脾脏T细胞凋亡及相关基因表达对脓毒症免疫功能的影响
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
目的观察脓毒症大鼠脾脏T淋巴细胞凋亡与免疫麻痹发生的相关性。观察高糖皮质激素血症及T淋巴细胞过度活化两种促凋亡因素对脾脏T淋巴细胞凋亡、凋亡相关基因mRNA表达及caspase3活性的影响,明确脓毒症时脾脏T淋巴细胞的凋亡机制及调节因素。探讨活血化瘀中药调节T淋巴细胞凋亡,改善脓毒症免疫功能的作用及机制。
     方法第一部分首先以盲肠结扎穿孔(CLP)法制备脓毒症大鼠模型,假手术组及模型组各10只,检测模型的各项生理及生化指标。然后将96只Wistar大鼠随机分为正常对照组(8只)、假手术组(8只)、脓毒症组(40只)和中药组(40只),中药组动物行CLP术后予活血化瘀中药注射。脓毒症组和中药组再分别分为4 h、8 h、24 h、36 h和48 h五个时间点。分别于术后各个时间点以ELISA法检测血清IL-2、IL-10水平,TUNEL法检测脾细胞凋亡情况,流式细胞仪检测脾脏淋巴细胞中CD_3~+细胞比例,分光光度法测定脾组织caspase3活性以及免疫组化法检测脾组织Fas、FasL、Bcl-2、Bax蛋白表达水平。第二部分提取BAB/C小鼠脾脏T淋巴细胞并培养,分别以地塞米松和活化诱导细胞凋亡(AICD)方法进行凋亡诱导。于地塞米松诱导6 h、16 h及活化诱导18 h后以流式细胞仪检测T淋巴细胞的凋亡率,并于地塞米松诱导6 h及活化诱导6 h、1 8 h后RT-PCR法检测T淋巴细胞内Fas、FasL、Bcl-2、Bax mRNA表达水平,分光光度法测定细胞内caspase3酶活性。同时观察活血化瘀中药对上述各项指标的影响。第三部分提取BAB/C小鼠脾脏T淋巴细胞并培养,观察活血化瘀中药对静息及活化T细胞增殖活性影响的MTT检测,流式细胞仪检测中药干预后静息T淋巴细胞的自然凋亡率。再分别以地塞米松和活化诱导法进行凋亡诱导,并以活血化瘀中药进行干预,RT-PCR法检测T淋巴细胞内IL-2 mRNA表达水平。
     结果第一部分实验中脓毒症组大鼠于造模后出现脾组织caspase3活性升高、细胞凋亡数增多,而脾细胞中CD_3~+细胞比例明显下降。并于造模后36 h、48 h,血清IL-2水平明显下降,IL-10水平显著升高,显示出免疫麻痹的表现。同时脓毒症组脾组织Fas、FasI、Bax表达明显增多,Bcl-2表达下降。活血化瘀中药干预后可提高IL-2水平,降低IL-10水平,减轻脾组织caspase3活化程度,减少脾细胞凋亡,并使CD_3~+细胞比例恢复正常。同时可明显降低脾组织Fas、FasL、Bax表达,促进Bcl-2表达。第二部分实验中地塞米松诱导6 h后T淋巴细胞凋亡率即明显增加,至16 h细胞较少存活。诱导6 h后T淋巴细胞内BaxmRNA表达升高,Bcl-2 mRNA表达下降,Fas mRNA表达无变化,无FasL mRNA表达。以活化诱导凋亡的T淋巴细胞于诱导18 h后细胞凋亡率明显增加,于诱导6 h时未见FasL、Bax mRNA表达,Fas、Bcl-2 mRNA表达无明显变化;于诱导1 8 h后Fas、FasL、Bax mRNA表达升高,Bcl-2mRNA表达下降,caspase3活性增高。活血化瘀中药可降低两种促凋亡因素诱导的T细胞凋亡,并可分别降低Fas、FasL、Bax mRNA表达,提高Bcl-2 mRNA表达,减轻caspase3酶活性。第三部分实验中活血化瘀中药可以促进静息及活化脾脏T淋巴细胞的增殖活性,降低静息T细胞的自然凋亡率。增加地塞米松诱导6 h后的T淋巴细胞内IL-2 mRNA表达。在活化诱导早期(6 h)促进T淋巴细胞内IL-2 mRNA表达,在晚期(18 h)减少IL-2 mRNA表达。
     结论脾脏T淋巴细胞的异常凋亡与脓毒症免疫麻痹的发生相关,并受凋亡相关蛋白调节。脓毒症状态下的高糖皮质激素血症及T淋巴细胞过度活化引起的AICD是脾脏T淋巴细胞异常凋亡的诱发因素,地塞米松诱导的凋亡受Bax、Bcl-2 mRNA表达的调节,而AICD的发生与Fas、FasL、Bax、Bcl-2 mRNA表达的改变有关。活血化瘀中药可通过调节IL-2 mRNA表达而减轻两种因素诱导的脾脏T淋巴细胞凋亡,同时可以促进T淋巴细胞的增殖活性,减轻T细胞的自然凋亡率,缓解脓毒症时的免疫麻痹。
Objective To observe the relationship between T lymphocytic apoptosis inspleen and immunoparalysis in sepsis. The effect of glucocorticoid and AICD on theT lymphocyte apoptosis in spleen, apoptotic related gene mRNA levels and theactivity of caspase3 in T lymphocyte were observed. To investigate the mechanism ofthe T lymphocyte apoptosis in sepsis and its influence factors. To investigate themechanism of HuoXueHuaYu injection regulating the apoptosis of T lymphocyte andameliorating the immunoparalysis in sepsis.
     Methods In the 1st part, the sepsis models were established by cecal ligationand puncture (CLP),and the parameters of physiology and biochemical in modelswere detected. After that, 96 wistar rats were divided into four groups: control group(n=8), sham operation group (n=8), sepsis group (n=40), and HuoXueHuaYutherapeutic group (n=40). The sepsis group and HuoXueHuaYu therapeutic groupthen divided into 4h, 8h, 24h, 36h, 48h points. The rats were killed at the point afterthe operation and evaluated the IL-2, IL-10 levels in serum by the methods of ELISA,the apoptotic cells by TUNEL, the CD_3~+ lymphocyte percent in spleen by flowcytometry, the activity of caspase3 in spleen by spectrophotometric method, and theexpression of Fas, FasL, Bcl-2, Bax proteins in spleen by immunohistochemistry. Inthe 2nd part, the T lymphocytes obtained from the spleens of BAB/C mice werecultured and induced apoptosis by dexamethasone and AICD. Apoptosis was assessedby flow cytometry at 6 h, 16 h after the stimulation of dexamethasone, and 18 hamong the AICD procesure. RT-PCR was used to evaluted the expression of Fas,FasL, Bcl-2, Bax mRNA, and the activity of caspase3 in T lymphocyte was detectedby spectrophotometric method at 6 h after the stimulation of dexamethasone, and 6 h,18 h among the AICD procesure. In the mean time the effect of HuoXueHuaYuinjection on those parameters was observed. In the 3rd part, the T lymphocytes wereobtained from the spleens of BAB/C mice and cultured with HuoXueHuaYu injectionThe MTT was measured to assessed the proliferation activity, and the natureapoptosis of T cells was investigated by flow cytometry. Dexamethasone and AICDwere used to induce apoptosis, and the IL-2 mRNA in T cells were dected by RT-PCR.
