Abstract

BackgroundThe purpose of this study was to establish a novel rat model for ligamentum flavum (LF) hypertrophy using increased motion of lumbar and to elucidate the etiology of (LFH).MethodsA total number of 30 male rats were used. The increased motion of lumbar was induced by surgical resection of L5/6 posterior elements (n = 15). The other rats underwent a sham operation (n = 15). After 8 weeks, all rats were taken lateral plain X-rays. The LF from L5/6 in both groups were harvested to investigate histological, immunohistological, and real-time PCR analysis.ResultsAccording to radiological results, the disc height ratio, flexion ratio, and extension ratio were larger in the rats in the experimental group than that of in the sham group. The HE staining showed that the LF thickness in the experimental group significantly increased in comparison to the sham group. The Masson trichrome staining showed that the ratio of elastic fibers to collagen fibers in experimental group was lower than that in the sham group. The protein and gene expression of TGF-β1, TNF-α, IL-1β, and Col 1 were significantly higher in the experimental group than that in the sham group.ConclusionA relatively safe, simple, and rapid rat model of LFH using increased motion of lumbar was established. The increased motion of lumbar could lead to high expression of inflammatory and fibrotic factors in LF, causing the accumulation of collagen fibers and decreasing of elastic fibers.

Highlights

  • The purpose of this study was to establish a novel rat model for ligamentum flavum (LF) hypertrophy using increased motion of lumbar and to elucidate the etiology of (LFH)

  • The disc height ratios (DHR) in flexion, extension ratio (ER), and flexion ratio (FR) were larger in the rats in the experimental group than that of in the sham group (Fig. 2b-d)

  • The increased motion of lumbar induced ligamentum flavum hypertrophy (LFH) In order to test whether increased motion of lumbar brought about LFH, we compared the L5/6 axial cross-sectional pathological section of all rats

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Summary

Introduction

The purpose of this study was to establish a novel rat model for ligamentum flavum (LF) hypertrophy using increased motion of lumbar and to elucidate the etiology of (LFH). There are approximately 250,000 to 500, 000 LSCS patients in the United States [2] In these patients with LSCS, protruded lumbar discs, ligamentum flavum hypertrophy (LFH) and bulged facet joints. Wang et al BMC Musculoskeletal Disorders (2021) 22:334 human hypertrophied LF The inflammatory factors such as Interleukin-1 (IL-1β), Tumor Necrosis Factor (TNFα), and fibrogenic cytokines such as Transforming Growth Factor-β1 (TGF-β1) were observed [7,8,9]. Whether such factors are causative or merely a consequence of LFH remains unknown. Basic research using an experimental animal model is necessary to clarify its pathomechanism

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