Cellular Physiology and Biochemistry

Original Paper

Antioxidant-Sensitive Triiodothyronine Effects on Characteristics of Rat Liver Mitochondrial Population

Venditti P. · Daniele M.C. · Masullo P. · Di Meo S.

Author affiliations

Dipartimento di Fisiologia Generale ed Ambientale, Università di Napoli ‘Federico II’, Napoli, Italia

Related Articles for ""

Cell Physiol Biochem 1999;9:38–52

Log in to MyKarger to check if you already have access to this content.


Buy

  • FullText & PDF
  • Unlimited re-access via MyKarger
  • Unrestricted printing, no saving restrictions for personal use
read more

CHF 38.00 *
EUR 35.00 *
USD 39.00 *

Select

KAB

Buy a Karger Article Bundle (KAB) and profit from a discount!


If you would like to redeem your KAB credit, please log in.


Save over 20% compared to the individual article price.

Learn more

Rent/Cloud

  • Rent for 48h to view
  • Buy Cloud Access for unlimited viewing via different devices
  • Synchronizing in the ReadCube Cloud
  • Printing and saving restrictions apply

Rental: USD 8.50
Cloud: USD 20.00

Select

Subscribe

For eJournal Archive and eJournal Backfiles information please contact Karger service

* The final prices may differ from the prices shown due to specifics of VAT rules.

Article / Publication Details

First-Page Preview
Abstract of Original Paper

Published online: May 28, 1999
Issue release date: 1999

Number of Print Pages: 15
Number of Figures: 3
Number of Tables: 7

ISSN: 1015-8987 (Print)
eISSN: 1421-9778 (Online)

For additional information: https://www.karger.com/CPB

Abstract

Whole mitochondrial population and three mitochondrial fractions were resolved by differential centrifugation from liver homogenates from euthyroid, hyperthyroid (ten daily i.p. injections of triiodothyronine (T3), 10 μg/100 g body weight) and hyperthyroid vitamin E-treated (ten daily i.m. vitamin E injections, 20 mg/100 g body weight) rats. Homogenates and mitochondrial preparations were examined for their protein content, oxidative capacity, lipid peroxidation, antioxidant status, and susceptibility to oxidative stress. In all groups, antioxidant level was smaller and oxidative capacity, lipid peroxidation, and susceptibility to oxidants were greater in the heavy mitochondrial fraction. T3 treatment was associated with increased oxidative capacity, lipid peroxidation, and susceptibility to oxidative stress, and decreased antioxidant levels in all preparations. It was also associated with increased mitochondrial protein content of homogenate and altered quantitative presence of the mitochondrial fractions. The vitamin E effects on the T3-induced changes were different for the different parameters. Vitamin E did not modify the mitochondrial protein content in liver and oxidative capacity of the various preparations, reduced the changes in both susceptibility to oxidants and contribution of each fraction to the whole mitochondrial population, and reinstated euthyroid values for antioxidant capacity and lipid peroxidation. The incomplete recovery of euthyroid resistance to oxidants in vitamin E-treated rats is due to the vitamin inability to reinstate the levels of both antioxidants and hemoproteins, on which such a resistance depends. The vitamin E effect on the composition of the mitochondrial population is more difficult to explain, because of the complexity of the mechanisms underlying the mitochondrial population modulation by thyroid hormone. However, available data suggest that such a modulation occurs through changes in the turnover of the mitochondrial fractions to which an induction of mitochondrial protein synthesis and accelerated antioxidant-sensitive degradation contribute in different measure.




Related Articles:


