3-hydroxybutyrate Promotes Longevity and Delays Senescence in Mice

Unveiling the Anti-Aging Potential of 3HB: Lifespan Extension and Cellular Senescence Delay

Yongpan An et al. Nutrients. 2025.

Abstract

Background/objective: Aging is a significant risk factor for chronic diseases and disability, yet effective anti-aging interventions remain elusive. We explored the potential of 3-hydroxybutyrate (3HB), an endogenous metabolite with established safety, to modulate longevity in mice.

Methods: In this study, we employed 2BS and WI-38 cell models, a yeast model, and naturally aging mouse models to investigate the effects of 3HB on aging in various systems. Additionally, we utilized RNA sequencing and metabolomics technologies to explore the potential mechanisms underlying the action of 3HB.

Results: Our findings demonstrate that 3HB supplementation effectively delays cellular senescence, extending yeast lifespan by 51.3% and the median lifespan of naturally senescent mice by 21.0%. Notably, 3HB prolonged healthy lifespan in mice while mitigating age-related tissue morphology changes and organ senescence. Mechanistically, we identified that 3HB’s anti-aging properties are mediated through its ability to delay cellular senescence and metabolic reprogramming, while promoting the production of beneficial metabolites like trigoneline and isoguvacine.

Conclusions: These findings highlight the promising therapeutic potential of 3HB as an anti-aging intervention and provide novel insights into its underlying mechanisms. [PMID: 40431385]

PubMed Abstract

Full Text - Open Access

From the full text:

“The results show that 3HB can delay cellular senescence and extend yeast lifespan, and it also increases the median lifespan of mice by 21.0%, while alleviating age-related tissue and organ decline. Mechanistically, we found that the anti-aging properties of 3HB are mediated by its ability to delay cellular senescence and reprogram metabolism, while also promoting the production of beneficial metabolites such as trigonelline and isoguvacine.”

“While promising anti-aging candidates, like senolytics and mTOR inhibitors, exist, concerns regarding safety and clinical translation due to side effects remain [27,28,29]. Endogenous metabolites, like 3HB, offer a safer alternative due to their natural presence in the body. In this study, we found that 3HB intervention extended the median lifespan of mice by 21% (123 days) and the mean lifespan by 8.4% (52 days) throughout their entire life cycle (as shown in Figure 2A). We then compared 3HB with other known compounds that delay aging. Our findings revealed that metformin can extend the mean lifespan of mice by 4.15% from the start of the intervention [6]; NMN/NR can extend the mean lifespan of mice by 30.2% from the start of the intervention, and the mean lifespan throughout the entire life cycle can be extended by 4.7% [4]; rapamycin can extend the mean lifespan throughout the entire life cycle by 7% to 16% [10,11]; dasatinib + quercetin can extend the mean lifespan of mice by 36% from the start of the intervention [3]. From these studies, we can see that the anti-aging effects of 3HB are comparable to or even more outstanding than those of these well-known anti-aging compounds.”

Notes: Treatment was started at 11 months. They used an outbred strain of mice, ICR. And they were male mice. Female mice were not tested. A published lifespan study with 300 mice found the median lifespan was around 16 months; approximately 490 days. The first graph above shows the effect on total lifespan. The graph below shows the survival curve for 11 months forward, giving a better indication of the interventional effect.

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I searched, but cannot find the dose in mice.

Yeah. Matt Kaeberlein 900 day rule. Next.

The impact of short-lived controls on the interpretation of lifespan experiments and progress in geroscience - Through the lens of the “900-day rule”

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Interesting…
Here are 3 previous threads on this (a ketone body).

https://www.rapamycin.news/t/hydroxybutyrate-is-a-metabolic-regulator-of-proteostasis-in-the-aged-and-alzheimer-disease-brain/8144

https://www.rapamycin.news/t/continuous-ketone-monitor-sibio/11495

https://www.rapamycin.news/t/ketone-bodies-mimic-the-life-span-extending-properties-of-caloric-restriction/14058

