TY - JOUR
T1 - Activity of methylgerambullin from Glycosmis species (Rutaceae) against Entamoeba histolytica and Giardia duodenalis in vitro
AU - Drinić, Mirjana
AU - Raninger, Adriane
AU - Zraunig, Andrea
AU - Astelbauer, Florian
AU - Leitsch, David
AU - Obwaller, Andreas
AU - Walochnik, Julia
AU - Greger, Harald
AU - Duchene, Michael
N1 - Copyright © 2019 The Authors. Published by Elsevier Ltd.. All rights reserved.
PY - 2019/8
Y1 - 2019/8
N2 - Entamoeba histolytica and Giardia duodenalis are widespread intestinal protozoan parasites which both spread via cysts that have to be ingested to infect a new host. Their environment, the small intestine for G. duodenalis and the colon for E. histolytica, contains only very limited amounts of oxygen, so both parasites generate energy by fermentation and substrate level phosphorylation rather than by oxidative phosphorylation. They both contain reducing agents able to reduce and activate nitroimidazole drugs such as metronidazole which is the gold standard drug to treat Entamoeba or Giardia infections. Although metronidazole works well in the majority of cases, it has a number of drawbacks. In animal models, the drug has carcinogenic activity, and concerns about a possible teratogenic activity remain. In addition, the treatment of G. duodenalis infections is hampered by emerging metronidazole resistance. Plant-derived drugs play a dominant role in human medicine, therefore we tested the activity of 14 isolated plant compounds belonging to seven different classes in vitro against both parasites. The tests were performed in a new setting in microtiter plates under anaerobic conditions. The compound with the highest activity was methylgerambullin, a sulphur-containing amide found in Glycosmis species of the family Rutaceae with an EC50 of 14.5 μM (6.08 μg/ml) after 24 h treatment for E. histolytica and 14.6 μM (6.14 μg/ml) for G. duodenalis. The compound was successfully synthesised in the laboratory which opens the door for the generation of new derivatives with higher activity.
AB - Entamoeba histolytica and Giardia duodenalis are widespread intestinal protozoan parasites which both spread via cysts that have to be ingested to infect a new host. Their environment, the small intestine for G. duodenalis and the colon for E. histolytica, contains only very limited amounts of oxygen, so both parasites generate energy by fermentation and substrate level phosphorylation rather than by oxidative phosphorylation. They both contain reducing agents able to reduce and activate nitroimidazole drugs such as metronidazole which is the gold standard drug to treat Entamoeba or Giardia infections. Although metronidazole works well in the majority of cases, it has a number of drawbacks. In animal models, the drug has carcinogenic activity, and concerns about a possible teratogenic activity remain. In addition, the treatment of G. duodenalis infections is hampered by emerging metronidazole resistance. Plant-derived drugs play a dominant role in human medicine, therefore we tested the activity of 14 isolated plant compounds belonging to seven different classes in vitro against both parasites. The tests were performed in a new setting in microtiter plates under anaerobic conditions. The compound with the highest activity was methylgerambullin, a sulphur-containing amide found in Glycosmis species of the family Rutaceae with an EC50 of 14.5 μM (6.08 μg/ml) after 24 h treatment for E. histolytica and 14.6 μM (6.14 μg/ml) for G. duodenalis. The compound was successfully synthesised in the laboratory which opens the door for the generation of new derivatives with higher activity.
KW - Aglafoline
KW - Entamoeba histolytica
KW - Giardia duodenalis
KW - Glycosmis spp.
KW - Methylgerambullin
KW - Sulphur-containing amide
KW - Sulfur Compounds/chemical synthesis
KW - Giardiasis/drug therapy
KW - Humans
KW - Amides/chemical synthesis
KW - Rutaceae/chemistry
KW - Entamoebiasis/drug therapy
KW - Acrylamides/chemical synthesis
KW - Giardia lamblia/drug effects
KW - Plant Extracts/chemistry
KW - Antiprotozoal Agents/chemical synthesis
KW - Entamoeba histolytica/drug effects
UR - http://www.scopus.com/inward/record.url?scp=85071334541&partnerID=8YFLogxK
U2 - 10.1016/j.ijpddr.2019.08.001
DO - 10.1016/j.ijpddr.2019.08.001
M3 - Article
C2 - 31472356
AN - SCOPUS:85071334541
SN - 2211-3207
VL - 10
SP - 109
EP - 117
JO - International Journal for Parasitology: Drugs and Drug Resistance
JF - International Journal for Parasitology: Drugs and Drug Resistance
ER -