Cargando…

Inhibition of Trypanosoma evansi Protein-Tyrosine Phosphatase by Myristic Acid Analogues Isolated from Khaya senegalensis and Tamarindus indica

BACKGROUND: Trypanosome infections still pose severe health and economic consequences, especially in the endemic regions of Sub-Saharan Africa. Trypanosome differentiation to the procyclic forms which lack the immune evasion mechanisms for survival in the bloodstream is prevented by tyrosine dephosp...

Descripción completa

Detalles Bibliográficos
Autores principales: Dingwoke, Emeka John, Adamude, Fatima Amin, Chukwuocha, Chimee Ethel, Ambi, Ahmed Adamu, Nwobodo, Nwobodo Ndubuisi, Sallau, Abdullahi Balarabe, Nzelibe, Humphrey Chukwuemeka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6927228/
https://www.ncbi.nlm.nih.gov/pubmed/31908547
http://dx.doi.org/10.2147/JEP.S226632
_version_ 1783482266700218368
author Dingwoke, Emeka John
Adamude, Fatima Amin
Chukwuocha, Chimee Ethel
Ambi, Ahmed Adamu
Nwobodo, Nwobodo Ndubuisi
Sallau, Abdullahi Balarabe
Nzelibe, Humphrey Chukwuemeka
author_facet Dingwoke, Emeka John
Adamude, Fatima Amin
Chukwuocha, Chimee Ethel
Ambi, Ahmed Adamu
Nwobodo, Nwobodo Ndubuisi
Sallau, Abdullahi Balarabe
Nzelibe, Humphrey Chukwuemeka
author_sort Dingwoke, Emeka John
collection PubMed
description BACKGROUND: Trypanosome infections still pose severe health and economic consequences, especially in the endemic regions of Sub-Saharan Africa. Trypanosome differentiation to the procyclic forms which lack the immune evasion mechanisms for survival in the bloodstream is prevented by tyrosine dephosphorylation which is catalyzed by protein-tyrosine phosphatase; thereby promoting survival of the parasites in the host. Inhibition of Protein-tyrosine phosphatase is a strategic therapeutic target that could attenuate trypanosomiasis. This study investigated the in vitro inhibitory effect of stem bark extracts of Khaya senegalensis and Tamarindus indica on the enzymatic activity of protein-tyrosine phosphatase. METHODS: All determinations were carried out following standard procedures for analytical experiments. The analogues of myristic acid that inhibited the enzymatic activity of protein-tyrosine phosphatase were isolated by bioassay-guided fractionation of stem bark extracts of Khaya senegalensis and Tamarindus indica. RESULTS: Analogues of myristic acid proved to be potent inhibitors of protein-tyrosine phosphatase. Double reciprocal (Lineweaver–Burk) plots of the initial velocity data indicated non-competitive inhibition with K(i) of 0.67 mg/mL for Khaya senegalensis and 2.17 mg/mL for Tamarindus indica. The kinetic parameters for the cleavage of para-nitrophenylphosphate by the enzyme showed a K(M) of 3.44 mM and V(max) of 0.19 µmol/min. Sodium orthovanadate, the enzymes’ specific inhibitor, inhibited the enzyme competitively with K(i) of 0.20 mg/mL. Gas chromatography-mass spectrometry analysis of the stem bark bioactive fractions of Khaya senegalensis and Tamarindus indica revealed the presence of myristic acid analogues. CONCLUSION: Analogues of myristic acid are potent inhibitors of protein-tyrosine phosphatase that could be developed as trypanocide to inhibit the enzymatic activity of protein-tyrosine phosphatase in order to prevent transmission of trypanosomes.
format Online
Article
Text
id pubmed-6927228
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Dove
record_format MEDLINE/PubMed
spelling pubmed-69272282020-01-06 Inhibition of Trypanosoma evansi Protein-Tyrosine Phosphatase by Myristic Acid Analogues Isolated from Khaya senegalensis and Tamarindus indica Dingwoke, Emeka John Adamude, Fatima Amin Chukwuocha, Chimee Ethel Ambi, Ahmed Adamu Nwobodo, Nwobodo Ndubuisi Sallau, Abdullahi Balarabe Nzelibe, Humphrey Chukwuemeka J Exp Pharmacol Original Research BACKGROUND: Trypanosome infections still pose severe health and economic consequences, especially in the endemic regions of Sub-Saharan Africa. Trypanosome differentiation to the procyclic forms which lack the immune evasion mechanisms for survival in the bloodstream is prevented by tyrosine dephosphorylation which is catalyzed by protein-tyrosine phosphatase; thereby promoting survival of the parasites in the