     Results In the 1 st part, the activity of caspase3 increased at 4h after the CLPoperation and there were more apoptosis appeared. Simultaneously the percent ofCD3~+ lymphocyte in spleen decreased. At 36 h, 48 h after the CLP operation, the IL-2in serum decreased and IL- 10 increased obviously. The immunoparalysis appeared. Inthe mean time, the expression of Fas, FasL, Bax in spleen increased obviously inmodel animals, otherwise the Bcl-2 decreased. After the intervention withHuoXueHuaYu injection, the IL-2 level in serum increased and the IL-10 in serumdecreased. The intervention also lightened the activity of caspase3 and the apoptosis,and made the percent of CD3~+ lymphocyte returned to normal level. The expressionof Fas, FasL, Bax reduced and Bax raised. In the 2nd part, the apoptosis of Tlymphocyte induced by dexamethasone was increased at 6 h, and there was little alivecells at 16 h. The expressions of Bax mRNA rised and the expression of Bcl-2 mRNAlessened at 6 h. There was no change in the expression of Fas mRNA, and theexpression of FasL mRNA was not detected. After the AICD, T lymphocyte apoptosisraised at 18 h. At 6 h after the AICD, there was no expression of FasL, Bax mRNA,and no change in the expression of Fas and Bcl-2 mRNA. At 18 h after the AICD, theexpressions of Fas, FasL, Bax mRNA rised and the expression of Bcl-2 mRNAlessened. The activity of caspase3 also ascended. HuoueHuaYu injection can cutdown the apoptosis induced by the two pro-apoptotic factors, make the expression ofFas, FasL, Bax mRNA decreased and Bcl-2 mRNA improved. The activity ofcaspase3 also fallen after the HuoueHuaYu injection treated. In the 3rd part,HuoXueHuaYu injection can improve the proliferation activity of T lymphocyte,lessen the nature apoptosis of T lymphocyte. HuoXueHuaYu injection can increasethe expressions of IL-2 mRNA in T lymphocyte induced by dexamethasone, promotethe expressions of IL-2 mRNA at early phase of AICD (6 h) and depress theexpressions at the late period (18 h).
     Conclusions There is a close relationship between T lymphocyte apoptosis inspleen and the immunoparalysis in sepsis models. The expression of apoptotic relatedproteins in spleen regulate the T lymphocyte apoptosis. T lymphocyte in spleen canbe induced to apoptotic by dexamethasone and AICD, and be regulated by the expression of apoptotic related gene. The apoptosis induced by dexamethasone wasregulated by the expression of Bax and Bcl-2 mRNA. The AICD of T lymophocytewas regulated by the change of Fas, FasL, Bcl-2, Bax mRNA expression.HuoueHuaYu injection can ameliorate the apoptosis through regulating the expressionof IL-2 mRNA which resulted in the improving the immune function of sepsis. It canimprove the proliferation activity of T lymphocyte, lessen the nature apoptosis of Tlymphocyte.
引文
1.Lang JD,Matute-Bello G.Lymphocytes,apoptosis and sepsis:making the jump from mice to humans]J].Critical Care,2009,13 (1):109.
    2.Shimaoka M,Park EJ.Advances in understanding sepsis]J].Eur J Anaesthesiol Suppl,2008,42:146-153.
    3.Poli-de-Figueiredo LF,Garrido AG,Nakagawa N,et al.Experimental models of sepsis and their clinical relevance]J].Shock,2008,30 (Suppl 1):53-59.
    4.姚咏明,王松柏,威力明,等.脓毒症大鼠多器官高迁移率族蛋白B1基因表达信号机制及意义[J].中华外科杂志,2006,44(13):916-920.
    5.Astiz ME,Rackow EC.Septic shock]J].Lancet,1998,351(9114):1501-1505.
    6.Oberholzer A,Oberholzer C,Moldawer LL.sepsis syndrome:understanding the role of innate and acquired immunity]J].Shock,2001,16(2):83-96.
    7.Levy MM,Fink MP,Marshall JC,et al.2001 SCCM/ESICM/ACCP/ATS/SIS International Sepsis Definitions Conference]J].Crit Care Med,2003,31(4):1250-1256.
    8.Dyson A,Singer M.Animal models of sepsis:why does preclinical efficacy fail to translate to the clinical setting?[J].Crit Care Med,2009,37(1 Suppl):S30-37.
    9.Esmon CT.Why do animal models (sometimes) fail to mimic human sepsis?[J].Crit Care Med,2004,32(5 Suppl):S219-222.
    10.Rittirsch D,Hoesel LM,Ward PA.The disconnect between animal models of sepsis and human sepsis]J].J Leukoc Biol,2007,81(1):137-143.
    11.姚咏明,盛志勇.脓毒症防治学[M].中国:科学技术文献出版社,2008:257-279.
