dr. erzsébet tóth - semmelweis...
TRANSCRIPT
![Page 1: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/1.jpg)
Cholinergic and adrenergic neurotransmission
Dr. Erzsébet Tóth
7. October 2015.
Department of Medical Biochemistry Semmelweis University
![Page 2: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/2.jpg)
![Page 3: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/3.jpg)
![Page 4: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/4.jpg)
![Page 5: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/5.jpg)
Formation of acetylcholin in the nerve terminal in the cytoplasm
Choline acetyltransferase
Kolin-acetiltranszferáz
Cholinergic neuorotransmission
![Page 6: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/6.jpg)
ph
osp
hatidyl ch
olin
e
sp
hin
go
mye
lin
ph
osp
hatidyl e
tha
no
am
ine
ph
osp
hatidyl se
rin
e
sources of choline:
absorption from food
plasma membrane degradation
uptake from synaptic gap
![Page 7: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/7.jpg)
PC
Voltage-operated
High affinity choline - Na+ symporter
action
potential
![Page 8: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/8.jpg)
Acetylcholinesterase
in synaptic cleft
- two important sites:
- one binding site for quaterner N
- at the active site carbonyl C is
attacked
- active site of enzyme contains:
Ser, His, Glu
- covalent ester bond intermediate
between Ser of enz. and acetate
- reaction mechanism of ACE is
similar to serine proteases
H2O
![Page 9: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/9.jpg)
Acetylcholinesterase inhibitors
Gyógyszerek = ideggázok = nerve gases,
medicines rovarölők = insectisides
![Page 10: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/10.jpg)
dohány
nicotine
Nicotiana tabacum
![Page 11: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/11.jpg)
Ligand-operated
cation channel is the
pentamer nicotinic
receptor:
Na+ and Ca2+ channel
Each nicotinic receptor contains
5 subunits, it is pentamer.
α-subunit have10 isotypes
β-subunit have 5 isotypes
In neurons there are
5α homopentamer, or
2 α and 3 β heteropentamer
In skeletal muscle there is
(2α)βγδ heterotetramer
Ach always binds to α-subunit
The No of α-subunits equal the No
of bound Ach
One subunit has 4 transmembrane
segments, 4 α-helices.
![Page 12: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/12.jpg)
Acetylcholine is an ancient signal transducing molecule:
found in bacteria, algae, protozoons, plants, animals, humans it has a regulatory role in: proliferation, migration, secretion, survival, apoptosis
Nicotinic receptor exist in the human cell, but the cell doesn’t produce acetylcholine: skeletal muscle: α1α1β1γδ neuromuscular junction macrophages, microglia: α7 pentamer (proliferation ↓, IL-6,12, TNF-α secretion) astrocyte: α7 pentamer (brain function) blood vessel smooth muscle: α 2-5,7,10 pentamers (proliferation)
Acetylcholine is synthetized, secreted, has receptor, has ACE: lymfocytes: T-lymph. proliferation, differentiation, selection, B-lymph. growth, Ab secretion ↓ keratinocytes: proliferation, apoptosis, differentiation, adhesion, motility blood vessel endothel: α3,5,7,10 + β2,4 pentamer: angiogenesis, smooth muscle proliferation respiratory tract: many kind of cells, receptors and effect CNS = central nervous system: transmitter liberation, exitability, sleeping, neural integration, awakeness, tiredness, pain, eating, cognitive functions α homopentamers and 2α3β heteropentamers
![Page 13: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/13.jpg)
Effect of Ach in respiratory tract – not to study
![Page 14: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/14.jpg)
Skeletal muscle contraction
1.) action potential →
Na+ channels and VOOC open →
Ach vesicles’ exocytosis
2.) Ach binds to N-type Ach receptor
3.) Na+ enters through nicotinic rec.
→ postsynaptic potential →
voltage operated Na+ channel opens →
action potential on sarcolemma →
T-tubules L-vocc and
SER ryanodin receptor (RR)
functional interaction allows
Ca2+ release from SER →
Ca2+ binding to troponin C →
conformational change in
troponin I, T, tropomyosin →
F-actin binding site becomes free
to interact with myosin → contraction
![Page 15: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/15.jpg)
We do not ask it in biochemistry
![Page 16: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/16.jpg)
Kerti susulyka
(Inocybe fastigata)
Every Inocybe species
is either poisonous or
not eatable
Inocybe lanuginella Clitocybe dealbata
Légyölő galóca
(Amanita muscaria)
Muscarine and muscarine
containing mushrooms
![Page 17: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/17.jpg)
M3 receptor
Muscarinic receptors are heterotrimer G protein-coupled
7 transmembrane segment type receptors, 5 isotypes exist
![Page 18: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/18.jpg)
INHIBITORY EFFECT OF ACETYLCHOLIN IN HEART – 1-2.
