Choose an application

• Reference Manager
• EndNote
• RefWorks (Direct export to RefWorks)

Membrane transporters are of vital importance for cells. They mediate the flux of many substances through the plasma membrane. In this book, the transporters for organic cations, a special class of membrane transporters, are presented. Transporters belonging to this class are important because they allow many neurotransmitters (e.g., histamine and serotonin) and many drugs (e.g., trospium and tofacitinib) to permeate the plasma membrane. Therefore, transporters for organic cations can modulate the action of neurotransmitters and drugs, having in this way important physiological and pharmacological implications. These aspects are illustrated in original works and reviews presented in this book. Using a system biology approach, the global significance of different transporters working together has been illustrated. Regulation mechanisms determining their expression in specific organs and modulating their function are also described in this book, also concerning their role for special drug toxicities. Such an aspect is also discussed in relationship to mutations (single nucleotide polymorphisms) of transporters for organic cations. Finally, the translational value of studies performed in flies, mice, and rats is discussed. Therefore, this book offers integrative information on transporters for organic cations, which may be of interest to beginners and specialized scientists in this field.

Medicine --- transporters --- endogenous metabolism --- functional subgroups --- SLC22 --- remote sensing and signaling --- drug transporters --- gut microbiome --- chronic kidney disease --- solute carrier 22 (SLC22) --- Remote Sensing and Signaling Theory --- interorgan communication --- organic anion transporter --- organic cation transporter --- SLC22A15 --- SLC22A16 --- SLC22A18 --- kidney --- Malpighian tubule --- TCGA --- human pathology atlas --- gene ontology --- organic cations --- transport --- kidneys --- regulation --- Nuclear receptor --- renal excretion --- bile acids --- organic cation transporters --- drug disposition --- genetic polymorphisms --- drug-induced kidney injury --- nephrotoxicity --- RA --- Tofacitinib --- Baricitinib --- MATE1 --- solute carrier (SLC) family --- OCT1 --- SLC22A1 --- species differences --- drugs --- pesticides --- cisplatin nephrotoxicity --- PPAR-alpha --- organic transporters --- serotonin transporter --- plasma membrane monoamine transporter --- ketamine --- isoflurane --- serotonin clearance --- antidepressant-like activity --- chronoamperometry --- tail suspension test --- forced swim test --- hepatotoxicity --- solute carrier --- pulmonary drug delivery --- SLC22A1-5 --- lung epithelium --- drug uptake --- β2-agonists --- chronic lung diseases --- anticholinergics --- trospium --- OCT --- MATE --- drug excretion --- drug transport --- transporters --- endogenous metabolism --- functional subgroups --- SLC22 --- remote sensing and signaling --- drug transporters --- gut microbiome --- chronic kidney disease --- solute carrier 22 (SLC22) --- Remote Sensing and Signaling Theory --- interorgan communication --- organic anion transporter --- organic cation transporter --- SLC22A15 --- SLC22A16 --- SLC22A18 --- kidney --- Malpighian tubule --- TCGA --- human pathology atlas --- gene ontology --- organic cations --- transport --- kidneys --- regulation --- Nuclear receptor --- renal excretion --- bile acids --- organic cation transporters --- drug disposition --- genetic polymorphisms --- drug-induced kidney injury --- nephrotoxicity --- RA --- Tofacitinib --- Baricitinib --- MATE1 --- solute carrier (SLC) family --- OCT1 --- SLC22A1 --- species differences --- drugs --- pesticides --- cisplatin nephrotoxicity --- PPAR-alpha --- organic transporters --- serotonin transporter --- plasma membrane monoamine transporter --- ketamine --- isoflurane --- serotonin clearance --- antidepressant-like activity --- chronoamperometry --- tail suspension test --- forced swim test --- hepatotoxicity --- solute carrier --- pulmonary drug delivery --- SLC22A1-5 --- lung epithelium --- drug uptake --- β2-agonists --- chronic lung diseases --- anticholinergics --- trospium --- OCT --- MATE --- drug excretion --- drug transport