党丹 吴芳 郭俊 李宏增 赵聪 汪杰 李川李柱一.非肥胖型糖尿病小鼠成年神经发生的实验研究[J].,2014,14(29):5605-5608 |
非肥胖型糖尿病小鼠成年神经发生的实验研究 |
Study on Adult Neurogenesis in an Animal Model of Non-obese Diabetes |
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DOI: |
中文关键词: 糖尿病 非肥胖型 神经干/ 祖细胞 增殖 |
英文关键词: Diabetes mellitus Non-obese Neural stem/progenitor cell Proliferation |
基金项目:国家自然科学基金项目(31200665) |
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中文摘要: |
目的:探讨异常免疫反应介导的糖尿病(DM)对大脑神经干/ 祖细胞(NSC/NPC)增殖的影响。方法:依据尿糖测定结果将
非肥胖型糖尿病(NOD)小鼠分为发病组和未发病组,观察两组小鼠的体重变化和胰岛炎的严重程度。通过5- 溴-2'- 脱氧尿苷
(BrdU)掺入和免疫荧光染色方法,观察两组小鼠海马齿状回(DG)和侧脑室下区(SVZ)的BrdU 阳性细胞数量的变化,以评估
NSC/NPC增殖情况。结果:发病组小鼠呈现出多饮、多食、多尿等糖尿病典型症状,体重较未发病组明显减低。发病组小鼠胰腺组
织中炎症评分为3 分的胰岛数量明显多于未发病组,且胰岛炎症的平均评分显著高于未发病组(P<0.05)。与未发病组比较,发病
组小鼠大脑海马DG区BrdU阳性细胞显著降低(P<0.01);SVZ区的BrdU阳性细胞数量亦明显少于未发病组(P<0.001)。结论:
异常免疫反应介导的DM可抑制小鼠大脑NSC/NPC 的增殖。 |
英文摘要: |
Objective:To investigate the changes of the proliferation of neural stem/progenitor cell (NSC/NPC) in diabetes
mellitus (DM) mediated by abnormal immune responses.Methods:Female non-obese diabetic (NOD) mice were divided into non-DMor
DM groups according to the results of glycosuria tests. The changes of body weight and the severity of insulitis were observed and
compared between the two groups. 5-bromo-2'-deoxyuridine (BrdU) incorporation and subsequent BrdU immunofluorescent staining
were used. The NSC/NPC proliferation was assessed by counting the number of BrdU-positive cells in the dentate gyrus (DG) of
hippocampus and in the subventricular zone (SVZ), respectively.Results:Diabetic NOD mice exhibited the classical symptoms of
hyperglycemia including polydipsia, polyuria, and weight loss. The number of islets with an inflammatory score of 3 was larger in DM
group than in non-DMgroup. The mean inflammatory score of insulitis is also higher in DMgroup (P < 0.05). Compared with non-DM
NOD mice, the number of BrdU-positive cells was significantly decreased in the DG of hippocampus in diabetic NOD mice (P<0.01).
Similarly, a reduced number of BrdU-positive cells also occurred in the SVZ of diabetic NOD mice (P<0.001).Conclusion:Abnormal
immune responses-mediated DMcontributes to an impaired NSC/NPC proliferation in female NOD mice. |
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