脓毒症早期大鼠肾上腺TLR4、TNF-α mRNA表达、超微结构变化及地塞米松干预影响
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摘要
目的:脓毒症合并相对肾上腺皮质功能不全与多器官功能障碍综合征的发生密切相关,显著增加脓毒症患者的病死率。Marik报道危重患者相对肾上腺皮质功能不全(relative adrenal insufficiency,RAI)的总体发病率为30% ~40%,脓毒症休克患者可高达60%,严重影响患者的预后。为此,早期识别及积极干预脓毒症及脓毒症休克合并RAI患者,对改善预后意义重大。但是,目前脓毒症合并RAI的发病机制尚不很清楚,伴随肾上腺皮质功能不全的发生是否存在相应的组织形态学改变,国内外尚无明确报道。小剂量糖皮质激素能显著降低脓毒症休克合并急性肾上腺皮质功能不全患者的病死率,改善预后。但目前糖皮质激素应用的时机、剂量、具体疗程均存在争议。本实验通过观察脓毒症早期大鼠的血清皮质醇浓度、肾上腺组织Toll样受体4(TLR4)、肿瘤坏死因子α(TNF-α) mRNA的表达、组织微观结构变化以及不同时间应用小剂量地塞米松对其干预的影响,判别脓毒症早期是否存在相对肾上腺皮质功能不全,并探讨其可能的发病机制,以及地塞米松替代治疗的时机,以期为临床积极治疗脓毒症及脓毒症休克,降低病死率提供有利的实验依据。
     方法:脓毒症动物模型采用盲肠结扎穿孔法(cecal liga- tion and puncture,CLP)复制,小剂量促肾上腺皮质激素(ad- renocor- ticotropic hormone,ACTH)刺激试验判断脓毒症早期大鼠肾上腺皮质的功能状态,以ACTH刺激前后血清皮质醇浓度无显著差异,定义为RAI。实验动物选择健康雄性清洁级Wistar大鼠260只(607123),体重250~300g,随机分为5组:(1)正常对照组(n=50);(2)假手术组(n=50):仅打开腹腔,不做CLP;(3)模型组(n=50):仅做CLP ;(4)地塞米松预先给药组(n=50):CLP术前腹腔注射地塞米10mg.kg-1;(5)地塞米松治疗组(n=50):CLP术后7h腹腔注射地塞米松10mg. kg-1。各组均分2h、4h、6h、8h、12h五个时间点,每个时间点10只大鼠。每组按时间点留取肾上腺,液氮保存做半定量RT-PCR检测TLR4、TNF-αmRNA的表达。各组8h、12h时间点动物做ACTH刺激试验,均于术后(CLP/单纯开腹术)6h腹腔注射ACTH 0.8μg.kg-1,于注射前、后30min经颈总动脉测压管采血,分别记做T0、T30,留取血清,-70℃冻存,采用液相平衡放射免疫分析法(radioimmunoa- ssay,RIA)测定血清中皮质醇浓度。此外,随机选取各组大鼠各2只,于CLP /开腹术后12h行1%多聚甲醛经主动脉灌注固定留取肾上腺皮质,做电镜切片。模型组、地塞米松预先给药组和治疗组动物做12h生存率的统计(按时间点处死的动物除外)。用SPSS11.5统计分析软件进行统计学分析,数据用均数±标准差(x±s)表示,计量资料行单因素方差分析及配对t检验,计数资料行多个样本率比较的x2检验,P<0.05为有统计学意义。
     结果:
     1各组ACTH刺激前血清皮质醇浓度的比较:
     模型组(13.84±4.42ng/ml)、地塞米松预先给药组(20.83±6.58ng/ml)和地塞米松治疗组(12.60±3.07ng/ml)ACTH注射前血清皮质醇浓度明显高于正常对照组(9.80±2.27ng/ml)和假手术组(8.32±2.09ng/ml)(P<0.05);而地塞米松预先给药组明显高于模型组和地塞米松治疗组(P<0.05)。
     2各组ACTH刺激前、后血清皮质醇浓度变化的比较:
     正常对照组和假手术组腹腔注射ACTH后30分钟血清皮质醇浓度(T30)较注射ACTH前(T0)明显升高(13.91±2.56 ng/ml vs 9.80±2.27ng/ml;9.41±2.83ng/ml vs8.10±1.86ng/ml),具有统计学差异(P<0.05);模型组、地塞米松预先给药组和地塞米松治疗组T30血清皮质醇浓度与T0无明显差异。
     3各组肾上腺组织TLR4、TNF-αmRNA表达的比较:
     模型组TLR4、TNF-αmRNA的表达均明显升高,TLR4于4h达高峰,TNF-α于2h即达高峰,12h两者均保持在较高水平。地塞米松预先给药组TLR4、TNF-αmRNA的表达2h均较模型组明显下降(P<0.05),但仍显著高于假手术组(P<0.05), 4h TLR4、TNF-αmRNA的表达与假手术组没有差异, 12h TLR4、TNF-αmRNA的表达明显高于假手术组(P<0.05);地塞米松治疗组TLR4、TNF-αmRNA于8、12h的表达较模型组明显下降,但仍显著高于假手术组(P<0.05)。
     4各组肾上腺组织超微结构变化的比较:
     模型组、地塞米松预先给药组和地塞米松治疗组大鼠肾上腺皮质束状带细胞均出现脂质耗减、髓鞘样小体以及管泡状嵴的线粒体嵴和膜部分或全部溶解消失的组织形态结构改变,其中以模型组为著。
     5各组大鼠12h生存率的比较:
     地塞米松预先给药组12h生存率(76.92%)明显高于模型组(33.33%)(P<0.01)和地塞米松治疗组(40%)(P<0.05),地塞米松治疗组12h生存率显著高于模型组(P<0.05)。
     结论:
     1脓毒症早期即存在相对肾上腺皮质功能不全。
     2脓毒症早期合并RAI大鼠肾上腺组织TLR4、TNF-αmRNA的表达明显升高,可能与脓毒症伴RAI的发生有关。
     3脓毒症早期合并RAI大鼠肾上腺组织TNF-αmRNA的表达高峰明显早于TLR4,由此推测,LPS引起炎性因子的释放可能并不完全依靠TLR4的识别。
     4脓毒症早期合并RAI大鼠肾上腺组织超微结构发生了代谢性改变,影响皮质醇的合成与分泌,可能参与了脓毒症早期相对肾上腺皮质功能不全的发生。
     5小剂量地塞米松治疗可以降低肾上腺组织TLR4、TNF-αmRNA的表达,减轻肾上腺组织超微结构变化,提高12h生存率,改善预后。
     6小剂量地塞米松早期应用效果更理想,为有效控制炎性反应,需重复给药。
Objective: Sepsis ensuing relative adrenal insufficiency was related closely to multiple organ dysfunction syndromes, increasing significantly case fatality of sepsis. Marik reported that the total morbility of relative adrenal insufficiency of critically ill patients was 30%~40%, while septic shock patients was 60%, influencing prognosis of patients. Therefor, it is important to discriminate and interfere with RAI in sepsis and septic shock patients and improve prognosis. But, now mechanisms of relative adrenal insufficiency with sepsis dot not understand yet, few definite studies both home and abroad have reported that whether the corresponding changes of morphologicfunctional status exsisted following the occurance of organ dysfunction.