host. Inhibition of Protein-tyrosine phosphatase is a strategic therapeutic target that could attenuate trypanosomiasis. This study investigated the in vitro inhibitory effect of stem bark extracts of Khaya senegalensis and Tamarindus indica on the enzymatic activity of protein-tyrosine phosphatase. METHODS: All determinations were carried out following standard procedures for analytical experiments. The analogues of myristic acid that inhibited the enzymatic activity of protein-tyrosine phosphatase were isolated by bioassay-guided fractionation of stem bark extracts of Khaya senegalensis and Tamarindus indica. RESULTS: Analogues of myristic acid proved to be potent inhibitors of protein-tyrosine phosphatase. Double reciprocal (Lineweaver–Burk) plots of the initial velocity data indicated non-competitive inhibition with K(i) of 0.67 mg/mL for Khaya senegalensis and 2.17 mg/mL for Tamarindus indica. The kinetic parameters for the cleavage of para-nitrophenylphosphate by the enzyme showed a K(M) of 3.44 mM and V(max) of 0.19 µmol/min. Sodium orthovanadate, the enzymes’ specific inhibitor, inhibited the enzyme competitively with K(i) of 0.20 mg/mL. Gas chromatography-mass spectrometry analysis of the stem bark bioactive fractions of Khaya senegalensis and Tamarindus indica revealed the presence of myristic acid analogues. CONCLUSION: Analogues of myristic acid are potent inhibitors of protein-tyrosine phosphatase that could be developed as trypanocide to inhibit the enzymatic activity of protein-tyrosine phosphatase in order to prevent transmission of trypanosomes. Dove 2019-12-18 /pmc/articles/PMC6927228/ /pubmed/31908547 http://dx.doi.org/10.2147/JEP.S226632 Text en © 2019 Dingwoke et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Dingwoke, Emeka John
Adamude, Fatima Amin
Chukwuocha, Chimee Ethel
Ambi, Ahmed Adamu
Nwobodo, Nwobodo Ndubuisi
Sallau, Abdullahi Balarabe
Nzelibe, Humphrey Chukwuemeka
Inhibition of Trypanosoma evansi Protein-Tyrosine Phosphatase by Myristic Acid Analogues Isolated from Khaya senegalensis and Tamarindus indica
title Inhibition of Trypanosoma evansi Protein-Tyrosine Phosphatase by Myristic Acid Analogues Isolated from Khaya senegalensis and Tamarindus indica
title_full Inhibition of Trypanosoma evansi Protein-Tyrosine Phosphatase by Myristic Acid Analogues Isolated from Khaya senegalensis and Tamarindus indica
title_fullStr Inhibition of Trypanosoma evansi Protein-Tyrosine Phosphatase by Myristic Acid Analogues Isolated from Khaya senegalensis and Tamarindus indica
title_full_unstemmed Inhibition of Trypanosoma evansi Protein-Tyrosine Phosphatase by Myristic Acid Analogues Isolated from Khaya senegalensis and Tamarindus indica
title_short Inhibition of Trypanosoma evansi Protein-Tyrosine Phosphatase by Myristic Acid Analogues Isolated from Khaya senegalensis and Tamarindus indica
title_sort inhibition of trypanosoma evansi protein-tyrosine phosphatase by myristic acid analogues isolated from khaya senegalensis and tamarindus indica
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6927228/
https://www.ncbi.nlm.nih.gov/pubmed/31908547
http://dx.doi.org/10.2147/JEP.S226632
work_keys_str_mv AT dingwokeemekajohn inhibitionoftrypanosomaevansiproteintyrosinephosphatasebymyristicacidanaloguesisolatedfromkhayasenegalensisandtamarindusindica
AT adamudefatimaamin inhibitionoftrypanosomaevansiproteintyrosinephosphatasebymyristicacidanaloguesisolatedfromkhayasenegalensisandtamarindusindica
AT chukwuochachimeeethel inhibitionoftrypanosomaevansiproteintyrosinephosphatasebymyristicacidanaloguesisolatedfromkhayasenegalensisandtamarindusindica
AT ambiahmedadamu inhibitionoftrypanosomaevansiproteintyrosinephosphatasebymyristicacidanaloguesisolatedfromkhayasenegalensisandtamarindusindica
AT nwobodonwobodondubuisi inhibitionoftrypanosomaevansiproteintyrosinephosphatasebymyristicacidanaloguesisolatedfromkhayasenegalensisandtamarindusindica
AT sallauabdullahibalarabe inhibitionoftrypanosomaevansiproteintyrosinephosphatasebymyristicacidanaloguesisolatedfromkhayasenegalensisandtamarindusindica
AT nzelibehumphreychukwuemeka inhibitionoftrypanosomaevansiproteintyrosinephosphatasebymyristicacidanaloguesisolatedfromkhayasenegalensisandtamarindusindica