{"title":"Protective Effects of Hydrothermal Extract of Crassula “Buddha's Temple” on Oxidative Stress and Lipid Metabolism in 2D and 3D Adipocyte Models","authors":"Eun Hye Park, Sung-Jo Kim","doi":"10.1002/cbf.70117","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p><i>Crassula</i> “Buddha's Temple” aqueous extract (BTAE), prepared via an optimized, reproducible hydrothermal extraction, exhibits protective antioxidant and lipid regulatory effects in adipocyte models subjected to oxidative stress. The phytochemical profile of BTAE revealed a chemically diverse composition enriched in polyphenols (chlorogenic acid, quercetin, kaempferol, catechin) alongside sulfur-containing metabolites, tricarboxylic acid cycle intermediates, nucleotides, and peptide-like compounds, indicating multifaceted biochemical activity. In both 2D monolayer and advanced 3D bioprinted 3T3-L1 adipocyte cultures exposed to <i>tert</i>-butyl hydroperoxide (tBHP), BTAE pretreatment (5.7 ng/mL) significantly attenuated cytotoxicity, reduced intracellular and mitochondrial reactive oxygen species accumulation, preserved mitochondrial membrane potential, and suppressed lipid peroxidation. Concurrently, BTAE modulated gene expression by downregulating proapoptotic (Bax, CASP3) and lipogenic genes (GPAT1, ABHD5) while upregulating the antiapoptotic gene Bcl2. Notably, BTAE's efficacy matched or exceeded that of <i>N</i>-acetylcysteine, a standard antioxidant control. Enhanced bioactivity of BTAE in 3D adipocyte constructs suggests physiological microenvironment-dependent potentiation of its cytoprotective and metabolic regulatory functions. These findings support BTAE's potential as a natural, safe, and cost-effective candidate for mitigating oxidative stress and lipid dysregulation in adipose tissues, with implications for metabolic disease therapeutics including nonalcoholic fatty liver disease.</p></div>","PeriodicalId":9669,"journal":{"name":"Cell Biochemistry and Function","volume":"43 9","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell Biochemistry and Function","FirstCategoryId":"99","ListUrlMain":"https://analyticalsciencejournals.onlinelibrary.wiley.com/doi/10.1002/cbf.70117","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Crassula “Buddha's Temple” aqueous extract (BTAE), prepared via an optimized, reproducible hydrothermal extraction, exhibits protective antioxidant and lipid regulatory effects in adipocyte models subjected to oxidative stress. The phytochemical profile of BTAE revealed a chemically diverse composition enriched in polyphenols (chlorogenic acid, quercetin, kaempferol, catechin) alongside sulfur-containing metabolites, tricarboxylic acid cycle intermediates, nucleotides, and peptide-like compounds, indicating multifaceted biochemical activity. In both 2D monolayer and advanced 3D bioprinted 3T3-L1 adipocyte cultures exposed to tert-butyl hydroperoxide (tBHP), BTAE pretreatment (5.7 ng/mL) significantly attenuated cytotoxicity, reduced intracellular and mitochondrial reactive oxygen species accumulation, preserved mitochondrial membrane potential, and suppressed lipid peroxidation. Concurrently, BTAE modulated gene expression by downregulating proapoptotic (Bax, CASP3) and lipogenic genes (GPAT1, ABHD5) while upregulating the antiapoptotic gene Bcl2. Notably, BTAE's efficacy matched or exceeded that of N-acetylcysteine, a standard antioxidant control. Enhanced bioactivity of BTAE in 3D adipocyte constructs suggests physiological microenvironment-dependent potentiation of its cytoprotective and metabolic regulatory functions. These findings support BTAE's potential as a natural, safe, and cost-effective candidate for mitigating oxidative stress and lipid dysregulation in adipose tissues, with implications for metabolic disease therapeutics including nonalcoholic fatty liver disease.
期刊介绍:
Cell Biochemistry and Function publishes original research articles and reviews on the mechanisms whereby molecular and biochemical processes control cellular activity with a particular emphasis on the integration of molecular and cell biology, biochemistry and physiology in the regulation of tissue function in health and disease.
The primary remit of the journal is on mammalian biology both in vivo and in vitro but studies of cells in situ are especially encouraged. Observational and pathological studies will be considered providing they include a rational discussion of the possible molecular and biochemical mechanisms behind them and the immediate impact of these observations to our understanding of mammalian biology.