     Low-dose glucocorticoid could degrade obviously case fatality of acute adrenal insufficiency with septic shock patients, improve prognosis.Howere, dispution exist yet on oppor- tunity,dosage, time of glucocorticoid therapy. This study investigate serum cortisol concentration, the expression of Toll-like receptor-4 and tumour necrosis factor-αmRNA, changes of tissue micstruture in adrenal glands in rat in the early phases of sepsis and effects of Dexamethasone with the same dosage (low-dose) at different time, discriminate relative adrenal insufficiency in the early phases of sepsis ,and approach probalble mechanisms of that and time of glucocorticoid replactment therapy, And looking forward to providing favorable exparimental evidence for the clinical treatment ,case fatality degression of sepsis and sepsis shock.
     Methods: The sepsis animal model used cecal ligation and puncture (CLP) to replicate and adopted the low-dose adrenocorticotropic hormone (ACTH) stimulated test to evaluate adrenal function of sepsis animals,it is difinfy RAI that serum cortisol concentration was not significant deviation between before and after ACTH stimulation. 260 healthy male wistar rats with weight 250~300g were chosen and divided into five groups on random: (1) normal control group (n=50); (2) sham group (n=50): only cut open the celiac without CLP;(3) model group (n=50): only CLP; (4) Dexprevention group (n=50): injected 10mg.kg-1 dexamethasone into the abdominal cavity before CLP; (5) Dextreatment group (n=50): injected 10mg.kg-1 dexamethasone into the abdominal cavity 7 hours after CLP. Every group sets up five time points of 2h, 4h, 6h, 8h and 12h, every of which had 10 rats, collected adrenal according to time points of every group, stored in liquid nitrogen and detected the expressions of TLR4 and TNF-αmRNA with semiquantitative RT-PCR. The rats of time points of 8h and 12h were all injected ACTH (0.8μg.kg-1) into the abdominal cavity 6h after CLP. Before injection and 30min later, collected blood samples from arteria carotis communis catheter as T0, T30. Blood serum was stored in - 70℃and detected cortisol with radioimmuno- assay(RIA). In addition, two rats of every group were chosen on random and fixed with 1% paraformaldehyde by aorta perfusion at 12h after CLP/ open the celiac. And adrenal were taken to be electron microscopic section. Add up the survival rate of 12h of model,Dexprevention and Dextreatment groups.(without rats executed according to points.) Measurement data were presen- ted as?x±s and analyzed with indendpent-sample One- Way ANOVA and paired-sample t test , numeration data analyzed with multiple-sample ratio x2-test using SPSS 11.5 statistical program. A level of P<0.05 was considered to be statistically significant.
