PHARMACOLOGY Flashcards
what drug class is chlorpromazine?
a phenothiazine based antipsychotic
what is chlorpromazine an antagonist for?
dopamine receptors, serotonin 1 and 2 receptors, H1 receptors, alpha 1 and alpha 2 receptors, M1 and M2 receptors
what is the mechanisms for chlorpromazine’s antipsychotic actions?
long-term adaptation by the brain to block dopamine receptors
what is chlorpromazine used for?
antipsychotic, intractable hiccup, antiemetic
note: no longer used as an antipsychotic
what drug class is clozapine?
a psychotropic agent
what are the indications for clozapine?
schizophrenia
what is clozapine’s mechanism of action?
D2 antagonism to relive positive symptoms and 5HT2A antagonism to alleviate negative symptoms
what drug class is haloperidol?
a dopamine receptor antgaonist
what is haloperidol used to treat?
schizophrenia
what are haloperidol effects?
antipsychotics
sedative
antiemetic
what are the possible mechanisms of haloperidol’s action?
1) Depressing the CNS at the subcortical level of the brain, midbrain, and brain stem reticular formation, via inhibition of the ascending reticular activating system of the brain stem (possibly through the caudate nucleus), thereby interrupting the impulse between the diencephalon and the cortex.
2) Antagonizing the actions of glutamic acid within the extrapyramidal system,
3) Inhibiting catecholamine receptors
4) Inhibiting the reuptake of various neurotransmitters in the midbrain
5) Directly affect the chemoreceptor trigger zone (CTZ) through the blocking of dopamine receptors.
what drug class is risperidone?
multitarget antipsychotic
what is risperidone used to treat?
delusional psychosis, bipolar disorder, psychotic depression
what is risperidones mechanism of action?
inhibition of D2 receptors in the limbic system which alleviates symptoms of schizophrenia.
inhibition of 5-HT2 receptors in the mesocortical tract. This causes an excess of dopamine and an increase in dopamine transmission and an elimination of core negative symptoms. Usefully dopamine receptors in the nigrostriatal pathway are not affected and therefore extrapyramidal effects are avoided.
and inhibition of Alpha (1), alpha (2) adrenergic receptors and H1 receptors