Selective glutathione repletion with oral oxothiazolidine carboxylate (OTZ) in the radiated tumor-bearing rat Journal Article


Authors: Rose, D. M.; Hochwald, S. N.; Harrison, L. E.; Burt, M.
Article Title: Selective glutathione repletion with oral oxothiazolidine carboxylate (OTZ) in the radiated tumor-bearing rat
Abstract: Oxothiazolidine carboxylate (OTZ) is a cysteine prodrug which augments intracellular glutathione (GSH) levels. We examined the effects of oral OTZ on tumor and host tissue reduced GSH levels in fasting and radiated models of GSH depletion. In addition, we studied the tumor's ability to utilize OTZ via the enzyme, oxoprolinase. Fischer 344 rats (n = 40) were implanted with MCA sarcoma and studied at 10% tumor burden. Treatment consisted of 10 mmol/kg OTZ or buffer orally. After a 24-hr fast, 16 animals were treated and tumor, kidney, jejunal, and colonic mucosa were collected after 4 hr. Significant increases in GSH with OTZ (n = 8) vs buffer (n = 8) were seen in kidney (5.6 ± 0.4 vs 4.3 ± 0.9; P < 0.01), jejunum (13.8 ± 1.3 vs 12.1 ± 1.1; P < 0.05), and colon (6.7 ± 1.2 vs 5.3 ± 0.6; P < 0.05), but not tumor (8.9 ± 2.4 vs 10.6 ± 1.4; P = 0.12). Sixteen animals were treated 4 hr before and 18 hr following 1100 cGy of abdominal radiation and at 4 days, tumor, jejunal, and colonic mucosa were collected. Significant increases in GSH with OTZ (n = 8) vs buffer (n = 8) were noted in jejunum (9.3 ± 1.1 vs 7.5 ± 1.8; P < 0.05) and colon (5.6 ± 1.1 vs 4.3 ± 0.9; P < 0.05) but not tumor (8.4 ± 1.6 vs 7.6 ± 1.4; P = 0.34). To determine tissue oxoprolinase activity, tumor, kidney, liver, jejunal, and colonic mucosa were collected from 8 animals. Oxoprolinase activity was highest in the kidney (814 ± 145) with no difference noted between liver and tumor (280 ± 117 and 324 ± 137, respectively). Oral OTZ selectively increases reduced GSH levels in normal tissues compared to tumor following fasting and whole abdominal radiation. This increase does not appear to be due to a differential activity of oxoprolinase. OTZ may have a role in protection against toxicity associated with oxidative injury by selective repletion of normal host tissue GSH levels.
Keywords: controlled study; drug efficacy; nonhuman; cancer radiotherapy; animal tissue; animal model; drug selectivity; radiation injury; sarcoma; liver; kidney; rat; glutathione; prodrug; oral drug administration; radiation protection; colon mucosa; 2 oxo 4 thiazolidinecarboxylic acid; male; priority journal; article; 5 oxoprolinase; jejunum mucosa
Journal Title: Journal of Surgical Research
Volume: 62
Issue: 2
ISSN: 0022-4804
Publisher: Academic Press Inc., Elsevier Science  
Date Published: 1996-05-01
Start Page: 224
End Page: 228
Language: English
DOI: 10.1006/jsre.1996.0199
PUBMED: 8632643
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 22 November 2017 -- Source: Scopus
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors
  1. Michael E. Burt
    187 Burt