Acta Pharmacologica Sinica (2009) 30:1666–1673; doi: 10.1038/aps.2009.163; published online 16 Nov 2009

 
Original Article
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In vivo assessment of mitochondrial toxicity of metacavir in Rhesus monkeys after three months of intravenous administration
 

Wen ZENG1, 3, #, An-chun CHENG1, 4, #,*, Zheng-li CHEN1,4, #,*, Qi-hui LUO1,4, Yu-bo SUN3, Zhan LI2, Feng-jun BI1

1Engineering and Technology Center for Laboratory Animals of Sichuan Agricultural University, Ya-an 625014, China; 2Nanjing Chang’ao Pharmaceutical Science; Technology Co Ltd, Nanjing 210022, China; 3Sinopharm Center for Safety Evaluation and Reserch, Cheng-du 610051, China; 4Key Laboratory of Animal Disease and Human Health of Sichuan Province, Ya-an 625014, China

 

Aim: To explore the potential mitochondrial toxicities and their severities of intravenously administered metacavir, a nucleoside analog, in rhesus monkeys.

 

Methods: Totally 21 rhesus monkeys were randomly divided into 4 groups: metacavir 120 mg/kg group, metacavir 40 mg/kg group, zidovudine(AZT) 50 mg/kg group, and blank control group.  Animals were killed after the completion of dosing or further observed in a 4-week recovery phase.  Changes of structure of mitochondria in liver, kidney, skeletal muscles, and cardiac muscles were observed under transmission electron microscope(TEM).  Changes of the activities of mitochondrial respiratory chain complexes and mitochondrial DNA were also determined. 

 

Results: In metacavir 120 mg/kg group, some mitochondrial injuries were found in skeletal muscle, cardiac muscle, and liver, including that some cristae was broken and became sparse in density in the skeletal muscle, the morphology and size of mitochondria remained unchanged.  Metacavir decreased the activities of respiratory chain complexes I and II and the mtDNA contents in three tissues in a dose-dependent manner; however, the extent of such decrease was lower than that in AZT 50 mg/kg group.  The mitochondrial injuries in metacavir 40 mg/kg group were mild in each tissue and no obvious change in mitochondrial function was noted.  On week 4 in the recovery phase, results showed that all these injuries were reversible after drug withdrawal.


Conclusion:
These results suggest that metacavir has not a high risk for potential mitochondrial-related effects in rhesus monkeys.

 

Keywords: metacavir; rhesus monkey; toxicity; mitochondria; mtDNA; respiratory chain

 

The research was supported by the Program for Changjiang Scholars and Innovative Research Team in University (IRT0853), the National and Sichuan Province Innovation Funds for moderate scale science and technology corporation ( 06C 26215101716/06CX1607002), Sichuan Province Basic Research Program (2008JO0003/2008JY0100/2008JY0102), the youth Foundation of Sichuan Province Sci & Tech Bureau, China (08ZQ026-061) and Program for Key Disciplines Construction of Sichuan Province (SZD0418).

# These authors contribute equally to this work.
* To whom correspondence should be addressed.
E-mail zengwen10@vip.163.com; chzhli75@163.com
Received 2009-07-30     Accepted 2009-10-09

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