Rodent Models of Aging Bone: An Update
Autor: | Terry Melim, Farhan A. Syed |
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Rok vydání: | 2011 |
Předmět: |
Male
Aging medicine.medical_specialty Stromal cell Endocrinology Diabetes and Metabolism Osteoporosis Population Bioinformatics medicine.disease_cause Bone and Bones Proinflammatory cytokine Mice Internal medicine medicine Animals education education.field_of_study Osteoblasts business.industry Mesenchymal stem cell Cell Differentiation medicine.disease Rats Disease Models Animal Endocrinology Models Animal Life expectancy Female business Oxidative stress Hormone |
Zdroj: | Current Osteoporosis Reports. 9:219-228 |
ISSN: | 1544-2241 1544-1873 |
DOI: | 10.1007/s11914-011-0074-z |
Popis: | With an increase in the average life span especially in the Western hemisphere, there is renewed interest in treating maladies of old age including osteoporosis. Age-related bone loss and resultant osteoporosis substantially increase risk of fractures and morbidity in the geriatric population leading to both a decline in the quality of life for the elderly as well as a substantial burden on the health care system. Herein, we review recent research in murine and rodent models looking at how both extrinsic and intrinsic factors such as hormones, biochemicals, neuromodulators, inflammatory cytokines, oxidative stress, nutrition, and exercise influence the skeleton with age. Recent studies on the relationship between bone and fat in the marrow, and the fate of the marrow mesenchymal stromal cell population, which can give rise to either bone-forming osteoblasts or fat-forming adipocytic cells as a function of age, have also been highlighted. An appreciable range of studies using aging murine as well as cellular models are discussed, as these studies have broadened our understanding of the pathways and players in the aging bone. Impactful information regarding aging and the bone may then allow the application of better pharmacologic as well as nonpharmacologic regimens to alleviate bone loss due to aging. |
Databáze: | OpenAIRE |
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