DEFECTS OF THE RESPIRATORY-CHAIN IN VARIOUS TISSUES OF OLD MONKEYS - A CYTOCHEMICAL-IMMUNOCYTOCHEMICAL STUDY

Citation
J. Mullerhocker et al., DEFECTS OF THE RESPIRATORY-CHAIN IN VARIOUS TISSUES OF OLD MONKEYS - A CYTOCHEMICAL-IMMUNOCYTOCHEMICAL STUDY, Mechanism of ageing and development, 86(3), 1996, pp. 197-213
Citations number
77
Categorie Soggetti
Geiatric & Gerontology",Biology,"Cell Biology
ISSN journal
00476374
Volume
86
Issue
3
Year of publication
1996
Pages
197 - 213
Database
ISI
SICI code
0047-6374(1996)86:3<197:DOTRIV>2.0.ZU;2-9
Abstract
The aim of the present study was to evaluate if defects of the respira tory chain known to occur in humans, also exist in lower primates. Cyt ochemical-immunocytochemical studies of the respiratory chain enzymes in five monkeys (10-25 years of age) showed defects of ubiquinone cyto chrome-c-oxidoreductase (complex III), of cytochrome-c-oxidase (comple x IV) and of ATP-synthase (complex V) in the limb muscles, diaphragm, heart muscle and extraocular muscles of three old animals (about 25 ye ars) and also in the heart muscle of two younger animals (10 and 15 ye ars). Characteristically! the defects were randomly distributed and th ere was no loss of succinate-dehydrogenase (complex II) in the fibres. Ultracytochemistry-immunocytochemistry of complex IV disclosed that i n an involved fibre segment all the mitochondria exhibited the defect. The highest number of defects was observed in the extraocular muscles (up to 340/cm(2)) while the lowest defect density was present in the limb muscles (2-5/cm(2)). Defects of complex IV occurred two to three times more often than defects of complex III and besides isolated defe cts of complex III and IV, combined defects of both complexes were als o observed. Defects of complex V occurred exclusively in combination a nd were rarely seen. rising subunit specific antisera against complex IV, it could be demonstrated at light and electron microscopic level t hat loss of activity of cytochrome-c-oxidase was associated with a los s both of mitochondrially and nuclearly coded subunits of the enzyme. In summary, aging in lower primates and humans is characterised by a h ighly similar defect expression of the respiratory chain enzymes, with intercellular and interorgan differences of the aging process, underl ining the universal nature of the involved pathogenetic mechanisms.