Cargando…

In Vivo Evaluation of the Anti-Schistosomal Potential of Ginger-Loaded Chitosan Nanoparticles on Schistosoma mansoni: Histopathological, Ultrastructural, and Immunological Changes

Chemotherapy is the most widely advocated method of Schistosome control. However, repeated chemotherapy leads to the emergence of drug-resistant Schistosoma strains. Therefore, efforts to find alternative drugs, especially those of natural origin, have risen globally. Nanoparticles (NPs) have receiv...

Descripción completa

Detalles Bibliográficos
Autores principales: El-Derbawy, Mona M., Salem, Hala S., Raboo, Mona, Baiuomy, Ibrahim R., Fadil, Sana A., Fadil, Haifa A., Ibrahim, Sabrin R. M., El Kholy, Walaa A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696985/
https://www.ncbi.nlm.nih.gov/pubmed/36362992
http://dx.doi.org/10.3390/life12111834
_version_ 1784838446541438976
author El-Derbawy, Mona M.
Salem, Hala S.
Raboo, Mona
Baiuomy, Ibrahim R.
Fadil, Sana A.
Fadil, Haifa A.
Ibrahim, Sabrin R. M.
El Kholy, Walaa A.
author_facet El-Derbawy, Mona M.
Salem, Hala S.
Raboo, Mona
Baiuomy, Ibrahim R.
Fadil, Sana A.
Fadil, Haifa A.
Ibrahim, Sabrin R. M.
El Kholy, Walaa A.
author_sort El-Derbawy, Mona M.
collection PubMed
description Chemotherapy is the most widely advocated method of Schistosome control. However, repeated chemotherapy leads to the emergence of drug-resistant Schistosoma strains. Therefore, efforts to find alternative drugs, especially those of natural origin, have risen globally. Nanoparticles (NPs) have received special interest as efficient drug delivery systems. This work aimed to investigate the anti-schistosomal potential of Zingiber officinale (ginger, Zingiberaceae)-loaded chitosan nanoparticles (GCsNPs) on Schistosoma mansoni experimentally infected mice that were exposed to 80 ± 10 cercariae/mouse. The study groups are: (G1) negative control; (G2) positive control; (G3) praziquantel in a dose of 500 mg/kg/day for two consecutive days; (G4) ginger in a dose of 500 mg/kg treated; (G5) chitosan nanoparticles in a dose 3 mg/kg (G6) GCsNPs in a dose 250 mg/kg; and (G7) GCsNPs in a dose 500 mg/kg. The anti-schistosome potential was assessed using histopathological scanning electron microscopically and immunological parameters. The results showed that there was a significant decrease in cellular granuloma count (p < 0.05) and granuloma diameter (p < 0.001) in all infected treated mice groups, in comparison to the infected non-treated group with the highest reduction in both G3 and G7. SEM of S. mansoni adult worm recovered from G3 showed mild edema of oral and ventral suckers with some peeling and blebs around them, while that recovered from G7 showed abnormal oedematous oral and retracted ventral sucker, edema of the tegument, rupture of many tubercles with vacuolation and complete loss of spines. All infected treated mice groups, in comparison to positive control G2, showed a significant reduction in IL-4, IL-10, and TNF-α levels (p-value < 0.001), especially groups G6 and G7 (p-value < 0.05); both G6 and G7 values were nearer to the normal that indicated recovery of the liver tissue.
format Online
Article
Text
id pubmed-9696985
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-96969852022-11-26 In Vivo Evaluation of the Anti-Schistosomal Potential of Ginger-Loaded Chitosan Nanoparticles on Schistosoma mansoni: Histopathological, Ultrastructural, and Immunological Changes El-Derbawy, Mona M. Salem, Hala S. Raboo, Mona Baiuomy, Ibrahim R. Fadil, Sana A. Fadil, Haifa A. Ibrahim, Sabrin R. M. El Kholy, Walaa A. Life (Basel) Article Chemotherapy is the most widely advocated method of Schistosome control. However, repeated chemotherapy leads to the emergence of drug-resistant Schistosoma strains. Therefore, efforts to find alternative drugs, especially those of natural origin, have risen globally. Nanoparticles (NPs) have received special interest as efficient drug delivery systems. This work aimed to investigate the anti-schistosomal potential of Zingiber officinale (ginger, Zingiberaceae)-loaded chitosan nanoparticles (GCsNPs) on Schistosoma mansoni experimentally infected mice that were exposed to 80 ± 10 cercariae/mouse. The study groups are: (G1) negative control; (G2) positive control; (G3) praziquantel in a dose of 500 mg/kg/day for two consecutive