<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>43(1)</volume><submitter>Huang J</submitter><pubmed_abstract>Harmine is a β-carboline alkaloid isolated from Banisteria caapi and Peganum harmala L with various pharmacological activities, including antioxidant, anti-inflammatory, antitumor, anti-depressant, and anti-leishmanial capabilities. Nevertheless, the pharmacological effect of harmine on cardiomyocytes and heart muscle has not been reported. Here we found a protective effect of harmine on cardiac hypertrophy in spontaneously hypertensive rats in vivo. Further, harmine could inhibit the phenotypes of norepinephrine-induced hypertrophy in human embryonic stem cell-derived cardiomyocytes in vitro. It reduced the enlarged cell surface area, reversed the increased calcium handling and contractility, and downregulated expression of hypertrophy-related genes in norepinephrine-induced hypertrophy o</pubmed_abstract><journal>Acta pharmacologica Sinica</journal><pagination>50-63</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8724320</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Harmine is an effective therapeutic small molecule for the treatment of cardiac hypertrophy.</pubmed_title><pmcid>PMC8724320</pmcid><pubmed_authors>Xun ZX</pubmed_authors><pubmed_authors>Zheng QY</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Sun N</pubmed_authors><pubmed_authors>Qin L</pubmed_authors><pubmed_authors>Li EM</pubmed_authors><pubmed_authors>Huang J</pubmed_authors><pubmed_authors>Chen HY</pubmed_authors><pubmed_authors>Xu C</pubmed_authors><pubmed_authors>Chen JX</pubmed_authors><pubmed_authors>Lu XY</pubmed_authors><pubmed_authors>Zhu WJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Harmine is an effective therapeutic small molecule for the treatment of cardiac hypertrophy.</name><description>Harmine is a β-carboline alkaloid isolated from Banisteria caapi and Peganum harmala L with various pharmacological activities, including antioxidant, anti-inflammatory, antitumor, anti-depressant, and anti-leishmanial capabilities. Nevertheless, the pharmacological effect of harmine on cardiomyocytes and heart muscle has not been reported. Here we found a protective effect of harmine on cardiac hypertrophy in spontaneously hypertensive rats in vivo. Further, harmine could inhibit the phenotypes of norepinephrine-induced hypertrophy in human embryonic stem cell-derived cardiomyocytes in vitro. It reduced the enlarged cell surface area, reversed the increased calcium handling and contractility, and downregulated expression of hypertrophy-related genes in norepinephrine-induced hypertrophy o</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2026-06-18T08:45:52.45Z</modification><creation>2025-04-06T09:41:32.947Z</creation></dates><accession>S-EPMC8724320</accession><cross_references><pubmed>33785860</pubmed><doi>10.1038/s41401-021-00639-y</doi></cross_references></HashMap>