Moderate traumatic brain injury causes acute dendritic and synaptic degeneration in the hippocampal dentate gyrus

• Published in: PloS one 2011-09, Vol.6 (9), p.e24566-e24566
• Main Authors: Gao, Xiang, Deng, Ping, Xu, Zao C, Chen, Jinhui
• Format: Article
• Language: English
• Subjects: Alzheimer's disease; Animals; Apoptosis; Beading; Biology; Brain; Brain injuries; Brain Injuries - pathology; Brain research; Cell death; Cortex; Degeneration; Dendritic spines; Dendritic structure; Dentate gyrus; Dentate Gyrus - injuries; Dentate Gyrus - pathology; Epilepsy; Golgi Apparatus - metabolism; Green Fluorescent Proteins - metabolism; Head injuries; Hippocampus; Hippocampus - metabolism; Immunohistochemistry; Laboratories; Learning; Male; Medicine; Memory; Mice; Mice, Inbred C57BL; Mice, Transgenic; Microscopy, Fluorescence - methods; Neurodegeneration; Neurodegenerative Diseases - pathology; Neurons; Neurons - metabolism; Neurons - pathology; Neurosciences; Neurosurgery; Perfusion; Physiological aspects; Rodents; Spinal cord; Synapses; Synapses - pathology; Time Factors; Topography; Transgenic animals; Trauma; Traumatic brain injury
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0024566

Hippocampal injury-associated learning and memory deficits are frequent hallmarks of brain trauma and are the most enduring and devastating consequences following traumatic brain injury (TBI). Several reports, including our recent paper, showed that TBI brought on by a moderate level of controlled cortical impact (CCI) induces immature newborn neuron death in the hippocampal dentate gyrus. In contrast, the majority of mature neurons are spared. Less research has been focused on these spared neurons, which may also be injured or compromised by TBI. Here we examined the dendrite morphologies, dendritic spines, and synaptic structures using a genetic approach in combination with immunohistochemistry and Golgi staining. We found that although most of the mature granular neurons were spared following TBI at a moderate level of impact, they exhibited dramatic dendritic beading and fragmentation, decreased number of dendritic branches, and a lower density of dendritic spines, particularly the mushroom-shaped mature spines. Further studies showed that the density of synapses in the molecular layer of the hippocampal dentate gyrus was significantly reduced. The electrophysiological activity of neurons was impaired as well. These results indicate that TBI not only induces cell death in immature granular neurons, it also causes significant dendritic and synaptic degeneration in pathohistology. TBI also impairs the function of the spared mature granular neurons in the hippocampal dentate gyrus. These observations point to a potential anatomic substrate to explain, in part, the development of posttraumatic memory deficits. They also indicate that dendritic damage in the hippocampal dentate gyrus may serve as a therapeutic target following TBI.