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1.
J Bone Miner Metab ; 31(1): 16-25, 2013 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-23011466

RESUMO

Methylsulfonylmethane (MSM), which is one of the popular ingredients of so-called health foods in Japan, is expected to relieve inflammation in arthritis and allergies. However, there is no scientific evidence to confirm the efficacy and safety of MSM in detail. In this study, we examined the effects of MSM on cartilage formation in growing rats (G) and cartilage degradation in STR/Ort mice (A), an accepted human osteoarthritis (OA) model. For cartilage formation study, 6-week-old growing male Wister rats were assigned to four groups to receive a control or MSM-containing diet. To examine the efficacy of MSM on the cartilage of OA model mouse, 10-week-old male STR/OrtCrlj mice were assigned to three groups to receive a control or MSM-containing diet. The dosages used were amounts equal to the recommended supplements for humans [0.06 g/kg body weight (BW)/day: MSM1G and MSM1A], 10 fold higher (0.6 g/kg BW/day: MSM10G and MSM10A), and 100 fold higher (6 g/kg BW/day: MSM100G). Intake of MSM for 4 weeks did not affect cartilage formation in the knee joint in growing rats. Body, liver, and spleen weight in the MSM100G group were significantly lower than those in the control group. Intake of MSM for 13 weeks decreased degeneration of the cartilage at the joint surface in the knee joints in STR/Ort mice in a dose-dependent manner. These results suggest that appropriate intake of MSM is possibly effective in OA model mice; however, intake of large amounts of MSM induced atrophy of several organs.


Assuntos
Anti-Inflamatórios/farmacologia , Dimetil Sulfóxido/farmacologia , Osteoartrite do Joelho/tratamento farmacológico , Sulfonas/farmacologia , Animais , Cartilagem/metabolismo , Cartilagem/patologia , Modelos Animais de Doenças , Relação Dose-Resposta a Droga , Avaliação Pré-Clínica de Medicamentos , Humanos , Articulação do Joelho/metabolismo , Articulação do Joelho/patologia , Masculino , Camundongos , Osteoartrite do Joelho/metabolismo , Osteoartrite do Joelho/patologia , Ratos
2.
Menopause ; 18(5): 563-74, 2011 May.
Artigo em Inglês | MEDLINE | ID: mdl-21252728

RESUMO

OBJECTIVE: Equol is a metabolite of the isoflavone daidzein and may play a critical role in preventing bone loss by soy isoflavones in postmenopausal women. However, results from clinical trials have not been published. The aim of this study was to investigate the effects of equol on bone metabolism and serum sex and thyroid hormone levels in postmenopausal Japanese women. METHODS: We performed a 1-year double-blind, randomized, placebo-controlled trial with natural S-equol supplements for 93 non-equol-producing menopausal Japanese women. Participants were randomly assigned to four groups receiving the following: placebo, 2 mg of equol supplement per day, 6 mg of equol supplement per day, and 10 mg of equol supplement per day. RESULTS: Equol intervention increased equol concentrations in serum and urine in a dose-dependent manner. Urinary deoxypyridinoline was significantly decreased, with a -23.94% change in the group that received 10 mg of equol supplement per day as compared with a -2.87% change in the group that received placebo after 12 months of intervention (P = 0.020). Thus, 10 mg/day of equol supplement markedly inhibited bone resorption. Treatment with 10 mg/day of equol prevented a decrease in bone mineral density in the entire body in postmenopausal women after 12 months. Sex and thyroid hormone concentrations in serum did not differ among the four groups after intervention. CONCLUSIONS: These findings suggest that 10 mg/day of natural S-equol supplementation contributes to bone health in non-equol-producing postmenopausal women without adverse effects.


