Effects of Tocotrienol and Lovastatin Combination on Osteoblast and Osteoclast Activity in Estrogen-Deficient Osteoporosis
Autor: | Ima Nirwana Soelaiman, Saif Abdul-Majeed, Norazlina Mohamed |
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Jazyk: | angličtina |
Rok vydání: | 2012 |
Předmět: |
Anabolism
Article Subject business.industry medicine.drug_class Osteoporosis Osteoblast lcsh:Other systems of medicine Pharmacology lcsh:RZ201-999 medicine.disease Bone resorption chemistry.chemical_compound medicine.anatomical_structure Complementary and alternative medicine chemistry Estrogen Osteoclast Medicine Tocotrienol Lovastatin business Research Article medicine.drug |
Zdroj: | Evidence-Based Complementary and Alternative Medicine, Vol 2012 (2012) Evidence-based Complementary and Alternative Medicine : eCAM |
ISSN: | 1741-427X |
DOI: | 10.1155/2012/960742 |
Popis: | Statins are HMGCoA reductase inhibitors and had been demonstrated to stimulate bone formation in rodents after high oral doses. Observational studies on patients treated with oral statins were varied. Delta-tocotrienol had been found to stimulate the cleavage of HMGCoA reductase and inhibit its activity. Tocotrienols were found to have both catabolic and anabolic effects on bone in different animal models of osteoporosis. The current study aimed to ascertain the effects of delta–tocotrienol and lovastatin combination on biochemical and static bone histomorphometric parameters in a postmenopausal rat model at clinically tolerable doses. 48 Sprague Dawley female rats were randomly divided into 6 groups: (1) baseline control group; (2) sham-operated control group; (3) ovariectomised control group; (4) ovariectomised and 11 mg/kg lovastatin; (5) ovariectomised and 60 mg/kg delta-tocotrienol; (6) ovariectomised and 60 mg/kg delta-tocotrienol + 11 mg/kg lovastatin. These treatments were given daily via oral gavage for 8 weeks. Delta-tocotrienol plus lovastatin treatment significantly increased bone formation and reduced bone resorption compared to the other groups. Therefore, the combined treatment may have synergistic or additive effects and have the potential to be used as an antiosteoporotic agent in patients who are at risk of both osteoporosis and hypercholesterolemia, especially in postmenopausal women. |
Databáze: | OpenAIRE |
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