PMID- 17143902 OWN - NLM STAT- MEDLINE DCOM- 20070302 LR - 20131121 IS - 1050-9631 (Print) IS - 1050-9631 (Linking) VI - 17 IP - 1 DP - 2007 TI - Neonatal isolation impairs neurogenesis in the dentate gyrus of the guinea pig. PG - 78-91 AB - In the current study we examined the effects of early isolation rearing on cell proliferation, survival and differentiation in the dentate gyrus of the guinea pig. Animals were assigned to either a standard (control) or an isolated environment a few days after birth (P5-P6), taking advantage of the precocious independence from maternal care of the guinea pig. On P14-P17 animals received one daily bromodeoxyuridine injection, to label dividing cells, and were sacrificed either on P18, to evaluate cell proliferation or on P45, to evaluate cell survival and differentiation. In P18 isolated animals we found a reduced cell proliferation (-35%) compared to controls and a lower expression of brain-derived neurotrophic factor (BDNF). Though in absolute terms P45 isolated animals had less surviving cells, they showed no differences in survival rate and phenotype percent distribution compared to controls. Looking at the location of the new neurons, we found that while in control animals 76% of them had migrated to the granule cell layer, in isolated animals only 55% of the new neurons had reached this layer. Examination of radial glia cells of P18 and P45 animals by vimentin immunohistochemistry showed that in isolated animals radial glia cells were reduced in density and had less and shorter processes. Granule cell count revealed that P45 isolated animals had less (-42%) granule cells than controls. Results show that isolation rearing reduces hippocampal cell proliferation, likely by reducing BDNF expression and hampers migration of the new neurons to the granule cell layer, likely by altering density/morphology of radial glia cells. The large reduction in granule cell number following isolation rearing emphasizes the role of environmental cues as relevant modulators of neurogenesis. FAU - Rizzi, Simona AU - Rizzi S AD - Dipartimento di Fisiologia Umana e Generale, Universita di Bologna, Bologna, Italy. FAU - Bianchi, Patrizia AU - Bianchi P FAU - Guidi, Sandra AU - Guidi S FAU - Ciani, Elisabetta AU - Ciani E FAU - Bartesaghi, Renata AU - Bartesaghi R LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Hippocampus JT - Hippocampus JID - 9108167 RN - 0 (Brain-Derived Neurotrophic Factor) RN - 0 (Glial Fibrillary Acidic Protein) RN - 0 (Vimentin) RN - EC 4.2.1.11 (Phosphopyruvate Hydratase) RN - G34N38R2N1 (Bromodeoxyuridine) SB - IM MH - Age Factors MH - Animals MH - Animals, Newborn MH - Body Weight/physiology MH - Brain-Derived Neurotrophic Factor/metabolism/pharmacology MH - Bromodeoxyuridine/metabolism MH - Cell Count/methods MH - Cell Death/physiology MH - Cell Differentiation/drug effects/physiology MH - Cell Proliferation MH - Dentate Gyrus/*cytology/growth & development MH - Glial Fibrillary Acidic Protein/metabolism MH - Guinea Pigs MH - Immunohistochemistry MH - In Situ Nick-End Labeling/methods MH - Male MH - Neurons/drug effects/*physiology MH - Organ Size MH - Organogenesis/*physiology MH - Phosphopyruvate Hydratase/metabolism MH - *Social Isolation MH - Vimentin/metabolism EDAT- 2006/12/05 09:00 MHDA- 2007/03/03 09:00 CRDT- 2006/12/05 09:00 PHST- 2006/12/05 09:00 [pubmed] PHST- 2007/03/03 09:00 [medline] PHST- 2006/12/05 09:00 [entrez] AID - 10.1002/hipo.20247 [doi] PST - ppublish SO - Hippocampus. 2007;17(1):78-91. doi: 10.1002/hipo.20247.