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STUDY ON THE MECHANISM OF DEAFNESS ASSOCIATED WITH MITOCHONDRIAL DNA ABNORMALITY

Research Project

Project/Area Number 11557125
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section展開研究
Research Field Otorhinolaryngology
Research InstitutionTHE UNIVERSITY OF TOKYO

Principal Investigator

YAMASOBA Tatsuya  DEPARTMENT OF OTOLARYNGOLOGY, ASSOCIATED PROFESSOR, 医学部附属病院, 助教授 (60251302)

Co-Investigator(Kenkyū-buntansha) GOTO Yuichi  NATIONAL CENTER OF NEUROLOGY AND PSYCHIATRY, DEPARTMENT OF MENTAL RETARDATION AND BIRTH DEFECT RESEARCH, DlRECTOR(Researcher), 部長(研究職) (20225668)
ASANO Tomoichiro  DEPARTMENT OF OTOLARYNGOLOGY, research associate, 医学部附属病院, 助手 (70242063)
ITOH Ken  DEPARTMENT OF OTOLARYNGOLOGY, Lecturer, 医学部附属病院, 講師 (50251286)
鈴木 光也  東京大学, 医学部・附属病院, 講師 (50302724)
Project Period (FY) 1999 – 2002
Project Status Completed (Fiscal Year 2002)
Budget Amount *help
¥13,000,000 (Direct Cost: ¥13,000,000)
Fiscal Year 2002: ¥2,600,000 (Direct Cost: ¥2,600,000)
Fiscal Year 2001: ¥2,600,000 (Direct Cost: ¥2,600,000)
Fiscal Year 2000: ¥2,300,000 (Direct Cost: ¥2,300,000)
Fiscal Year 1999: ¥5,500,000 (Direct Cost: ¥5,500,000)
KeywordsMITOCHONDRIAL DNA / DEAFNESS / COCHLEA / STRIA VASCULARIS / HAIR CELL / ENCEPHALOMYOPATHY / 脳節症 / mitochondrial DNA / deafness / cochlea / germanium / guinea pig
Research Abstract

(1) Albino guinea pigs were orally given germanium at different concentrations (0.15%, 0.5%, and 1%). Animals treated with 1% germanium died within a few weeks. Animals treated with 0.15% germanium did not die until 6 months and showed no abnormalities in the skeletal muscle, inner ear, heart, kidney or liver. Approximately two-thirds animals treated with 0.5 % germanium survived for two months. These animals did not gain body weight, and their skeletal muscles were apparently atrophic. TEM observation revealed degeneration and germanium inclusion in a lot of mitochondria in the skeletal muscle and kidney, some mitochondria in the heart, and a few mitochondria in the liver. ABR measurements revealed moderate threshold shifts at all frequencies. A lot of germanium inclusion and degenerative changes were found in the mitochondria in the stria vascularis and its adjacent areas. Germanium was also scattered in the supporting cells, the sensory epithelium in the utricle and semicircular can … More als, and areas around the cochlear and vestibular nerve fibers, but these tissues showed virtually normal appearance. These findings indicate that 0.5% germanium administration induces mitochondrial damages in multiple organs including the cochlea in the guinea pigs, suggesting that this experimental model is useful to investigate cochlear damage in mitochondrial encephalomyopathy. The threshold shifts may be due chiefly to damage to me stria vascularis. (2) We detected an A-to-G point mutation at np 3243 from temporal bone of a patient with maternally inherited diabetes and deafness using dot-blotting method. In this temporal bone, severe degeneration was observed in the stria vascularis and outer hair cells throughout the cochlea and spiral ganglion cells in the base. In contrast, the inner hair cells and sensory epithelium in the vestibulum and semicircular canals were well preserved. (3) We did not detect cis-mutations in the whole mitochondrial DNAs in three patients who harbored an A1555G point mutation and had developed aminoglycoside-induced deafness. In one of them and his mother, reduced COX activities and mitochondrial inclusion bodies were found in muscle biopsies, suggesting that this mutation itself may affect mitochondrial function. Less

Report

(5 results)
  • 2002 Annual Research Report   Final Research Report Summary
  • 2001 Annual Research Report
  • 2000 Annual Research Report
  • 1999 Annual Research Report
  • Research Products

    (46 results)

All Other

All Publications (46 results)

  • [Publications] Yamasoba T, Tsukuda K, Oka Y, Kobayashi T, Kaga K: "Cochlear histopathology associated with mitochondrial transfer RNA Leu(UUR) gene mutation"Neurology. 52. 1705-1707 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Yamasoba T, Goto Y, Oka Y, Nishino I, Tsukuba K et al.: "Atypical muscle pathology and a survey of cis-mutation in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene"Neuromusc Disord. 12. 506-512 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Yamasoba T., Tsukuda K.: "Matemally inherited hearing loss associated with T7511C mutation in the mitochondrial DNA tRNA Ser(UCN) gene"(in press).