    12.Redl H,Bahrami S.Large animal models:baboons for trauma,shock,and sepsis studies]J].Shock,2005,24(Suppl 1):88-93.
    13.Entleutner M,Traeger T,Westerholt A,et al.Impact of interleukin-12,oxidative burst,and iNOS on the survival of murine fecal peritonitis]J].Int J Colorectal Dis,2006,21 (1):64-70.
    14.Hubbard W J,Choudhry M,Schwacha MG,et al.Cecal ligation and puncture]J].Shock,2005,24(Suppl 1):52-57.
    15.Song M,Kellum JA.Interleukin-6]J].Crit Care Med,2005,33(12 Suppl):S463-S465.
    16.Turnbull IR,Javadi P,Buchman TG,et al.Antibiotics improve survival in sepsis independent of injury severity but do not change mortality in mice with markedly elevated interleukin 6 levels]J].Shock,2004,21 (2):121-125.
    17.Riedemann NC,Neff TA,Guo RF,et al.Protective effects of IL-6 blockade in sepsis are linked to reduced C5a receptor expression]J].J Immunol,2003,170(1):503-507.
    18.Singleton KD,Wischmeyer PE.Distance of cecum ligated influences mortality,tumor necrosis factor-alpha and interleukin-6 expression following cecal ligation and puncture in the rat]J].Eur Surg Res,2003,35(6):486-491.
    19.Hotchkiss RS,Tinsley KW,Swanson PE,et al.Sepsis-induced apoptosis causes progressive profound depletion of B and CD4~+ T lymphocytes in humans]J].J Immunol,2001,166(11):6952-6963.
    20.姚咏明.免疫功能紊乱在脓毒症发病中的作用及意义[J].中国危重病急救医学,2007,19(3):138-141.
    21.Su BH,Chiu HY,Soga T,et al.Ulinastatin alone does not reduce caspase 3-mediated apoptosis in protease-positive Aeromonas hydrophilia-induced sepsis[J].J Formos Med Assoc,2007,106(2):97-104.
    22.Delogu G,Famularo G,Tellan G,et al.Lymphocyte apoptosis,caspase activation and inflammatory response in septic shock]J].Infection,2008,36(5):485-487.
    23.Angus DC,Wax RS.Epidemiology of sepsis:an update]J].Crit Care Med,2001,29(7 Suppl):S109-S116.
    24.Brun-Buisson C,Meshaka P,Pinton P,et al.EPISEPSIS:a reappraisal of the epidemiology and outcome of severe sepsis in French intensive care units]J].Intensive Care Med,2004,30(4):580-588.
    25.Dombrovskiy VY,Martin AA,Sunderram J,et al.Rapid increase in hospitalization and mortality rates for severe sepsis in the United States:a trend analysis from 1993 to 2003]J].Crit Care Med,2007,35(5):1244-1250.
    26.王鸣,彭炜,蔡敏,等.外科重症监护室645例脓毒症患者临床流行病学调查[J].中国危重病急救医学,2006,18(2):74-77.
    27.Remick DG.Pathophysiology of sepsis]J].Am J Pathol,2007,170(5):1435-1444.
    28.Annane D,Bellissant E,Cavaillon JM.Septic shock]J].Lancet,2005,365(9453):63-78.
    29.Monneret G,Venet F,Pachot A,et al.Monitoring Immune Dysfunctions in the Septic Patient:A New Skin for the Old Ceremony]J].Mol Med,2008,14(1-2):64-78.
    30.Monneret G,Lepape A,Voirin N,et al.Persisting low monocyte human leukocyte antigen-DR expression predicts mortality in septic shock]J].Intensive Care Med,2006,32(8):1175-1183.
    31.Pachot A,Lepape A,Vey S,et al.Systemic transcriptional analysis in survivor and non-survivor septic shock patients:a preliminary study]J].Immunol Lett,2006,106(1):63-71.
    32.Pugin J.Immunostimulation is a rational therapeutic strategy in sepsis]J].Novartis Found Symp,2007,280:21-27.
    33.Remick DG.Pathophysiology of sepsis]J].Am J Pathol,2007,170(5):1435-1444.
    34.Prass K,Meisel C,H(?)flich C,et al.Stroke-induced immunodeficiency promotes spontaneous bacterial infections and is mediated by sympathetic activation reversal by poststroke T helper cell type l-like immunostimulation]J].J Exp Med,2003,198(5):725-736.
    35.刘毅,邓小明.脓毒症与机体免疫状态紊乱[J].中国急救医学,2003,23(10):710-711.
    36.Annane D,Cavaillon JM.Corticosteroids in sepsis:from bench to beside?]J].Shock,2003,20(3):197-207.
    37.Scumpia PO,Moldawer LL.Biology of interleukin-10 and its regulatory roles in sepsis syndromes]J].Crit Care Med,2005,33(12 Suppl):S468-S471.
    38.Hotchkiss RS,Nicholson DW.Apoptosis and caspases regulate death and inflammation in sepsis]J].Nat Rev Immunol,2006,6(11):813-822.
    39.Wesche DE,Lomas-Neira JL,Perl M,et al.Leukocyte apoptosis and its significance in sepsis and shock]J].J Leukoc Biol,2005,78(2):325-337.
    40. Le Tulzo Y, Pangault C, Gacouin A, et al. Early circulating lymphocyte apoptosis in human septic shock is associated with poor outcome [J]. Shock,2002,18(6):487-494.
    
