Effect of Medicago sativa compared To 17β-oestradiol on osteoporosis in ovariectomized mice

References

• Baltaci, A.K., et al., 2004. The effects of zinc deficiency and supplementation on lipid peroxidation in bone tissue of ovariectomized rats. Toxicology, 203, 77–82.
   PubMed Web of Science ®Google Scholar
• Aebi, A., 1984. Catalase in vitro. Methods in enzymology, 105, 121–126.
   PubMed Web of Science ®Google Scholar
• Arai, M., et al., 2007. Effect of reactive oxygen species (ROS) on antioxidant system and osteoblastic differentiation in MC3T3-E1 cells. IUBMB life, 59 (1), 27–33.
   PubMed Web of Science ®Google Scholar
• Asada, K., Takahashi, M., and Nagate, M., 1974. Assay and inhibitors of spinach superoxide dismutase. Agricultural and biological chemistry, 38 (2), 471–473.
   Web of Science ®Google Scholar
• Baek, K.H., et al., 2010. Association of oxidative stress with postmenopausal osteoporosis and the effect of hydrogen peroxide on osteoclast formation in human bone marrow cell cultures. Calcified tissue international, 87 (3), 226–235.
   PubMed Web of Science ®Google Scholar
• Beauchamp, C., and Fridovich, I., 1971. Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Analytical biochemistry, 44 (1), 276–287.
   PubMed Web of Science ®Google Scholar
• Behr, G.A., et al., 2012. Increased cerebral oxidative damage and decreased antioxidant defenses in ovariectomized and sham-operated rats supplemented with vitamin A. Cell biology and toxicology, 28 (5), 317–330.
   PubMed Web of Science ®Google Scholar
• Bingham, S.A., et al., 1998. Phytoestrogens: where are we now? British journal of nutrition, 79 (5), 393–406.
   PubMed Web of Science ®Google Scholar
• Borrelli, F., and Ernst, E., 2010. Alternative and complementary therapies for the menopause. Maturitas, 66 (4), 333–343.
   PubMed Web of Science ®Google Scholar
• Castelao, J.E., and Gago-Dominguez, M., 2008. Risk factors for cardiovascular disease in women: relationship to lipid peroxidation and oxidative stress. Medical hypotheses, 71 (1), 39–44.
   PubMed Web of Science ®Google Scholar
• Chairman, W.A., and Peck, U.S., 1993. Consensus development conference: diagnosis, prophylaxis and treatment of osteoporosis. American journal of medicine, 94, 646–650.
   PubMed Web of Science ®Google Scholar
• Cho, J.W., Lee, K.S., and Kim, C.W., 2007. Curcumin attenuates the expression of IL-1β, IL-6, and TNF-α as well as cyclin E in TNF-α-treated HaCaT cells; NF-κB and MAPKs as potential upstream targets. International journal of molecular medicine, 19 (3), 469–474.
   PubMed Web of Science ®Google Scholar
• Choi, E.M., Kim, G.H., and Lee, Y.S., 2009. Protective effects of dehydrocostus lactone against hydrogen peroxide-induced dysfunction and oxidative stress in osteoblastic MC3T3-E1 cells. Toxicology in vitro, 23 (5), 862–867.
   PubMed Web of Science ®Google Scholar
• Delmas, P. D., 1988. Biochemical markers of bone turnover in osteoporosis. In: B.L. Riggs, L.J. Melton III, eds. Osteoporosis, etiology, diagnosis and management. New York, NY: Raven Press, 297–316.
   Google Scholar
• Dike, N., Kalu, C., and Cang, C., 1999. Ovariectomized murine model of postmenopausal calcium malabsorption. Journal of bone and mineral research, 14 (4), 593–601.
   PubMed Web of Science ®Google Scholar
• Ellman, M., 1959. A spectrophotometric method for determination of reduced glutathione in tissues. Analytical biochemistry, 74, 214–226.
   Google Scholar
• Finkel, T., and Holbrook, N.J., 2000. Oxidants, oxidative stress and biology of ageing. Nature, 408 (6809), 239–239.
   PubMed Web of Science ®Google Scholar
• Heaney, R.P., Recker, R.R., and Saville, P.D., 1978. Menopausal changes in calcium balance performance. Journal of laboratory and clinical medicine, 92 (6), 953–963.
