mTORC1 inhibitors

mTORC1 inhibitors has been studied in 8 papers since 2019: 1 observational study in people, 2 in animals, 1 in cells, 4 reviews; 1 in the past year. The newest paper, Sep 7, 2026: “Strengthening muscle for healthy ageing: innovative treatments for sarcopenia”.

Intervention

8 papers study it5 findingsUpdated

See all 8 papers on mTORC1 inhibitors

At a glance

The findings reach mice, none yet in people. 3 independent labs in 4 countries.

None of its findings points the other way.

Cells and mice: a single group. Worms or flies and humans: nothing yet.
  • 3 independent labs in 4 countries
  • Funders: Japan Orthopaedics and Traumatology Foundation and others
  • Humans1
  • Animals2
  • Cells1

What did studies of mTORC1 inhibitors find?

5

Studies of mTORC1 inhibitors measured 5 outcomes; the most studied are muscle quality (1 study), metabolic defects (1) and glomerulosclerosis (1).

Muscle quality

upin A. animals1

1 study
  1. mTORC1 inhibitors improve muscle quality in aged animals.

    “Pharmaceutical inhibition of mTORC1 as well as caloric restriction significantly improves muscle quality in aged animals”

    Reviewin aged animalsskeletal muscle

    Age-Related Dysfunction in Proteostasis and Cellular Quality Control in the Development of Sarcopenia

    Cells

Metabolic defects

downin mice1

1 study
  1. mTORC1 inhibitors decrease metabolic defects in RagAGTP mice.

    “and revert by pharmacological inhibition of mTORC1”

    Animalsin RagAGTP mice

    Limited survival and impaired hepatic fasting metabolism in mice with constitutive Rag GTPase signaling

    Nature communications

Glomerulosclerosis

downin mice1

1 study
  1. mTORC1 inhibitors decrease glomerulosclerosis in Ercc1-deficient mice.

    “Moreover, pharmacological inhibition of mTORC1 modulated the development of glomerulosclerosis in Ercc1 -deficient mice.”

    Animalsin Ercc1-deficient micekidney

    Loss of genome maintenance accelerates podocyte damage and aging

    bioRxiv (Cold Spring Harbor Laboratory)Preprint

More on Glomerulosclerosis

extracellular matrix catabolism

downin human cells1

1 study
  1. mTORC1 inhibitors protect against extracellular matrix catabolism in human cells (inflammation-induced).

    “protect against inflammation-induced apoptosis, senescence, and matrix catabolism in human disc cells”

    Cellsinflammation-inducednucleus pulposus cells

    Pharmacological inhibition of mTORC1 but not mTORC2 protects against human disc cellular apoptosis, senescence, and extracellular matrix catabolism through Akt and autophagy induction

    Osteoarthritis and cartilage

Autophagy

upin human cells1

1 study
  1. mTORC1 inhibitors activate autophagy in human cells.

    “promoted autophagy with light chain 3 (LC3)-II increases and p62/sequestosome 1 (p62/SQSTM1) decreases”

    Cellsnucleus pulposus cells

    Pharmacological inhibition of mTORC1 but not mTORC2 protects against human disc cellular apoptosis, senescence, and extracellular matrix catabolism through Akt and autophagy induction

    Osteoarthritis and cartilage

More on Autophagy

Latest

Dec 2025: 0Jan 2026: 0Feb 2026: 0Mar 2026: 0Apr 2026: 0May 2026: 0Jun 2026: 0Jul 2026: 0Aug 2026: 0Sep 2026: 1Oct 2026: 0Nov 2026: 01 paper in 12 months