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Khamira Marwarid Khas, a herbo-mineral prescription, as mucosal immunopotentiator in murine model

机译:矿物质处方药Khamira Marwarid Khas,作为鼠模型中的粘膜免疫增强剂

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Khamira Marwarid khas (KMK) is a compound herbo-mineral preparation consisting of pearl extract and 7 plant extracts, widely prescribed by Unani physicians for various ailments related with immune suppression. Though it is a known Unani formulation, no attempts have been made to validate its mechanism of action. In this regard, we attempted to elucidate its role in modulation of the immune response. KMK was administered to mice orally at a dose level of 2 g/kg body weight for 15 days, following which hematology and immune function including the lymphoid organ weight and cellularity of lymphoid organs were analyzed. Humoral and cell mediated immune responses were evaluated by assessing the IgG levels and titres, IgG subtypes, comparative levels of IgG and IgE, delayed type of hypersensitivity, lymphocyte proliferation using 3H-thymidine incorporation assay and cytokine analysis. Innate immune responses were analyzed using production of nitrogen oxide (NO) by macrophages and phagocytosis. KMK treated mice showed a significant increase (p < 0.05) in the cellularity of the bone marrow. Ovalbumin-specific serum IgG level (p<0.05) and levels of IgG2a and IgG2b increased significantly. KMK enhanced significantly (p < 0.05) lymphocyte proliferation and delayed type of hypersensitivity response. An upregulation in the production of Th-1 cytokine (IFN-γ) by concavalin A (Con A) stimulated splenocytes was observed while the level of inflammatory cytokines like TNF-α and IL-1β were non-significantly increased. Oral administration of KMK by itself did not induce the production of NO by macrophages and suppressed the production of NO in response to LPS.? Increased phagocytic rate and phagocytic index was observed. Taken together, the results suggest the immunostimulatory effect of KMK through a mechanism, leading to a Th1 dominant immune state.
机译:Khamira Marwarid khas(KMK)是一种由草药提取物组成的复合矿物质制剂,由珍珠提取物和7种植物提取物组成,被Unani医师广泛用于治疗与免疫抑制有关的各种疾病。尽管这是一种已知的Unani配方,但尚未尝试验证其作用机理。在这方面,我们试图阐明其在调节免疫应答中的作用。以2g / kg体重的剂量口服KMK 15天,然后分析血液学和免疫功能,包括淋巴器官重量和淋巴器官的细胞性。通过评估IgG水平和滴度,IgG亚型,IgG和IgE的相对水平,迟发型超敏反应类型,使用3H-胸苷掺入法和细胞因子分析的淋巴细胞增殖来评估体液和细胞介导的免疫反应。使用巨噬细胞产生的一氧化氮(NO)和吞噬作用分析先天免疫反应。 KMK处理的小鼠显示出骨髓细胞的显着增加(p <0.05)。卵清蛋白特异性血清IgG水平(p <0.05)以及IgG2a和IgG2b的水平显着增加。 KMK显着增强(p <0.05)淋巴细胞增殖和迟发型超敏反应。观察到由伴刀豆球蛋白A(Con A)刺激的脾细胞产生的Th-1细胞因子(IFN-γ)上调,而TNF-α和IL-1β等炎性细胞因子的水平却没有明显增加。口服KMK本身不会诱导巨噬细胞产生NO,也不会抑制LPS引起的NO产生。吞噬率和吞噬指数增加。两者合计,结果表明KMK通过一种机制的免疫刺激作用,导致Th1主导的免疫状态。

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