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Docente
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NISTICO ROBERT
(programma)
Pharmacodynamics: relationship dose/effects; series of doses; ED50, LD50, Therapeutic window; Receptors: Classification, Structural, Functional
Organization And Pharmacological Modulation; Ionotropic Receptors And Metabotropic Receptors; Methods For The Study Of Membrane Receptors;Protein
Kinases And Their Role In Signal Transduction; Regulation Of Intracellular Calcium Homeostasis; Voltage-Deprendent Ion Channels; Neurotransporters:
Molecular Structure, Activation Mechanisms And Pharmacological Modulation Of Neurotransporters; Neurotransmitters: Cholinergic Transmission,
Catecholaminergic Transmission, Serotonergic Transmission, Gabaergic Transmission, Excitatory Amino Acid Transmission, Nitric Oxide, Opioid System,
Cannabinoids; Tolerance, Drug Dependence, Prescription Medicines And Otc Medicines; Clinical Trials (placebo, randomization, blind design, ethics);
Homeopathic School; Introduction To Toxicology; Toxicokinetics, Mechanisms Of Toxicity, Cellular Toxicity, Genetic Toxicology, Carcinogenesis,
Mechanisms And Pathogenesis Of Developmental Toxicity; Basis Of Adverse Drug Reaction: Drug Allergy, Drug Idiosyncrasy; Target Organ Toxicity
Induced By Drugs.
Scope and aims of pharmacokinetics; Utility of pharmacokinetics in pharmacotherapy and drug development; Pharmacokinetic parameters (Ke, Clearance,
Vd, t1/2); Steady-state; Relationship between persistence in the body and effect; Passage through biological membranes; Cell barriers; Absorption,
Biological dosage (bioassay), Bioavailability, Pre-systemic elimination; Binding to plasma proteins and Pharmaco-toxicological consequences of plasma
protein binding displacement, Drug interactions; Accumulation and storage tissues; Renal and biliary excretion; Dose-concentration relationship, saturation
kinetics; Kinetic variability: influence of genetic factors, interactions, pathologies; Metabolism of drugs; Enzymatic induction: mechanisms and kinetics,
pharmacological and toxicological consequences; Enzymatic inhibition: mechanisms and kinetics, pharmacological and toxicological consequences, main
inhibitors of CYP450; Genetic polymorphism of metabolizing enzymes.
 Goodman and Gilman: The pharmacological basis of therapeutics, XI ed. McGraw-Hill; Clementi F., Fumagalli G.: Farmacologia generale e molecolare, III ed. UTET.
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