Treatment with dehydroepiandrosterone (DHEA) stimulates oxidative energy metabolism in the liver mitochondria from developing rats

Molecular and Cellular Biochemistry

Volumn 293, Issue 1-2, 2006, Pages 193-201

  Patel, Minal A ^a   Katyare, Surendra S ^a  

^a M S UNIVERSITY OF BARODA   (India)

Author keywords

ATPase activity; Cytochrome; Dehydroepiandrosterone (DHEA); Dehydrogenases; Liver mitochondria; Oxidative energy metabolism

Indexed keywords

ADENOSINE TRIPHOSPHATASE; CYTOCHROME B; CYTOCHROME C; CYTOCHROME C OXIDASE; CYTOCHROME C1; OXIDOREDUCTASE; PRASTERONE;

AGE; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BODY WEIGHT; BREATHING RATE; DOSE RESPONSE; ENERGY METABOLISM; ENZYME ACTIVITY; LIVER DEVELOPMENT; LIVER MITOCHONDRION; LIVER WEIGHT; MALE; NONHUMAN; RAT; SIMULATION;

ADENOSINE TRIPHOSPHATASES; ANIMALS; CELL RESPIRATION; CYTOCHROMES; DEHYDROEPIANDROSTERONE; ENERGY METABOLISM; LIVER; MALE; MITOCHONDRIA, LIVER; OXIDATIVE PHOSPHORYLATION; RATS; RATS, INBRED STRAINS;

ANIMALIA;

EID: 33750720074     PISSN: 03008177     EISSN: 15734919     Source Type: Journal    
DOI: 10.1007/s11010-006-9242-3     Document Type: Article

References (39)