days; (G4) ginger in a dose of 500 mg/kg treated; (G5) chitosan nanoparticles in a dose 3 mg/kg (G6) GCsNPs in a dose 250 mg/kg; and (G7) GCsNPs in a dose 500 mg/kg. The anti-schistosome potential was assessed using histopathological scanning electron microscopically and immunological parameters. The results showed that there was a significant decrease in cellular granuloma count (p < 0.05) and granuloma diameter (p < 0.001) in all infected treated mice groups, in comparison to the infected non-treated group with the highest reduction in both G3 and G7. SEM of S. mansoni adult worm recovered from G3 showed mild edema of oral and ventral suckers with some peeling and blebs around them, while that recovered from G7 showed abnormal oedematous oral and retracted ventral sucker, edema of the tegument, rupture of many tubercles with vacuolation and complete loss of spines. All infected treated mice groups, in comparison to positive control G2, showed a significant reduction in IL-4, IL-10, and TNF-α levels (p-value < 0.001), especially groups G6 and G7 (p-value < 0.05); both G6 and G7 values were nearer to the normal that indicated recovery of the liver tissue. MDPI 2022-11-09 /pmc/articles/PMC9696985/ /pubmed/36362992 http://dx.doi.org/10.3390/life12111834 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
El-Derbawy, Mona M.
Salem, Hala S.
Raboo, Mona
Baiuomy, Ibrahim R.
Fadil, Sana A.
Fadil, Haifa A.
Ibrahim, Sabrin R. M.
El Kholy, Walaa A.
In Vivo Evaluation of the Anti-Schistosomal Potential of Ginger-Loaded Chitosan Nanoparticles on Schistosoma mansoni: Histopathological, Ultrastructural, and Immunological Changes
title In Vivo Evaluation of the Anti-Schistosomal Potential of Ginger-Loaded Chitosan Nanoparticles on Schistosoma mansoni: Histopathological, Ultrastructural, and Immunological Changes
title_full In Vivo Evaluation of the Anti-Schistosomal Potential of Ginger-Loaded Chitosan Nanoparticles on Schistosoma mansoni: Histopathological, Ultrastructural, and Immunological Changes
title_fullStr In Vivo Evaluation of the Anti-Schistosomal Potential of Ginger-Loaded Chitosan Nanoparticles on Schistosoma mansoni: Histopathological, Ultrastructural, and Immunological Changes
title_full_unstemmed In Vivo Evaluation of the Anti-Schistosomal Potential of Ginger-Loaded Chitosan Nanoparticles on Schistosoma mansoni: Histopathological, Ultrastructural, and Immunological Changes
title_short In Vivo Evaluation of the Anti-Schistosomal Potential of Ginger-Loaded Chitosan Nanoparticles on Schistosoma mansoni: Histopathological, Ultrastructural, and Immunological Changes
title_sort in vivo evaluation of the anti-schistosomal potential of ginger-loaded chitosan nanoparticles on schistosoma mansoni: histopathological, ultrastructural, and immunological changes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696985/
https://www.ncbi.nlm.nih.gov/pubmed/36362992
http://dx.doi.org/10.3390/life12111834
work_keys_str_mv AT elderbawymonam invivoevaluationoftheantischistosomalpotentialofgingerloadedchitosannanoparticlesonschistosomamansonihistopathologicalultrastructuralandimmunologicalchanges
AT salemhalas invivoevaluationoftheantischistosomalpotentialofgingerloadedchitosannanoparticlesonschistosomamansonihistopathologicalultrastructuralandimmunologicalchanges
AT raboomona invivoevaluationoftheantischistosomalpotentialofgingerloadedchitosannanoparticlesonschistosomamansonihistopathologicalultrastructuralandimmunologicalchanges
AT baiuomyibrahimr invivoevaluationoftheantischistosomalpotentialofgingerloadedchitosannanoparticlesonschistosomamansonihistopathologicalultrastructuralandimmunologicalchanges
AT fadilsanaa invivoevaluationoftheantischistosomalpotentialofgingerloadedchitosannanoparticlesonschistosomamansonihistopathologicalultrastructuralandimmunologicalchanges
AT fadilhaifaa invivoevaluationoftheantischistosomalpotentialofgingerloadedchitosannanoparticlesonschistosomamansonihistopathologicalultrastructuralandimmunologicalchanges
AT ibrahimsabrinrm invivoevaluationoftheantischistosomalpotentialofgingerloadedchitosannanoparticlesonschistosomamansonihistopathologicalultrastructuralandimmunologicalchanges
AT elkholywalaaa invivoevaluationoftheantischistosomalpotentialofgingerloadedchitosannanoparticlesonschistosomamansonihistopathologicalultrastructuralandimmunologicalchanges