Biochemical and ultrastructural changes of the liver and kidney of the phytoplanktivorous silver carp feeding naturally on toxic Microcystis blooms in Taihu Lake, China

Toxicon. 2007 Jun 1;49(7):1042-53. doi: 10.1016/j.toxicon.2007.01.013. Epub 2007 Feb 8.

Abstract

Many experimental studies have documented the impact of microcystins (MC) on fish based on either intraperitoneal injection, or oral gavaging via the diet, but few experiments were conducted by MC exposure through natural food uptake in lakes. In this study, the phytoplanktivorous silver carp were stocked in a large pen set in Meiliang Bay of Taihu Lake where toxic Microcystis blooms occurred in the warm seasons. Fish samples were collected monthly and MC concentrations in liver and kidney of the fish were determined by LC-MS. The maximum MC concentrations in liver and kidney were present in July when damages in ultrastructures of the liver and kidney were revealed by electron microscope. In comparison with previous studies on common carp, silver carp showed less damage and presence of lysosome proliferation in liver and kidney. Silver carp might eliminate or lessen cell damage caused by MC through lysosome activation. Recovery in the ultrastructures of liver and kidney after Microcystis blooms was companied with a significant decrease or even disappearance of MC. Catalase and glutathione S-transferase in liver and kidney of silver carp during Microcystis blooms were significantly higher than before and after Microcystis blooms. The high glutathione pool in liver and kidney of silver carp suggests their high resistance to MC exposure. The efficient antioxidant defence may be an important mechanism of phytoplanktivorous fish like silver carp to counteract toxic Microcystis blooms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomass
  • Carps / metabolism*
  • Carps / physiology
  • China
  • Environmental Monitoring
  • Feeding Behavior
  • Kidney / drug effects*
  • Kidney / metabolism
  • Kidney / ultrastructure
  • Liver / drug effects*
  • Liver / metabolism
  • Liver / ultrastructure
  • Lysosomes / drug effects
  • Lysosomes / physiology
  • Lysosomes / ultrastructure
  • Microcystins / toxicity*
  • Microcystis / growth & development*
  • Microcystis / metabolism
  • Microscopy, Electron, Transmission
  • Seasons

Substances

  • Microcystins