{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["11(20)"],"submitter":["Oh HJ"],"pubmed_abstract":["Since skeletal muscle atrophy resulting from various causes accelerates the progression of several diseases, its prevention should help maintain health and quality of life. A range of natural materials have been investigated for their potential preventive effects against muscle atrophy. Here, ethanol extracts of <i>Angelica gigas</i> and <i>Artemisia dracunculus</i> were concentrated and dried, and mixed at a ratio of 7:3 to create the mixture CHDT. We then evaluated the potential for CHDT to prevent muscle atrophy and explored the mechanisms involved. CHDT was orally administered to C57BL/6 mice daily for 30 days, and dexamethasone (Dex) was intraperitoneally injected daily to induce muscle atrophy from 14 days after the start of oral administration. We found that CHDT prevented the Dex-i"],"journal":["Cells"],"pagination":["3245"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9600779"],"repository":["biostudies-literature"],"pubmed_title":["A Combined <i>Angelica gigas</i> and <i>Artemisia dracunculus</i> Extract Prevents Dexamethasone-Induced Muscle Atrophy in Mice through the Akt/mTOR/FoxO3a Signaling Pathway."],"pmcid":["PMC9600779"],"pubmed_authors":["Oh HJ","Jin H","Lee OH","Lee BY","Kim BY"],"additional_accession":[]},"is_claimable":false,"name":"A Combined <i>Angelica gigas</i> and <i>Artemisia dracunculus</i> Extract Prevents Dexamethasone-Induced Muscle Atrophy in Mice through the Akt/mTOR/FoxO3a Signaling Pathway.","description":"Since skeletal muscle atrophy resulting from various causes accelerates the progression of several diseases, its prevention should help maintain health and quality of life. A range of natural materials have been investigated for their potential preventive effects against muscle atrophy. Here, ethanol extracts of <i>Angelica gigas</i> and <i>Artemisia dracunculus</i> were concentrated and dried, and mixed at a ratio of 7:3 to create the mixture CHDT. We then evaluated the potential for CHDT to prevent muscle atrophy and explored the mechanisms involved. CHDT was orally administered to C57BL/6 mice daily for 30 days, and dexamethasone (Dex) was intraperitoneally injected daily to induce muscle atrophy from 14 days after the start of oral administration. We found that CHDT prevented the Dex-i","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Oct","modification":"2025-04-03T21:29:37.565Z","creation":"2025-04-03T21:29:37.565Z"},"accession":"S-EPMC9600779","cross_references":{"pubmed":["36291111"],"doi":["10.3390/cells11203245"]}}