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Effects and mechanisms of glucosides of chaenomeles speciosa on collagen-induced arthritis in rats.

机译:木瓜蛋白苷对大鼠胶原性关节炎的作用及其机制。

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摘要

Effects of glucosides of chaenomeles speciosa (GCS)-a Chinese traditional herbal medicine (CTM) on inflammatory and immune responses and its mechanisms in collagen-induced arthritis (CIA) rat were studied. Hind paw volumes of rats were measured by volume meter; lymphocyte proliferation, interleukin-1, interleukin-2, TNF-alpha level was determined by 3-(4,5-2dimethylthiazal-2yl)2,5-diphenyltetrazoliumbromide (MTT) assay; cAMP level in synoviocytes was analyzed by competitive protein binding assay (CPBA). mRNA expression of G(i,), G(s), and TNF-alpha of synoviocytes in CIA rats was measured by RT-PCR and antibodies to collagen type II (CII) were determined by enzyme-linked immunosorbent assay (ELISA), respectively. There was a marked secondary inflammatory response in CIA model, which accompanied with the decrease of body weight and the weight of immune organs simultaneously. The administration of GCS (30, 60, 120 mg kg(-1), igx7 days) inhibited the inflammatory response and restored body weight and the weight of immune organs of CIA rats. Lymphocyte proliferation and IL-2 production of CIA rats increases, together with IL-1 and TNF-alpha in peritoneal macrophages and synoviocytes. The administration of GCS (30, 60, 120 mg kg(-1), igx7 days) reduced above changes significantly. GCS at the concentration of 0.5, 2.5, 12.5, 62.5, 125 mg l(-1) increased cAMP level of synoviocytes, which decreased in CIA rats in vitro. At the same time, GCS inhibited mRNA expression of G(i,) and TNF-alpha of synoviocytes and increased mRNA expression of G(s) of synoviocytes in CIA rats. GCS had no effect on the concentration of antibodies to CII. GCS possesses anti-inflammatory and immunoregulatory actions and has a therapeutic effect on CIA rats due to G protein-AC-cAMP transmembrane signal transduction of synoviocytes, which play a crucial role in pathogenesis of this disease.
机译:研究了中草药木瓜木糖苷(GCS)对胶原性关节炎(CIA)大鼠炎症和免疫反应的影响及其机制。用体积计测量大鼠后爪的体积。通过3-(4,5-2二甲基噻唑-2基)2,5-二苯基四唑溴化物(MTT)测定法测定淋巴细胞增殖,白细胞介素-1,白细胞介素-2,TNF-α水平;滑膜细胞中的cAMP水平通过竞争性蛋白结合分析(CPBA)进行分析。通过RT-PCR测量CIA大鼠滑膜细胞G(i,),G(s)和TNF-α的mRNA表达,并通过酶联免疫吸附测定(ELISA)确定II型胶原(CII)的抗体,分别。在CIA模型中有明显的继发性炎症反应,伴随着体重的减少和免疫器官重量的减少。 GCS的给药(30、60、120 mg kg(-1),igx7天)抑制了炎症反应并恢复了CIA大鼠的体重和免疫器官的重量。 CIA大鼠的淋巴细胞增殖和IL-2的产生以及腹膜巨噬细胞和滑膜细胞中的IL-1和TNF-α均增加。 GCS的管理(30、60、120 mg kg(-1),igx7天)显着降低了上述变化。 GCS的浓度为0.5、2.5、12.5、62.5、125 mg l(-1)时,滑膜细胞的cAMP水平升高,在CIA大鼠中降低。同时,GCS抑制了CIA大鼠滑膜细胞G(i,)和TNF-α的mRNA表达,并增加了滑膜细胞G(s)的mRNA表达。 GCS对CII抗体的浓度没有影响。由于滑膜细胞的G蛋白-AC-cAMP跨膜信号转导,GCS具有抗炎和免疫调节作用,并且对CIA大鼠具有治疗作用,其在该疾病的发病机理中起关键作用。

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