AZT inhibition of the ADP/ATP antiport in isolated rat heart mitochondria.

Author(s):  
D Valenti ◽  
M Barile ◽  
S Passarella
2012 ◽  
Vol 443 (1) ◽  
pp. 113-117 ◽  
Author(s):  
S. M. Korotkov ◽  
L. V. Emel’yanova ◽  
I. V. Brailovskaya ◽  
V. P. Nesterov

2011 ◽  
Vol 74 (7) ◽  
pp. 1640-1644 ◽  
Author(s):  
Julius Liobikas ◽  
Daiva Majiene ◽  
Sonata Trumbeckaite ◽  
Lolita Kursvietiene ◽  
Ruta Masteikova ◽  
...  

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 Today, valdecoxib and rofecoxib have been withdrawn on the market but celecoxib remains.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.


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