Drug - exam questions (multichoice) Flashcards
1
Q
- Isoprenoids are synthesized in:
- Only cytosol
- Only plastid
- Only mitochondrium
- Mitochondrium and plastid
- Plastid and cytosol
A
Plastid and cytosol
2
Q
- The cation channel TRPM8 is activated by
- Menthol
- Flavonoids
- Artemisin
A
Menthol
3
Q
- Which compounds are synthesized in the MEP-Pathway
- Carotenoids
- Flavonoids
- Brassinosteroids
A
Carotenoids
4
Q
- Betalains are:
- Inhibitors of glycine receptors
- Blue-colored pigments that absorb UV light
- Dopamine-derived alkaloids
A
C-Dopamine-derived alkaloids
5
Q
- Caffeine kills the larvae of the tobacco hornworm by:
- Competative inhibition of phosphodiesterase
- Blocking of the glutamate receptor
- Depolarization of microtubules
- Or is not toxic to animals
A
A-Competative inhibition of phosphodiesterase
6
Q
- Resiniferatoxin
- Binds to human TPRV1 channels
- Is an antidote to muscarin
- Is a volatile metabolite used to attract insects for pollination
- Induces a cold sensation by shifting the TRPM8 activation unit?
A
A-Binds to human TPRV1 channels
7
Q
- The M-Phase of the plant cell cycle does not involve:
- Microtubules
- Alignment of chromosomes at the spindle equator
- Centrosomes
- Break down of nuclear envelope
A
C-Centrosomes
- Centrosomes replicate during S-phase, but move during prophase
8
Q
- Tobacco hornworm is not killed by nicotine
- Because the binding site of its nicotine acetylcholine (…)
- Nicotine is converted to a harmless metabolite
- It only feeds on non-nicotine containing tobacco s…
A
B-Nicotine is converted to a harmless metabolite
9
Q
- Cannabinoids are found predominantly
- In root cortical cells
- In glandular trichomes
- In cells of vascular bundle
- In buds of male plants
A
B-In glandular trichomes
10
Q
- Aristolochic acid - X - not sure on answer to this one
- Can depolarize microtubules
- Causes point mutations, gaps and chromosome breaks
- Activates intrinsic and extrinsic apoptotic pathways
- Inhibits BCRP/ABCG2 (ABC transporters)
A
B-Causes point mutations, gaps and chromosome breaks
- Wikipedia says potentially works by mutating p53 gene, so maybe this one?
Not sure on answer to this one,
11
Q
- Plant secondary metabolites are
- Always specific to plants
- Always found also in animals or bacteria
- Often employed for plant defense against biotic stress
- Specifically made as an attractant for humans to assist seed dispersion
A
C-Often employed for plant defense against biotic stress
12
Q
- Which of the following plant secondary metabolites affect the GABAA/G receptors?
- Thujone
- Coniine
- Salvinorin A
- Kainic acid
A
A-Thujone
13
Q
- Which of the following substance class does not contribute to plant secondary metabolism?
- Polysaccharides
- Ribonucleic acids
- Terpenoids
- Amino acids
- Alkaloids
- All of the above contribute
A
A - Polysaccharides
B - Ribonucleic acids
D - Amino acids
14
Q
- Which properties are not found in plant heterotrimeric G-Proteins?
- Fast nucleotide exchanging and slow GTP-Hydrolysis activity
- Self-activation
- Spontaneous loading with GTP
- Usage of GPCRs as GEFs
A
- Fast nucleotide exchanging and slow GTP-Hydrolysis activity
- Self-activation
- Spontaneous loading with GTP
-
Usage of GPCRs as GEFs
- not found in plant heterotrimeric g-proteins (is found in animals)
15
Q
- Plant secondary metabolism is
- Associated with essential cellular functions
- Usually species specific and dispensable
- Important to increase plant fitness under laboratory conditions
- Detrimental to survival and reproduction in the natural environment
A
- Associated with essential cellular functions
- Usually species specific and dispensable
- Important to increase plant fitness under laboratory conditions
- Detrimental to survival and reproduction in the natural environment
16
Q
- Brazzein is
- An alkaloid
- A diterpene
- A protein
- A polyacetylene
A
- An alkaloid
- A diterpene
- A protein
- A polyacetylene
17
Q
- Tyrosine is a precursor molecule for the formation of
- Monoterpenoid indole alkaloids
- Berberine
- Nicotine
- Scopolamine
- Caffeine
A
- Tyrosine is a precursor molecule for the formation of
- Monoterpenoid indole alkaloids
- Berberine
- Nicotine
- Scopolamine
- Caffeine
18
Q
- Polyploidy in plants can be induced by:
- Colchicine
- Combrestatins
- Falcarinol
- Safranol
A
-
Colchicine
- Chromosome segregation driven by microtubules. Inhibits chromosome segregation during meiosis, inducing polyploidy.
