| Literature DB >> 14698483 |
Dong Hoon Shin1, Eunju Lee, Jong-Wan Kim, Bum-Sun Kwon, Mi Kyung Jung, Youn Hee Jee, Jaehyup Kim, Su-ryeon Bae, Young Pyo Chang.
Abstract
Recent studies have shown that growth hormone (GH) can reduce neuronal loss after hypoxic-ischemic injury (HI) in neonatal and juvenile rat brains. Here, we investigated whether GH exerts its neuroprotective role through an anti-apoptotic effect in neonatal rat brains damaged by severe HI. Gross and histological observations showed that the extent of brain damage was found to be reduced in GH-treated brain at E7 after injury. In a terminal transferase-mediated dUTP nick-end-labeling (TUNEL) study, TUNEL-positive apoptotic cells were localized only at the damaged region in animals treated with saline, which was confirmed by an electron microscopy. In an immunohistochemical study with anti-bcl-2, -bax, -bad, -neuronal nitric oxide synthase (nNOS), -inducible NOS (iNOS) and -endothelial NOS (eNOS) antibodies, we observed that bax, bad, iNOS and eNOS were elevated in the saline-treated group. This study thus suggests that the protective role of GH against HI injury is mediated thorough an anti-apoptotic effect, which offers the possibility of a GH application for the treatment of neonatal HI encephalopathy.Entities:
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Year: 2004 PMID: 14698483 DOI: 10.1016/j.neulet.2003.09.070
Source DB: PubMed Journal: Neurosci Lett ISSN: 0304-3940 Impact factor: 3.046