Jamdar S C
Biochem J. 1978 Jan 15;170(1):153-60. doi: 10.1042/bj1700153.
The rates of lipid formation were compared in different fat-depots from lean and obese rats by using [14C]glycerol 3-phosphate, [14C]glucose or [14C]acetate as substrates. In lean animals, subcutaneous adipose tissue showed significantly lower rates of lipid synthesis than did perirenal and gonadal fat-tissue. In obese animals, the rates of lipid synthesis were significantly higher and did not vary from one fat-depot to another. Differences in the rates of lipid formation between lean and obese rats disappeared during dietary restriction of obese animals. The isolated adipocyte preparation did not reflect the true metabolic activity of the adipose organ, since this preparation was mainly derived from smaller adipocytes that were metabolically less active than larger adipocytes. The present study suggests that it is better to use whole tissue preparations to measure lipogenesis and esterification reactions, because these measurements represent the contribution of both larger and smaller adipocytes towards lipid formation.
通过使用[14C]甘油3 - 磷酸、[14C]葡萄糖或[14C]乙酸盐作为底物,比较了瘦鼠和肥胖大鼠不同脂肪储存部位的脂质生成速率。在瘦动物中,皮下脂肪组织的脂质合成速率明显低于肾周和性腺脂肪组织。在肥胖动物中,脂质合成速率明显更高,且在不同脂肪储存部位之间没有差异。在对肥胖动物进行饮食限制期间,瘦鼠和肥胖大鼠之间的脂质生成速率差异消失。分离的脂肪细胞制剂不能反映脂肪器官的真实代谢活性,因为这种制剂主要来源于较小的脂肪细胞,其代谢活性低于较大的脂肪细胞。本研究表明,最好使用全组织制剂来测量脂肪生成和酯化反应,因为这些测量代表了较大和较小脂肪细胞对脂质形成的贡献。