Fluoroquinolones suppress gluconeogenesis by inhibiting fructose 1, 6-bisphosphatase in primary monkey hepatocytes. (June 2020)
- Record Type:
- Journal Article
- Title:
- Fluoroquinolones suppress gluconeogenesis by inhibiting fructose 1, 6-bisphosphatase in primary monkey hepatocytes. (June 2020)
- Main Title:
- Fluoroquinolones suppress gluconeogenesis by inhibiting fructose 1, 6-bisphosphatase in primary monkey hepatocytes
- Authors:
- Iguchi, Takuma
Goto, Koichi
Watanabe, Kyoko
Hashimoto, Kazuyuki
Suzuki, Takami
Kishino, Hiroyuki
Fujimoto, Kazunori
Mori, Kazuhiko - Abstract:
- Abstract: Dysglycemia is one of the most serious adverse events associated with the clinical use of certain fluoroquinolones. The purpose of this study was to investigate the effects of the representative fluoroquinolones moxifloxacin and gatifloxacin on hepatic gluconeogenesis using primary monkey hepatocytes. Glucose production was induced after the cells were incubated for 4 h with 10 mM sodium lactate and 1 mM sodium pyruvate as gluconeogenic substrates. Under these conditions, moxifloxacin and gatifloxacin dose-dependently suppressed gluconeogenesis at concentrations of 100 μM or higher. Transcriptome analysis of rate-limiting enzymes involved in hepatic gluconeogenesis revealed that moxifloxacin and gatifloxacin at a concentration of 1000 μM did not affect the expression of key gluconeogenic enzymes such as phosphoenolpyruvate carboxykinase, glucose 6-phosphatase, and fructose 1, 6-bisphosphatase. Furthermore, metabolome analysis, in vitro glucose production assay using additional gluconeogenic substrates, and fructose 1, 6-bisphosphatase assay using the cell extracts showed that fluoroquinolones enzymatically suppressed hepatic gluconeogenesis by inhibiting fructose 1, 6-bisphosphatase. These inhibitory effects may involve in the clinically relevant dysglycemia associated with fluoroquinolones in human. Highlights: Fluoroquinolones suppressed gluconeogenesis in primary monkey hepatocytes. Fluoroquinolones did not affect the gene expression levels of gluconeogenicAbstract: Dysglycemia is one of the most serious adverse events associated with the clinical use of certain fluoroquinolones. The purpose of this study was to investigate the effects of the representative fluoroquinolones moxifloxacin and gatifloxacin on hepatic gluconeogenesis using primary monkey hepatocytes. Glucose production was induced after the cells were incubated for 4 h with 10 mM sodium lactate and 1 mM sodium pyruvate as gluconeogenic substrates. Under these conditions, moxifloxacin and gatifloxacin dose-dependently suppressed gluconeogenesis at concentrations of 100 μM or higher. Transcriptome analysis of rate-limiting enzymes involved in hepatic gluconeogenesis revealed that moxifloxacin and gatifloxacin at a concentration of 1000 μM did not affect the expression of key gluconeogenic enzymes such as phosphoenolpyruvate carboxykinase, glucose 6-phosphatase, and fructose 1, 6-bisphosphatase. Furthermore, metabolome analysis, in vitro glucose production assay using additional gluconeogenic substrates, and fructose 1, 6-bisphosphatase assay using the cell extracts showed that fluoroquinolones enzymatically suppressed hepatic gluconeogenesis by inhibiting fructose 1, 6-bisphosphatase. These inhibitory effects may involve in the clinically relevant dysglycemia associated with fluoroquinolones in human. Highlights: Fluoroquinolones suppressed gluconeogenesis in primary monkey hepatocytes. Fluoroquinolones did not affect the gene expression levels of gluconeogenic enzymes. Fluoroquinolones enzymatically suppressed fructose 1, 6-bisphosphatase. … (more)
- Is Part Of:
- Toxicology in vitro. Volume 65(2020)
- Journal:
- Toxicology in vitro
- Issue:
- Volume 65(2020)
- Issue Display:
- Volume 65, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 65
- Issue:
- 2020
- Issue Sort Value:
- 2020-0065-2020-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-06
- Subjects:
- Gluconeogenesis -- Fructose 1, 6-bisphosphatase -- Fluoroquinolones -- Hepatocyte -- Cynomolgus monkey
Toxicity testing -- In vitro -- Periodicals
Toxicology -- Periodicals
615.9 - Journal URLs:
- http://www.sciencedirect.com/science/journal/08872333 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.tiv.2020.104786 ↗
- Languages:
- English
- ISSNs:
- 0887-2333
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8873.043400
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13354.xml