A Liposomal Formulation Enhances the Anti-Senescence Properties of Nicotinamide Adenine-Dinucleotide (NAD+) in Endothelial Cells and Keratinocytes
- Curr Issues Mol Biol. 2025 Sep 5;47(9):722. doi: 10.3390/cimb47090722.
- 1. Center for Molecular Cardiology, Schlieren Campus, University of Zurich, Wagistrasse 12, 8952 Schlieren, Switzerland.
- 2. First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, 6 Viale Benedetto XV, 16132 Genoa, Italy.
- 3. IRCCS Ospedale Policlinico San Martino Genoa-Italian Cardiovascular Network, L.go R. Benzi 10, 16132 Genoa, Italy.
- 4. Independent Researcher, Chemin des Macherettes 28, 1172 Bougy Villars, Switzerland.
- 5. Eurofins BIO-EC Laboratory, Chemin de Saulxier 1, 91160 Longjumeau, France.
- 6. Unité Universitaire Interdisciplinaire Lip (Sys), Lipides, Systèmes Analytiques et Biologiques, Faculté de Pharmacie, Université Paris-Saclay, 17 Avenue des Sciences, 91400 Orsay, France.
- 7. Sovida Solutions Limited, Michelin House, 81 Fulham Road, London SW3 6RD, UK.
- 8. Department of Research and Education, University Hospital Zurich, Rämistrasse 100, 8092 Zurich, Switzerland.
Nicotinamide adenine-dinucleotide (NAD+) supplementation is a promising strategy to delay cellular aging in different areas, including cosmetic dermatology. However, low bioavailability and stability of NAD+ formulations are the main factors limiting its effectiveness as an Anti-aging treatment. In light of the above, a liposomal formulation of NAD+ (LF-NAD+) was tested in this study and compared to NAD+ alone in primary human aortic endothelial cells (HAECs) and primary human epidermal keratinocytes (HEKas). Intracellular NAD+ was measured using a colorimetric assay. Cell survival was derived from Lactate Dehydrogenase release in supernatants. Cell senescence was measured by senescence-associated β-galactosidase staining. Molecular mechanisms underlying the reported effects were analyzed by Western blot. Skin penetration of NAD+ was measured ex vivo in skin explants, using infrared spectroscopy. Compared to control NAD+ alone, the LF-NAD+ formulation increased the intracellular NAD+ content and cell survival in HAECs, but not in HEKas. Instead, a significant reduction in the number of senescent cells was observed in both HAECs and HEKas. LF-NAD+ treatment was associated with a reduced expression of p16 in both HAECs and HEKas, and to a significant reduction in p21 in HEKas alone. Finally, LF-NAD+ increases the skin penetration of the active substance NAD+ by 30% compared to the application of NAD+ alone. LF-NAD+, enhances the Anti-aging effects of NAD+ on vascular and skin cells. Such in vitro findings might indicate a potential Anti-aging role in the microcirculation and in the epidermidis.
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Cat. No.Product NameDescriptionTargetResearch Area
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target: LiposomeResearch Areas: Metabolic Disease