Apr 27.
3
Cecal ligation and puncture.盲肠结扎穿刺术
Shock. 2005 Dec;24 Suppl 1:52-7. doi: 10.1097/01.shk.0000191414.94461.7e.
4
Pathophysiology of polytrauma.多发伤的病理生理学
Injury. 2005 Jun;36(6):691-709. doi: 10.1016/j.injury.2004.12.037.
5
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
6
Chemical sympathectomy increases numbers of inflammatory cells in the peritoneum early in murine listeriosis.化学性交感神经切除术在小鼠李斯特菌病早期会增加腹膜中炎症细胞的数量。
Brain Behav Immun. 2002 Dec;16(6):654-62. doi: 10.1016/s0889-1591(02)00016-8.
7
Six at six: interleukin-6 measured 6 h after the initiation of sepsis predicts mortality over 3 days.六小时的六指标:脓毒症开始后6小时测量的白细胞介素-6可预测3天内的死亡率。
Shock. 2002 Jun;17(6):463-7. doi: 10.1097/00024382-200206000-00004.
8
Cytokines regulate alpha(1)-adrenergic receptor mRNA expression in human monocytic cells and endothelial cells.细胞因子调节人单核细胞和内皮细胞中α(1)-肾上腺素能受体mRNA的表达。
J Neuroimmunol. 2002 Apr;125(1-2):66-72. doi: 10.1016/s0165-5728(02)00034-6.
9
Impact of alcohol intoxication on hemodynamic, metabolic, and cytokine responses to hemorrhagic shock.酒精中毒对失血性休克时血流动力学、代谢及细胞因子反应的影响。
J Trauma. 2002 Apr;52(4):675-82. doi: 10.1097/00005373-200204000-00010.
10
Noradrenergic inhibition of TNF upregulation in hemorrhagic shock.去甲肾上腺素能对失血性休克中肿瘤坏死因子上调的抑制作用。
Neuroimmunomodulation. 2001;9(3):125-33. doi: 10.1159/000049016.

在从出血中恢复期间,感染性挑战对宿主防御反应的交感神经调节。

Sympathetic modulation of the host defense response to infectious challenge during recovery from hemorrhage.

机构信息

Department of Physiology, Louisiana State University Health Science Center, and Alcohol and Drug Abuse Center of Excellence, New Orleans, LA 70112-1393, USA.

出版信息

Neuroimmunomodulation. 2010;17(6):349-58. doi: 10.1159/000292039. Epub 2010 May 27.

DOI:10.1159/000292039
PMID:20516716
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3214917/
Abstract

BACKGROUND

Trauma/hemorrhage (TxHem) is associated with an immediate pro-inflammatory response that, if exaggerated or prolonged, is thought to contribute to the subsequent immunosuppression that characterizes the period after injury. Previously we have demonstrated that chemical sympathectomy (SNSx) accentuates this immediate pro-inflammatory response to TxHem. These findings suggest that the noradrenergic system plays a critical role in limiting the magnitude of the inflammatory response during TxHem and preserving the integrity of the host defense response to a subsequent infectious challenge during the period after TxHem.

OBJECTIVE

To examine the contribution of tissue norepinephrine to the host defense response to an infectious challenge during recovery from TxHem.

METHODS

Male Sprague-Dawley rats underwent SNSx (6-hydroxydopamine, i.p. daily for 3 days) prior to vascular catheter implantation. Conscious, unrestrained rats were subjected to traumatic injury (muscle crush) prior to a fixed-pressure hemorrhage (40 mm Hg for 60 min) and fluid resuscitation followed 24 h later by cecal ligation and puncture (CLP).

RESULTS

SNSx impaired the hemodynamic and thermoregulatory response to hemorrhage as indicated by decreased basal blood pressure, impaired blood pressure recovery during fluid resuscitation, and greater hypothermia after CLP. Furthermore, SNSx accentuated the TNF-alpha, IL-1, IL-6, and IL-10 response to TxHem + infection in plasma 6 h after CLP and in peritoneal lavage fluid 24 h after CLP.

CONCLUSION

These results indicate that the integrity of the noradrenergic system is necessary for adequate hemodynamic, thermoregulatory, and inflammatory responses to infection during the period following TxHem.

摘要

背景

创伤/出血(TxHem)与即刻的促炎反应有关,如果这种反应被夸大或延长,据认为会导致随后的免疫抑制,这是损伤后时期的特征。我们之前已经证明,化学性交感神经切除术(SNSx)会加剧 TxHem 对这种即刻促炎反应的影响。这些发现表明,去甲肾上腺素能系统在限制 TxHem 期间炎症反应的幅度以及在 TxHem 后期间维持宿主防御反应对随后感染挑战的完整性方面起着关键作用。

目的

研究组织去甲肾上腺素在从 TxHem 恢复期间对感染挑战的宿主防御反应的贡献。

方法

雄性 Sprague-Dawley 大鼠在血管导管植入前接受 SNSx(6-羟多巴胺,腹腔内每日一次,连续 3 天)。清醒、不受限制的大鼠在固定压力出血(40mmHg 持续 60 分钟)和液体复苏之前进行创伤性损伤(肌肉挤压),然后在 24 小时后进行盲肠结扎和穿孔(CLP)。

结果

SNSx 损害了出血时的血流动力学和体温调节反应,表现为基础血压降低、液体复苏期间血压恢复受损以及 CLP 后体温过低更严重。此外,SNSx 加剧了 TxHem+感染后 6 小时血浆和 24 小时腹腔灌洗液中 TNF-α、IL-1、IL-6 和 IL-10 的反应。

结论

这些结果表明,去甲肾上腺素能系统的完整性对于 TxHem 后期间感染时适当的血流动力学、体温调节和炎症反应是必要的。