Literature DB >> 21275886

Investigating mitochondrial dysfunction to increase drug safety in the pharmaceutical industry.

Sashi Nadanaciva1, Yvonne Will.   

Abstract

Drug-induced mitochondrial dysfunction is a contributor to both late-stage compound attrition and post-market drug withdrawals. This review outlines the mechanisms which lead to drug-induced mitochondrial dysfunction and discusses the tremendous advances that have been made in the development of in vitro methods to identify mitochondrial impairment. Potentially useful animal models and in vivo methods to detect drug-induced mitochondrial impairment are also discussed.

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Year:  2011        PMID: 21275886     DOI: 10.2174/138945011795528985

Source DB:  PubMed          Journal:  Curr Drug Targets        ISSN: 1389-4501            Impact factor:   3.465


  10 in total

1.  Mitochondrial dysfunction induced by leflunomide and its active metabolite.

Authors:  Jiekun Xuan; Zhen Ren; Tao Qing; Letha Couch; Leming Shi; William H Tolleson; Lei Guo
Journal:  Toxicology       Date:  2018-02-08       Impact factor: 4.221

2.  In vitro cardiotoxicity assessment of environmental chemicals using an organotypic human induced pluripotent stem cell-derived model.

Authors:  Oksana Sirenko; Fabian A Grimm; Kristen R Ryan; Yasuhiro Iwata; Weihsueh A Chiu; Frederick Parham; Jessica A Wignall; Blake Anson; Evan F Cromwell; Mamta Behl; Ivan Rusyn; Raymond R Tice
Journal:  Toxicol Appl Pharmacol       Date:  2017-03-01       Impact factor: 4.219

3.  Systematic study of mitochondrial toxicity of environmental chemicals using quantitative high throughput screening.

Authors:  Matias S Attene-Ramos; Ruili Huang; Srilatha Sakamuru; Kristine L Witt; Gyda C Beeson; Louie Shou; Rick G Schnellmann; Craig C Beeson; Raymond R Tice; Christopher P Austin; Menghang Xia
Journal:  Chem Res Toxicol       Date:  2013-08-15       Impact factor: 3.739

4.  Effects of mid-respiratory chain inhibition on mitochondrial function in vitro and in vivo.

Authors:  Ashley J Broom; Jeffrey Ambroso; Gino Brunori; Angie K Burns; James R Armitage; Ian Francis; Mitul Gandhi; Richard A Peterson; Timothy W Gant; Alan R Boobis; Jonathan J Lyon
Journal:  Toxicol Res (Camb)       Date:  2015-09-17       Impact factor: 3.524

5.  Intact Cell Lipidomics Reveal Changes to the Ratio of Cardiolipins to Phosphatidylinositols in Response to Kanamycin in HeLa and Primary Cells.

Authors:  Sonia Rebollo-Ramirez; Sina Krokowski; Damian Lobato-Márquez; Michael Thomson; Ivana Pennisi; Serge Mostowy; Gerald Larrouy-Maumus
Journal:  Chem Res Toxicol       Date:  2018-07-11       Impact factor: 3.739

6.  Hepatotoxicity reports in the FDA adverse event reporting system database: A comparison of drugs that cause injury via mitochondrial or other mechanisms.

Authors:  Payal Rana; Michael D Aleo; Xuerong Wen; Stephen Kogut
Journal:  Acta Pharm Sin B       Date:  2021-06-07       Impact factor: 11.413

Review 7.  Versatile Functional Energy Metabolism Platform Working From Research to Patient: An Integrated View of Cell Bioenergetics.

Authors:  Sylvain Loric; Marc Conti
Journal:  Front Toxicol       Date:  2022-02-03

8.  Profiling of the Tox21 chemical collection for mitochondrial function to identify compounds that acutely decrease mitochondrial membrane potential.

Authors:  Matias S Attene-Ramos; Ruili Huang; Sam Michael; Kristine L Witt; Ann Richard; Raymond R Tice; Anton Simeonov; Christopher P Austin; Menghang Xia
Journal:  Environ Health Perspect       Date:  2014-10-10       Impact factor: 9.031

9.  Florfenicol-induced Mitochondrial Dysfunction Suppresses Cell Proliferation and Autophagy in Fibroblasts.

Authors:  Dongfang Hu; Shengliang Cao; Guihua Zhang; Yihong Xiao; Sidang Liu; Yingli Shang
Journal:  Sci Rep       Date:  2017-10-19       Impact factor: 4.379

Review 10.  Mitochondria as the Target of Hepatotoxicity and Drug-Induced Liver Injury: Molecular Mechanisms and Detection Methods.

Authors:  Milos Mihajlovic; Mathieu Vinken
Journal:  Int J Mol Sci       Date:  2022-03-18       Impact factor: 5.923

  10 in total

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