- Combrestatins
- Falcarinol
- Safranol
19
Q
- Cholera toxin
- Inhibits receptor tyrosine kinases
- Blocks ion channels
- Inhibits GTPase activity of stimulatory G-Protein alpha subunit
- Inhibits phosphodiesterases
A
- Inhibits receptor tyrosine kinases
- Blocks ion channels
-
Inhibits GTPase activity of stimulatory G-Protein alpha subunit
- Produces ADP-ribosyltransferase specific for Galpha
- ADP ribosyl transferred to active site Arg
- Galpha activity inhibited
- Inhibits phosphodiesterases
20
Q
- The so-called pyschodelic drugs mescalin and psilocin
- Are tyrosine kinase inhibitors
- Bind to a subclass of serotonin receptors
- Bind to steroid hormone receptors
- Are dopamine receptor antagonists
A
- Are tyrosine kinase inhibitors
-
Bind to a subclass of serotonin receptors
- Hallucinogens bind 5HT2A receptors, a type of serotonin receptor
- Bind to steroid hormone receptors
- Are dopamine receptor antagonists
21
Q
- Notch signaling
- Occurs between two adjacent cells and is important for the formation of tissue boundaries
- Occurs in cells when the receptor is bound by an endocrine signaling molecule
- Regulates hormone production in plants
A
- Occurs between two adjacent cells and is important for the formation of tissue boundaries
- Occurs in cells when the receptor is bound by an endocrine signaling molecule
- Regulates hormone production in plants
22
Q
- Cocaine binds
- The dopamine receptor D2
- The dopamine transporter
- The dopamine gated ion channel
- The serotonin receptor
A
- The dopamine receptor D2
-
The dopamine transporter
- Blocks dopamine transporter DAT
- The dopamine gated ion channel
- The serotonin receptor
23
Q
- Protein kinase A
- Is activated by cAMP
- Is inhibited by cAMP
- Is activated by phospholipids
- Is inhibited by phospholipids
A
- Is activated by cAMP
- Is inhibited by cAMP
- Is activated by phospholipids
- Is inhibited by phospholipids
24
Q
- Curare
- Is a dopamine receptor antagonist
- Is an inhibitor of acetylcholine esterase
- Is a competative antagonist of the acetylcholine receptor
- Is a glycine receptor agonist
A
- Is a dopamine receptor antagonist
- Is an inhibitor of acetylcholine esterase
- Is a competative antagonist of the acetylcholine receptor
- Is a glycine receptor agonist
25
Q
- 7-transmembrane domain receptors
- Serve as GEFs (guanyl nucleotide exchange factors) for trimeric G-proteins
- Serve as GAP (GTPase activating protein) for trimeric G-Protein alpha-subunits
- Phosphorylate other 7-transmembrane receptors
A
- Serve as GEFs (guanyl nucleotide exchange factors) for trimeric G-proteins
- Serve as GAP (GTPase activating protein) for trimeric G-Protein alpha-subunits
- Phosphorylate other 7-transmembrane receptors
26
Q
- Wnt signaling
- Is involved in the visual system to transduce light signals
- Is involved in many developmental processes in plants
- Is important for stem cell differentiation and maintenance in animals
- Involves beta-catenin secretion and binding to frizzles-receptors
A
- Is involved in the visual system to transduce light signals
- Is involved in many developmental processes in plants
- Is important for stem cell differentiation and maintenance in animals
- Involves beta-catenin secretion and binding to frizzles-receptors
27
Q
- Vinblastine or its derivatives are used in tumor therapy because
- They block topoisomerase and cause DNA damage in dividing cells
- They bind to the actin cytoskeleton and prevent cell shape changes that would be important for metastatisation
- They block tumor cell dividing during S-phase of the cell cycle
- They buind microtubules and block mitosis
A
- They block topoisomerase and cause DNA damage in dividing cells
- They bind to the actin cytoskeleton and prevent cell shape changes that would be important for metastatisation
- They block tumor cell dividing during S-phase of the cell cycle
- They bind microtubules and block mitosis
28
Q
