Molecules
March 14, 2023
Timur Zanikov, Marta Gerasymchuk, Gregory Ian Robinson et al.
48 citations
In a mouse model of systemic inflammation induced by lipopolysaccharide injection, psilocybin combined with eugenol reduced brain levels of several inflammatory cytokines. Pre-treatment with psilocybin alone or in a 1:50 combination with eugenol most effectively lowered COX-2 and TNF-α mRNA expression. Post-treatment with the 1:50 combination produced the strongest reductions across multiple markers, including IL-6 and IL-8, as measured by ELISA. Western blot confirmed decreased COX-2 and IL-1β proteins. The findings suggest that psilocybin and eugenol together have anti-inflammatory effects in the brain, potentially relevant to disorders like depression and PTSD.
Biocatalysis and Agricultural Biotechnology
January 25, 2024
Timur Zanikov, Marta Gerasymchuk, Gregory Ian Robinson et al.
10 citations
Oral psilocybin and eugenol, given after inflammation was induced in a colitis mouse model, each reduced pro-inflammatory cytokines and mediators in the brain, including IL-1β, IL-6, and COX-2. The combined treatment produced the strongest reduction in IL-6 levels compared to the colitis group. However, across all markers, the combination did not show synergistic anti-inflammatory effects. These findings support the therapeutic potential of both compounds for psychiatric and neurodegenerative inflammatory disorders, though further research is needed to clarify mechanisms and clinical efficacy.
Pharmaceuticals
March 23, 2025
Gregory Ian Robinson, Marta Gerasymchuk, Timur Zanikov et al.
4 citations
Psilocybin and eugenol, both individually and combined, reduced inflammation in a mouse model of liver injury induced by lipopolysaccharides. Post-treatment administration produced stronger anti-inflammatory effects than pre-treatment. Psilocybin alone showed the most pronounced reduction of pro-inflammatory cytokines IL-1β, IL-6, and MCP-1, while the combination with eugenol (1:50 ratio) also strongly reduced COX-2 and TNF-α. Histological analysis indicated improved nuclear circularity and less inflammatory infiltration. Eugenol alone increased MCP-1 and GM-CSF, an adverse effect that was mitigated by co-administration with psilocybin. The findings suggest psilocybin and its combination with eugenol as potential therapies for hepatic inflammation.
Biochemistry and Cell Biology
January 1, 2025
Farzaneh Norouzkhani, Esmaeel Ghasemi Gojani, Bo Wang et al.
1 citation
A high-glucose and high-lipid diet accelerates cellular aging through oxidative stress, mitochondrial dysfunction, and inflammation, contributing to collagen degradation and skin aging. Psilocybin, a naturally occurring compound, was tested on BJ-5ta fibroblasts exposed to such conditions. Post-treatment with 15 µmol/L psilocybin and co-treatment with 10 µmol/L preserved cell viability and reduced senescence markers. The 10 µmol/L co-treatment most effectively lowered apoptosis and alleviated cell cycle arrest in S phase. Psilocybin also decreased inflammatory cytokines IL-1β, IL-6, and COX-2, and co-treatment significantly upregulated elastin gene expression, though fibroblast migration increased nonsignificantly. Psilocybin shows promise as a natural compound for reducing skin aging under oxidative stress.