Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Sep;66(3):812-826.
doi: 10.1007/s11686-020-00326-8. Epub 2021 Feb 2.

Evaluation of In vitro and In vivo Protective Efficacy of Bauhinia variegata Against Leishmania donovani in Murine Model

Affiliations

Evaluation of In vitro and In vivo Protective Efficacy of Bauhinia variegata Against Leishmania donovani in Murine Model

Gurpreet Kaur et al. Acta Parasitol. 2021 Sep.

Abstract

Purpose: Visceral leishmaniasis is one of the ignored parasitic infection affecting millions of people globally. Currently, available treatment options are unsatisfactory because of high cost and side effects of the leishmanicidal drugs. Therefore, herbal medicines provide a promising choice for the detection of efficient and novel leishmanicidal therapeutics which can rejuvenate the immune response of the host with less adverse effects. The objective of the present study was to determine the in vitro and in vivo effect of hydroethanolic extract of Bauhinia variegata (HEBV) against Leishmania donovani.

Methods: The in vitro efficacy and cytotoxicity of HEBV was checked against L. donovani and THP1 human macrophages. Further HEBV (500 and 1000 mg/kg b.wt.) were given orally to inbred BALB/c mice infected with L. donovani for 2 weeks and euthanized on 14th post treatment day. Various parameters like parasite load, delayed-type hypersensitivity (DTH) responses, T cells, Th1/Th2 cytokines, histological and biochemical tests were investigated.

Results: HEBV showed marked antileishmanial activity with cell cycle arrest at sub-G0/G1 phase. HEBV was found to be more effective at higher dose in declining parasite concentration in the spleen as compared to the lower dose. Moreover, the extract augmented the DTH reaction and T cell responses in the infected mice. Oral administration of HEBV caused the enhancement of disease-suppressing Th1 cytokines and suppression of disease-progressing Th2 cytokines with no toxicities.

Conclusion: Thus, HEBV showed the antileishmanial efficacy through the generation of pro-inflammatory immunity of the host which further suggests the mechanistic exploration of it as a leishmanicidal therapeutic.

Keywords: Bauhinia variegata; CD8+ T cells; DTH responses; Sub-G0/G1 phase; Th1 cytokines; Visceral leishmaniasis.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Álvarez-Velilla R, del Camino G-C, Punzón C, Pérez-Pertejo MY, Balaña-Fouce R, Fresno M, Reguera RM (2019) A chronic bioluminescent model of experimental visceral leishmaniasis for accelerating drug discovery. Plos Neglect Trop D 13:e0007133. https://doi.org/10.1371/journal.pntd.0007133 - DOI
    1. Freitas-Junior LH, Chatelain E, Kim HA, Siqueira-Neto JL (2012) Visceral leishmaniasis treatment: what do we have, what do we need and how to deliver it? Int J Parasitol Drugs Drug Resist 2:11–19. https://doi.org/10.1016/j.ijpddr.2012.01.003 - PMC - DOI - PubMed
    1. Monge-Maillo B, López-Vélez R (2013) Therapeutic options for visceral leishmaniasis. Drugs 73:1863–1888. https://doi.org/10.1007/s40265-013-0133-0 - PMC - DOI - PubMed
    1. Ponte-Sucre A, Gamarro F, Dujardin JC, Barrett MP, López-Vélez R, García-Hernández R, Pountain AW, Mwenechanya R, Papadopoulou B (2017) Drug resistance and treatment failure in leishmaniasis: a 21st century challenge. Plos Neglect Trop D 11:0006052. https://doi.org/10.1371/journal.pntd.0006052 - DOI
    1. Berger BJ, Fairlamb AH (1992) Interactions between immunity and chemotherapy in the treatment of the trypanosomiases and leishmaniases. Parasitology 105:S71–S78. https://doi.org/10.1017/S0031182000075375 - DOI - PubMed

LinkOut - more resources