     Results
     1 Comparion of serum cortisol concentration before ACTH stimulation of rats.
     The levels of T0 of model(13.84±4.42ng/ml), Dex- prevention(20.83±6.58ng/ml) and Dextreatment groups (12.60±3.07ng/ml) were respectively higher than that of normal control and sham groups; and the levels of that of Dexprevention group was higher than that of model and Dextreatment groups respectively(P<0.05).
     2 Comparion of changes of serum cortisol concentration of rats between before and after ACTH stimulation.
     The cortisol levels of blood serum at 30min after ACTH stimulation(T30) of normal control and sham groups were higher than that of before ACTH stimulation(T0)(13.91±2.56 ng/ml vs 9.80±2.27 ng/ml;9.41±2.83 ng/ml vs8.10±1.86 ng/ml), there was statistical significance(P<0.05); While there was no statistical significance to differencite the cortisol levels of blood serum at T30 after ACTH stimulation and that at T0 of model, Dexprevention and Dextreatment groups.
     3 Comparion of the expressions of TLR4 and TNF-αmRNA in adrenal glands of rats.
     The expressions of TLR4 and TNF-αmRNA of model group obviously elevated, TLR4 reached the peak 4 hours after CLP, TNF-αreached the peak 2 hours , maintaining high level at 12 hours after CLP.the expressions of TLR4、TNF-αmRNA of Dexprevention group both were lower significantly than model group at 2h(P<0.05),but was higher than sham group, there was no statistics difference witn sham group at 4h, it was higher than sham group at 12h too(P<0.05); The expressions of TLR4、TNF-αmRNA of Dextreatment group both degraded obviously than model group at 8h and 12h,but it was higher than that of sham group (P<0.05).
     4 Comparion of the changes of ultramicrostructure of adrenal cortex of rats.
     In the groups of model, Dexprevention and Dextreatment, adrenocortical fascicular zone of rats presented the histological changes of lipid droplets lossing and myelin bodies as well as the mitochondrial tracheid crista and intima partly or completely dissolved and disappeared. especially model group.
     5 Comparion of survival rate of 12h of rats.
     The survival rate of 12h in Dexprevention group(76.92%) was higher than Dextreatment group(40%) and Model group(33.33%) (P<0.05),Dextreatment group was higher than model group(P<0.05).
     Conclusion:
     1 The rats had adrenal insufficiency at early stage of sepsis.
     2 The expressions of TLR4、TNF-αmRNA in adrenal glands of rats with early stage of sepsis complicating adrenal insufficiency evidently ascended, was concerned with the occurrence of relatve adrenal insufficiency with sepsis possibly.
     3 The peak of expression of TNF-αmRNA is higher obviously than TLR4 of rats with early stage of sepsis complicating relative adrenal insufficiency, it is supposed that releasing of inflammatory factor by LPS didn,t at all dependent on identification by TLR4.
     4 Adrenal gland would have metabolic structural changes in the rats with early stage of sepsis complicating relative adrenal insufficiency, influence synthesis and secretion of cortisol, participate in the occurrence of relative adrenal insufficiency at early stage of sepsis.
     5 low-dose Dexamethasone therapy could effectively increase the survival rate of 12 hours, improve outcome through down-regulating the expression changes of TLR4,TNF-αmRNA and lessening changes of ultramicro-structure of adrenal glands.
     6 Low-dose Dexamethasone application early showed best effects, in order to control effectively inflammatory reaction, this need to dosage again and again.
