<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fan X</submitter><funding>National Natural Science Foundation of China</funding><pagination>892643</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9294374</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13</volume><pubmed_abstract>Diabetes mellitus (DM) often involves cardiovascular complications; however, treatment regimens are limited. ROCK1 (rho-associated coiled-coil containing protein kinase 1) serves as a pathological factor in several diabetic complications. Herein, we aimed to explore the effect of Fasudil (a ROCK1 inhibitor) on the progress of cardiac dysfunction in type 2 DM (T2DM), and to explore the possible mechanisms. Type II diabetic mice models were established by inducing insulin resistance through a high-fat diet combined with low-dose streptozotocin (STZ) injection. NMCMs (neonatal mouse ventricular cardiac myocytes) in the control group were treated with 5.5 mM glucose, while those in the High Glucose (HG) group were treated with 33 mM glucose and 10 nmol/L insulin. &lt;i>In vivo&lt;/i>, we found that </pubmed_abstract><journal>Frontiers in pharmacology</journal><pubmed_title>A ROCK1 Inhibitior Fasudil Alleviates Cardiomyocyte Apoptosis in Diabetic Cardiomyopathy by Inhibiting Mitochondrial Fission in a Type 2 Diabetes Mouse Model.</pubmed_title><pmcid>PMC9294374</pmcid><funding_grant_id>82070388 82170442</funding_grant_id><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Fan X</pubmed_authors><pubmed_authors>Ji X</pubmed_authors><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Xu F</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>A ROCK1 Inhibitior Fasudil Alleviates Cardiomyocyte Apoptosis in Diabetic Cardiomyopathy by Inhibiting Mitochondrial Fission in a Type 2 Diabetes Mouse Model.</name><description>Diabetes mellitus (DM) often involves cardiovascular complications; however, treatment regimens are limited. ROCK1 (rho-associated coiled-coil containing protein kinase 1) serves as a pathological factor in several diabetic complications. Herein, we aimed to explore the effect of Fasudil (a ROCK1 inhibitor) on the progress of cardiac dysfunction in type 2 DM (T2DM), and to explore the possible mechanisms. Type II diabetic mice models were established by inducing insulin resistance through a high-fat diet combined with low-dose streptozotocin (STZ) injection. NMCMs (neonatal mouse ventricular cardiac myocytes) in the control group were treated with 5.5 mM glucose, while those in the High Glucose (HG) group were treated with 33 mM glucose and 10 nmol/L insulin. &lt;i>In vivo&lt;/i>, we found that </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-07-14T14:51:17.462Z</modification><creation>2024-11-20T22:11:57.994Z</creation></dates><accession>S-EPMC9294374</accession><cross_references><pubmed>35865967</pubmed><doi>10.3389/fphar.2022.892643</doi></cross_references></HashMap>