Palm Tocotrienol Exerted Better Antioxidant Activities in Bone than α-Tocopherol
Sandra Maniam
Department of Pharmacology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia
Search for more papers by this authorNorazlina Mohamed
Department of Pharmacology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia
Search for more papers by this authorAhmad Nazrun Shuid
Department of Pharmacology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia
Search for more papers by this authorIma Nirwana Soelaiman
Department of Pharmacology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia
Search for more papers by this authorSandra Maniam
Department of Pharmacology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia
Search for more papers by this authorNorazlina Mohamed
Department of Pharmacology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia
Search for more papers by this authorAhmad Nazrun Shuid
Department of Pharmacology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia
Search for more papers by this authorIma Nirwana Soelaiman
Department of Pharmacology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia
Search for more papers by this authorAbstract
Abstract: The aim of this study was to investigate the effects of vitamin E on the levels of lipid peroxidation and antioxidant enzymes in rat bones. Fifty-six normal male Sprague-Dawley rats, aged 3 months, were randomly divided into seven groups with eight rats in each group. The age-matched control group was given the vehicle olive oil, by oral gavage daily. Six of the treatment groups received either palm tocotrienol or pure α-tocopherol at the dose of 30, 60 or 100 mg/kg body weight, by oral gavage daily, 6 days a week for 4 months. Thiobarbituric acid-reactive substance (TBARS) that is an index to measure the level of lipid peroxidation and the antioxidant enzymes, glutathione peroxidase and superoxide dismutase levels were measured in the femur at the end of the study. Palm tocotrienol at the dose of 100 mg/kg body weight significantly reduced the TBARS level in the femur with a significant increase in glutathione peroxidase activity compared to the age-matched control group. These were not observed in the α-tocopherol groups. Palm tocotrienol was more effective than pure α-tocopherol acetate in suppressing lipid peroxidation in bone. Palm tocotrienol showed better protective effect against free radical damage in the femur compared to α-tocopherol. This study suggests that palm tocotrienol plays an important role in preventing imbalance in bone metabolism due to free radicals.
References
- 1 Steven DA, Williams GR. Hormone regulation of chondrocyte differentiation and endochondral bone formation. Mol Cell Endocrinol 1999; 151: 195–204.
- 2 Roux S, Orcel P. Bone loss: factors that regulates osteoclast differentiation. Arthritis Res 2000; 24: 451–6.
- 3 Yang S, Madyastha P, Bingel S, Ries W, Key L. A new superoxide-generating oxidase in murine osteoclasts. J Biol Chem 2001; 276: 5452–8.
- 4 Muthusami S, Ramachandra I, Muthusamy B, Vasudevan G, Prabhu V, Subramaniam V et al . Ovariectomy induces oxidative stress and impairs bone antioxidant system in adult rats. Clin Chim Act 2005; 360: 81–6
- 5 Suda N, Morita I, Kuroda T, Murota S. Participation of oxidative stress in the process of osteoclast differentiation. Biochimica et Biophysica Acta 1993; 1157: 318–23.
- 6 Khalkali-Ellis Z, Collin-Osdoby P, Li L, Brandi ML, Osdoby P. A human homolog of the 150 kD avian osteoclast membrane antigen related to superoxide dismutase and essential for bone resorption is induced by developmental agents and opposed by estrogen in FLG 29. Calcif Tissue Int 1997; 60: 187–93.
- 7 Packer L, Weber SU, Rimbach G. Molecular mechanism of protective effect of vitamin E in atherosclerosis: Molecular aspect of α-tocotrienol antioxidant action and cell signaling. J Nutr 2001; 131: 369–73.
- 8 Serbinova E, Kagan V, Han D, Packer L. Free radical recycling and intramembrane mobility in the antioxidant properties of α-tocopherol and α-tocotrienol. Free Radic Biol Med 1991; 10: 263–75.
- 9 Yoshida Y, Niki E, Noguchi N. Comparative study on the action of tocopherol and tocotrienols as antioxidant: chemical and physical effects. Chem Phys Lipids 2003; 123: 63–75.
- 10 Sen CK, Khanna S, Roy S, Packer L. Molecular basis of vitamin E action: tocotrienol potently inhibits glutamate-induced pp60c-src kinase activation and death of HT4 neuronal cells. J Biol Chem 2000; 275: 13049–55.
- 11 Norazlina M, Ima-Nirwana S, Abd Gapor MT, Khalid BAK. Tocotrienols are needed for normal bone calcification in growing female rats. Asia Pac J Clin Nutr 2002; 11: 194–9.
- 12 Norazlina M, Ling HLR, Ima-Nirwana S. The effects of vitamin E or calcium supplementation on bone mineral composition in vitamin E deficient rats. Malays J Biochem Biol 2002; 7: 1–5.
- 13
Kessenich CR.
Calcium and vitamin D supplementation for postmenopausal bone health.
J Nur Pra
2007; 2 (Suppl): 155–9.
10.1016/j.nurpra.2007.01.017 Google Scholar
- 14 Ima-Nirwana S, Kiftiah A, Zainal AG, Norazlina M, Gapor MT, Khalid BAK. Palm vitamin E prevents osteoporosis in orchidectomized growing male rats. Nat Prod Sci 2000; 6: 155–60.
