Influence of microcystin-LR on the activity of membrane enzymes in rat intestinal mucosa

J Physiol Biochem. 2003 Dec;59(4):293-9. doi: 10.1007/BF03179887.

Abstract

The objective of the present study was to evaluate the effects of microcystin-LR (MCLR) on the activity of membrane enzymes from intestinal mucosa. In addition, serum chemistry and peroxidative status of both serum and intestinal homogenate were evaluated after treatment with MCLR. Wistar rats were treated with intraperitoneal injection of either 100 microg pure MCLR/Kg body weight or saline solution. A significant increase in liver weight and altered serum enzyme activities were found in MCLR-treated rats, indicating damage to the liver in these rats, as previously suggested. A higher specific activity of sucrase (1.5-fold) was observed after the administration of MCLR, whereas other intestinal apical membrane enzymes, such as lactase, maltase and alkaline phosphatase were not modified by the treatment. The specific activities of acid phosphatase and succinate dehydrogenase, markers for lysosomal and mitochondrial membranes, respectively, were also increased (32% and 60%, respectively) in treated rats. The analysis of lipid peroxidation showed that the peroxidative status was increased in both serum and intestinal mucosa from MCLR-treated rats, reflecting an excess production of oxygen free radicals induced by this cyanobacterial toxin. In conclusion, this study shows that acute exposure to MCLR affects the intestinal physiology by modifying the intestinal peroxidation status as well as the activity of membrane enzymes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Toxins / metabolism
  • Bacterial Toxins / pharmacology
  • Blood Chemical Analysis
  • Cell Membrane / drug effects
  • Cell Membrane / enzymology*
  • Enzyme Inhibitors / metabolism*
  • Intestinal Mucosa / cytology
  • Intestinal Mucosa / drug effects*
  • Intestinal Mucosa / enzymology*
  • Lipid Peroxidation
  • Male
  • Marine Toxins
  • Microcystins
  • Peptides, Cyclic / metabolism*
  • Peptides, Cyclic / pharmacology*
  • Rats
  • Rats, Wistar

Substances

  • Bacterial Toxins
  • Enzyme Inhibitors
  • Marine Toxins
  • Microcystins
  • Peptides, Cyclic
  • cyanoginosin LR