Abstract

BackgroundChronic low back pain (LBP) is the most common cause of disability worldwide. New ideas surrounding LBP are emerging that are based on interactions between mechanical, biological and chemical influences on the human IVD. The degenerate IVD is proposed to be innervated by sensory nerve fibres and vascularised by blood vessels, and it is speculated to contribute to pain sensation. However, the incidence of nerve and blood vessel ingrowth, as well as whether these features are always associated, is unknown. We investigated the presence of nerves and blood vessels in the nucleus pulposus (NP) of the IVD in a large population of human discs.MethodsImmunohistochemistry was performed with 61 human IVD samples, to identify and localise nerves (neurofilament 200 [NF200]/protein gene product 9.5) and blood vessels (CD31) within different regions of the IVD.ResultsImmunopositivity for NF200 was identified within all regions of the IVD within post-mortem tissues. Nerves were seen to protrude across lamellar ridges and through matrix towards NP cells. Nerves were identified deep within the NP and were in many cases, but not always, seen in close proximity to fissures or in areas where decreased matrix was seen. Fifteen percent of samples were degenerate and negative for nerves and blood vessels, whilst 16 % of all samples were degenerate with nerves and blood vessels. We identified 52 % of samples that were degenerate with nerves but no blood vessels. Interestingly, only 4 % ofall samples were degenerate with no nerves but positive for blood vessels. Of the 85 samples investigated, only 6 % of samples were non-degenerate without nerves and blood vessels and 7 % had nerves but no blood vessels.ConclusionsThis study addresses the controversial topic of nerve and blood vessel ingrowth into the IVD in a large number of human samples. Our findings demonstrate that nerves are present within a large proportion of NP samples from degenerate IVDs. This study shows a possible link between nerve ingrowth and degeneration of the IVD and suggests that nerves can migrate in the absence of blood vessels.

Highlights

  • Chronic low back pain (LBP) is the most common cause of disability worldwide

  • Analysis revealed that % of all samples were degenerate and negative for nerves and blood vessels (NF200−/cluster of differentiation factor 31 (CD31) −), whilst % of all samples were degenerate with nerves and blood vessels (NF200+/CD31+) (Fig. 3a)

  • We identified 52 % of samples that were degenerate with nerves but no blood vessels (NF200 +/CD31−) (Fig. 3a)

Read more

Summary

Introduction

New ideas surrounding LBP are emerging that are based on interactions between mechanical, biological and chemical influences on the human IVD. We investigated the presence of nerves and blood vessels in the nucleus pulposus (NP) of the IVD in a large population of human discs. New ideas surrounding LBP are slowly emerging that are based on studies demonstrating interactions between mechanical, biological and chemical influences on the human IVD. Studies using animal models to identify the innervation patterns of the lumbar discs have revealed that the dorsal portion of L5-S1 is innervated by the dorsal root ganglion (DRG) from L2 by the paravertebral trunk, whereas L3-L5 DRG innervate through the sinuvertebral nerve, these patients feel non-specific pain [4, 5]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call