    41. Cristaldi M, Rovati M, Elli M, et al. Lymphocytic subpopulation changes after open and laparoscopic cholecystectomy: a prospective and comparative study on 38 patients [J]. Surg Laparosc Endosc, 1997,7(3):255-261.
    
    42. Tschoeke SK, Oberholzer C, LaFace D, et al. Hutchins B Endogenous IL-10 regulates sepsis-induced thymic apoptosis and improves survival in septic IL-10 null mice [J]. Scand J Immunol, 2008,68(6):565-571.
    
    43. Weber SU, Schewe JC, Lehmann LE, et al. Induction of Bim and Bid gene expression during accelerated apoptosis in severe sepsis [J]. Crit Care,2008,12(5):R128.
    
    44. Le Tulzo Y, Pangault C, Gacouin A, et al. Early circulating lymphocyte apoptosis in human septic shock is associated with poor outcome [J]. Shock,2002,18(6):487-494.
    
    45. Roth G, Moser B, Krenn C, et al. usceptibility to programmed cell death in T-lymphocytes from septic patients: a mechanism for lymphopenia and Th2 predominance [J]. Biochem Biophys Res Commun, 2003,308(4):840-846.
    
    46. Coopersmith CM, Stromberg PE, Dunne WM, et al. Inhibition of intestinal epithelial apoptosis and survival in a murine model of pneumonia-induced sepsis [J]. JAMA, 2002,287(13):1716-1721.
    
    47. Green DR, Droin N, Pinkoski M. Activation-induced cell death in T cells [J].Immunol Rev, 2003,193:70-81.
    
    48. Maher S, Toomey D, Condron C, et al. Activation -induced cell death: the controversial role of Fas and Fas ligang in immune privilege and tumour counterattack [J]. Immunol Cell Biol, 2002,80(2):131-137.
    
    49. Krueger A, Fas SC, Baumann S, et al. The role of CD95 in the regulation of peripheral T-cell apoptosis [J]. Immunpl Rev, 2003,193:58-69.
    
    50. Hotchkiss RS, Coopersmith CM, Karl IE. Prevention of lymphocyte apoptosis—a potential treatment of sepsis? [J]. Clin Infect Dis, 2005,41(Suppl 7):S465- S469.
    
