TY - JOUR
T1 - Milk basic protein supplementation enhances fracture healing in mice
AU - Yoneme, Hiroshi
AU - Hatakeyama, Junko
AU - Danjo, Atsushi
AU - Oida, Hanako
AU - Yoshinari, Masao
AU - Aijima, Reona
AU - Murata, Naohisa
AU - Watanabe, Toshiyuki
AU - Oki, Yuji
AU - Kido, Mizuho A.
PY - 2015/2/1
Y1 - 2015/2/1
N2 - Objectives: There is an unmet need for agents that can stimulate bone healing. The goal of this study was to evaluate the effects of basic proteins from milk whey (milk basic protein [MBP]) on fracture healing in mice. Methods: Closed tibial transverse fractures were generated in 6-wk-old male C3 H/HeJ mice given either tap water or MBP-supplemented water for 3, 7, 14, 28, and 56d after fracture generation. The tibial tissues were analyzed by radiography, μCT, and a three-point bending test. The expression levels of genes associated with bone metabolism were analyzed by real-time reverse transcription-polymerase chain reaction. Results: Quantitative μCT analysis showed that MBP-treated fractured tibiae had a larger hard callus in the sectional area and a larger volume compared with fractured tibiae without MBP treatment. The expression levels of genes associated with chondrogenesis and osteogenesis showed greater increases in fractured tibiae with MBP treatment. Significant increases in the callus mechanical properties were found in MBP-treated tibiae. Conclusions: MBP supplementation has the potential to improve fracture healing and bone strength in mouse tibiae. MBP could be a potential safe, low-cost, and easily administered nutritional element to prevent secondary fractures in patients with bone fractures.
AB - Objectives: There is an unmet need for agents that can stimulate bone healing. The goal of this study was to evaluate the effects of basic proteins from milk whey (milk basic protein [MBP]) on fracture healing in mice. Methods: Closed tibial transverse fractures were generated in 6-wk-old male C3 H/HeJ mice given either tap water or MBP-supplemented water for 3, 7, 14, 28, and 56d after fracture generation. The tibial tissues were analyzed by radiography, μCT, and a three-point bending test. The expression levels of genes associated with bone metabolism were analyzed by real-time reverse transcription-polymerase chain reaction. Results: Quantitative μCT analysis showed that MBP-treated fractured tibiae had a larger hard callus in the sectional area and a larger volume compared with fractured tibiae without MBP treatment. The expression levels of genes associated with chondrogenesis and osteogenesis showed greater increases in fractured tibiae with MBP treatment. Significant increases in the callus mechanical properties were found in MBP-treated tibiae. Conclusions: MBP supplementation has the potential to improve fracture healing and bone strength in mouse tibiae. MBP could be a potential safe, low-cost, and easily administered nutritional element to prevent secondary fractures in patients with bone fractures.
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U2 - 10.1016/j.nut.2014.08.008
DO - 10.1016/j.nut.2014.08.008
M3 - Article
C2 - 25592019
AN - SCOPUS:84920896763
VL - 31
SP - 399
EP - 405
JO - Nutrition
JF - Nutrition
SN - 0899-9007
IS - 2
ER -