Assuntos
Conservadores da Densidade Óssea/uso terapêutico , Densidade Óssea/efeitos dos fármacos , Reabsorção Óssea/tratamento farmacológico , Isoflavonas/uso terapêutico , Fitoestrógenos/uso terapêutico , Pós-Menopausa/metabolismo , Adulto , Aminoácidos/urina , Povo Asiático , Suplementos Nutricionais , Equol , Feminino , Hormônios Esteroides Gonadais/sangue , Humanos , Isoflavonas/sangue , Isoflavonas/urina , Pessoa de Meia-Idade , Fitoestrógenos/sangue , Fitoestrógenos/urina , Projetos Piloto , Placebos , Hormônios Tireóideos/sangue
3.
J Nutr Sci Vitaminol (Tokyo) ; 55(1): 15-21, 2009 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-19352059

RESUMO

It has been reported that treatment with a pharmacological dose (45 mg/d) of menaquinone-4 (MK-4) prevents bone loss in postmenopausal women. However, it is not known whether supplementation with low dose MK-4 has beneficial effects on bone metabolism in healthy women. The aim of this study is to examine the effects of the supplementation of 1.5 mg/d MK-4 for 4 wk on bone and lipid metabolism in healthy postmenopausal Japanese women. The study was performed as a randomized double blind placebo-controlled trial. The participants aged 53-65 y were randomly assigned to 2 groups and supplemented with 1.5 mg/d of MK-4 or a placebo for 4 wk (n=20 for each group). The most marked effects of MK-4 intake were observed on serum osteocalcin (OC) concentrations. Serum undercarboxylated OC (ucOC) concentration decreased, and the gamma-carboxylated OC (GlaOC) and GlaOC/GlaOC+ucOC ratio that indicates the degree of OC gamma-carboxylation increased significantly at 2 and 4 wk compared with that at baseline in the MK-4 group. The serum ucOC and GlaOC concentrations in the MK-4 group were significantly different from those in the placebo group at 2 wk. These results suggest that supplementation with 1.5 mg/d MK-4 accelerated the degree of OC gamma-carboxylation. The concentrations of serum lipids and other indices were not different between the groups at either intervention period. Thus, the additional intake of MK-4 might be beneficial in the maintenance of bone health in postmenopausal Japanese women.


Assuntos
Osso e Ossos/efeitos dos fármacos , Suplementos Nutricionais , Lipídeos/sangue , Osteocalcina/sangue , Osteoporose Pós-Menopausa/tratamento farmacológico , Vitamina K 2/uso terapêutico , Vitaminas/uso terapêutico , Biomarcadores/sangue , Pressão Sanguínea/efeitos dos fármacos , Osso e Ossos/metabolismo , Método Duplo-Cego , Estradiol/sangue , Feminino , Humanos , Japão , Pessoa de Meia-Idade , Osteoporose Pós-Menopausa/sangue , Pós-Menopausa/sangue , Vitamina D/análogos & derivados , Vitamina D/sangue , Vitamina K 1/sangue , Vitamina K 2/sangue , Vitamina K 2/farmacologia , Vitaminas/sangue
4.
Biomed Environ Sci ; 21(5): 357-64, 2008 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-19133608

RESUMO

OBJECTIVE: To investigate the effects of isoflavone on body weight, fat mass, and gene expression in relation to lipid metabolism. METHODS: Thirty-six female SD rats were ovariectomized or sham-operated and fed on a high-fat diet. Two months later, abdominal incision was made, blood was collected to separate serum, and the liver and adipose tissue were immediately collected and weighed. Some portions of these tissues were frozen in liquid nitrogen and stored at -80 degrees C. RESULTS: Ovariectomy (OVX) with a high-fat diet could induce obesity in rats, while treatment with isoflavone significantly inhibited the increase in body weight and fat mass in abdomen. Serum total cholesterol and leptin were significantly decreased in isoflavone group, compared with the OVX group. The mRNA expression of liver fatty acid synthase (FAS) in the OVX group was significantly higher than that in sham-operated group, while this difference was not observed in the isoflavone group. The mRNA expression of liver hormone-sensitive lipase (HSL) in the OVX rats tended to be lower than that in the sham-operated rats. Furthermore, a large amount of isoflavone maintained the mRNA expression at a sham level. CONCLUSION: Isoflavone may prevent obesity induced by ovariectomy with a high-fat diet, in part by modulating gene expression related to lipid metabolism.