1. Milgrom E, Steroid hormone. In Hormones From molecues to disease: Baulieu EE and Kelly PA, (Ed.), Hermann Publishers and Hall. New York and London, pp. 387-438, 1990
2. Buvat J, Androgen therapy with dehydroepiandrosterone. World J Urol 21: 346-355, 2004
3. Hinson JP, Raven PW, DHEA deficiency syndrome: A new term for old age? J Endocrinol 163: 1-5, 1999
4. Celec P, Starka L, Dehydroepiandrosterone-Is the fountain of fouth drying out? Physiol Res 52: 397-407, 2003
5. Miller BC, Lau HW, Tyler NE, Cottam GL, Liver composition and lipid metabolism in NZB/W F1 female mice fed dehydroisoandrosterone. Biochem Biophys Acta 962: 25-36, 1988
6. Cleary MP, Effect of dehydroisoandrosterone treatment on liver metabolism in rats. Int J Biochem 22: 205-210, 1990
7. McIntosh MK, Pan JS, Berdanier CD, In vitro studies on the effects of dehydroisoandrosterone and corticosterone on hepatic steroid receptor binding and mitochondrial respiration. Comp. Bichem Physiol Comp Physiol 104: 147-153, 1993
8. Oliver TW, Clemens K, Action of dehydroepiandrosterone and its sulfate in the central nervous system: Effects on cognition and emotion in animals and humans. Brain Res Rev 30: 264-288, 1999
9. Natawa H, Toshihiko Y, Kiminobu G, Taijiro OKA, Mechanism of action of anti-aging DHEA-S and the replacement of DHEA-S. Mech Age Dev 123: 1101-1106, 2002
10. Patel MA, Katyare SS, (2005) Effect of dehydroepiandrosterone (DHEA) treatment on oxidative energy metabolism in rat liver and brain mitochondria. A dose response study Arch Biochem Physiol, 2005 (Communicated)
11. Katewa SD, Katyare SS, Treatment with antimalarials adversely affects the oxidative energy metabolism in rat liver mitochondria. Drug Chem Toxicol 27: 41-53, 2004
12. Pandya JD, Agarwal NA, Katyare SS, Effect of Dexamethasone treatment on oxidative energy metabolism in rat liver mitochondria during postnatal developmental periods. Drug Chem Toxicol 27: 389-403, 2004
13. Kaushal R., Dave KR, Katyare SS, Paracetamol hepatotoxicity and microsomal function. Environ Toxicol Pharmacol 7: 67-74, 1999
14. Katyare SS, Satav JG, Impaired mitochondrial energy metabolism following paracetamol-induced hepatotoxicity in the rat. Br J Pharmacol 96: 51-58, 1989
15. Ferreira J, Gil L, Nutriotional effects on mitochondrial bioenergetics: Alterations in oxidative phosphorylation by rat liver mitochondria. Biochem J 218: 61-67, 1984
16. Katyare SS, Joshi MV, Fatterpaker P, Sreenivasan A, Effect of thyroid deficiency on oxidative phosphorylation in rat liver, kidney and brain mitochondria. Arch Biochem Biophys 182: 155-163, 1977
17. Chance B, Williams GR, The respiratory chain and oxidative phosphorylation. Nature 173: 1094-1095, 1954
18. Subramaniam M, Katyare SS, Oxidative phosphorylation in mouse liver mitochondria during weaning. Mech Age Dev 54: 121-129, 1990
19. Leighton F, Poole B, Beaufay H, Baudhuin P, Coffer JW, Flower S, de Duve C, The large scale separation of peroxisome, mitochondria and lysosomes from livers of rats injected with Triton X-100: Improved isolation procedures, analysis and biochemical properties of fractions. J Cell Biol 37: 482-513, 1968
20. Ochoa S, Malic dehydrogenase from pig heart, In: Colowick SP, Kaplan NO, (Ed), Methods Enzymol. vol. 1, Academic Press, New York, pp. 735-739, 1955
21. King TE, Preparation of succinate-cytochrome c-reductase and the cytochrome b-c1 particle and the reconstitution of cytochrome c-reductase, In: Estabrook RW, Pullman ME, (Ed.), Methods Enzymol., Academic Press, New York, pp. 216-225, 1967
22. Katewa SD, Katyare SS, A Simplified method for inorganic phosphate determination and its application for phosphate analysis in enzyme assays, Anal Biochem 323: 180-187, 2003
23. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ, Protein measurement with Folin-phenol reagent. J Biol Chem 193: 265-275, 1951
24. Jani MS, Telang SD, Katyare SS, Effect of corticosterone treatment on energy metabolism in rat liver mitochondria. J Steroid Biochem Mol Biol 38: 587-591, 1991
25. Katyare SS, Balasubramanian S, Parmar DV, Effect of corticosterone treatment on mitochondrial oxidative energy metabolism in developing rat brain. Exp Neurol 183: 241-248, 2003
26. Rajan RR, Katyare SS,. Is the first site of phosphoryrlation operative in rat brain mitochondria in early neonatal life: A critical reevaluation. Mech Age Dev 61:149-.161.1991
27. Golovachev AF, Nadal'yak EA, Respiration and glycolysis in the liver of developing chick embryos and chicks. Zh Evol Biokhim Fiziol 11: 353-359, 1975
28. Okada Y, Energy metabolism and neural activity in hippocampal slices of developing rat brain. No To Hattatsu 26: 113-118, 1994
29. Rust RS, Energy metabolism of developing brain. Curr Opin Neurol 7: 160-165, 1994
30. Poyton RO, Mc Ewen JE, Crosstalk between nuclear and mitochondrial genomes. Annu Rev Biochem 65: 563-607, 1996
31. Parker CR Jr, Dehydroepiandrosterone and dehydroepiandrosterone sulfate production in the human adrenal during development and aging. Steroids 64: 640-647, 1999
32. Steckelbroeck S, Watzka M, Lutjohall D, Makiola P, Nassen A,. Hans VH, Clusmann H,. Reissinger A, Ludwig M, Siekmann L, Klingmuller D, Characterization of the dehydroepiandrosterone (DHEA) metabolism via oxysterol 7 alpha-hyroxylase and 17-ketosteroid reductase activity in human brain. J Neurochem 83: 713-726.
33. Weill-Engerer S, David JP, Sazdovitch V, Liere P, Schumacher M, Delacourte A, Baulieu EE, Akwa Y, In vitro metabolism of dehydroepiandrosterone (DHEA) to 7 alpha-hyroxy- DHEA and Delta 5 androstene 3 beta, 17 beta-diol in specific regions of the aging brain from Alzheimer's and non-demented patients. Brain Res 969: 117-125, 2003
34. Mamczka M, Jung Y, Park BS, Partovi D, Reddy PH, Time-course of mitochondrial gene expressions in mice brains: Implications for mitochondrial dysfunction, oxidative damage, and cytochrome c in aging. J Neurochem 92: 494-504, 2005
35. Formoso G, Chen H, Kim JA, Montagnani M, Consoli A, Quon MJ, DHEA mimics acute actions of insulin to stimulate production of both NO and ET-1 via distinct PI 3-kinase and MAP-kinase-dependent pathways in vascular endothelium. Mol Endocrinol., 20: 1153-1163, 2006
36. Wang MJ, Huang HM, Chen HL, Kuo JS, Jeng KC, Dehydroepiandrosterone inhibits lipopolysaccharide-induced nitric oxide production in BV-2 microglia. J Neurochem 77:830-838, 2001
37. Kadenbach B, Intrinsic and extrinsic uncoupling of oxidative phosphorylation. Biochim Biophys Acta 1604: 77-94, 2003
38. Brunori M, Giuffre A, Forte E, Mastronicola D, Barone MC, Sarti P, Control of cytochrome c oxidase activity by nitric oxide. Biochim Biophys Acta 1655: 365-371, 2005
39. Aragno M, Cutrin JC, Mastrocola R, Perrelli MG, Restivo F, Poli G, Danni O, Boccuzzi G. Oxidative stress and kidney dysfunction due to ischemia/ reperfusion in rat: Attenuation by dehydroepiandrosterone. Kidney Int 64:836-843, 2003