• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Low-calorie sweetener use and energy balance: Results from experimental studies in animals, and large-scale prospective studies in humans.低热量甜味剂的使用与能量平衡:来自动物实验研究及人类大规模前瞻性研究的结果。
Physiol Behav. 2016 Oct 1;164(Pt B):517-523. doi: 10.1016/j.physbeh.2016.04.047. Epub 2016 Apr 26.
2
A randomized controlled trial contrasting the effects of 4 low-calorie sweeteners and sucrose on body weight in adults with overweight or obesity.一项随机对照试验比较了 4 种低热量甜味剂和蔗糖对超重或肥胖成年人体重的影响。
Am J Clin Nutr. 2019 May 1;109(5):1288-1301. doi: 10.1093/ajcn/nqy381.
3
Do low-calorie sweeteners promote weight gain in rodents?低热量甜味剂会促进啮齿动物体重增加吗?
Physiol Behav. 2016 Oct 1;164(Pt B):509-513. doi: 10.1016/j.physbeh.2016.01.043. Epub 2016 Feb 4.
4
Characterization of Non-Nutritive Sweetener Intake in Rural Southwest Virginian Adults Living in a Health-Disparate Region.弗吉尼亚州西南部农村地区健康状况存在差异的成年人非营养性甜味剂摄入量的特征分析
Nutrients. 2017 Jul 14;9(7):757. doi: 10.3390/nu9070757.
5
Metabolic Effects of Low-Calorie Sweeteners: A Brief Review.低卡路里甜味剂的代谢效应:简要综述。
Obesity (Silver Spring). 2018 Oct;26 Suppl 3:S25-S31. doi: 10.1002/oby.22252. Epub 2018 Aug 1.
6
Low-Calorie Sweetened Beverages and Cardiometabolic Health: A Science Advisory From the American Heart Association.低热量甜味饮料与心血管代谢健康:美国心脏协会科学咨询声明
Circulation. 2018 Aug 28;138(9):e126-e140. doi: 10.1161/CIR.0000000000000569.
7
Beverages containing low energy sweeteners do not differ from water in their effects on appetite, energy intake and food choices in healthy, non-obese French adults.含低能量甜味剂的饮料在健康、非肥胖的法国成年人中,对食欲、能量摄入和食物选择的影响与水并无差异。
Appetite. 2018 Jun 1;125:557-565. doi: 10.1016/j.appet.2018.03.007. Epub 2018 Mar 9.
8
Rationale, Design and Participants Baseline Characteristics of a Crossover Randomized Controlled Trial of the Effect of Replacing SSBs with NSBs versus Water on Glucose Tolerance, Gut Microbiome and Cardiometabolic Risk in Overweight or Obese Adult SSB Consumer: Strategies to Oppose SUGARS with Non-Nutritive Sweeteners or Water (STOP Sugars NOW) Trial and Ectopic Fat Sub-Study.采用非营养性甜味剂或水替代 SSB 对超重或肥胖 SSB 消费者的葡萄糖耐量、肠道微生物组和心血管代谢风险影响的交叉随机对照试验的原理、设计和参与者基线特征:用非营养性甜味剂或水来对抗糖(STOP Sugars NOW 试验)和异位脂肪子研究。
Nutrients. 2023 Feb 28;15(5):1238. doi: 10.3390/nu15051238.
9
Low-calorie sweeteners and body weight and composition: a meta-analysis of randomized controlled trials and prospective cohort studies.低热量甜味剂与体重及身体组成:随机对照试验和前瞻性队列研究的荟萃分析
Am J Clin Nutr. 2014 Sep;100(3):765-77. doi: 10.3945/ajcn.113.082826. Epub 2014 Jun 18.
10
Low-calorie- and calorie-sweetened beverages: diet quality, food intake, and purchase patterns of US household consumers.低热量和高热量甜味饮料:美国家庭消费者的饮食质量、食物摄入量和购买模式。
Am J Clin Nutr. 2014 Mar;99(3):567-77. doi: 10.3945/ajcn.113.072132. Epub 2013 Dec 18.

