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Biogenic Selenium Nanoparticles Target Chronic Toxoplasmosis With Minimal Cytotoxicity in a Mouse Model Publisher Pubmed



Keyhani A1 ; Ziaali N2 ; Shakibaie M3 ; Kareshk AT4 ; Shojaee S5 ; Asadishekaari M6 ; Sepahvand M7 ; Mahmoudvand H8
Authors
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Authors Affiliations
  1. 1. Department of Disease Prevention, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
  2. 2. Research Center of Tropical and Infectious Diseases, Kerman University of Medical Sciences, Kerman, Iran
  3. 3. Pharmaceutics Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran
  4. 4. Infectious Diseases Research Center, Birjand University of Medical Sciences, Birjand, Iran
  5. 5. Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  6. 6. Neuroscience Research Center, Kerman University of Medical Sciences, Kerman, Iran
  7. 7. Student Research Committee, Lorestan University of Medical Sciences, Khorramabad, Iran
  8. 8. Razi Herbal Medicines Research Center, Lorestan University of Medical Sciences, Khorramabad, Iran

Source: Journal of Medical Microbiology Published:2020


Abstract

Introduction. Nanoparticles (NPs) have numerous biological benefits due to their large surface-volume ratio and convenient entry into cells compared to other particles. Previous research has shown the antimicrobial properties of biogenic selenium NPs (SeNps) and their effects on cellular immunomodulatory cytokines that play a key role in controlling infections. Aim. This study aimed to evaluate the therapeutic effects of SeNPs against chronic toxoplasmosis in mice. Methodology. Infected mice with Toxoplasma gondii (Tehran strain) were orally treated with SeNPs at doses of 2.5, 5 and 10 mg kg−1 once a day for 14 days. On the fifthteenth day, the mean number of brain-tissue cysts and the mRNA levels of TNF-α, IL-12, IL-10, IFN-γ and inducible nitric oxide synthase (iNOS) in the mice of each group were recorded. Moreover, serum clinical chemistry factors in the treated mice were examined to determine the safety of SeNPs. Results. The mean number of tissue cysts was significantly (P<0.001) decreased in mice treated with SeNPs in a dose-dependent manner compared with the control group. The mRNA levels of inflammatory cytokines were significantly increased in mice treated with SeNPs at a dose of 10 mg kg−1 compared with the control subgroup (P<0.05). No significant variation (P>0.05) observed in clinical chemistry parameters among the mice in the control subgroup compared with those treated with SeNPs. Conclusion. The findings demonstrated the therapeutic effects of SeNPs with no considerable toxicity against latent toxoplasmosis in the mouse model. Nevertheless, further studies are obligatory to reveal the exact anti-Toxoplasma mechanisms of SeNPs. © 2020 The Authors
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