Jin Xin, Sun Jing, Xie Wenli, Wan Zongming, Jin Yuzhang, Zhu Jiang
Department of Pharmacology, Medical College of Chinese People's Armed Police Forces, Tianjin 300162, China.
Zhongguo Zhong Yao Za Zhi. 2009 Dec;34(23):3082-6.
To study the effect of geniposide-acid(GA) on the anti-inflammatory action for adjuvant-induced arthritis (AA) rats and the proliferation of synoviocytes in AA rats and the feasible mechanism of apoptosis in vitro.
Forty-eight health male Wistar rats were divided randomly into six groups and were administered respectively with 200, 100, 50 mg x kg(-1) GA and 0.75 mg x kg(-1) MTX and normal sodium (normal or model control group) for four weeks when right posterior paw pads of rats excluding normal control group were injected intrademally with complete Freund's adjuvant after 19 days. The left posterior paws swelling degree, swelling inhibition ratio and arthritis index of secondary inflamation were detected. The TNF-alpha and IL-1beta proteins in serum of rats were assayed by enzyme linked immunosorbent assay (ELISA) kits. The synovial fibroblasts of AA rats were exposed to 1-4 micromol x L(-1) GA or 4 micromol x L(-1) MTX. The effect of GA on the proliferation of synoviocytes was detected by MTT assay. The morphologic change of apoptosis cells was observed by Hoechst/PI double stainning and fluorescence microscope. The rate of apoptosis cells was analyzed by flow cytometry. The mRNA expresstion of Bcl-2 and Bax gene was detected by reverse transcription PCR (RT-PCR).
200 mg kg(-1) or 100 mg kg(-1) GA could decrease significantly the paw swelling degree, arthritis index and the level of TNF-alpha and IL-1beta proteins in serum of AA rats (P < 0.05 or P < 0.01) with 25.4%, 21.37% of the swelling inhibition ratio respectivly, 34.61%, 28% of protein inhibition ratio of TNF-alpha and 29.05%, 21.65% of that of IL-1beta. GA(1-4 micromol x L(-1)) inhibitated significantly the proliferation of synoviocytes culcured for 5 days. Flow cytometry showed that 1, 2, 4 micromol x L(-1) GA increased obviously the rate of apoptosis cells, the apoptosis ratios were 15.8%, 24.3%, 40.7% respectivly (P < 0.01). RT-PCR showed GA could decrease the expression level of Bcl-2 gene but increase that of Bax gene (P < 0.05 or P < 0.01).
GA could inhibit the secondary inflamation of AA rats and decrease the level of TNF-alpha and IL-1beta protein in the AA rats serum. GA could inhibit the proliferation of AA rat synoviocytes in vitro and induce apoptosis which mechanism was concerned with down-regulating the mRNA expression of Bcl-2 and up-regulating that of Bax.
研究京尼平苷酸(GA)对佐剂性关节炎(AA)大鼠的抗炎作用、AA大鼠滑膜细胞增殖及体外细胞凋亡的可能机制。
48只健康雄性Wistar大鼠随机分为6组,分别给予200、100、50mg·kg⁻¹GA及0.75mg·kg⁻¹甲氨蝶呤(MTX)和生理盐水(正常或模型对照组),连续灌胃4周。于第19天除正常对照组外,其余大鼠右后足跖皮内注射完全弗氏佐剂。检测大鼠左后足肿胀度、肿胀抑制率及继发性炎症的关节炎指数。采用酶联免疫吸附测定(ELISA)试剂盒检测大鼠血清中肿瘤坏死因子-α(TNF-α)和白细胞介素-1β(IL-1β)蛋白水平。将AA大鼠的滑膜成纤维细胞分别暴露于1~4μmol·L⁻¹GA或4μmol·L⁻¹MTX。采用MTT法检测GA对滑膜细胞增殖的影响。通过Hoechst/PI双重染色及荧光显微镜观察凋亡细胞的形态变化。采用流式细胞术分析凋亡细胞率。通过逆转录聚合酶链反应(RT-PCR)检测Bcl-2和Bax基因的mRNA表达。
200mg·kg⁻¹或100mg·kg⁻¹GA可显著降低AA大鼠足肿胀度、关节炎指数及血清中TNF-α和IL-1β蛋白水平(P<0.05或P<0.01),肿胀抑制率分别为25.4%、21.37%,TNF-α蛋白抑制率分别为34.61%、28%,IL-1β蛋白抑制率分别为29.05%、21.65%。GA(1~4μmol·L⁻¹)显著抑制培养5天的滑膜细胞增殖。流式细胞术显示,1、2、4μmol·L⁻¹GA明显增加凋亡细胞率,凋亡率分别为15.8%、24.3%、40.7%(P<0.01)。RT-PCR显示GA可降低Bcl-2基因表达水平,但增加Bax基因表达水平(P<0.05或P<0.01)。
GA可抑制AA大鼠的继发性炎症,降低AA大鼠血清中TNF-α和IL-1β蛋白水平。GA可体外抑制AA大鼠滑膜细胞增殖并诱导凋亡,其机制与下调Bcl-2 mRNA表达及上调Bax mRNA表达有关。