    51. Finkel E. The mitochondrion: is it central to apoptosis? [J]. Science, 2001,291 (5504):585.
    52.Messaris E,Memos N,Chatzigianni E,et al.Time-dependent mitochondrial-mediated programmed neuronal cell death prolongs survival in sepsis]J].Crit Care Med,2004,32(8):1764-1770.
    53.Fazal N,A1-Ghoul WM.Thermal injury-plus-sepsis contributes to a substantial deletion of intestinal mesenteric lymph node CD_4 T cell via apoptosis]J].Int J Biol Sci,2007,3(6):393-401.
    54.Suzuki T,Shimizu T,Szalay L,et al.Androstenediol ameliorates alterations in immune cells cytokine production capacity in a two-hit model of trauma-hemorrhage and sepsis]J].Cytokine,2006,34(1-2):76-84.
    55.王振猛,俞卫锋.白介素-10在脓毒症中的作用[J].《国外医学》麻醉学与复苏分册,2003,24(5):281-284.
    56.Maier JK,Lahoua Z,Gendron NH,et al.The neuronal apoptosisinhibitory protein is a direct inhibitor of caspases 3 and 7]J].J Neuro Sci,2002,22 (6):2035-2043.
    57.刘伟,李庆军,卢绮萍.Caspase与细胞凋亡[J].新乡医学院学报,2005,22(1):67-70.
    58.Kriebel F,Wittemann S,Hsu HY,et al.Caspase-3 activation,Bcl-2 contents,and soluble FAS-ligand are not related to the inflammatory marker profile in patients with sepsis and septic shock]J].Ann N YAcad Sci,2006,1090:168-176.
    59.Omokaro SO,Desierto MJ,Eckhaus MA,et al.Lymphocytes with aberrant expression of Fas or Fas ligand attenuate immune bone marrow failure in a mouse model]J].Immunol,2009,182(6):3414-3422.
    60.Bilbault P,Lavaux T,Launoy A,et al.Influence of drotrecogin alpha (activated) infusion on the variation of Bax/Bcl-2 and Bax/Bcl-xl ratios in circulating mononuclear cells:a cohort study in septic shock patients]J].Crit Care Med,2007,35(1):69-75.
    61.Ha T,Hua F,Grant D,et al.Glucan phosphate attenuates cardiac dysfunction and inhibits cardiac MIF expression and apoptosis in septic mice]J].Am J Physiol Heart Circ Physiol,2006,291 (4):H 1910-H1918
    62.Yi C,Cao Y,Wang SR,et al.Beneficial effect of recombinant human growth hormone on the intestinal mucosa barrier of septic rats]J].Braz J Med Biol Res,2007,40(1):41-48.
    63.Groesdonk HV,Wagner F,Hoffarth B,et al.Enhancement of NF-kappaB activation in lymphocytes prevents T cell apoptosis and improves survival in murine sepsis]J].J Immunol,2007,179(12):8083-8089.
    64.Hotchkiss RS,Swanson PE,Cobb JP,et al.Apoptosis in lymphoid and parenchymal cells during sepsis:findings in normal and T-and B-cell-deficient mice]J].Crit Care Med,1997,25(8):1298-1307.
    65.Hotchkiss RS,Osmon SB,Chang KC,et al.Accelerated lymphocyte death in sepsis occurs by both the death receptor and mitochondrial pathways]J].J Immunol,2005,174(8):5110-5118.
    66.Kinloch RA,Treherne JM,Furness LM,et al.The pharmacology of apoptosis]J].Trends Pharmacol Sci,1999,20(1):35-42.
    67.马涛,尤胜义.淋巴细胞凋亡、免疫抑制和脓毒症[J].《国外医学》外科学分册,2005,32(1):35-38.
    68.Habib KE,Gold PW,Chrousos GP.Neuroendocrinology of stress]J].Endocrinol Metab Clin North Am,2001,30(3):695-728.
    69.Miller DB,O'Callaghan JP.Neuroendocrine aspects of the response to stress]J].Metabolism,2002,51 (6 Suppl 1):5-10.
    70.Pac(?)k K,Palkovits M.Stressor specificity of central neuroendocrine responses:implications for stress-related disorders]J].Endocr Rev,2001,22(4):502-548.
    71.Tsigos C,Chrousos GP.Hypothalamic-pituitary-adrenal axis,neuroendocrine factors and stress]J].J Psychosom Res,2002,53(4):865-871.
    72.Widmer IE,Puder JJ,K(?)nig C,et al.Cortisol response in relation to the severity of stress and illness]J].J Clin Endocrinol Metab,2005,90(8):4579-4586.
    73.Oppert M,Reinicke A,Gr(?)f K J,et al.Plasma cortisol levels before and during“low-dose” hydrocortisone therapy and their relationship to hemodynamic improvement in patients with septic shock]J].Intensive Care Med,2000,26(12):1747-1755.
    74.Beishuizen A,Thijs LG,Vermes I.Patterns of corticosteroid-binding globulin and the free cortisol index during septic shock and multitrauma]J].Intensive Care Med, 2001,27(10):1584-1591.
    
    75. 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 [J].JAMA, 2002,288(7):862-871.
    
    76. Keh D, Boehnke T, Weber-Cartens S, et al. Immunologic and hemodynamic effects of "low-dose" hydrocortisone in septic shock: a double-blind, randomized,placebo-controlled, crossover study [J]. Am J Respir Crit Care Med,2003,167(4):512-520.
    
    77. Maxime V, Lesur O, Annane D. Adrenal insufficiency in septic shock [J]. Clin Chest Med, 2009,30(1): 17-27.
    
    78. Sam S, Corbridge TC, Mokhlesi B, et al. Cortisol levels and mortality in severe sepsis [J]. Clin Endocrinol (Oxf), 2004,60(1):29-35.
    
    79. Annane D, Sebille V, Troche G, et al. A 3-level prognostic classification in septic shock based on cortisol levels and cortisol response to corticotrophin [J]. JAMA,2000,283(8):1038-1045.
    
    80. Ho JT, Al-Musalhi H, Chapman MJ, et al. Septic shock and sepsis: a comparison of total and free plasma cortisol levels [J]. J Clin Endocrinol Metab,2006,91(1):105-114.
    
    81. Rivers EP, Gaspari M, Saad GA, et al. Adrenal insufficiency in high-risk surgical ICU patients [J]. Chest, 2001,119(3):889-896.
    
    82. Hamrahian AH, Oseni TS, Arafah BM. Measurements of serum free cortisol in critically ill patients [J]. N Engl J Med, 2004,350(16): 1629-1638.
    
    83. Marik PE, Gayowski T, Starzl TE. The hepatoadrenal syndrome: a common yet unrecognized clinical condition [J]. Crit Care Med, 2005,33(6): 1254-1259.
    
