Ginger (Zingiber Officinale)-derived nanoparticles in Schistosoma mansoni infected mice: Hepatoprotective and enhancer of etiological treatment

Autor: Yaser A. El-Badry, Ayman A. El-Badry, Soheir Mahmoud, Wegdan Mohamed Abd El Wahab, Doaa A. Hamdy, Mohamed A. El-Badry
Jazyk: angličtina
Rok vydání: 2021
Předmět:
Male
0301 basic medicine
Schistosoma Mansoni
Physiology
Eggs
RC955-962
Administration
Oral

Pharmacology
medicine.disease_cause
Biochemistry
Antioxidants
Praziquantel
Mice
Animal Cells
Reproductive Physiology
Arctic medicine. Tropical medicine
Medicine and Health Sciences
Nanotechnology
Public and Occupational Health
Anthelmintics
Antioxidant Therapy
Granuloma
biology
Pharmaceutics
Mefloquine
Eukaryota
030108 mycology & parasitology
Infectious Diseases
Liver
Granulomas
Schistosoma
Engineering and Technology
Drug Therapy
Combination

Schistosoma mansoni
Cellular Types
Public aspects of medicine
RA1-1270
Research Article
medicine.drug
Immune Cells
Immunology
Schistosomiasis
Ginger
03 medical and health sciences
Drug Therapy
Helminths
parasitic diseases
medicine
Animals
Parasite Egg Count
Prophylaxis
Plant Extracts
business.industry
Therapeutic effect
Organisms
Public Health
Environmental and Occupational Health

Biology and Life Sciences
Cell Biology
medicine.disease
biology.organism_classification
Invertebrates
Schistosomiasis mansoni
030104 developmental biology
Nanoparticles
Pre-Exposure Prophylaxis
Preventive Medicine
business
Zoology
Oxidative stress
Zdroj: PLoS Neglected Tropical Diseases, Vol 15, Iss 5, p e0009423 (2021)
PLoS Neglected Tropical Diseases
ISSN: 1935-2735
1935-2727
Popis: Background Nanotechnology has been manufactured from medicinal plants to develop safe, and effective antischistosmal alternatives to replace today’s therapies. The aim of the study is to evaluate the prophylactic effect of ginger-derived nanoparticles (GNPs), and the therapeutic effect of ginger aqueous extract, and GNPs on Schistosoma mansoni (S. mansoni) infected mice compared to praziquantel (PZQ), and mefloquine (MFQ). Methodology/principal findings Eighty four mice, divided into nine different groups, were sacrificed at 6th, 8th, and 10th week post-infection (PI), with assessment of parasitological, histopathological, and oxidative stress parameters, and scanning the worms by electron microscope. As a prophylactic drug, GNPs showed slight reduction in worm burden, egg density, and granuloma size and number. As a therapeutic drug, GNPs significantly reduced worm burden (59.9%), tissue egg load (64.9%), granuloma size, and number at 10th week PI, and altered adult worm tegumental architecture, added to antioxidant effect. Interestingly, combination of GNPs with PZQ or MFQ gave almost similar or sometimes better curative effects as obtained with each drug separately. The highest therapeutic effect was obtained when ½ dose GNPs combined with ½ dose MFQ which achieved 100% reduction in both the total worm burden, and ova tissue density as early as the 6th week PI, with absence of detected eggs or tissue granuloma, and preservation of liver architecture. Conclusions/significance GNPs have a schistosomicidal, antioxidant, and hepatoprotective role. GNPs have a strong synergistic effect when combined with etiological treatments (PZQ or MFQ), and significantly reduced therapeutic doses by 50%, which may mitigate side effects and resistance to etiological drugs, a hypothesis requiring further research. We recommend extending this study to humans.
Author summary Schistosomiasis is one of the most important tropical diseases that yearly causes millions of morbidities and mortalities. Several researchers are interested in trying variable chemical and herbal drugs for treating the disease. This research introduced a trial for prophylaxis and treating schistosomiasis mansoni in mice using ginger-derived nanoparticles (GNPs). GNPs have antischistosmal, antioxidant and hepatoprotective features. The nano-formulation of ginger provides a safer therapeutic and restorative enhancer to etiological treatments. GNPs may reduce infection complications, reduce required therapeutic doses of Schistosoma-standard drugs, and may help mitigate the side effects of and resistance to standard drugs; hypotheses which require further studies.
Databáze: OpenAIRE