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Bovine colostrum supplementation improves bone metabolism in an osteoporosis-induced animal model

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Autore
Kydonaki E.K., Freitas L., Fonseca B.M., Reguengo H., Simón C.R., Bastos A.R., Fernandes E.M., Canadas R.F., Oliveira J.M., Correlo V.M., Reis R.L., Vliora M., Gkiata P., Koutedakis Y., Ntina G., Pinto R., Carrillo A.E., Marques F., Amorim T.
Data
2021
Language
en
DOI
10.3390/nu13092981
Soggetto
fibroblast growth factor 2
messenger RNA
osteocalcin
osteoclast differentiation factor
receptor activator of nuclear factor kappa B
vasculotropin A
animal experiment
animal model
Article
bone density
bone metabolism
bone microarchitecture
bone strength
colostrum
controlled study
cortical bone
gene expression
in vivo study
nonhuman
ossification
osteolysis
osteoporosis
rat
real time polymerase chain reaction
supplementation
trabecular bone
animal
bone
bovine
colostrum
dietary supplement
disease model
drug effect
female
metabolism
osteoporosis
ovariectomy
Wistar rat
Animals
Bone and Bones
Bone Density
Cattle
Colostrum
Dietary Supplements
Disease Models, Animal
Female
Osteoporosis
Ovariectomy
Rats
Rats, Wistar
MDPI
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Abstract
Osteoporosis is characterized by bone loss. The present study aims to investigate the effects of bovine colostrum (BC) on bone metabolism using ovariectomized (OVX) and orchidec-tomized (ORX) rat models. Twenty-seven-week-old Wistar Han rats were randomly assigned as: (1) placebo control, (2) BC supplementation dose 1 (BC1: 0.5 g/day/OVX, 1 g/day/ORX), (3) BC sup-plementation dose 2 (BC2: 1 g/day/OVX, 1.5 g/day/ORX) and (4) BC supplementation dose 3 (BC3: 1.5 g/day/OVX, 2 g/day/ORX). Bone microarchitecture, strength, gene expression of VEGFA, FGF2, RANKL, RANK and OPG, and bone resorption/formation markers were assessed after four months of BC supplementation. Compared to the placebo, OVX rats in the BC1 group exhibited significantly higher cortical bone mineral content and trabecular bone mineral content (p < 0.01), while OVX rats in the BC3 group showed significantly higher trabecular bone mineral content (p <0.05). ORX rats receiving BC dose 2 demonstrated significantly higher levels of trabecular bone mineral content (p < 0.05). Serum osteocalcin in the ORX was pointedly higher in all BC supplementation groups than the placebo (BC1: p < 0.05; BC2, BC3: p < 0.001). Higher doses of BC induced significantly higher relative mRNA expression of OPG, VEGFA, FGF2 and RANKL (p < 0.05). BC supplementation improves bone metabolism of OVX and ORX rats, which might be associated with the activation of the VEGFA, FGF2 and RANKL/RANK/OPG pathways. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
URI
http://hdl.handle.net/11615/75551
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