Lauren Wimer, Elena Goncharova, Sofiya Galkina, Edna Nyangau, Mahalakshmi Shankaran, Asia Davis, Leandro Prado, Maria Castro Munoz, Sharon Epstein, Cavan Patterson, Nicholas Shaum, Mark Hellerstein, William Evans, Simon Melov
{"title":"3d -肌酸稀释法无创测量小鼠肌肉质量","authors":"Lauren Wimer, Elena Goncharova, Sofiya Galkina, Edna Nyangau, Mahalakshmi Shankaran, Asia Davis, Leandro Prado, Maria Castro Munoz, Sharon Epstein, Cavan Patterson, Nicholas Shaum, Mark Hellerstein, William Evans, Simon Melov","doi":"10.1111/acel.13897","DOIUrl":null,"url":null,"abstract":"<p>Developing accurate methods to quantify age-related muscle loss (sarcopenia) could greatly accelerate development of therapies to treat muscle loss in the elderly, as current methods are inaccurate or expensive. The current gold standard method for quantifying sarcopenia is dual-energy X-ray absorptiometry (DXA) but does not measure muscle directly—it is a composite measure quantifying “lean mass” (muscle) excluding fat and bone. In humans, DXA overestimates muscle mass, which has led to erroneous conclusions about the importance of skeletal muscle in human health and disease. In animal models, DXA is a popular method for measuring lean mass. However, instrumentation is expensive and is potentially limited by anesthesia concerns. Recently, the D<sub>3</sub>-creatine (D<sub>3</sub>Cr) dilution method for quantifying muscle mass was developed in humans and rats. This method is faster, cheaper, and more accurate than DXA. Here, we demonstrate that the D<sub>3</sub>Cr method is a specific assay for muscle mass in mice, and we test associations with DXA and body weight. We evaluated the D<sub>3</sub>Cr method compared to DXA-determined lean body mass (LBM) in aged mice and reported that DXA consistently overestimates muscle mass with age. Overall, we provide evidence that the D<sub>3</sub>Cr dilution method directly measures muscle mass in mice. Combined with its ease of use, accessibility, and non-invasive nature, the method may prove to more quickly advance development of preclinical therapies targeting sarcopenia.</p>","PeriodicalId":119,"journal":{"name":"Aging Cell","volume":"22 8","pages":""},"PeriodicalIF":7.1000,"publicationDate":"2023-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/acel.13897","citationCount":"0","resultStr":"{\"title\":\"The D3-creatine dilution method non-invasively measures muscle mass in mice\",\"authors\":\"Lauren Wimer, Elena Goncharova, Sofiya Galkina, Edna Nyangau, Mahalakshmi Shankaran, Asia Davis, Leandro Prado, Maria Castro Munoz, Sharon Epstein, Cavan Patterson, Nicholas Shaum, Mark Hellerstein, William Evans, Simon Melov\",\"doi\":\"10.1111/acel.13897\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Developing accurate methods to quantify age-related muscle loss (sarcopenia) could greatly accelerate development of therapies to treat muscle loss in the elderly, as current methods are inaccurate or expensive. The current gold standard method for quantifying sarcopenia is dual-energy X-ray absorptiometry (DXA) but does not measure muscle directly—it is a composite measure quantifying “lean mass” (muscle) excluding fat and bone. In humans, DXA overestimates muscle mass, which has led to erroneous conclusions about the importance of skeletal muscle in human health and disease. In animal models, DXA is a popular method for measuring lean mass. However, instrumentation is expensive and is potentially limited by anesthesia concerns. Recently, the D<sub>3</sub>-creatine (D<sub>3</sub>Cr) dilution method for quantifying muscle mass was developed in humans and rats. This method is faster, cheaper, and more accurate than DXA. Here, we demonstrate that the D<sub>3</sub>Cr method is a specific assay for muscle mass in mice, and we test associations with DXA and body weight. We evaluated the D<sub>3</sub>Cr method compared to DXA-determined lean body mass (LBM) in aged mice and reported that DXA consistently overestimates muscle mass with age. Overall, we provide evidence that the D<sub>3</sub>Cr dilution method directly measures muscle mass in mice. 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The D3-creatine dilution method non-invasively measures muscle mass in mice
Developing accurate methods to quantify age-related muscle loss (sarcopenia) could greatly accelerate development of therapies to treat muscle loss in the elderly, as current methods are inaccurate or expensive. The current gold standard method for quantifying sarcopenia is dual-energy X-ray absorptiometry (DXA) but does not measure muscle directly—it is a composite measure quantifying “lean mass” (muscle) excluding fat and bone. In humans, DXA overestimates muscle mass, which has led to erroneous conclusions about the importance of skeletal muscle in human health and disease. In animal models, DXA is a popular method for measuring lean mass. However, instrumentation is expensive and is potentially limited by anesthesia concerns. Recently, the D3-creatine (D3Cr) dilution method for quantifying muscle mass was developed in humans and rats. This method is faster, cheaper, and more accurate than DXA. Here, we demonstrate that the D3Cr method is a specific assay for muscle mass in mice, and we test associations with DXA and body weight. We evaluated the D3Cr method compared to DXA-determined lean body mass (LBM) in aged mice and reported that DXA consistently overestimates muscle mass with age. Overall, we provide evidence that the D3Cr dilution method directly measures muscle mass in mice. Combined with its ease of use, accessibility, and non-invasive nature, the method may prove to more quickly advance development of preclinical therapies targeting sarcopenia.
Aging CellBiochemistry, Genetics and Molecular Biology-Cell Biology
自引率
2.60%
发文量
212
期刊介绍:
Aging Cell is an Open Access journal that focuses on the core aspects of the biology of aging, encompassing the entire spectrum of geroscience. The journal's content is dedicated to publishing research that uncovers the mechanisms behind the aging process and explores the connections between aging and various age-related diseases. This journal aims to provide a comprehensive understanding of the biological underpinnings of aging and its implications for human health.
The journal is widely recognized and its content is abstracted and indexed by numerous databases and services, which facilitates its accessibility and impact in the scientific community. These include:
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Being indexed in these databases ensures that the research published in Aging Cell is discoverable by researchers, clinicians, and other professionals interested in the field of aging and its associated health issues. This broad coverage helps to disseminate the journal's findings and contributes to the advancement of knowledge in geroscience.