{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,8,2]],"date-time":"2025-08-02T00:11:32Z","timestamp":1754093492108,"version":"3.41.2"},"reference-count":52,"publisher":"Wiley","issue":"8","license":[{"start":{"date-parts":[[2025,5,19]],"date-time":"2025-05-19T00:00:00Z","timestamp":1747612800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["J of Diabetes Invest"],"published-print":{"date-parts":[[2025,8]]},"abstract":"<jats:title>ABSTRACT<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>Canagliflozin (Cana) has protected against diabetes\u2010related cardiovascular disease. This study was intended to explore the effect and molecular mechanism of Cana on cardiovascular protection in type 2 diabetic coronary atherosclerotic heart disease (CAD).<\/jats:p><\/jats:sec><jats:sec><jats:title>Materials and Methods<\/jats:title><jats:p>We constructed a rat model of type 2 diabetic CAD and examined its physiological and biochemical indices before and after Cana treatment. Next\u2010generation transcriptome sequencing was performed on rat cardiac tissue. Various functional and molecular experiments involving Cana treatment and the natriuretic peptide B (<jats:italic>NPPB<\/jats:italic>) gene were performed on human cardiomyocytes (AC16 cells).<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>The physiological, biochemical, and imaging parameters of the model rats were abnormal. Cana treatment reversed these injuries. In all, 369 differentially expressed genes were discovered by next\u2010generation transcriptome sequencing; <jats:italic>NPPB<\/jats:italic> was identified as the target gene. Cana treatment significantly improved the function of AC16 cells treated with high glucose and significantly upregulated the expression level of the <jats:italic>NPPB<\/jats:italic> gene. The <jats:italic>NPPB<\/jats:italic> gene significantly increased the viability of AC16 cells and significantly decreased the apoptosis rate and reactive oxygen species (ROS) level. In addition, <jats:italic>NPPB<\/jats:italic> significantly upregulated the expression of B\u2010cell lymphoma 2 (Bcl\u20102) and downregulated the expression of Bcl\u20102 associated X protein (Bax). Cana treatment further improved these cellular functions and protein expression levels. Furthermore, the <jats:italic>NPPB<\/jats:italic> gene significantly upregulated protein kinase 1\u2010\u03b1 (PKG1\u03b1) expression level and Cana treatment enhanced the regulatory effect of <jats:italic>NPPB<\/jats:italic> on PKG1\u03b1.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>The cardiovascular protective effect of Cana in diabetes mellitus was mediated by upregulating the expression of <jats:italic>NPPB<\/jats:italic> and upregulating the level of PKG1\u03b1, which in turn regulated the viability, apoptosis rate, and ROS level of AC16 cells.<\/jats:p><\/jats:sec>","DOI":"10.1111\/jdi.70056","type":"journal-article","created":{"date-parts":[[2025,5,20]],"date-time":"2025-05-20T05:53:38Z","timestamp":1747720418000},"page":"1430-1444","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Canagliflozin protects cardiovascular function in type 2 diabetic coronary artery disease by 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