Development of Novel Animal Model for Studying Scoliosis Using a Noninvasive Method and Its Validation through Gene-Expression Analysis
- Author:
Rajkiran Reddy BANALA
1
;
Satish Kumar VEMURI
;
Murahari PENKULINTI
;
Gurava Reddy AV
;
Subbaiah GPV
Author Information
- Publication Type:Original Article
- Keywords: Adolescent idiopathic scoliosis; Noninvasive method; Inflammation; Histopathology
- MeSH: Animals; Braces; Brain; Congenital Abnormalities; Female; Fibrosis; Gene Expression; Humans; Inflammation; Interleukins; Kidney; Liver; Matrix Metalloproteinase 2; Methods; Models, Animal; Necrosis; Pancreas; Rats; Rats, Wistar; Real-Time Polymerase Chain Reaction; Retina; Scoliosis; Spine; Up-Regulation
- From:Asian Spine Journal 2019;13(1):126-134
- CountryRepublic of Korea
- Language:English
- Abstract: STUDY DESIGN: To induce scoliosis in young female Wistar rats using a noninvasive method and to validate this model. PURPOSE: To induce scoliosis in a rat model noninvasively by bracing and to study the corresponding gene-expression profile in the spine and different organs. OVERVIEW OF LITERATURE: Scoliosis involves abnormal lateral curvature of the spine, the causes of which remain unclear. In the literature, it is suggested that scoliosis is genetically heterogeneous, as there are multiple factors involved directly or indirectly in its pathogenesis. Clinical and experimental studies were conducted to understand the etiology of anatomical alterations in the spine and internal organs, as the findings could help clinicians to establish new treatment approaches. METHODS: Twelve female Wistar rats aged 21 days were chosen for this study. Customized braces and real-time polymerase chain reaction (RT-PCR) primers for rats were designed using Primer 3 software. Radiological analysis (X-rays), histopathological studies, SYBR green, and RT-PCR analysis were performed. RESULTS: The spines of six rats were braced in a deformed position, which resulted in a permanent structural deformity as confirmed by X-ray studies. The remaining rats were used as controls. Quantitative studies of the expression of various genes (osteocalcin, pleiotrophins, matrix metalloproteinase-2 [MMP2] and MMP9, TIMP, interleukins 1 and 6, tumor necrosis factor-α) showed their differential expression and significant upregulation (p < 0.05) in different organs of scoliotic rats in comparison to those in control rats. Histopathological findings showed tissue necrosis and fibrosis in the brain, retina, pancreas, kidney, liver, and disc of scoliotic rats. CONCLUSIONS: Bracing is a noninvasive method for inducing scoliosis in an animal model with 100% reliability and with corresponding changes in gene expression. Scoliosis does not just involve a spine deformity, but can be referred to as a systemic disease on the basis of the pathological changes observed in various internal organs.