引文
1 Marik PE, Kiminyo K, Olexo S, et al: Occult adrenal insufficiency in critically ill patients :An underdiagnosed entity. Crit Care Med,1999, 27:141
    2 Annane D,Sebille V,Charpentier C,et al.Effect of treatment with low doses of hydrocortisone and fludrocortisoneon mortality in patients with septic shock〔J〕.JA MA, 2002, 288:862-871
    3 Douglas J. Koo, BA; David Jackman, MD. Adrenal insufficiency during the late stage of polymicrobial sepsis Crit Care Med 2001; 29:618–622
    4 Bollaert P, Charpentier C, Levy B, et al: Reversal of late septic shock with suprap-hysiologic doses of hydrocor- tisone. Crit Care Med,1998,26:645–650
    5 Bollaert P, Fieux F, Charpentier C, et al: Baseline cortisol levels, cortisol response to corticotropin and prognosis in late septic shock. Shock, 2003,19:13–15
    6 Annane D, Sebille V, Charpentier C, et al: Effect of treatment with low doses of hydrocortisone and fludroco- rtisone on mortality in patients with septic shock. JAMA, 2002, 288: 862–871
    7 Angus DC,Wax RS.Epidemiology of sepsis: unupdate〔J〕. Crit Care Med, 2001,29: 109-116
    8 Lien E,Ingalls RR.Toll-like receptors.Crit Care Med, 2002, 30:S1-S11
    9 Betancur C, Borrell J, Guaza C: Cytokine regulation of corticosteroid receptors in the rat hippocampus: Effects of interleukin-1, interleukin-6, tumor necrosis factor and lipopolysaccharide. Neuroendocrinology ,1995,62:47–54
    10 Briegel J, Kellermann W, Forst H, et al: Low dose hydrocortisone infusion attenuates the systemic inflamm- atory response syndrome.Clin Investig, 1994, 72: 782 – 787.
    11 William J. Hubbard, Mashkoor Choudhry, Martin G. Schwacha et al. Cecal Ligation and Puncture. Shock, 2005, 24: 52-57
    12 Watts JA, Kline JA, Thornton LR, et al.Metabolic dysfunction and depletion of mitochondria in hearts of septic rats. J Mol Cell Cardiol , 2004,36:141–150
    13 Chaudry IH , Wichterman KA , Baue AE. Effect of sepsis on tissue adenine nucleotide levels. Surgery, 1979, 85: 205- 211
    14 Valérie Siraux, MD. Relative adrenal insufficiency in patients with septic hock: Comparison of low-dose and conventional corticotropin tests Crit Care Med 2005; 33: 2479– 2486
    15 Lowniak JV, Loriaux DL.Adouble-blind study of perioperative steroid requirements in secortdary adrenal insufficiency [J].Surgery,1999, 121:123-129
    16 Zaloga GP , Marik P. Hypothalamic-pituitary-adrenal insufficiency[J] Critical Care Clinicl,2001,17: 25-42
    17 Marik PE, Zaloga GP: Adrenal insufficiency during septic shock. Crit Care Med , 2003, 31: 141– 145
    18 Range-Frausto MS,Pitte tD,Costigan M,etal.The natural History of the systemic inflammatory response syndrome (SIRS) . A prospective study [J]. JAMA, 1995, 273: 117 -123
    19 Zaloga GP, Bhatt B, Marik PE. Critical illness and systemic inflammation. In: Becker K, Nylen E, eds. Practice and principles of endocrinology and metablism. Philadelphia, PA: Lippincott, Williams, and Wilkins, 2001,2068-2076
    20 周涛,樊寻梅.急性呼吸窘迫综合征及脓毒症的机体防御反应与糖皮质激素.中华儿科杂志,2003,41(8):632-635
    21 Turnbull AV, Rivier CL. Regulation of the hypothalamic -pituitary-adrenal axis by cytokines:actions and mechanis- ms of action. Physiol Rev ,1999,79:1-71
    22 Gaillard RC, Turnill D, Sappino P, et al. Tumor necrosis factor α inhibits the hormonal response of the pituitary gland to hypothalamic releasing factors. Endocrinology, 1990,127:101-106
    23 Mastrorakos G, Chrousos GP, Weber JS. Recombinant interleukin 6 activate the hypothalamic -pituitary- adrenal axis in humans. J Clin Endocrinol Metab, 1993, 77: 1690- 1694
    24 Sharshar T, Gray F, Lorin de la Grandmaison G, et al: Apoptosis of neurons in cardiovascular autonomic centres triggered by inducible nitric oxide synthase after death from septic shock. Lancet 2003, 362:1799-1805
    25 Kai Zacharowsk Paula A et al. Toll-like receptor 4 plays acrucial role in theimmune–adrenal response to systemic inflammatory response syndrome. Samuel M. McCann, April 18, 2006 103 (16) :6392–6397
    26 Fan I, Kapus A, Marsden PA etal. Regulation of toll-like receptor4 expression in the lung following hemorrhagic shock and lipopolysaccharide. J Immunol, 2002,168 5252 – 5259
    27 李红云,姚咏明,盛志勇.Toll 样受体与脓毒症的研究进展.中华烧伤杂志,2002,18:314-317
    28 Kirschning CJ, Bauer S.Toll-like receptors:cellular signal Transducers for exogenous molecular patterns causing immune responses. Int J Med Microbiol 2001, 291: 251-260.
