Boon Niels, Hul Gabby B J, Viguerie Nathalie, Sicard Audrey, Langin Dominique, Saris Wim H M
Nutrition and Toxicology Research Institute Maastricht, University of Maastricht, Maastricht, Netherlands.
Am J Clin Nutr. 2005 Dec;82(6):1244-52. doi: 10.1093/ajcn/82.6.1244.
Evidence from molecular and animal research and epidemiologic investigations indicates that calcium intake may be inversely related to body weight, possibly through alterations in 1,25-dihydroxyvitamin D(3) [1,25(OH)(2)D(3)] metabolism.
We tested whether energy and substrate metabolism and adipose tissue enzyme messenger RNA (mRNA) expression can be altered by dietary calcium intake in healthy, nonobese, human volunteers consuming an isocaloric diet.
Twelve healthy men [age: 28 +/- 2 y; body mass index (BMI; in kg/m(2)): 25.2 +/- 06] received 3 isocaloric diets [high calcium (1259 +/- 9 mg/d), high dairy (high/high); high calcium (1259 +/- 9 mg/d), low dairy (high/low); and low calcium (349 +/- 8 mg/d), low dairy (low/low)] in a randomized crossover design. At the end of the 7-d dietary periods, 24-h energy expenditure and substrate metabolism were measured, and fat biopsy specimens were obtained to determine mRNA expression in genes involved in the lipolytic and lipogenic pathways.
The 24-h energy expenditure was 11.8 +/- 0.3, 11.6 +/- 0.3, and 11.7 +/- 0.3 MJ/24 h in the high/high, high/low, and low/low conditions, respectively. Fat oxidation in these conditions was 108 +/- 7, 105 +/- 9, and 100 +/- 6 g/24 h. These differences were not statistically significant. mRNA concentrations of UCP2, FAS, GPDH2, HSL, and PPARG did not differ significantly. Serum 1,25(OH)(2)D(3) concentrations changed from 175 +/- 16 to 138 +/- 15, 181 +/- 23 to 159 +/- 19, and 164 +/- 13 to 198 +/- 19 pmol/L in the high/high, high/low, and low/low conditions, respectively, and was significantly different between the high/high and low/low conditions (P < 0.05).
Altering the dietary calcium content for 7 d does not influence substrate metabolism, energy metabolism, or gene expression in proteins related to fat metabolism, despite significant changes in 1,25(OH)(2)D(3) concentrations.
分子研究、动物研究及流行病学调查的证据表明,钙摄入量可能与体重呈负相关,这可能是通过改变1,25 - 二羟基维生素D(3)[1,25(OH)₂D₃]的代谢实现的。
我们测试了在摄入等热量饮食的健康、非肥胖人类志愿者中,饮食钙摄入量是否会改变能量和底物代谢以及脂肪组织酶信使核糖核酸(mRNA)的表达。
12名健康男性[年龄:28±2岁;体重指数(BMI;单位:kg/m²):25.2±0.6]采用随机交叉设计接受3种等热量饮食[高钙(1259±9毫克/天)、高乳制品(高/高);高钙(1259±9毫克/天)、低乳制品(高/低);以及低钙(349±8毫克/天)、低乳制品(低/低)]。在7天饮食期结束时,测量24小时能量消耗和底物代谢,并获取脂肪活检标本以确定参与脂解和脂肪生成途径的基因中的mRNA表达。
在高/高、高/低和低/低条件下,24小时能量消耗分别为11.8±0.3、11.6±0.3和11.7±0.3兆焦/24小时。这些条件下的脂肪氧化分别为108±7、105±9和100±6克/24小时。这些差异无统计学意义。UCP2、FAS、GPDH2、HSL和PPARG的mRNA浓度无显著差异。在高/高、高/低和低/低条件下,血清1,25(OH)₂D₃浓度分别从175±16变为138±15、181±23变为159±19和164±13变为198±19皮摩尔/升,高/高和低/低条件之间有显著差异(P<0.05)。
尽管1,25(OH)₂D₃浓度有显著变化,但改变7天的饮食钙含量不会影响底物代谢、能量代谢或与脂肪代谢相关蛋白质的基因表达。