» Articles » PMID: 6707710

Regeneration of Long Spinal Axons in the Rat

Overview
Journal J Neurocytol
Specialty Cell Biology
Date 1984 Feb 1
PMID 6707710
Citations 73
Authors
Affiliations
Soon will be listed here.
Abstract

To investigate regeneration of long spinal axons, the right lateral column of the rat spinal cord was cut at high cervical, low cervical, midthoracic or lumbar level, and one end of an autologous sciatic nerve segment was grafted to the spinal cord at the site of incision. Three to six months after operation, the origin of axons in the grafts was traced retrogradely with horseradish peroxidase injected into the grafts and, in some cases, anterogradely with radioautography of tritiated amino acids injected into the brainstem. Axons from each of the major lateral spinal tracts arising in the brainstem as well as axons ascending from the lower spinal cord succeeded in growing into low cervical grafts. However, long descending axons rarely regenerated after midthoracic or lumbar injury; axons ascending from lumbar segments of the spinal cord usually failed to enter high cervical grafts. Differences in axonal regrowth at the four segmental levels were not simply attributable to dwindling of axonal number in fibre tracts. Axonal regeneration from Clarke's column or the red nucleus was observed only with lesions causing atrophy of many neurons. There was no obvious example of a fibre tract in the lateral spinal columns from which axons failed to regenerate nor from which axons regenerated exceptionally well. Under the conditions of these experiments, the distance from cell body to injury appeared to be an important determinant of axonal regeneration.

Citing Articles

Targeting Spinal Interneurons for Respiratory Recovery After Spinal Cord Injury.

Paracha M, Brezinski A, Singh R, Sinson E, Satkunendrarajah K Cells. 2025; 14(4).

PMID: 39996760 PMC: 11854602. DOI: 10.3390/cells14040288.


Neurons Are Not All the Same: Diversity in Neuronal Populations and Their Intrinsic Responses to Spinal Cord Injury.

Siebert J, Kennedy K, Osterhout D ASN Neuro. 2025; 17(1):2440299.

PMID: 39819292 PMC: 11877619. DOI: 10.1080/17590914.2024.2440299.


Single-Nuclei Sequencing Reveals a Robust Corticospinal Response to Nearby Axotomy But Overall Insensitivity to Spinal Injury.

Wang Z, Kumaran M, Batsel E, Testor-Cabrera S, Beine Z, Alvarez Ribelles A J Neurosci. 2025; 45(8).

PMID: 39746824 PMC: 11841758. DOI: 10.1523/JNEUROSCI.1508-24.2024.


Injury distance limits the transcriptional response to spinal injury.

Wang Z, Kumaran M, Batsel E, Testor-Cabrera S, Beine Z, Alvarez Ribelles A bioRxiv. 2024; .

PMID: 38854133 PMC: 11160615. DOI: 10.1101/2024.05.27.596075.


Development of neural repair therapy for chronic spinal cord trauma: soluble Nogo receptor decoy from discovery to clinical trial.

Howard E, Strittmatter S Curr Opin Neurol. 2023; 36(6):516-522.

PMID: 37865850 PMC: 10841037. DOI: 10.1097/WCO.0000000000001205.