Okamoto Yuji, Higashiyama Hiroyuki, Inoue Hiroki, Kanematsu Masahiro, Kinoshita Mine, Asano Satoshi
Pharmacology Department, Tsukuba Research Laboratories, GlaxoSmithKline, Wadai, Tsukuba, Japan.
Pathol Int. 2007 Jun;57(6):369-77. doi: 10.1111/j.1440-1827.2007.02109.x.
Morphometric analysis of adipocytes is widely used to demonstrate the effects of antiobesity drugs or anti-diabetic drugs on adipose tissues. However, adipocyte morphometry has been quantitatively performed by manual object extraction using conventional image analysis systems. The authors have developed an automated quantitative image analysis method for adipose tissues using an innovative object-based quantitative image analysis system (eCognition). Using this system, it has been shown quantitatively that morphological features of adipose tissues of mice treated with peroxisome proliferator-activated receptor (PPAR) agonists differ dramatically depending on the type of PPAR agonist. Marked alteration of morphological characteristics of brown adipose tissue (BAT) treated with GI259578A, a PPAR-alpha agonist, was observed in AKR/J (AKR) obese mice. Furthermore, there was a 22.8% decrease in the mean size of adipocytes in white adipose tissue (WAT) compared with vehicle. In diabetic db/db mice, the PPAR-gamma agonist GW347845X decreased the mean size of adipocytes in WAT by 15.4% compared with vehicle. In contrast to changes in WAT, GW347845X increased the mean size of adipocytes in BAT greatly by 96.1% compared with vehicle. These findings suggest that GI259578A may activate fatty acid oxidation in BAT and that GW347845X may cause adipocyte differentiation in WAT and enhancement of lipid storage in BAT.
脂肪细胞的形态计量分析被广泛用于证明抗肥胖药物或抗糖尿病药物对脂肪组织的作用。然而,脂肪细胞形态计量学一直是通过使用传统图像分析系统手动提取对象来进行定量分析的。作者开发了一种使用创新的基于对象的定量图像分析系统(eCognition)对脂肪组织进行自动定量图像分析的方法。使用该系统已定量显示,用过氧化物酶体增殖物激活受体(PPAR)激动剂治疗的小鼠脂肪组织的形态特征因PPAR激动剂的类型而异。在AKR/J(AKR)肥胖小鼠中观察到用PPAR-α激动剂GI259578A处理的棕色脂肪组织(BAT)的形态特征发生了明显改变。此外,与载体相比,白色脂肪组织(WAT)中脂肪细胞的平均大小减少了22.8%。在糖尿病db/db小鼠中,与载体相比,PPAR-γ激动剂GW347845X使WAT中脂肪细胞的平均大小减少了15.4%。与WAT的变化相反,与载体相比,GW347845X使BAT中脂肪细胞的平均大小大幅增加了96.1%。这些发现表明,GI259578A可能激活BAT中的脂肪酸氧化,而GW347845X可能导致WAT中的脂肪细胞分化并增强BAT中的脂质储存。