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1.
Sci Rep ; 6: 21343, 2016 Feb 11.
Article in English | MEDLINE | ID: mdl-26867002

ABSTRACT

Bone loss caused by ionizing radiation is a potential health concern for radiotherapy patients, radiation workers and astronauts. In animal studies, exposure to ionizing radiation increases oxidative damage in skeletal tissues, and results in an imbalance in bone remodeling initiated by increased bone-resorbing osteoclasts. Therefore, we evaluated various candidate interventions with antioxidant or anti-inflammatory activities (antioxidant cocktail, dihydrolipoic acid, ibuprofen, dried plum) both for their ability to blunt the expression of resorption-related genes in marrow cells after irradiation with either gamma rays (photons, 2 Gy) or simulated space radiation (protons and heavy ions, 1 Gy) and to prevent bone loss. Dried plum was most effective in reducing the expression of genes related to bone resorption (Nfe2l2, Rankl, Mcp1, Opg, TNF-α) and also preventing later cancellous bone decrements caused by irradiation with either photons or heavy ions. Thus, dietary supplementation with DP may prevent the skeletal effects of radiation exposures either in space or on Earth.


Subject(s)
Bone Resorption , Dietary Supplements , Fruit , Gamma Rays/adverse effects , Gene Expression Regulation/radiation effects , Radiation Injuries, Experimental , Animals , Bone Resorption/metabolism , Bone Resorption/pathology , Bone Resorption/prevention & control , Male , Mice , Prunus domestica , Radiation Injuries, Experimental/metabolism , Radiation Injuries, Experimental/pathology , Radiation Injuries, Experimental/prevention & control
2.
Osteoporos Int ; 22(8): 2283-93, 2011 Aug.
Article in English | MEDLINE | ID: mdl-20941479

ABSTRACT

UNLABELLED: Diabetic obesity is associated with increased fracture risk in adults and adolescents. We find in both adolescent and adult mice dramatically inferior mechanical properties and structural quality of cortical bone, in agreement with the human fracture data, although some aspects of the response to obesity appear to differ by age. INTRODUCTION: The association of obesity with bone is complex and varies with age. Diabetic obese adolescents and adult humans have increased fracture risk. Prior studies have shown reduced mechanical properties as a result of high-fat diet (HFD) but do not fully address size-independent mechanical properties or structural quality, which are important to understand material behavior. METHODS: Cortical bone from femurs and tibiae from two age groups of C57BL/6 mice fed either HFD or low-fat diet (LFD) were evaluated for structural and bone turnover changes (SEM and histomorphometry) and tested for bending strength, bending stiffness, and fracture toughness. Leptin, IGF-I, and non-enzymatic glycation measurements were also collected. RESULTS: In both young and adult mice fed on HFD, femoral strength, stiffness, and toughness are all dramatically lower than controls. Inferior lamellar and osteocyte alignment also point to reduced structural quality in both age groups. Bone size was largely unaffected by HFD, although there was a shift from increasing bone size in obese adolescents to decreasing in adults. IGF-I levels were lower in young obese mice only. CONCLUSIONS: While the response to obesity of murine cortical bone mass, bone formation, and hormonal changes appear to differ by age, the bone mechanical properties for young and adult groups are similar. In agreement with human fracture trends, adult mice may be similarly susceptible to bone fracture to the young group, although cortical bone in the two age groups responds to diabetic obesity differently.


Subject(s)
Aging , Bone and Bones/physiopathology , Diet, High-Fat/adverse effects , Obesity/physiopathology , Aging/pathology , Aging/physiology , Animals , Biomechanical Phenomena , Blood Glucose/metabolism , Body Composition , Bone Density/physiology , Bone and Bones/pathology , Diabetes Mellitus, Experimental/blood , Diabetes Mellitus, Experimental/complications , Diabetes Mellitus, Experimental/pathology , Diabetes Mellitus, Experimental/physiopathology , Femur/physiopathology , Femur/ultrastructure , Glycation End Products, Advanced/blood , Insulin-Like Growth Factor I/metabolism , Leptin/blood , Male , Mice , Mice, Inbred C57BL , Microscopy, Electron, Scanning , Obesity/blood , Obesity/pathology , Osteoporotic Fractures/etiology , Osteoporotic Fractures/pathology , Osteoporotic Fractures/physiopathology , Tibia/physiopathology , Tibia/ultrastructure , Weight Gain/physiology
3.
Calcif Tissue Int ; 80(3): 160-6, 2007 Mar.
Article in English | MEDLINE | ID: mdl-17340224

ABSTRACT

Genetic selection for rapid body growth in broiler chickens has resulted in adverse effects on the skeletal system exemplified by a higher rate of cortical fractures in leg bones. Strontium (Sr) has been reported to have beneficial effects on bone formation and strength. We supplemented the diet of 300-day-old chicks with increasing dosages of Sr (0%, 0.12%, or 0.24%) to study the capacity of the element to improve bone quality and mechanical integrity. Treatment with Sr increased cortical bone volume and reduced bone porosity as measured by micro-computed tomography. The higher level of Sr significantly reduced bone Ca content (34.7%) relative to controls (37.2%), suggesting that Sr replaced some of the Ca in bone. Material properties determined by the three-point bending test showed that bone in the Sr-treated groups withstood greater deformation prior to fracture. Load to failure and ultimate stress were similar across groups. Our results indicate that Sr treatment in rapidly growing chickens induced positive effects on bone volume but did not improve the breaking strength of long bones.


Subject(s)
Bone and Bones/metabolism , Strontium/administration & dosage , Animals , Biomechanical Phenomena , Body Weight , Bone Density , Bone Development , Calcification, Physiologic , Chickens , Densitometry , Dietary Supplements , Fractures, Bone , Male , Stress, Mechanical , Strontium/pharmacology
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