Ali Ganji
* , Iman Farahani
, Amir Mohammad Saeedifar
, Ali Ghazavi, Ghasem Mosayebi
Abstract
Detoxification drugs used for opium (OPM) withdrawal, such as Buprenorphine (BUP), Naltrexone (NTX), and Methadone (MTD), can have adverse inhibitory effects. In a recent study, the impact of opium and these detoxification drugs on cytokines secreted by RAW 264.7 macrophages was examined. The M1 model (positive control) used LPS-stimulated macrophages, while the M0 model (negative control) used DMSO-treated macrophages. The study measured the ratios of inflammatory (IFN-γ, TNF-α, IL-6) to Anti-inflammatory cytokines (IL-10, TGF-β) secreted by RAW 264.7 macrophages exposed to OPM and the detoxification drugs using Real-time PCR. The results showed that in the M1 model, the ratio of IFN-γ/IL-10 significantly increased with OPM+MTD (P<0.001) and OPM+BUP (P<0.05). Similarly, the INF-γ/TGF-β ratio increased significantly with OPM+MTD (P<0.001), OPM+BUP (P<0.01), and OPM+NTX (P<0.05) compared to the negative control. Compared to the M0 model, the TNF-α/IL-10 and TNF-α/TGF-β ratios showed the highest increase with OPM+BUP (P<0.001) and OPM+MTD (P<0.01). Additionally, OPM+BUP (P<0.001) and OPM+MTD (P<0.05) exhibited the greatest increase in the IL-6/IL-10 ratio, and OPM+BUP (P<0.001) also showed a significant upward trend in the IL-6/TGF-β ratio. These findings suggest that buprenorphine and methadone may have potential as therapies for reducing inflammation in opium-treated macrophages by increasing M1 cytokines and enhancing immune responses.
Keywords: Opium, Macrophage, Inflammation, Buprenorphine, Naltrexone, Methadone