Charles D Brennan, Nathan R Kerr, Jose A Viteri, Zachary Williard, Harper Snyder, Gabriella Meier, Sam Cairns, Fereshteh B Darvishi, Anna R Dashtmian, Peter J Moore, Sindhuja N Ayyagari, Meifang Wang, W David Arnold
{"title":"加权推车拉:一种新的结果测量持续运动功能的小鼠。","authors":"Charles D Brennan, Nathan R Kerr, Jose A Viteri, Zachary Williard, Harper Snyder, Gabriella Meier, Sam Cairns, Fereshteh B Darvishi, Anna R Dashtmian, Peter J Moore, Sindhuja N Ayyagari, Meifang Wang, W David Arnold","doi":"10.1113/EP092658","DOIUrl":null,"url":null,"abstract":"<p><p>Sarcopenia, the pathological age-related decline in muscle mass and strength, compromises independence and quality of life in older adults. Currently, no effective treatments are available. To enhance translational research using aged mouse models, we developed and validated the weighted cart pull (WCP) as a novel assessment of sustained motor function. The WCP test involved attaching a weighted cart to the tail of a mouse as it climbed a ramp to a 'resting house'. Mass was increased incrementally until failure, defined as either five consecutive hindquarter pokes without progress or sliding backwards. In experiment 1, reliability (inter- and intra-rater) was evaluated in middle-aged mice (9 months, n = 10, 50% female). In experiment 2, young (n = 8, 50% female) and old (n = 8, 50% female) mice were tested on WCP, all-limb grip and rotarod. In experiment 3, middle-aged mice (7-9 months, n = 20, 50% female) underwent behavioural tests, in vivo electrophysiology and muscle physiology to correlate WCP with assessments of neuromuscular function. WCP showed high intra-rater repeatability [intraclass correlation coefficient = 0.611, P = 0.018, 95% confidence interval (CI) = (0.046, 0.885)]. WCP demonstrated phenotypic differences between young and old mice (Student's unpaired t-test, P < 0.0001). WCP was significantly correlated with all-limb grip [Pearson's r = 0.5820, P = 0.0071, 95% CI = (0.1878, 0.8147)], percentage decrement upon repetitive nerve stimulation at 50 Hz [Pearson's r = 0.4613, P = 0.0468, 95% CI = (0.008973, 0.7569)], twitch torque [Pearson's r = 0.6241, P = 0.0033, 95% CI = (0.2509, 0.8358)], tetanic torque [Pearson's r = 0.5100, P = 0.0216, 95% CI = (0.08718, 0.7771)] and bilateral gastrocnemius and soleus muscle mass [Pearson's r = 0.5878, P = 0.0064, 95% CI = (0.1964, 0.8177)]. The WCP provides a cost-effective, comprehensive measure of strength and sustained motor function, improving preclinical assessments.</p>","PeriodicalId":12092,"journal":{"name":"Experimental Physiology","volume":" ","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Weighted cart pull: A novel outcome measure for sustained motor function in mice.\",\"authors\":\"Charles D Brennan, Nathan R Kerr, Jose A Viteri, Zachary Williard, Harper Snyder, Gabriella Meier, Sam Cairns, Fereshteh B Darvishi, Anna R Dashtmian, Peter J Moore, Sindhuja N Ayyagari, Meifang Wang, W David Arnold\",\"doi\":\"10.1113/EP092658\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Sarcopenia, the pathological age-related decline in muscle mass and strength, compromises independence and quality of life in older adults. Currently, no effective treatments are available. To enhance translational research using aged mouse models, we developed and validated the weighted cart pull (WCP) as a novel assessment of sustained motor function. The WCP test involved attaching a weighted cart to the tail of a mouse as it climbed a ramp to a 'resting house'. Mass was increased incrementally until failure, defined as either five consecutive hindquarter pokes without progress or sliding backwards. In experiment 1, reliability (inter- and intra-rater) was evaluated in middle-aged mice (9 months, n = 10, 50% female). In experiment 2, young (n = 8, 50% female) and old (n = 8, 50% female) mice were tested on WCP, all-limb grip and rotarod. In experiment 3, middle-aged mice (7-9 months, n = 20, 50% female) underwent behavioural tests, in vivo electrophysiology and muscle physiology to correlate WCP with assessments of neuromuscular function. WCP showed high intra-rater repeatability [intraclass correlation coefficient = 0.611, P = 0.018, 95% confidence interval (CI) = (0.046, 0.885)]. WCP demonstrated phenotypic differences between young and old mice (Student's unpaired t-test, P < 0.0001). WCP was significantly correlated with all-limb grip [Pearson's r = 0.5820, P = 0.0071, 95% CI = (0.1878, 0.8147)], percentage decrement upon repetitive nerve stimulation at 50 Hz [Pearson's r = 0.4613, P = 0.0468, 95% CI = (0.008973, 0.7569)], twitch torque [Pearson's r = 0.6241, P = 0.0033, 95% CI = (0.2509, 0.8358)], tetanic torque [Pearson's r = 0.5100, P = 0.0216, 95% CI = (0.08718, 0.7771)] and bilateral gastrocnemius and soleus muscle mass [Pearson's r = 0.5878, P = 0.0064, 95% CI = (0.1964, 0.8177)]. 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Weighted cart pull: A novel outcome measure for sustained motor function in mice.
Sarcopenia, the pathological age-related decline in muscle mass and strength, compromises independence and quality of life in older adults. Currently, no effective treatments are available. To enhance translational research using aged mouse models, we developed and validated the weighted cart pull (WCP) as a novel assessment of sustained motor function. The WCP test involved attaching a weighted cart to the tail of a mouse as it climbed a ramp to a 'resting house'. Mass was increased incrementally until failure, defined as either five consecutive hindquarter pokes without progress or sliding backwards. In experiment 1, reliability (inter- and intra-rater) was evaluated in middle-aged mice (9 months, n = 10, 50% female). In experiment 2, young (n = 8, 50% female) and old (n = 8, 50% female) mice were tested on WCP, all-limb grip and rotarod. In experiment 3, middle-aged mice (7-9 months, n = 20, 50% female) underwent behavioural tests, in vivo electrophysiology and muscle physiology to correlate WCP with assessments of neuromuscular function. WCP showed high intra-rater repeatability [intraclass correlation coefficient = 0.611, P = 0.018, 95% confidence interval (CI) = (0.046, 0.885)]. WCP demonstrated phenotypic differences between young and old mice (Student's unpaired t-test, P < 0.0001). WCP was significantly correlated with all-limb grip [Pearson's r = 0.5820, P = 0.0071, 95% CI = (0.1878, 0.8147)], percentage decrement upon repetitive nerve stimulation at 50 Hz [Pearson's r = 0.4613, P = 0.0468, 95% CI = (0.008973, 0.7569)], twitch torque [Pearson's r = 0.6241, P = 0.0033, 95% CI = (0.2509, 0.8358)], tetanic torque [Pearson's r = 0.5100, P = 0.0216, 95% CI = (0.08718, 0.7771)] and bilateral gastrocnemius and soleus muscle mass [Pearson's r = 0.5878, P = 0.0064, 95% CI = (0.1964, 0.8177)]. The WCP provides a cost-effective, comprehensive measure of strength and sustained motor function, improving preclinical assessments.
期刊介绍:
Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged.
Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.