    84. Braams R, Koppeschaar HP, van de Pavoordt HD, et al. Adrenocortical function in patients with ruptured aneurysm of the abdominal aorta [J]. Intensive Care Med, 1998,24(2):124-127.
    
    85. Munck A, Naray-Fejes-Toth A. The ups and downs of glucocorticoid physiology.Permissive and suppressive effects revisited [J]. Mol Cell Endocrinol,1992,90(1):C1-4.
    
    86. Charmandari E, Kino T, Chrousos GP. Glucocorticoids and their actions: an introduction]J].Ann N Y Acad Sci,2004,1024:1-8.
    87.Sionov RV,Cohen O,Kfir S,et al.Role of mitochondrial glucocorticoid receptor in glucocorticoid-induced apoptosis]J].J Exp Med,2006,203(1):189-201.
    88.Kizawa Y,Furuya M,Saito K,Effects of dexamethasone and aminophylline on survival of Jurkat and HL-60 cells]J].Biol Pharm Bull,2006,29(2):281-285.
    89.Arafah BM.Hypothalamic pituitary adrenal function during critical illness:limitations of current assessment methods]J].J Clin Endocrinol Metab,2006,91 (10):3725-3745.
    90.Mesotten D,Vanhorebeek I,Van den Berghe G.The altered adrenal axis and treatment with glucocorticoids during critical illness]J].Nat Clin Pract Endocrinol Metab,2008,4(9):496-505.
    91.Miller DB,O'Callaghan JP.Neuroendocrine aspects of the response to stress]J].Metabolism,2002,51 (6 Suppl 1):5-10.
    92.Pac(?)k K,Palkovits M.Stressor specificity of central neuroendocrine responses:implications for stress-related disorders]J].Endocr Rev,2001,22(4):502-48.
    93.Tsigos C,Chrousos GP.Hypothalamic-pituitary-adrenal axis,neuroendocrine factors and stress]J].J Psychosom Res,2002,53(4):865-71.
    94.Schuld A,Mullington J,Friess E,et al.Changes in dehydroepiandrosterone (DHEA) and DHEA-sulfate plasma levels during experimental endotoxinemia in healthy volunteers]J].J Clin Endocrinol Metab,2000,85(12):4624-4629.
    95.Dandona P,Aljada A,Garg R,et al.Increase in plasma interleukin-10 following hydrocortisone injection]J].J Clin Endocrinol Metab,1999,84(3):1141-1144.
    96.Distelhorst CW.Recent insights into the mechanism of glucocorticosteroid-induced apoptosis]J].Cell Death Differ,2002,9(1):6-19.
    97.包倪荣,赵建宁,王与荣.糖皮质激素诱导淋巴细胞凋亡的细胞学机制[J].中国组织化学与细胞化学杂志,2003,12(1):94-98.
    98.Sionov RV,Cohen O,Kfir S,et al.Role of mitochondrial glucocorticoid receptor in glucocorticoid-induced apoptosis]J].J Exp Med,2006,203(1):189-201.
    99.Wang D,M(?)ller N,McPherson KG,et al.Glucocorticoids engage different signal transduction pathways to induce apoptosis in thymocytes and mature T cells]J].J Immunol,2006,176(3):1695-1702.
    100.Kasprowicz DJ, Droin N, Soper DM, et al. Dynamic regulation of FoxP3 expression controls the balance between CD4+ T cell activation and cell death [J].Eur J Immunol, 2005,35(12):3424-3432.
    101.Zhang J, Xu X, Liu Y. Activation-induced cell death in T cells and autoimmunity [J]. Cell Mol Immunol, 2004,1(3):186-192.
    102.Miller AT, Berg LJ. Defective Fas ligand expression and activation-induced cell death in the absence of IL-2-inducible T cell kinase [J]. J Immunol,2002,168(5):2163-2172.
    103.Maher SG, Condron CE, Bouchier-Hayes DJ, et al. Taurine attenuates CD3/interleukin-2-induced T cell apoptosis in an in vitro model of activation-induced cell death (AICD) [J]. Clin Exp Immunol,2005,139(2):279-286.
    104.Kasibhatla S, Genestier L, Green DR. Regulation of fas-ligand expression during activation-induced cell death in T lymphocytes via nuclear factor kappaB [J]. J Biol Chem, 1999,274(2): 987-992.
    105.Ragin MJ, Hu J, Henderson AJ, et al. A role for the Tec family kinase ITK in regulating SEB-induced interleukin-2 production in vivo via c-jun phosphorylation [J]. BMC Immunol, 2005,6:19.
    106.Delogu G, Famularo G, Tellan G, et al. Lymphocyte apoptosis, caspase activation and inflammatory response in septic shock [J]. Infection, 2008,36(5):485-487.
    107.Lukaszewski RA, Yates AM, Jackson MC, et al. Presymptomatic prediction of sepsis in intensive care unit patients [J]. Clin Vaccine Immunol,2008,15(7):1089-1094.
    108.Tannahill CL, Fukuzuka K, Marum T, et al. Discordant tumor necrosis factor-alpha superfamily gene expression in bacterial peritonitis and endotoxemic shock [J]. Surgery, 1999,126(2):349-357.
    109.Ertel W, Keel M, Stocker R, et al. Detectable concentrations of Fas ligand in cerebrospinal fluid after severe head injury [J]. J Neuroimmunol,1997,80(l-2):93-96.
    110.Matute-Bello G, Liles WC, Steinberg KP, et al. Soluble Fas ligand induces epithelial cell apoptosis in humans with acute lung injury (ARDS) [J]. J Immunol, 1999,163(4):2217-2225.
    111.Ayala A,Chung CS,Xu YX,et al.Increased inducible apoptosis in CD4+ T lymphocytes during polymicrobial sepsis is mediated by Fas ligand and not endotoxin]J].Immunology,1999,97(1):45-55.
    112.Woodside K J,Spies M,Wu XW,et al.Decreased lymphocyte apoptosis by anti-tumor necrosis factor antibody in Peyer's patches after severe burn]J].Shock,2003,20(1):70-73.
    113.黄建华,沈自尹,刘小雨,等.淫羊藿总黄酮拮抗皮质酮大鼠肾上腺皮质细胞凋亡的研究[J].中医药学刊,2006,24(9):1664-1666.
    114.张淑文,孙成栋,文燕,等.血必净注射液对脓毒症大鼠血清内毒素及脾脏特异性免疫功能的影响[J].中国中西医结合急救杂志,2007,14(2):91-94.
    115.常文秀,高红梅,曹书华.血必净对多器官功能障碍综合征内皮细胞的保护作用[J].天津医药,2005,33(11):685-687.
    116.曹书华,高红梅,王勇强,等.“神农33号”对多器官功能衰竭综合征大鼠细胞因子的影响[J].中华急诊医学杂志,2003,12(12):94-96.
    117.Zeerleder S,Hack CE,Wuillemin WA.Disseminated intravascular coagulation in sepsis]J].Chest,2005,128(4):2864-2875.
    118.Slofstra SH,ten Cate H,Spek CA.Signal transduction induced by activated protein C:no role in protection against sepsis?]J].Trends Mol Med,2006,12(8):374-381.
    119.Dahlb(?)ck B,Villoutreix BO.Regulation of blood coagulation by the protein C anticoagulant pathway:novel insights into structure-function relationships and molecular recognition]J].Arterioscler Thromb Vasc Biol,2005,25 (7):1311-1320.
    120.Yuksel M,Okajima K,Uchiba M,et al.Activated protein C inhibits lipopolysaccharide-induced tumor necrosis factor-alpha production by inhibiting activation of both nuclear factor-kappa B and activator protein-1 in human monocytes]J].Thromb Haemost,2002,88(2):267-273.
    121.Zeng W,Matter WF,Yan SB,et al.Effect of drotrecogin alfa (activated) on human endothelial cell permeability and Rho kinase signaling]J].Crit Care Med,2004,32(5 Suppl):S302-S308.
    122.Ayala A,Chung CS,Song GY,et al.IL-10 mediation of activation-induced TH1 cell apoptosis and lymphoid dysfunction in polymicrobial sepsis [J]. Cytokine,2001,14(1):37-48.
    
