Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 2139-2163 |
| Number of pages | 25 |
| Journal | The Journal of Physiology |
| Volume | 601 |
| Issue number | 11 |
| Early online date | 9 Sept 2022 |
| DOIs | |
| Publication status | Published - 30 Jun 2023 |
Data Availability Statement
Source data for all figures are available in the Supplementary Data, with the exception of sensitive human data. Human data are available for qualified investigators upon request from Dr Kristen Malecki and the Survey of Health of Wisconsin. A fee for service model may apply for access to restricted data.UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Male
- Humans
- Animals
- Mice
- Aged
- Histidine/metabolism
- Thinness
- Mice, Inbred C57BL
- Diet
- Obesity/metabolism
- Proteins
- Energy Metabolism
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