Neurochemistry Flashcards
Which of the following neurotransmitters can be called catecholamines?
Select one:
1. Serotonin only
2. Dopamine only
3. Noradrenalin only
4. Dopamine and serotonin
5. Dopamine and noradrenalin
Dopamine and noradrenaline
All the three are monoamines, but dopamine and noradrenaline are catecholamines while serotonin is an indolamine.
Which of the following type of glutamate receptors is crucial for the normal function of inhibitory interneurons?
Select one:
1. AMPA
2. GABA-B
3. NMDA
4. Sigma
5. Kainate
NMDA
Inhibitory interneurons comprise only about 20% of cortical neurons but have influential roles in cortical
maturation, function, and plasticity. NMDA receptors are predominantly located on these GABA interneurons.
The neural mechanism of memory formation may include changes in physical properties of neurons and
synapses. One such change called LTP or Long Term Potentiation is mediated by
Select one:
1. Cannabinoid receptor CB1
2. NMDA receptor
3. GABA receptor
4. Adenosine A1
5. Serotonin 5HT2A
NMDA receptor
NMDA has a role in memory acquisition, developmental plasticity, epilepsy, and ischemic brain injury. NMDA receptor mediates long-term potentiation
Which of the following best fits glucocorticoid receptor?
Select one:
1. Ionotropic
2. Ligand dependent regulators of nuclear transcription
3. Receptors with intrinsic enzyme activity
4. Metabotropic
5. G protein coupled
Ligand dependent regulators of nuclear transcription
Glucocorticoids act via their binding to the intracellular GR (Glucocorticoid Receptor) which translocates to
the nucleus to modulate gene expression. The GR belongs to a nuclear receptor superfamily of
transcription factors.
Which of the following receptors increase adenylate cyclase to stimulate cell machinery?
Select one:
1. Dopamine D2
2. Dopamine D3
3. Alpha 1
4. Dopamine D4
5. Beta adrenergic
Beta adrenergic
Alpha1 receptors phospholipase C coupled; Alpha 2 are Gi-coupled(inhibitory). Beta receptors Gs coupled -
so they increase adenylate cyclase.
D1 and D2 receptors are mainly located in which of the following structures?
Select one:
1. Nucleus accumbens
2. Amygdala
3. Caudate-putamen
4. Prefrontal cortex
5. Hippocampus
Caudate and putamen
There are two families of DA receptors. D1 and D5 receptors (D1-like), which are positively coupled to
Cyclic AMP, increase cyclic AMP. D2, D3, D4 (D2-like) that inhibit and decreases cyclic AMP. D1 and D2 are
predominant in the caudate and putamen, D3-nucleus accumbens, D4– the prefrontal cortex, D5-
Hippocampus. Both D1 and D 2 have wide distribution (striatal, mesolimbic and hypothalamic) while D3 and
D4 are more localised (mesolimbic, cortical and hippocampal).
Which neurotransmitter plays an important role in the neurochemical changes seen in Huntington’s
disease?
Select one:
1. Dopamine
2. Endorphins
3. Serotonin
4. GABA
5. Noradrenaline
GABA
Reduced GABA, Reduced glutamic acid decarboxylase, reduced acetyl choline, reduced substance P,
Raised somatostatin and reduced corticotrophin releasing factor are seen in Huntington’s disease.
Which of the following substances serve as a precursor for GABA?
Select one:
1. Adrenaline
2. Dopamine
3. Glucagon
4. Butyrylcholinesterase
5. Glutamate
Glutamate
GABA is one of the most ubiquitous inhibitory neurotransmitters in the CNS, and an estimated 40% of all brain synapses use it. Within the cerebellum, Purkinje cells produce GABA. GABA projections are found arising in the striatum, terminating in the substantia nigra and Globus pallidus. Loss of these GABA neurones in the caudate and putamen occurs in Huntington’s chorea. Underactivity of the GABAergic
system would theoretically result in epilepsy and reduction in GABA-BDZ receptors have been
demonstrated in seizure foci.
