Lipid Peroxidation, Tissue Necrosis, and Metabolic and Mechanical Recovery of Isolated Reperfused Rat Heart as a Function of Increasing Ischemia

1998 ◽  
Vol 28 (1) ◽  
pp. 25-37 ◽  
Author(s):  
Barbara Tavazzi ◽  
Donato Di Pierro ◽  
Marco Bartolini ◽  
Mario Marino ◽  
Stefanla Distefano ◽  
...  
1994 ◽  
Vol 47 (3) ◽  
pp. 549-553 ◽  
Author(s):  
Yu-Chiang Lo ◽  
Teng Che-Ming ◽  
Chen Chieh-Fu ◽  
Chen Chien-Chih ◽  
Hong Chuang-Ye

Pharmacology ◽  
1996 ◽  
Vol 52 (1) ◽  
pp. 1-7 ◽  
Author(s):  
Etienne Tatou ◽  
Claude Mossiat ◽  
Véronique Maupoil ◽  
François Gabrielle ◽  
Michel David ◽  
...  

1997 ◽  
Vol 97 (1) ◽  
pp. 1-7 ◽  
Author(s):  
Hector Molina ◽  
Miriam Garcı́a
Keyword(s):  

2020 ◽  
Author(s):  
Saman Atashbar ◽  
Elham Mohammad Khanlou ◽  
Saleh Khezri ◽  
Peyman Kurdpour ◽  
Ahmad Salimi

Abstract Background In spite of the cardiotoxic effect of selective cyclooxygenase-2 inhibitors, they are most widely used as anti-inflammatory and analgesic drugs. Today, valdecoxib and rofecoxib have been withdrawn on the market but celecoxib remains. In this study, we focused on an analysis of celecoxib toxic effects on isolated mitochondrial. Methods isolated rat heart mitochondria were obtained using differential centrifugation. Using flowcytometry and biochemical assays we searched succinate dehydrogenases (SDH), mitochondrial membrane potential (MMP), reactive oxygen species (ROS) formation, mitochondrial swelling, lipid peroxidation and mitochondrial complexes activity in rat heart isolated mitochondria. Results In here our results indicated a significant decrease in activity of complexes IV after exposure with celecoxib (16 µg/ml). This decrease in activity of complexes IV is paralleled by the MMP collapse, ROS formation, mitochondrial swelling and lipid peroxidation. Conclusion For the first time, this introductory study has showed a significant decrease in activity of complexes IV and mitochondrial dysfunction after exposure with celecoxib in rat heart isolated mitochondria.


Author(s):  
T. Oguro ◽  
T. Onodera ◽  
M. Ashraf

Previously we reported that hydrogen peroxide (H2O2) is primarily cytotoxic to the cardiac cell membranes presumably through lipid peroxidation (LP). However, the effect of LP on the altered cell membrane permeability remains unknown. In this study, we evaluated the ultrastructural effects of LP on the sarcolemma of the isolated rat heart using H2O2 and N,N’-diphenyl-p-phenylene diamine (DPPD), an antilipid peroxidative agent.The hearts were perfused with 300 μM H2O2 for 15 minutes. In the other experiment the hearts were perfused with 2.5 μM DPPD for 20 minutes prior to perfusion with H2O2 for 15 minutes. Coronary effluent was collected at the end of the equilibration period and during H2O2 treatment for malondialdehyde (MDA) determination. Two minutes prior to the termination of the experiment, horseradish peroxidase (HRP: 220 U/mg × 55 mg) was perfused to assess the enhanced permeability of the cell membranes. The tissue slices were incubated in Graham-Karnovsky medium for one hour followed by postfixation with buffered 1% OsO4.


1995 ◽  
Vol 47 (2) ◽  
pp. 138-142 ◽  
Author(s):  
CHUANG-YE HONG ◽  
CHEIN-PING WANG ◽  
SHIANG-SUO HUANG ◽  
FENG-LIN HSU

1981 ◽  
Vol 30 (20) ◽  
pp. 2797-2804 ◽  
Author(s):  
Edward G. Mimnaugh ◽  
Michael A. Trush ◽  
Theodore E. Gram
Keyword(s):  

2014 ◽  
Vol 1837 ◽  
pp. e63
Author(s):  
Martin Modrianský ◽  
Aleš Dvořák ◽  
David Biedermann ◽  
Vladimír Křen ◽  
Petr Ježek ◽  
...  

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