[Effects of microcystins on expression of apoptosis-associated hepatocyte genes]

Zhonghua Yu Fang Yi Xue Za Zhi. 2007 Jan;41(1):13-6.
[Article in Chinese]

Abstract

Objective: To deeply explore the effects of microcystins (MC-LR) on Bax and Bcl-2 during the course of MC-LR promoting liver tumor.

Methods: applied to set up the animal model, and the effect of MC-LR promoting liver tumor was evaluated by the Albertgamma-GT methods. And then, the immunohistochemical technique, RT-PCR and image analysis were used to study the expression of the Bcl-2 and Bax during the course of promoting tumor.

Results: (1) MC-LR might enhance the positive reaction rate of GGT. The positive reaction rate of GGT in DEN + pure toxin group was 100%, it was significantly higher than the DEN control group 22.22% (P < 0.05). (2) The intension and areas of the protein expression of Bcl-2 in DEN + pure toxin group were 0.0977 and 0.0315, and in DEN control group were 0.0460 and 0.0205, respectively. The expression level of Bcl-2 protein in DEN + pure toxin group were significantly higher than in DEN control group (P < 0.05). Simultaneously, the protein expression of Bax was significantly decreased by MC-LR (P < 0.05). The intension and areas of the expression of Bax in DEN + pure toxin group were 0.0283 and 0.0073, and in DEN control group were 0.0655 and 0.0244 respectively. (3) The mRNA expression of Bcl-2 was significantly increased by MC-LR. The intension of Bcl-2 mRNA expression in DEN + pure toxin group was 2.244, being significantly higher than in the other groups (P < 0.05). However, the mRNA expression of Bax showed no significant difference between DEN + pure toxin and the other groups.

Conclusion: The expression change of Bcl-2 and Bax should possibly play an important role in the course of MC-LR promoting liver tumor.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Carcinogens / toxicity*
  • Hepatocytes / metabolism*
  • Liver Neoplasms / chemically induced*
  • Liver Neoplasms / metabolism*
  • Male
  • Microcystins / toxicity*
  • RNA, Messenger / genetics
  • Rats
  • Rats, Wistar
  • bcl-2-Associated X Protein / biosynthesis*
  • bcl-Associated Death Protein / biosynthesis*

Substances

  • Carcinogens
  • Microcystins
  • RNA, Messenger
  • bcl-2-Associated X Protein
  • bcl-Associated Death Protein