Pharm 1: Drug receptors and pharmacodynamics

Define Pharmacology

Study of the manner in which function of living systems is affected by chemical agents

Define Pharmacodynamics

the study of effects of drugs and their mechanisms of action

Pharmacokinetics

the study of absorption, distribution, biotransformation and excretion of drugs

Pharmacotherapy

study of the use of drugs in prevention and treatment of disease

Toxicology

aspect of pharmacology that deals with the adverse effects of drugs

Define selectivity

drugs act on particular cells and tissues -> must show high degree of binding-site specificity.

Define specificity

proteins that function as drug targets will only recognize ligands of a certain type

Receptor

the component of the organism with which a chemical agent interacts

List the different classes of receptors with which drugs interact

physiological receptors, enzymes, transporters, ion channels, structural proteins

Drugs that are not mediated by binding to receptors

interact with small molecules or ions that are found in the body -> ex. therapeutic neutralization of gastric acid by antacids, Mesma, mannitol, cholestyramine/colestipol/colesevelam, Dimercaprol, Structural analogs of pyrimidines and purines

Mesma

acts in the bladder with acroline (reactive metabolite of the anticancer drug cyclophosphamide to prevent hemorrhagic cystitis),

Cholestyramine/colestipol/colesevelam

binds bile acids to prevent reabsorption (treats hyperlipidemia)

Mannitol

administered to increase osmolarity of body fluids -> can promote diuresis, catharsis, expansion of circulating volume or reduction of cerebral edema

Dimercaprol

chelates heavy metals to decrease their toxicity

Structural analogs of pyrimidines and purines

can be incorporated into nucleic acids and alter their function; such drugs have clinical utility in cancer and antiviral chemo