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Principles of Safety Pharmacology

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Cover of 'Principles of Safety Pharmacology'

Table of Contents

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    Book Overview
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    Chapter 1 A Historical View and Vision into the Future of the Field of Safety Pharmacology
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    Chapter 2 In Vitro Early Safety Pharmacology Screening: Perspectives Related to Cardiovascular Safety
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    Chapter 3 Safety Pharmacology in Drug Discovery and Development
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    Chapter 4 CNS Adverse Effects: From Functional Observation Battery/Irwin Tests to Electrophysiology
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    Chapter 5 Preclinical Abuse Potential Assessment
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    Chapter 6 Overview of Respiratory Studies to Support ICH S7A
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    Chapter 7 Biophysics and Molecular Biology of Cardiac Ion Channels for the Safety Pharmacologist
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    Chapter 8 Sensitivity and Specificity of the In Vitro Guinea Pig Papillary Muscle Action Potential Duration for the Assessment of Drug-Induced Torsades De Pointes Liability in Humans
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    Chapter 9 Haemodynamic Assessment in Safety Pharmacology
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    Chapter 10 High Definition Oscillometry: Non-invasive Blood Pressure Measurement and Pulse Wave Analysis
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    Chapter 11 The Safety Pharmacology of Auditory Function
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    Chapter 12 Principles of Safety Pharmacology
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    Chapter 13 Principles of Safety Pharmacology
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    Chapter 14 Inclusion of Safety Pharmacology Endpoints in Repeat-Dose Toxicity Studies
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    Chapter 15 Safety Pharmacology Evaluation of Biopharmaceuticals.
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    Chapter 16 Safety Pharmacology of Anticancer Agents
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    Chapter 17 Clinical ECG Assessment
Attention for Chapter 4: CNS Adverse Effects: From Functional Observation Battery/Irwin Tests to Electrophysiology
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Chapter title
CNS Adverse Effects: From Functional Observation Battery/Irwin Tests to Electrophysiology
Chapter number 4
Book title
Principles of Safety Pharmacology
Published in
Handbook of experimental pharmacology, January 2015
DOI 10.1007/978-3-662-46943-9_4
Pubmed ID
Book ISBNs
978-3-66-246942-2, 978-3-66-246943-9
Authors

Carlos Fonck, Alison Easter, Mark R. Pietras, Russell A. Bialecki, Fonck, Carlos, Easter, Alison, Pietras, Mark R., Bialecki, Russell A.

Abstract

This chapter describes various approaches for the preclinical assessment of drug-induced central nervous system (CNS) adverse effects. Traditionally, methods to evaluate CNS effects have consisted of observing and scoring behavioral responses of animals after drug is administered. Among several behavioral testing paradigms, the Irwin and the functional observational battery (FOB) are the most commonly used assays for the assessment of CNS effects. The Irwin and FOB are considered good first-tier assays to satisfy the ICH S7A guidance for the preclinical evaluation of new chemical entities (NCE) intended for humans. However, experts have expressed concern about the subjectivity and lack of quantitation that is derived from behavioral testing. More importantly, it is difficult to gain insight into potential mechanisms of toxicity by assessing behavioral outcomes. As a complement to behavioral testing, we propose using electrophysiology-based assays, both in vivo and in vitro, such as electroencephalograms and brain slice field-potential recordings. To better illustrate these approaches, we discuss the implementation of electrophysiology-based techniques in drug-induced assessment of seizure risk, sleep disruption, and cognitive impairment.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 34 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 34 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 7 21%
Student > Master 5 15%
Researcher 5 15%
Student > Ph. D. Student 3 9%
Other 3 9%
Other 2 6%
Unknown 9 26%
Readers by discipline Count As %
Medicine and Dentistry 5 15%
Biochemistry, Genetics and Molecular Biology 3 9%
Agricultural and Biological Sciences 3 9%
Chemistry 3 9%
Immunology and Microbiology 2 6%
Other 7 21%
Unknown 11 32%