    29 Wolfs TG ,Buurman WA , van Schadewijk A , et al . In vivo expression of Toll-like receptor 2 and 4 by renal epithelial cells : IFN-gamma and TNF-αlpha mediated up-regulation during inflammation. J Immunol,2002 ,168 (16): 1286-1292
    30 鄢小建,姚咏明,董宁等.腹腔感染所致多器官损害与 Toll样受体 2 基因表达的关系.中华实验外科杂志, 2003, 20(1):36-38
    31 Philip E. Knapp, Seth M. Arum and James C. Melby. Relative adrenal insufficiency in critical illness: a reviewof the evidence. Current Opinion in Endocrinology & Diabetes 2004; 11:147 – 152
    32 Merryn singer, Vincenzo DE Santis, Domenico Vitale, William Jeffeoate. Multiorgan failure is an adaptive, endocrine-mediated, metabolicresponse to overwhelmingsystemic inflammation. Lancet, 2004, 64: 545-548
    33 许贤豪.神经免疫学.湖北科学技术出版社,2000,429-430
    34 成苓如.组织学人民卫生出版社, 1992 , 787
    35 Briegel J,Forst H,Haller M,etal. Stress doses of hydrocortisone to reverse hyperdynamic septic shock: a prospective, randomized, double-blind,single-center study. Crit Care Med, 1999, 27: 723- 732
    36 Keh D, Boehnke T, Weber-Cartens S,et al. Immunologic and hemodynamic effects of“low-dose”hydrocortisone in septic shock.Am J Respir Crit Care Med, 2003, 167: 512 – 520
    37 Dellinger RP, Carlet JM, Masur H, et al.: Surviving Sepsis Campaign guidelines for management of severe sepsis and septic shock. Crit Care Med 2004, 32:858-873
    38 Annane D, Bellissant E, Bollaert PE, Briegel J, Keh D, Kupfer Y: Corticosteroids for severe sepsis and septic shock: a system-atic review and meta-analysis. BMJ. 2004 August 28; 329(7464): 480
    39 Annane D, Sebille V, Charpentier C, et al: Effect of treatment with low doses of hydrocortisone and fludrocortisone on mortality in patients with septic shock. JAMA, 2002, 288: 862–871
    40 Peter C. Minneci, MD; Katherine J. Deans, MD; Steven M. Banks, PhD,et al. Meta-analysis: The effect of steroids on survival and shock during sepsis depends on the dose. Ann Intern Med. 2004;141:47-56
    41 Marik PE. Mechanisms and clinical consequences of critical illness associated adrenal insufficiency. Curr Opin Crit Care. 2007 Aug;13(4):363-9
    42 Wolfs TG, Buurman WA,van Schadewijk A,et al.In vivo expression of Toll-like receptor 2 and 4 by renal epithelial cells: IFN-gamma and TNF-αlpha mediated up-regulation during inflammation [J]. J Immunol, 2002 ,168:1286
    43 Rivers E,Nguyen B,Havstad S,et al.Early goal-directed therapy in the treatment of severe sepsis and septic sho(J).N Engl J Med,2001,345:1368-1377 
    1 Bollaert P, Fieux F, Charpentier C, et al: Baseline cortisol levels, cortisol response to corticotropin and prognosis in late septic shock. Shock, 2003,19:13–15
    2 Annane D, Sebille V, Charpentier C, et al: Effect of treatment with low doses of hydrocortisone and fludrocortisone on mortality in patients with septic shock. JAMA, 2002, 288: 862–871
    3 Langer M, Modi PB, Agus M. Adrenal insufficiency in the critically ill neonate and child. Curr Opin Pediatr. 2006;18:448-53
    4 齐宇洁 樊寻梅 严重脓毒症及脓毒症休克患者的相对肾上腺功能不全的研究进展。中华儿科杂志 2004 年 9 月第
    42 卷 第 9 期 Chin J Pediatr, Septmber 2004, Vo l42,No 19 673 -676
    5 Augus DC,Linde Z warble WT,Lidicker J,et al. pidemiology of severe Sepsis in the United States: analysis of incidence, utcome,and associated costs of care.Crit Care Med, 2001, 29: 1303-1310
    6 Alberti C,Brun Buisson C,Burchardi H,et al.Epidemiology of sepsis And infectionin ICU patients from an international lmulticenter cohort Study. Intensive Care Med, 2002, 28: 108-121
    7 NICE: An Appraisal of Drotrecogin Alpha (activated) and Sepsis 2004
    8 Flaatten H. Epidemiology of sepsis in Norway in 1999..Crit Care. 2004; 8:R180 –R 184.: 321-324
    9 Silva E, de Almeida Pedro M, Sogayar ACB, et al. Brazil-ian Sepsis Epidemiological Study (BASES study). Crit Care. 2004;8:R251–R260
    10 van Gestel A, Bakker J, Veraart CPWM, van Hout BA.Prevalence and incidence of severe sepsis in Dutch in-tensive care units. Crit Care. 2004; 8: R153–R162