   PubMed Web of Science ®Google Scholar
• Ingberg, E., et al., 2012. Methods for long term 17β -estradiol administration to mice. General and comparative endocrinology, 175 (1), 188–193.
   PubMed Web of Science ®Google Scholar
• Jakob, O., Ström1, E.T., and Annette, T., 2008. Order of magnitude differences between methods for maintaining physiological 17boestradiol concentrations in ovariectomized rats. Journal of clinical and laboratory investigation, 68 (8), 814–822.
   Web of Science ®Google Scholar
• Jdidi, H., et al., 2019. Effects of estrogen deficiency on liver function and uterine development: assessments of Medicago sativa’s activities as estrogenic, anti-lipidemic, and antioxidant agents using an ovariectomized mouse model. Archives of physiology and biochemistry, 12, 1–12.
   Google Scholar
• Justine, A., et al., 2003. Safe and effective method for chronic 17β-estradiol administration to mice. Journal of the American association for laboratory animal, 42, 33–35.
   Google Scholar
• Nakaoka, K., et al., 2018. Vitamin D-restricted high-fat diet down regulates expression of intestinal alkaline phosphatase isozymes in ovariectomized rats. Nutrition research, 53, 23.
   PubMed Web of Science ®Google Scholar
• Kenichiro, K., et al., 2015. Anti-osteoporosis effects of 1,4-dihydroxy-2-naphthoic acid in ovariectomized mice with increasing of bone density. Journal of oral and maxillofacial surgery, medicine, 28, 66–72.
   Web of Science ®Google Scholar
• Komrakova, M., et al., 2014. Evaluation of twelve vibration regimes applied to improve spine properties in ovariectomized rats. Bone reports, 7 (14), 172–180.
   Google Scholar
• Leal, M., et al., 2000. Hormone replacement therapy for oxidative stress in postmenopausal women with hot flushes. Obstetrics & gynecology, 95 (6), 804–809.
   PubMed Web of Science ®Google Scholar
• LEE, Y.-B., et al., 2004. Evaluation of the preventive effect of isoflavone extract on bone loss in ovariectomized rats. Bioscience, biotechnology and biochemestry, 68 (5), 1040–1045.
   PubMed Web of Science ®Google Scholar
• Lorden, J.F., and Caudle, A., 1986. Behavioral and endocrinological effects of single injections of monosodium glutamate in the mouse. Neurobehavioural toxicology and teratology, 8, 509–519.
   PubMedGoogle Scholar
• Lowry, O.H., Rosenbrough, N.J., and Randall, R., 1951. Protein measurement with the folin phenol reagent. Journal of biological and chemistry, 193, 265–275.
   PubMed Web of Science ®Google Scholar
• Martin, C., Watson, R., and Preedy, V., 2013. Nutrition and diet in menopause. New York, NY: Humana Press, Springer Publishing Company.
   Google Scholar
• Mazur, J.A., et al., 2013. Glycine max (L) Merr. Vigna radiata L. and Medicago sativa L. sprouts: a natural source of bioactive compounds. Food research international, 50, 167–175.
   Web of Science ®Google Scholar
• Mi Hye, K., et al., 2017. Improvement of osteoporosis by Lycium chinense administration in ovariectomized mice. Journal of the Chinese medical association, 80, 222–226.
   PubMed Web of Science ®Google Scholar
• Miquel, J., et al., 2006. Menopause: a review on the role of oxygen stress and favorable effects of dietary antioxidants. Archives of gerontology and geriatrics, 42 (3), 289–306.
   PubMed Web of Science ®Google Scholar
• Mohammed, S., 2012. In vitro and in vivo antioxidant activity of Alfalfa (Medicago sativa L.) on carbon tetrachloride intoxicated rats. Journal of the Chinese medicine, 40 (4), 779–793.
   Web of Science ®Google Scholar
• Muller, F.L., et al., 2006. Absence of CuZn superoxide dismutase leads to elevated oxidative stress and acceleration of agedependent skeletal muscle atrophy. Free radical biology and medicine, 40 (11), 1993–2004.
   PubMed Web of Science ®Google Scholar
• Nazıroglu, M., et al., 2011. Capparis ovata modulates ovariectomize inducedoxidative toxicity in brain, kidney and liver of aged mice. Free radicals, membrane damage and cell-research, 3, 186–193.
