银杏二萜内酯调控Toll样受体4/核因子-κB通路对糖尿病大鼠肾脏病变的影响及机制研究

    Efficacy and mechanism of ginkgo diterpenoid lactoneon on renal lesions in diabetes mellitus rats by regulating Toll-like receptor 4/nuclear factor-κB signal pathway

    • 摘要:
      目的  研究银杏二萜内酯对糖尿病(diabetic mellitus,DM)大鼠肾脏病变的影响,并基于Toll样受体4(toll like receptor 4,TLR4)/核因子-κB(nuclear factor-κB,NF-κB)通路探讨其可能的作用机制。
      方法  采用高糖高脂饮食4周后腹腔注射30 mg/kg链脲佐菌素的方法构建DM大鼠模型,设模型组、银杏二萜内酯组、瑞沙托维(TLR4抑制剂)组、银杏二萜内酯+瑞沙托维组,另设正常对照组。各组分别1次/d腹腔注射给药治疗14 d后,测定空腹血糖(fasting blood glucose,FBG)、血肌酐(serum creatinine,Scr)、尿素氮(blood urea nitrogen,BUN)和24 h尿蛋白定量(24 h urine protein,24 h-UTP)水平,通过苏木精-伊红染色和马松染色观察肾脏病变,透射电子显微镜观察肾小球足细胞超微结构病变,末端标记法观察细胞凋亡状况,酶联免疫吸附法检测肾组织炎症因子白细胞介素(interleukin,IL)1β、IL-6、IL-8、肿瘤坏死因子α(tumor necrosis factor-α,TNF-α)含量,蛋白质印迹法检测TLR4、NF-κB p65、p-NF-κB p65、NF-κB抑制因子(inhibitor α of NF-κB,IκBα)、p-IκBα、B淋巴细胞瘤2(b-cell lymphoma-2,Bcl-2)、Bcl-2相关X蛋白(bcl-2 assaciated X protein,Bax)表达。
      结果  与模型组相比,银杏二萜内酯组、瑞沙托维组和银杏二萜内酯+瑞沙托维组FBG(9.51 ± 1.13) mmol/L、(12.17 ± 1.42)mmol/L、(8.09 ± 1.05)mmol/L比(21.08 ± 3.49) mmol/L、Scr(45.69 ± 5.78)μmol/L、(51.02 ± 6.91)μmol/L、(38.57 ± 4.28)μmol/L比(91.44 ± 12.50) μmol/L、BUN(9.28 ± 1.54)mmol/L、(10.96 ± 1.80)mmol/L、(7.01 ± 0.78)mmol/L比(16.13 ± 1.72) mmol/L、24 h-UTP(17.69 ± 2.03)mg、(19.75 ± 2.16)mg、(13.54 ± 1.39)mg比(45.28 ± 4.71)mg水平明显降低(P均<0.05);肾小球萎缩、系膜扩张、胶原沉积、炎性浸润等肾脏病变明显改善;足细胞足突融合变宽,基底膜弥漫性增厚,线粒体肿胀、嵴断裂等超微结构病变明显改善;细胞凋亡指数(16.75 ± 2.06)%、(20.19 ± 2.50)%、(8.07 ± 1.14)%比(38.45 ± 4.61)%明显降低(P<0.05);IL-1β(37.42 ± 4.81)ng/L、(40.95 ± 5.27)ng/L、(32.17 ± 4.30)ng/L比(54.16 ± 7.03)ng/L、IL-6(49.37 ± 6.02)ng/L、(54.83 ± 6.53)ng/L、(43.26 ± 5.51)ng/L比(74.22 ± 9.48)ng/L、IL-8(28.04 ± 3.53)ng/L、(32.11 ± 3.98)ng/L、(20.47 ± 2.45)ng/L比(41.86 ± 5.12)ng/L、TNF-α(461.57 ± 62.85)ng/L、(510.83 ± 69.21)ng/L、(351.29 ± 43.08)ng/L比(772.63 ± 120.92)ng/L含量明显降低(P均<0.05);TLR4(0.19 ± 0.04)、(0.28 ± 0.05)、(0.13 ± 0.03)比(0.43 ± 0.06)、p-NF-κB p65(0.22 ± 0.04)、(0.56 ± 0.11)、(0.14 ± 0.03)比(0.94 ± 0.17)、p-IκBα(0.17 ± 0.04)、(0.26 ± 0.05)、(0.12 ± 0.03)比(0.45 ± 0.07)、Bax(0.18 ± 0.04)、(0.32 ± 0.07)、(0.14 ± 0.03)比(1.14 ± 0.19)表达量及p-NF-κB p65/NF-κB p65 (0.27 ± 0.06)、(0.69 ± 0.14)、(0.17 ± 0.04)比(1.22 ± 0.24)、p-IκBα/IκBα(0.81 ± 0.17)、(1.36 ± 0.22)、(0.54 ± 0.10)比(2.25 ± 0.41)、Bax/Bcl-2(0.82 ± 0.17)、(1.59 ± 0.24)、(0.29 ± 0.06)比(22.78 ± 3.64)比值明显降低,Bcl-2(0.22 ± 0.05)、(0.20 ± 0.04)、(0.48 ± 0.10)比(0.05 ± 0.01)表达量明显升高(P均<0.05)。银杏二萜内酯+瑞沙托维组对DM大鼠上述指标的影响明显优于银杏二萜内酯组和瑞沙托维组(P均<0.05)。
      结论  银杏二萜内酯可减轻DM大鼠肾脏病变和足细胞超微结构病变,改善肾功能,其机制可能与抑制TLR4/NF-κB通路活化,降低炎症反应和细胞凋亡有关。

