Johnsen L, Lyckegaard N B, Khanal P, Quistorff B, Raun K, Nielsen M O
Department of Large Animal SciencesFaculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Department of Biomedical SciencesFaculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Endocr Connect. 2018 May;7(5):777-790. doi: 10.1530/EC-18-0014.
We aimed to test, whether fetal under- or overnutrition differentially program the thyroid axis with lasting effects on energy metabolism, and if early-life postnatal overnutrition modulates implications of prenatal programming.
Twin-pregnant sheep ( = 36) were either adequately (NORM), under- (LOW; 50% of NORM) or overnourished (HIGH; 150% of energy and 110% of protein requirements) in the last-trimester of gestation. From 3 days-of-age to 6 months-of-age, twin lambs received a conventional (CONV) or an obesogenic, high-carbohydrate high-fat (HCHF) diet. Subgroups were slaughtered at 6-months-of-age. Remaining lambs were fed a low-fat diet until 2½ years-of-age (adulthood).
Serum hormone levels were determined at 6 months- and 2½ years-of-age. At 2½ years-of-age, feed intake capacity (intake over 4-h following 72-h fasting) was determined, and an intravenous thyroxine tolerance test (iTTT) was performed, including measurements of heart rate, rectal temperature and energy expenditure (EE).
In the iTTT, the LOW and nutritionally mismatched NORM:HCHF and HIGH:CONV sheep increased serum T, T:T and T:TSH less than NORM:CONV, whereas TSH was decreased less in HIGH, NORM:HCHF and LOW:HCHF. Early postnatal exposure to the HCHF diet decreased basal adult EE in NORM and HIGH, but not LOW, and increased adult feed intake capacity in NORM and LOW, but not HIGH.: The iTTT revealed a differential programming of central and peripheral HPT axis function in response to late fetal malnutrition and an early postnatal obesogenic diet, with long-term implications for adult HPT axis adaptability and associated consequences for adiposity risk.
我们旨在测试胎儿营养不足或营养过剩是否会对甲状腺轴产生不同的编程作用,并对能量代谢产生持久影响,以及生命早期的产后营养过剩是否会调节产前编程的影响。
36只怀有双胞胎的绵羊在妊娠晚期分别接受充足营养(正常组,NORM)、营养不足(低营养组,LOW;正常营养的50%)或营养过剩(高营养组,HIGH;能量需求的150%和蛋白质需求的110%)。从3日龄到6月龄,双胞胎羔羊分别接受常规(CONV)或致肥胖的高碳水化合物高脂肪(HCHF)饮食。在6月龄时宰杀亚组。其余羔羊喂食低脂饮食直至2.5岁(成年)。
在6月龄和2.5岁时测定血清激素水平。在2.5岁时,测定采食量(72小时禁食后4小时内的摄入量),并进行静脉注射甲状腺素耐量试验(iTTT),包括测量心率、直肠温度和能量消耗(EE)。
在iTTT中,低营养组以及营养不匹配的正常组:HCHF组和高营养组:CONV组绵羊血清T、T:T和T:TSH的升高幅度小于正常组:CONV组,而高营养组、正常组:HCHF组和低营养组:HCHF组中TSH的降低幅度较小。产后早期接触HCHF饮食会降低正常组和高营养组成年后的基础能量消耗,但低营养组不受影响,并且会增加正常组和低营养组成年后的采食量,但高营养组不受影响。iTTT显示,胎儿晚期营养不良和产后早期致肥胖饮食会对中枢和外周HPT轴功能产生不同的编程作用,对成年HPT轴适应性具有长期影响,并对肥胖风险产生相关后果。