- Receptor tyrosine kinases
- Are activated by DNA-damaging drugs
- Are activated by growth and survival factors
- Are a target for nicotine to protect tobacco plants from insects
- Are activated by the small GTPase: Ras
A
- Are activated by DNA-damaging drugs
- Are activated by growth and survival factors
- Are a target for nicotine to protect tobacco plants from insects
- Are activated by the small GTPase: Ras
29
Q
- The acetylcholine gated ion channel at the neuromuscular junction
- Closes when acetylcholine is secreted from presynaptic cells
- Opens when acetylcholine binds at the extracellular surface and allows sodium ion efflex and potassium ion influx into the postsynaptic cell
- Opens, when acetylcholine binds and this leads to a change in membrane potential from -85 mV to -60 mV in the muscle cell membrane
A
- The acetylcholine gated ion channel at the neuromuscular junction
- Closes when acetylcholine is secreted from presynaptic cells
- Opens when acetylcholine binds at the extracellular surface and allows sodium ion efflex and potassium ion influx into the postsynaptic cell
- Opens, when acetylcholine binds and this leads to a change in membrane potential from -85 mV to -60 mV in the muscle cell membrane
30
Q
- The endogenous ligands for opiate receptors in animal are
- Trimeric G-proteins
- Small peptides
- Arachidonic acid derivatives
A
- Trimeric G-proteins
- Small peptides
- Arachidonic acid derivatives
31
Q
- The nicotinic acetylcholine receptor is
- A 7-transmembrane domain receptor
- A voltage gated ion channel
- A ligand gated ion channel
- A calcium ion channel on the membrane of the endoplasmic reticulum
A
- A 7-transmembrane domain receptor
- A voltage gated ion channel
- A ligand gated ion channel
- A calcium ion channel on the membrane of the endoplasmic reticulum
32
Q
- Lipophilic steroid hormones
- Are soluble in the blood
- Bind to steroid receptors on the cell membrane of target cells
- Bind to steroid receptors in the cytoplasm
A
- Are soluble in the blood
- Bind to steroid receptors on the cell membrane of target cells
-
Bind to steroid receptors in the cytoplasm
- Can diffuse directly into cell and activate intracellular targets directly
33
Q
- Smads are
- Transcription factors
- Serine/threonine kinases
- Tyrosine kinases
- Membrane receptors for TGF-beta
A
- Transcription factors
- Serine/threonine kinases
- Tyrosine kinases
- Membrane receptors for TGF-beta
34
Q
- Caffeine is a receptor antagonist for
- Muscarinic acetylcholine receptor
- Cannabinoid receptors
- Serotonin receptors
- Adenosine receptors
A
- Caffeine is a receptor antagonist for
- Muscarinic acetylcholine receptor
- Cannabinoid receptors
- Serotonin receptors
- Adenosine receptors
35
Q
- Cannabinoids bind to single transmembrane domain receptors and:
- activate transcription in the nervous system
- Activate 7-transmembrane domain receptors on presynaptic cells and inhibit neurotransmitter release
- Bind ion channels on presynaptic cells and inhibit neurotransmitter release
A
- activate transcription in the nervous system
-
Activate 7-transmembrane domain receptors on presynaptic cells and inhibit neurotransmitter release
- CB1 localized at presynapses, manly coupled to G1 (GPCR), binding causes inhibition of adenylylcyclase
- Bind ion channels on presynaptic cells and inhibit neurotransmitter release
36
Q
- Muscarine and atropine
- Are both antagonists of the dopamine receptor
- Are both agonists for the G-protein couples acetylcholine receptor
- Counteract each other on the G-protein coupled acetylcholine receptor
- Are both agonists for glutamate receptors
A
- Are both antagonists of the dopamine receptor
- Are both agonists for the G-protein couples acetylcholine receptor
-
Counteract each other on the G-protein coupled acetylcholine receptor
- Muscarine stimulates it, atropine blocks (antagonizes) it
- Are both agonists for glutamate receptors
37
Q
A