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Mitochondrial Pathogenesis

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Cover of 'Mitochondrial Pathogenesis'

Table of Contents

  1. Altmetric Badge
    Book Overview
  2. Altmetric Badge
    Chapter 1 Overview
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    Chapter 2 Mitochondrial Genome Single Nucleotide Polymorphisms and Their Phenotypes in the Japanese
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    Chapter 3 Mitochondrial DNA variation in the aboriginal populations of the Altai-Baikal region: implications for the genetic history of North Asia and America.
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    Chapter 4 Mitochondrial ALDH2 deficiency as an oxidative stress.
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    Chapter 5 Mitochondrial reactive oxygen species generation and calcium increase induced by visible light in astrocytes.
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    Chapter 6 Radical Metabolism Is Partner to Energy Metabolism in Mitochondria
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    Chapter 7 Mitochondrial Nucleoid and Transcription Factor A
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    Chapter 8 Regulation of Mitochondrial Transcription Factor A Expression by High Glucose
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    Chapter 9 Regulation and Role of the Mitochondrial Transcription Factor in the Diabetic Rat Heart
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    Chapter 10 The Mitochondrial Production of Reactive Oxygen Species in Relation to Aging and Pathology
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    Chapter 11 Biological Significance of the Defense Mechanisms against Oxidative Damage in Nucleic Acids Caused by Reactive Oxygen Species
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    Chapter 12 Mitochondrial Swelling and Generation of Reactive Oxygen Species Induced by Photoirradiation Are Heterogeneously Distributed
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    Chapter 13 Mitochondrial Dysfunction via Disruption of Complex II Activity during Iron Chelation—Induced Senescence-like Growth Arrest of Chang Cells
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    Chapter 14 Mitochondrial DNA Mutation and Depletion Increase the Susceptibility of Human Cells to Apoptosis
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    Chapter 15 Resistance of ρ 0 Cells against Apoptosis
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    Chapter 16 Mitochondrial DNA 4,977-bp Deletion in Paired Oral Cancer and Precancerous Lesions Revealed by Laser Microdissection and Real-Time Quantitative PCR
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    Chapter 17 Role of oxidative stress in pancreatic beta-cell dysfunction.
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    Chapter 18 Initiation of Apoptotic Signal by the Peroxidation of Cardiolipin of Mitochondria
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    Chapter 19 Diabetes Mellitus with Mitochondrial Gene Mutations in Japan
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    Chapter 20 Accumulation of Somatic Mutation in Mitochondrial DNA and Atherosclerosis in Diabetic Patients
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    Chapter 21 Changes of Mitochondrial DNA Content in the Male Offspring of Protein-Malnourished Rats
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    Chapter 22 Mitochondrial Encephalomyopathies
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    Chapter 23 Mitochondrial Encephalomyopathies
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    Chapter 24 Comprehensive Molecular Diagnosis of Mitochondrial Disorders
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    Chapter 25 Molecular Pathogenetic Mechanism of Maternally Inherited Deafness
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    Chapter 26 Genetic and functional analysis of mitochondrial DNA-encoded complex I genes.
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    Chapter 27 Genome-Wide Analysis of Signal Transducers and Regulators of Mitochondrial Dysfunction in Saccharomyces cerevisiae
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    Chapter 28 Enhanced Detection of Deleterious Mutations by TTGE Analysis of Mother and Child’s DNA Side by Side
  30. Altmetric Badge
    Chapter 29 Quantitative PCR Analysis of Mitochondrial DNA Content in Patients with Mitochondrial Disease
  31. Altmetric Badge
    Chapter 30 Somatic mitochondrial DNA mutations in oral cancer of betel quid chewers.
  32. Altmetric Badge
    Chapter 31 Association of the Mitochondrial DNA 16189 T to C Variant with Lacunar Cerebral Infarction
  33. Altmetric Badge
    Chapter 32 Mechanisms of Cell Death Induced by Cadmium and Arsenic
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    Chapter 33 Cadmium-Induced Nephropathy in Rats Is Mediated by Expression of Senescence-Associated Beta-Galactosidase and Accumulation of Mitochondrial DNA Deletion
  35. Altmetric Badge
    Chapter 34 Investigation of Common Mitochondrial Point Mutations in Korea
  36. Altmetric Badge
    Chapter 35 Leber’s Hereditary Optic Neuropathy: The Spectrum of Mitochondrial DNA Mutations in Iranian Patients
Attention for Chapter 17: Role of oxidative stress in pancreatic beta-cell dysfunction.
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Chapter title
Role of oxidative stress in pancreatic beta-cell dysfunction.
Chapter number 17
Book title
Mitochondrial Pathogenesis
Published in
Annals of the New York Academy of Sciences, May 2004
DOI 10.1007/978-3-662-41088-2_17
Pubmed ID
Book ISBNs
978-1-57331-491-6, 978-3-66-241088-2
Authors

Kajimoto Y, Kaneto H, Kajimoto, Yoshitaka, Kaneto, Hideaki

Abstract

Oxidative stress is produced under diabetic conditions and is likely involved in progression of pancreatic beta-cell dysfunction found in diabetes. Possibly caused by low levels of antioxidant enzyme expressions, pancreatic beta-cells are vulnerable to oxidative stress. When beta-cell-derived HIT-T15 cells or isolated rat islets were exposed to oxidative stress, insulin gene expression was markedly decreased. To investigate the significance of oxidative stress in the progression of pancreatic beta-cell dysfunction in type 2 diabetes, we evaluated the effects of antioxidants in diabetic C57BL/KsJ-db/db mice. According to an intraperitoneal glucose tolerance test, the treatment with antioxidants retained glucose-stimulated insulin secretion and moderately decreased blood glucose levels. Histological analyses of the pancreata revealed that the beta-cell mass was significantly larger in the mice treated with the antioxidants, and the antioxidant treatment suppressed apoptosis in beta-cells without changing the rate of beta-cell proliferation. The antioxidant treatment also preserved the amounts of insulin content and insulin mRNA, making the extent of insulin degranulation less evident. As possible mechanism underlying the phenomena, expression of pancreatic and duodenal homeobox factor-1 (also known as IDX-1/STF-1/IPF1), an important transcription factor for the insulin gene, was more clearly visible in the nuclei of islet cells after the antioxidant treatment. Under diabetic conditions, JNK is activated by oxidative stress and involved in the suppression of insulin gene expression. This JNK effect appears to be mediated in part by nucleocytoplasmic translocation of PDX-1, which is also downstream of JNK activation. Taken together, oxidative stress and consequent activation of the JNK pathway are involved in progression of beta-cell dysfunction found in diabetes. Antioxidants may serve as a novel mechanism-based therapy for type 2 diabetes.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 10 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 10 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 5 50%
Other 1 10%
Lecturer > Senior Lecturer 1 10%
Student > Bachelor 1 10%
Student > Master 1 10%
Other 0 0%
Unknown 1 10%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 2 20%
Chemistry 2 20%
Social Sciences 1 10%
Medicine and Dentistry 1 10%
Unknown 4 40%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 04 July 2012.
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#17,660,193
of 22,669,724 outputs
Outputs from Annals of the New York Academy of Sciences
#10,529
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Outputs of similar age
#54,999
of 58,129 outputs
Outputs of similar age from Annals of the New York Academy of Sciences
#148
of 161 outputs
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