Literature DB >> 27031804

Microcalorimetric studies on the energy release of isolated rat mitochondria under different concentrations of gadolinium (III).

Jie Zhao1, Long Ma1, Xun Xiang1, Qing-Lian Guo2, Feng-Lei Jiang1, Yi Liu3.   

Abstract

Gadolinium-based compounds are most widely utilized for paramagnetic contrast agents, but, the toxicological mechanism of gadolinium (Gd) had not been fully elucidated since the first report about Gd anomaly. In this work, we analyzed the effect of Gd(3+) on mitochondria in vitro by microcalorimetry. Microcalorimetry can provide detailed kinetic and thermodynamic information from thermogenic curve. At the tested concentration, Gd(3+) induced the increase of growth rate constant (k1). At high concentration (100-500 μM), the maximum power output time (tm), the decline rate constant (-k2) and the time of activity recovery phase (tR) decreased with the addition of Gd(3+) and the maximum power output (Pm) increased. At low concentration (0-100 μM), the changes were different from high concentration. From the results we concluded that the effect of different concentrations of Gd(3+) had a relationship with time, high concentration of Gd(3+) induced mitochondrial energy metabolism disturb however low concentration may promote mitochondrial adaption to physiological stresses. The effect of low concentration of Gd(3+) need more work to elucidate the mechanism. The results of total heat output (Q) and mitochondrial respiratory activities suggested high concentrations of Gd(3+) could accelerate adenosine triphosphate (ATP) consumption under respiratory system damaged.
Copyright © 2016 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Gadolinium; Microcalorimetry; Mitochondria; Respiration; Thermokinetics

Mesh:

Substances:

Year:  2016        PMID: 27031804     DOI: 10.1016/j.chemosphere.2016.03.082

Source DB:  PubMed          Journal:  Chemosphere        ISSN: 0045-6535            Impact factor:   7.086


  5 in total

1.  In vitro modulation of mercury-induced rat liver mitochondria dysfunction.

Authors:  Long Ma; Kai-Dong Bi; Yu-Meng Fan; Zi-Yi Jiang; Xiao-Yi Zhang; Jing-Wen Zhang; Jie Zhao; Feng-Lei Jiang; Jia-Xin Dong
Journal:  Toxicol Res (Camb)       Date:  2018-07-10       Impact factor: 3.524

2.  Toxicity of Pb2+ on rat liver mitochondria induced by oxidative stress and mitochondrial permeability transition.

Authors:  Long Ma; Jun-Yi Liu; Jia-Xin Dong; Qi Xiao; Jie Zhao; Feng-Lei Jiang
Journal:  Toxicol Res (Camb)       Date:  2017-09-25       Impact factor: 3.524

3.  Spectroscopic, Polarographic, and Microcalorimetric Studies on Mitochondrial Dysfunction Induced by Ethanol.

Authors:  Long Ma; Jia-Xin Dong; Can Wu; Xue-Yi Li; Jing Chen; Hong Zhang; Yi Liu
Journal:  J Membr Biol       Date:  2017-02-21       Impact factor: 1.843

4.  Mitochondrial morphology and function impaired by dimethyl sulfoxide and dimethyl Formamide.

Authors:  Long Ma; Jia-Xin Dong; Wen-Rong Fu; Xue-Yi Li; Jing Chen; Yi Liu
Journal:  J Bioenerg Biomembr       Date:  2018-05-17       Impact factor: 2.945

5.  Mitochondrial toxicity of organic arsenicals: membrane permeability transition pore opening and respiratory dysfunction.

Authors:  Xiao-Yang Fan; Lian Yuan; Can Wu; Yu-Jiao Liu; Feng-Lei Jiang; Yan-Jun Hu; Yi Liu
Journal:  Toxicol Res (Camb)       Date:  2017-12-19       Impact factor: 3.524

  5 in total

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