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年轻血液对衰老相关认知功能障碍的改善作用 被引量:2

The young blood improves the aging-related cognitive impairments
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摘要 目的通过建立异时或同时连体模型,探讨年轻血液对衰老相关认知功能障碍的改善。方法用C57BL/6小鼠、EGFP转基因小鼠建立EGFP-C57BLJ6异时或同时连体模型。通过脾脏细胞分离和荧光显微镜技术检测连体模型血液嵌合情况。通过场景恐惧实验和新物体识别实验检测连体模型组中的年老C57BL/6小鼠的学习记忆能力。结果 EGFP-C57BL/6连体模型形成稳定的血液嵌合。场景恐惧实验的关联测试中,异时连体模型组中的年老C57BL/6小鼠的学习记忆能力得到显著改善(P<0.05)。新物体识别实验中,异时连体模型组中的年老鼠对新物体的辨别能力和短期及长期记忆能力明显增强(P<0.05)。结论年轻血液可显著提高年老鼠的学习和记忆能力,改善衰老相关认知功能障碍。 Objective To investigate the improving effects of young blood on aging-related cognitive disorder through the establishment of heterochronic parabiosis models. Methods EGFP-C57BL/6 heterochronic or isochronic parabiosis models were established using C57BL/6 mice and EGFP transgenic mice. The blood chimerism of parabiosis model was analyzed by the isolation of spleen cells and subsequent fluorescence microscopy. The learning and memory of the old C57BL/6 mice in parabiosis model groups was evaluated by contextual fear conditioning test and novel object recognition test. Results Stable blood chimerism was established successfully in parabiosis models. In contextual memory testing of the contextual fear conditioning test, the learning and memory abilities of the old C57BL/6 mice in heterochronic parabiosis model group were obviously improved (p〈0.05). In the novel object recognition test, the capacity of recognizing novel object and short-term and long-term memory of the old C57BL/6 mice in heterochronic parabiosis model group were significantly enhanced (p〈0.05). Conclusion Young blood can evidently improve the learning and memory of the old mice and ameliorate aging-related cognitive disorders.
出处 《解剖科学进展》 CAS 2015年第1期63-67,共5页 Progress of Anatomical Sciences
基金 黑龙江省卫生厅科研课题(No.2302242002133) 国家自然基金面上项目(No.81073162) 黑龙江省留学归国基金(No.Lc201016/C090301) 黑龙江省教育厅面上项目(No.115511811) 黑龙江省博士后启动基金(No.LBH-Q11027)
关键词 衰老 年轻血液 C57BL/6小鼠 EGFP转基因小鼠 连体模型 aging young blood C57BL/6 mouse EGFP transgenic mouse parabiosis model
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同被引文献12

  • 1陈向荣,游思维,金大地.BBB评分评估脊髓损伤大鼠后肢运动功能的探讨[J].中国脊柱脊髓杂志,2004,14(9):547-549. 被引量:52
  • 2Finerty JC.Parabiosis in physiological studies[J].Physiol Rev,1952,32:277-302.
  • 3Katsimpardi L,Litterman NK,Schein PA,et al.Vascular and neurogenic rejuvenation of the aging mouse brain by young systemic factors[J].Science,2014,344(10):630-634.
  • 4Conboy MJ,Conboy IM,Thomas A.Heterochronic parabiosis:historical perspective and methodological considerations for studies of aging and longevity[J].Aging Cell,2013,12(10):525-530.
  • 5Conboy MJ,Conboy IM,Rando TA.Heterochronic parabiosis:historical perspective and methodological considerations for studies of aging and longevity[J].Aging cell,2013,12:525-530.
  • 6Duyverman AMMJ,Kohno M,Duda DG,et al.A transient parabiosis skin transplantation model in mice[J].Nature Protocols,2013,7(4):763-770.
  • 7Finerty JC.Parabiosis in physiological studies[J].Physiol Rev,1952,32:277-302.
  • 8Katsimpardi L,Litterman NK,Schein PA,et al.Vascular and neurogenic rejuvenation of the aging mouse brain by young systemic factors[J].Science,2014,344(10),630-634.
  • 9Conboy MJ,Conboy IM,Thomas A.Heterochronic parabiosis:historical perspective and methodological considerations for studies of aging and longevity[J].Aging Cell,2013,12(10):525-530.
  • 10Conboy MJ,Conboy IM,Rando TA.Heterochronic parabiosis:historical perspective and methodological considerations for studies of aging and longevity[J].Aging cell,2013,12:525-530.

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