<i>Garcinia cowa</i> bark extract induces oxidative stress mediated cellular apoptosis in <i>Leishmania donovani</i> parasite modulated by its active phytosterol constituent

Visceral leishmaniasis still remains a leading cause of parasitic deaths, with modern pentavalent antimonials showing limited efficacy and health risks. The methanolic bark extract of the Northeastern Indian plant, <i>Garcinia cowa</i>, demonstrated potent leishmanicidal effects against the parasite <i>Leishmania donovani</i>, demonstrating IC<sub>50</sub> values of 20-36 µg/ml, with selective toxicity for parasites over healthy cells. It induced parasite death through elevated oxidative and nitrosative stress elements, reduced arginase activity, nuclear fragmentation, cell cycle arrest, and apoptosis. A GC-MS study and molecular docking identified stigmasterol as a primary component, an antileishmanial compound that inhibits <i>Leishmania donovani</i> parasite efficiently.

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Journal
Journal of Asian Natural Products Research
Published
2024-11-20
DOI
https://doi.org/10.1080/10286020.2024.2429145
Primary Topic
Research on Leishmaniasis Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Garcinia cowa bark extract induces oxidative stress mediated cellular apoptosis in Leishmania donovani parasite modulated by its active phytosterol constituent

Santanu Paul, Nibedita Pyne, Ishita Bhattacharya
Journal of Asian Natural Products Research
Research on Leishmaniasis Studies
article

Garcinia cowa bark extract induces oxidative stress mediated cellular apoptosis in Leishmania donovani parasite modulated by its active phytosterol constituent

Santanu Paul, Nibedita Pyne, Ishita Bhattacharya
article en

Abstract

Visceral leishmaniasis still remains a leading cause of parasitic deaths, with modern pentavalent antimonials showing limited efficacy and health risks. The methanolic bark extract of the Northeastern Indian plant, <i>Garcinia cowa</i>, demonstrated potent leishmanicidal effects against the parasite <i>Leishmania donovani</i>, demonstrating IC<sub>50</sub> values of 20-36 µg/ml, with selective toxicity for parasites over healthy cells. It induced parasite death through elevated oxidative and nitrosative stress elements, reduced arginase activity, nuclear fragmentation, cell cycle arrest, and apoptosis. A GC-MS study and molecular docking identified stigmasterol as a primary component, an antileishmanial compound that inhibits <i>Leishmania donovani</i> parasite efficiently.

Journal of Asian Natural Products ResearchVol. 27(5)
University of Calcutta (IN)
University Grants Commission of Bangladesh
Zero hunger
Openalex Percentile: Top 68%
Research on Leishmaniasis Studies
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