The solubility of the MgAlO 2.5 component in bridgmanite was measured at pressures of 27, 35 and 40 GPa and a temperature of 2000 o K using an ultra-high pressure multi-anvil press. Compositional analysis of recovered samples demonstrated that the MgAlO 2.5 component decreases with increasing pressure, and approaches virtually zero at 40 GPa. Above this pressure, the MgAlO 2.5 component, i.e. the oxygen-vacancy substitution, becomes negligible, and Al is incorporated in bridgmanite by the charge-coupled substitution only. These results are supported by the volume change associated with the change from the oxygen-vacancy substitution to charge-coupled substitution. The present result may explain the seismically observed slab stagnation in the mid-lower mantle. Although bridgmanite has been put forward as a potential host for water and argon in the lower mantle by trapping them in oxygen vacancies, such capabilities will rapidly decrease with depth and be lost in regions deeper than 1000 km.