Bovine Colostrum Supplementation Improves Bone Metabolism in an Osteoporosis-Induced Animal Model

Autor: Vitor M. Correlo, Raphaël F. Canadas, Laura Freitas, Andres E. Carrillo, Parakevi Gkiata, Maria Vliora, Tânia Amorim, Franklim Marques, Georgia Ntina, Ana R. N. Bastos, Rui Pinto, Henrique Reguengo, Bruno M. Fonseca, Yiannis Koutedakis, Rui L. Reis, Joaquim M. Oliveira, Eirini K. Kydonaki, Carlos Simón, Emanuel M. Fernandes
Přispěvatelé: Universidade do Minho
Jazyk: angličtina
Předmět:
Supplementation
Osteoporosis
bone
Bone remodeling
0302 clinical medicine
Bone Density
TX341-641
0303 health sciences
Nutrition and Dietetics
biology
medicine.anatomical_structure
RANKL
Ovariectomized rat
Female
Bovine colostrum
Ciências Agrárias::Biotecnologia Agrária e Alimentar
medicine.medical_specialty
Biotecnologia Agrária e Alimentar [Ciências Agrárias]
Ovariectomy
030209 endocrinology & metabolism
Placebo
Bone resorption
Bone and Bones
Article
03 medical and health sciences
Internal medicine
medicine
Animals
Rats
Wistar

Bone
030304 developmental biology
Science & Technology
business.industry
Nutrition. Foods and food supply
Colostrum
medicine.disease
osteoporosis
Rats
bovine colostrum
Disease Models
Animal

Endocrinology
Dietary Supplements
supplementation
biology.protein
Cortical bone
Cattle
business
Food Science
Zdroj: Nutrients
Volume 13
Issue 9
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Nutrients, Vol 13, Iss 2981, p 2981 (2021)
ISSN: 2072-6643
DOI: 10.3390/nu13092981
Popis: 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 orchidectomized (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 supplementation 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.
Databáze: OpenAIRE