戴景月,赵宇飞,江洋,陈月,唐兴喆,崔颖,彭新桂.MRI脂质定量评估Irisin干预后小鼠肩胛间棕色脂肪激活[J].中国医学影像技术,2023,39(3):321~325
MRI脂质定量评估Irisin干预后小鼠肩胛间棕色脂肪激活
MRI quantitative lipid content for assessment activation of interscapular brown adipose tissue in mice after Irisin intervention
投稿时间:2022-11-04  修订日期:2022-12-07
DOI:10.13929/j.issn.1003-3289.2023.03.001
中文关键词:  脂肪组织  小鼠  磁共振成像
英文关键词:adipose tissue  mice  magnetic resonance imaging
基金项目:国家自然科学基金面上项目(81871412、82272064)、江苏省科技厅面上项目(BK20221461)。
作者单位E-mail
戴景月 东南大学附属中大医院放射科 江苏省分子影像与功能影像重点实验室, 江苏 南京 210009  
赵宇飞 东南大学附属中大医院放射科 江苏省分子影像与功能影像重点实验室, 江苏 南京 210009  
江洋 东南大学附属中大医院放射科 江苏省分子影像与功能影像重点实验室, 江苏 南京 210009  
陈月 东南大学附属中大医院放射科 江苏省分子影像与功能影像重点实验室, 江苏 南京 210009  
唐兴喆 东南大学附属中大医院放射科 江苏省分子影像与功能影像重点实验室, 江苏 南京 210009  
崔颖 东南大学附属中大医院放射科 江苏省分子影像与功能影像重点实验室, 江苏 南京 210009  
彭新桂 东南大学附属中大医院放射科 江苏省分子影像与功能影像重点实验室, 江苏 南京 210009 xingui2005peng@126.com 
摘要点击次数: 2669
全文下载次数: 806
中文摘要:
      目的 探讨MR化学位移选择成像活体定量评估Irisin干预后小鼠肩胛间棕色脂肪组织(iBAT)脂质含量与其活性的相关性。方法 以12只小鼠构建高脂饮食(HFD)诱导肥胖模型(HFD组),随机将其分为磷酸盐缓冲液(PBS)亚组(HFDPBS亚组)、Irisin干预2周亚组(HFDIrisin2w亚组)及干预4周亚组(HFDIrisin4w亚组),每亚组4只;另以正常饮食(CD)饲养4只小鼠(CD组)。对各组对应注射PBS或Irisin溶液予以干预4周后行7.0T Micro MR化学位移成像,测量小鼠iBAT脂质含量MRI;以HE染色测量iBAT细胞内脂滴面积和脂质含量HE,以免疫组织化学法检测iBAT解耦联蛋白1(UCP-1)表达水平。比较各指标组(亚组)间差异,评价MR化学位移成像定量小鼠iBAT脂质含量MRI与病理学检测结果的相关性。结果 HFDPBS亚组小鼠iBAT脂质含量MRI、脂滴面积及脂质含量HE均大于CD组小鼠(P均<0.05),而UCP-1表达水平低于CD组(P<0.05)。HFDIrisin2w亚组小鼠iBAT脂质含量HE低于、而UCP-1表达水平高于HFDPBS亚组小鼠(P均<0.05)。HFDIrisin4w亚组iBAT脂质含量MRI及脂质含量HE显著低于HFDPBS亚组、HFDIrisin2w亚组(P均<0.05),脂滴面积明显小于HFDIrisin2w亚组(P<0.05),UCP-1表达水平高于HFDPBS亚组(P<0.05)。小鼠iBAT脂质含量MRI与通过组织病理学测定的iBAT脂滴面积及脂质含量HE呈正相关(r=0.750、0.974,P均<0.05),与UCP-1表达水平呈负相关(r=-0.681,P=0.01)。结论 Irisin可激活HFD小鼠iBAT活性;MR化学位移选择成像定量小鼠iBAT脂质含量与组织病理学iBAT活性具有相关性。
英文摘要:
      Objective To investigate the correlation between the lipid content quantified with MR chemical shift-selective imaging and the activity of interscapular brown adipose tissue (iBAT) in mice after Irisin intervention. Methods Twelve high-fat diet (HFD) induced obese mice (HFD group) were equally assigned to phosphate buffer solution (PBS) subgroup (HFDPBS subgroup), 2 weeks Irisin intervention subgroup (HFDIrisin2w subgroup) and 4 weeks Irisin intervention subgroup (HFDIrisin4w subgroup), respectively (each n=4), while normal control diet (CD) mice were assigned to CD group (n=4). The mice were intraperitoneally injected with PBS or Irisin solution for 4 weeks, respectively. 7.0T Micro MR chemical shift-selective imaging was used to measure lipid contentMRI of iBAT. HE staining was used to measure the area of lipid droplets and lipid contentHE in brown adipocytes, and the expression level of uncoupling protein-1 (UCP-1) in iBAT was explored with immunohistochemistry. Then the above indexes were compared between group/subgroups, and the correlations of lipid contentMRI detected with MR chemical shift-selective imaging and the pathological indicators were assessed. Results The lipid contentMRI, lipid area and lipid contentHE of iBAT in HFDPBS group were higher than those in CD group (all P<0.05), while the expression levels of UCP-1 was lower than that in CD group (P<0.05). The lipid contentHE in HFDIrisin2w subgroup was lower than that in HFDPBS subgroup (P<0.05), while the expression level of UCP-1 was higher than that in HFDPBS subgroup (P<0.05). The lipid contentMRI and the lipid contentHE of iBAT were significantly lower in HFDIrisin4w subgroup than those in HFDPBS and HFDIrisin2w subgroup (all P<0.05), and the lipid area in HFDIrisin4w subgroup was smaller than that in HFDIrisin2w subgroup (P<0.05), the expression level of UCP-1 in HFDIrisin4w was higher than that in HFDPBS subgroup (P<0.05). The quantity of iBAT lipid contentMRI was positive correlated with iBAT lipid droplet area and lipid contentHE measured histopathologically (r=0.750, 0.974, both P<0.05) and negative correlated with the expression level of UCP-1 (r=-0.681, P=0.01). Conclusion Irisin could activate iBAT activity in HFD mice. The lipid content of iBAT quantified by MR chemical shift-selective imaging was correlated with the iBAT activity assessed histopathologically in mice.
查看全文  查看/发表评论  下载PDF阅读器