Chinese Journal of Chromatography ›› 2024, Vol. 42 ›› Issue (2): 131-141.DOI: 10.3724/SP.J.1123.2023.12018
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LIU Huinan1,2, SUN Zhendong3, LIU Qian S.1, ZHOU Qunfang1,2,3,*(
), JIANG Guibin1,2,3
Received:2023-12-17
Online:2024-02-08
Published:2024-02-20
Supported by:CLC Number:
LIU Huinan, SUN Zhendong, LIU Qian S., ZHOU Qunfang, JIANG Guibin. Synthetic phenolic compounds perturb lipid metabolism and induce obesogenic effects[J]. Chinese Journal of Chromatography, 2024, 42(2): 131-141.
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URL: https://www.chrom-china.com/EN/10.3724/SP.J.1123.2023.12018
| Chemical | Test tissue | Model | Effects | Mechanisms |
|---|---|---|---|---|
| BPA | adipocytes | 3T3-L1 | ↑ lipid storage[ | lipogenesis[ autophagosome-lysosome fusion[ |
| insulin resistant[ | inflammation[ | |||
| C3H10T1/2 | — adipogenesis[ | |||
| rASCs | ↑ adipose differentiation[ | |||
| hASCs | ↑ lipid storage[ | lipogenesis[ | ||
| zebrafish | ↑ lipid storage, ↑appetite[ | CB1 signal[ | ||
| hepatic tissue | HepG2 | ↑ lipid storage[ | inflammation, ER signal[ | |
| HUH-7 | ↑ lipid storage[ | oxidation[ | ||
| mouse | ↑ lipid storage[ | inflammation[ methylation patterns[ | ||
| zebrafish | ↑ lipid storage[ | lipogenesis, ↓TG degradation[ | ||
| male Gobiocypris rarus | ↑ lipid storage[ | lipogenesis, ↓TG degradation[ | ||
| chicken | ↑ lipid storage, ferroptosis[ | fatty acid synthesis/uptake, inflammation, GPER signal[ | ||
| BPA-G | adipocytes | 3T3-L1 and primary human preadipocytes | ↑ lipid storage, ↑ adipose differentiation[ | non-classical ER transcriptional activation[ |
| BPAF | adipocytes | hASCs | ↑ adipogenesis at a low dose[ | |
| hepatic tissue | mouse | ↓ lipid storage[ | PPAR signal[ | |
| BPB | adipocytes | 3T3-L1 | ↑ lipid storage[ | |
| BPE | adipocytes | 3T3-L1 | ↑ lipid storage[ | |
| BPF | adipocytes | 3T3-L1 | ↑ lipid storage[ | lipogenesis[ |
| — adipogenesis, ↓ insulin-stimulated glucose metabolism[ | inhibiting IRS-1/PI3K/AKT pathway[ | |||
| ↓ differentiation genes expression[ | ||||
| ↓ expressions of leptin, adiponectin and apelin[ | ||||
| hASCs | ↑ lipid storage, ↓ adipogenic markers[ | ER signal[ | ||
| hepatic tissue | mouse | ↓ lipid storage[ | PPAR signal[ | |
| zebrafish | ↑ lipid storage[ | intestinal cell heterogeneous response[ | ||
| BPS | adipocytes | 3T3-L1 | ↑ lipid storage[ | |
| primary human preadipocytes | ↑ lipid storage, ↑ adipose differentiation[ | PPARγ, GR signal[ | ||
| hASCs | ↑ lipid storage[ | |||
| perinatal exposure in mouse | ↑ weight, ↑ TG and T-cholesterol accumulation[ | inflammation[ | ||
| multigenerational obesogenic effect[ | ||||
| zebrafish | ↑ lipid storage[ | De novo synthesis[ | ||
| hepatic tissue | zebrafish | ↑ TG, T-cholesterol accumulation, ↑ ALT, AST[ | endoplasmic reticulum stress response[ | |
| TMBPF | adipocytes | hASCs | ↓ adipogenesis, cytotoxicity[ |
Table 1 Studies related to lipid metabolism of bisphenol A (BPA) and its analogues
| Chemical | Test tissue | Model | Effects | Mechanisms |
|---|---|---|---|---|
| BPA | adipocytes | 3T3-L1 | ↑ lipid storage[ | lipogenesis[ autophagosome-lysosome fusion[ |
| insulin resistant[ | inflammation[ | |||
| C3H10T1/2 | — adipogenesis[ | |||
| rASCs | ↑ adipose differentiation[ | |||
| hASCs | ↑ lipid storage[ | lipogenesis[ | ||
| zebrafish | ↑ lipid storage, ↑appetite[ | CB1 signal[ | ||
| hepatic tissue | HepG2 | ↑ lipid storage[ | inflammation, ER signal[ | |
| HUH-7 | ↑ lipid storage[ | oxidation[ | ||
| mouse | ↑ lipid storage[ | inflammation[ methylation patterns[ | ||
| zebrafish | ↑ lipid storage[ | lipogenesis, ↓TG degradation[ | ||
| male Gobiocypris rarus | ↑ lipid storage[ | lipogenesis, ↓TG degradation[ | ||
| chicken | ↑ lipid storage, ferroptosis[ | fatty acid synthesis/uptake, inflammation, GPER signal[ | ||
| BPA-G | adipocytes | 3T3-L1 and primary human preadipocytes | ↑ lipid storage, ↑ adipose differentiation[ | non-classical ER transcriptional activation[ |
| BPAF | adipocytes | hASCs | ↑ adipogenesis at a low dose[ | |
| hepatic tissue | mouse | ↓ lipid storage[ | PPAR signal[ | |
| BPB | adipocytes | 3T3-L1 | ↑ lipid storage[ | |
| BPE | adipocytes | 3T3-L1 | ↑ lipid storage[ | |
| BPF | adipocytes | 3T3-L1 | ↑ lipid storage[ | lipogenesis[ |
| — adipogenesis, ↓ insulin-stimulated glucose metabolism[ | inhibiting IRS-1/PI3K/AKT pathway[ | |||
| ↓ differentiation genes expression[ | ||||
| ↓ expressions of leptin, adiponectin and apelin[ | ||||
| hASCs | ↑ lipid storage, ↓ adipogenic markers[ | ER signal[ | ||
| hepatic tissue | mouse | ↓ lipid storage[ | PPAR signal[ | |
| zebrafish | ↑ lipid storage[ | intestinal cell heterogeneous response[ | ||
| BPS | adipocytes | 3T3-L1 | ↑ lipid storage[ | |
| primary human preadipocytes | ↑ lipid storage, ↑ adipose differentiation[ | PPARγ, GR signal[ | ||
| hASCs | ↑ lipid storage[ | |||
| perinatal exposure in mouse | ↑ weight, ↑ TG and T-cholesterol accumulation[ | inflammation[ | ||
| multigenerational obesogenic effect[ | ||||
| zebrafish | ↑ lipid storage[ | De novo synthesis[ | ||
| hepatic tissue | zebrafish | ↑ TG, T-cholesterol accumulation, ↑ ALT, AST[ | endoplasmic reticulum stress response[ | |
| TMBPF | adipocytes | hASCs | ↓ adipogenesis, cytotoxicity[ |
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