1985
DOI: 10.1055/s-2007-969454
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Toxicity of the Sesquiterpene Lactone Parthenin to Cultured Bovine Kidney Cells

Abstract: The cytotoxic effect of the sesquiterpene lactone, parthenin was studied in vitro using cultured bovine kidney cells. The drug inhibited macromolecular synthesis. Fifty percent inhibitions in RNA, DNA and protein synthesis were observed when the cells were treated with parthenin at a final concentration of 1 g/ml. The cytotoxic effect of parthenin was also evident by its ability to markedly inhibit the activities of key cellular enzymes after treatment of the cells with the toxin for 24 h.

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Cited by 15 publications
(9 citation statements)
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“…The strong correlation between parthenin and cytotoxicity observed in this study is consistent with previous reports [ 15 , 46 , 47 ]. Parthenin itself was highly cytotoxic to bovine kidney cells by inhibiting the synthesis of RNA, DNA and key cellular enzymes within 24 h after exposure [ 47 ].…”
Section: Discussionsupporting
confidence: 93%
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“…The strong correlation between parthenin and cytotoxicity observed in this study is consistent with previous reports [ 15 , 46 , 47 ]. Parthenin itself was highly cytotoxic to bovine kidney cells by inhibiting the synthesis of RNA, DNA and key cellular enzymes within 24 h after exposure [ 47 ].…”
Section: Discussionsupporting
confidence: 93%
“…The strong correlation between parthenin and cytotoxicity observed in this study is consistent with previous reports [ 15 , 46 , 47 ]. Parthenin itself was highly cytotoxic to bovine kidney cells by inhibiting the synthesis of RNA, DNA and key cellular enzymes within 24 h after exposure [ 47 ]. Similarly, other sesquiterpene lactones including ambrosin, coronopilin, tetraneurin A and hysterone D, and some acetylated pseudoguaianolides have been associated with the cytotoxicity of aerial parts of parthenium weed [ 15 , 48 , 49 ].…”
Section: Discussionsupporting
confidence: 93%
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“…The structure of t-DCTN contains three highly reactive functional groups: O = C-C = C (ring A), a lactone (ring C) and cyclopentenone (ring D). Since the structure of t-DCTN is not planar, the most available group is O = C-C = C, which can function as a Michael acceptor to interact with the SH groups of proteins, GSH and nitrogen bases, mainly guanine, through nucleophilic attack [5], [6]. Other diterpenes isolated from C. incanus and Laetia corymbulosa also exhibited cytotoxic effect on several tumor cell lines, and the authors suggested that their effect was due to interaction with macromolecules [7], [8].…”
mentioning
confidence: 99%
“…goats [297]. Parthenin, a compound characteristic to Parthenium species, inhibited RNA, DNA and protein synthesis in vitro in cultured bovine kidney cells [298]. In a repeated dose toxicity study in rats, the administration of sesquiterpene lactone containing extracts of Smallanthus sonchifolius resulted in alterations of creatinine, glucose and albumin levels, implying renal damage.…”
Section: Toxicological Evaluation Of Common Ragweedmentioning
confidence: 99%