Fowler Sharon P G
Department of Medicine, The University of Texas Health Science Center at San Antonio, Texas, United States.
Physiol Behav. 2016 Oct 1;164(Pt B):517-523. doi: 10.1016/j.physbeh.2016.04.047. Epub 2016 Apr 26.
For more than a decade, pioneering animal studies conducted by investigators at Purdue University have provided evidence to support a central thesis: that the uncoupling of sweet taste and caloric intake by low-calorie sweeteners (LCS) can disrupt an animal's ability to predict the metabolic consequences of sweet taste, and thereby impair the animal's ability to respond appropriately to sweet-tasting foods. These investigators' work has been replicated and extended internationally. There now exists a body of evidence, from a number of investigators, that animals chronically exposed to any of a range of LCSs - including saccharin, sucralose, acesulfame potassium, aspartame, or the combination of erythritol+aspartame - have exhibited one or more of the following conditions: increased food consumption, lower post-prandial thermogenesis, increased weight gain, greater percent body fat, decreased GLP-1 release during glucose tolerance testing, and significantly greater fasting glucose, glucose area under the curve during glucose tolerance testing, and hyperinsulinemia, compared with animals exposed to plain water or - in many cases - even to calorically-sweetened foods or liquids. Adverse impacts of LCS have appeared diminished in animals on dietary restriction, but were pronounced among males, animals genetically predisposed to obesity, and animals with diet-induced obesity. Impacts have been especially striking in animals on high-energy diets: diets high in fats and sugars, and diets which resemble a highly-processed 'Western' diet, including trans-fatty acids and monosodium glutamate. These studies have offered both support for, and biologically plausible mechanisms to explain, the results from a series of large-scale, long-term prospective observational studies conducted in humans, in which longitudinal increases in weight, abdominal adiposity, and incidence of overweight and obesity have been observed among study participants who reported using diet sodas and other LCS-sweetened beverages daily or more often at baseline. Furthermore, frequent use of diet beverages has been associated prospectively with increased long-term risk and/or hazard of a number of cardiometabolic conditions usually considered to be among the sequelae of obesity: hypertension, metabolic syndrome, diabetes, depression, kidney dysfunction, heart attack, stroke, and even cardiovascular and total mortality. Reverse causality does not appear to explain fully the increased risk observed across all of these studies, the majority of which have included key potential confounders as covariates. These have included body mass index or waist circumference at baseline; total caloric intake and specific macronutrient intake; physical activity; smoking; demographic and other relevant risk factors; and/or family history of disease. Whether non-LCS ingredients in diet beverages might have independently increased the weight gain and/or cardiometabolic risk observed among frequent consumers of LCS-sweetened beverages deserves further exploration. In the meantime, however, there is a striking congruence between results from animal research and a number of large-scale, long-term observational studies in humans, in finding significantly increased weight gain, adiposity, incidence of obesity, cardiometabolic risk, and even total mortality among individuals with chronic, daily exposure to low-calorie sweeteners - and these results are troubling.
十多年来,普渡大学的研究人员开展的开创性动物研究提供了证据,支持一个核心论点:低热量甜味剂(LCS)使甜味与热量摄入脱钩,会破坏动物预测甜味代谢后果的能力,从而损害动物对甜味食物做出适当反应的能力。这些研究人员的工作已在国际上得到重复和扩展。现在,许多研究人员提供了一系列证据,表明长期接触多种LCS(包括糖精、三氯蔗糖、乙酰磺胺酸钾、阿斯巴甜或赤藓糖醇+阿斯巴甜的组合)的动物出现了以下一种或多种情况:食物摄入量增加、餐后产热降低、体重增加、体脂百分比升高、葡萄糖耐量测试期间胰高血糖素样肽-1释放减少,以及空腹血糖显著升高、葡萄糖耐量测试期间曲线下葡萄糖面积增加和高胰岛素血症,与饮用白开水的动物相比,在许多情况下,甚至与摄入高热量甜味食物或液体的动物相比也是如此。LCS的不利影响在饮食受限的动物中似乎有所减轻,但在雄性动物、具有肥胖遗传倾向的动物以及饮食诱导肥胖的动物中表现明显。在高能饮食的动物中影响尤为显著:高脂肪和高糖饮食,以及类似高度加工的“西方”饮食(包括反式脂肪酸和味精)的饮食。这些研究既支持了在人类中进行的一系列大规模、长期前瞻性观察研究的结果,也提供了生物学上合理的机制来解释这些结果。在这些人类研究中,据报告在基线时每天或更频繁饮用无糖汽水和其他LCS甜味饮料的研究参与者中,观察到体重、腹部肥胖以及超重和肥胖发生率的纵向增加。此外,前瞻性研究表明,频繁饮用无糖饮料与多种通常被认为是肥胖后遗症的心脏代谢疾病的长期风险和/或危害增加有关:高血压、代谢综合征、糖尿病、抑郁症、肾功能障碍、心脏病发作、中风,甚至心血管疾病和全因死亡率。反向因果关系似乎并不能完全解释所有这些研究中观察到的风险增加,其中大多数研究已将关键的潜在混杂因素作为协变量纳入。这些因素包括基线时的体重指数或腰围;总热量摄入和特定宏量营养素摄入;身体活动;吸烟;人口统计学和其他相关风险因素;和/或疾病家族史。无糖饮料中的非LCS成分是否可能独立增加了频繁饮用LCS甜味饮料者的体重增加和/或心脏代谢风险,值得进一步探索。然而,与此同时,动物研究结果与人类的一些大规模、长期观察研究结果惊人地一致,即长期每日接触低热量甜味剂的个体体重增加、肥胖、肥胖发生率、心脏代谢风险甚至全因死亡率显著增加——这些结果令人担忧。