2007
DOI: 10.1016/j.jep.2007.08.028
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Hibiscus sabdariffa L. water extract inhibits the adipocyte differentiation through the PI3-K and MAPK pathway

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Cited by 73 publications
(56 citation statements)
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“…Effect of ADE extract to inhibit the differentiation of 3T3L1 preadipocyte to mature adipocyte was carried out based on reported protocol (Kim et al 2007). Briefly, 3T3L1 preadipocyte cells were maintained by 10 % FBS in DMEM containing 4.5 g/L glucose, 100 U/mL penicillin, 0.1 mg/mL streptomycin and 0.25 mg/mL amphotericin B at 37°C in 5 % CO 2 incubator.…”
Section: Adipocyte Differentiation Assaymentioning
confidence: 99%
“…Effect of ADE extract to inhibit the differentiation of 3T3L1 preadipocyte to mature adipocyte was carried out based on reported protocol (Kim et al 2007). Briefly, 3T3L1 preadipocyte cells were maintained by 10 % FBS in DMEM containing 4.5 g/L glucose, 100 U/mL penicillin, 0.1 mg/mL streptomycin and 0.25 mg/mL amphotericin B at 37°C in 5 % CO 2 incubator.…”
Section: Adipocyte Differentiation Assaymentioning
confidence: 99%
“…[48][49][50] Evidence shows the influence of plant compounds in cell-signaling pathways that may lead to regulation of cell differentiation 50 and function. 51 The establishment and function of the human placenta depend on the proliferation, migration, and invasion of trophoblasts into the maternal deciduas and myometrium.…”
Section: Discussionmentioning
confidence: 99%
“…Cells were seeded in 9.2-cm 2 Petri plates (1.8 · 10 5 cell/plate) and incubated for 24 hours in 5% CO 2 and 95% humidity. Then, cells were treated with (1) the MAPK inhibitors PD98059 (50 lM) or SB203580 (10 lM), (2) plant extract (50,250, and 500 lg/mL) with or without FKL (50 lM), (3) FKL (50 lM), and (4) DMSO only (concentration of vehicle present in PD98059/SB203580-treated cells < 0.1%). Doses of MAPK inhibitors were established by dose-dependent tests (data not shown) and reports in the literature.…”
Section: Morphologic Evaluation Of Trophoblast Differentiation By Immmentioning
confidence: 99%
“…The PBEE-induced decrease in PPARγ and C/EBPα expression suggested that another PBEE target molecule lay upstream of PPARγ and C/EBPα. To elucidate the signaling pathway through which PBEE affected preadipocyte proliferation, we first examined the possible involvement of ERKs, which have been linked to adipocyte differentiation [23,24]. However, PBEE treatment did not affect ERK phosphorylation.…”
Section: Discussionmentioning
confidence: 99%