<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tong HY</submitter><funding>National Major New Drugs Innovation and Development</funding><pagination>5023654</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8843775</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>2022</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Anshen Buxin Liuwei pill (ABLP) is a Mongolian medicinal formula which has a therapeutic effect on the symptoms such as coronary heart disease, angina pectoris, arrhythmia, depression and irritability, palpitation, and short breath. However, its bioactivity against cardiac injury remains unclear.&lt;h4>Methods&lt;/h4>The protective effect of ABLP was evaluated using H9c2 cells. Cell viability, intracellular Ca&lt;sup>2+&lt;/sup>, reactive oxidative indices, and mitochondrial membrane potential (∆ψ) were assessed, respectively. The mRNA levels of Ca&lt;sup>2+&lt;/sup> channel-related genes (DHPR, RyR2, and SCN5A) and oxidative stress-related genes (Keap1, Nrf2, and HO-1) were measured by RT-PCR.&lt;h4>Results&lt;/h4>0.5-50 &lt;i>μ&lt;/i>g/mL ABLP could significantly decrease H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub>-induced cell injury by suppressing cell necrosis/apoptosis and excess oxidative stress, ameliorating the collapse of ∆ψ, and reducing intracellular Ca&lt;sup>2+&lt;/sup> concentration. Furthermore, 0.5-50 &lt;i>μ&lt;/i>g/mL ABLP reversed H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub>-induced imbalance in the mRNA levels of DHPR, RyR2, SCN5A, Keap1, Nrf2, and HO-1 gene in H9c2 cells, which further illustrate the mechanism.&lt;h4>Conclusion&lt;/h4>ABLP provided protective and therapeutic benefits against H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub>-induced H9c2 cell injury, indicating that this formula can effectively treat coronary disease. In addition, the present study also provides an in-depth understanding of the pharmacological functions of ABLP, which may lead to further successful applications of Mongolian medicine.</pubmed_abstract><journal>Evidence-based complementary and alternative medicine : eCAM</journal><pubmed_title>Anshen Buxin Liuwei Pill, a Mongolian Medicinal Formula, Could Protect H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub>-Induced H9c2 Myocardial Cell Injury by Suppressing Apoptosis, Calcium Channel Activation, and Oxidative Stress.</pubmed_title><pmcid>PMC8843775</pmcid><funding_grant_id>2018YFC1708206</funding_grant_id><pubmed_authors>Murtaza G</pubmed_authors><pubmed_authors>Dong Y</pubmed_authors><pubmed_authors>Huang XJ</pubmed_authors><pubmed_authors>Huang YJ</pubmed_authors><pubmed_authors>Tong HY</pubmed_authors><pubmed_authors>Sarfaraz Iqbal M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Anshen Buxin Liuwei Pill, a Mongolian Medicinal Formula, Could Protect H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub>-Induced H9c2 Myocardial Cell Injury by Suppressing Apoptosis, Calcium Channel Activation, and Oxidative Stress.</name><description>&lt;h4>Background&lt;/h4>Anshen Buxin Liuwei pill (ABLP) is a Mongolian medicinal formula which has a therapeutic effect on the symptoms such as coronary heart disease, angina pectoris, arrhythmia, depression and irritability, palpitation, and short breath. However, its bioactivity against cardiac injury remains unclear.&lt;h4>Methods&lt;/h4>The protective effect of ABLP was evaluated using H9c2 cells. Cell viability, intracellular Ca&lt;sup>2+&lt;/sup>, reactive oxidative indices, and mitochondrial membrane potential (∆ψ) were assessed, respectively. The mRNA levels of Ca&lt;sup>2+&lt;/sup> channel-related genes (DHPR, RyR2, and SCN5A) and oxidative stress-related genes (Keap1, Nrf2, and HO-1) were measured by RT-PCR.&lt;h4>Results&lt;/h4>0.5-50 &lt;i>μ&lt;/i>g/mL ABLP could significantly decrease H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub>-induced cell injury by suppressing cell necrosis/apoptosis and excess oxidative stress, ameliorating the collapse of ∆ψ, and reducing intracellular Ca&lt;sup>2+&lt;/sup> concentration. Furthermore, 0.5-50 &lt;i>μ&lt;/i>g/mL ABLP reversed H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub>-induced imbalance in the mRNA levels of DHPR, RyR2, SCN5A, Keap1, Nrf2, and HO-1 gene in H9c2 cells, which further illustrate the mechanism.&lt;h4>Conclusion&lt;/h4>ABLP provided protective and therapeutic benefits against H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub>-induced H9c2 cell injury, indicating that this formula can effectively treat coronary disease. In addition, the present study also provides an in-depth understanding of the pharmacological functions of ABLP, which may lead to further successful applications of Mongolian medicine.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2024-11-14T20:01:00.702Z</modification><creation>2024-11-14T20:01:00.702Z</creation></dates><accession>S-EPMC8843775</accession><cross_references><pubmed>35178104</pubmed><doi>10.1155/2022/5023654</doi></cross_references></HashMap>