Gender differences in the inflammatory response and survival following haemorrhage and subsequent sepsis

被引:218
作者
Diodato, MD
Knöferl, MW
Schwacha, MG
Bland, KI
Chaudry, IH
机构
[1] Univ Alabama Birmingham, Surg Res Ctr, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Surg, Birmingham, AL 35294 USA
[3] Brown Univ, Sch Med, Surg Res Ctr, Providence, RI 02903 USA
关键词
IL-6; TNF-alpha; PGE(2); cyclooxygenase-2;
D O I
10.1006/cyto.2001.0861
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Studies have shown gender dimorphism in cell-mediated immune responses following haemorrhage, with depressed responses in young males and maintained or enhanced responses in proestrus females. However, it remains unknown whether or not the sexually dimorphic immune response to haemorrhage provides any protection against a subsequent in vivo polymicrobial septic challenge. To study this, male and proestrus female C3H/HeN mice were subjected to haemorrhage (35 +/- 5 mmHg for 90 min followed by fluid resuscitation) or sham operation. Twenty-four hours thereafter, all mice were subjected to polymicrobial sepsis by cecal ligation and puncture (CLP) and survival was assessed over a 10 day period. Haemorrhage prior to CLP significantly increased mortality in males as compared to shams. In contrast, mortality in females following CLP was comparable between the sham and haemorrhage groups. Plasma levels of interleukin (IL-)6, tumour necrosis factor (TNF)-alpha and prostaglandin E-2(PGE(2)) at 5 h after CLP mere significantly increased in males subjected to prior haemorrhage. In contrast, plasma levels of IL-6 and TNF-alpha in females did not increase under such conditions. PGE(2) levels were comparable in males and females following CLP, however prior haemorrhage significantly reduced PGE(2) levels in females, whereas no change was observed in males. Liver and splenic expression of cyclooxygenase-2 protein paralleled the changes in plasma PGE(2). Female sex hormones, therefore, appear to play an important role not only in maintaining immune function following haemorrhage, but also provide a survival advantage against subsequent septic challenge. (C) 2001 Academic Press.
引用
收藏
页码:162 / 169
页数:8
相关论文
共 55 条
[1]
AHMED SA, 1985, AM J PATHOL, V121, P531
[2]
Testosterone: the culprit for producing splenocyte immune depression after trauma hemorrhage [J].
Angele, MK ;
Ayala, A ;
Cioffi, WG ;
Bland, KI ;
Chaudry, IH .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1998, 274 (06) :C1530-C1536
[3]
Gender dimorphism in trauma-hemorrhage-induced thymocyte apoptosis [J].
Angele, MK ;
Xu, YX ;
Ayala, A ;
Schwacha, MG ;
Catania, RK ;
Cioffi, WG ;
Bland, KI ;
Chaudry, IH .
SHOCK, 1999, 12 (04) :316-322
[4]
Sex steroids regulate pro- and anti-inflammatory cytokine release by macrophages after trauma-hemorrhage [J].
Angele, MK ;
Knöferl, MW ;
Schwacha, MG ;
Ayala, A ;
Cioffi, WG ;
Bland, KI ;
Chaudry, IH .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1999, 277 (01) :C35-C42
[5]
Effect of gender and sex hormones on immune responses following shock [J].
Angele, MK ;
Schwacha, MG ;
Ayala, A ;
Chaudry, IH .
SHOCK, 2000, 14 (02) :81-90
[6]
Immune dysfunction in murine polymicrobial sepsis: Mediators, macrophages, lymphocytes and apoptosis [J].
Ayala, A ;
Chaudry, IH .
SHOCK, 1996, 6 :S27-S38
[7]
AYALA A, 1994, ARCH SURG-CHICAGO, V129, P1172
[8]
AYALA A, 1992, CIRC SHOCK, V36, P191
[9]
BAKER CC, 1983, SURGERY, V94, P331
[10]
Interleukin-6 in the injured patient marker of injury or mediator of inflammation? [J].
Biffl, WL ;
Moore, EE ;
Moore, FA ;
Peterson, VM .
ANNALS OF SURGERY, 1996, 224 (05) :647-664