Table 2.
Autophagy inducers | Mechanism of action | References |
---|---|---|
FDA-approved-drugs | ||
Rapamycin | Induces autophagy by inhibiting mTORC1 | [194,195,196] |
Metformin | Upregulates AMPK, which promotes autophagy by inducing ULK1 phosphorylation | [197,198] |
Isoniazid | Activates autophagy flux, oxidative stress and upregulates AMPK | [199] |
Vitamin D3 | Upregulates cathelicidin | [200,201] |
Vitamin C | Antioxidant | [202] |
Vitamin E | Antioxidant | [203] |
Lithium | Lowers inositol and Ins(1,4,5)P" levels | [204] |
Sodium valproate | Lowers inositol and Ins(1,4,5)P" levels | [196,204] |
Carbamazepine | Lowers inositol and Ins(1,4,5)P" levels | [196,204] |
Verapamil | Lowers intracytosolic Ca2+ levels | [196] |
Clonidine and rilmenidine | Lower cAMP levels | [196] |
Anti-psychotic drugs | Inhibit autophagy | [205] |
Statins | Lower membrane cholesterol levels, thereby preventing cholesterol-dependent pore-forming toxins from forming pores | [206] |
Pharmacological agents | ||
17-hydroxy-jolkinolide B | Activates heme oxygenase-1 expression | [207] |
L-NAME | Decreases nitric oxide formation to induce autophagy | [208] |
Nutritional compounds | ||
Resveratrol | Activates sirtuin 1 (histone deacetylase) | [209,210,211] |
Epicatechins | Inhibit LPS-induced HMGB1 upregulation by stimulating its autophagic degradation | [212,213] |
Catalase | Antioxidant | [214] |
Chloroquine | Inhibits autophagosome-lysosome fusion | [215,216] |
Vinblastine | Inhibits microtubule formation | [217] |
Nocodazole | Inhibits microtubule formation and inhibits autophagosome-lysosome fusion | [218,219] |
3-methyladenine, Wortmannin and LY294002 | Inhibit phosphatidylinositol 3-3-kinase | [220] |
AMPK: AMP-activated protein kinase; cAMP cyclic AMP; Ins(1,4,5)P3: inositol-1,4,5-triphosphate; L-NAME: N-l-arginine methyl ester; mTOR, mammalian target of rapamycin; mTORC1, mTOR complex 1; ULK1, Uncoordinated 51-like kinase 1; HMGB1, high mobility group B-1.