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Changes in mitochondrial morphology and organization can enhance energy supply from mitochondrial oxidative phosphorylation in diabetic cardiomyopathy.
Jarosz, Jan; Ghosh, Shouryadipta; Delbridge, Lea M D; Petzer, Amorita; Hickey, Anthony J R; Crampin, Edmund J; Hanssen, Eric; Rajagopal, Vijay.
Afiliação
  • Jarosz J; Cell Structure and Mechanobiology Group, Department of Mechanical Engineering, University of Melbourne, Parkville, Australia.
  • Ghosh S; Systems Biology Laboratory, Melbourne School of Engineering, University of Melbourne, Parkville, Australia.
  • Delbridge LM; Cell Structure and Mechanobiology Group, Department of Mechanical Engineering, University of Melbourne, Parkville, Australia.
  • Petzer A; Systems Biology Laboratory, Melbourne School of Engineering, University of Melbourne, Parkville, Australia.
  • Hickey AJ; Department of Physiology, University of Melbourne, Parkville, Australia.
  • Crampin EJ; School of Biological Sciences, University of Auckland, Aukland, New Zealand.
  • Hanssen E; School of Biological Sciences, University of Auckland, Aukland, New Zealand.
  • Rajagopal V; Systems Biology Laboratory, Melbourne School of Engineering, University of Melbourne, Parkville, Australia.
Am J Physiol Cell Physiol ; 312(2): C190-C197, 2017 Feb 01.
Article em En | MEDLINE | ID: mdl-27903587
ABSTRACT
Diabetic cardiomyopathy is accompanied by metabolic and ultrastructural alterations, but the impact of the structural changes on metabolism itself is yet to be determined. Morphometric analysis of mitochondrial shape and spatial organization within transverse sections of cardiomyocytes from control and streptozotocin-induced type I diabetic Sprague-Dawley rats revealed that mitochondria are 20% smaller in size while their spatial density increases by 53% in diabetic cells relative to control myocytes. Diabetic cells formed larger clusters of mitochondria (60% more mitochondria per cluster) and the effective surface-to-volume ratio of these clusters increased by 22.5%. Using a biophysical computational model we found that this increase can have a moderate compensatory effect by increasing the availability of ATP in the cytosol when ATP synthesis within the mitochondrial matrix is compromised.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Trifosfato de Adenosina / Cardiomiopatias Diabéticas / Mitocôndrias Cardíacas / Modelos Cardiovasculares Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Trifosfato de Adenosina / Cardiomiopatias Diabéticas / Mitocôndrias Cardíacas / Modelos Cardiovasculares Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article