{"title":"周围亚急性治疗鸢尾素对海马树突发生和星形胶质细胞分泌因子的影响。","authors":"Mun-Hee Kim, Yea-Hyun Leem","doi":"10.20463/jenb.2019.0029","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Fibronectin type III domain containing 5 (FNDC5)/irisin is an exercise-induced myokine, which contributes to cognitive functions. However, the relationship between the neuroprotective effects of FNDC5/irisin and hippocampal dendritic remodeling and astrocyte-secreted factors remains unclear. Therefore, we explored whether subchronic recombinant irisin treatment affected hippocampal morphology and some astrocyte-derived molecules.</p><p><strong>Methods: </strong>Mice were intraperitoneally injected with irisin (0.5 μg/kg/day) for seven days, followed by their sacrifice two days later. Hippocampal morphometric parameters were analyzed and pgc-1a, fndc5, bdnf, and some astrocyte-derived factors mRNA levels were measured.</p><p><strong>Results: </strong>Dendritic length, arborization, and spine density were enhanced by irisin regimen in hippocampal CA1 and CA3 areas. Hippocampal pgc-1a, fndc5, and bdnf mRNA levels were significantly increased by irisin treatment. Moreover, hevin mRNA levels were significantly enhanced, whereas tgf-b1 levels downregulated by irisin treatment.</p><p><strong>Conclusion: </strong>FNDC5/irisin has dendritogenic activity probably through hevin induction and TGF-β1 suppression.</p>","PeriodicalId":15795,"journal":{"name":"Journal of Exercise Nutrition & Biochemistry","volume":"23 4","pages":"32-35"},"PeriodicalIF":0.0000,"publicationDate":"2019-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004566/pdf/","citationCount":"5","resultStr":"{\"title\":\"The effects of peripherally-subacute treatment with irisin on hippocampal dendritogenesis and astrocyte-secreted factors.\",\"authors\":\"Mun-Hee Kim, Yea-Hyun Leem\",\"doi\":\"10.20463/jenb.2019.0029\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>Fibronectin type III domain containing 5 (FNDC5)/irisin is an exercise-induced myokine, which contributes to cognitive functions. However, the relationship between the neuroprotective effects of FNDC5/irisin and hippocampal dendritic remodeling and astrocyte-secreted factors remains unclear. Therefore, we explored whether subchronic recombinant irisin treatment affected hippocampal morphology and some astrocyte-derived molecules.</p><p><strong>Methods: </strong>Mice were intraperitoneally injected with irisin (0.5 μg/kg/day) for seven days, followed by their sacrifice two days later. Hippocampal morphometric parameters were analyzed and pgc-1a, fndc5, bdnf, and some astrocyte-derived factors mRNA levels were measured.</p><p><strong>Results: </strong>Dendritic length, arborization, and spine density were enhanced by irisin regimen in hippocampal CA1 and CA3 areas. Hippocampal pgc-1a, fndc5, and bdnf mRNA levels were significantly increased by irisin treatment. Moreover, hevin mRNA levels were significantly enhanced, whereas tgf-b1 levels downregulated by irisin treatment.</p><p><strong>Conclusion: </strong>FNDC5/irisin has dendritogenic activity probably through hevin induction and TGF-β1 suppression.</p>\",\"PeriodicalId\":15795,\"journal\":{\"name\":\"Journal of Exercise Nutrition & Biochemistry\",\"volume\":\"23 4\",\"pages\":\"32-35\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-12-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004566/pdf/\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Exercise Nutrition & Biochemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.20463/jenb.2019.0029\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Exercise Nutrition & Biochemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20463/jenb.2019.0029","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5
摘要
目的:Fibronectin type III domain containing 5 (FNDC5)/irisin是一种运动诱导的肌因子,有助于认知功能。然而,FNDC5/鸢尾素的神经保护作用与海马树突重塑和星形胶质细胞分泌因子之间的关系尚不清楚。因此,我们探讨了亚慢性重组鸢尾素治疗是否影响海马形态和一些星形胶质细胞衍生分子。方法:小鼠腹腔注射鸢尾素(0.5 μg/kg/d) 7 d, 2 d后处死。分析海马形态计量学参数,测定pgc-1a、fndc5、bdnf及部分星形胶质细胞衍生因子mRNA水平。结果:鸢尾素可增强海马CA1和CA3区的树突长度、树突化和脊柱密度。鸢尾素处理后,海马pgc-1a、fndc5和bdnf mRNA水平显著升高。鸢尾素显著提高了hevin mRNA水平,降低了tgf-b1水平。结论:FNDC5/鸢尾素可能通过诱导hevin和抑制TGF-β1而具有树突生成活性。
The effects of peripherally-subacute treatment with irisin on hippocampal dendritogenesis and astrocyte-secreted factors.
Purpose: Fibronectin type III domain containing 5 (FNDC5)/irisin is an exercise-induced myokine, which contributes to cognitive functions. However, the relationship between the neuroprotective effects of FNDC5/irisin and hippocampal dendritic remodeling and astrocyte-secreted factors remains unclear. Therefore, we explored whether subchronic recombinant irisin treatment affected hippocampal morphology and some astrocyte-derived molecules.
Methods: Mice were intraperitoneally injected with irisin (0.5 μg/kg/day) for seven days, followed by their sacrifice two days later. Hippocampal morphometric parameters were analyzed and pgc-1a, fndc5, bdnf, and some astrocyte-derived factors mRNA levels were measured.
Results: Dendritic length, arborization, and spine density were enhanced by irisin regimen in hippocampal CA1 and CA3 areas. Hippocampal pgc-1a, fndc5, and bdnf mRNA levels were significantly increased by irisin treatment. Moreover, hevin mRNA levels were significantly enhanced, whereas tgf-b1 levels downregulated by irisin treatment.
Conclusion: FNDC5/irisin has dendritogenic activity probably through hevin induction and TGF-β1 suppression.