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Drug Safety Evaluation

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Cover of 'Drug Safety Evaluation'

Table of Contents

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    Book Overview
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    Chapter 1 Nonclinical Development of Combination Drugs
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    Chapter 2 Juvenile Nonclinical Safety Studies in Support of Pediatric Drug Development
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    Chapter 3 Procedures of Necropsy and Tissue Sampling
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    Chapter 4 Tissue Sampling and Processing for Histopathology Evaluation
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    Chapter 5 Principles and Methods of Immunohistochemistry
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    Chapter 6 Applications of Mass Spectrometry Imaging for Safety Evaluation
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    Chapter 7 In Vivo Rat T-Lymphocyte Pig-a Assay: Detection and Expansion of Cells Deficient in the GPI-Anchored CD48 Surface Marker for Analysis of Mutation in the Endogenous Pig-a Gene
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    Chapter 8 Detection of In Vivo Mutation in the Pig-a Gene of Mouse Bone Marrow Erythroids
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    Chapter 9 The Use of Bacterial Repair Endonucleases in the Comet Assay
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    Chapter 10 Automated Patch-Clamp Methods for the hERG Cardiac Potassium Channel
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    Chapter 11 Impedance Measurement in Induced Pluripotent Stem Cell-Derived Cardiomyocytes
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    Chapter 12 Target Safety Assessment: Strategies and Resources
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    Chapter 13 NMR and MS Methods for Metabolomics
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    Chapter 14 Protocols and Applications of Cellular Metabolomics in Safety Studies Using Precision-Cut Tissue Slices and Carbon 13 NMR
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    Chapter 15 Statistical Analysis of Quantitative RT-PCR Results
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    Chapter 16 Evaluation of Mitochondrial Respiration in Cultured Rat Hepatocytes
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    Chapter 17 FETAX Assay for Evaluation of Developmental Toxicity
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    Chapter 18 Evaluation of Embryotoxicity Using the Zebrafish Model
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    Chapter 19 Absolute Quantification of Toxicological Biomarkers via Mass Spectrometry
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    Chapter 20 Next-Generation Sequencing to Investigate Urinary microRNAs from Macaca fascicularis (Cynomolgus Monkey)
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    Chapter 21 Quantitative RT-PCR for MicroRNAs in Biofluids
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    Chapter 22 Chromogenic In Situ Hybridization Methods for microRNA Biomarker Monitoring of Drug Safety and Efficacy
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    Chapter 23 Urine Exosome Isolation and Characterization
Attention for Chapter 14: Protocols and Applications of Cellular Metabolomics in Safety Studies Using Precision-Cut Tissue Slices and Carbon 13 NMR
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Chapter title
Protocols and Applications of Cellular Metabolomics in Safety Studies Using Precision-Cut Tissue Slices and Carbon 13 NMR
Chapter number 14
Book title
Drug Safety Evaluation
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-7172-5_14
Pubmed ID
Book ISBNs
978-1-4939-7170-1, 978-1-4939-7172-5
Authors

Gabriel Baverel, Maha El Hage, Guy Martin

Abstract

Numerous xenobiotics are toxic to human and animal cells by interacting with their metabolism, but the precise metabolic step affected and the biochemical mechanism behind such a toxicity remain often unknown. In an attempt to reduce the ignorance in this field, we have developed a new approach called cellular metabolomics. This approach, developed in vitro, provides a panoramic view not only of the pathways involved in the metabolism of physiological substrates of any normal or pathological human or animal cell but also of the beneficial and adverse effects of xenobiotics on these metabolic pathways. Unlike many cell lines, precision-cut tissue slices, for which there is a renewed interest, remain metabolically differentiated for at least 24-48 h and allow to study the effect of xenobiotics during short-term and long-term incubations. Cellular metabolomics (or metabolic flux analysis), which combines enzymatic and carbon 13 NMR measurements with mathematical modeling of metabolic pathways, is illustrated in this brief chapter for studying the effect of insulin on glucose metabolism in rat liver precision-cut slices and of valproate on glutamine metabolism in human renal cortical precision-cut slices. The use of very small amounts of test compounds allows to predict their toxic effect and eventually their beneficial effects very early in the research and development processes. Cellular metabolomics is complementary to other omics approaches, but, unlike them, provides functional, mechanistic, and dynamic pieces of information by measuring enzymatic fluxes.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 6 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 1 17%
Unknown 5 83%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 2 33%
Unspecified 1 17%
Student > Bachelor 1 17%
Other 1 17%
Student > Doctoral Student 1 17%
Other 0 0%
Readers by discipline Count As %
Pharmacology, Toxicology and Pharmaceutical Science 2 33%
Unspecified 1 17%
Agricultural and Biological Sciences 1 17%
Medicine and Dentistry 1 17%
Engineering 1 17%
Other 0 0%