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Pharmacology of Mitochondria

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Cover of 'Pharmacology of Mitochondria'

Table of Contents

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    Book Overview
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    Chapter 1 Leber Hereditary Optic Neuropathy: A Mitochondrial Disease Unique in Many Ways
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    Chapter 1 The Mitochondrial Ca2+ Uniporter: Structure, Function, and Pharmacology
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    Chapter 2 Toxicity of Antiepileptic Drugs to Mitochondria
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    Chapter 2 Leber Hereditary Optic Neuropathy: Exemplar of an mtDNA Disease
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    Chapter 3 Nuclear Transcription Factors in the Mitochondria: A New Paradigm in Fine-Tuning Mitochondrial Metabolism
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    Chapter 3 Mitochondria in Alzheimer’s Disease and Diabetes-Associated Neurodegeneration: License to Heal!
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    Chapter 4 MITO-Porter for Mitochondrial Delivery and Mitochondrial Functional Analysis
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    Chapter 5 The Mitochondrial Permeability Transition Pore and ATP Synthase
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    Chapter 6 The Emerging Role of Mitochondrial Targeting in Kidney Disease
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    Chapter 7 Mitochondrial Dynamics as a Therapeutic Target for Treating Cardiac Diseases
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    Chapter 37 Mitochondria-Targeted Agents: Mitochondriotropics, Mitochondriotoxics, and Mitocans
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    Chapter 38 Mitochondrial Fission in Human Diseases
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    Chapter 39 Anion Channels of Mitochondria
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    Chapter 40 Mitochondrial Changes in Cancer
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    Chapter 79 Guide to the Pharmacology of Mitochondrial Potassium Channels
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    Chapter 87 Erratum to: The Mitochondrial Permeability Transition Pore and ATP Synthase
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    Chapter 92 The Roles of Mitochondrial Cation Channels Under Physiological Conditions and in Cancer
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    Chapter 93 Equipping Physiologists with an Informatics Tool Chest: Toward an Integerated Mitochondrial Phenome
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    Chapter 110 Mitochondrial Cholesterol and the Paradox in Cell Death
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    Chapter 117 Role of Mitochondrial Reactive Oxygen Species in the Activation of Cellular Signals, Molecules, and Function
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    Chapter 129 Mitochondrial Flashes: Elemental Signaling Events in Eukaryotic Cells
Attention for Chapter 7: Mitochondrial Dynamics as a Therapeutic Target for Treating Cardiac Diseases
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Chapter title
Mitochondrial Dynamics as a Therapeutic Target for Treating Cardiac Diseases
Chapter number 7
Book title
Pharmacology of Mitochondria
Published in
Handbook of experimental pharmacology, January 2016
DOI 10.1007/164_2016_7
Pubmed ID
Book ISBNs
978-3-31-957311-3, 978-3-31-957313-7
Authors

Sang-Bing Ong, Derek J. Hausenloy

Abstract

Mitochondria are dynamic in nature and are able to shift their morphology between elongated interconnected mitochondrial networks and a fragmented disconnected arrangement by the processes of mitochondrial fusion and fission, respectively. Changes in mitochondrial morphology are regulated by the mitochondrial fusion proteins - mitofusins 1 and 2 (Mfn1 and 2), and optic atrophy 1 (Opa1) as well as the mitochondrial fission proteins - dynamin-related peptide 1 (Drp1) and fission protein 1 (Fis1). Despite having a unique spatial arrangement, cardiac mitochondria have been implicated in a variety of disorders including ischemia-reperfusion injury (IRI), heart failure, diabetes, and pulmonary hypertension. In this chapter, we review the influence of mitochondrial dynamics in these cardiac disorders as well as their potential as therapeutic targets in tackling cardiovascular disease.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 35 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 35 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 7 20%
Student > Master 4 11%
Student > Doctoral Student 3 9%
Student > Bachelor 3 9%
Other 3 9%
Other 6 17%
Unknown 9 26%
Readers by discipline Count As %
Medicine and Dentistry 8 23%
Biochemistry, Genetics and Molecular Biology 7 20%
Agricultural and Biological Sciences 5 14%
Immunology and Microbiology 1 3%
Neuroscience 1 3%
Other 0 0%
Unknown 13 37%