Literature DB >> 9261776

Ultrastructural characteristics of glutamatergic and GABAergic terminals in cat lamina IX before and after spinal cord injury.

Q Tai1, K Palazzolo, A Mautes, W Nacimiento, J P Kuhtz-Buschbeck, A C Nacimiento, H G Goshgarian.   

Abstract

The present study was designed to: 1) morphologically characterize cat glutamate and GABAergic synaptic terminals in lamina IX in the intact spinal cord at the electron microscopic level using postembedding immunochemical techniques and .2), begin an analysis of how the synaptic architecture of glutamate and GABAergic terminals changes after an ipsilateral spinal cord hemisection. The present study shows that glutamate immunoreactive terminals are characterized by a wide synaptic cleft, asymmetric synaptic membrane densities and spherical synaptic vesicles. Most of the glutamatergic terminals are presynaptic to small or medium size dendrites. In contrast, GABAergic terminals display typical pleomorphic synaptic vesicles, a narrow synaptic cleft and a symmetrical membrane density. Qualitative analysis indicated that 13-17 months after hemisection, the length of the synaptic active zones in both glutamatergic and GABAergic terminals ipsilateral to hemisection is longer than those observed in the terminals contralateral to hemisection orfin normal control cats. Furthermore, the perimeters of both dendrites and either glutamate or GABA immunoreactive terminals are longer on the hemisected side compared with those observed in the nonhemisected side of the spinal cord. The results are important for complete understanding of the mechanisms which underlie locomotor recovery in mammals following spinal cord injury.

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Year:  1997        PMID: 9261776     DOI: 10.1080/10790268.1997.11719481

Source DB:  PubMed          Journal:  J Spinal Cord Med        ISSN: 1079-0268            Impact factor:   1.985


  6 in total

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Authors:  David Parker
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2006-01-29       Impact factor: 6.237

2.  Phrenic motoneuron discharge patterns following chronic cervical spinal cord injury.

Authors:  Kun-Ze Lee; Brendan J Dougherty; Milapjit S Sandhu; Michael A Lane; Paul J Reier; David D Fuller
Journal:  Exp Neurol       Date:  2013-08-13       Impact factor: 5.330

3.  Use-dependent modulation of inhibitory capacity in the feline lumbar spinal cord.

Authors:  Niranjala J K Tillakaratne; Ray D de Leon; Thao X Hoang; Roland R Roy; V Reggie Edgerton; Allan J Tobin
Journal:  J Neurosci       Date:  2002-04-15       Impact factor: 6.167

4.  Serotonin receptors 5-HT1A and 5-HT3 reduce hyperexcitability of dorsal horn neurons after chronic spinal cord hemisection injury in rat.

Authors:  Bryan C Hains; William D Willis; Claire E Hulsebosch
Journal:  Exp Brain Res       Date:  2003-01-25       Impact factor: 1.972

Review 5.  Synaptic plasticity, neurogenesis, and functional recovery after spinal cord injury.

Authors:  Corinna Darian-Smith
Journal:  Neuroscientist       Date:  2009-04       Impact factor: 7.519

Review 6.  GABAergic Mechanisms Can Redress the Tilted Balance between Excitation and Inhibition in Damaged Spinal Networks.

Authors:  Graciela Lujan Mazzone; Atiyeh Mohammadshirazi; Jorge Benjamin Aquino; Andrea Nistri; Giuliano Taccola
Journal:  Mol Neurobiol       Date:  2021-04-07       Impact factor: 5.590

  6 in total

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