Leibowitz S F, Chang G-Q, Dourmashkin J T, Yun R, Julien C, Pamy P P
The Rockefeller University, 1230 York Ave., New York, NY, USA.
Am J Physiol Endocrinol Metab. 2006 Feb;290(2):E258-67. doi: 10.1152/ajpendo.00609.2004.
The objective of this study was to investigate meal-related endocrine changes that permit one to identify Sprague-Dawley rats at normal weight that are prone (OP) vs. resistant (OR) to obesity. In blood collected via chronic cardiac catheters, a 2-h high-fat meal (HFM, 50% fat, 40 kcal) at dark onset caused a significant increase in leptin, insulin, and triglycerides compared with premeal levels. Similar to patterns in already obese compared with lean rats on a high-fat diet, these meal-induced endocrine changes in normal-weight rats on lab chow were almost twofold larger in OP rats that, compared with OR rats, subsequently accumulated 100% more fat mass on a chronic high-fat diet. These exaggerated endocrine changes were similarly observed in blood collected using a simpler tail vein puncture procedure. In three separate experiments, the HFM-induced rise in leptin was found to be the strongest, positive correlate (r = +0.58, +0.62 and +0.64) of long-term body fat accrual. The lowest (2-5 ng/ml) vs. highest (6-9 ng/ml) scores for this post-HFM leptin measurement identified distinct OR and OP subgroups, respectively, when they were similar in body weight (340-350 g), premeal leptin (2.6-3.4 ng/ml), and meal size (40 kcal). Subsequent tests in these normal-weight OP rats revealed a distinct characteristic compared with OR rats, namely, exaggerated HFM-induced rise in expression of the orexigenic peptide galanin in the paraventricular nucleus. Thus, with this HFM-induced leptin measurement, OP rats can be identified while still at normal weight and then investigated for mechanisms that contribute to their excessive body fat accrual on a high-fat diet.
本研究的目的是调查与进食相关的内分泌变化,以便能够识别正常体重下易患肥胖(OP)和抗肥胖(OR)的斯普拉格-道利大鼠。通过慢性心脏导管采集的血液样本显示,在黑暗开始时给予2小时的高脂餐(HFM,50%脂肪,40千卡)后,与餐前水平相比,瘦素、胰岛素和甘油三酯显著增加。与高脂饮食的肥胖大鼠和瘦大鼠的模式相似,正常体重、食用实验室普通饲料的大鼠在进食高脂餐诱导的内分泌变化方面,OP大鼠比OR大鼠几乎大两倍,随后在慢性高脂饮食中积累的脂肪量比OR大鼠多100%。使用更简单的尾静脉穿刺程序采集的血液中也观察到了这些夸张的内分泌变化。在三个独立实验中,发现高脂餐诱导的瘦素升高与长期体脂增加之间存在最强的正相关(r = +0.58、+0.62和+0.64)。当高脂餐后瘦素测量值最低(2-5 ng/ml)与最高(6-9 ng/ml)时,在体重(340-350克)、餐前瘦素(2.6-3.4 ng/ml)和餐量(40千卡)相似的情况下,分别确定了不同的OR和OP亚组。随后对这些正常体重的OP大鼠进行的测试显示,与OR大鼠相比,它们具有一个明显特征,即在室旁核中,高脂餐诱导的食欲肽甘丙肽表达升高更为夸张。因此,通过这种高脂餐诱导的瘦素测量,可以在OP大鼠仍处于正常体重时将其识别出来,然后研究导致它们在高脂饮食中过度积累体脂的机制。