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低温可诱导内毒素血症大鼠肺组织产生白细胞介素-10并减轻肺损伤。

Hypothermia induces interleukin-10 and attenuates injury in the lungs of endotoxemic rats.

作者信息

Sarcia Paul J, Scumpia Philip O, Moldawer Lyle L, DeMarco Vincent G, Skimming Jeffrey W

机构信息

Department of Pediatrics, University of Florida, Gainesville, Florida, USA.

出版信息

Shock. 2003 Jul;20(1):41-5. doi: 10.1097/01.shk.0000071080.50028.f2.

Abstract

We recently reported that hypothermia protects against intrapulmonary nitric oxide overproduction and nitric oxide-mediated lung injury in endotoxemic rats. Few studies have been performed to investigate whether hypothermia reduces inflammation by affecting favorable changes in chemokine and pro- and anti-inflammatory cytokine profiles. In this study, we tested the hypothesis that hypothermia decreases concentrations of growth-related oncogene/cytokine-induced neutrophil chemoattractant-1 (GRO/CINC-1), interleukin (IL)-1beta, IL-6, and myeloperoxidase and increases concentration of IL-10 in the lungs endotoxemic rats. Twelve rats were anesthetized and randomized to treatment with either hypothermia (T = 18-24 degrees C; n = 6) or normothermia (T = 36-38 degrees C, n = 6). Endotoxin (15 mg/kg of Escherichia coli lipopolysaccharide) was administered intravascularly and lung tissue was harvested 150 min later. Three additional rats were sham instrumented and maintained as normothermic but not given endotoxin. Hematoxylin & eosin staining was performed for qualitative inspection of tissues. Quantitative analyses of lung homogenates were performed using enzyme-linked immunosorbent assays for IL-1beta, IL-6, IL-10, and GRO/CINC-1. Myeloperoxidase concentrations were determined using a colorimetric assay. Hypothermia attenuated the induction of intrapulmonary IL-1beta (P < 0.05), IL-6 (P < 0.05), GRO/CINC-1 (P < 0.05), and myeloperoxidase (P < 0.05) caused by endotoxin. Inspection of the lungs revealed that hypothermia similarly attenuated histological signs of injury, such as interstitial edema and neutrophil accumulation. Hypothermia increased the intrapulmonary concentration of IL-10 more than 3-fold over that measured in the normothermia (endotoxin-exposed) group (P < 0.05). Hypothermia inhibits neutrophil recruitment in the lungs of endotoxemic rats in part by decreasing proinflammatory cytokine expression. Additionally, hypothermia induces intrapulmonary IL-10 expression. Further studies are needed to investigate whether IL-10 mediates the anti-inflammatory effects of hypothermia.

摘要

我们最近报道,低温可防止内毒素血症大鼠肺内一氧化氮过量产生及一氧化氮介导的肺损伤。很少有研究探讨低温是否通过影响趋化因子以及促炎和抗炎细胞因子谱的有利变化来减轻炎症。在本研究中,我们验证了以下假设:低温可降低内毒素血症大鼠肺内生长相关癌基因/细胞因子诱导的中性粒细胞趋化因子-1(GRO/CINC-1)、白细胞介素(IL)-1β、IL-6和髓过氧化物酶的浓度,并增加IL-10的浓度。将12只大鼠麻醉后随机分为低温组(T = 18 - 24℃;n = 6)或正常体温组(T = 36 - 38℃,n = 6)。经血管内注射内毒素(15 mg/kg大肠杆菌脂多糖),150分钟后采集肺组织。另外3只大鼠进行假手术,维持正常体温但不给予内毒素。采用苏木精-伊红染色对组织进行定性检查。使用酶联免疫吸附测定法对肺匀浆进行定量分析,检测IL-1β、IL-6、IL-10和GRO/CINC-1。使用比色法测定髓过氧化物酶浓度。低温减弱了内毒素引起的肺内IL-1β(P < 0.05)、IL-6(P < 0.05)、GRO/CINC-1(P < 0.05)和髓过氧化物酶(P < 0.05)的诱导。对肺的检查显示,低温同样减轻了损伤的组织学征象,如间质水肿和中性粒细胞聚集。低温使肺内IL-10浓度比正常体温(暴露于内毒素)组测量值增加了3倍多(P < 0.05)。低温部分通过降低促炎细胞因子表达来抑制内毒素血症大鼠肺内中性粒细胞募集。此外,低温诱导肺内IL-10表达。需要进一步研究来探讨IL-10是否介导低温的抗炎作用。

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