Abstract

BackgroundImpaired lumbar artery flow has been reported in clinical and epidemiological studies to be associated with low back pain and lumbar disc degeneration. However, it has not been experimentally demonstrated that impaired lumbar artery flow directly induces intervertebral disc (IVD) degeneration by affecting IVD matrix metabolism. The purpose of this study was to evaluate whether ligation of the lumbar artery can affect degenerative changes in the rabbit IVD.MethodsNew Zealand White rabbits (n = 20) were used in this study. Under general anesthesia, the third and fourth lumbar arteries were double-ligated using vascular clips. The blood flow to the L3/L4 disc (cranial disc) was reduced by ligation of the third lumbar artery and that of the L5/L6 disc (caudal disc) by ligation of the fourth lumbar artery. The blood flow to the L4/L5 disc (bilateral disc) was decreased by ligation of both the third and fourth lumbar arteries. The L2/L3 disc was used as the control. Disc height was radiographically monitored biweekly until 12 weeks after surgery. The rabbits were sacrificed at 4, 8, and 12 weeks after surgery and magnetic resonance imaging (MRI) T2-mapping, histology and immunohistochemistry were assessed.ResultsLumbar artery ligation did not induce significant changes in disc height between control and ischemic discs (cranial, bilateral and caudal discs) during the 12-week experimental period. T2-values of ischemic discs had no significant trend to be lower than those of the control L2/L3 discs. Histologically, Safranin-O staining changed following ligation of corresponding IVD lumbar arteries. Histological grading scores for disc degeneration, which correlated significantly with MRI T2-values, had significant changes after the surgery. Immunohistochemical analysis showed that the ligation of lumbar arteries significantly affected a change in the percentage of HIF-1α immunoreactive cells of ischemia discs compared to that of control discs four weeks after the surgery (p < 0.05).ConclusionsThe MRI and histology results suggest that diminished flow in lumbar arteries induce mild changes in the extracellular matrix metabolism of rabbit IVDs. These matrix changes, however, were not progressive and differed from the degenerative disc changes seen in the process of human IVD degeneration.

Highlights

  • Impaired lumbar artery flow has been reported in clinical and epidemiological studies to be associated with low back pain and lumbar disc degeneration

  • The %disc height index (DHI) of each experimental group significantly decreased during the observation period (p < 0.01, 2-way repeated measures ANOVA), the analysis of variance showed no significant interaction between disc level and time-point (p = 0.83)

  • T2-values of the control, cranial, bilateral, and caudal discs (n = 5, respectively at each time point) showed significant decreases during the experimental period (p < 0.01, 2-way repeated measures ANOVA), the analysis of variance showed no significant interaction between disc level and time-point (p = 0.58)

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Summary

Introduction

Impaired lumbar artery flow has been reported in clinical and epidemiological studies to be associated with low back pain and lumbar disc degeneration. It has not been experimentally demonstrated that impaired lumbar artery flow directly induces intervertebral disc (IVD) degeneration by affecting IVD matrix metabolism. Intervertebral disc (IVD) degeneration, clinically characterized by radiographic findings including the decreased signal intensity of magnetic resonance imaging (MRI) T2-weighted imaging [2] and disc height narrowing [3], is a proven major contributor to discogenic low back pain [4]. The IVD is anatomically classified as a symphysis It consists of the gelatinous nucleus pulposus (NP) surrounded by the annulus fibrosus (AF), a concentrically organized lamella structure of collagen fibers. A definitive biochemical feature of IVD degeneration is degradation of the ECM resulting from loss of PGs and collagens caused by the homeostatic imbalance between anabolism and catabolism [7]

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