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亚马逊榕树皮提取物的免疫生物学和抗炎特性。

Immunobiologic and antiinflammatory properties of a bark extract from Ampelozizyphus amazonicus Ducke.

机构信息

Departamento de Imunologia, Instituto de Microbiologia Paulo de Goes, Universidade Federal do Rio de Janeiro, CCS Bloco I, 2° andar, 21941-590 Rio de Janeiro, RJ, Brazil.

出版信息

Biomed Res Int. 2013;2013:451679. doi: 10.1155/2013/451679. Epub 2013 Feb 28.

DOI:10.1155/2013/451679
PMID:23555087
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3600244/
Abstract

Ampelozizyphus amazonicus is used in the treatment and prevention of malaria. The effect of an aqueous extract from this plant (SART) on the immune response was investigated by measuring immunoglobulin production induced by immunization with the antigen TNP-Ficoll in Plasmodium chabaudi-infected mice. SART treatment increased antigen-specific IgM and IgG levels in TNP-Ficoll-immunized mice. The B cell response during malarial infection was also modified by SART. There was an increase in total serum IgM and IgG and a decrease in the percentage of splenic plasma cells (CD138+ cells) in P. chabaudi-infected, SART-treated animals. SART (1, 3 or 10 mg/kg, p.o.) and the reference drug dexamethasone (5 mg/kg) were also tested in carrageenan-induced leukocyte migration to the subcutaneous air pouch (SAP). All SART doses significantly reduced leukocyte migration into the SAP. The protein concentration resulting from extravasation into the peritoneum was also significantly reduced. Our data indicate that SART possesses immunomodulatory properties, inducing an in vivo modification of the B lymphocyte response and anti-inflammatory properties, which are partly due to a reduction in cell migration and are most likely due to an inhibition of the production of inflammatory mediators. Preliminary HPLC-ESI-MS/MS analysis of SART shows a complex saponin profile with deprotonated molecule M-H ions in the range of m/z 800-1000.

摘要

亚马孙枸杞用于治疗和预防疟疾。通过测量用抗原 TNP-Ficoll 免疫接种感染疟原虫的小鼠引起的免疫球蛋白产生,研究了该植物(SART)的水提取物对免疫反应的影响。SART 处理增加了 TNP-Ficoll 免疫接种小鼠的抗原特异性 IgM 和 IgG 水平。SART 还改变了疟原虫感染期间的 B 细胞反应。在感染疟原虫的 SART 处理动物中,总血清 IgM 和 IgG 增加,而脾浆细胞(CD138+细胞)的百分比降低。还测试了 SART(1、3 或 10mg/kg,口服)和参考药物地塞米松(5mg/kg)在卡拉胶诱导的白细胞向皮下气囊中迁移(SAP)中的作用。所有 SART 剂量均显著减少白细胞向 SAP 的迁移。漏入腹腔的蛋白质浓度也显著降低。我们的数据表明,SART 具有免疫调节特性,诱导体内 B 淋巴细胞反应的修饰和抗炎特性,这部分归因于细胞迁移减少,很可能归因于炎症介质产生的抑制。SART 的初步 HPLC-ESI-MS/MS 分析显示,其具有复杂的皂苷特征,在 m/z 800-1000 范围内具有去质子分子[M-H](-)离子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ee2/3600244/fb2bf8ac377b/BMRI2013-451679.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ee2/3600244/208c468cb392/BMRI2013-451679.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ee2/3600244/832f2cdde9ae/BMRI2013-451679.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ee2/3600244/87827fe862f9/BMRI2013-451679.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ee2/3600244/98e4aa4df7bb/BMRI2013-451679.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ee2/3600244/a2cdedaf0e17/BMRI2013-451679.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ee2/3600244/fb2bf8ac377b/BMRI2013-451679.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ee2/3600244/208c468cb392/BMRI2013-451679.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ee2/3600244/832f2cdde9ae/BMRI2013-451679.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ee2/3600244/87827fe862f9/BMRI2013-451679.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ee2/3600244/98e4aa4df7bb/BMRI2013-451679.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ee2/3600244/a2cdedaf0e17/BMRI2013-451679.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ee2/3600244/fb2bf8ac377b/BMRI2013-451679.006.jpg

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