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THE RELATIONSHIP BETWEEN THE STRUCTURE AND ACTIVITY OF RAT SKELETAL MUSCLE MITOCHONDRIA AFTER THYROIDECTOMY AND THYROID HORMONE TREATMENT
Open accessAbstract
The fine structure of rat gastrocnemius muscle fibers has been studied after changes were induced in the basal metabolic rate (BMR) by thyroidectomy and L-thyroxine administration under anabolic conditions. Biochemical analysis of skeletal muscle mitochondrial respiration and phosphorylation from the same tissue preparations has been summarized, details having been published earlier (3). As estimated from electron micrographs, the total amount of mitochondria from thyroidectomized animals was enlarged 1.5 times over that from normal controls. The total amount of mitochondria from thyroidectomized or normal animals made hypermetabolic with thyroxine was increased 2.5 to 3.5 times over that from their corresponding controls. In all cases, there was an increase in the mitochondrial population and the profile ratio of cristae to matrix was also considerably increased, thus indicating both relative and absolute enlargements of the entire surface of the cristae per unit fiber. The major structural changes persisted for at least 3 weeks after the cessation of thyroxine treatment, by which time the elevated mitochondrial respiratory and phosphorylative activity had declined to normal values. The hypertrophy and increase in mitochondrial population was more prominent in the perinuclear and subsacrolemmic regions near blood vessels than in the interstices of the fibrils. The very long interfibrillar mitochondria found in both the hypo- and hypermetabolic tissues are more likely to be derived from outgrowths of the original mitochondria rather than from a fusion of smaller ones. These findings are compatible with the ideas expressed elsewhere (see 1, 3, 10) that, under conditions close to the physiological, thyroid hormones control mitochondrial metabolic activity by a subtle alteration in mitochondrial composition with respect to their respiratory and phosphorylative constituents. The possible application of using thyroid hormones in the study of biogenesis of mitochondria and the synthesis of mitochondrial constituents are discussed.
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Citations
Cited by
Cellular energy utilization and molecular origin of standard metabolic rate in mammals
Rolfe, D. F., & Brown, G. C. (1997) · Physiological Reviews · doi:10.1152/physrev.1997.77.3.731 · Cited by 2,021
Biochemical Adaptations in Muscle
Holloszy, J. O. (1967) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)96046-1 · Cited by 1,517
Palmer, J. W., Tandler, B., & Hoppel, C. L. (1977) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)75283-1 · Cited by 829
The Mechanism of the Calorigenic Action of Thyroid Hormone
Ismail-Beigi, F., & Edelman, I. S. (1971) · The Journal of General Physiology · doi:10.1085/jgp.57.6.710 · Cited by 373
Mitochondrial framework (reticulum mitochondriale) in rat diaphragm muscle
Bakeeva, L. E., Chentsov, Y. S., & Skulachev, V. P. (1978) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(78)90104-4 · Cited by 227
Metadata
- Authors
- Gustafsson, R., Tata, J. R., Lindberg, O., & Ernster, L.
- Venue
- The Journal of Cell Biology
- Publisher
- Rockefeller University Press
- Published
- 1965-08-01
- Volume
- 26
- Issue
- 2
- Pages
- 555-578
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- OpenAlex
- W2146591693
- Cited by
- 216
- References
- 0
- FWCI
- 5.22
- Type
- journal article
- Language
- en
- Open access
- green
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- CoChat. (2026). Citation check: THE RELATIONSHIP BETWEEN THE STRUCTURE AND ACTIVITY OF RAT SKELETAL MUSCLE MITOCHONDRIA AFTER THYROIDECTOMY AND THYROID HORMONE TREATMENT. https://app.cochat.ai/papers/10.1083/jcb.26.2.555
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- Gustafsson, R., Tata, J. R., Lindberg, O., & Ernster, L. (1965). THE RELATIONSHIP BETWEEN THE STRUCTURE AND ACTIVITY OF RAT SKELETAL MUSCLE MITOCHONDRIA AFTER THYROIDECTOMY AND THYROID HORMONE TREATMENT. The Journal of Cell Biology. https://doi.org/10.1083/jcb.26.2.555
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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