Effect of dapagliflozin, a sodium‐glucose co‐transporter‐2 inhibitor, on gluconeogenesis in proximal renal tubules. Issue 3 (16th December 2019)
- Record Type:
- Journal Article
- Title:
- Effect of dapagliflozin, a sodium‐glucose co‐transporter‐2 inhibitor, on gluconeogenesis in proximal renal tubules. Issue 3 (16th December 2019)
- Main Title:
- Effect of dapagliflozin, a sodium‐glucose co‐transporter‐2 inhibitor, on gluconeogenesis in proximal renal tubules
- Authors:
- Kim, Jin Hee
Ko, Hae Young
Wang, Hye Jin
Lee, Hyangkyu
Yun, MiJin
Kang, Eun Seok - Abstract:
- Abstract: Aims: To investigate the effect of dapagliflozin, a sodium‐glucose co‐transporter‐2 (SGLT2) inhibitor, on renal gluconeogenesis in vitro, ex vivo and in vivo . Materials and methods: We treated HK‐2 cells (human renal proximal tubule cells) and mouse primary renal proximal tubule cells with dapagliflozin, and evaluated the process of renal gluconeogenesis. We also examined the effect of dapagliflozin on renal gluconeogenesis in normoglycaemic and hyperglycaemic mice. Results: Dapagliflozin enhanced renal gluconeogenesis in vitro, ex vivo and in vivo . It increased phosphoenolpyruvate carboxykinase (PEPCK), glucose‐6‐phosphatase (G6Pase), peroxisome proliferative activated receptor‐gamma co‐activator 1α (PGC‐1α) and phosphorylated cyclic‐AMP response element binding protein (CREB) expression and decreased phosphorylated Forkhead Box O1 (FOXO1) expression in HK‐2 cells, mouse primary renal proximal tubule cells, and the mouse renal cortex. Glutamine enhanced the gluconeogenic effect of dapagliflozin in HK‐2 cells. Also, dapagliflozin increased 14 C‐glutamine utilization in HK‐2 cells. Glucagon did not affect dapagliflozin‐induced enhancement in renal gluconeogenesis in HK‐2 cells. SGLT2 gene knockdown with siRNA resulted in an increase of gluconeogenic gene expression and associated transcription factors in HK‐2 cells. Dapagliflozin reduced fasting plasma glucose levels and improved oral glucose tolerance and insulin tolerance in high‐fat diet‐fed hyperglycaemicAbstract: Aims: To investigate the effect of dapagliflozin, a sodium‐glucose co‐transporter‐2 (SGLT2) inhibitor, on renal gluconeogenesis in vitro, ex vivo and in vivo . Materials and methods: We treated HK‐2 cells (human renal proximal tubule cells) and mouse primary renal proximal tubule cells with dapagliflozin, and evaluated the process of renal gluconeogenesis. We also examined the effect of dapagliflozin on renal gluconeogenesis in normoglycaemic and hyperglycaemic mice. Results: Dapagliflozin enhanced renal gluconeogenesis in vitro, ex vivo and in vivo . It increased phosphoenolpyruvate carboxykinase (PEPCK), glucose‐6‐phosphatase (G6Pase), peroxisome proliferative activated receptor‐gamma co‐activator 1α (PGC‐1α) and phosphorylated cyclic‐AMP response element binding protein (CREB) expression and decreased phosphorylated Forkhead Box O1 (FOXO1) expression in HK‐2 cells, mouse primary renal proximal tubule cells, and the mouse renal cortex. Glutamine enhanced the gluconeogenic effect of dapagliflozin in HK‐2 cells. Also, dapagliflozin increased 14 C‐glutamine utilization in HK‐2 cells. Glucagon did not affect dapagliflozin‐induced enhancement in renal gluconeogenesis in HK‐2 cells. SGLT2 gene knockdown with siRNA resulted in an increase of gluconeogenic gene expression and associated transcription factors in HK‐2 cells. Dapagliflozin reduced fasting plasma glucose levels and improved oral glucose tolerance and insulin tolerance in high‐fat diet‐fed hyperglycaemic mice, although renal gluconeogenesis was enhanced. Conclusions: Dapagliflozin increased levels of gluconeogenic enzyme in the renal cortex and consequently increased renal gluconeogenesis, which is mediated by SGLT2 inhibition. … (more)
- Is Part Of:
- Diabetes, obesity & metabolism. Volume 22:Issue 3(2020)
- Journal:
- Diabetes, obesity & metabolism
- Issue:
- Volume 22:Issue 3(2020)
- Issue Display:
- Volume 22, Issue 3 (2020)
- Year:
- 2020
- Volume:
- 22
- Issue:
- 3
- Issue Sort Value:
- 2020-0022-0003-0000
- Page Start:
- 373
- Page End:
- 382
- Publication Date:
- 2019-12-16
- Subjects:
- antidiabetic drug -- dapagliflozin -- SGLT2 inhibitor -- glycaemic control
Diabetes -- Periodicals
Obesity -- Periodicals
Metabolism -- Disorders -- Periodicals
Clinical pharmacology -- Periodicals
616.462 - Journal URLs:
- http://www.blackwellpublishing.com/journal.asp?ref=1462-8902&site=1 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1463-1326 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/dom.13905 ↗
- Languages:
- English
- ISSNs:
- 1462-8902
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3579.601970
British Library DSC - BLDSS-3PM
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- 17596.xml