Davidson Marson T, Deitch Edwin A, Lu Qi, Osband Adena, Feketeova Eleonora, Németh Zoltán H, Haskó Gyorgy, Xu Da-Zhong
Department of Surgery, University of Medicine and Dentistry of New Jersey, Newark, 07103, USA.
Surgery. 2004 Jul;136(1):32-41. doi: 10.1016/j.surg.2003.12.012.
Gut-derived factors in intestinal lymph have been recently shown to cause lung injury, activate neutrophils, and injure endothelial cells in rats subjected to hemorrhagic shock (T/HS). However, the time course of the appearance and disappearance of these factors in intestinal lymph is unclear. Thus the goal of this study was to characterize the biologic activity of T/HS lymph collected at various times during and after shock.
Male rats subjected to trauma (laparotomy) plus hemorrhagic shock (mean arterial pressure, 90 mm Hg x 90 min) (T/HS) or trauma plus sham shock (T/SS) had their mesenteric lymph duct catheterized. Mesenteric lymph collected before shock, during shock, and hourly for 6 hours after shock was assayed for cytokine levels (tumor necrosis factor, granulocyte-macrophage colony-stimulating factor, interleukin-1, and transforming growth factor-beta) as well as biologic activity on endothelial cells (cytotoxicity and permeability) and neutrophils (CD11b adhesion molecule expression and respiratory burst activity).
T/HS, but not T/SS, lymph injured endothelial cells and activated neutrophils, although the cytokine levels did not differ between the T/HS and T/SS lymph samples. The biologic activity of T/HS lymph appeared during the shock (gut ischemic) period. The temporal pattern of activity varied on the basis of the biologic activity being tested, with the neutrophil-activating properties of the T/HS lymph persisting longest.
These results suggest that gut ischemia itself is sufficient to induce the production of biologically active T/HS lymph and that the temporal pattern of biologic activity varies over time on the basis of the property being tested. Consequently, studies directed at identifying the active factors in T/HS lymph must take these temporal patterns of activity into account.
最近研究表明,肠道淋巴液中的肠道源性因子可导致肺损伤、激活中性粒细胞并损伤失血性休克(创伤/失血性休克,T/HS)大鼠的内皮细胞。然而,这些因子在肠道淋巴液中出现和消失的时间进程尚不清楚。因此,本研究的目的是描述在休克期间及休克后不同时间采集的T/HS淋巴液的生物活性。
对雄性大鼠进行创伤(剖腹术)加失血性休克(平均动脉压90mmHg,持续90分钟)(T/HS)或创伤加假手术休克(T/SS),并将其肠系膜淋巴管插管。在休克前、休克期间以及休克后每小时采集6小时的肠系膜淋巴液,检测细胞因子水平(肿瘤坏死因子、粒细胞-巨噬细胞集落刺激因子、白细胞介素-1和转化生长因子-β)以及对内皮细胞的生物活性(细胞毒性和通透性)和中性粒细胞的生物活性(CD11b黏附分子表达和呼吸爆发活性)。
T/HS淋巴液可损伤内皮细胞并激活中性粒细胞,而T/SS淋巴液则无此作用,尽管T/HS和T/SS淋巴液样本中的细胞因子水平并无差异。T/HS淋巴液的生物活性在休克(肠道缺血)期间出现。活性的时间模式因所检测的生物活性而异,T/HS淋巴液激活中性粒细胞的特性持续时间最长。
这些结果表明,肠道缺血本身足以诱导具有生物活性的T/HS淋巴液的产生,并且生物活性的时间模式会根据所检测的特性随时间而变化。因此,旨在鉴定T/HS淋巴液中活性因子的研究必须考虑这些活性的时间模式。