Literature DB >> 3085790

Deficiency of thiosulphate sulphurtransferase (rhodanese) in Leber's hereditary optic neuropathy.

C J Poole, P R Kind.   

Abstract

Leber's hereditary optic neuropathy is a rare cause of progressive visual failure. Its cause is unknown, but one hypothesis is that patients have a defect in the detoxication of cyanide. One of the enzymes used in this detoxication is thiosulphate sulphurtransferase (rhodanese). The activity of this enzyme was measured in the rectal mucosa of a group of subjects with Leber's hereditary optic neuropathy, and it was found to be considerably reduced compared with that in a group of controls (p less than 0.001). This finding supports the hypothesis of an inborn error of cyanide detoxication in this condition.

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Year:  1986        PMID: 3085790      PMCID: PMC1340241          DOI: 10.1136/bmj.292.6530.1229

Source DB:  PubMed          Journal:  Br Med J (Clin Res Ed)        ISSN: 0267-0623


  5 in total

1.  A new micromethod for determination of protein in cerebrospinal fluid and urine.

Authors:  M A Pesce; C S Strande
Journal:  Clin Chem       Date:  1973-11       Impact factor: 8.327

2.  Plasma-cobalamins in neuro-ophthalmological diseases.

Authors:  J Wilson; J C Linnell; D M Matthews
Journal:  Lancet       Date:  1971-02-06       Impact factor: 79.321

3.  Leber's hereditary optic neuroretinopathy, a mitochondrial disease?

Authors:  E Nikoskelainen; I E Hassinen; L Paljärvi; H Lang; H Kalimo
Journal:  Lancet       Date:  1984-12-22       Impact factor: 79.321

4.  Thiosulphate-sulphur transferase (rhodanese) deficiency in Leber's hereditary optic atrophy.

Authors:  B Cagianut; K Rhyner; W Furrier; H P Schnebli
Journal:  Lancet       Date:  1981-10-31       Impact factor: 79.321

5.  Ophthalmoscopic findings in Leber's hereditary optic neuropathy. II. The fundus findings in the affected family members.

Authors:  E Nikoskelainen; W F Hoyt; K Nummelin
Journal:  Arch Ophthalmol       Date:  1983-07
  5 in total
  9 in total

Review 1.  Neuro-ophthalmology.

Authors:  M D Sanders
Journal:  Br J Ophthalmol       Date:  1990-08       Impact factor: 4.638

2.  Histochemical, ultrastructural and biochemical study of muscle mitochondria in Leber's hereditary optic atrophy.

Authors:  A Federico; L Manneschi; M Meloni; C Alessandrini; A M Bardelli; M T Dotti; P Sabatelli
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

3.  Leber's hereditary optic atrophy: further evidence for a defect of cyanide metabolism?

Authors:  T A Berninger; L von Meyer; E Siess; O Schon; F D Goebel
Journal:  Br J Ophthalmol       Date:  1989-04       Impact factor: 4.638

4.  Restriction endonuclease analysis of leukocyte mitochondrial DNA in Leber's optic atrophy.

Authors:  I J Holt; D H Miller; A E Harding
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-08       Impact factor: 10.154

5.  Rhodanese isozymes in three subjects with Leber's optic neuropathy.

Authors:  D B Whitehouse; C J Poole; P R Kind; D A Hopkinson
Journal:  J Med Genet       Date:  1989-02       Impact factor: 6.318

Review 6.  Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations.

Authors:  P Riordan-Eva; A E Harding
Journal:  J Med Genet       Date:  1995-02       Impact factor: 6.318

Review 7.  Optic neuropathy and chronic cyanide intoxication: a review.

Authors:  A G Freeman
Journal:  J R Soc Med       Date:  1988-02       Impact factor: 18.000

Review 8.  Thiosulfate-Cyanide Sulfurtransferase a Mitochondrial Essential Enzyme: From Cell Metabolism to the Biotechnological Applications.

Authors:  Silvia Buonvino; Ilaria Arciero; Sonia Melino
Journal:  Int J Mol Sci       Date:  2022-07-30       Impact factor: 6.208

9.  The Expression and Activity of Rhodanese, 3-Mercaptopyruvate Sulfurtransferase, Cystathionine γ-Lyase in the Most Frequently Chosen Cellular Research Models.

Authors:  Marta Kaczor-Kamińska; Kamil Kaminski; Maria Wróbel
Journal:  Biomolecules       Date:  2021-12-10
  9 in total

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