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Yamasoba T.: "Hearing loss"Nippon Rinsho. 60(Suppl 4). 530-534 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Yamasoba T.: "Amynoglycoside-induced hearing loss"Nippon Rinsho. 60(Suppl 4). 332-336 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Fujitake J, Mizuta H, Fujii H, Ishikawa Y, Sasamoto K et al.: "Leber's hereditary optic neuropathy with intracranial arteriovenous malformation : a case report"Acta Neurol Belg. 102. 82-86 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Komaki H, Fukazawa T, Houzen H, Yoshida K, Nonaka, I et al.: "A novel D104G mutation in the adenine nucleotide translocator I gene in autosomal dominant progressive external ophthalmoplegia patients with mitochondrial DNA with multiple deletions"Ann Neurol. 51. 645-648 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Ikezoe K, Nakagawa M, Yan C, Kira J et al.: "Apoptosis is suspended in muscle of mitochondrial encephalomyopathies"Acta Neuropathol (Berl). 103. 531-540 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Akagi M, Inui K, Tsukamoto H et al.: "A point mutation of mitochondrial ATPase 6 gene in Leigh syndrome"Neuromuscul Disord. 12. 53-55 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Nagashima T, Kato H, Maguchi S, Chuma T et al.: "A mitochondrial encephalo-myo-neuropathy with a nucleotide position 3271 (T-C) point mutation in the mitochondrial DNA"Neuromuscul Disord. 11. 470-476 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Toyono M, Nakano K, Kicuchi M et al.: "Sugie H.A case of MERRF associated with chronic pancreatitis"Neuromuscul Disord. 11. 300-304 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Akanuma J, Muraki K, Komaki H, Nonaka I: "Two pathogenic point mutations exist in the autheic mitochondrial genome, not in the nuclear pseudogene"J Hum Genet. 45. 337-341 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Amemiya S, Hamamoto M, Goto Y, Komaki H et al.: "Psychosis and progressing dementia ; presenting features of a mitochondriopathy"Neurology. 55. 600-601 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Goto Y.: "Clinical and molecular studies of mitochondrial disease"Inherit Metab Dis. 24. 181-188 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Makino M, Horai S, Goto Y et al.: "Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implications"J Hum Genet. 45. 69-75 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Goto Y.: "Mitochondrial DNA deletion and duplication in human disease and mouse model"Acta Myologic. 20. 110-114 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Yamasoba T, Tsukuda K, Oka Y, Kobayashi T, Kaga K.: "Cochlear histopathology associated with mitochondrial transfer RNA Leu(UUR) gene mutation"Neurology. 52. 1705-1707 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Yamasoba T, Goto Y, Oka Y, Nishino I, Tsukuda K, Nonaka I.: "Atypical muscle pathology and a survey of cis-mutation in deaf patients harboring a 1555 A-to-G point mutation in the ribosomal RNA gene"Neuromusc Disord.. 12. 506-512 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Yamasoba T, Tsukuda K.: "Maternally inherited hearing loss associated with T7511C mutation in the mitochondrial DNA tRNA Ser(UCN) gene"in press.

