首页> 美国卫生研究院文献>Journal of Visualized Experiments : JoVE >Functional Imaging of Brown Fat in Mice with 18F-FDG micro-PET/CT
【2h】

Functional Imaging of Brown Fat in Mice with 18F-FDG micro-PET/CT

机译:18F-FDG micro-PET / CT对小鼠棕色脂肪的功能成像

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Brown adipose tissue (BAT) differs from white adipose tissue (WAT) by its discrete location and a brown-red color due to rich vascularization and high density of mitochondria. BAT plays a major role in energy expenditure and non-shivering thermogenesis in newborn mammals as well as the adults 1. BAT-mediated thermogenesis is highly regulated by the sympathetic nervous system, predominantly via β adrenergic receptor 2, 3. Recent studies have shown that BAT activities in human adults are negatively correlated with body mass index (BMI) and other diabetic parameters 4-6. BAT has thus been proposed as a potential target for anti-obesity/anti-diabetes therapy focusing on modulation of energy balance 6-8. While several cold challenge-based positron emission tomography (PET) methods are established for detecting human BAT 9-13, there is essentially no standardized protocol for imaging and quantification of BAT in small animal models such as mice. Here we describe a robust PET/CT imaging method for functional assessment of BAT in mice. Briefly, adult C57BL/6J mice were cold treated under fasting conditions for a duration of 4 hours before they received one dose of 18F-Fluorodeoxyglucose (FDG). The mice were remained in the cold for one additional hour post FDG injection, and then scanned with a small animal-dedicated micro-PET/CT system. The acquired PET images were co-registered with the CT images for anatomical references and analyzed for FDG uptake in the interscapular BAT area to present BAT activity. This standardized cold-treatment and imaging protocol has been validated through testing BAT activities during pharmacological interventions, for example, the suppressed BAT activation by the treatment of β-adrenoceptor antagonist propranolol 14, 15, or the enhanced BAT activation by β3 agonist BRL37344 16. The method described here can be applied to screen for drugs/compounds that modulate BAT activity, or to identify genes/pathways that are involved in BAT development and regulation in various preclinical and basic studies.
机译:棕色脂肪组织(BAT)与白色脂肪组织(WAT)的不同之处在于其离散的位置和棕红色,这归因于丰富的血管形成和线粒体的高密度。 BAT在新生哺乳动物以及成年动物 1 的能量消耗和不发抖的产热中起着重要作用。 BAT介导的生热受到交感神经系统的高度调节,主要通过β肾上腺素受体 2,3 来调节。最近的研究表明,成年人中的BAT活性与体重指数(BMI)和其他糖尿病参数 4-6 呈负相关。因此,以调节能量平衡 6-8 为重点,BAT被认为是抗肥胖/抗糖尿病治疗的潜在靶点。虽然建立了几种基于冷挑战的正电子发射断层扫描(PET)方法来检测人BAT 9-13 ,但基本上没有标准化协议可在小鼠等小型动物模型中对BAT进行成像和定量。在这里,我们描述了一种强大的PET / CT成像方法,用于小鼠中BAT的功能评估。简而言之,成年C57BL / 6J小鼠在禁食条件下进行了4小时的冷处理,然后再接受一剂 18 F-氟脱氧葡萄糖(FDG)。 FDG注射后,小鼠在寒冷中再呆一个小时,然后用小型动物专用的micro-PET / CT系统扫描。将获取的PET图像与CT图像共同配准,以提供解剖参考,并分析肩s间BAT区域的FDG摄取情况,以展现BAT活性。通过测试药理干预过程中的BAT活性,已经验证了这种标准化的冷疗和成像方案,例如,通过治疗β-肾上腺素受体拮抗剂普萘洛尔 14、15 或增强的BAT抑制了BAT活化。 β3激动剂BRL37344 16 活化。本文所述方法可用于筛选可调节BAT活性的药物/化合物,或用于鉴定各种临床前和基础研究中与BAT开发和调节有关的基因/途径。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号