1. In vitro anthelmintic activity of ethanol and aqueous extracts of Terminalia macroptera and Bridelia micrantha against Heligmosomoides polygyrus, Caenorhabditis elegans and in-silico molecular docking evaluation of some isolated phytoconstituents.
- Author
-
Cédric, Yamssi, Yaghoobi, Mahdi, Nadia, Noumedem Anangmo Christelle, Besati, Masoud, Che, Siri Trifosia, Sidiki, Ngouyamsa Nsapkain Aboubakar, Azizi, Mounvera Abdel, and Payne, Vincent Khan
- Subjects
- *
MOLECULAR docking , *CAENORHABDITIS elegans , *ETHANOL , *TERMINALIA , *PROTEIN receptors , *LARVAE , *GLUTAMIC acid , *GLYCINE receptors - Abstract
• Caenorhabditis elegance and Heligmosomoides polygyrus are great model of parasitic nematodes for the identification of anthelminthic drugs. • By tracking the larvae's movement, the worm microtracker was used to assess the anthelminthic activity in a 96-well microplate. • The calculations of the interaction of the ligands of Terminalia macroptera and Bridelia micrantha with the tubulin alpha-1B protein receptor indicate that the ligands rich in hydroxyl groups interact better with the amino acids of protein. • The aqueous and ethanolic extracts of Terminalia macroptera and Bridelia micrantha have potent anthelmintic activity against the 4 life stage cycle stages of H. polygyrus and on the L4 stage of C. elegance. In tropical and subtropical African nations, helminthiases are widespread and devastating to school-aged children. This study was undertaken in order to objectively support the ethnobotanical use of the stem bark of Terminalia macroptera and the leaves of Bridelia micrantha as anthelminthic agent, using Heligmosomoides polygyrus and Caenorhabditis elegans. The flotation technique was used to obtain fresh eggs of H. polygyrus from the feces of experimentally infected mice and culture to different stages of the larvae. Caenorhabditis elegans L4 larvae were obtained after bleaching adult worms to create a synchronized medium and then was cultured until the L4 larval stage. By tracking the larvae's movement, the worm micro tracker was used to assess the anthelminthic activity in a 96-well microplate. The extract was tested at various concentrations and distilled water served as the negative control, and albendazole as the positive control. The percentage of larvae motility inhibition was calculated. The Glide module of the Schrodinger Maestro software was used to conduct the docking studies. The software's score function was used to rank and classify several potentials adduct patterns produced by molecular docking. For the ethanol and aqueous extracts of T. macroptera, the IC 50 of the ovicidal activity was 0.013 and 0.042 mg/ml, respectively, whereas for the ethanol and aqueous extracts of B. micrantha , it was 0.38 and 0.63 mg/ml. This demonstrates that ethanol extracts are more effective than water extracts in preventing hatching inside the host. T. macroptera larvicidal activity against L1, L2, and L3 larvae resulted in IC 50 values of 0.47, 0.29, and 0.004 mg/ml for the ethanol extract, respectively, while B. micrantha's had IC 50 values of 0.154, 1.4, and 0.047 mg/ml. Caenorhabditis elegans was very sensitive with IC 50 values of, 4.733, and 2.8 µg̸ mL, respectively, for the ethanol and aqueous extract. In B. micrantha , Isoquercetin has the most interaction with amino acids, Asparagine, Phenylalanine, Glycine, Glutamic acid, and Tyrosine, because of its abundant hydroxyl functional group as well as carbonyl group and benzene ring, which makes it have a better inhibitory effect on the receptor protein while that of T. macroptera was Orientin. These findings imply that B. micrantha and T. macroptera may be effective as an anthelminthic agent. However, additional in vivo research is required to verify this biological activity. In addition, the hydroxyl groups as well as the flavonoid backbone of these compounds are the reason for the good effect of these proteins on the receptor protein, and the in silico studies of these compounds on the receptor protein and its interactions with amino acids confirm this claim. [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
- View/download PDF