The Phytoalexin Resveratrol Ameliorates Ochratoxin A Toxicity in Human Embryonic Kidney (HEK293) Cells. Issue 12 (8th October 2015)
- Record Type:
- Journal Article
- Title:
- The Phytoalexin Resveratrol Ameliorates Ochratoxin A Toxicity in Human Embryonic Kidney (HEK293) Cells. Issue 12 (8th October 2015)
- Main Title:
- The Phytoalexin Resveratrol Ameliorates Ochratoxin A Toxicity in Human Embryonic Kidney (HEK293) Cells
- Authors:
- Raghubeer, Shanel
Nagiah, Savania
Phulukdaree, Alisa
Chuturgoon, Anil - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <sec id="jcb25242-sec-0001" sec-type="section"> <p>Ochratoxin A (OTA) is a nephrotoxic mycotoxin produced by <italic>Aspergillus</italic> and <italic>Penicillium</italic> fungi. It contaminates human and animal food products, and chronic exposure is associated with renal fibrosis in humans (Balkan endemic nephropathy). Resveratrol, a phytoalexin, possesses anti‐cancer and antioxidant properties. We investigated the mechanism of cellular oxidative stress induced by OTA, and the effect of resveratrol in human embryonic kidney (HEK293) cells over 24 and 48 h. Cells were exposed to OTA [IC50 = 1.5 μM (24 h) and 9.4 μM (48 h) determined using MTT assay] and 25 μM resveratrol. Glutathione was quantified by luminometry and gene expression of Nrf2 and OGG1 was determined by qPCR. Protein expression of Nrf2, LonP1, SIRT3, and pSIRT1 was assessed by Western blot, DNA damage (comet assay), and intracellular reactive oxygen species (flow cytometry). At 24 h, resveratrol increased mRNA expression of the DNA repair enzyme, OGG1 (<italic>P</italic> &lt; 0.05), whereas OTA and OTA+resveratrol significantly decreased OGG1 expression (<italic>P</italic> &lt; 0.05). OGG1 expression increased during 48‐h exposure to resveratrol and OTA+resveratrol (<italic>P</italic> &lt; 0.05). Comet tail lengths doubled in 48‐h OTA‐treated cells, whereas at both time periods, OTA+resveratrol yielded shorter comet tails<abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <sec id="jcb25242-sec-0001" sec-type="section"> <p>Ochratoxin A (OTA) is a nephrotoxic mycotoxin produced by <italic>Aspergillus</italic> and <italic>Penicillium</italic> fungi. It contaminates human and animal food products, and chronic exposure is associated with renal fibrosis in humans (Balkan endemic nephropathy). Resveratrol, a phytoalexin, possesses anti‐cancer and antioxidant properties. We investigated the mechanism of cellular oxidative stress induced by OTA, and the effect of resveratrol in human embryonic kidney (HEK293) cells over 24 and 48 h. Cells were exposed to OTA [IC50 = 1.5 μM (24 h) and 9.4 μM (48 h) determined using MTT assay] and 25 μM resveratrol. Glutathione was quantified by luminometry and gene expression of Nrf2 and OGG1 was determined by qPCR. Protein expression of Nrf2, LonP1, SIRT3, and pSIRT1 was assessed by Western blot, DNA damage (comet assay), and intracellular reactive oxygen species (flow cytometry). At 24 h, resveratrol increased mRNA expression of the DNA repair enzyme, OGG1 (<italic>P</italic> &lt; 0.05), whereas OTA and OTA+resveratrol significantly decreased OGG1 expression (<italic>P</italic> &lt; 0.05). OGG1 expression increased during 48‐h exposure to resveratrol and OTA+resveratrol (<italic>P</italic> &lt; 0.05). Comet tail lengths doubled in 48‐h OTA‐treated cells, whereas at both time periods, OTA+resveratrol yielded shorter comet tails (<italic>P</italic> &lt; 0.0001). During 24‐ and 48‐h exposure, OTA, resveratrol, and OTA+resveratrol significantly decreased mRNA expression of Nrf2 (<italic>P</italic> &lt; 0.05). Luminometry analysis of GSH revealed an increase by OTA+resveratrol for 24 and 48 h (<italic>P</italic> &lt; 0.05 and <italic>P</italic> &lt; 0.001, respectively). Western blot analysis showed decreased Nrf2 protein expression during 24‐h exposure, but increased Nrf2 expression during 48 h. LonP1 protein expression increased during 24‐h exposure to OTA (<italic>P</italic> &lt; 0.05) and OTA+resveratrol (<italic>P</italic> &lt; 0.0011) and during 48‐h exposure to resveratrol (<italic>P</italic> &lt; 0.0005). J. Cell. Biochem. 116: 2947–2955, 2015. © 2015 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of cellular biochemistry. Volume 116:Issue 12(2015:Dec.)
- Journal:
- Journal of cellular biochemistry
- Issue:
- Volume 116:Issue 12(2015:Dec.)
- Issue Display:
- Volume 116, Issue 12 (2015)
- Year:
- 2015
- Volume:
- 116
- Issue:
- 12
- Issue Sort Value:
- 2015-0116-0012-0000
- Page Start:
- 2947
- Page End:
- 2955
- Publication Date:
- 2015-10-08
- Subjects:
- Cytochemistry -- Periodicals
572 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4644 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jcb.25242 ↗
- Languages:
- English
- ISSNs:
- 0730-2312
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4955.010000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3135.xml