PROPHYLACTIC ANTICRYPTOSPORIDIAL ACTIVITY OF ATORVASTATIN VERSUS NITAZOXANIDE ON EXPERIMENTALLY INFECTED IMMUNOSUPPRESSED MURINE MODELS

Autor: Asmaa Mohammed Yousef, Hytham K. Ahmed, Tahani Ismail Farag, Al-Sayed M. Tealeb, Rasha M. S. M. Mohamed, Hanaa A. Atwa, Asmaa M. Farouk Al-Ghandour
Rok vydání: 2020
Předmět:
Zdroj: Journal of the Egyptian Society of Parasitology. 50:535-546
ISSN: 2090-2549
DOI: 10.21608/jesp.2020.131084
Popis: This study investigated the possible prophylactic and curative role of Atorvastatin (ATV) intreatment of cryptosporidiosis in immunosuppressed cases. Immunosuppression was done usingoral dexamethasone (0.25μg/g/day) for 14 days before infection till last scarification. Thestudy included 150 immunosuppressed mice in 5 major groups (N=30): G1: Normal controlgroup, G2: Infected control group, G3: ATV (40mg/kg/day), G4: Nitazoxanide (NTZ; 500-mg/kg/day), G5: combination group. Each one was divided into 3 subgroups of 10 mice each:prophylaxis ones received drug daily for 5 consecutive days before infection only, 1st and 2ndtherapeutic dose groups: mice received the drug for 1 week and 2 weeks after prophylaxis andinfection, respectively. Assessment was done parasitological by formol-ether concentrationand Modified Ziehl-Neelsen staining of stool pellets gathered weekly, immunological by serumIFN-ɣ levels and histopathological by haematoxyline and eosin staining to determine thedrug regimens and parasite impacts on tissues.The results showed a significant reduction in inflammatory changes of ileum, stomach andliver histopathology and in oocysts shed on the 7th day post infection (PI) by 62.08%, 40.55%& 71.78%, on the 14th day (PI) by 78.53%, 53.4%, 87.43% & 90.41%, 57.21%, 94.71% on21st day (PI) in all treated groups respectively, compared to infected untreated control ones.Sera IFN-ɣ levels showed significant increase in combination followed by ATV prophylacticdrug regimens compared to NTZ alone or infected control ones. Combined ATV and NTZprophylaxis gave a good synergistic anticryptosporidial efficacy in immunosuppressed mice.
Databáze: OpenAIRE