   Google Scholar
• Noor, R., Mittal, S., and Iqbal, J., 2002. Superoxide dismutase-applications and relevance to human diseases. Medical science monitor, 8, 210–215.
   Google Scholar
• Oyaizu, M., 1986. Studies on products of browning reaction: antioxidative activity of products of browning reaction. The Japanese journal of nutrition and dietetics, 44, 307–315.
   Web of Science ®Google Scholar
• Paglia, D.E., and Valentine, W.N., 1967. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidise. Journal of laboratory and clinical medicine, 70 (1), 158–169.
   PubMed Web of Science ®Google Scholar
• Pinta, M., 1973. Méthodes de références pour détermination des éléments dans végétaux: Détermination des éléments Ca, Mg, Fe, Mn, Zn et Cu Par absorption atomique. Oléagineuse, 28, 87–92.
   Google Scholar
• Reznick, A., and Packer, Z.L., 1994. Oxidative damage to proteins: spectrophotometric method for carbonyl assy. Methods enzymology, 233, 257–263.
   Web of Science ®Google Scholar
• Ruch, R.J., Cheng, S.J., and Klaunig, J.E., 1989. Prevention of cytotoxicity and inhibition of intercellular communication by antioxidant catechins isolated from Chinese green tea. Carcinogenesis, 10 (6), 1003–1008.
   PubMed Web of Science ®Google Scholar
• Sedlak, I.K., et al., 2016. Effect of dietary flavonoid naringenin on bones in rats with ovariectomy induced osteoporosis. Acta poloniae pharmaceutica, 73 (4), 1073–1081.
   PubMed Web of Science ®Google Scholar
• Sener, G., et al., 2005. Protective effects of MESNA (2-mercaptoethane sulphonate) against acetaminophen-induced hepatorenal oxidative damage in mice. Journal of applied toxicology, 25 (1), 20–29.
   PubMed Web of Science ®Google Scholar
• Setchell, K.D., and Lydeking-Olsen, E., 2003. Dietary phytoestrogens and their effect on bone: evidence from in vitro and in vivo, human observational and dietary intervention studies. The American journal of clinical nutrition, 78 (3), 593S–609S.
   PubMed Web of Science ®Google Scholar
• Svanberg, M., and Knuuttila, M., 1994. Dietary xylitol prevents ovariectomy induced changes of bone inorganic fraction in rats. Bone and mineral, 26 (1), 81–88.
   PubMedGoogle Scholar
• Swami, N.R., 2001. Biochemical markers of bone turnover. Clinica chimica acta, 313, 95–105.
   PubMed Web of Science ®Google Scholar
• Turner, R.T., Riggs, B.L., and Spelsberg, T.C., 1994. Skeletal effects of estrogen. Endocrine Reviews, 15, 275–300.
   PubMed Web of Science ®Google Scholar
• Wauquier, F., et al., 2009. Oxidative stress in bone remodelling and disease. Trends in molecular medicine, 15 (10), 468–477.
   PubMed Web of Science ®Google Scholar
• Witko, S.V., et al., 1996. Advanced oxidation protein products as a novel marker of oxidative stress in uremia. Kidney international, 49, 1304–1313.
   PubMed Web of Science ®Google Scholar
• Yagi, K., 1976. A simple fluorometric assay for lipoperoxide in blood plasma. Biomedical medicine, 15, 212–216.
   Google Scholar
• Zemel, M.B., 2002. Regulation of adiposity and obesity risk by dietary calcium: mechanisms and implications. Journal of the American college of nutrition, 21 (2), 146S–151S.
   PubMed Web of Science ®Google Scholar
• Zhang, D., et al., 2014. The effects of Cordyceps sinensis phytoestrogen on estrogen deficiency-induced osteoporosis in ovariectomized rats. Complementary and alternative medicine, 14, 472–484.
   PubMed Web of Science ®Google Scholar
• Zhong, Y.Z., et al., 2006. Effect of ethanol extract of Lepidium meyenii Walp. on osteoporosis in ovariectomized rat. Journal of ethnopharmacology, 105, 274–279.
   PubMed Web of Science ®Google Scholar
• Zhou, S., et al., 2003. Estrogens activate bone morphogenetic protein-2 gene transcription in mouse mesenchymal stem cells. Molecular endocrinology, 17 (1), 56–66.
   PubMedGoogle Scholar