    11 The Intensive Care National Audit and Research Centre (ICN-ARC): Prevalence of Severe Sepsis Between 1995 and 2000 from 91 Adult ICUs in England, Wales and Northern Ireland 2003
    12 Annane D,Sebille V,Troche G,et al.A 3-level prognostic classification in sepsis shock based on cortisol level and cortisol response to corticotropin.JAMA,2000,283(8):1038-1045
    13 Didier Keh,Charlse L.Use of corticosteroid therapy in patients with sepsis and septic shock:an evidence-based review.Crit Care Med,2004,32(1):527-533
    14 Hatherill M,Tibby SM,Hilliard T,etal. Adrenal insufficiencyin septic shock.Arch Dis Child,1999,80:51-55
    15 Menon K,Clarson C.Adrenal function in pediatric critical illness Pediatr Crit Care Med,2002,3:112-116
    16 Pizarro CF, Troster EJ, Damiani D, Carcillo JA. Absolute and relative adrenal insufficiency in children with septic shock. Crit Care Med. 2005;33:855-859
    17 Pizarro CF. Insuficiência adrenal absoluta e relativa emcri an?ascom sepse grave e choque séptico [disserta??o]. S?o Paulo:Faculdade de Medicina da Universidade de S?o Paulo; 2004
    18 Lamberts SW, Bruining HA, deJong FH. Corticosteroid therapy in severe illness. N Engl J Med, 1997, 337: 1285- 1292
    19 Mackenzie JS, Burrows L, Burchard KW. Transient hypo- adrenalism during surgical critical illness.Arch Surg, 1998, 133:199-204
    20 Hamrahian A H, Oseni T S, Arafah B M. Measurements of serum free cortisol in critically ill patients [J].N Engl J Med, 2004,350:1629-1638
    21 Chrousos GP. The hypothalamic-pituitary-adrenal axis and immune mediated inflammation.N Engl J Med, 1995, 332: 1351-1362
    22 Wang P, Ba ZF, Jarrar D, Cioffi WG, Bland KI, Chaudry IH. Mechanism of adrenal insufficiency following trauma and severe haemorrhage. Role of hepatic 11 b-hydroxysteroid dehydrogenase. Arch Surg 1999; 134: 394-401
    23 Turnbull AV, Rivier CL. Regulation of the hypothalamic -pituitary-adrenal axis by cytokines: actions and mechanis- ms of action. Physiol Rev ,1999,79:1-71
    24 Gaillard RC, Turnill D, Sappino P, et al. Tumor necrosis factor α inhibits the hormonal response of the pituitary gland to hypothalamic releasing factors. Endocrinology, 1990, 127: 101-106
    25 Jaattela M, Ilvesmaki V, Voutilainen R,et al. Tumor necrosis factor as a potent inhibitor of adrenocorticotropin-induced cortisol production and steroid- ogenic P450 enzyme gene expression in cultured human fetal adrenal cells. End- ocrinology , 1991, 128: 623 -629
    26 Girardin E , Grau G , Dayer JM , et al. Tumor necrosis factor and interleukin-1 in the serum of children with severe infectious purpura [J].N Engl Med,1988,319:397
    27 Sharshar T, Gray F, Lorin de la Grandmaison G, Hopkinson NS,Ross E, Dorandeau A, Orlikowski D, Raphael JC, Gajdos P,Annane D: Apoptosis of neurons in cardiovascular autonomic centres triggered by inducible nitric oxide synthase after death from septic shock. Lancet 2003, 362:1799-1805
    28 Mastrorakos G, Chrousos GP, Weber JS. Recombinant interleukin 6 activate the hypothalamic-pituitary-adrenal axis in humans. J Clin Endocrinol Metab, 1993, 77: 1690- 1694
    29 Soni A,Pepper GM, Wyrwinski PM,etal.Adrenalinsufficiency occurring during septic shock: Incidence, outcome,and relation ship to peripheral cytokine levels. Am J Med,1995,98:266-271
    30 Gonzalez-Hernandez JA, Bornstein SR, Ehrhart- Bornstein M,etal.Interleukin-6 messenger ribonucleic acid expression in human adrenalgland in vivo: new clue to a paracrine or autocrine regulation of adrenal function. J Clin Endocrinol Metab,1994,79:1492-1497
    31 Gonzalez-Hernandez JA, Ehrhart-Bornstein M, Spath- schwalbe E,etal. Human adrenal cells express tumor necrosis factor-alpha messenger ribonucleic acid: evidence for paracrine control of adrenal function.J Clin Endocrinol Metab, 1996,81:807-813
    32 Melby JC, Egdahl RH, Spink WW. Secretion and metabolism of cortisol after injection of endotoxin. J Lab Clin Med 1960;56:50-62
