Literature DB >> 19125408

Extensive spinal decussation and bilateral termination of cervical corticospinal projections in rhesus monkeys.

Ephron S Rosenzweig1, John H Brock, Maya D Culbertson, Paul Lu, Rod Moseanko, V Reggie Edgerton, Leif A Havton, Mark H Tuszynski.   

Abstract

To examine neuroanatomical mechanisms underlying fine motor control of the primate hand, adult rhesus monkeys underwent injections of biotinylated dextran amine (BDA) into the right motor cortex. Spinal axonal anatomy was examined using detailed serial-section reconstruction and modified stereological quantification. Eighty-seven percent of corticospinal tract (CST) axons decussated in the medullary pyramids and descended through the contralateral dorsolateral tract of the spinal cord. Eleven percent of CST axons projected through the dorsolateral CST ipsilateral to the hemisphere of origin, and 2% of axons projected through the ipsilateral ventromedial CST. Notably, corticospinal axons decussated extensively across the spinal cord midline. Remarkably, nearly 2-fold more CST axons decussated across the cervical spinal cord midline (approximately 12,000 axons) than were labeled in all descending components of the CST (approximately 6,700 axons). These findings suggest that CST axons extend multiple segmental collaterals. Furthermore, serial-section reconstructions revealed that individual axons descending in either the ipsilateral or contralateral dorsolateral CST can: 1) terminate in the gray matter ipsilateral to the hemisphere of origin; 2) terminate in the gray matter contralateral to the hemisphere of origin; or 3) branch in the spinal cord and terminate on both sides of the spinal cord. These results reveal a previously unappreciated degree of bilaterality and complexity of corticospinal projections in the primate spinal cord. This bilaterality is more extensive than that of the rat CST, and may resemble human CST organization. Thus, augmentation of sprouting of these extensive bilateral CST projections may provide a novel target for enhancing recovery after spinal cord injury.

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Year:  2009        PMID: 19125408      PMCID: PMC2706096          DOI: 10.1002/cne.21940

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  57 in total

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  67 in total

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Authors:  Marie-Francoise Chesselet; S Thomas Carmichael
Journal:  Neurotherapeutics       Date:  2012-04       Impact factor: 7.620

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Authors:  Rafer Willenberg; Katherine Zukor; Kai Liu; Zhigang He; Oswald Steward
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Journal:  J Neurosci       Date:  2014-10-15       Impact factor: 6.167

Review 5.  Animal models of neurologic disorders: a nonhuman primate model of spinal cord injury.

Authors:  Yvette S Nout; Ephron S Rosenzweig; John H Brock; Sarah C Strand; Rod Moseanko; Stephanie Hawbecker; Sharon Zdunowski; Jessica L Nielson; Roland R Roy; Gregoire Courtine; Adam R Ferguson; V Reggie Edgerton; Michael S Beattie; Jacqueline C Bresnahan; Mark H Tuszynski
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Journal:  J Physiol       Date:  2013-02-04       Impact factor: 5.182

7.  Volumetric effects of motor cortex injury on recovery of ipsilesional dexterous movements.

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8.  Enhanced axonal transport: A novel form of "plasticity" after primate and rodent spinal cord injury.

Authors:  J H Brock; E S Rosenzweig; H Yang; M H Tuszynski
Journal:  Exp Neurol       Date:  2017-12-22       Impact factor: 5.330

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Journal:  Front Mol Neurosci       Date:  2009-10-30       Impact factor: 5.639

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