Your browser doesn't support javascript.
loading
Characterization of neuromas in peripheral nerves and their effects on heterotopic bone formation.
Minarelli, Jordan; Davis, Eleanor L; Dickerson, Austin; Moore, William C; Mejia, Julio A; Gugala, Zbigniew; Olmsted-Davis, Elizabeth A; Davis, Alan R.
Affiliation
  • Minarelli J; 1 Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital and Houston Methodist Hospital, Houston, TX, USA.
  • Davis EL; 1 Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital and Houston Methodist Hospital, Houston, TX, USA.
  • Dickerson A; 1 Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital and Houston Methodist Hospital, Houston, TX, USA.
  • Moore WC; 1 Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital and Houston Methodist Hospital, Houston, TX, USA.
  • Mejia JA; 1 Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital and Houston Methodist Hospital, Houston, TX, USA.
  • Gugala Z; 2 Department of Orthopedic Surgery and Rehabilitation, University of Texas Medical Branch, Galveston, TX, USA.
  • Olmsted-Davis EA; 1 Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital and Houston Methodist Hospital, Houston, TX, USA.
  • Davis AR; 3 Department of Pediatrics - Section Hematology/Oncology, Baylor College of Medicine, Houston, TX, USA.
Mol Pain ; 15: 1744806919838191, 2019.
Article in En | MEDLINE | ID: mdl-30813850
The formation of neuromas involves expansion of the cellular components of peripheral nerves. The onset of these disorganized tumors involves activation of sensory nerves and neuroinflammation. Particularly problematic in neuroma is arborization of axons leading to extreme, neuropathic pain. The most common sites for neuroma are the ends of transected nerves following injury; however, this rodent model does not reliably result in neuroma formation. In this study, we established a rodent model of neuroma in which the sciatic nerve was loosely ligated with two chromic gut sutures. This model formed neuromas reliably (∼95%), presumably through activation of the neural inflammatory cascade. Resulting neuromas had a disorganized structure and a significant number of replicating cells. Quantification of changes in perineurial and Schwann cells showed a significant increase in these populations. Immunohistochemical analysis showed the presence of ß-tubulin 3 in the rapidly expanding nerve and a decrease in neurofilament heavy chain compared to the normal nerve, suggesting the axons forming a disorganized structure. Measurement of the permeability of the blood-nerve barrier shows that it opened almost immediately and remained open as long as 10 days. Studies using an antagonist of the ß3-adrenergic receptor (L-748,337) or cromolyn showed a significant reduction in tumor size and cell expansion as determined by flow cytometry, with an improvement in the animal's gait detected using a Catwalk system. Previous studies in our laboratory have shown that heterotopic ossification is also a result of the activation of neuroinflammation. Since heterotopic ossification and neuroma often occur together in amputees, they were induced in the same limbs of the study animals. More heterotopic bone was formed in animals with neuromas as compared to those without. These data collectively suggest that perturbation of early neuroinflammation with compounds such as L-748,337 and cromolyn may reduce formation of neuromas.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sciatic Nerve / Neuroma Limits: Animals Language: En Journal: Mol Pain Journal subject: BIOLOGIA MOLECULAR / NEUROLOGIA / PSICOFISIOLOGIA Year: 2019 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sciatic Nerve / Neuroma Limits: Animals Language: En Journal: Mol Pain Journal subject: BIOLOGIA MOLECULAR / NEUROLOGIA / PSICOFISIOLOGIA Year: 2019 Document type: Article Affiliation country: United States Country of publication: United States