    33 Catalano RD, Parameswaran V, Ramachandran J,et al. Mechanism of adrenocortical depression during Escherichia coli shock. Arch Surg 1984;119:145-150
    34 Keri G, Parameswaran V, Trunkey DD, et al. Effects of septic shock plasma on adrenocortical cell function.Life Sci 1981;28:1917-1923
    35 Marik PE,Zaloga GP.Adrenal insufficiency during septic shock.Crit Care Med,2003,31(1):141-145
    36 Reichardt HM, Umland T,Bauer A,et al.Mice with an increased Glucocorticoid receptor gene dosage showenhance dresistance to stress And endotoxic shock. Mol Cell Biol,2000,20:9009-9017
    37 Meduri GU,Tolley EA,Chrousos GP,et al.Prolonged methyl-prednisolone treatment suppresses systemic inflame- mation in patients with unresolving acute respiratory distress syndrome:evidence for inadequate endogenous glucocor- ticoid secretion and inflammationinduced immune cell resistance to glucocorticoids. Am J Respir Crit Care Med,2002,165(7):983-991
    38 Beishuizen A,Thijs LG,Vermes I.Patterns of corticosteroid -binding globulin and the free cortisol index during septic shock and multitrauma.Intensive Care Med,2001,27(10):1584-1591
    39 McCallum RE, Stith RD. Endotoxin-induced inhibition of steroid binding by mouse liver cytosol.Circ shock 1982; 9:357-367
    40 刘大为,崔娜. 糖皮质激素在严重感染和感染性休克中的应用. 中国危重病急救医学.2005;17:241-243
    41 Biffl WL, Moore EE, Moore FA, et al: Interleukin-6 in the injured patient: Marker of injury or mediator of inflammation. Ann Surg 1996; 224:647–664
    42 Melby JC, Spink WW. Comparative studies of adrenal cortisol function and cortisol metabolism in healthy adults and in patients with septic shock due to infection. J Clin Invest 1958;37:1791-1798
    43 KNUEFERMANN P,NEMOTO S,BAUMGARTEN G,etal.Cardiac inflammation and innate immunity in septic shock:is there a role for Toll-like receptors? [J]. Chest, 2002, 121(4):1329-1336
    44 Wolfs TG, Buurman WA, Van Schadewijk A, et al. In vivo expression of Toll-like receptor 2 and 4 by renal epithelial cells: IFN-gamma and TNF-alpha mediated up-regulation during inflammation.J Immunol, 2002, 168: 1286~1293
    45 鄢小建,姚咏明,董宁,等.腹腔感染所致多器官损害与 Toll样受体 2 基因表达的关系.中华实验外科杂志,2003,20: 36~38
    46 Kai Zacharowsk Paula A et al. Toll-like receptor 4 plays a crucial role in theimmune–adrenal response to systemic inflammatory response syndrome. Samuel M. McCann, April 18, 2006 103 (16) :6392–6397
    47 Briegel Meduri GU, Chrousos GP. Duration of gluco- corticoid treatment and outcome in sepsis: istheright drug used the wrong way (editorial)? Chest, 1998, 114: 355-360
    48 Bennett N,Gabrielli A.Hypotension and adrenal insufficiency. J Clin Anesth, 1999, 11:425-430
    49 Beishuizen A , Thijs LG , Vermes I.Decreased levels of dehydroepiandrosterone sulphate in severe critical illness::a sign of exhausted adrenal reserve ? Critical Care , 2002, 6: 434-438
    50 Marik PE,Zaloga GP. Adrenal insufficiency in the critically ill:a new look at an old problem〔J〕.Chest, 2002, 122: 1784- 1796
    51 Burry LD,Wax RS.Role of corticosteroid in septic shock[J]. Ann Pharmacother,2004,38:464-472
    52 Richards ML, Caplan RH,Wickus GC, etal. The rapid low-dose (1mg)cosynthropin test in the immediate post- operative peroid:Results in elderly subjects after major abdominal surgery [J]. Surgery, 1999, 125: 431-440
    53 Zaloga GP,Marik P.Hypothalamic-pituitary-adrenal insuffici- ency [J].Critical Care Clinicl, 2001, 17:.25-41
    54 Nicholson G,Bunin JM,Hall GM.Peri-operative steroid supplementation [J]. Anaesthesia, 1998, 53: 1091 -1104
    55 Dickstein G: The assessment of the hypothalamo-pituitary- adrenal axis in pituitary disease: Are there short cuts? J Endocrinol Invest 2003; 26:25–30
    56 Oelkers W. The role of high and low–dose corticotropin tests in the dagnosis of secondary adrenal insufticiency [J] .Eur J Endocrino. 1998; 139: 567- 570
