Literature DB >> 3241467

Pathological findings of the sural nerve in mitochondrial encephalomyopathy.

S Katsuragi1, A Shimoji, K Watanabe, T Miyakawa.   

Abstract

We examined the muscle and peripheral nerve of a 55-year-old woman with familial mitochondrial encephalomyopathy. In the gastrocnemius muscle, many ragged red fibers and mitochondria containing paracrystalline inclusions in those fibers were observed by light and electron microscopy, respectively. Histopathological studies of the sural nerve revealed a marked decrease in the number of large myelinated fibers. Electron microscopic studies showed an accumulation of glycogen particles and mitochondria containing abnormal, structurally obscure cristae in the Schwann cell cytoplasm. These results suggest that the cause of loss of the large myelinated fibers may be some disturbance of metabolism in the Schwann cells due to mitochondrial dysfunction.

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Year:  1988        PMID: 3241467     DOI: 10.1111/j.1440-1819.1988.tb01981.x

Source DB:  PubMed          Journal:  Jpn J Psychiatry Neurol        ISSN: 0912-2036


  3 in total

1.  Acute peripheral neuropathy, rhabdomyolysis, and severe lactic acidosis associated with 3243 A to G mitochondrial DNA mutation.

Authors:  H Hara; Y Wakayama; Y Kouno; H Yamada; M Tanaka; T Ozawa
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-12       Impact factor: 10.154

2.  Schwann cell glycogen selectively supports myelinated axon function.

Authors:  Angus M Brown; Richard D Evans; Joel Black; Bruce R Ransom
Journal:  Ann Neurol       Date:  2012-09       Impact factor: 10.422

Review 3.  Emerging Roles for Glycogen in the CNS.

Authors:  Alice E Waitt; Liam Reed; Bruce R Ransom; Angus M Brown
Journal:  Front Mol Neurosci       Date:  2017-03-16       Impact factor: 5.639

  3 in total

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