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61 Cards in this Set

  • Front
  • Back

ligand gated channel

ionotropic receptor/ open by ligand

g- protein coupled receptor

do not work on its own/ work by coupling with g protein/ some work independent of g protein

Gs protein

stimulatory receptor- Gs- activates enzyme- reacts- ATP- protein

Gi protein

Gi- inhibitory- turn off protein

Gq protein

Gq- diff. system of activation ( no interaction with adenylyl- interacts with phosphal lipid...)

PIP2

PIP2- one specie phosphallypose cuts head off (that likes water)

IP3

IP3- result, calcium channels, calcium goes out to the cell

DAG

DAG- fatty part now exposed interact with protein

Neurotransmitter

we use to communicate with brain

EPSP(depolarization)

bigger when more channels

IPSP(hyperpolarization)

when cell slightly activated, makes cell negative kept away from treshold

sumation

total of... inputs on cell (spatial-multiple inputs at diff. places)

Agonists

A chem. that binds to and activates a receptor

antagonists

a chemical that binds to a receptor and prevents its activation

Direct

competitive binding

Indirect

non-competitive binding

Neurotransmitter criteria

1. in terminal 2. Ca2+ dependent release 3. Subject to inactivation 4. synaptic mimicry 5. receptors exist

acetylcholine

broken down(inactivate) by acetylcholinesterase (AChE).


acetyl-CoA = cofactor that supplies acetate for the synthesis of acetylcholine

Amino Acid neurotransmittes

1. Workhorses of the CNS 2. Overall roll 3. receptors

Glutamate

13 types of receptors

NMDA

of great interest correlates with learning. sodium + calcium comes in. ball in pore is Mg(magnesium)- if there no ions can flow through/activate cell and make it less negative and Mg+ goes away

GABA

y-aminbutyric acid. GAD turns glutamate into GABA and CO2

Two families of GABA

GABAa receptors and GABAb receptors

GABAa receptors

-allows Cl- ions in result in hypolarization -alot of binding sites

GABAb receptors

-G- protein coupled - K+ hypolarization

Acetylcholine

- first discovered/ many diff. receptors for acetylcholine

psychopharmacology

the study of drugs on the ns and on behavior

Drug effect

the changes a drug produces in animals physiological processes and behavior

site of action

a location at which molecules of drug interact with molecules located on or in cells of the body, thus affecting some biochemical processes of these cells

pharmacokinetics

process by which drugs are absorbed, distributed within the body, metabolized, and excreted

exogenous

outside of body

endogenous

inside the body(used to test hypothesis of whats going on inside the body)

precursor

a substance from which another substance is formed (tb says its a agonist)

peptides

string of amino acids

intravenous (iv) injection

injection to the vein/ fastest/ disadvantage increased skill and care required

intraperitoneal l(IP) injection

injected to abdominal wall into the peritoneal cavity- space surrounds stomach, intestines, liver, abdominal organs( most common for lab animals)

intramusclar (IM) injection

direct to muscle(capillaries that supply the muscle)

subcutaneous (SC) injection

injected into space beneath skin(small amounts)

oral administration

most common to humans/ some cannot because stomach acid could destroy it

sublingual administration

placing them beneath tongue/ absorbed into bloodstream by capillaries that supply the mucous membrane that lines the mouth

intrarectal administration

rarely used/ drugs up the butt in the form of suppositories

inhalation

smoke/inhale weed nicotine cocaine

topical administration

creams ex. sunscreen

insuffation

cocaine/ mucous membrane lining the nasal passages different than inhalation because ends up in nasal passages not lungs

intracerebral administration

inject small amount of drug in brain/ study effects a drug has to specific region of the brain

intracerebroventricular (ICV) administration

inject drug into cerebral ventricle, absorbed into brain tissue/ rare to humans unless to treat people with antibiotics in the brain

blood-brain barrier

only for water soluble molecules/ lipids get through heroin > morphine

excretion

many drugs are deactivated by enzymes and excreted by kidneys/liver plays a role in enzymatic deactivation of drugs some also in blood also the brain/ transformed molecule is even more active than the one administered

dose-response curve

various drugs and amounts and effects plotted/ heavier needs more amount/ doses reach a limit after equals no effect

therapeutic index

Drug margain of safety

Drug effectiveness

different sites of action/ drug affinity(readiness with which the two molecules join together) with its site of action/ high affinity produce effects at low concentration

tolerance

effects of a drug not constant and soon diminish

sensitization

Drug becomes more effective

withdrawal symptoms

opposite effects of drugs when taken too much

direct agonist

drug binds and activates receptor

receptor blocker(DIRECT ANTAGONISTS)

a drug that binds with a receptor but does not activate it

non-competitive binding(Indirect)

binding of a drug to a site on a receptor, does not interfere with the binding site for the principal ligand

indirect antagonists

a drug that attaches to a binding site on a receptor and interferes with the action of the receptor/ does not interfere with the binding site for the principal ligand

indirect agonist

attaches to one of the alternative sites and facilitates the opening of the ion channel

choline acetyltransferase (ChAT)

enzyme that transfers the acetate ion from acetyl coenzyme A to choline, producing the neurotransmitter acetylcholine

botulinum toxin

an acetylcholine