| Literature DB >> 30255215 |
Eduardo Farias Sanches1, Lauren Valentim2,3, Felipe de Almeida Sassi2,3, Lisiane Bernardi2, Nice Arteni3, Simone Nardin Weis3, Felipe Kawa Odorcyk3, Patricia Pranke2,4, Carlos Alexandre Netto3.
Abstract
Neonatal hypoxia-ischemia (HI) is associated to cognitive and motor impairments and until the moment there is no proven treatment. The underlying neuroprotective mechanisms of stem cells are partially understood and include decrease in excitotoxicity, apoptosis and inflammation suppression. This study was conducted in order to test the effects of intracardiac transplantation of human dental pulp stem cells (hDPSCs) for treating HI damage. Seven-day-old Wistar rats were divided into four groups: sham-saline, sham-hDPSCs, HI-saline, and HI-hDPSCs. Motor and cognitive tasks were performed from postnatal day 30. HI-induced cognitive deficits in the novel-object recognition test and in spatial reference memory impairment which were prevented by hDPSCs. No motor impairments were observed in HI animals. Immunofluorescence analysis showed human-positive nuclei in hDPSC-treated animals closely associated with anti-GFAP staining in the lesion scar tissue, suggesting that these cells were able to migrate to the injury site and could be providing support to CNS cells. Our study evidence novel evidence that hDPSC can contribute to the recovery following hypoxia-ischemia and highlight the need of further investigation in order to better understand the exact mechanisms underlying its neuroprotective effects.Entities:
Keywords: Cellular therapy; Dental pulp stem cells; Memory; Neonatal hypoxia-ischemia; hDPSCs
Mesh:
Year: 2018 PMID: 30255215 DOI: 10.1007/s11064-018-2647-z
Source DB: PubMed Journal: Neurochem Res ISSN: 0364-3190 Impact factor: 3.996