CYP3A suppression during diet-induced nonalcoholic fatty liver disease is independent of PXR regulation. (1st August 2019)
- Record Type:
- Journal Article
- Title:
- CYP3A suppression during diet-induced nonalcoholic fatty liver disease is independent of PXR regulation. (1st August 2019)
- Main Title:
- CYP3A suppression during diet-induced nonalcoholic fatty liver disease is independent of PXR regulation
- Authors:
- Zeng, Hang
Lin, Yiming
Gong, Jiande
Lin, Sisi
Gao, Jianguo
Li, Chunxiao
Feng, Zemin
Zhang, Hong
Zhang, Jie
Li, Youming
Yu, Chaohui - Abstract:
- Abstract: Cytochrome P450 3A (CYP3A) activity is inhibited, and its expression is suppressed during many diseases, including nonalcoholic fatty liver disease (NAFLD). However, the mechanism is controversial. Here, we report that PXR may not take part in the downregulation of CYP3A during NAFLD. Hepatic CYP3A11 (major subtype of mouse CYP3A) mRNA and protein expression was significantly decreased in both mice fed a high-fat diet (HFD) for 8 weeks and palmitate (PA)-treated mouse primary hepatocytes. Similarly, in HepG2 cells, PA treatment significantly suppressed the CYP3A4 (major subtype of human CYP3A) mRNA level and promoter transcription activity. However, Western blotting analysis found an induction of PXR nuclear translocation during NAFLD in both in vivo and in vitro models. Moreover, immunofluorescence determination also found nuclear translocation effect of PXR by PA stimulation in HepG2 cells. In addition, the siRNA knockdown of PXR did not affect the suppressive effects of PA on the CYP3A4 promoter transcription activity and mRNA levels in HepG2 cells. Similarly, PXR knockdown also did not affect the suppressive effects of PA on CYP3A11 mRNA and protein expression levels in mouse primary hepatoctyes. Taken together, the results showed that the suppressive effect of CYP3A transcription was independent of PXR regulation. Highlights: CYP3A expression is suppressed by NAFLD modelling. PXR translocation is induced by NAFLD modelling. PXR silence did not affect theAbstract: Cytochrome P450 3A (CYP3A) activity is inhibited, and its expression is suppressed during many diseases, including nonalcoholic fatty liver disease (NAFLD). However, the mechanism is controversial. Here, we report that PXR may not take part in the downregulation of CYP3A during NAFLD. Hepatic CYP3A11 (major subtype of mouse CYP3A) mRNA and protein expression was significantly decreased in both mice fed a high-fat diet (HFD) for 8 weeks and palmitate (PA)-treated mouse primary hepatocytes. Similarly, in HepG2 cells, PA treatment significantly suppressed the CYP3A4 (major subtype of human CYP3A) mRNA level and promoter transcription activity. However, Western blotting analysis found an induction of PXR nuclear translocation during NAFLD in both in vivo and in vitro models. Moreover, immunofluorescence determination also found nuclear translocation effect of PXR by PA stimulation in HepG2 cells. In addition, the siRNA knockdown of PXR did not affect the suppressive effects of PA on the CYP3A4 promoter transcription activity and mRNA levels in HepG2 cells. Similarly, PXR knockdown also did not affect the suppressive effects of PA on CYP3A11 mRNA and protein expression levels in mouse primary hepatoctyes. Taken together, the results showed that the suppressive effect of CYP3A transcription was independent of PXR regulation. Highlights: CYP3A expression is suppressed by NAFLD modelling. PXR translocation is induced by NAFLD modelling. PXR silence did not affect the suppressive effect of PA on CYP3A in vitro . … (more)
- Is Part Of:
- Chemico-biological interactions. Volume 308(2019)
- Journal:
- Chemico-biological interactions
- Issue:
- Volume 308(2019)
- Issue Display:
- Volume 308, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 308
- Issue:
- 2019
- Issue Sort Value:
- 2019-0308-2019-0000
- Page Start:
- 185
- Page End:
- 193
- Publication Date:
- 2019-08-01
- Subjects:
- CYP3A -- NALFD -- PXR
Biochemistry -- Periodicals
Toxicological chemistry -- Periodicals
Biochemistry -- Periodicals
Biologie moléculaire -- Périodiques
Biochimie -- Périodiques
Toxicologie biochimique -- Périodiques
572 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00092797 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.cbi.2019.05.038 ↗
- Languages:
- English
- ISSNs:
- 0009-2797
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3155.500000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 25190.xml