2017
DOI: 10.1007/s10811-017-1215-2
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Ethanolic extract of Sargassum serratifolium inhibits adipogenesis in 3T3-L1 preadipocytes by cell cycle arrest

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Cited by 17 publications
(16 citation statements)
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“…Cellular TYR activity was measured as l -DOPA oxidase activity by a previously described method [26] with some modifications. Cells were seeded at 1 × 10 4 cells/well in a 24-well plate, incubated for 24 h and then stimulated with α-MSH (3 μM) in the presence or absence of 974-A, phlorofucofuroeckol-A, or eckol for 24 h. After treatment, the cells were washed with cold PBS and lysed with RIPA buffer.…”
Section: Methodsmentioning
confidence: 99%
“…Cellular TYR activity was measured as l -DOPA oxidase activity by a previously described method [26] with some modifications. Cells were seeded at 1 × 10 4 cells/well in a 24-well plate, incubated for 24 h and then stimulated with α-MSH (3 μM) in the presence or absence of 974-A, phlorofucofuroeckol-A, or eckol for 24 h. After treatment, the cells were washed with cold PBS and lysed with RIPA buffer.…”
Section: Methodsmentioning
confidence: 99%
“…The adipocyte differentiation is regulated by several adipogenicspecific genes, such as peroxisome proliferator-activated receptorγ (PPARγ), CCAA/enhancer-binding protein (C/ EBP) family members and fatty acid binding protein (FABP) [20][21][22][23]. Moreover, the adipocyte differentiation is extensively regulated through crosstalk between the cell cycle regulators and adipogenic transcription factors [12,24,25]. The process of adipogenesis is divided into several phases, including growth arrest, mitotic clonal expansion (MCE), lipid accumulation, and late phase of differentiation [26].…”
Section: Introductionmentioning
confidence: 99%
“…The cellular TYR activity was measured as the L-DOPA oxidase activity using a previously described method with some modifications [11,12]. The B16F10 cells were seeded and incubated for 24 h in a 24 well plate in the presence or absence of the sample for 72 h. After treatment, the cells were washed with cold PBS and lysed with lysis buffer (0.1 M sodium phosphate buffer, 1% Triton X-100 and 0.1 mM PMSF).…”
Section: Cellular Tyr Activity Assaymentioning
confidence: 99%