<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Munier JJ</submitter><funding>National Institute on Alcohol Abuse and Alcoholism</funding><funding>National Institute of Diabetes and Digestive and Kidney Diseases</funding><funding>NIDDK NIH HHS</funding><funding>NIDA NIH HHS</funding><funding>NIAAA NIH HHS</funding><funding>National Institutes of Health</funding><funding>National Institute on Drug Abuse</funding><funding>NIH HHS</funding><pagination>16428</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9525296</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(1)</volume><pubmed_abstract>Grip strength is a valuable preclinical assay to study muscle physiology in disease and aging by directly determining changes in muscle force generation in active laboratory mice. Existing methods to statistically evaluate grip strength, however, have limitations in the power and scope of the physiological features that are assessed. We therefore designed a microcontroller whose serial measure of resistance-based force enables the simultaneous readout of (1) peak grip strength, (2) force profile (the non-linear progress of force exerted throughout a standard grip strength trial), and (3) cumulative force profile (the integral of force with respect to time of a single grip strength trial). We hypothesized that muscle pathologies of different etiologies have distinct effects on these paramet</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Simultaneous monitoring of mouse grip strength, force profile, and cumulative force profile distinguishes muscle physiology following surgical, pharmacologic and diet interventions.</pubmed_title><pmcid>PMC9525296</pmcid><funding_grant_id>U54 DK120342</funding_grant_id><funding_grant_id>F31AA028183</funding_grant_id><funding_grant_id>T32DA024635</funding_grant_id><funding_grant_id>P50 GM115318</funding_grant_id><pubmed_authors>Severino A</pubmed_authors><pubmed_authors>Pank JT</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Munier JJ</pubmed_authors><pubmed_authors>Reue K</pubmed_authors><pubmed_authors>Zhang P</pubmed_authors><pubmed_authors>Vergnes L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Simultaneous monitoring of mouse grip strength, force profile, and cumulative force profile distinguishes muscle physiology following surgical, pharmacologic and diet interventions.</name><description>Grip strength is a valuable preclinical assay to study muscle physiology in disease and aging by directly determining changes in muscle force generation in active laboratory mice. Existing methods to statistically evaluate grip strength, however, have limitations in the power and scope of the physiological features that are assessed. We therefore designed a microcontroller whose serial measure of resistance-based force enables the simultaneous readout of (1) peak grip strength, (2) force profile (the non-linear progress of force exerted throughout a standard grip strength trial), and (3) cumulative force profile (the integral of force with respect to time of a single grip strength trial). We hypothesized that muscle pathologies of different etiologies have distinct effects on these paramet</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2025-04-22T03:41:17.321Z</modification><creation>2025-04-05T20:45:17.418Z</creation></dates><accession>S-EPMC9525296</accession><cross_references><pubmed>36180720</pubmed><doi>10.1038/s41598-022-20665-y</doi></cross_references></HashMap>