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Background p38 mitogen-activated protein kinases (MAPK) in ischemic preconditioning (IPC) may be essential tocardioprotection.We assessed whether protective effect of morphine-induced preconditioning (MPG) on myocardialischemia and reperfusion injury in rat hearts involved p38 MAPK activation.Methods Male Spargue-Dawley rats (weighing 300—350 g) were randomly assigned to 1 of the following 8 groups:control (CON,saline vehicle,n=9),SB 203580 (SB,a p38 MAPK inhibitor,n=6),MPC (n=6),IPC (n=9),SB+MPC,SB+IPC,MPC+SB,and IPC+SB (n=6).Infarct sizes (IS),a percentage of the area at risk (AAR),were determined bytriphenyltetrazolium (TTC) staining.Tissue samples were processed from the entire AAR of left ventricle for thedetermination of p38 MAPK protein expression (5 hearts/group).The bands representing the proteins were visualizedusing an enhanced chemiluminescence detection system.Results The I S/AAR was significantly reduced by I PC (12.9±1.6)% or M PC (25.3±2.9)% compared to the control(52.7±5.5)%.SB 203580 administered prior to preconditioning abolished the effect of IPC (SB+IPC:(43.8±2.6)%,P>0.05 vs CON,P<0.01 vs IPC),but not MPC (SB+MPC:(30.7±0.9)%,P<0.01 vs CON,P>0.05 vs MPC).Treatmentwith SB 203580 prior to sustained ischemia diminished the protective effect of both MPC (MPC+SB:(42.4±2.9)%,P>0.05 vs CON) and IPC (IPC+SB:(52.0±2.5)%,P>0.05 vs CON) on IS/AAR.In the IPC group,phospho-p38 MAPKprotein increased significantly within 5 minutes into ischemia and remained elevated at 30 minutes into repeffusion,while phospho-p38 MAPK protein in the MPC group only increased significantly at 30 minutes into reperfusion.Conclusion The activation of p38 MAPK just acts as a mediator of MPC,whereas it acts as both a trigger and amediator in IPC.
Background p38 mitogen-activated protein kinases (MAPK) in ischemic preconditioning (IPC) may be essential tocardioprotection. We assessed either protective effect of morphine-induced preconditioning (MPG) on myocardialischemia and reperfusion injury in rat hearts p38 MAPK activation. Methods Male Spargue Dawley rats weighing 300-350 g were randomly assigned to 1 of the following 8 groups: control (CON, saline vehicle, n = 9), SB 203580 (SB, a p38 MAPK inhibitor, n = 6) (n = 6), IPC (n = 9), SB + MPC, SB + IPC, MPC + SB, and IPC + SB (n = 6) .Infarct sizes (IS) , were determined bytriphenyltetrazolium (TTC) staining. Tissue samples were processed from the entire AAR of left ventricle for the determination of p38 MAPK protein expression (5 hearts / group). The bands were visualizedusingusing an enhanced chemiluminescence detection system. Results of The IS / AAR was significantly reduced by I PC (12.9 ± 1.6)% or M PC (25.3 ± 2.9)% compared to the control ( 52.7 ± 5.5)%. SB 203580 ablished the effect of IPC (SB + IPC: (43.8 ± 2.6)%, P> 0.05 vs. CON, (30.7 ± 0.9)%, P <0.01 vs. CON, P> 0.05 vs MPC) .Treatmentwith SB 203580 prior to sustained ischemia diminished the protective effect of both MPC (MPC + SB: (42.4 ± 2.9)%, P> 0.05 vs CON) and IPC (IPC + SB: (52.0 ± 2.5)%, P> 0.05 vs. CON) on IS / AAR.In the IPC group, phospho-p38 MAPK protein increased significantly within 5 minutes into ischemia and remained elevated at 30 minutes into repeffusion, while phospho-p38 MAPK protein in the MPC group only increased significantly 30 minutes into reperfusion. Confluence The activation of p38 MAPK just acts as a mediator of MPC, and it acts as both a trigger and amediator in IPC.