Assuntos
Gorduras na Dieta/metabolismo , Regulação da Expressão Gênica/efeitos dos fármacos , Isoflavonas/farmacologia , Metabolismo dos Lipídeos/efeitos dos fármacos , Tecido Adiposo , Animais , Composição Corporal , Peso Corporal , Comportamento Alimentar , Feminino , Fígado/anatomia & histologia , Tamanho do Órgão , Ovariectomia , Ratos , Ratos Sprague-Dawley
5.
Menopause ; 14(5): 866-74, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17464237

RESUMO

OBJECTIVE: Equol is more biologically active than its precursor daidzein, which is the principal isoflavone found in soybean. There are interindividual differences in the ability to produce equol; these may lead to differences in the effects of isoflavone intervention on human health. This study aimed to investigate whether the effects of soy isoflavones on bone and fat mass are related to an individual's equol status. DESIGN: We performed a 1-year double-blind, randomized trial to compare the effects of isoflavone (75 mg of isoflavone conjugates/day) with those of placebo on bone mineral density, fat mass, and serum isoflavone concentrations in early postmenopausal Japanese women who were classified based on their equol-producer phenotype. RESULTS: After 1 year, the isoflavone intervention significantly increased the serum equol concentration in the equol producers but not in the nonproducers. In the isoflavone group, the annualized changes in the bone mineral density of the total hip and intertrochanteric regions were -0.46% and -0.04%, respectively, in the equol producers and -2.28% and -2.61%, respectively, in the nonproducers; these values were significantly different (P<0.05 for both the regions). Significant differences were observed between the equol producers and nonproducers in the isoflavone group with regard to the annualized changes in the fat mass. No significant difference in the annualized changes in bone mineral density and fat mass was observed between the equol producers and nonproducers in the placebo group. CONCLUSIONS: Our data suggest that the preventive effects of isoflavones on bone loss and fat accumulation in early postmenopausal women depend on an individual's equol-producing capacity.


Assuntos
Adiposidade/efeitos dos fármacos , Composição Corporal/efeitos dos fármacos , Osso e Ossos/metabolismo , Isoflavonas/farmacologia , Fitoestrógenos/farmacologia , Povo Asiático , Densidade Óssea/efeitos dos fármacos , Método Duplo-Cego , Equol , Feminino , Humanos , Isoflavonas/administração & dosagem , Japão , Pessoa de Meia-Idade , Osteoporose Pós-Menopausa/prevenção & controle , Fitoestrógenos/administração & dosagem , Inquéritos e Questionários , Resultado do Tratamento
6.
J Bone Miner Metab ; 24(6): 439-46, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-17072735

RESUMO

It is well known that skeletal unloading induces bone loss. It has been shown that soybean isoflavones are effective in preventing bone loss in osteoporotic animals. We investigated the ability of isoflavones to protect bone loss induced by hindlimb unloading by using a tail-suspension mouse model. Eight-week-old female mice were divided into five groups: (1) normal housed group (Normal), (2) sham unloaded group fed a control diet (Sham-UL), (3) hindlimb unloaded group fed a control diet (UL-C), (4) hindlimb unloaded group fed a 0.25% isoflavone conjugates diet (UL-ISO 0.25), and (5) hindlimb unloaded group fed a 0.5% isoflavone conjugates diet (UL-ISO 0.5). After 3 weeks, bone mineral density (BMD) of the femur was significantly decreased in UL-C, and this bone loss was prevented by isoflavone treatment. Histomorphometric analysis revealed a decrease in the cancellous bone of the distal femur in the UL-C group, and isoflavone prevented this change. Serum corticosterone increased in the UL-C group, and isoflavones inhibited the elevation. These results suggest that isoflavones might be promising food components that provide protection from bone loss and normalize stress-induced serum corticosterone during skeletal unloading.


