Table 1.
Disease | Subjects | Pathways | Effects | Reference |
---|---|---|---|---|
Scleroderma | Mice | mTOR-STAT3 signaling | ↓IL-6, IL-1β, IL-17, TNF-α, TGF-β, Col1a, Th17 ↑p-AMPK |
[60] |
Silica-induced pulmonary fibrosis | Human and rats | AMPK-mTOR signaling | ↓TGF-β1, TNF-α, IL-1β, α-SMA, p62 ↑E-cadherin, p-AMPK, autophagy |
[61] |
Thyroid-associated ophthalmopathy | Human | AMPK-mTOR signaling | ↓IL6, IL-8, CXCL1, CXCL2, CCL2, HA,α-SMA, ITGA5, COL1A1, COL2A1, COL3A1, FN1, ITGB1, and p-Smad2 ↑Autophagy |
[62] |
Gout | Human | mTOR signaling | ↓The rate of monocyte death, inflammation, and frequency of gout flares ↑Autophagy |
[63] |
Polycystic ovary syndrome | Human and mice | AMPK-PI3K-mTOR signaling | ↓TNF-α, mitochondrial membrane potential (MMP), ROS Reverse ovulatory dysfunction, disturbed estrous cycle, and abnormal ovarian morphology, and restore the impaired glucose tolerance |
[57] |
Psoriasis | HaCaT cells | mTOR signaling | ↓Proliferation, p-p70S6K, IL-6, TNF-α, and VEGF ↑Apoptosis |
[64] |
Liver injury | Rats | mTOR-HIF-1α signaling | ↓α-SMA, TIMP-1, hs-CRP, TNF-α, IL-6,ALT and AST | [65] |
Spinal cord injury | Rats and microglial cells | AMPK-mTOR signaling | ↓Apoptosis, inflammation ↑Axon regeneration, M1 to M2 phenotype polarization, and autophagy |
[66] |
Intestinal injury | HUVECs, HIECs, and BALB/c mice | mTOR signaling | ↓Senescence, intestinal canal inflammation, and oxidative stress | [67] |
Sepsis-associated myocardial injury | C57BL/6J mice and H9c2 cells | AMPK-mTOR signaling | ↓Cardiac dysfunction, myocardial enzymes, and cardiac hydroncus ↑Autophagy |
[68] |