Ischemic preconditioning produces systemic protective and adoptively transferable effects
Author(s) -
Anja ReutzelSelke,
Johann Pratschke,
Paulo N. Martins,
Christian Denecke,
Anke Jurisch,
Katja Kotsch,
Andreas Pascher,
P. Neuhaus,
Stefan G. Tullius
Publication year - 2008
Publication title -
kidney international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.499
H-Index - 276
eISSN - 1523-1755
pISSN - 0085-2538
DOI - 10.1038/ki.2008.208
Subject(s) - medicine , ischemic preconditioning , denervation , ischemia , heme oxygenase , kidney , systemic inflammation , inflammation , heme , pharmacology , anesthesia , chemistry , biochemistry , enzyme
Ischemic preconditioning directly protects organs from subsequent non-specific injuries. To test for systemic protective effects kidneys from F-344 donor rats went through a short warm ischemic time. Both, clamped and contralateral unclamped kidneys were procured after either a short (15 min) or long (24 h) reperfusion period and transplanted into Lewis rats following a prolonged cold ischemia. To test for transferable effects serum from preconditioned rats was infused either into native donors or recipients. Following a short reperfusion interval protective effects were only evident in previously clamped grafts. However, after a long reperfusion interval protective effects were observed in previously clamped and contralateral unclamped kidneys promoting improved survival, structure, function and reduced inflammation. These effects were not related to heme oxygenase-1 induction or neural transmission as heme oxygenase-1 inhibition or denervation prior to preconditioning did not affect organ protection. These results show that renal ischemic preconditioning is associated with time-dependent local and systemically transferable protection.
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