Assuntos
Densidade Óssea/efeitos dos fármacos , Glycine max/química , Membro Posterior/efeitos dos fármacos , Isoflavonas/farmacologia , Animais , Peso Corporal/efeitos dos fármacos , Corticosterona/sangue , Feminino , Membro Posterior/diagnóstico por imagem , Membro Posterior/fisiologia , Isoflavonas/sangue , Vértebras Lombares/efeitos dos fármacos , Camundongos , Radiografia , Suporte de Carga
7.
J Bone Miner Res ; 21(5): 780-9, 2006 May.
Artigo em Inglês | MEDLINE | ID: mdl-16734394

RESUMO

UNLABELLED: The combined intervention of isoflavone intake and walking exercise over 1 year in postmenopausal Japanese women exhibited a trend for a greater effect on prevention of bone loss at the total hip and Ward's triangle regions. INTRODUCTION: The additive effects of isoflavones and exercise on bone and lipid metabolism have been shown in estrogen-deficient animals. In this study, we determined the effects of isoflavone intake, walking exercise, and their interaction on bone, fat mass, and lipid metabolism over 1 year in postmenopausal Japanese women. MATERIALS AND METHODS: A total of 136 postmenopausal women at <5 years after the onset of menopause were randomly assigned to four groups: (1) placebo, (2) walking (45 minutes/day, 3 days/week) with placebo, (3) isoflavone intake (75 mg of isoflavone conjugates/day), and (4) combination of isoflavone plus walking. BMD, fat mass, serum lipid, and serum and urinary isoflavone concentrations were assessed. RESULTS: A significant main effect of isoflavone on the reduction in trunk fat mass was obtained at 12 months. Significant main effects of walking on the reduction in fat mass in the whole body and the trunk were observed at 3, 6, and 12 months and that in the legs and arms at 6 and 12 months. Serum high-density lipoprotein (HDL)-cholesterol concentration significantly increased by 12 months after the walking and the combined intervention. After 12 months, a significant main effect of isoflavone on BMD was observed only at Ward's triangle. Walking prevented bone loss at the total hip and the Ward's triangle to significant degrees. The effect of the combined intervention on BMD at total hip and Ward's triangle regions was greater than that of either alone. No significant interaction was observed between isoflavone and walking in any measurements recorded during the study. CONCLUSIONS: Our study suggest that combined intervention of 75 mg/day of isoflavone intake and walking exercise 3 times/week for 1 year showed a trend for a greater effect on BMD at total hip and Ward's triangle regions than either alone. Intervention with isoflavone in postmenopausal Japanese women showed a modest effect on BMD compared with those in Westerners. Further studies over longer treatment duration that include assessment of BMD at various regions are necessary to ascertain the clinical significance of the combined intervention of isoflavone plus walking in postmenopausal women.


Assuntos
Adiposidade/efeitos dos fármacos , Densidade Óssea/efeitos dos fármacos , Exercício Físico , Isoflavonas/farmacologia , Pós-Menopausa , Biomarcadores/sangue , Estradiol/sangue , Feminino , Humanos , Isoflavonas/sangue , Isoflavonas/urina , Lipídeos/sangue , Pessoa de Meia-Idade , Placebos , Inquéritos e Questionários
8.
Biosci Biotechnol Biochem ; 70(2): 363-8, 2006 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-16495651

RESUMO

The safety and effectiveness were examined of the spirulina alga on bone metabolism in ovariectomized estrogen-deficient rats and hindlimb-unloaded mice. The dosage range was from an amount equal to that recommended in so-called health foods for humans (0.08 g/kg BW/day) to a 100-fold higher dose. The bone mineral density (BMD) of the whole femur and tibia of ovariectomized rats in the any spirulina-treated groups was not significantly different from that of the ovariectomized group, although BMD of the distal femur and proximal tibia was significantly lower in the spirulina-treated groups than in the ovariectomized group after a 6 week-experimental period. BMD of the femur and tibia was not affected by treatment with any dose of spirulina in hindlimb-unloaded mice. These results suggest that the intake of spirulina decreased BMD in the trabecular bone of rodents under estrogen-deficient conditions.


Assuntos
Proteínas de Bactérias/farmacologia , Densidade Óssea/fisiologia , Osso e Ossos/efeitos dos fármacos , Osso e Ossos/metabolismo , Cianobactérias/metabolismo , Elevação dos Membros Posteriores , Membro Posterior/efeitos dos fármacos , Membro Posterior/fisiologia , Envelhecimento/efeitos dos fármacos , Envelhecimento/fisiologia , Animais , Biomarcadores/sangue , Peso Corporal/efeitos dos fármacos , Feminino , Camundongos , Ovariectomia , Ratos , Ratos Wistar , Spirulina , Suporte de Carga
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