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Background: Excessive fat deposition in localized adiposity is known to induce severe medical diseases as well as aesthetic problems. Of late, LIPOSA-T pharmacopuncture, a new herbal pharmacopuncture consisting of the cortex of and bark of , is developed as a non-surgical injection for dissolving localized fat deposits.
Methods: The network pharmacology analysis was carried out with the target gene sets of constituents of and . Male C57BL/6 J mice were induced obesity and injected LIPOSA-T pharmacopuncture into inguinal fat pad. The fat weight and size were analyzed using dual energy X-ray absorptiometry.
Results: The possible pathways and mechanism of action of LIPOSA-T were found to be mainly related to the fatty acid biosynthesis, glycolysis and glycogenesis in KEGG Pathways database. Subcutaneous injection of the LIPOSA-T pharmacopuncture significantly reduced the inguinal fat tissues weight and enlarged adipocyte size. In addition, the phosphorylated IRS with the PEPCK and G6p expressions were increased by the LIPOSA-T injection. Following the increase of AMPK expression, the fatty acid synthesis enzyme and lipolytic enzymes were regulated by the LIPOSA-T.
Conclusions: Taken together, LIPOSA-T exerted the catabolic effects on fat deposition in obesity by regulating the glucose production, lipid synthesis and TAG hydrolysis in consistent with the prediction results. Based on the findings, LIPOSA-T pharmacopuncture is expected to be a dissolving injection for localized fat.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12391440 | PMC |
http://dx.doi.org/10.1016/j.imr.2025.101201 | DOI Listing |
Integr Med Res
December 2025
Department of Convergence Korean Medical Science, College of Korean Medicine, Kyung Hee University, Seoul, Korea.
Background: Excessive fat deposition in localized adiposity is known to induce severe medical diseases as well as aesthetic problems. Of late, LIPOSA-T pharmacopuncture, a new herbal pharmacopuncture consisting of the cortex of and bark of , is developed as a non-surgical injection for dissolving localized fat deposits.
Methods: The network pharmacology analysis was carried out with the target gene sets of constituents of and .