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暴露于硒和南非醉茄的哮喘小鼠血小板及纤维蛋白网络的超微结构

Ultrastructure of platelets and fibrin networks of asthmatic mice exposed to selenium and Withania somnifera.

作者信息

Pretorius Etheresia, Oberholzer Hester Magdalena, Vieira Warren A, Smit Eureka

机构信息

Department of Anatomy, University of Pretoria, PO Box 2034, Pretoria, 0001, Gauteng, South Africa.

出版信息

Anat Sci Int. 2009 Sep;84(3):210-7. doi: 10.1007/s12565-008-0010-1. Epub 2009 Feb 13.

Abstract

Platelets and fibrin play an important role in allergic processes, including allergic asthma. The asthmatic BALB/c mouse model was used to induce asthma, and asthmatic mice were treated with the anti-inflammatory plant Withania somnifera, separately and in combination with the antioxidant selenium. Selenium is an important supplement in asthma, because asthmatics may have a selenium deficiency. Hydrocortisone was used as positive control. Results indicate control mice possess major thick fibers, minor thin fibers, and tight round activated platelets with typical pseudopodia formation. Minor fibers of asthmatic mice have a netlike appearance covering the major fibers whereas the platelets form loosely connected, granular aggregates. Hydrocortisone made the fibrin more fragile and platelet morphology changes from a tight activated platelet to a more granular activated platelet, not closely fused to each other. The plant extracts, separately and in combination with selenium did not affect the fragility of the fibrin and reversed the formation of the dense minor netlike layer over the major fibers, and the platelets formed a dense aggregate. Asthmatic mice treated with selenium showed a dense minor fibrin layer; however, the platelets formed a dense aggregate. We conclude that the anti-inflammatory products affect the stability of fibrin networks but not platelet stability (seen with hydrocortisone). Selenium does not affect the stability of the fibrin networks, but affects platelet stability. These results suggests that asthmatic patients should indeed use an antioxidant supplement, e.g. selenium, because it stabilizes activated platelets, together with anti-inflammatory products.

摘要

血小板和纤维蛋白在包括过敏性哮喘在内的过敏过程中发挥着重要作用。采用哮喘BALB/c小鼠模型诱导哮喘,分别用抗炎植物睡茄单独或与抗氧化剂硒联合治疗哮喘小鼠。硒是哮喘治疗中的一种重要补充剂,因为哮喘患者可能存在硒缺乏。氢化可的松用作阳性对照。结果表明,对照小鼠有主要的粗纤维、少量细纤维以及紧密的圆形活化血小板,伴有典型的伪足形成。哮喘小鼠的细纤维呈网状外观覆盖在粗纤维上,而血小板形成松散连接的颗粒状聚集体。氢化可的松使纤维蛋白更易碎,血小板形态从紧密的活化血小板变为更颗粒状的活化血小板,彼此之间融合不紧密。植物提取物单独或与硒联合使用均不影响纤维蛋白的易碎性,并逆转了粗纤维上致密的细网状层的形成,且血小板形成致密聚集体。用硒治疗的哮喘小鼠显示有致密的细纤维蛋白层;然而,血小板形成致密聚集体。我们得出结论,抗炎产物影响纤维蛋白网络的稳定性,但不影响血小板稳定性(氢化可的松则有此作用)。硒不影响纤维蛋白网络的稳定性,但影响血小板稳定性。这些结果表明,哮喘患者确实应该使用抗氧化剂补充剂,如硒,因为它与抗炎产物一起能稳定活化血小板。

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