<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Huang YW</submitter><funding>Yunnan Science and Technology Talents support plan</funding><funding>Applied Basic Research Key Project of Yunnan</funding><pagination>45-57</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11230660</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>84(1)</volume><pubmed_abstract>&lt;h4>Abstract&lt;/h4>Atherosclerosis (AS) is a chronic progressive disease caused by various factors and causes various cerebrovascular and cardiovascular diseases (CVDs). Reducing the plasma levels of low-density lipoprotein cholesterol is the primary goal in preventing and treating AS. Proprotein convertase subtilisin/kexin type 9 (PCSK9) plays a crucial role in regulating low-density lipoprotein cholesterol metabolism. Panax notoginseng has potent lipid-reducing effects and protects against CVDs, and its saponins induce vascular dilatation, inhibit thrombus formation, and are used in treating CVDs. However, the anti-AS effect of the secondary metabolite, 20( S )-protopanaxatriol (20( S )-PPT), remains unclear. In this study, the anti-AS effect and molecular mechanism of 20( S )-PPT were inv</pubmed_abstract><journal>Journal of cardiovascular pharmacology</journal><pubmed_title>20( S )-Protopanaxatriol Improves Atherosclerosis by Inhibiting Low-Density Lipoprotein Receptor Degradation in ApoE KO Mice.</pubmed_title><pmcid>PMC11230660</pmcid><funding_grant_id>YNWR-QNBJ-2018-083</funding_grant_id><funding_grant_id>202301BD070001-029</funding_grant_id><pubmed_authors>Huang YW</pubmed_authors><pubmed_authors>Yang J</pubmed_authors><pubmed_authors>Hu D</pubmed_authors><pubmed_authors>Sheng J</pubmed_authors><pubmed_authors>Luo F</pubmed_authors><pubmed_authors>Zhang M</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Wang L</pubmed_authors><pubmed_authors>Meng W</pubmed_authors></additional><is_claimable>false</is_claimable><name>20( S )-Protopanaxatriol Improves Atherosclerosis by Inhibiting Low-Density Lipoprotein Receptor Degradation in ApoE KO Mice.</name><description>&lt;h4>Abstract&lt;/h4>Atherosclerosis (AS) is a chronic progressive disease caused by various factors and causes various cerebrovascular and cardiovascular diseases (CVDs). Reducing the plasma levels of low-density lipoprotein cholesterol is the primary goal in preventing and treating AS. Proprotein convertase subtilisin/kexin type 9 (PCSK9) plays a crucial role in regulating low-density lipoprotein cholesterol metabolism. Panax notoginseng has potent lipid-reducing effects and protects against CVDs, and its saponins induce vascular dilatation, inhibit thrombus formation, and are used in treating CVDs. However, the anti-AS effect of the secondary metabolite, 20( S )-protopanaxatriol (20( S )-PPT), remains unclear. In this study, the anti-AS effect and molecular mechanism of 20( S )-PPT were inv</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2025-04-04T11:26:05.564Z</modification><creation>2025-04-04T11:26:05.564Z</creation></dates><accession>S-EPMC11230660</accession><cross_references><pubmed>38922585</pubmed><doi>10.1097/FJC.0000000000001566</doi></cross_references></HashMap>