Literature DB >> 7228016

Ultrastructure of hepatic mitochondria in a child with hyperornithinemia, hyperammonemia, and homocitrullinuria.

M D Haust, P D Gatfield, B A Gordon.   

Abstract

Ultrastructural studies of hepatic tissue obtained at biopsy from a nine year old severely retarded boy with hyperornithinemia, hyperammonemia, and homocitrullinuria showed mitochondria of bizarre shapes and unusual internal features. Among the latter were tubules extending throughout the length of the large mitochondria that on cross section had a rosette-like arrangement; the presence of a periodic, approximately 300 A thick, sievelike membrane interposed between the tubules and the inner mitochondrial membrane; and "bulges" of mitochondrial matrix occasionally formed between these two membranes. Since to be metabolized ornithine must enter the mitochondria, the hyperornithinemia is regarded as a reflection of its inability to reach the mitochondrial interior. It is speculated that among other possible causes, the unusual sievelike membrane may be the barrier to ornithine's access to the mitochondrion.

Entities:  

Mesh:

Substances:

Year:  1981        PMID: 7228016     DOI: 10.1016/s0046-8177(81)80121-9

Source DB:  PubMed          Journal:  Hum Pathol        ISSN: 0046-8177            Impact factor:   3.466


  9 in total

1.  Ornithine and Homocitrulline Impair Mitochondrial Function, Decrease Antioxidant Defenses and Induce Cell Death in Menadione-Stressed Rat Cortical Astrocytes: Potential Mechanisms of Neurological Dysfunction in HHH Syndrome.

Authors:  Ângela Zanatta; Marília Danyelle Nunes Rodrigues; Alexandre Umpierrez Amaral; Débora Guerini Souza; André Quincozes-Santos; Moacir Wajner
Journal:  Neurochem Res       Date:  2016-05-09       Impact factor: 3.996

2.  Argininosuccinic aciduria: long-term treatment with arginine.

Authors:  H G Parsons; R B Scott; A Pinto; R J Carter; F F Snyder
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

3.  HHH syndrome (hyperornithinaemia, hyperammonaemia, homocitrullinuria), with fulminant hepatitis-like presentation.

Authors:  S Fecarotta; G Parenti; P Vajro; A Zuppaldi; R Della Casa; M T Carbone; A Correra; G Torre; S Riva; C Dionisi-Vici; F M Santorelli; G Andria
Journal:  J Inherit Metab Dis       Date:  2006-02       Impact factor: 4.982

4.  Ornithine In Vivo Administration Disrupts Redox Homeostasis and Decreases Synaptic Na(+), K (+)-ATPase Activity in Cerebellum of Adolescent Rats: Implications for the Pathogenesis of Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) Syndrome.

Authors:  Ângela Zanatta; Carolina Maso Viegas; Fernanda Hermes Hickmann; Wagner de Oliveira Monteiro; Angela Sitta; Daniela de Moura Coelho; Carmen Regla Vargas; Guilhian Leipnitz; Moacir Wajner
Journal:  Cell Mol Neurobiol       Date:  2015-03-13       Impact factor: 5.046

5.  The pH of mitochondria of fibroblasts from a hyperornithinaemia, hyperammonaemia, homocitrullinuria-syndrome patient.

Authors:  K Metoki; F A Hommes
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

6.  Ultrastructural changes in fibroblast mitochondria of a patient with HHH-syndrome.

Authors:  K Metoki; F A Hommes; P Dyken; C Kelloes; J Trefz
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

7.  Ultrastructural findings in citrullinaemia in Holstein-Friesian calves.

Authors:  P A Harper; P J Healy; J A Dennis; A B Martin
Journal:  Acta Neuropathol       Date:  1988       Impact factor: 17.088

8.  Impairment of brain redox homeostasis caused by the major metabolites accumulating in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome in vivo.

Authors:  Carolina Maso Viegas; Anelise Miotti Tonin; Angela Zanatta; Bianca Seminotti; Estela Natacha Brandt Busanello; Carolina Gonçalves Fernandes; Alana Pimentel Moura; Guilhian Leipnitz; Moacir Wajner
Journal:  Metab Brain Dis       Date:  2012-07-15       Impact factor: 3.584

Review 9.  The hyperornithinemia-hyperammonemia-homocitrullinuria syndrome.

Authors:  Diego Martinelli; Daria Diodato; Emanuela Ponzi; Magnus Monné; Sara Boenzi; Enrico Bertini; Giuseppe Fiermonte; Carlo Dionisi-Vici
Journal:  Orphanet J Rare Dis       Date:  2015-03-11       Impact factor: 4.123

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.