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. 2020 Jan 30;2020:5457049. doi: 10.1155/2020/5457049

Table 5.

Agents that can inhibit the autophagy-lysosome pathway in ischemic stroke models.

Agents Effects on ischemic stroke Possible mechanisms Models References
miR-207 mimics Protective Decreasing the expression of cellular lysosome and autophagosome In vivo [90]
DDS Protective Inhibiting lysosome accumulation In vivo and in vitro [91]
DMBC Protective Inhibiting the release of cathepsin B from the lysosomes into the cytoplasm In vivo and in vitro [92]
Clik148 Protective Inhibiting the release of cathepsin L from the lysosomes into the cytoplasm and activation of caspase-3 In vivo and in vitro [93]
3-MA and Wort Protective Inhibiting autophagy and stabilizing lysosomal membranes In vivo and in vitro [94]
CA074-me Protective Inhibiting the release of cathepsin B, preserving lysosomal membrane integrity, and suppressing lysosomal rupture In vivo [93, 95]
Fingolimod Protective Inhibiting autophagy via the mTOR/p70S6K pathway In vivo [96]
Lycium barbarum polysaccharide Protective Inhibiting apoptosis and autophagy through the PI3K/Akt/mTOR pathway In vitro [97]
Cornin Protective Inhibiting autophagy through the PI3K/Akt/mTOR pathway In vitro [98]

Abbreviations: DDS: dapsone; DMBC: 2-(3′,5′-dimethoxybenzylidene) cyclopentanone; 3-MA: 3-methyladenine; Wort: wortmannin.