草药-矿物质制剂卡米拉-玛尔沃德的免疫增强作用。

Farah Khan, S Ali, B A Ganie, I Rubab
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引用次数: 18

摘要

本研究在动物模型上研究了一种草药-矿物质乌纳尼制剂——卡米拉·玛瓦尔德(KM)的免疫增强作用。小鼠按2 g/kg体重口服KM 5、10、15和30天,处死动物进行血液学和免疫功能检测,包括淋巴器官重量和细胞结构。KM组相对脏器(脾脏和胸腺)重量显著增加(P < 0.05)。脾脏和骨髓细胞数量也显著增加(P < 0.01)。KM组血红蛋白、红细胞(rbc)和总白细胞(wbc)均显著升高(P < 0.01)。在用山羊红细胞刺激小鼠后,通过斑块形成细胞(PFC)测定来评估体液免疫反应,与对照组相比,所有治疗组的免疫反应都更好。小鼠经KM处理15天后血凝滴度达到最大值。小鼠卵清蛋白特异性血清IgG水平显著升高(P < 0.01),提示该制剂具有免疫增强作用。KM可导致IgG2a和IgG2b水平升高。比较抗卵清蛋白IgE和IgG;抗卵清蛋白IgE降低,同时抗卵清蛋白IgG升高。给药10或15天可引起延迟型超敏反应(DTH)的增加。综上所述,结果表明,通过导致th1主导免疫状态的机制,KM具有免疫刺激作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunopotentiating effect of Khamira Marwarid, an herbo-mineral preparation.

This study investigated the immunopotentiating effect of Khamira Marwarid (KM), an herbo-mineral Unani preparation, in an animal model. KM was administered to mice orally at a dose level of 2 g/kg body weight for 5, 10, 15 or 30 days, following which the animals were sacrificed for hematology and immune function testing, including lymphoid organ weight and cellularity. The group of animals receiving KM showed a significant increase (P < 0.05) in the relative organ (spleen and thymus) weight. Cellularity of the spleen and bone marrow also increased significantly (P < 0.01). Groups receiving KM for 10 and 15 days showed an increase in hemoglobin, red blood cells (RBCs) and total white blood cells (WBCs) (P < 0.01). The humoral immune response, evaluated by the plaque-forming cell (PFC) assay after challenging the mice with goat RBCs, was better in all treated groups when compared to controls. Maximum hemagglutination titer was obtained in mice treated with KM for 15 days. Ovalbumin-specific serum IgG levels in the treated mice also increased significantly (P < 0.01), suggesting an immunopotentiating effect for the preparation. Administration of KM resulted in elevated levels of IgG2a and IgG2b. A comparison of anti-ovalbumin IgE and IgG was also done; anti-ovalbumin IgE decreased, with a concomitant increase in anti-ovalbumin IgG. Administration of KM for 10 or 15 days elicited an increase in the delayed-type hypersensitivity (DTH) response. Taken together, the results suggest an immunostimulatory effect for KM through a mechanism leading to a Th1-dominant immune state.

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