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Chronic Nerve Compression Accelerates the Progression of Diabetic Peripheral Neuropathy in a Rat Model: A Study of Gene Expression Profiling.
Tu, Yiji; Chen, Zenggan; Hu, Junda; Ding, Zuoyou; Lineaweaver, William C; Dellon, A Lee; Zhang, Feng.
Afiliação
  • Tu Y; Department of Orthopedics, Zhongshan Hospital, Fudan University, Shanghai, China.
  • Chen Z; Joseph M. Still Burn and Reconstructive Center, Jackson, Mississippi.
  • Hu J; Department of Orthopedics, Zhongshan Hospital, Fudan University, Shanghai, China.
  • Ding Z; Department of Orthopedics, Zhongshan Hospital, Fudan University, Shanghai, China.
  • Lineaweaver WC; Department of Orthopedics, Zhongshan Hospital, Fudan University, Shanghai, China.
  • Dellon AL; Joseph M. Still Burn and Reconstructive Center, Jackson, Mississippi.
  • Zhang F; Department of Plastic Surgery, Johns Hopkins University, Baltimore, Maryland.
J Reconstr Microsurg ; 34(7): 537-548, 2018 Sep.
Article em En | MEDLINE | ID: mdl-29695014
ABSTRACT

OBJECTIVE:

This article investigates the role of chronic nerve compression in the progression of diabetic peripheral neuropathy (DPN) by gene expression profiling.

METHODS:

Chronic nerve compression was created in streptozotocin (STZ)-induced diabetic rats by wrapping a silicone tube around the sciatic nerve (SCN). Neurological deficits were evaluated using pain threshold test, motor nerve conduction velocity (MNCV), and histopathologic examination. Differentially expressed genes (DGEs) and metabolic processes associated with chronic nerve compression were analyzed.

RESULTS:

Significant changes in withdrawal threshold and MNCV were observed in diabetic rats 6 weeks after diabetes induction, and in DPN rats 4 weeks after diabetes induction. Histopathologic examination of the SCN in DPN rats presented typical changes of myelin degeneration in DPN. Function analyses of DEGs demonstrated that biological processes related to inflammatory response, extracellular matrix component, and synaptic transmission were upregulated after diabetes induction, and chronic nerve compression further enhanced those changes. While processes related to lipid and glucose metabolism, response to insulin, and apoptosis regulation were inhibited after diabetes induction, chronic nerve compression further enhanced these inhibitions.

CONCLUSION:

Our study suggests that additional silicone tube wrapping on the SCN of rat with diabetes closely mimics the course and pathologic findings of human DPN. Further studies are needed to verify the effectiveness of this rat model of DPN and elucidate the roles of the individual genes in the progression of DPN.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças do Sistema Nervoso Periférico / Neuropatias Diabéticas / Síndromes de Compressão Nervosa Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças do Sistema Nervoso Periférico / Neuropatias Diabéticas / Síndromes de Compressão Nervosa Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article