Erstellt von Dan McArthur
vor etwa 8 Jahre
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Frage | Antworten |
Nifedipine | - Blocks Calcium Channels - Reduces blood vessel constriciton - Reduces Blood Pressure |
Fluoxitine | - Blocks 5-HT reuptake - Prolongs effects of 5-HT |
Aspirin | - Inhibits Cyclo-Oxygenase (COX) - Reduces inflammatory response - Binds covalently |
L-Dopa | - Increases synthesis of Dopamine |
Morphine | - Activates opioid receptors for pain relief |
Naloxone | - Opioid receptor antagonist - Used for heroin overdoses |
Ionotropic Receptors | Agonists bind and directly regulate the opening of the ion channel |
Metabotropic Receptors | Agonist binding causes series of intracellular events to indirectly produce effects |
Nicotinic Receptors | Located on skeletal muscle, and at the preganglionic junction of Para and Sympa neurons. Ach binds and causes Sodium Channels to open |
Kinase-Linked Receptors | Agonist binding causes the activation of the cytoplasmic domain that has Kinase Activity |
Cytoplasmic Receptors | Receptors for lipid-soluble agonists Agonist-receptor binds and enters the nucleus Regulates gene expression e.g. Glucocorticoid Receptors |
G-Protein Coupled Receptors | Largest receptor family Linked to an effector protein by a G-protein e.g. Muscarinic Receptors |
GPCR: Adenylate Cyclase | Produces cAMP which has activation activity in the cell |
GPCR: Phospholipase C | Catalyzes PIP2 into Inositol Triphosphate and DAG Increases intracellular Calcium levels in the cell Used by Beta Adrenoceptors and Alpha1 |
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