引用本文的文献

1
Experts contributions to the development of a non-sugar sweeteners warning label for Brazilian food products.专家对巴西食品非糖类甜味剂警示标签制定的贡献。
PLoS One. 2025 Sep 3;20(9):e0331302. doi: 10.1371/journal.pone.0331302. eCollection 2025.
2
Dietary Guidance, Sensory, Health and Safety Considerations When Choosing Low and No-Calorie Sweeteners.选择低热量和无热量甜味剂时的饮食指南、感官、健康与安全考量
Nutrients. 2025 Feb 25;17(5):793. doi: 10.3390/nu17050793.
3
Effect of Replacing Sucrose in Beverages with Nonnutritive Sweetener Sucralose on Cardiometabolic Risk Factors Among Asian Indian Adults with Type 2 Diabetes: A 12-Week Randomized Controlled Trial.用非营养性甜味剂三氯蔗糖替代亚洲印度裔 2 型糖尿病成年患者饮料中的蔗糖对心血管代谢危险因素的影响:一项为期 12 周的随机对照试验。
Diabetes Ther. 2024 Sep;15(9):2061-2077. doi: 10.1007/s13300-024-01622-6. Epub 2024 Jul 24.
4
Physiological Integration of Taste and Metabolism.味觉与新陈代谢的生理整合
N Engl J Med. 2024 May 9;390(18):1699-1710. doi: 10.1056/NEJMra2304578.
5
The Cardiometabolic Impact of Rebaudioside A Exposure during the Reproductive Stage.生育期接触莱鲍迪苷A对心脏代谢的影响。
Biology (Basel). 2024 Mar 2;13(3):163. doi: 10.3390/biology13030163.
6
Effects of long-term high dose aspartame on body mass, bone strength, femoral geometry, and microbiota composition in a young and aged cohort of male and female mice.长期高剂量阿斯巴甜对年轻和老年雌雄小鼠队列的体重、骨强度、股骨几何形态及微生物群组成的影响
bioRxiv. 2024 Jan 3:2024.01.02.573970. doi: 10.1101/2024.01.02.573970.
7
Sugar substitutes and taste enhancers need more science, sensitivity- and allergy-guided labeling.糖替代品和增味剂需要更多基于科学、敏感度及过敏信息的标签标注。
NPJ Sci Food. 2023 Dec 9;7(1):64. doi: 10.1038/s41538-023-00240-z.
8
Long-term aspartame and saccharin intakes are related to greater volumes of visceral, intermuscular, and subcutaneous adipose tissue: the CARDIA study.长期摄入阿斯巴甜和糖精与内脏、肌肉间和皮下脂肪组织体积增大有关:CARDIA 研究。
Int J Obes (Lond). 2023 Oct;47(10):939-947. doi: 10.1038/s41366-023-01336-y. Epub 2023 Jul 13.
9
Maternal low-calorie sweetener consumption rewires hypothalamic melanocortin circuits via a gut microbial co-metabolite pathway.母体低热量甜味剂摄入通过肠道微生物共代谢物途径重塑下丘脑黑皮质素回路。
JCI Insight. 2023 May 22;8(10):e156397. doi: 10.1172/jci.insight.156397.
10
The Effect of Non-Nutritive Sweetened Beverages on Postprandial Glycemic and Endocrine Responses: A Systematic Review and Network Meta-Analysis.非营养性甜味饮料对餐后血糖和内分泌反应的影响:系统评价和网络荟萃分析。
Nutrients. 2023 Feb 20;15(4):1050. doi: 10.3390/nu15041050.

本文引用的文献

1
Interactions between Gut Microbiota, Host Genetics and Diet Modulate the Predisposition to Obesity and Metabolic Syndrome.肠道微生物群、宿主遗传学和饮食之间的相互作用调节肥胖和代谢综合征的易感性。
Cell Metab. 2015 Sep 1;22(3):516-530. doi: 10.1016/j.cmet.2015.07.007. Epub 2015 Aug 20.
2
Non-caloric artificial sweeteners and the microbiome: findings and challenges.非热量人工甜味剂与微生物群:研究结果与挑战
Gut Microbes. 2015;6(2):149-55. doi: 10.1080/19490976.2015.1017700. Epub 2015 Apr 1.
3
TLR4 at the Crossroads of Nutrients, Gut Microbiota, and Metabolic Inflammation.TLR4 在营养素、肠道微生物群和代谢炎症的十字路口。
Endocr Rev. 2015 Jun;36(3):245-71. doi: 10.1210/er.2014-1100. Epub 2015 Mar 26.
4
Diet soda intake is associated with long-term increases in waist circumference in a biethnic cohort of older adults: the San Antonio Longitudinal Study of Aging.在一个老年双种族队列(圣安东尼奥衰老纵向研究)中,饮用无糖汽水与腰围的长期增加有关。
J Am Geriatr Soc. 2015 Apr;63(4):708-15. doi: 10.1111/jgs.13376. Epub 2015 Mar 17.
5
Obesity and cardiovascular disease: weight loss is not the only target.肥胖与心血管疾病:减肥并非唯一目标。
Can J Cardiol. 2015 Feb;31(2):216-22. doi: 10.1016/j.cjca.2014.12.009. Epub 2014 Dec 11.
6
Metabolic and feeding behavior alterations provoked by prenatal exposure to aspartame.产前暴露于阿斯巴甜引起的代谢和摄食行为改变。
Appetite. 2015 Apr;87:168-74. doi: 10.1016/j.appet.2014.12.213. Epub 2014 Dec 24.
7
Diet drink consumption and the risk of cardiovascular events: a report from the Women's Health Initiative.饮用低热量饮料与心血管事件风险:来自女性健康倡议的一份报告。
J Gen Intern Med. 2015 Apr;30(4):462-8. doi: 10.1007/s11606-014-3098-0. Epub 2014 Dec 17.
8
A view of obesity as a learning and memory disorder.将肥胖视为一种学习和记忆障碍的观点。
J Exp Psychol Anim Learn Cogn. 2014 Jul;40(3):261-79. doi: 10.1037/xan0000029.
9
Low-dose aspartame consumption differentially affects gut microbiota-host metabolic interactions in the diet-induced obese rat.低剂量阿斯巴甜摄入对饮食诱导肥胖大鼠的肠道微生物群-宿主代谢相互作用有不同影响。
PLoS One. 2014 Oct 14;9(10):e109841. doi: 10.1371/journal.pone.0109841. eCollection 2014.
10
Artificial sweeteners induce glucose intolerance by altering the gut microbiota.人工甜味剂通过改变肠道微生物群诱导葡萄糖不耐受。
Nature. 2014 Oct 9;514(7521):181-6. doi: 10.1038/nature13793. Epub 2014 Sep 17.

低热量甜味剂的使用与能量平衡:来自动物实验研究及人类大规模前瞻性研究的结果。

Low-calorie sweetener use and energy balance: Results from experimental studies in animals, and large-scale prospective studies in humans.

作者信息

Fowler Sharon P G

机构信息

Department of Medicine, The University of Texas Health Science Center at San Antonio, Texas, United States.

出版信息

Physiol Behav. 2016 Oct 1;164(Pt B):517-523. doi: 10.1016/j.physbeh.2016.04.047. Epub 2016 Apr 26.

DOI:10.1016/j.physbeh.2016.04.047
PMID:27129676
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5045440/
Abstract

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.

摘要

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。