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皮内注射肝素对豚鼠皮肤炎症反应中嗜酸性粒细胞聚集的抑制作用,但对水肿形成无抑制作用。

Suppression by intradermal administration of heparin of eosinophil accumulation but not oedema formation in inflammatory reactions in guinea-pig skin.

作者信息

Teixeira M M, Hellewell P G

机构信息

Department of Applied Pharmacology, National Heart and Lung Institute, London.

出版信息

Br J Pharmacol. 1993 Dec;110(4):1496-500. doi: 10.1111/j.1476-5381.1993.tb13991.x.

Abstract
  1. Heparin is widely used in the treatment of thrombotic disorders and as an aid in surgery. Anti-inflammatory effects of heparin have also been described. In this study, we have investigated the effects of locally-injected heparin on the oedema formation and eosinophil accumulation induced by various inflammatory stimuli in guinea-pig skin. 2. Heparin dose-dependently suppressed the accumulation of 111In-labelled eosinophils induced by i.d. injection of zymosan-activated plasma (ZAP). The 111In-eosinophil accumulation induced by other inflammatory stimuli (compound 48/80, platelet activating factor, interleukin-8 and in a passive cutaneous anaphylaxis reaction) was also suppressed by locally-injected heparin. 3. Oedema formation in response to these same stimuli was not altered by the local injection of heparin. 4. Fucoidin, a negatively-charged sulphated algal polymer, had no effect on the 111In-eosinophil accumulation or oedema formation induced by ZAP. Nevertheless, fucoidin significantly suppressed the oedema formation induced by i.d. injection of cationic protein-containing extracts of Schistosoma mansoni larvae. Heparin also inhibited oedema induced by the extracts, suggesting that both fucoidin and heparin were effectively neutralizing the cationic protein of the extracts to inhibit their oedema-inducing activity. 5. Thus, heparin significantly inhibited the accumulation of 111In-eosinophils, but not oedema formation, induced by various inflammatory stimuli. This, taken together with the lack of effect of fucoidin, suggests that heparin interferes with the process of eosinophil trafficking by a mechanism that does not depend on neutralisation of the charge of the stimulatory molecules.
摘要
  1. 肝素广泛用于血栓性疾病的治疗及手术辅助。肝素的抗炎作用也已得到描述。在本研究中,我们研究了局部注射肝素对豚鼠皮肤中由各种炎症刺激诱导的水肿形成和嗜酸性粒细胞聚集的影响。2. 肝素剂量依赖性地抑制了皮下注射酵母聚糖激活血浆(ZAP)诱导的111In标记嗜酸性粒细胞的聚集。局部注射肝素也抑制了由其他炎症刺激(化合物48/80、血小板活化因子、白细胞介素-8以及在被动皮肤过敏反应中)诱导的111In嗜酸性粒细胞聚集。3. 局部注射肝素对这些相同刺激引起的水肿形成没有影响。4. 岩藻依聚糖,一种带负电荷的硫酸化藻类聚合物,对ZAP诱导的111In嗜酸性粒细胞聚集或水肿形成没有影响。然而,岩藻依聚糖显著抑制了皮下注射曼氏血吸虫幼虫含阳离子蛋白提取物诱导的水肿形成。肝素也抑制了提取物诱导的水肿,这表明岩藻依聚糖和肝素都有效地中和了提取物的阳离子蛋白以抑制它们的水肿诱导活性。5. 因此,肝素显著抑制了由各种炎症刺激诱导的111In嗜酸性粒细胞的聚集,但不抑制水肿形成。这与岩藻依聚糖缺乏作用一起表明,肝素通过一种不依赖于刺激分子电荷中和的机制干扰嗜酸性粒细胞的迁移过程。

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