Anthelmintic Activity and Cytotoxic Effects of Compounds Isolated from the Fruits of Ozoroa insignis Del. (Anacardiaceae)

被引:8
|
作者
Dube, Mthandazo [1 ]
Saoud, Mohamad [1 ]
Rennert, Robert [1 ]
Fotso, Ghislain Wabo [2 ]
Andrae-Marobela, Kerstin [3 ]
Imming, Peter [4 ]
Haeberli, Cecile [5 ,6 ]
Keiser, Jennifer [5 ,6 ]
Arnold, Norbert [1 ]
机构
[1] Leibniz Inst Plant Biochem, Dept Bioorgan Chem, D-06120 Halle, Saae, Germany
[2] Univ Yaounde I, Dept Organ Chem, Fac Sci, POB 812, Yaounde, Cameroon
[3] Univ Botswana, Dept Biol Sci, Fac Sci, POB 0022, Gaborone, Botswana
[4] Martin Luther Univ Halle Wittenberg, Inst Pharm, Fac Nat Sci, D-06120 Halle, Saale, Germany
[5] Swiss Trop & Publ Hlth Inst, CH-4051 Basel, Switzerland
[6] Univ Basel, CH-4051 Basel, Switzerland
关键词
Ozoroa insignis Del; fruits; anthelmintic properties; cytotoxicity; Caenorhabditis elegans; parasitic worms; GINKGOLIC ACID; PRINCIPLES; INHIBITORS; ROOTS;
D O I
10.3390/biom11121893
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ozoroa insignis Del. is an ethnobotanical plant widely used in traditional medicine for various ailments, including schistosomiasis, tapeworm, and hookworm infections. From the so far not investigated fruits of Ozoroa insignis, the anthelmintic principles could be isolated through bioassay-guided isolation using Caenorhabditis elegans and identified by NMR spectroscopic analysis and mass spectrometric studies. Isolated 6-[8(Z)-pentadecenyl] anacardic (1), 6-[10(Z)-heptadecenyl] anacardic acid (2), and 3-[7(Z)-pentadecenyl] phenol (3) were evaluated against the 5 parasitic organisms Schistosoma mansoni (adult and newly transformed schistosomula), Strongyloides ratti, Heligmosomoides polygyrus, Necator americanus, and Ancylostoma ceylanicum, which mainly infect humans and other mammals. Compounds 1-3 showed good activity against Schistosoma mansoni, with compound 1 showing the best activity against newly transformed schistosomula with 50% activity at 1 mu M. The isolated compounds were also evaluated for their cytotoxic properties against PC-3 (human prostate adenocarcinoma) and HT-29 (human colorectal adenocarcinoma) cell lines, whereby compounds 2 and 3 showed antiproliferative activity in both cancer cell lines, while compound 1 exhibited antiproliferative activity only on PC-3 cells. With an IC50 value of 43.2 mu M, compound 3 was found to be the most active of the 3 investigated compounds.
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页数:12
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