    57 Kozyra EF, Wax RS, Burry LD. Can 1 microg of cosyntropin beused to evaluate adrenal insufficiency in critically ill patients [J]?Ann Pharma-cother, 2005, 39(4): 691-698
    58 Siraux V, DeBacker D,Yalavatti G,et al. Relative adrenal insufficiency in patients with septic shock: comparison of low-dose and conventional corticotrophin tests [J]. Crit Care Med, 2005, 33(11): 2479-2486
    59 Cooper MS, Stewart PM. Corticosteroids insufficiency in acutely ill patients. N Engl J Med. 2003;348:727-34
    60 Ligtenberg JJ,Zijlstra JG.The relative adrenal insufficiency syndrome revisited:which patients will benefit from low-dose steroids[J]?Curr Opin Crit Care, 2004, 10(6): 456- 460
    61 任少华,胡华成.急性呼吸窘迫综合征患者防御反应和糖皮质激素治疗的研究[J].中国危重病急救医学,2001, 13:121-123
    62 Matsumura M,Kakishita H,Suzuki M,et al.Dexamethasone suppresses iNOS gene expression by inhibiting NF-κB in vascular smooth muscle cells[J].Life Sci,2001, 69: 1067- 1077
    63 Annane D,Cavaillon J M. Corticosteroids in sepsis:from bench to bedsid〔J〕? Shock, 2003, 20:197-207
    64 Perla D, Marmorston J. Suprarenal cortical hormone and salt in the treatment of pneumonia nd other severe infections.Endocrinology. 1940;27:367-74
    65 Hahn EO, Houser HB, Rammelkamp CH Jr, Denny FW,Wannamaker LW. Effect of cortisone on acute streptococcal infections and post-streptococcal compli- cations. J Clin Invest. 1951; 30:274-81
    66 Matot I, Sprung CL. Corticosteroids in septic shock: ressurrection of the last rites? Crit Care Med. 1998; 26: 627-30
    67 Sessler CN. Steroids for septic shock: back from the dead? (Con). Chest. 2003;123:482S-9S
    68 Luce JM, Montgomery AB, Marks JD, Turner J, Metz CA,Murray JF. Ineffectiveness of high-dose methyl- prednisolone in preventing parenchymal lung injury and improving mortality in patients with septic shock. Am Rev Resp Dis. 1988;138:62-8
    69 Bone RC, Fisher CJ Jr, Clemmer TP, Slotman GJ, Metz CA,Balk RA. A controlled clinical trial of high-dose methylprednisolone in the treatment of severe sepsis and septic shock. N Engl J Med. 1987;317:653-8
    70 Cronin L,Kook DJ,CarletJ,et al. Corticosteroid treatment for sepsis: acritical appraisal and meta-analysis of the literature. Crit Care Med 1995,23:1430–1439
    71 Lefering R, Neugebauer EAM: Steroid controversy in sepsis and septicshock: a meta-analysis. Crit Care Med 1995, 23: 1294–1303
    72 Keh D, Boehnke T, Weber-Cartens S, Schulz C, Ahlers O,Bercker S, et al. Immunologic and hemodynamic effects of “lowdose” hydrocortisone in septic shock: a double- blind,randomized, placebo-controlled, crossover study. Am J Respir Crit Care Med. 2003;167:512-20
    73 Oppert M, Schindler R, Husung C, Offermann K, Gr?f KJ, BoenischO, et al. Low-dose hydrocortisone improves shock reversal and reduces cytokine level in early hyperdinamic septic shock. Crit Care Med. 2005;33:2457-64
    74 Keh D, Sprung CL. Use of corticosteroid therapy in patients with sepsis and septic shock: an evidence- based review. Crit Care Med. 2004;32:S527-33
    75 Rivers EP, Gaspari M, AbiSaad G, etal.Adrenal insufficiency inhigh risk surgical ICU patients〔J〕. Chest, 2001, 119: 889- 896
    76 Annane D, Bellissant E, Bollaert PE, Briegel J, Keh D, Kupfer Y.Corticosteroids for severe sepsis and septic shock: a systematic review and meta-analysis. BMJ. 2004; 329: 480- 489
    77 Annane D. Glucocorticoids in the treatment of severe sepsis and septic shock [J].Curr Opin Crit Care,2005,11:449-453
    78 Minneci P C. Deans K I. Banks SM, etal. meta-analysis The effect of steroids on survival and shock during sepsis depends on the dose[J]. Intem Med. 2004,141:47-56
    79 Loisa P,Rinne T,Kaukinen S.Adrenocortical function and multiple organ failure in severe sepsis.Acta Anaesthesiol Scand,2002,46(2):145-151
    80 Shapiro NI, Howell M,Talmor D.A blueprint for a sepsis protocol [J].Acad Emerg Med. 2005; 12(4): 352-359 .

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