SIRT2 and NAD+ Boosting Broadly Suppress Aging-Associated Inflammation
Marine Barthez1, Zehan Song1,2, Yufan Feng1
1Department of Nutritional Sciences and Toxicology, University of California, Berkeley, California, USA.
Aging causes chronic inflammation and tissue decline. Boosting NAD+ levels, potentially by targeting SIRT2, can reduce this inflammation and improve tissue function in older individuals.
Area of Science:
- Immunology
- Gerontology
- Biochemistry
Background:
- Aging is characterized by chronic inflammation, termed
- inflammaging,
- which contributes to age-related diseases.
- Multiple immune pathways are activated during aging, complicating therapeutic interventions.
- Sirtuin 2 (SIRT2), an NAD+-dependent deacetylase, plays a role in regulating immune responses.
Purpose of the Study:
- To investigate the role of SIRT2 in aging-associated inflammation.
- To evaluate the potential of NAD+ boosting as a strategy to counteract aging-related inflammation and tissue dysfunction.
Main Methods:
- Studied the effects of SIRT2 deficiency on inflammation and tissue function in aged models.
- Administered an NAD+ boosting compound (78c) to aged models.
- Assessed multiple immune pathways and tissue function markers.
Main Results:
- SIRT2 deficiency exacerbated inflammation and led to tissue function decline in aged individuals.
- NAD+ boosting with 78c effectively suppressed aging-associated inflammation.
- NAD+ boosting improved tissue function in aged individuals.
Conclusions:
- SIRT2 acts as a key regulator of aging-associated inflammation.
- NAD+ boosting is a promising therapeutic strategy to mitigate age-related inflammation and preserve tissue function.
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