Please use this identifier to cite or link to this item: http://repositorio.ufc.br/handle/riufc/66457
Type: Artigo de Periódico
Title: Vitamin K supplementation modulates bone metabolism and ultra-structure of ovariectomized mice
Authors: Rangel, Letícia Batista Azevedo
Siqueira, Daniel de
Soares, Olívia do Rosário
Santana, Higor Scardini
Miguel, Emilio de Castro
Cunha, Maura da
Oliveira, Andre Lacerda de Abreu
Pedrosa, Diego França
Resgala, Ludmilla Carvalho Rangel
Rangel Neto, Helder Azevedo
Rochette, Neuza Felix Gomes
Eish, Sérgio Ragi
Graceli, Jones Bernardes
Silva, Ian Victor
Keywords: Ovariectomized;Vitamin K;Bone mineral density;Bone microarchitecture;Mineral metabolism
Issue Date: 2018
Publisher: Cellular Physiology and Biochemistry
Citation: RANGEL, Letícia Batista Azevedo et al. Vitamin K supplementation modulates bone metabolism and ultra-structure of ovariectomized mice. Cellular Physiology and Biochemistry, [s.l.], v. 51, p. 356-374, 2018.
Abstract: Osteoporosis is a bone metabolic disease that affects mostly postmenopausal women. There has been shown that vitamin K (VK) supplementation during menopause may decrease bone loss as well as risk of bone breaking. Aiming to clarify the beneficial role of VK in bone metabolism during menopause, we investigated mineral metabolism and bone ultrastructure of ovariectomized (OVX) mice. Methods: To determine the effects chronic use of VK in bone structure and mineral metabolism in OVX mice, we used several methods, such as DXA, µCTScan, and SEM as well as biomolecular techniques, such as ELISA and qRT-PCR. In addition, complete analysis of serum hormonal and other molecules associated to bone and lipid metabolism were evaluated overview the effects of VK in menopause murine model. Results: VK treatment significantly affects Pi metabolism independently of OVX, changing Pi plasma, urinary output, balance, and Pi bone mass. Interestingly, VK also increased VLDL in mice independently of castration. In addition, VK increased compact bone mass in OVX mice when we evaluated it by DXA, histomorphometry, µCTScanning. VK increased bone formation markers, osteocalcin, HYP- osteocalcin, and AP whereas it decreased bone resorption markers, such as urinary DPD/creatinine ratio and plasmatic TRAP. Surprisingly, SEM images revealed that VK treatment led to amelioration of microfractures observed in OVX untreated controls. In addition, SHAM operated VK treated mice exhibited higher number of migrating osteoblasts and in situ secretion of AP. OVX led to decreased to in situ secretion of AP that was restored by VK treatment. Moreover, VK treatment increased mRNA expression of bone Calbindin 28KDa independently of OVX. Conclusion: VK treatment in OVX mice exhibited beneficial effects on bone ultrastructure, mostly by altering osteoblastic function and secretion of organic bone matrix. Therefore, VK could be useful to treat osteopenic/osteoporotic patients.
URI: http://www.repositorio.ufc.br/handle/riufc/66457
ISSN: 1421-9778
Appears in Collections:DEMM - Artigos publicados em revista científica

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