Differential regulation of the growth-associated proteins GAP-43 and superior cervical ganglion 10 in response to lesions of the cortex and substantia nigra in the adult rat
| Autor: | E.J. Hughes-Davis, C.K. Meshul, J.P. Cogen, Thomas H. McNeill, G. Grenningloh, Heng Wei Cheng, Michael W. Jakowec |
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| Rok vydání: | 2005 |
| Předmět: |
Male
Superior cervical ganglion Pathology medicine.medical_specialty Central nervous system Blotting Western Gene Expression Substantia nigra Striatum Motor Activity Functional Laterality Lesion GAP-43 Protein Basal ganglia medicine Animals Nerve Growth Factors RNA Messenger Gap-43 protein In Situ Hybridization Denervation Cerebral Cortex biology General Neuroscience Membrane Proteins Rats Inbred F344 Rats Up-Regulation Substantia Nigra medicine.anatomical_structure Brain Injuries biology.protein Microtubule Proteins medicine.symptom Carrier Proteins Neuroscience |
| Zdroj: | Neuroscience. 135(4) |
| ISSN: | 0306-4522 |
| Popis: | Investigation of the elements underlying synapse replacement after brain injury is essential for predicting the neural compensation that can be achieved after various types of damage. The growth-associated proteins superior cervical ganglion-10 and growth-associated protein-43 have previously been linked with structural changes in the corticostriatal system in response to unilateral deafferentation. To examine the regulation of this response, unilateral cortical aspiration lesion was carried out in combination with ipsilateral 6-hydroxydopamine lesion of the substantia nigra, and the time course of the contralateral cortical molecular response was followed. Unilateral cortical aspiration lesion in rats corresponds with an upregulation of superior cervical ganglion-10 mRNA at 3 and 10 days post-lesion, and protein, sustained from three to at least 27 days following lesion. With the addition of substantia nigra lesion, the response shifts to an upregulation of growth-associated protein-43 mRNA at 3 and 10 days post-lesion, and protein after 10 days. Nigral lesion alone does not alter contralateral expression of either gene. Likewise, motor function assessment using the rotorod test revealed no significant long-term deficits in animals that sustained only nigrostriatal damage, but cortical lesion was associated with a temporary deficit which was sustained when nigrostriatal input was also removed. Growth-associated protein-43 and superior cervical ganglion-10, two presynaptic genes that are postulated to play roles in lesion-induced sprouting, are differentially upregulated in corticostriatal neurons after cortical versus combined cortical/nigral lesions. The shift in contralateral gene response from superior cervical ganglion-10 to growth-associated protein-43 upregulation and associated behavioral deficit following combined cortical and nigral denervation suggest that nigrostriatal afferents regulate cortical lesion-induced gene expression and ultimate functional outcome. |
| Databáze: | OpenAIRE |
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