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Bernard
Testa and Stefanie D. Krämer
The Biochemistry of Drug Metabolism: Conjugations, Consequences of
Metabolism, Influencing Factors
Volume 2

February 2010
620 Pages, Softcover
ISBN-10: 3-906390-54-3
ISBN-13: 978-3-906390-54-3
Softcover
Description
Volume Two contains the last four parts of this work. Part
4 is devoted to the huge field of conjugation reactions, with much information
being given on transferases. As in the two preceding parts, each
drug-metabolizing enzyme or enzyme family begins with an Enzyme Identity Card
summarizing its nomenclature and biochemical essentials. The reactions examined
here include methylation, sulfation, glucuronidation, acetylation, conjugation
with glutathione, while there is also a rigorous presentation of the pivotal
role of xenobiotic-coenzyme A conjugates as a crossroads to various metabolic
reactions.
The next part examines the consequences of drug and xenobiotic metabolism in a
pharmacological and toxicological perspective, with due attention paid to full
activation, as is found with prodrugs, and to the worrying case of xenobiotic
toxification.
Parts 6 and 7 cover the inter-individual and intra-individual factors that
influence drug metabolism, starting with an introduction to evolutionary events
leading to species differences in the metabolism of xenobiotics and to
polymorphisms within a particular species. Focusing on humans, the most relevant
polymorphic drug-metabolizing enzymes are discussed, concentrating on ethnic
differences and on the consequences for the pharmacokinetic behavior of affected
drugs, while also introducing sex-dependent metabolic reactions.
The final part introduces the mechanisms leading to increases or decreases in
enzyme activities as the concept of enzyme induction via nuclear receptors and
the different mechanisms of enzyme inhibition are explained. With these basics
in mind, various influencing factors are discussed, including physiological and
pathological conditions, as well as drugs, nutrients and environmental agents
with a special focus on drug-drug interactions.
With a foreword by Prof Leslie Z. Benet -- the best and best-known
biopharmaceutical scientist worldwide.
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