<HashMap><database>biostudies-literature</database><scores/><additional><submitter>He Q</submitter><funding>National Natural Science Foundation of China</funding><pagination>24</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10773052</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>There are accumulating type 2 diabetes patients who have osteoporosis simultaneously. More effective therapeutic strategies should be discovered. Biochanin A (BCA) has been indicated that can play a role in improving metabolic disorders of type 2 diabetes and preventing osteoporosis. But whether BCA can treat type 2 diabetic osteoporosis has not been studied.&lt;h4>Purpose&lt;/h4>To investigate if the BCA can protect against type 2 diabetic osteoporosis and clarify the mechanism.&lt;h4>Methods&lt;/h4&gt;Micro-CT and histology assays were performed to detect the trabecular bone and analyze the bone histomorphology effect of BCA. CCK-8 assay was performed to detect the toxicity of BCA. TRAcP staining, immunofluorescence and hydroxyapatite resorption assay were used to observe osteoclasts</pubmed_abstract><journal>BMC complementary medicine and therapies</journal><pubmed_title>Biochanin A abrogates osteoclastogenesis in type 2 diabetic osteoporosis via regulating ROS/MAPK signaling pathway based on integrating molecular docking and experimental validation.</pubmed_title><pmcid>PMC10773052</pmcid><funding_grant_id>NO. 82074462</funding_grant_id><funding_grant_id>82374470</funding_grant_id><pubmed_authors>Yang J</pubmed_authors><pubmed_authors>Pan Z</pubmed_authors><pubmed_authors>Chen P</pubmed_authors><pubmed_authors>Zhang N</pubmed_authors><pubmed_authors>Lin Y</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>He Q</pubmed_authors><pubmed_authors>Chen C</pubmed_authors><pubmed_authors>Chen B</pubmed_authors><pubmed_authors>Li M</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Xiao J</pubmed_authors><pubmed_authors>Chen W</pubmed_authors><pubmed_authors>Zeng J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Biochanin A abrogates osteoclastogenesis in type 2 diabetic osteoporosis via regulating ROS/MAPK signaling pathway based on integrating molecular docking and experimental validation.</name><description>&lt;h4>Background&lt;/h4>There are accumulating type 2 diabetes patients who have osteoporosis simultaneously. More effective therapeutic strategies should be discovered. Biochanin A (BCA) has been indicated that can play a role in improving metabolic disorders of type 2 diabetes and preventing osteoporosis. But whether BCA can treat type 2 diabetic osteoporosis has not been studied.&lt;h4>Purpose&lt;/h4>To investigate if the BCA can protect against type 2 diabetic osteoporosis and clarify the mechanism.&lt;h4>Methods&lt;/h4&gt;Micro-CT and histology assays were performed to detect the trabecular bone and analyze the bone histomorphology effect of BCA. CCK-8 assay was performed to detect the toxicity of BCA. TRAcP staining, immunofluorescence and hydroxyapatite resorption assay were used to observe osteoclasts</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jan</publication><modification>2026-06-02T06:59:56.303Z</modification><creation>2025-04-04T19:22:30.751Z</creation></dates><accession>S-EPMC10773052</accession><cross_references><pubmed>38191438</pubmed><doi>10.1186/s12906-023-04332-x</doi></cross_references></HashMap>