U.S. flag An official website of the United States government.
Official websites use .gov

A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS

A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

i

Toxicokinetics of Monochloroacetic Acid: A Whole-Body Autoradiography Study



Details

  • Personal Author:
  • Description:
    Monochloroacetic acid (MCA) is a toxic chemical used as a herbicide and in the synthesis of various organic compounds. MCA has also been shown to be present in chlorinated drinking waters. In order to understand the mechanism of MCA toxicity, we studied the tissue distribution of [1-14C]MCA in rats, by whole-body autoradiography technique. Male Sprague-Dawley rats were given a tracer dose of [1-14C]MCA [6.8 ug/100 g (40 uCi) body weight] by tail vein and euthanized at different time intervals (5 min, 1, 4, 12, 24 and 48 h). The animals were embedded in carboxymethyl cellulose and frozen immediately. Frozen animals were sectioned and processed using whole-body autoradiographic techniques. Analysis of developed sections showed that at 5 min, there was a rapid accumulation of 14C-activity in the kidney cortex and stomach walls. The radioactivity was rapidly removed from the circulation. There was high accumulation of 14C-activity in the myocardial tissues. The liver was also loaded with MCA and/or its metabolites. After 1 h following administration of [14C]MCA, radioactivity was extensively excreted into the small intestinal lumen. The accumulation of 14C-activity in the brain, thymus, salivary glands and tongue was prominent at 1 h. After 4 h the liver and other tissues started to eliminate most of the radioactivity. Contrary to other tissues, however, the central nervous system, thymus and pancreas started to accumulate the radioactivity at later time periods. These observations suggest the accumulation of MCA and/or its metabolites into hydrophilic tissues at earlier time periods and into lipophilic tissues at later times. [Description provided by NIOSH]
  • Subjects:
  • Keywords:
  • ISSN:
    0300-483X
  • Document Type:
  • Funding:
  • Genre:
  • Place as Subject:
  • CIO:
  • Topic:
  • Location:
  • Pages in Document:
    35-43
  • Volume:
    63
  • Issue:
    1
  • NIOSHTIC Number:
    nn:20058141
  • Citation:
    Toxicology 1990 Jul; 63(1):35-43
  • Contact Point Address:
    Ahmed E. Ahmed, Division of Biochemistry and Pharmacokinetics Laboratory of Cancer Center, University of Texas Medical Branch, Galveston, TX 77550 U.S.A.
  • CAS Registry Number:
  • Federal Fiscal Year:
    1990
  • Performing Organization:
    University of Texas Medical Branch at Galveston
  • Peer Reviewed:
    True
  • Start Date:
    19860101
  • Source Full Name:
    Toxicology
  • End Date:
    19960630
  • Collection(s):
  • Main Document Checksum:
    urn:sha-512:6471e6c52c5456f90bb9511683fa2a539346b520b3f876982fc256c07a1277e1d72100f64800123b55918208aeb710414db8fafde62d5ee0ca827c19caf17495
  • Download URL:
  • File Type:
    Filetype[PDF - 1.27 MB ]
ON THIS PAGE

CDC STACKS serves as an archival repository of CDC-published products including scientific findings, journal articles, guidelines, recommendations, or other public health information authored or co-authored by CDC or funded partners.

As a repository, CDC STACKS retains documents in their original published format to ensure public access to scientific information.