    123.Tschoeke SK, Oberholzer C, LaFace D, et al. Endogenous IL-10 regulates sepsis-induced thymic apoptosis and improves survival in septic IL-10 null mice [J]. Scand J Immunol, 2008,68(6):565-571.
    1、Angus DC,Linde-Zwirble WT,Lidicker J,et al.Epidemiology of severe sepsis in the United States:analysis of incidence,outcome,and associated costs of care]J].Crit Care Med,2001,29:1303-1310.
    2、Doreen E,Wesche-Soldato,Ryan Z,et al.The Apoptotic Pathway as a Therapeutic Target in Sepsis]J].Curr Drug Targets,2007,8(4):493-500
    3、Hotchkis RS,ChangKC,GmysonMH,et al.Adoptive transfer of apoptotic splenocytes worsens survival,whereas adoptive transfer of necrotic splenoeytes improves survival in sepsis]J].Proc Natl Acad Sci USA,2003,100:6724-6729.
    4、Messaris E,Memos N,Chatzigianni E,et al.Apoptotic death of renal tubular cells in experimental sepsis]J].Surg Infect (Larchmt),2008,9(3):377-388.
    5、 Cantaluppi V, Assenzio B, Pasero D, et al. Polymyxin-B hemoperfusion inactivates circulating proapoptotic factors [J]. Intensive Care Med, 2008,8:1240-1259.
    6、 Mariano F, Cantaluppi V, Stella M, et al. Circulating plasma factors induce tubular and glomerular alterations in septic burns patients [J]. Crit Care,2008,12(2):R42.
    7、 Buerke U, Carter JM, Schlitt A, et al. Apoptosis contributes to septic cardiomyopathy and is improved by simvastatin therapy [J]. Shock,2007,16:27-32
    8、 Dhanantwari P, Nadaraj S, Kenessey A, et al. Macrophage migration inhibitory factor induces cardiomyocyte apoptosis [J]. Biochem Biophys Res Commun,2008,371(2):298-303.
    9、 Chen LW, Chang WJ, Chen PH, et al. TLR ligand decreases mesenteric ischemia and reperfusion injury-induced gut damage through TNF-alpha signaling [J]. Shock,2008,11:145-152.
    10、 Kuckleburg CJ, Tiwari R, Czuprynski CJ. Endothelial cell apoptosis induced by bacteria-activated platelets requires caspase-8 and -9 and generation of reactive oxygen species [J]. Thromb Haemost, 2008,99(2):363-372.
    11、 Gambim MH, do Carmo Ade O, Marti L, et al. Platelet-derived exosomes induce endothelial cell apoptosis through peroxynitrite generation: experimental evidence for a novel mechanism of septic vascular dysfunction [J]. Crit Care,2007,11(5):R107.
    12、 Zdychova J, Komers R. Emerging role of Akt kinase/protein kinase B signaling in pathophysiology of diabetes and its complications [J]. Physiol Res,2005,54:1-16.
    13、 Bommhardt U, Chang KC, Swanson PE, et al. Akt decreases lymphocyte apoptosis and improves survival in sepsis [J]. J Immunol, 2004,172:7583-7591.
    14、 Nielsen JS, Larsson A, Brix-Christensen V, et al. Endotoxemiainduced lymphocyte apoptosis is augmented by a hyperinsulinemic-euglycemic clamp [J]. Anesthesiology,2005,102:768-773.
    