The drug ‘khat’ (Catha edulis) has effects comparable to
Select one:
1. Cannabis
2. Benzodiazepines
3. Alcohol
4. Amphetamine
5. LSD
Amphetamine
Cathinone is an alkaloid present in the leaves of the khat bush that grows in East Africa and southern
Arabia and is often chewed because of its stimulating properties. Cathinone, which is S(-)-alphaaminopropiophenone, has a pharmacological profile closely resembling that of amphetamine; indeed, in a wide variety of in vitro and in vivo experiments it was demonstrated that cathinone shares the action of amphetamine on CNS as well as its sympathomimetic effects; thus, for example, drug-conditioned animals will not distinguish between cathinone and amphetamine. It operates through the same mechanism as amphetamine; i.e. it acts by releasing catecholamines from presynaptic storage sites. Thus, much experimental evidence indicates that cathinone is the main psychoactive constituent of the khat leaf and that, in fact, this alkaloid is a natural amphetamine (Excerpt from Cathinone, a natural amphetamine.
Where do phospholipids get produced in a cell?
Select one:
- Ribosomes
- Lysosomes
- Smooth endoplasmic reticulum
- Nucleus
- Rough Endoplasmic reticulum
Smooth endoplasmic reticulum
Throughout the human body, especially in those cells that produce hormones and other secretory products,
a vast network of membrane-bound vesicles and tubules called the endoplasmic reticulum, or ER is
present. Smooth ER plays different functions depending on the specific cell type including lipid
(incl.phospholipid) and steroid hormone synthesis, breakdown of lipid-soluble toxins in liver cells, and
control of calcium release in muscle cell contraction.
Glycine and d-serine both act as co-agonists at
Select one:
1. Dopamine receptors
2. NMDA receptors
3, GABA receptors
4. Adrenaline receptors
5. Acetylcholine receptors
NMDA receptors
Glycine and D-serine both act as co-agonists at NMDA receptors. The excitatory glycine site on the NMDA
receptor is called non-strychnine-sensitive glycine receptor.
Which of the following neurotransmitters are not correctly matched with their precursors?
Select one:
1. Adrenaline-Noradrenaline
2. Dopamine-Tyrosine
3. Serotonin-Histidine
4. Noradrenaline-Dopamine
5. The Noradrenaline neurones originate in the brain stem, from a series of nuclei including the locus cereleus
Serotonin-Histidine
The biosynthesis of catecholamines starts from the conversion of tyrosine into L-dihydroxyphenylalanine (LDOPA) by tyrosine hydroxylase. L-DOPA is then decarboxylated by DOPA decarboxylase to form
dopamine. The conversion of dopamine to norepinephrine comes about by the action of the enzyme dopamine ß-hydroxylase. The rate-limiting enzyme in the biosynthesis of serotonin is tryptophan
hydroxylase. Here, tryptophan is converted to 5-hydroxytryptophan by tryptophan hydroxylase and by 5- hydroxytryptophan decarboxylase into serotonin. Histidine is the precursor of histamine not serotonin.
The neurochemical changes in the brain reported in Alzheimer’s disease include
Select one:
1. Increased DOPA decarboxylase
2. Increased levels of choline acetyl transferase
3. Increased levels of acetyl cholinesterase
4. Increased GABA levels
5. Decreased levels of acetyl cholinesterase
Decreased levels of acetyl cholinesterase
The neurochemical changes in the brain reported in Alzheimers disease would include decreased levels of
acetylcholinesterase (AChE), decreased levels of choline acetyltransferase, decreased GABA levels and
decreased levels of noradrenaline.
Acetylcholinesterase, the enzyme that inactivates acetylcholine and thus inhibits cholinergic neurotransmission, is consistently decreased in the brains of patients with Alzheimer’s dementia. Such a decrease is also seen in the CSF and plasma of these patients. But note that despite this overall decrease, levels of this enzyme appears to be high in the vicinity of β-amyloid plaques - thus contributes to amyloidogenesis. Thus AChE Inhibitors are useful to treat this illness.
Which of the following enzymes mediate several catalytic reactions involving amino acids that synthesize neurotransmitters such as dopamine, serotonin and tryptamine?
Select one:
1. Hydrolase
2. Reductase
3. Oxidase
4. Decarboxylase
5. Hydroxylase
Oxidase
Monoamine Oxidases are a family of enzymes that catalyze the oxidation of monoamines. They are present on the outer membrane of mitochondria.
Which of the following is an ionotropic receptor?
Select one:
1. 5HT2A receptor
2. Dopamine D2 receptor
3. GABA-B receptor
4. GABA-A receptor
5. Norepinephrine receptor
GABA-A receptor
GABA-A - opens chloride channel; inhibitory - leads to hyperpolarization; made of five subunits and at least
14 subunit subtypes
All others are G-coupled protein receptors