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The in vitro effect of pancuronium bromide on lymphocyte apoptosis was investigated at a clinically relevant concentration of 0.136 micromol/l for 3 hours. Treatment with pancuronium resulted in a tenfold increase in the frequency of apoptotic lymphocytes compared to control cultures. Pancuronium significantly upregulated the expression of Fas with a sixfold increase, Fas ligand with a fourfold increase, and ICEp20 with a fivefold increase.
Pancuronium exposure also led to a sevenfold increase in the percentage of cells exhibiting dissipation of mitochondrial membrane potential and a sevenfold increase in the generation of mitochondrial reactive oxygen species. These changes were associated with a decrease in glutathione levels. The findings suggest that pancuronium induces lymphocyte apoptosis through both death receptor and mitochondrial pathways, which may contribute to the transient immune suppression observed in the post-surgical period.
Fig. 1 Effect of pancuronium on Fas, FasL and ICEp20 expression of CD4 cells. (Delogu G.; et al. 2003)
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