References

  1. Freeman BA, Crapo JD: Biology of disease. Free radicals and tissue injury. Lab Invest 1982;47:412–426.
  2. Schwartz HL, Oppenheimer JH: Physiologic and biochemical actions of thyroid hormone. Pharmacol Ther 1978;3:349–376.
  3. Asayama K, Dobashi K, Hayashibe H, Megata Y, Kato K: Lipid peroxidation and free radical scavengers in thyroid dysfunction in the rat: A possible mechanism of injury to heart and skeletal muscle in hyperthyroidism. Endocrinology 1987;121:2112–2118.
    External Resources
  4. Fernandez V, Llesuy S, Solari L, Kipreos K, Videla LA, Boveris A: Chemiluminescent and respiratory responses related to thyroid hormone-induced liver oxidative stress. Free Radic Res Commun 1988;5:77–84.
    External Resources
  5. Venditti P, Balestrieri M, Di Meo S, De Leo T: Effect of thyroid state on lipid peroxidation, antioxidant defences, and susceptibility to oxidative stress in rat tissues. J Endocrinol 1997;155:151–157.
  6. Boveris A, Cadenas E, Stoppani AOM: Role of ubiquinone in the mitochondrial generation of hydrogen peroxide. Biochem J 1976;156:435–444.
  7. Nohl H, Hegner D: Do mitochondria produce oxygen radical in vivo? Eur J Biochem 1978;82:563–567.
  8. Turrens JF, Boveris A: Generation of superoxide anion by the NADH dehydrogenase of bovine heart mitochondria. Biochem J 1980;191:421–427.
  9. Lanni A, Moreno M, Lombardi A, Goglia F: Biochemical and functional differences in rat liver mitochondrial subpopulations obtained at different gravitational forces. Int J Biochem Cell Biol 1996;28:337–343.
  10. Venditti P, Di Meo S, De Leo T: Effect of thyroid state on characteristics determining the susceptibility to oxidative stress of mitochondrial fractions from rat liver. Cell Physiol Biochem 1996;6:283–295.
  11. Di Meo S, Venditti P, De Leo T: Tissue protection against oxidative stress. Experientia 1996;52:786–794.
  12. Stadtman ER: Oxidation of proteins by mixed-function oxidation system. Implication in protein turnover, ageing and neutrophil function. Trends Biochem Sci 1986;11:11–12.
    External Resources
  13. Rivett AJ: Regulation of intracellular protein turnover: Covalent modifications as a mechanism of marking proteins for degradation. Curr Top Cell Regul 1986;38:291–336.
  14. Wolff SP, Dean RT: Fragmentation of proteins by free radicals and its effect on their susceptibility to enzymic hydrolysis. Biochem J 1986;234:399–403.
  15. Gornall AG, Bardawill CJ, David MM: Determination of serum proteins by mean of the biuret reaction. J Biol Chem 1949;177:751–766.
  16. Buege JA, Aust SD: Microsomal lipid peroxidation. Methods Enzymol 1978;52:306–307.
  17. Heath RL, Tappel AL: A new sensitive assay for the measurement of hydroperoxides. Anal Biochem 1976;76:184–191.
  18. Aulie A, Grav HJ: Effect of cold acclimation on the oxidative capacity of skeletal muscles and liver in young bantam chicks. Comp Biochem Physiol 1979;62A:335–338.
  19. Barré H, Bailly L, Rouanet JL: Increased oxidative capacity in skeletal muscles from cold-acclimated ducklings: A comparison with rats. Comp Biochem Physiol 1987;88B:519–522.
  20. Simon LM, Robin ED: Relationship of cytochrome oxidase activity to vertebrate total and organ oxygen consumption. Int J Biochem 1971;2:569–573.
    External Resources
  21. Lang JK, Gohil K, Packer L: Simultaneous determination of tocopherols, ubiquinols and ubiquinones in blood, plasma, tissue homogenates and subcellular fractions. Anal Biochem 1986;157:106–116.
  22. Griffith OW: Determination of glutathione and glutathione disulphide using glutathione reductase and 2-vinylpyridine. Anal Biochem 1980;106:207–212.
  23. Di Meo S, Venditti P, Piro MC, De Leo T: Enhanced luminescence study of liver homogenate response to oxidative stress. Arch Physiol Biochem 1995;103:187–195.
  24. Venditti P, Di Meo S, de Martino Rosaroll P, De Leo T: Determination by enhanced luminescence technique of liver antioxidant capacity. Arch Physiol Biochem 1995;103:484–491.
    External Resources
  25. Oppenheimer JH: Thyroid hormone action at the cellular level. Science 1979;203:971–979.
  26. Asayama K, Kato K: Oxidative muscular injury and its relevance to hyperthyroidism. Free Radic Biol Med 1990;8:293–303.
  27. Fernandez V, Simizu K, Barros SBM, Azzalis LA, Pimentel R, Junqueira VBC, Videla LA: Effects of hyperthyroidism on rat liver glutathione metabolism: Related enzymes’ activities, efflux, and turnover. Endocrinology 1991;129:85–91.
    External Resources
  28. Sanford CF, Griffin EE, Wildenthal K: Synthesis and degradation of myocardial protein during the development and regression of thyroxine-induced cardiac hypertrophy in rats. Circ Res 1978;43:688–694.
    External Resources
  29. Siehl D, Chua BH, Lautensack-Belser N, Morgan HE: Faster protein and ribosome synthesis in thyroxine-induced hypertrophy of rat heart. Am J Physiol 1985;248:C309–C319.
    External Resources
  30. Mutvei A, Kuzela S, Nelson BD: Control of mitochondrial transcription by thyroid hormone. Eur J Biochem 1989;180:235–240.
  31. Venditti P, De Leo T, Di Meo S: Vitamin E administration attenuates the tri-iodothyronine-induced modification of heart electrical activity on the heart. J Exp Biol 1997;200:909–914.
    External Resources
  32. Yu BP: Cellular defenses against damage from reactive oxygen species. Physiol Rev 1994;74:139–162.
  33. Boveris A, Oshino N, Chance B: The cellular production of hydrogen peroxide. Biochem J 1972;128:617–630.
  34. Horrum MA, Tobin RB, Ecklund RE: Thyroid-induced changes in rat liver mitochondrial cytochromes. Mol Cell Endocrinol 1985;41:163–169.
  35. Swaroop A, Ramasarma T: Heat exposure and hyperthyroid conditions decrease peroxide generation in liver mitochondria. Biochem J 1985;226:403–408.
    External Resources
  36. Gutteridge JMC: Iron promoters of the Fenton reaction and lipid peroxidation can be released from haemoglobin by peroxides. FEBS Lett 1986;20:291–295.
    External Resources
  37. Raywade MS, Katyare SS, Fatterpaker P, Sreenivasan A: Regulation of mitochondrial protein turnover by thyroid hormone(s). Biochem J 1975;152:379–385.
    External Resources
  38. Gross NJ: Control of mitochondrial turnover under the influence of thyroid hormone. J Cell Biol 1971;48:29–40.
  39. Goglia F, Liverini G, Lanni A, Iossa S, Barletta A: The effect of thyroid state on respiratory activities of three liver mitochondrial fractions. Mol Cell Endocrinol 1989;62:41–46.
  40. Katyare SS, Fatterpaker P, Sreenivasan A: Heterogeneity of rat liver mitochondrial fractions and the effect of tri-iodothyronine on their protein turnover. Biochem J 1970;118:111–121.
    External Resources

Article / Publication Details

First-Page Preview
Abstract of Original Paper

Published online: May 28, 1999
Issue release date: 1999

Number of Print Pages: 15
Number of Figures: 3
Number of Tables: 7

ISSN: 1015-8987 (Print)
eISSN: 1421-9778 (Online)

For additional information: https://www.karger.com/CPB


Copyright / Drug Dosage / Disclaimer

Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher.
Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.
TOP