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血小板活化因子在幼鼠肠道免疫屏障功能损伤中的作用

[Role of platelet activating factor in the injury of intestinal immuno-barrier function in young rats].

作者信息

Wang Li-Jie, Liu Chun-Ying, Sun Mei, Lu Qing-Jie

机构信息

Department of Pediatrics, Second Clinical College, China Medical University, Shenyang 110004, China.

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2006 Feb;8(1):59-62.

Abstract

OBJECTIVE

Gastrointestinal dysfunction is closely correlated with the destruction of intestinal barrier function induced by serious infection. Platelet activating factor (PAF) may induce intestinal injuries. This study aimed to investigate the effect of PAF on the injury of intestinal mucosal immuno-barrier function in young rats.

METHODS

Eighteen-day-old Wistar rats were randomized to lipopolysaccharide (LPS) (5 mg/kg), LPS plus PAF receptor antagonist and normal saline injection (Control). PAF receptor antagonist BN52021 5 mg/kg was administered before or 30 minutes after LPS injection (pretreatment or treatment). The ileum specimens (n=8) were harvested at 1.5, 3, 6, 24, 48 and 72 hrs after LPS injection. Double antibody-PEG radioimmunoassay was used to determine the secretory IgA (sIgA) content in intestinal mucosa. Hematoxylin and erosin staining was used for histological evaluation. The ratio of wet and dry weight (W/D) of ileum tissues was calculated.

RESULTS

Intestinal villi edema, capillary congestion, extension of the subepithelial lympho channel, and polymorphonuclear infiltration in enteric cavity were noted in the LPS group at 1.5, 3, 6 and 24 hrs after LPS injection. In the PAF receptor antagonist group only villi edema was found. The W/D ratio in the LPS group was significantly higher than that in the Control group at all time points, but it was slightly reduced by the PAF receptor antagonist pretreatment or treatment. The sIgA content was obviously decreased after 1.5, 3, 6, 24 and 48 hrs of LPS challenge compared with that in the Control group (P < 0.01). It reached to a nadir at 6 hrs (0.15 +/- 0.04 microg/mL). The level of sIgA in the PAF receptor antagonist group was higher than that in the LPS group at each time point. There was no statistical difference in the sIgA level between the PAF receptor pretreatment and treatment groups.

CONCLUSIONS

PAF plays roles in the injury of intestinal immuno-barrier function. Preventive and remedial use of PAF receptor antagonist BN52021 may relieve intestinal injury.

摘要

目的

胃肠功能障碍与严重感染所致肠屏障功能破坏密切相关。血小板活化因子(PAF)可能诱发肠道损伤。本研究旨在探讨PAF对幼鼠肠黏膜免疫屏障功能损伤的影响。

方法

将18日龄Wistar大鼠随机分为脂多糖(LPS)组(5mg/kg)、LPS加PAF受体拮抗剂组和生理盐水注射对照组。在注射LPS前或注射后30分钟给予PAF受体拮抗剂BN52021 5mg/kg(预处理或治疗)。在注射LPS后1.5、3、6、24、48和72小时采集回肠标本(n = 8)。采用双抗体-聚乙二醇放射免疫分析法测定肠黏膜中分泌型IgA(sIgA)含量。采用苏木精-伊红染色进行组织学评估。计算回肠组织的湿重与干重之比(W/D)。

结果

LPS组在注射LPS后1.5、3、6和24小时可见肠绒毛水肿、毛细血管充血、上皮下淋巴通道增宽以及肠腔内多形核细胞浸润。PAF受体拮抗剂组仅见绒毛水肿。LPS组在所有时间点的W/D比值均显著高于对照组,但PAF受体拮抗剂预处理或治疗后略有降低。与对照组相比,LPS攻击后1.5、3、6、24和48小时sIgA含量明显降低(P < 0.01)。在6小时时降至最低点(0.15±0.04μg/mL)。PAF受体拮抗剂组在各时间点的sIgA水平均高于LPS组。PAF受体预处理组和治疗组的sIgA水平无统计学差异。

结论

PAF在肠免疫屏障功能损伤中起作用。预防性和补救性使用PAF受体拮抗剂BN52021可能减轻肠道损伤。

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