Hepatic and intestine alterations in mice after prolonged exposure to low oral doses of Microcystin-LR. (15th September 2015)
- Record Type:
- Journal Article
- Title:
- Hepatic and intestine alterations in mice after prolonged exposure to low oral doses of Microcystin-LR. (15th September 2015)
- Main Title:
- Hepatic and intestine alterations in mice after prolonged exposure to low oral doses of Microcystin-LR
- Authors:
- Sedan, Daniela
Laguens, Martín
Copparoni, Guido
Aranda, Jorge Oswaldo
Giannuzzi, Leda
Marra, Carlos Alberto
Andrinolo, Darío - Abstract:
- Abstract: Oral intake of Microcystin-LR (MC-LR) is the principal route of exposure to this toxin, with prolonged exposure leading to liver damage of unspecific symptomatology. The aim of the present paper was therefore to investigate the liver and intestine damage generated by prolonged oral exposure to low MC-LR doses (50 and 100 μg MC-LR/kg body weight, administrated every 48 h during a month) in a murine model. We found alterations in TBARS, SOD activity and glutathione content in liver and intestine of mice exposed to both doses of MC-LR. Furthermore, the presence of MC-LR was detected in both organs. We also found hepatic steatosis (3.6 ± 0.6% and 15.3 ± 1.6%) and a decrease in intraepithelial lymphocytes (28.7 ± 5.0% and 44.2 ± 8.7%) in intestine of 50- and 100-μg MC-LR/kg treated animals, respectively. This result could have important implications for mucosal immunity, since intraepithelial lymphocytes are the principal effectors of this system. Our results indicate that prolonged oral exposure at 50 μg MC-LR/kg every 48 h generates significant damage not only in liver but also in intestine. This finding calls for a re-appraisal of the currently accepted NOAEL (No Observed Adverse Effect Level), 40 μg MC-LR/kg body weight, used to derive the guideline value for MC-LR in drinking water. Highlights: MC-LR prolonged oral exposure to low doses generates hepatic steatosis. MC-LR prolonged oral exposure to low doses cause decrease in intestinal intraepithelial lymphocytes.Abstract: Oral intake of Microcystin-LR (MC-LR) is the principal route of exposure to this toxin, with prolonged exposure leading to liver damage of unspecific symptomatology. The aim of the present paper was therefore to investigate the liver and intestine damage generated by prolonged oral exposure to low MC-LR doses (50 and 100 μg MC-LR/kg body weight, administrated every 48 h during a month) in a murine model. We found alterations in TBARS, SOD activity and glutathione content in liver and intestine of mice exposed to both doses of MC-LR. Furthermore, the presence of MC-LR was detected in both organs. We also found hepatic steatosis (3.6 ± 0.6% and 15.3 ± 1.6%) and a decrease in intraepithelial lymphocytes (28.7 ± 5.0% and 44.2 ± 8.7%) in intestine of 50- and 100-μg MC-LR/kg treated animals, respectively. This result could have important implications for mucosal immunity, since intraepithelial lymphocytes are the principal effectors of this system. Our results indicate that prolonged oral exposure at 50 μg MC-LR/kg every 48 h generates significant damage not only in liver but also in intestine. This finding calls for a re-appraisal of the currently accepted NOAEL (No Observed Adverse Effect Level), 40 μg MC-LR/kg body weight, used to derive the guideline value for MC-LR in drinking water. Highlights: MC-LR prolonged oral exposure to low doses generates hepatic steatosis. MC-LR prolonged oral exposure to low doses cause decrease in intestinal intraepithelial lymphocytes. We report MC-LR lowest dose which cause intestinal alterations by oral prolonged exposure. Our results suggest that the NOAEL currently accepted shall be discussed. … (more)
- Is Part Of:
- Toxicon. Volume 104(2015)
- Journal:
- Toxicon
- Issue:
- Volume 104(2015)
- Issue Display:
- Volume 104, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 104
- Issue:
- 1
- Issue Sort Value:
- 2015-0104-0001-0000
- Page Start:
- 26
- Page End:
- 33
- Publication Date:
- 2015-09-15
- Subjects:
- Oral exposure -- Microcystin-LR -- Prolonged intoxication -- Intraepithelial lymphocytes
Toxins -- Periodicals
Venom -- Periodicals
615.9 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00410101 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.toxicon.2015.07.011 ↗
- Languages:
- English
- ISSNs:
- 0041-0101
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8873.050000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 9016.xml