2017
DOI: 10.1016/j.cbpc.2017.04.003
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PPARα, PPARγ and SREBP-1 pathways mediated waterborne iron (Fe)-induced reduction in hepatic lipid deposition of javelin goby Synechogobius hasta

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Cited by 23 publications
(12 citation statements)
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References 51 publications
(51 reference statements)
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“…Thus, the present study indicated that PPAR α , PPAR γ and SREBP-1 mediated the regulation of lipid deposition and metabolism in the fore- and mid-intestine in yellow catfish. Similarly, several studies reported that these signalling pathways widely mediated mineral element-induced changes in hepatic lipid deposition in fish ( 36 , 38 ) .…”
Section: Discussionmentioning
confidence: 88%
See 1 more Smart Citation
“…Thus, the present study indicated that PPAR α , PPAR γ and SREBP-1 mediated the regulation of lipid deposition and metabolism in the fore- and mid-intestine in yellow catfish. Similarly, several studies reported that these signalling pathways widely mediated mineral element-induced changes in hepatic lipid deposition in fish ( 36 , 38 ) .…”
Section: Discussionmentioning
confidence: 88%
“…Zinc content. For the determination of Zn content, the fore-and mid-intestinal samples were digested in 3 ml concentrated nitric acid at 110°C for 72 h, and diluted to appropriate concentrations for Zn content using ICP-MS (36) . Quality assurance/quality control procedures included analysis of three method blanks (purified water), two certified biological reference tissues (DORM-2 and DORM-4; National Research Council of Canada) and two randomly selected duplicate samples per twenty samples.…”
Section: Samples Analysismentioning
confidence: 99%
“…PPARγ and SREBP1 are two transcription factors that activate numerous downstream genes in the adipogenesis signalling pathway for lipid synthesis and storage (Chen et al, 2017; Lefterova & Lazar, 2009). Here, only intestinal ppar γ abundance was suppressed in response to starvation, but srebp1 transcription remained unaffected (Figure 4f, g).…”
Section: Discussionmentioning
confidence: 99%
“…Five treatments were designed as follows: the control, 20μg/mL nano-ZnO (nano-ZnO group), 2 μM TPEN (TPEN group), 20 μg/mL nano-ZnO + 2 μM TPEN (nano-ZnO + TPEN group), 2 μM Dynasore (Dynasore group), and 20 μg/mL nano-ZnO + 2 μM Dynasore (nano-ZnO + Dynasore group). The concentrations of Zn and the corresponding inhibitors were selected according to our and other studies [ 39 , 40 ]. Each treatment had triplicate groups.…”
Section: Methodsmentioning
confidence: 99%