Havel P J, Kasim-Karakas S, Mueller W, Johnson P R, Gingerich R L, Stern J S
Department of Nutrition, School of Medicine, University of California, Davis 95616, USA.
J Clin Endocrinol Metab. 1996 Dec;81(12):4406-13. doi: 10.1210/jcem.81.12.8954050.
Leptin, the product of the human homologue of the ob gene, which is defective in the obese (ob/ob) mouse, may be a humoral regulator of human adiposity. Plasma leptin concentrations were measured by RIA in 19 normal weight [body mass index (BMI) = 24.5 +/- 0.6 kg/m2] and 19 overweight to obese (BMI = 34.7 +/- 1.2 kg/m2) nondiabetic postmenopausal women on sequential controlled weight-maintaining diets containing 31%, 23%, and 14% of energy as fat, each for 4-6 weeks. Thereafter, the subjects ate a very low fat diet (< 15%) ad libitum; plasma leptin and insulin concentrations, BMI, percent body fat (%BF), and resting energy expenditure were determined after 6 and 8 months. Absolute and adiposity-corrected plasma leptin levels were higher in overweight/obese women (37.7 +/- 3.5 ng/mL; 1.01 +/- 0.07 ng.mL-1.%BF-1) than in normal weight women (16.9 +/- 2.2 ng/mL; 0.57 +/- 0.06 ng.mL-1.%BF-1, both P < 0.005 vs. obese), but were not different between the 31%, 23%, and 14% fat diets when body weight was stable. Plasma leptin was highly correlated with BMI (r = 0.81, P < 0.0001), %BF (r = 0.80, P < 0.0001), and fasting plasma insulin (r = 0.61, P < 0.0001). After 8 months on the ad libitum low fat diet, the women had lost an average of 6.9 +/- 1.0% of body mass (-2.0 +/- 0.3 kg/m2, P < 0.0001). In 15 subjects who lost more than 7% of body mass (-12.3 +/- 1.0%), plasma leptin concentrations decreased (-9.6 +/- 1.9 ng/mL, P < 0.0005), and the decrease of plasma leptin per change of adiposity (delta leptin/delta %BF) was greater in overweight/obese women (3.6 +/- 0.5) than in normal weight women (0.9 +/- 0.4, P < 0.01 vs. obese). In 18 other subjects who lost less than 7% of body mass (-2.7 +/- 0.6%), plasma leptin was unchanged (+1.4 +/- 1.4 ng/mL). Overall, the change of plasma leptin was significantly correlated with change of BMI (r = 0.43, P < 0.02), the change of %BF (r = 0.49, P < 0.005), the change of resting energy expenditure (r = 0.40, P < 0.02), and with the change of plasma insulin independently of changes of body adiposity (r = 0.45, P < 0.01). We conclude that plasma leptin concentrations are: 1) not affected by dietary fat content per se; 2) highly correlated with BMI, %BF, and plasma insulin in both overweight/obese and normal weight women; 3) decreased in parallel with plasma insulin after sustained weight loss; and 4) decreased more in overweight/obese than in normal weight women.
瘦素是肥胖(ob/ob)小鼠中存在缺陷的ob基因的人类同源物的产物,可能是人体肥胖的一种体液调节因子。采用放射免疫分析法(RIA)测定了19名体重正常[体重指数(BMI)=24.5±0.6kg/m²]和19名超重至肥胖(BMI=34.7±1.2kg/m²)的非糖尿病绝经后女性的血浆瘦素浓度。这些女性按顺序食用能量分别为31%、23%和14%来自脂肪的控制体重饮食,每种饮食持续4 - 6周。此后,受试者随意食用极低脂肪饮食(<15%);在6个月和8个月后测定血浆瘦素和胰岛素浓度、BMI、体脂百分比(%BF)以及静息能量消耗。超重/肥胖女性的绝对血浆瘦素水平和经肥胖校正后的血浆瘦素水平(37.7±3.5ng/mL;1.01±0.07ng·mL⁻¹·%BF⁻¹)高于体重正常女性(16.9±2.2ng/mL;0.57±0.06ng·mL⁻¹·%BF⁻¹,与肥胖组相比,P均<0.(此处原文有误,推测应为P均<0.005)),但在体重稳定时,31%、23%和14%脂肪饮食组之间无差异。血浆瘦素与BMI(r = 0.81,P<0.0001)、%BF(r = 0.80,P<0.0001)和空腹血浆胰岛素(r = 0.61,P<0.0001)高度相关。在随意食用低脂肪饮食8个月后,这些女性平均体重减轻了6.9±1.0%(-2.0±0.3kg/m²,P<0.0001)。在15名体重减轻超过7%(-12.3±1.0%)的受试者中,血浆瘦素浓度下降(-9.6±1.9ng/mL,P<0.0005),超重/肥胖女性中每单位体脂变化引起的血浆瘦素下降幅度(δ瘦素/δ%BF)(3.6±0.5)大于体重正常女性(0.9±0.4,与肥胖组相比,P<0.(此处原文有误,推测应为P<0.01))。在另外18名体重减轻少于7%(-2.7±0.6%)的受试者中,血浆瘦素无变化(+1.4±1.4ng/mL)。总体而言,血浆瘦素的变化与BMI的变化(r = 0.43,P<0.02)、%BF的变化(r = 0.49,P<0.005)、静息能量消耗的变化(r = 0.40,P<0.02)以及与血浆胰岛素的变化显著相关,且独立于体脂的变化(r = 0.45,P<0.01)。我们得出结论:血浆瘦素浓度:1)本身不受饮食脂肪含量影响;2)在超重/肥胖和体重正常女性中均与BMI、%BF和血浆胰岛素高度相关;3)在持续体重减轻后与血浆胰岛素平行下降;4)超重/肥胖女性下降幅度大于体重正常女性。