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3‐nitropropionic acid‐induced mitochondrial permeability transition: Comparative study of mitochondria from different tissues and brain regions
Author(s) -
Mirandola Sandra R.,
Melo Daniela R.,
Saito Ângela,
Castilho Roger F.
Publication year - 2009
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.22239
Subject(s) - mitochondrion , mitochondrial permeability transition pore , striatum , biology , succinate dehydrogenase , neurodegeneration , cerebellum , pharmacology , biochemistry , chemistry , medicine , endocrinology , dopamine , apoptosis , disease , programmed cell death
The adult rat striatum is particularly vulnerable to systemic administration of the succinate dehydrogenase inhibitor 3‐nitropropionic acid (3NP), which is known to induce degeneration of the caudate‐putamen, as occurs in Huntington's disease. The aim of the present study was to compare the susceptibility of isolated mitochondria from different rat brain regions (striatum, cortex, and cerebellum) as well as from the liver, kidney, and heart to mitochondrial permeability transition (MPT) induced by 3NP and Ca 2+ . In the presence of micromolar Ca 2+ concentrations, 3NP induces MPT in a dose‐dependent manner, as estimated by mitochondrial swelling and a decrease in the transmembrane electrical potential. A 3NP concentration capable of promoting a 10% inhibition of ADP‐stimulated, succinate‐supported respiration was sufficient to stimulate Ca 2+ ‐induced MPT. Brain and heart mitochondria were generally more sensitive to 3NP and Ca 2+ ‐induced MPT than mitochondria from liver and kidney. In addition, a partial inhibition of mitochondrial respiration by 3NP resulted in more pronounced MPT in striatal mitochondria than in cortical or cerebellar organelles. A similar inhibition of succinate dehydrogenase activity was observed in rat tissue homogenates obtained from various brain regions as well as from liver, kidney, and heart 24 hr after a single i.p. 3NP dose. Mitochondria isolated from forebrains of 3NP‐treated rats were also more susceptible to Ca 2+ ‐induced MPT than those of control rats. We propose that the increased susceptibility of the striatum to 3NP‐induced neurodegeneration may be partially explained by its susceptibility to MPT, together with the greater vulnerability of this brain region to glutamate receptor‐mediated Ca 2+ influx. © 2009 Wiley‐Liss, Inc.