Mitochondrial creatine kinase: a key enzyme of aerobic energy metabolism

1992 ◽  
Vol 1102 (2) ◽  
pp. 119-166 ◽  
Author(s):  
Markus Wyss ◽  
Jan Smeitink ◽  
Ron A. Wevers ◽  
Theo Wallimann
1989 ◽  
Vol 20 (2) ◽  
pp. 113-114
Author(s):  
W Biermans ◽  
M De Bie ◽  
I Bernaert ◽  
A Bakker ◽  
W Jacob

1997 ◽  
Vol 7 (6) ◽  
pp. 811-818 ◽  
Author(s):  
Wolfgang Kabsch ◽  
Karin Fritz-Wolf

Author(s):  
Jadriane Fontoura Friedrich ◽  
Jessica Tadiello dos Santos ◽  
Ariane Ribas Pohl ◽  
Vivian Shinobu Kishimoto Nishihira ◽  
Morgana Brondani ◽  
...  

Naringin and naringenin are flavonoids found in citrus fruits and have several health benefits, however these compounds are susceptible to degradation, limiting their therapeutic application. To solve this problem, an alternative is to incorporate them into nanocapsules. The aim of this work was to evaluate the toxicity of these nanocapsules against renal and hepatic serum markers and also on the activities of pyruvate kinase, Mg2+-ATPase, and creatine kinase. Nanocapsules containing naringin and naringenin, nanocapsules without the active compounds and the compounds in their free form were administered orally, once a day, for 28 days. After treatment, the serum levels of hepatic and renal markers were not altered, nor the activities of pyruvate kinase tissue, however, the treatment of nanocapsules with flavonoids increased the activities of mitochondrial creatine kinase in the kidney and hepatic Mg2+-ATPase. Thus, renal and hepatic serum markers, which are normally used as indicators of toxicity, did not change after the period of administration of the nanoparticles. However, the activities of important enzymes of the energy metabolism in these organs were affected. Our findings reinforce that nanomaterial testing for toxicity needs to go beyond traditional methods to ensure the safe use of nanoparticles for therapeutic purposes.


1994 ◽  
Vol 91 (11) ◽  
pp. 5089-5093 ◽  
Author(s):  
A. M. Stadhouders ◽  
P. H. Jap ◽  
H. P. Winkler ◽  
H. M. Eppenberger ◽  
T. Wallimann

Author(s):  
Uwe Schlattner ◽  
Michael Forstner ◽  
Michael Eder ◽  
Olaf Stachowiak ◽  
Karin Fritz-Wolf ◽  
...  

1987 ◽  
Vol 26 (05) ◽  
pp. 220-223 ◽  
Author(s):  
L. Hadaš ◽  
J. VižĎa ◽  
P. Kafka ◽  
Y. Mazurová ◽  
V. Palicka ◽  
...  

Experimental cardiomyopathy was provoked in 24 dogs with high intravenous doses of adrenaline and theophylline. These lesions were studied by means of the new agent 99mTc-AHDP and 99mTc-PYP in comparison. Cardiomyopathy could be imaged as early as 4 h after the onset of involvement but not later than 7 days. A maximum accumulation occurred in lesions 24 h old. 99mTc uptake in the myocardium was graded scintigraphically. 99mTc-AHDP was accumulated in the altered’myocardium to a greater extent than 99mTc-PYP. Scintigraphic findings were in good agreement with plasma levels of creatine- kinase. A comparison with histology demonstrated that the maximum accumulation of radiopharmaceuticals occurred at the time when the development of myocardium involvement reached the stage of myocytolysis.


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