Literature DB >> 12958032

Myocardial contractile function during postischemic low-flow reperfusion: critical thresholds of NADH and O2 delivery.

Jason D Stoner1, Mark G Angelos, Thomas L Clanton.   

Abstract

The degree of myocardial oxygen delivery (Do2) that is necessary to reestablish functional contractile activity after short-term global ischemia in heart is not known. To determine the relationship between Do2 and recovery of contractile and metabolic functions, we used tissue NADH fluorometric changes to characterize adequacy of reperfusion flow. Isolated perfused rat hearts were subjected to global ischemia and were reperfused at variable flow rates that ranged from 1 to 100% of baseline flow. Myocardial function and tissue NADH changes were continuously measured. NADH fluorescence rapidly increased and plateaued during ischemia. A strong inverse logarithmic correlation between NADH fluorescence and reperfusion Do2 was demonstrated (r = -0.952). Left ventricular function (rate-pressure product) was inversely related to NADH fluorescence at reperfusion flows from 25 to 100% of baseline (r = -0.922) but not at lower reperfusion flow levels. An apparent reperfusion threshold of 25% of baseline Do2 was necessary to resume contractile function. At very low reperfusion flows (1% of baseline), another threshold flow was identified at which NADH levels increased beyond that observed during global ischemia (3.4 +/- 3.0%, means +/- SE, n = 9), which suggests further reduction of the cellular redox state. This NADH increase at 1% of baseline reperfusion flow was blocked by removing glucose from the perfusate. NADH fluorescence is a sensitive indicator of myocardial cellular oxygen utilization over a wide range of reperfusion Do2 values. Although oxygen is utilized at very low flow rates, as indicated by changes in NADH, a critical threshold of approximately 25% of baseline Do2 is necessary to restore contractile function after short-term global ischemia.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12958032     DOI: 10.1152/ajpheart.00436.2003

Source DB:  PubMed          Journal:  Am J Physiol Heart Circ Physiol        ISSN: 0363-6135            Impact factor:   4.733


  6 in total

1.  Modulation of p38 kinase by DUSP4 is important in regulating cardiovascular function under oxidative stress.

Authors:  Alma Barajas-Espinosa; Ariel Basye; Mark G Angelos; Chun-An Chen
Journal:  Free Radic Biol Med       Date:  2015-07-14       Impact factor: 7.376

2.  Co-Polarized [1-13C]Pyruvate and [1,3-13C2]Acetoacetate Provide a Simultaneous View of Cytosolic and Mitochondrial Redox in a Single Experiment.

Authors:  Gaurav Sharma; Xiaodong Wen; Nesmine R Maptue; Thomas Hever; Craig R Malloy; A Dean Sherry; Chalermchai Khemtong
Journal:  ACS Sens       Date:  2021-11-11       Impact factor: 7.711

Review 3.  Redox signaling in cardiovascular health and disease.

Authors:  Nageswara R Madamanchi; Marschall S Runge
Journal:  Free Radic Biol Med       Date:  2013-04-11       Impact factor: 7.376

4.  Prognostic value of minimal blood flow restoration in patients with acute myocardial infarction after reperfusion therapy.

Authors:  Gjin Ndrepepa; Dritan Keta; Stefanie Schulz; Robert A Byrne; Julinda Mehilli; Jürgen Pache; Melchior Seyfarth; Albert Schömig; Adnan Kastrati
Journal:  Clin Res Cardiol       Date:  2009-09-10       Impact factor: 5.460

5.  The potential of dual camera systems for multimodal imaging of cardiac electrophysiology and metabolism.

Authors:  Mark R Holcomb; Marcella C Woods; Ilija Uzelac; John P Wikswo; Jonathan M Gilligan; Veniamin Y Sidorov
Journal:  Exp Biol Med (Maywood)       Date:  2009-08-05

6.  Nocturnal hypoxia and the success rate of standard atrial fibrillation treatment: a case report.

Authors:  Bülent Güçyetmez; Hakan Korkut Atalan; Hikmet Aloglu; Adnan Kelebek; Tayfun Açıl
Journal:  J Med Case Rep       Date:  2015-06-06
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.