Back to Search Start Over

Inhibition of the pentose phosphate pathway decreases ischemia–reperfusion-induced creatine kinase release in the heart

Authors :
Zuurbier, C.J.
Eerbeek, O.
Goedhart, P.T.
Struys, E.A.
Verhoeven, N.M.
Jakobs, C.
Ince, C.
Source :
Cardiovascular Research. Apr2004, Vol. 62 Issue 1, p145. 9p.
Publication Year :
2004

Abstract

Objective: The oxidative pentose phosphate pathway (oxPPP) produces NADPH, which can be used to maintain glutathione in its reduced state (anti-oxidant; beneficial effects) or to produce radicals or nitric oxide (NO) through NADPH oxidase/NO synthase (detrimental effects). Changes in cytosolic redox status have been implicated in ischemic preconditioning (PC). This study investigates whether (1) PC affects mitochondrial redox state, (2) the oxPPP plays a protective or detrimental role in ischemia (I)–reperfusion (R) injury in the intact heart and (3) PPP is altered with PC. Methods: Isolated rat hearts were subjected to 40-min global I and 30-min R (CO, control). Ischemia was either preceded by three 5-min I/R periods (PC) and/or oxPPP inhibition by 6-aminonicotinamide (6AN) or NADPH oxidase/NO synthase inhibition by diphenyleneiodonium (DPI). NADH videofluorometry was used to determine mitochondrial redox state. PPP intermediates were determined in CO and PC hearts using tandem mass spectrometry. Results: PC reduced ischemic damage (creatine kinase, CK, release from 337±64 to 147±41 U/R/gdw) and contracture (from 59±5 to 31±3 mm Hg) and increased recovery of contractility (from 48±10% to 88±8%), as compared to CO. PC was without effect on NADH fluorometry. Inhibition of the oxPPP reduced injury (CK release: 91±24 U/R/gdw) to similar levels as PC, without improving contractility. Inhibition of NADPH oxidase/NO synthase mimicked the effects of oxPPP inhibition on injury (CK release: 140±22 U/R/gdw). Although levels of ribose-5P and (ribulose-5P+xylulose-5P) rose several fold during ischemia with minor changes in sedoheptulose-7P, demonstrating an active PPP in the heart, PC did not affect these levels. Conclusions: (1) PC can attenuate cardiac reperfusion injury without alterations in mitochondrial redox state; (2) inhibition of the oxPPP protects the heart against I/R-induced CK release; and (3) PC does not result in altered activity of the PPP. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
00086363
Volume :
62
Issue :
1
Database :
Academic Search Index
Journal :
Cardiovascular Research
Publication Type :
Academic Journal
Accession number :
12503013
Full Text :
https://doi.org/10.1016/j.cardiores.2004.01.010