Skip to main content Accessibility help
×
Hostname: page-component-77c89778f8-gq7q9 Total loading time: 0 Render date: 2024-07-23T20:23:33.415Z Has data issue: false hasContentIssue false
This chapter is part of a book that is no longer available to purchase from Cambridge Core

6 - Consolidation and maturation of regeneration

Douglas W. Zochodne
Affiliation:
University of Calgary
Get access

Summary

Regeneration is an ongoing process. Once axons form growth cones that cross injury zones, navigate distal stumps and approach former targets, they encounter additional challenges. The interaction of new axons with their targets involves a new series of events with new molecular requirements. Similarly axons are not fully effective the moment they reach their target. They must grow in caliber and may need to myelinate. This chapter will address these events.

Forming new nerve trunks after transection

After the transection of a nerve stump, the proximal and distal stump retract apart because they are normally under some degree of tension. Retraction leaves a gap. In some cases, the gap can be repaired by suturing nerve stumps together, but this is not always possible. Early studies successfully connected the stumps with conduits, tubes, or in one report, synovium propped open by a stainless steel spiral. Various surgical innovations are reviewed in more detail in other texts and sources [421,422,660,775]. They include nerve grafts, silicone tubes, vein–muscle conduits, fibronectin mats, veins, synthetic longitudinal filaments, collagen tubes, polymer biodegradable tubes, and others. With these strategies, eventual complete reconstitution of a severed new nerve trunk from the proximal to the distal stump can occur. This was initially described by Lundborg and colleagues [424–427].

When proximal and distal stumps are connected by tubes, an eventual connection therefore does develop as discussed in the previous chapter [610,740]. In the first week, extracellular exudative fluid and a fibrin matrix clot form within the tubes.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2008

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Armati, P. J. (2007). The Biology of Schwann Cells, Cambridge, UK: Cambridge University Press [23].CrossRefGoogle Scholar
Lundborg, G. (2004). Nerve Injury and Repair. Regeneration, Reconstruction and Cortical Remodeling. Elsevier [421].Google Scholar
Mirsky, R. & Jessen, K. R. (1999). The neurobiology of Schwann cells. Brain Pathology, 9, 293–311 [475].CrossRefGoogle ScholarPubMed

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×