- 15 Norazlina M, Ima-Nirwana S, Gapor MT, Khalid BAK. Palm vitamin E is comparable in maintaining bone mineral density in ovariectomized rats. Exp Clin Endocrinol Diabetes 2000; 108: 1–6.
- 16 Ahmad NS, Khalid BAK, Luke DA, Ima-Nirwana S. Tocotrienol offers better protection than tocopherol from free radical-induced damage on rat bone. Clin Exp Pharmacol Physiol 2005; 32: 761–70.
- 17 Ahmad NS, Khalid BAK, Ima-Nirwana S. Effects of vitamin E on interleukin-1 in ferric-nitrilotriacetate treated rats. Malays J Biochem Biol 2004; 9: 43–7.
- 18 Yee JK, Ima-Nirwana S. Palm Vitamin E protects against ferric nitrilotriacetate induced impairment of bone calcification. Asia Pac J Pharmacol 1998; 13: 35–41.
- 19 Parhami F, Marrow AD, Balucan J, Leitinger N, Watson AD, Tintut Y et al . Lipid oxidation products have opposite effects on calcifying vascular cell and bone cell differentiation, a possible explanation for the paradox of arterial calcification in osteoporotic patients. Aterioscler Thromb Vasc Biol 1997; 17: 680–7.
- 20 Demer LL. Vascular calcification and osteoporosis: inflammatory responses to oxidized lipids. Int J Epidemiol 2002; 31: 737–41.
- 21 Garret IR, Boyce BF, Oretto ROC, Bonewald L, Poser J, Mundy GR. Oxygen-derived free radicals stimulate osteoclastic bone resorption in rodent bone in vitro and in vivo. J Clin Invest 1990; 85: 632–9.
- 22 Parhami F, Garfinkel A, Demer LL. Role of lipids in osteoporosis. Aterioscler Thromb Vasc Biol 2000; 20: 2346–8.
- 23 Del Rio D, Stewart AJ, Pellegrini N. A review of recent studies on malondialdehyde as toxic molecule and biological marker of oxidative stress. Nutr Metab (Lond) 2005; 15: 316–28.
- 24 Bird RP, Hung SO, Hadley M, Draper HH. Determination of malondialdehyde in biological materials by high performance liquid chromatography. Anal Biochem 1983; 128: 240–4.
- 25 Esterbaue H, Schaur RJ, Zallner H. Chemistry and biochemistry of 4-hydroxynonenal, malondialdehyde and related aldehydes. Free Radic Biol Med 1991; 11: 81–128.
- 26 Baltaci AK, Sunar F, Mogulkoc R, Oztekin E. The effects of zinc deficiency and supplementation on lipid peroxidation in bone tissue of ovariectomized rats. Toxicology 2004; 203: 77–82.
- 27 Sazuka Y, Tanizawa H, Takino Y. Effect of adriamycin on the activities superoxide dismutase, glutathione peroxidase and catalase in tissues of mice. Jpn J Cancer Res 1989; 80: 89–94.
- 28 Marklund S, Marklund G. Involvement of the superoxide anion in radical in the autooxidation of pyrogallol and a convenient assay of superoxide dismutase. Eur J Biochem 1974; 47: 469–74.
- 29 Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem 1951; 193: 265–75.
- 30 Wang L, Banu J, McMahan CA, Kalu DN. Male rodent model of age-related bone loss in men. Bone 2001; 29: 141–8.
- 31 Meydani M. Vitamin E. Lancet 1995; 345: 170–5.
- 32 Kamat JP, Devasagayam TPA. Tocotrienols from palm oil as a potent inhibitor of lipid peroxidation and protein oxidation in rat brain mitochondria. Neurosci Lett 1995; 195: 179–82.
- 33 Mates JM. Effects of antioxidant enzymes in the molecular control of reactive oxygen species toxicology. Toxicology 2000; 153: 83–104.
- 34 Niki E, Yoshida Y, Saito Y, Noguchi N. Lipid peroxidation: mechanism, inhibition, and biological effects. Biochem Biophys Res Commun 2005; 338: 668–76.
- 35 Lean JM, Davies JT, Fuller K, Jagger CJ, Krstein B, Partington GA et al . A crucial role for thiol antioxidants in estrogen deficiency. J Clin Invest 2003; 112: 915–23.
- 36 Lean JM, Jagger CJ, Kirstein B, Fuller K, Chambers TJ. Hydrogen peroxide is essential for estrogen-deficiency bone loss and osteoclast formation. Endocrinology 2005; 146: 728–35.
- 37 Ozgocmen S, Kaya H, Fadilioglu E, Aydogan R, Yilmaz Z. Role of antioxidant systems, lipid peroxidation and nitric oxide in postmenopausal osteoporosis. Mol Cell Biochem 2007; 295: 45–52.
- 38 Li R, Cowan DB, Mickle DAG, Weisel RD, Burton GW. Effect of vitamin E on human glutathione peroxidase (GSH-Px1) expression in cardiomyocytes. Free Radic Biol Med 1996; 21: 419–26.
- 39 Hu WL, Goldring CEP, Rao NR, Rice-Evens C, Burdon RH, Diplock AT. Variable α-tocopherol and protection of glutathione peroxidase activity in established and malignant fibroblast. Biofactors 1992; 4: 47–9.