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李金平, 侯海峰, 丁国永, 王晶, 王欣农, 李群伟. 脱氧雪腐镰刀菌烯醇对幼鼠关节软骨代谢影响[J]. 中国公共卫生, 2012, 28(3): 347-348. DOI: 10.11847/zgggws2012-28-03-40
引用本文: 李金平, 侯海峰, 丁国永, 王晶, 王欣农, 李群伟. 脱氧雪腐镰刀菌烯醇对幼鼠关节软骨代谢影响[J]. 中国公共卫生, 2012, 28(3): 347-348. DOI: 10.11847/zgggws2012-28-03-40
LI Jin-ping, HOU Hai-feng, DING Guo-yong, . Metabolism and mechanism of articular chondrocytes in young Wistar rats exposed to deoxynivalenol[J]. Chinese Journal of Public Health, 2012, 28(3): 347-348. DOI: 10.11847/zgggws2012-28-03-40
Citation: LI Jin-ping, HOU Hai-feng, DING Guo-yong, . Metabolism and mechanism of articular chondrocytes in young Wistar rats exposed to deoxynivalenol[J]. Chinese Journal of Public Health, 2012, 28(3): 347-348. DOI: 10.11847/zgggws2012-28-03-40

脱氧雪腐镰刀菌烯醇对幼鼠关节软骨代谢影响

Metabolism and mechanism of articular chondrocytes in young Wistar rats exposed to deoxynivalenol

  • 摘要: 目的 观察脱氧雪腐镰刀菌烯醇(DON)对Wistar幼鼠关节软骨胶原合成和分解代谢的影响.方法 24只健康Wistar幼鼠,随机分为对照组、DON低剂量和高剂量组,低剂量和高剂量组隔日灌胃染毒,处理80 d后,免疫组织化学法检测软骨内Ⅱ型胶原、诱导型一氧化氮合酶(iNOS)、基质金属蛋白酶13(MMP-13)表达;ELISA法检测鼠尿液中脱氧吡啶啉(DPD)含量;电镜观察胶原纤维变化情况.结果 对照组、低、高剂量DON组Ⅱ型胶原表达量分别为(7.42±1.12)%、(4.79±0.96)%、(2.82±0.68)%,组间差异有统计学意义(P<0.05);对照组、低、高剂量DON组iNOS与MMP-13表达量分别为(6.90±1.61)%、(8.52±1.90)%、(11.78±2.51)%和(3.06±1.13)%、(6.45±1.56)%、(12.47±2.45)%,随DON浓度增高而增加(P<0.05);ELISA结果显示,DPD表达量随DON浓度增高呈上升趋势;电镜显示,胶原纤维空隙增大,稀疏,呈老化现象,网络结构破坏较明显.结论 DON可增加软骨细胞iNOS表达,提高NO合成,促进MMP-13合成并增加Ⅱ型胶原降解,进而导致软骨损伤.

     

    Abstract: Objective To examine the expression of collagen type Ⅱ,inducible nitric oxide synthase(iNOS),and matrix metalloproteinase(MMP-13) in articular chondrocytes induced by deoxynivalenol(DON).Methods The young healthy Wistar rats were divided into three groups:normal control,low and high-dosage of DON treatment groups.DON saline solution was injected into stomach of the rat on alternative day.The levels of collagen type Ⅱ,iNOS,MMP-13,and deoxypyridinoline(DPD) were determined by immunohistochemical technique,enzym-linked immunosorbent assay,and transmission electron microscope 80 days after the treatments.Results The content of collagen Ⅱ was 7.43%±1.12%,4.79%±0.96%,and 2.82%±0.68% for the control,low dose DON,and high dose DON group,respectively,with significant differences among the groups(P < 0.05 for all).The level of iNOS and MMP-13 had significant differences among the 3 groups(P < 0.05 for all),with higher levels in low and high-dosage of DON treatment groups compared to that of the control.The level of DPD was increased.The transmission electron microscope observation revealed the damage of collagen network of articular cartilage.Conclusion DON could increase the expression of iNOS in articular cartilage cells and promote the anabolism of mitic oxide,the expression of MMP-13,and the degradation of articular cartilage matrix such as collagen type Ⅱ; all these processes induce the damage of articular cartilage.

     

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