Cargando…

Enhanced cytostatic activity of the sesquiterpene lactone eupatoriopicrin by glutathione depletion.

Eupatoriopicrin (EUP), a sesquiterpene lactone from Eupatorium cannabinum L., possesses cytostatic activity. This was demonstrated for FIO 26 cells in vitro with the aid of a clonogenic assay and in vivo by tumour growth delay in FIO 26 and Lewis lung tumour-bearing mice. In vitro the IC50 for 1 h e...

Descripción completa

Detalles Bibliográficos
Autores principales: Woerdenbag, H. J., Lemstra, W., Malingré, T. M., Konings, A. W.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246971/
https://www.ncbi.nlm.nih.gov/pubmed/2757925
_version_ 1782150881686323200
author Woerdenbag, H. J.
Lemstra, W.
Malingré, T. M.
Konings, A. W.
author_facet Woerdenbag, H. J.
Lemstra, W.
Malingré, T. M.
Konings, A. W.
author_sort Woerdenbag, H. J.
collection PubMed
description Eupatoriopicrin (EUP), a sesquiterpene lactone from Eupatorium cannabinum L., possesses cytostatic activity. This was demonstrated for FIO 26 cells in vitro with the aid of a clonogenic assay and in vivo by tumour growth delay in FIO 26 and Lewis lung tumour-bearing mice. In vitro the IC50 for 1 h exposure to EUP was 1.5 microgram ml-1 (4.1 nmol ml-1). This concentration depleted about 25% of its cellular GSH concentration. Pretreatment of FIO 26 cells with BSO, resulting in greater than 99%. GSH depletion, enhanced the cytotoxic effect of EUP. The dose-enhancement factor at the level of 10% cell survival was 2.3. Growth inhibition of the Lewis lung carcinoma and the FIO 26 fibrosarcoma, solidly growing in C57Bl mice, was found after i.v. injection of 20 or 40 mg kg-1 EUP, at a tumour volume of about 500 microliters. Pretreatment with BSO at a dose of 4 mmol kg-1 i.p., 6 h before EUP administration, resulted in a significantly stronger growth delay of both tumours compared with EUP only. At the time of EUP treatment, cellular GSH in the tumours was reduced by BSO treatment to about 60%. It is concluded that EUP possesses antitumour activity in vivo and that chemosensitisation of EUP may be accomplished by pretreatment with BSO, indicating that endogenous GSH protects against the cytostatic action of EUP.
format Text
id pubmed-2246971
institution National Center for Biotechnology Information
language English
publishDate 1989
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-22469712009-09-10 Enhanced cytostatic activity of the sesquiterpene lactone eupatoriopicrin by glutathione depletion. Woerdenbag, H. J. Lemstra, W. Malingré, T. M. Konings, A. W. Br J Cancer Research Article Eupatoriopicrin (EUP), a sesquiterpene lactone from Eupatorium cannabinum L., possesses cytostatic activity. This was demonstrated for FIO 26 cells in vitro with the aid of a clonogenic assay and in vivo by tumour growth delay in FIO 26 and Lewis lung tumour-bearing mice. In vitro the IC50 for 1 h exposure to EUP was 1.5 microgram ml-1 (4.1 nmol ml-1). This concentration depleted about 25% of its cellular GSH concentration. Pretreatment of FIO 26 cells with BSO, resulting in greater than 99%. GSH depletion, enhanced the cytotoxic effect of EUP. The dose-enhancement factor at the level of 10% cell survival was 2.3. Growth inhibition of the Lewis lung carcinoma and the FIO 26 fibrosarcoma, solidly growing in C57Bl mice, was found after i.v. injection of 20 or 40 mg kg-1 EUP, at a tumour volume of about 500 microliters. Pretreatment with BSO at a dose of 4 mmol kg-1 i.p., 6 h before EUP administration, resulted in a significantly stronger growth delay of both tumours compared with EUP only. At the time of EUP treatment, cellular GSH in the tumours was reduced by BSO treatment to about 60%. It is concluded that EUP possesses antitumour activity in vivo and that chemosensitisation of EUP may be accomplished by pretreatment with BSO, indicating that endogenous GSH protects against the cytostatic action of EUP. Nature Publishing Group 1989-01 /pmc/articles/PMC2246971/ /pubmed/2757925 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Woerdenbag, H. J.
Lemstra, W.
Malingré, T. M.
Konings, A. W.
Enhanced cytostatic activity of the sesquiterpene lactone eupatoriopicrin by glutathione depletion.
title Enhanced cytostatic activity of the sesquiterpene lactone eupatoriopicrin by glutathione depletion.
title_full Enhanced cytostatic activity of the sesquiterpene lactone eupatoriopicrin by glutathione depletion.
title_fullStr Enhanced cytostatic activity of the sesquiterpene lactone eupatoriopicrin by glutathione depletion.
title_full_unstemmed Enhanced cytostatic activity of the sesquiterpene lactone eupatoriopicrin by glutathione depletion.
title_short Enhanced cytostatic activity of the sesquiterpene lactone eupatoriopicrin by glutathione depletion.
title_sort enhanced cytostatic activity of the sesquiterpene lactone eupatoriopicrin by glutathione depletion.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246971/
https://www.ncbi.nlm.nih.gov/pubmed/2757925
work_keys_str_mv AT woerdenbaghj enhancedcytostaticactivityofthesesquiterpenelactoneeupatoriopicrinbyglutathionedepletion
AT lemstraw enhancedcytostaticactivityofthesesquiterpenelactoneeupatoriopicrinbyglutathionedepletion
AT malingratm enhancedcytostaticactivityofthesesquiterpenelactoneeupatoriopicrinbyglutathionedepletion
AT koningsaw enhancedcytostaticactivityofthesesquiterpenelactoneeupatoriopicrinbyglutathionedepletion