       

      Abstract:
      Objective  To explore the efficacy of ginkgo diterpene lactone on renal lesions and explore its mechanism based upon signal pathway of toll-like receptor 4/nuclear factor-κB (TLR4/NF-κB) in diabetic mellitus (DM) rats.
      Methods  DM rat model was established by a daily intraperitoneal injection of 30 mg/kg streptozotocin after a 4-week diet of high sugar and high fat. The animals were assigned into model, ginkgo diterpene lactone, resatorvid (TLR4 inhibitor) and ginkgo diterpene lactone plus resatorvid and normal. After 14-day injection, the levels of fasting blood glucose(FBG), serum creatinine(Scr), urea nitrogen(BUN) and 24 h urinary totalprotein(24 h UTP) were measured. Renal pathological changes were observed after hematoxylin eosin (HE) and Masson staining. And ultrastructural changes of glomerular podocytes were examined by transmission electron microscopy. Apoptosis was observed after TdT-mediated dUTP nick-end labeling(TUNEL) staining. The contents of interleukin-1β(IL-1β), interleukin-6(IL-6), interleukin-8(IL-8) and tumor necrosis factor-α(TNF-α) were detected by enzyme-linked immunosorbent assay(ELISA). And the expressions of TLR4, NF-κB p65, p-NF-κB p65, NF-κB inhibitor α(IκBα), p-IκBα, B-cell lymphoma-2 (Bcl-2) and Bcl-2 associated X protein(Bax) were detected by Western blot.
      Results As compared with model group, the levels of FBG(9.51 ± 1.13) mmol/L,(12.17 ± 1.42) mmol/L, (8.09 ± 1.05) mmol/L vs (21.08 ± 3.49) mmol/L, Scr (45.69 ± 5.78) μmol/L, (51.02 ± 6.91) μmol/L, (38.57 ± 4.28) μmol/L vs (91.44 ± 12.50) μmol/L, BUN (9.28 ± 1.54) mmol/L , (10.96 ± 1.80) mmol/L, (7.01 ± 0.78) mmol/L vs (16.13 ± 1.72) mmol/L and 24h UTP (17.69 ± 2.03) mg, (19.75 ± 2.16) mg, (13.54 ± 1.39) mg vs (45.28 ± 4.71) mg declined markedly(all P<0.05). There were marked improvements of glomerular atrophy, mesangial expansion, collagen deposition, inflammatory infiltration and podocyte shrinkage. And foot process fusion of podocytes widening, basement membrane thickening, mitochondrial swelling and crista rupturing lessened greatly. Apoptotic index dropped markedly(16.75 ± 2.06)% , (20.19 ± 2.50)%, (8.07 ± 1.14)% vs (38.45 ± 4.61)%(P<0.05). The contents of IL-1β (37.42 ± 4.81) ng/L , (40.95 ± 5.27) ng/L, (32.17 ± 4.30) ng/L vs (54.16 ± 7.03) ng/L, IL-6(49.37 ± 6.02) ng/L, (54.83 ± 6.53) ng/L, (43.26 ± 5.51) ng/L vs (74.22 ± 9.48) ng/L, IL-8 (28.04 ± 3.53) ng/L, (32.11 ± 3.98) ng/L, (20.47 ± 2.45) ng/L vs (41.86 ± 5.12) ng/L and TNF-α (461.57 ± 62.85) ng/L, (510.83 ± 69.21) ng/L, (351.29 ± 43.08) ng/L vs (772.63 ± 120.92) ng/L decreased markedly (all P<0.05). The expressions of TLR4(0.19 ± 0.04) vs (0.28 ± 0.05), (0.13 ± 0.03) vs (0.43 ± 0.06), p-NF-κB p65(0.22 ± 0.04) vs (0.56 ± 0.11), (0.14 ± 0.03) vs (0.94 ± 0.17), p-IκBα(0.17 ± 0.04) vs (0.26 ± 0.05), (0.12 ± 0.03) vs (0.45 ± 0.07), Bax(0.18 ± 0.04) vs (0.32 ± 0.07), (0.14 ± 0.03) vs (1.14 ± 0.19) and ratio of p-NF-κB p65/NF-κB p65(0.27 ± 0.06) vs (0.69 ± 0.14), (0.17 ± 0.04) vs (1.22 ± 0.24), p-IκBα/IκBα(0.81 ± 0.17) vs (1.36 ± 0.22), (0.54 ± 0.10) vs (2.25 ± 0.41) and Bax/Bcl-2(0.82 ± 0.17) vs (1.59 ± 0.24), (0.29 ± 0.06) vs (22.78 ± 3.64) dropped markedly. The expression of Bcl-2 was up-regulated (0.22 ± 0.05) vs (0.20 ± 0.04), (0.48 ± 0.10) vs (0.05 ± 0.01)(all P<0.05). The efficacies of ginkgo diterpene lactone plus resatovi group on the above parameters were significantly better than those of ginkgo diterpene lactone and resatovi groups (all P<0.05).
      Conclusion  Ginkgo diterpene lactone may alleviate podocyte ultrastructural lesions and improve renal function in DM rats. Its mechanism may be correlated with an inhibition of TLR4/NF-κB and lessening of inflammatory response and apoptosis.

       

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