Melittin attenuates imiquimod-induced psoriatic dermatitis in mice: a role for autophagy activation via PI3K/Akt/mTOR pathway suppression.
What this study shows
Melittin (bee venom, 80 mg/kg i.p.) reduces psoriatic dermatitis severity by 60% in an imiquimod mouse model by suppressing PI3K/Akt/mTOR signaling and activating autophagy.
At a glance
| Evidence type | A Animal model Marked A because it is an animal intervention or observation study measuring an organismal outcome (model: Mouse (psoriasis model)); the code names the system studied -- animal work can be rigorous and still not be human data. |
| Study type | 4 - Animal Study |
| Model system | Mouse (psoriasis model) |
| Journal | Saudi pharmaceutical journal |
| Year | 2026 |
| Peer reviewed | Yes |
| Record last updated | 2026-10-01 |
| Source | DOI 10.1007/s44446-026-00105-y · PMID 42560464 · Free full text (PMC13447632) |
Extracted findings
These fields were extracted from the paper with AI assistance and have not been checked against the source. Read them as a pointer into the paper, not as curated claims; where they disagree with the curated summary above, the curated summary stands.
| Intervention | Melittin |
| Target | PI3K/Akt/mTOR |
| Model | Mouse |
| Effect | Reduces psoriatic inflammation via mTOR suppression and autophagy activation |
In the Atlas
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