Zonal distribution of protein-acetaldehyde adducts in the liver of rats fed alcohol for long periods

Authors

  • Renee C. Lin Ph.D.,

    Corresponding author
    1. Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana 46202
    2. Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana 46202
    3. Veterans Affairs Medical Center, Indianapolis, Indiana 46202
    • Research (151), Veteran Affairs Medical Center, 1481 West Tenth Street, Indianapolis, IN 46202
    Search for more papers by this author
  • Feng C. Zhou,

    1. Department of Anatomy, Indiana University School of Medicine, Indianapolis, Indiana 46202
    Search for more papers by this author
  • Michael J. Fillenwarth,

    1. Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana 46202
    Search for more papers by this author
  • Lawrence Lumeng

    1. Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana 46202
    2. Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana 46202
    3. Veterans Affairs Medical Center, Indianapolis, Indiana 46202
    Search for more papers by this author

Abstract

Acetaldehyde, a highly reactive intermediate of alcohol metabolism, has been shown to form adducts with liver proteins in rats fed alcohol for long periods. In this report, the zonal distribution of liver proteinacetaldehyde adducts that formed in vivo was studied by means of histoimmunostaining. Rats were pair-fed alcohol-containing and alcohol-free AIN'76 liquid diets for 2 or 11 wk before they were killed and subjected to whole body perfusion with paraformaldehyde. Each liver was cut into 60-μm-thick slices. Slices were first treated with 10% hydrogen peroxide to eliminate endogenous peroxidase activity. They were then incubated sequentially with rabbit antihemocyanin–acetaldehyde adduct, goat antirabbit serum IgG and rabbit peroxidase-antiperoxidase complex. The liver slices were stained with diaminobenzidine and counterstained with methylgreen. In the livers of rats fed alcohol for 2 wk, peroxidase activity was evident in the perivenous zone but not the periportal zone. No staining was obtained when the primary antibody had been preabsorbed with immobilized hemocyanin–acetaldehyde adduct or if the liver slices were incubated with the unimmunized rabbit IgG. Slight staining of the perivenous zone was seen in the livers of control rats, presumably because of minimal protein-acetaldehyde adduct formation emanating from endogenous acetaldehyde. When rats were fed alcohol for longer periods (e.g., 11 wk), protein-acetaldehyde adducts were still seen predominantly in the perivenous zone, but the distribution pattern was more diffuse than that observed in the livers of rats fed alcohol for only 2 wk. More liver cells produced protein-acetaldehyde adducts when rats were fed the alcohol-containing diet supplemented with cyanamide. However, these protein-acetaldehyde adduct–positive cells were still found mainly in the perivenous area. The zonation in the formation of protein-acetaldehyde adducts in the liver may in part explain the preferential damage of perivenous hepatocytes induced by long-term alcohol consumption. (HEPATOLOGY 1993;18:864-869).

Ancillary