Protective effect of pyruvate against ethanol-induced apoptotic neurodegeneration in the developing rat brain
- Authors
- Ullah, Najeeb; Naseer, Muhammad Imran; Ullah, Ikram; Lee, Hae Young; Koh, Phil Ok; Kim, Myeong Ok
- Issue Date
- Dec-2011
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD
- Keywords
- Ethanol; Apoptotic neurodegeneration; Pyruvate; Neuroprotection; Fetal alcohol syndrome; Fetal alcohol effects
- Citation
- NEUROPHARMACOLOGY, v.61, no.8, pp.1248 - 1255
- Indexed
- SCIE
SCOPUS
- Journal Title
- NEUROPHARMACOLOGY
- Volume
- 61
- Number
- 8
- Start Page
- 1248
- End Page
- 1255
- URI
- https://scholarworks.bwise.kr/gnu/handle/sw.gnu/23475
- DOI
- 10.1016/j.neuropharm.2011.06.031
- ISSN
- 0028-3908
- Abstract
- Exposure to alcohol during the early stages of brain development can lead to neurological disorders in the CNS. Apoptotic neurodegeneration due to ethanol exposure is a main feature of alcoholism. Exposure of developing animals to alcohol (during the growth spurt period in particular) elicits apoptotic neuronal death and causes fetal alcohol effects (FAE) or fetal alcohol syndrome (FAS). A single episode of ethanol intoxication (at 5 g/kg) in a seven-day-old developing rat can activate the apoptotic cascade, leading to widespread neuronal death in the brain. In the present study, we investigated the potential protective effect of pyruvate against ethanol-induced neuroapoptosis. After 4 h, a single dose of ethanol induced upregulation of Bax, release of mitochondrial cytochrome-c into the cytosol, activation of caspase-3 and cleavage of poly (ADP-ribose) polymerase (PARP-1), all of which promote apoptosis. These effects were all reversed by co-treatment with pyruvate at a well-tolerated dosage (1000 mg/kg). Histopathology performed at 24 and 48 h with Fluoro-Jade-B and cresyl violet stains showed that pyruvate significantly reduced the number of dead cells in the cerebral cortex, hippocampus and thalamus. Immunohistochemical analysis at 24 h confirmed that ethanol-induced cell death is both apoptotic and inhibited by pyruvate. These findings suggest that pyruvate treatment attenuates ethanol-induced neuronal cell loss in the developing rat brain and holds promise as a safe therapeutic and neuroprotective agent in the treatment of neurodegenerative disorders in newborns and infants.
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