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Hippocampal neurotrophic factor: characterization and response to denervation
Brain Research
|January 22, 1986
Summary
A neurotrophic factor (NTF) in the rat hippocampus supports neuron survival. Its levels increase with age and rise when hippocampal inputs are disrupted, suggesting a glial origin.
Area of Science:
- Neuroscience
- Molecular Biology
- Cell Biology
Background:
- The rat hippocampus contains an acidic macromolecular neurotrophic factor (NTF).
- This NTF supports the survival of cultured chick ciliary ganglion cells.
- Hippocampal NTF concentration increases significantly from birth to adulthood.
Purpose of the Study:
- To investigate the regulation and origin of hippocampal neurotrophic factor (NTF).
- To determine how extrinsic inputs and intrinsic neuronal integrity affect hippocampal NTF levels.
Main Methods:
- Lesioning studies involving entorhinal cortex, locus coeruleus, contralateral hippocampus, and septum.
- Kainic acid treatment to destroy intrinsic hippocampal neurons.
- Administration of methotrexate to inhibit gliosis.
Main Results:
- Disruption of extrinsic inputs (except from the septum) increased hippocampal NTF concentration.
- Destruction of intrinsic hippocampal neurons led to a significant increase in hippocampal NTF.
- Methotrexate suppressed the lesion-induced rise in NTF, indicating reduced gliosis.
Conclusions:
- Hippocampal NTF concentration increases with age and is modulated by extrinsic inputs.
- Evidence suggests a glial origin for hippocampal NTF.
- The factor's production is linked to gliosis, a reactive process in glial cells.