Antimalarial Activity of Piperine

Malaria remains a public health problem in tropical and subtropical regions. Resistance of Plasmodium falciparum to artemisinins in Southeast Asia is a great concern for disease control and research on discovery and development of new alternative antimalarial drugs is urgently required. In a previou...

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Main Authors: Artitaya Thiengsusuk, Phunuch Muhamad, Wanna Chaijaroenkul, Kesara Na-Bangchang
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:Journal of Tropical Medicine
Online Access:http://dx.doi.org/10.1155/2018/9486905
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author Artitaya Thiengsusuk
Phunuch Muhamad
Wanna Chaijaroenkul
Kesara Na-Bangchang
author_facet Artitaya Thiengsusuk
Phunuch Muhamad
Wanna Chaijaroenkul
Kesara Na-Bangchang
author_sort Artitaya Thiengsusuk
collection DOAJ
description Malaria remains a public health problem in tropical and subtropical regions. Resistance of Plasmodium falciparum to artemisinins in Southeast Asia is a great concern for disease control and research on discovery and development of new alternative antimalarial drugs is urgently required. In a previous study, the fruit of Piper chaba Hunt. was demonstrated to exhibit promising antimalarial activity against the asexual stage of 3D7 (chloroquine-sensitive) and K1 (chloroquine-resistant) P. falciparum clones. The aim of the present study was to further investigate the antimalarial activity of piperine, the major isolated constituent of Piper chaba Hunt. fruits against both P. falciparum clones. The antimalarial activity was determined using SYBR green-I-based assay and morphological change was observed under the light microscope with Giemsa staining. The median IC50 (concentration that inhibits parasite growth by 50%) values of piperine against 3D7 and K1 P. falciparum were 111.5 and 59 μM, respectively. A marked change in parasite morphology was observed within 48 hours of piperine exposure. Results of real-time PCR showed no effect of piperine on modulating the expression of the three genes associated with antimalarial drug resistance in P. falciparum, i.e., pfcrt, pfmdr1, and pfmrp1. Piperine could be a promising candidate for further development as an antimalarial drug based on its antimalarial potency and low risk of resistance development.
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spelling doaj-art-e922797fcd2b47589fb8f7cf6ea77f022025-02-03T06:11:16ZengWileyJournal of Tropical Medicine1687-96861687-96942018-01-01201810.1155/2018/94869059486905Antimalarial Activity of PiperineArtitaya Thiengsusuk0Phunuch Muhamad1Wanna Chaijaroenkul2Kesara Na-Bangchang3Drug Discovery and Development Center, Thammasat University (Rangsit Campus), Pathumtani 12121, ThailandDrug Discovery and Development Center, Thammasat University (Rangsit Campus), Pathumtani 12121, ThailandCenter of Excellence in Pharmacology and Molecular Biology of Malaria and Cholangiocarcinoma, Chulabhorn International College of Medicine, Thammasat University, Pathumthani 12121, ThailandCenter of Excellence in Pharmacology and Molecular Biology of Malaria and Cholangiocarcinoma, Chulabhorn International College of Medicine, Thammasat University, Pathumthani 12121, ThailandMalaria remains a public health problem in tropical and subtropical regions. Resistance of Plasmodium falciparum to artemisinins in Southeast Asia is a great concern for disease control and research on discovery and development of new alternative antimalarial drugs is urgently required. In a previous study, the fruit of Piper chaba Hunt. was demonstrated to exhibit promising antimalarial activity against the asexual stage of 3D7 (chloroquine-sensitive) and K1 (chloroquine-resistant) P. falciparum clones. The aim of the present study was to further investigate the antimalarial activity of piperine, the major isolated constituent of Piper chaba Hunt. fruits against both P. falciparum clones. The antimalarial activity was determined using SYBR green-I-based assay and morphological change was observed under the light microscope with Giemsa staining. The median IC50 (concentration that inhibits parasite growth by 50%) values of piperine against 3D7 and K1 P. falciparum were 111.5 and 59 μM, respectively. A marked change in parasite morphology was observed within 48 hours of piperine exposure. Results of real-time PCR showed no effect of piperine on modulating the expression of the three genes associated with antimalarial drug resistance in P. falciparum, i.e., pfcrt, pfmdr1, and pfmrp1. Piperine could be a promising candidate for further development as an antimalarial drug based on its antimalarial potency and low risk of resistance development.http://dx.doi.org/10.1155/2018/9486905
spellingShingle Artitaya Thiengsusuk
Phunuch Muhamad
Wanna Chaijaroenkul
Kesara Na-Bangchang
Antimalarial Activity of Piperine
Journal of Tropical Medicine
title Antimalarial Activity of Piperine
title_full Antimalarial Activity of Piperine
title_fullStr Antimalarial Activity of Piperine
title_full_unstemmed Antimalarial Activity of Piperine
title_short Antimalarial Activity of Piperine
title_sort antimalarial activity of piperine
url http://dx.doi.org/10.1155/2018/9486905
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AT phunuchmuhamad antimalarialactivityofpiperine
AT wannachaijaroenkul antimalarialactivityofpiperine
AT kesaranabangchang antimalarialactivityofpiperine