William S. Middleton Memorial Veterans Hospital, Madison, WI, USA.
Department of Medicine, University of Wisconsin-Madison, Madison, WI, USA.
J Physiol. 2023 Jun;601(11):2139-2163. doi: 10.1113/JP283261. Epub 2022 Sep 27.
Low-protein (LP) diets are associated with a decreased risk of diabetes in humans, and promote leanness and glycaemic control in both rodents and humans. While the effects of an LP diet on glycaemic control are mediated by reduced levels of the branched-chain amino acids, we have observed that reducing dietary levels of the other six essential amino acids leads to changes in body composition. Here, we find that dietary histidine plays a key role in the response to an LP diet in male C57BL/6J mice. Specifically reducing dietary levels of histidine by 67% reduces the weight gain of young, lean male mice, reducing both adipose and lean mass without altering glucose metabolism, and rapidly reverses diet-induced obesity and hepatic steatosis in diet-induced obese male mice, increasing insulin sensitivity. This normalization of metabolic health was associated not with caloric restriction or increased activity, but with increased energy expenditure. Surprisingly, the effects of histidine restriction do not require the energy balance hormone Fgf21. Histidine restriction that was started in midlife promoted leanness and glucose tolerance in aged males but not females, but did not affect frailty or lifespan in either sex. Finally, we demonstrate that variation in dietary histidine levels helps to explain body mass index differences in humans. Overall, our findings demonstrate that dietary histidine is a key regulator of weight and body composition in male mice and in humans, and suggest that reducing dietary histidine may be a translatable option for the treatment of obesity. KEY POINTS: Protein restriction (PR) promotes metabolic health in rodents and humans and extends rodent lifespan. Restriction of specific individual essential amino acids can recapitulate the benefits of PR. Reduced histidine promotes leanness and increased energy expenditure in male mice. Reduced histidine does not extend the lifespan of mice when begun in midlife. Dietary levels of histidine are positively associated with body mass index in humans.
低蛋白 (LP) 饮食与人类患糖尿病的风险降低有关,并促进啮齿动物和人类的苗条和血糖控制。虽然 LP 饮食对血糖控制的影响是通过降低支链氨基酸的水平来介导的,但我们已经观察到,降低其他六种必需氨基酸的饮食水平会导致身体成分发生变化。在这里,我们发现饮食组氨酸在雄性 C57BL/6J 小鼠对 LP 饮食的反应中起着关键作用。具体来说,通过将饮食中的组氨酸水平降低 67%,可以减少年轻、苗条的雄性小鼠的体重增加,同时减少脂肪和瘦肉量,而不改变葡萄糖代谢,并迅速逆转肥胖雄性小鼠的饮食诱导肥胖和肝脂肪变性,增加胰岛素敏感性。这种代谢健康的正常化不是通过热量限制或增加活动来实现的,而是通过增加能量消耗来实现的。令人惊讶的是,组氨酸限制的效果不需要能量平衡激素 Fgf21。从中年开始的组氨酸限制促进了老年雄性的苗条和葡萄糖耐量,但对雌性没有影响,也不影响两性的脆弱性或寿命。最后,我们证明饮食中组氨酸水平的变化有助于解释人类体重指数的差异。总的来说,我们的研究结果表明,饮食组氨酸是雄性小鼠和人类体重和身体成分的关键调节剂,并表明减少饮食组氨酸可能是肥胖治疗的一种可转化的选择。 关键点:蛋白质限制 (PR) 促进了啮齿动物和人类的新陈代谢健康,并延长了啮齿动物的寿命。限制特定的单个必需氨基酸可以重现 PR 的益处。减少组氨酸可促进雄性小鼠的苗条和增加能量消耗。从中年开始的减少组氨酸不会延长老鼠的寿命。饮食中组氨酸的水平与人类的体重指数呈正相关。