In animal and bacterial cells 3-hydroxybutyrate is an important metabolite with mainly energetic functions. Another important function of this metabolite is the supply of acetoacetyl-CoA and acetyl-CoA for the synthesis of other important metabolites. It should be emphasized that the role of 3-hydroxybutyrate does not end with its metabolic function, but it is a molecule that exhibits a number of signaling and regulatory properties. 3-HB can perform regulatory functions directly by inhibiting HDAC and binding to cell surface receptors and indirectly by altering the levels of other regulatory metabolites. The multitude of functions of 3-HB make it a compound that enjoys interest in many aspects of human life, including in medicine, as a therapeutic compound in diseases such as those of the circulatory and nervous systems or cancer, in dietetics, as the basis of a ketogenic diet to fight, among other diseases, epilepsy and obesity.

https://pmc.ncbi.nlm.nih.gov/articles/PMC8000602/#sec10-biomolecules-11-00402

Highlights

3-Hydroxybutyrate, produced by gut epithelial cells, is an essential energy substrate for gut microbiota.

Butyrate, produced by the gut microbiotas, regulates the integrity of gut epithelial cells.

The shuttle system by use of 3-hydroxybutyrate and butyrate that activates gut epithelial cells and microbiota may be essential for gut health.

https://www.sciencedirect.com/science/article/abs/pii/S030698772300213X

3-Hydroxybutyrate (3HB), predominantly found in the liver, muscles, and brain, is the most important endogenous ketone body in humans. During prolonged fasting and starvation, 3HB can partially replace glucose to meet some of the body’s energy needs. In recent years, the resurgence of the ketogenic diet (KD) and systematic exploration of the favorable biocompatibility of polyhydroxyalkanoates (PHAs), the precursor polymer to 3HB, have led to numerous reports indicating that the benefits of exogenous 3HB supplementation outweigh the drawbacks, particularly for middle-aged and elderly individuals.

3HB holds considerable promise as a therapeutic agent capable of addressing various age-related diseases and extending the health span. However, substantial challenges persist in fully elucidating its mechanisms of action, optimizing its administration, and ensuring its safety, particularly within elderly populations. As research advances, overcoming these obstacles will be essential to unlocking the complete therapeutic potential of 3HB.

https://www.sciencedirect.com/science/article/abs/pii/S0141813024091396

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“As a solution, we emphasize the importance of long-lived controls in mouse studies which should reach a median lifespan of around 900 ±50 days, or the comparison to appropriate historical controls.”

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“We selected 11-month-old male ICR mice, dissolved 3HB-Na in drinking water (1 g/L), and administered 3HB-Na to 11-month-old mice in drinking water until the mice died naturally, and recorded the body weights and survival conditions.”

Dose Administered: 1 g/L of 3HB (as 3HB-Na) in drinking water. Taking an estimate of 5 mL daily intake of water, this would be about 5 mg per day. The mice had an average weight of 47 grams.

5 mg / 0.047 kg = 106 mg/kg

Conversion factor from mouse to human = 12.3

106 / 12.3 = 8.62 mg/kg

8.62 x (your weight in kg) = total daily dose in mg.

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NMN/NR can extend the mean lifespan of mice by 30.2% from the start of the intervention, and the mean lifespan throughout the entire life cycle can be extended by 4.7%

The recentmost study by Sinclair showed NMN had a very modest, bordering on statistically insignificant effect on lifespan so where are they getting the data? If anything he had the most to prove and the most incentives to make NMN look good.

Thank you. That is about 500 mg for my 60kg weight.

Seems to be readily available from BulkSupplements

The study referenced by Vlasko cited a 2016 study from Switzerland.

https://www.science.org/doi/10.1126/science.aaf2693

Although the lead author’s name is Chinese, he is affiliated with the École Polytechnique Fédérale de Lausanne. The other authors are also affiliated with schools from Lausanne, or Zurich.

The 30% difference seems to be semantic. This time, the authors are Chinese from the Mainland. They may have stated it differently in Mandarin. I don’t think it was meant to mislead, because the full statement states both facts -extension of life after intervention, and extension of total lifespan.

NMN/NR can extend the mean lifespan of mice by 30.2% from the start of the intervention, and the mean lifespan throughout the entire life cycle can be extended by 4.7%

NMN/NR can extend the mean lifespan of mice by 30.2% from the start of the intervention

The controls lived to 829 days. The NR mice lived to 868 days. The start of the intervention occurred at 700 days age.

829 - 700 = 129
868 - 700 = 168

168 - 129 = 39
39/129 = 30.23%

For many here, beyond 40, the life extension after intervention is relevant. For the few here, who are in their 20s, the increase seems modest.