Heba Elsayed Abd Elhaliam Baioumy
Lecturer
Filgrastim protects the cerebellar cortex against TNF-α/Bax enhanced apoptosis after aluminum toxicity in albino rats. Histological and immunohistochemical study
EJH • 2024
Publication Information
Authors
هبة بيومي*- منى عطيه*- هاله طه شعلان**- ابتسام بدير *** -ايناس الجندي
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Journal
EJH
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publication.type
International
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Abstract
Aluminum (Al) is a strong toxicant affecting the brain neurons. Filgrastim can be a promising protective drug.
Aim of the work: Evaluation of the neuro-alleviating role of Filgrastim on the Aluminum-induced neuronal toxicity in the cerebellar cortex.
Material and methods: Thirty-two adult male albino rats were used in this study. The rats were divided into sets; group I (control group): rats received no drugs. Group II (Aluminum Chloride group): rats received AlCl3 at a dose of (150 mg/kg/bw; orally) dissolved in normal saline for 21 days, group III (Filgrastim +AlCl3 group): rats were trated with aluminum chloride (AlCl3) as in group II for 21 days, and were injected subcutaneously with Filgrastim at a dose of (40 μg/kg/day) for three days before AlCl3 and continued for another 21 days with AlCl3 (Filgrastim was injected 30 minutes before AlCl3). Following fixation, skulls were opened and the cerebellar cortex samples were directly handled for light and electron microscopic examination.
Outcomes: The results of this study lead to the conclusion that Filgrastim protects the cerebellar cortex against aluminum toxicity. The histological observations showed that group II revealed extensive cerebellar cortex affection with vacuolated apoptotic cells and degenerated nerve fibers. Calbindin immunoreactivity showed a significant down-regulation (P
Aim of the work: Evaluation of the neuro-alleviating role of Filgrastim on the Aluminum-induced neuronal toxicity in the cerebellar cortex.
Material and methods: Thirty-two adult male albino rats were used in this study. The rats were divided into sets; group I (control group): rats received no drugs. Group II (Aluminum Chloride group): rats received AlCl3 at a dose of (150 mg/kg/bw; orally) dissolved in normal saline for 21 days, group III (Filgrastim +AlCl3 group): rats were trated with aluminum chloride (AlCl3) as in group II for 21 days, and were injected subcutaneously with Filgrastim at a dose of (40 μg/kg/day) for three days before AlCl3 and continued for another 21 days with AlCl3 (Filgrastim was injected 30 minutes before AlCl3). Following fixation, skulls were opened and the cerebellar cortex samples were directly handled for light and electron microscopic examination.
Outcomes: The results of this study lead to the conclusion that Filgrastim protects the cerebellar cortex against aluminum toxicity. The histological observations showed that group II revealed extensive cerebellar cortex affection with vacuolated apoptotic cells and degenerated nerve fibers. Calbindin immunoreactivity showed a significant down-regulation (P