    15、 Macias WL, Yan SB, Williams MD, et al. New insights into the protein C pathway: potential implications for the biological activities of drotrecogin alfa (activated) [J]. Crit Care,2005,9 (Suppl 4):S38- S45.
    16、 Riewald M, Petrovan RJ, Donner A, et al. Activated protein C signals through the thrombin receptor PAR1 in endothelial cells [J]. J Endotoxin Res,2003,9:317-321.
    17、 Cheng T, Liu D, Griffin JH, et al. Activated protein C blocks p53-mediated apoptosis in ischemic human brain endothelium and is neuroprotective [J]. Nat Med,2003,9:338-342.
    18、 Esmon CT. Inflammation and the activated protein C anticoagulant pathway [J].Semin Thromb Hemost, 2006, 32(Suppl 1): 49-60.
    19、 O'Brien LA, Gupta A, Grinnell BW. Activated protein C and sepsis [J]. Front Biosci,2006,1(1):676-98.
    
    20、 Joyce DE, Nelson DR, Grinnell BW. Leukocyte and endothelial cell interactions in sepsis: relevance of the protein C pathway [J]. Crit Care Med, 2004,32(5 Suppl):S280- S286.
    
    21、 Stephenson DA, Toltl LJ, Beaudin S, et al. Modulation of monocyte function by activated protein C, a natural anticoagulant [J]. J Immunol,2006,177(4):2115-2122.
    
    22、 Gupta A, Berg DT, Gerlitz B, et al. Role of protein C in renal dysfunction after polymicrobial sepsis [J]. J Am Soc Nephrol, 2007,18(3):860-867.
    
    23、 Sturn DH, Kaneider NC, Feistritzer C, et al. Expression and function of the endothelial protein C receptor in human neutrophils [J]. Blood,2003,102(4): 1499-1505.
    24、 O'Brien LA, Gupta A, Grinnell BW. Activated protein C and sepsis [J]. Front Biosci,2006,1(11):676-698.
    25、 Mosnier LO, Griffin JH. Inhibition of staurosporine-induced apoptosis of endothelial cells by activated protein C requires protease-activated receptor-1 and endothelial cell protein C receptor [J]. Blood, 2003,1(373):65-70.
    26、 Cheng T, Liu D, Griffin JH, et al. Activated protein C blocks p53-mediated apoptosis in ischemic human brain endothelium and is neuroprotective [J]. Nat Med, 2003,9(3):338-342.
    27、 Yesilirmak DC, Kumral A, Tugyan K, et al. Effects of activated protein C on neonatal hypoxic ischemic brain injury [J]. Brain Res, 2008,1210:56-62.
    28、 Riewald M, Ruf W. J Biol Chem. Protease-activated receptor-1 signaling by activated protein C in cytokine-perturbed endothelial cells is distinct from thrombin signaling [J]. Nat Med, 2005, 280(20):19808-19814.
    29、 Uchiba M, Okajima K, Oike Y, et al. Activated protein C induces endothelial cell proliferation by mitogen-activated protein kinase activation in vitro and angiogenesis in vivo [J]. Circ Res,2004,95(l):34-41.
    30、 Gautier EL, Huby T, Saint-Charles F, et al. Enhanced dendritic cell survival attenuates lipopolysaccharide-induced immunosuppression and increases resistance to lethal endotoxic shock [J]. J Immunol, 2008,180(10):6941-6946.
    31、 Zhou Z, Gengaro P, Wang W, et al. Role of NF-{kappa}B and PI 3-kinase/Akt in TNF-{alpha}-induced cytotoxicity in microvascular endothelial cells [J]. Am J Physiol Renal Physiol, 2008,15:132-147.
    32、 McDunn JE, Muenzer JT, Rachdi L, et al. Peptide-mediated activation of Akt and extracellular regulated kinase signaling prevents lymphocyte apoptosis [J].FASEB J, 2008,22(2):561-568.
    33、 Schwulst SJ, Muenzer JT, Peck-Palmer OM, et al. Bim siRNA decreases lymphocyte apoptosis and improves survival in sepsis [J]. Shock,2008,16:254-271.
    34、 Flierl MA, Rittirsch D, Chen AJ, et al. The complement anaphylatoxin C5a induces apoptosis in adrenomedullary cells during experimental sepsis [J]. PLoS ONE, 2008,3(7):e2560.
    35、 Guo RF, Ward PA. C5a, a therapeutic target in sepsis . [J] Recent Patents Anti-Infect Drug Disc,2006 ,1(1):57-65.