D-pinitol
- 3 independent labs in 1 country
- Funders: Key Technologies Research and Development Program and 4 more
- Animals2
- Model organisms2
Outcomes
9Lifespan
upin worms2+29% mean lifespan
2 studies
Lifespan
upin worms2+29% mean lifespan
D-pinitol extends lifespan in worms (+28.6% mean lifespan).
“200 μM of DP increased mean lifespan of C. elegans by 28.6%”
Model organisms200 μM
npj aging27 Apr 2026
D-pinitol extends lifespan in worms.
“In C. elegans, DP treatment enhanced lifespan, stress capacity, antioxidant capacity (T-SOD/CAT/GSH-Px/MDA/ROS), and altered aging-related indicators”
Model organisms
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP20 Sep 2023
Autophagy
upin worms1
1 study
Autophagy
upin worms1
D-pinitol activates autophagy in worms.
“DP further enhanced HLH-30-dependent autophagy and mitophagy activities, which are essential for lifespan extension.”
Model organismsHLH-30-dependent
npj aging27 Apr 2026
Cellular senescence
downin mammals cells1
1 study
Cellular senescence
downin mammals cells1
D-pinitol decreases cellular senescence in mammals cells.
“Moreover, DP suppressed cellular senescence in multiple mammalian cell types.”
Cellsmultiple mammalian cell types
npj aging27 Apr 2026
Proteotoxicity
downin worms1
1 study
Proteotoxicity
downin worms1
D-pinitol decreases proteotoxicity in worms.
“DP also attenuated proteotoxicity and delays functional decline in C. elegans models of Parkinson's, Huntington's, and Alzheimer's diseases.”
Model organismsModels of Parkinson's, Huntington's, and Alzheimer's diseases
npj aging27 Apr 2026
Locomotor function
upin worms1
1 study
Locomotor function
upin worms1
D-pinitol improves locomotor function in worms.
“200 μM of DP increased mean lifespan of C. elegans by 28.6%, as well as healthspan phenotypes including preserved locomotor function and delayed lipofuscin accumulation.”
Model organisms200 μM
npj aging27 Apr 2026
Lean mass
upin mice1
1 study
Lean mass
upin mice1
D-pinitol increases lean mass in mice (8.47 ± 0.81 g vs. 7.08 ± 1.64 g).
“increased lean mass (8.47 ± 0.81 g vs. 7.08 ± 1.64 g)”
Animalsin STZ-induced diabetic SAM-P8 mice150 mg/kg per day6 weeks
Journal of cachexia, sarcopenia and muscle29 Mar 2024
Muscle cross-sectional area
upin mice1
1 study
Muscle cross-sectional area
upin mice1
D-pinitol increases muscle cross-sectional area in mice (1912.17 ± 535.61 μm2 vs. 1557.19 ± 588.38 μm2).
“muscle cross-sectional area (CSA) (1912.17 ± 535.61 μm2 vs. 1557.19 ± 588.38 μm2)”
Animalsin STZ-induced diabetic SAM-P8 micegastrocnemius muscle150 mg/kg per day6 weeks
Journal of cachexia, sarcopenia and muscle29 Mar 2024
Grip strength
upin mice1
1 study
Grip strength
upin mice1
D-pinitol improves grip strength in mice (208.62 ± 39.45 g vs. 160.87 ± 26.95 g).
“DP exerted protective effects on sarcopenia and mitophagy (DP + STZ-P8 vs. STZ-P8; all P < 0.01), such as increased lean mass (8.47 ± 0.81 g vs. 7.08 ± 1.64 g), grip strength (208.62 ± 39.45 g vs. 160.87 ± 26.95 g)”
Animalsin STZ-induced diabetic SAM-P8 miceskeletal muscle150 mg/kg per day6 weeks
Journal of cachexia, sarcopenia and muscle29 Mar 2024
Amyloid-beta toxicity
downin worms1
1 study
Amyloid-beta toxicity
downin worms1
D-pinitol decreases amyloid-beta toxicity in worms.
“Moreover, DP could reduce the toxicity Aβ in transgenic C. elegans CL4176, CL2355, and CL2331.”
Model organismsin transgenic C. elegans CL4176, CL2355, and CL2331
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP20 Sep 2023