<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Haam CE</submitter><funding>Myoung-Sun Kim Memorial Foundation</funding><pagination>2711</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9104054</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>27(9)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>&lt;i>Alpinia officinarum&lt;/i> (&lt;i>A. officinarum&lt;/i>) is known to exhibit a beneficial effect for anti-inflammatory, anti-oxidant, and anti-hyperlipidemic effects. However, no sufficient research data are available on the cardiovascular effect of &lt;i>A. officinarum&lt;/i>. Thus, in this study, we investigate whether &lt;i>A. officinarum&lt;/i> extract has direct effects on vascular reactivity.&lt;h4>Methods&lt;/h4>To examine whether &lt;i>A. officinarum&lt;/i> extract affects vascular functionality, we measured isometric tension in rat mesenteric resistance arteries using a wire myograph. After arteries were pre-contracted with high-K&lt;sup>+&lt;/sup> (70 mM), phenylephrine (5 µM), or U46619 (1 µM), &lt;i>A. officinarum&lt;/i> extract was treated.&lt;h4>Results&lt;/h4>&lt;i>A. officinarum&lt;/i> extract induced vasodilation in a concentration-dependent manner, and this effect was endothelium independent. To further investigate the mechanism, we incubated arteries in a Ca&lt;sup>2+&lt;/sup>-free and high-K&lt;sup>+&lt;/sup> solution, followed by the cumulative addition of CaCl&lt;sub>2&lt;/sub> (0.01-2.5 mM) with or without &lt;i>A. officinarum&lt;/i> extract (30 µg/mL). Pre-treatment of &lt;i>A. officinarum&lt;/i> extract reduced the contractile responses induced by cumulative administration of Ca&lt;sup>2+&lt;/sup>, which suggests that extracellular Ca&lt;sup>2+&lt;/sup> influx was inhibited by the treatment of &lt;i>A. officinarum&lt;/i> extract. These results were associated with a reduction in phosphorylated MLC&lt;sub>20&lt;/sub> in VSMCs treated with &lt;i>A. officinarum&lt;/i> extract. Furthermore, eucalyptol, an active compound of &lt;i>A. officinarum&lt;/i> extract, had a similar effect as &lt;i>A. officinarum&lt;/i> extract, which causes vasodilation in mesenteric resistance arteries.&lt;h4>Conclusion&lt;/h4>&lt;i>A. officinarum&lt;/i> extract and its active compound eucalyptol induce concentration-dependent vasodilation in mesenteric resistance arteries. These results suggest that administration of &lt;i>A. officinarum&lt;/i> extract could exert beneficial effects to treat high blood pressure.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Vasodilatory Effect of &lt;i>Alpinia officinarum&lt;/i> Extract in Rat Mesenteric Arteries.</pubmed_title><pmcid>PMC9104054</pmcid><funding_grant_id>2020</funding_grant_id><pubmed_authors>Haam CE</pubmed_authors><pubmed_authors>Lim S</pubmed_authors><pubmed_authors>Byeon S</pubmed_authors><pubmed_authors>Choi SK</pubmed_authors><pubmed_authors>Choi SJ</pubmed_authors><pubmed_authors>Lee YH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Vasodilatory Effect of &lt;i>Alpinia officinarum&lt;/i> Extract in Rat Mesenteric Arteries.</name><description>&lt;h4>Background&lt;/h4>&lt;i>Alpinia officinarum&lt;/i> (&lt;i>A. officinarum&lt;/i>) is known to exhibit a beneficial effect for anti-inflammatory, anti-oxidant, and anti-hyperlipidemic effects. However, no sufficient research data are available on the cardiovascular effect of &lt;i>A. officinarum&lt;/i>. Thus, in this study, we investigate whether &lt;i>A. officinarum&lt;/i> extract has direct effects on vascular reactivity.&lt;h4>Methods&lt;/h4>To examine whether &lt;i>A. officinarum&lt;/i> extract affects vascular functionality, we measured isometric tension in rat mesenteric resistance arteries using a wire myograph. After arteries were pre-contracted with high-K&lt;sup>+&lt;/sup> (70 mM), phenylephrine (5 µM), or U46619 (1 µM), &lt;i>A. officinarum&lt;/i> extract was treated.&lt;h4>Results&lt;/h4>&lt;i>A. officinarum&lt;/i> extract induced vasodilation in a concentration-dependent manner, and this effect was endothelium independent. To further investigate the mechanism, we incubated arteries in a Ca&lt;sup>2+&lt;/sup>-free and high-K&lt;sup>+&lt;/sup> solution, followed by the cumulative addition of CaCl&lt;sub>2&lt;/sub> (0.01-2.5 mM) with or without &lt;i>A. officinarum&lt;/i> extract (30 µg/mL). Pre-treatment of &lt;i>A. officinarum&lt;/i> extract reduced the contractile responses induced by cumulative administration of Ca&lt;sup>2+&lt;/sup>, which suggests that extracellular Ca&lt;sup>2+&lt;/sup> influx was inhibited by the treatment of &lt;i>A. officinarum&lt;/i> extract. These results were associated with a reduction in phosphorylated MLC&lt;sub>20&lt;/sub> in VSMCs treated with &lt;i>A. officinarum&lt;/i> extract. Furthermore, eucalyptol, an active compound of &lt;i>A. officinarum&lt;/i> extract, had a similar effect as &lt;i>A. officinarum&lt;/i> extract, which causes vasodilation in mesenteric resistance arteries.&lt;h4>Conclusion&lt;/h4>&lt;i>A. officinarum&lt;/i> extract and its active compound eucalyptol induce concentration-dependent vasodilation in mesenteric resistance arteries. These results suggest that administration of &lt;i>A. officinarum&lt;/i> extract could exert beneficial effects to treat high blood pressure.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-19T16:20:14.424Z</modification><creation>2025-04-19T16:20:14.424Z</creation></dates><accession>S-EPMC9104054</accession><cross_references><pubmed>35566064</pubmed><doi>10.3390/molecules27092711</doi></cross_references></HashMap>