TY - JOUR
T1 - Ischemic preconditioning activates phosphatidylinositol-3-kinase upstream of protein kinase C
AU - Tong, Haiyan
AU - Chen, Weina
AU - Steenbergen, Charles
AU - Murphy, Elizabeth
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2000/8/18
Y1 - 2000/8/18
N2 - The present study is designed to test whether phosphatidylinositol 3-kinase (PI3-kinase) has a role in the signaling pathway in ischemic preconditioning (PC) and whether it is proximal or distal to protein kinase C (PKC). Before 20 minutes of global ischemia, Langendorff-perfused rat hearts were perfused for 20 minutes (control); preconditioned with 4 cycles of 5-minute ischemia and 5-minute reflow (PC); treated with either wortmannin (WM) or LY 294002 (LY), each of which is a PI3-kinase inhibitor, for 5 minutes before and throughout PC; treated with 1,2-dioctanoyl-sn-glycerol (DOG), an activator of PKC for 10 minutes (DOG); treated identically to the DOG group except with WM added 10 minutes before and during perfusion with DOG; or treated with either WM or LY for 25 minutes. Recovery of left ventricular developed pressure (LVDP; percentage of initial preischemic LVDP), measured after 30 minutes of reflow, was improved by PC (72±2% versus 36±4% in control; P<0.001), and this was blocked by WM and LY (41±4% and 43±5%, respectively; P<0.05 compared with PC). DOG addition improved postischemic LVDP (67±6%; P<0.001 compared with control), but in contrast to its effect on PC, WM did not completely eliminate the protective effect of DOG (52±4%; P>0.05 compared with DOG; P<0.05 compared with control). PC induced phosphorylation of protein kinase B and translocation of PKCε, and it increased NO production, and these effects were blocked by WM, which suggests a role for PI3-kinase in PC upstream of PKC and NO.
AB - The present study is designed to test whether phosphatidylinositol 3-kinase (PI3-kinase) has a role in the signaling pathway in ischemic preconditioning (PC) and whether it is proximal or distal to protein kinase C (PKC). Before 20 minutes of global ischemia, Langendorff-perfused rat hearts were perfused for 20 minutes (control); preconditioned with 4 cycles of 5-minute ischemia and 5-minute reflow (PC); treated with either wortmannin (WM) or LY 294002 (LY), each of which is a PI3-kinase inhibitor, for 5 minutes before and throughout PC; treated with 1,2-dioctanoyl-sn-glycerol (DOG), an activator of PKC for 10 minutes (DOG); treated identically to the DOG group except with WM added 10 minutes before and during perfusion with DOG; or treated with either WM or LY for 25 minutes. Recovery of left ventricular developed pressure (LVDP; percentage of initial preischemic LVDP), measured after 30 minutes of reflow, was improved by PC (72±2% versus 36±4% in control; P<0.001), and this was blocked by WM and LY (41±4% and 43±5%, respectively; P<0.05 compared with PC). DOG addition improved postischemic LVDP (67±6%; P<0.001 compared with control), but in contrast to its effect on PC, WM did not completely eliminate the protective effect of DOG (52±4%; P>0.05 compared with DOG; P<0.05 compared with control). PC induced phosphorylation of protein kinase B and translocation of PKCε, and it increased NO production, and these effects were blocked by WM, which suggests a role for PI3-kinase in PC upstream of PKC and NO.
KW - Ischemic preconditioning
KW - Nitric oxide
KW - Phosphatidylinositol 3-kinase
KW - Protein kinase C
UR - http://www.scopus.com/inward/record.url?scp=0034683064&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0034683064&partnerID=8YFLogxK
U2 - 10.1161/01.RES.87.4.309
DO - 10.1161/01.RES.87.4.309
M3 - Article
C2 - 10948065
AN - SCOPUS:0034683064
VL - 87
SP - 309
EP - 315
JO - Circulation Research
JF - Circulation Research
SN - 0009-7330
IS - 4
ER -