The Distributions and Changes of Nerve Fiber in Human Nucleus Pulposus According to the Degenerative Changes.
10.4184/jkss.2004.11.1.24
- Author:
Jun Young YANG
1
;
June Kyu LEE
;
Ui Sung CHOI
;
Hyun Ho LEE
;
Se Min WOO
;
Jung Bum LEE
Author Information
1. Department of Orthopedic Surgery, School of Medicine, Chungnam National University, Taejon, Korea. jyyang@cnuh.co.kr
- Publication Type:Original Article
- Keywords:
Degenerative disc disease;
Nerve fiber;
S-100;
Synaptophysin;
CD-31
- MeSH:
Back Pain;
Blood Vessels;
Chondrocytes;
Diagnosis;
Humans*;
Intervertebral Disc;
Magnetic Resonance Imaging;
Nerve Fibers*;
Nociceptors;
Retrospective Studies;
Synaptophysin
- From:Journal of Korean Society of Spine Surgery
2004;11(1):24-30
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
STUDY DESIGN: This was a retrospective study to evaluate the nerve fibers in human nucleus pulposus. OBJECTIVE: To study the changes in the pain receptor, including the nerve fiber of the disc, immunohistologic studies were performed for S-100, synaptophysin and CD 31. SUMMARY OF LITERATURE REVIEW: Degeneration in a human intervertebral disc is one of the most important causes of back pain. MATERIALS AND METHODS: This study used disc materials obtained from patients that had undergone an operation. According to the patient`s age and diagnoses, the disc materials were subdivided into 3 groups. Group 1; HNP patients aged in their twenties and thirties, with a mean age of 28.3 years. Group 2; HNP patients aged above forty, with a mean age of 43.8 years. Group 3; patients diagnosed with degenerative disc disease through preoperative MRI or discogram, with a mean age of 40.2 years. There were ten in each group. H & E staining, immunohistologic studies for S-100, synaptophysin and CD 31 staining were investigated to find the relationship between blood vessels and nerve fibers. RESULTS: From the H & E staining, inflammatory cells were detected in groups 1 and 2, and partially detected in group 3, but no significant differences were detected between the groups. The chondrocyte morphologies were similar in groups 1 and 2, but the number of chondrocyte in group 3 was significantly decreased, and degeneration was also detected. From the S-100 staining, 0, 10 and 40% positive findings were detected in groups 1, 2 and 3, respectively. For the synaptophysin staining, no positive findings were detected in groups 1 and 2, whereas, 30% positive findings were detected in group 3. No positive results for the CD 31 staining were seen in any of the three groups. CONCLUSION: Pain due to a degenerative disc can be explained by the above results, but its relationship to blood vessels was insufficient. Further study on the changes in the vertebral endplate and annulus fibrosus is recommended.
