1. Abnormalities of ADP/ATP carrier protein in J-2-N cardiomyopathic hamsters
- Author
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Akira Tanamura, Jie Yang, Osamu Kawashima, Takaaki Iwai, Nobuakira Takeda, Mitsutoshi Kato, and Toru Arino
- Subjects
medicine.medical_specialty ,Clinical Biochemistry ,Hamster ,Cell Biology ,General Medicine ,biochemical phenomena, metabolism, and nutrition ,Mitochondrion ,Biology ,Cardiomyopathy, Hypertrophic ,Mitochondria, Heart ,Staining ,Pathogenesis ,Disease Models, Animal ,Endocrinology ,Cytoplasm ,Adenine nucleotide ,Internal medicine ,Cricetinae ,medicine ,Animals ,Inner mitochondrial membrane ,Molecular Biology ,Mitochondrial ADP, ATP Translocases ,Golden hamster - Abstract
ADP/ATP carrier protein (AAC) is located in the mitochondrial inner membrane and has an important function in mitochondrial energy supply. This protein transports ATP to the cytoplasm and counter transports ADP into the mitochondria. J-2-N cardiomyopathic hamsters were investigated to determine the AAC content in cardiac mitochondria. After recording an electrocardiogram and collecting blood, the cardiac mitochondria were isolated. The mitochondrial membranes were labelled with eosin-5-maleimide (EMA) and separated on SDS polyacrylamide gels. The position of the AAC component was identified by exposing the gel under UV light, and the AAC content was determined by densitometry after staining with Coomassie blue. The AAC content ratio was significantly decreased in both 10-week-old and 1-year survived J-2-N hamsters when compared to control Golden hamster. Among 10-week-old J-2-N hamsters, the decrease in the AAC content ratio was more marked for the animals with more severe myocardial damage. The H(+)-ATPase activities of mitochondrial membrane were higher in 10-week-old J-2-N hamsters than in control hamsters. These results suggest that the decrease of AAC in J-2-N hamster plays an important role in the pathogenesis of cardiomyopathy in J-2-N hamsters.
- Published
- 1993