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Yamasoba T.: "Hearing loss"Nippon Rinsho. 60 Suppl 4. 530-534 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Yamasoba T.: "Amynoglycoside-induced hearing loss"Nippon Rinsho. 60 Suppl 4. 332-336 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Fujitake J, Mizuta H, Fujii H, Ishikawa Y, Sasamoto K, Goto Y, Nonaka I, Tatsuoka Y.: "Leber's hereditary optic neuropathy with intracranial arteriovenous malformation"Acta Neurol Belg. 102. 82-86 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Komaki H, Fukazawa T, Houzen H, Yoshida K, Nonaka I, Goto Y.: "A novel D104G mutation in the adenine nucleotide translocator 1 gene in autosomal dominant progressive external ophthalmoplegia patients with mitochondrial DNA with multiple deletions"Ann Neurol. 51. 645-648 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Ikezoe K, Nakagawa M, Yan C, Kira J, Goto Y, Nonaka I.: "Apoptosis is suspended in muscle of mitochondrial encephalomyopathies"Acta Neuropathol (Berl). 103. 531-540 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Akagi M, Inui K, Tsukamoto H, Sakai N, Muramatsu T, Yamada M, Matsuzaki K, Goto Y, Nonaka I, Okada S.: "A point mutation of mitochondrial ATPase 6 gene in Leigh syndrome"Neuromuscul Disord. 12. 53-55 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Nagashima T, Kato H, Maguchi S, Chuma T, Mano Y, Goto Y, Nonaka I, Nagashima K.: "A mitochondrial encephalo-myo-neuropathy with a nucleotide position 3271 (T-C) point mutation in the mitochondrial DNA"Neuromuscul Disord. 11. 470-476 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Toyono M, Nakano K, Kiuchi M, Imai K, Suzuki H, Shishikura K, Osawa M, Shiratori K, Goto Y, Nonaka I, Sugie H.: "A case of MERRF associated with chronic pancreatitis"Neuromuscul Disord. 11. 300-304 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Akanuma J, Muraki K, Komaki H, Nonaka I: "Two pathogenic point mutations exist in the authentic mitochondrial genome, not in the nuclear pseudogene"J Hum Genet. 45. 337-341 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Amemiya S, Hamamoto M, Goto Y, Komaki H, Nishino I, Nonaka I, Katayam: "Psychosis and progressing dementia : presenting features of a mitochondriopathy"Neurology. 55. 600-601 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Goto Y.: "Clinical and molecular studies of mitochondrial disease"Inherit Metab Dis. 24. 181-188 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Makino M, Horai S, Goto Y, Nonaka I.: "Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implications"J Hum Genet. 45. 69-75 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Goto Y.: "Mitochondrial DNA deletion and dupilication in human disease and mouse model"Acta Myologica. 20. 110-114 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Yamasoba T.et al.: "Atypical muscle pathology and a survey of cis-mutatious in deat patients narboring a 1555 A-to-G point mutation in the mutochondrial ribosomal RNA gene"Neuromuscular Disordors. 12. 506-512 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] Komaki H et al.: "A novel D104 G mutation in the adenosine nucleotude translocator 1 gene in autosomal dominant progressive external ophthalmoplegia patients with mtDNA with multiple deletions"Annals of Neurology. 51. 645-648 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] Lkezoek et al.: "Apoptosis is suspended in muscle of mutochondnal eucepholony pathes"Acta Neuropathology. 103. 531-540 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] Sugimoto J. et al.: "A patient with mitochondrial myopathy associated with isolated succinate dehyrogenase deficiency."Brain and Development. 22. 158-162 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] Goto Y.: "Mitochondrial myopathy"Neuroscience News. 3. 46-50 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] Amemiya S. et al.: "Psychosis and progressing features of mitochondriopathy"Neurology. 55. 600-601 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] Goto Y.: "Mitochondrial eucephalomyopathy"Neuropathol. 20. 82-84 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] Akanuma J. et al: "Two pathogenic point mutations exist in the authentic mitochondrial genome, not in the nuclear pseudogene"J.Hum Genet. 45. 337-341 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] Yamasoba T, et al.: "Cochlear pathology associated with mitochondrial +RNALeu(VVR) gene mutation"Neurology. 52. 1705-1707 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Tamasoba T, et al.: "Attennation of cochlear damage from noise trauma by an iron chelator, afree radial scavenger and GDNF in vivo"Brain Research. 815. 317-325 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Asano T, et al.: "Clinical relevance of heteroplasmic concentration of mitochondrial A32X3G mutation in leucocytes"Diabetologia. 42. 1439-1440 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Nagashima T, et al. (Goto Y): "Adult Leigh syndrome with mitochondrial DNA mutation at 8993"Acta Neuropathology. 97. 416-422 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Kubota Y. et al. (Goto Y): "Skin manifestation of a patient with mitochondrial endepholo myopathy with lactic acidosis and stroke like episodes(MELAS)"J Am Acad Dermatology. 41. 469-473 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Makino M et.al. (Goto Y).: "Mitochondrial DNA mutation in Leigh syndrome and their phylogenetic implications"J. Hum Genetics. 45. 69-75 (2000)

    • Related Report
      1999 Annual Research Report

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Published: 1999-04-01   Modified: 2016-04-21  

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