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Journal ArticleDOI

Hematotoxicity and blood glutathione levels after cisplatin treatment of tumor-bearing mice.

D. Khynriam, +1 more
- 01 Jan 2001 - 
- Vol. 17, Iss: 6, pp 357-370
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TLDR
It is noted that the glutathione levels in blood and abnormalities in erythrocytes and other hematological parameters are inversely related in cisplatin-mediated cancer chemotherapy.
Abstract
The involvement of glutathione, a major cellular antioxidant, in cisplatin-mediated development of various hematological changes in mice bearing ascites Dalton lymphoma tumor was investigated With tumor growth, glutathione levels decreased in blood but increased in tumor cells Cisplatin treatment of tumor-bearing mice caused a decrease in glutathione levels in blood, ascites supernatant, and tumor cells Blood hemoglobin, erythrocytes, packed cell volume and leukocytes (eosinophils, basophils, and lymphocytes) were also decreased along with the development of various morphological abnormalities in erythrocytes (microcytes, macrocytes, echinocytes, acanthocytes, etc) after cisplatin treatment All these hematotoxic features were noted to be increased more when buthionine sulfoximine (a specific glutathione-depleting agent) was also given prior to cisplatin treatment However, combination treatment of cysteine (precursor for glutathione synthesis) plus cisplatin resulted in an improvement in the glutathione levels and decrease in hematological toxicities It is noted that the glutathione levels in blood and abnormalities in erythrocytes and other hematological parameters are inversely related in cisplatin-mediated cancer chemotherapy It is suggested that blood glutathione may play an important role in the development of cisplatin-mediated hematological toxicity in the host

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Citations
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Journal ArticleDOI

Changes in endogenous tissue glutathione level in relation to murine ascites tumor growth and the anticancer activity of cisplatin

TL;DR: Lower doses of cisplatin in combination with buthionine sulfoximine (an inhibitor of glutathione synthesis) may be useful in cancer chemotherapy with decreased toxicity in the host and could be an important contributory factor to cis platin's anticancer activity leading to tumor regression.
Journal ArticleDOI

Antileishmanial effect of cisplatin against murine visceral leishmaniasis

TL;DR: The in vivo effect of cisplatin is characterized for the first time in murine experimental visceral leishmaniasis by significant reduction in the parasite burden and increased DTH responses in infected and treated animals.
Journal ArticleDOI

Changes in glutathione-related enzymes in tumor-bearing mice after cisplatin treatment.

TL;DR: It is suggested that the changes in various glutathione-related enzymes and glutATHione levels in the tissues of the host during cisplatin-mediated chemotherapy could affect cellular antioxidant defense potential, which may play an important contributory role in cisplasin-mediated toxicity, particularly nephrotoxicity, and anticancer activity in the host.
Journal ArticleDOI

Cisplatin-induced genotoxic effects and endogenous glutathione levels in mice bearing ascites Dalton's lymphoma.

TL;DR: Findings support the possible involvement of glutathione as an important intracellular protective agent and suggest that differences in its levels may be one of the factors in the varying sensitivity of cells to cisplatin-induced genotoxic effects in the mice bearing ascites Dalton's lymphoma.
Journal ArticleDOI

Evaluation of nephroprotective and immunomodulatory activities of antioxidants in combination with cisplatin against murine visceral leishmaniasis.

TL;DR: Results are promising as antioxidants reduced the potential toxicity of high doses of cisplatin, making the combination a potential anti-leishmanial therapy, especially in resistant cases.
References
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Journal ArticleDOI

Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman's reagent

TL;DR: A simple spectrophotometric method for the routine concomitant determination of sulfhydryl groups in PB- SH, NP-SH, and T-SH fractions in various tissues is reported.
Journal Article

Production of Large Amounts of Hydrogen Peroxide by Human Tumor Cells

TL;DR: Constitutive generation of large amounts of reactive oxygen intermediates, if it occurs in vivo, might contribute to the ability of some tumors to mutate, inhibit antiproteases, injure local tissues, and therefore promote tumor heterogeneity, invasion, and metastasis.
Journal ArticleDOI

Potent and specific inhibition of glutathione synthesis by buthionine sulfoximine (S-n-butyl homocysteine sulfoximine).

TL;DR: The findings support the conclusion that the S-alkyl moiety of the sulfoximine binds at the enzyme site that normally binds the acceptor amino acid and increases in a manner which is parallel to those of the corresponding isosteric accepter amino acid substrates, i.e. glycine, alanine, and alpha-aminobutyrate.
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