“…But conceptually, the early window of protection for IPC is predominately dependent on immediate effects especially on the mitochondria, whereas the late-phase protection is mediated through modulation of key transcription factors (NF-κB, STAT1/3, HIF-1α, AP-1, Nrf2 etc.) and de novo protein synthesis (COX-2, HO-1, iNOS, MnSOD and HSPs; see Appendix for a list of molecular abbreviations) [12,26,27] (fig. 2).…”