Marine Drugs · 2024 · 12 citations · 31 references
Life SciencesBiochemistryPhysiologyCell SignalingMetabolismSignal TransductionAdipocyte DifferentiationAdipose TissueFatty Acid MetabolismLipid Biosynthesis InhibitionLipid MetabolismMetabolic SignalingAdipocyte BiologyAdipocyte MetabolismAdipose Tissue BrowningLipid AccumulationLipogenesis RegulationLipolytic ActivityNrf2 Pathway ActivationNrf2 Signaling Pathway
(EC-ETAC) on 3T3-L1 preadipocytes, focusing on its impact on adipogenesis, lipolysis, and adipose browning via the HO-1/Nrf2 pathway. Western blot analysis revealed that EC-ETAC significantly inhibited adipogenic transcription factors (PPARγ, C/EBPα, SREBP-1) and lipogenesis-related proteins (FAS, LPL). Concurrently, EC-ETAC enhanced lipolytic markers (p-AMPK, p-HSL) and adipose browning-related proteins (UCP-1, PGC-1α), indicating its role in promoting lipolysis and adipose browning. The inhibition of HO-1 by zinc protoporphyrin (ZnPP) significantly reversed these effects, underscoring the critical role of HO-1 in mediating the anti-obesity properties of EC-ETAC. Additionally, fluorescence measurements and Oil Red O staining confirmed the reduction of lipid accumulation and oxidative stress upon EC-ETAC treatment. These findings suggest that EC-ETAC exerts its anti-obesity effects by modulating the HO-1/Nrf2 pathway, which is crucial for regulating adipogenesis, lipolysis, and adipose browning. This study highlights the potential of EC-ETAC as a natural therapeutic agent for obesity management and supports further research into its clinical applications. By targeting the HO-1/Nrf2 pathway, EC-ETAC could offer a novel approach to enhancing energy expenditure and reducing fat mass, thereby improving metabolic health.
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IRF4 Is a Key Thermogenic Transcriptional Partner of PGC-1α
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Resveratrol induces apoptosis and inhibits adipogenesis in 3T3‐L1 adipocytes
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