+ inotropic, + chronotropic, + dromotropic effect
hyperpolarization,
slower heart beat =
bradycardia =
lassabb szívverés
- chronotropic: pacemaker frequency↓
in sinoatrial node
- dromotropic: conduction velocity in
AV-node ↓
- inotropic : force of contraction ↓
especially in atria
![Page 19: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/19.jpg)
• Contraction effect of acetylcholine in
gastrointestinal smooth muscle,
• secretion in digesting glands, • narrowing of pupil phincters (opening of
Schlemm channels and
decreasing of inner pressure in eye)
Acetylcholine activates secretion of
digesting juice in digesting glands during
signal transduction of vagus nerve (X brain
nerve), Ach bind to M3 (muscarinic 3)
receptors
![Page 20: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/20.jpg)
Acetylcholine causes smooth muscle contraction in certain
muscles
MLC = myosine light chain
![Page 21: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/21.jpg)
Smooth muscle contraction and relaxation
Ach
M3,5-rec
Gq
IP3
in SR
:adrenalin,
noradrenalin
GI=
gastrointestinal tract
longitudinal muscles,
pupilla sphincter
GI tract,
bronchi, genitourinal tract,
blood vessel smooth
muscle
AC
PKA
Figure 15-12a
Molecular Biology of the Cell
(© Garland Science 2008)
![Page 22: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/22.jpg)
.
M3/M5 muscarinic rec. = GPCR = G-protein-coupled receptor
![Page 23: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/23.jpg)
cGMP activates protein kinase G.
PKG phosphorylates and activates plasmamembrane Ca2+-ATPase and Na+/Ca2+ antiporter and SER
Ca2+ -ATP-ase, which removes Ca2+ from cytoplasm.
PKG phosphorylates Rho-dependent kinase inhibitory protein, it stops inhibition, myosin light chain
phosphatase can dephosphorylate MLC, so inactivates it, no contraction.
Ca2+ channel is inactivated, the ion does not enter.
PKG phosphorylates K+ channel, it opens, cell is hyperpolarized,
Smooth muscle is relaxed.
![Page 24: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/24.jpg)
and Erabutoxin
(from sea snake)
are blockers
in skeletal muscle,
κ-bungarotoxin inhibits
in neurons
Toxins of some
animals and bacteria
effecting on
cholinergic signal
transduction
Botulismus:
![Page 25: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/25.jpg)
recep
tor
localization signal
transduction
effect agonist antagonist
M1 Postsynaptic neuron:
striatum, cortex, hippocampus
Gq, PLC +
Ca2+
transmitter
release
atropin
M2 heart, bronchus
presyn. parasymp.neur.
hypothalamus, brain
Gi, AC –
Gi, K-channel.
- chronotr. bronchoconstr.
transm.liberation inhib,
hypothermia, anelgesia
atropin
M3 GI tract longitud. muscle,
bronchus
digestive glands, brain,
pupilla sphincter,
Gq, PLC +,
Ca2+
contraction
secretio, anelgesia
pupilla narrowing
neostigmin
physostigmin
pilocarpin
atropin
M4 striatum,hippocampus, cortex,
spinal cord pre- and postsyn.
Gi, AC –
Gi, K-channel.
DA liberation regulation
anelgesia…
atropin
M5 dopaminergic neurons, basal
ganglions, blood vessels
Gq, PLC +
Ca2+
DA liberation regul.
brain arthery relax.
atropin
Nm skeletal muscle Na+-channel contraction tubocurarin,
cobrotoxin,
α-bungarotoxin
Nn nervous system,
ganglion, adrenal gland
Na+/Ca2+ -
channel
action potential Κ-bungarotoxin
Nn macrophage
astrocyte,
smooth muscle.
Na+/Ca2+ -
channel
proliferation↓,
brain function
prolif.↑
Κ-bungarotoxin
Nn lymphocyte,
keratinocyte
endothel
respiratory tract
Na+/Ca2+ -
channel
prolif. diff. selection
prolif. diff. adhesion
angiogenesis
different effects
Κ-bungarotoxin
![Page 26: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/26.jpg)
Catecholamines,
adrenergic and noradrenergic signal transduction
= catechol
![Page 27: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/27.jpg)
Syntehsis of
catecholamines:
dopamine,
noradrenaline,
adrenaline
dopamine is a
neurotransmitter
in brain stem in
basal ganglions:
striatum,
substantia nigra
![Page 28: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/28.jpg)
most important
sympathetic
neurotransmitter
Mainly hormon in
adrenal medulla,
but neurotransmitter
in brain, too
![Page 29: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/29.jpg)
Noradrenerg idegvégződés
Noradrenergic nerve terminal
Na+
![Page 30: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/30.jpg)
stress
↓
hypothalamus
↓
CRH
↓
ACTH
↓
adrenal cortex
↓
side chain cleavage enz. act.
induction of tyrosine hydroxylase
↓
cortisol synth. and secr.
↓
blood in adrenal gland
↓
adrenal medulla
↓
induction of phenyletahnolamine
N-methyltransferase
↓
synthesis of adrenaline ↑
slowest process
sympathetic
activation
Ach
↓
adrenal medulla
↓
action potential
↓
IC [Ca2+] ↑
↓
adrenaline
liberation
fast, but
short duration
of effect
sympathetic fibers
↓
action potential
↓
IC [Ca2+] ↑
↓
Ca2+-camodulin
dependent
protein kinase
is activated
↓
tyrosine hydroxylase act. ↑
↓
synthesis of chatecholamines
(noradrenaline) ↑
release of NA
↓ effects
in organs
fastest
Regulation of
synthesis of stress
hormons and
sympathetic
neurotransmitters
effects in other organs
effects in other
organs
![Page 31: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/31.jpg)
MAO = monoamine oxidase
COMT = catechol
oxymethyltransferase
and either
aldehyde dehydrogenase
or aldehyde reductase
O2 + H2O
H2O2 + NH3
Degradation of
catecholamines
![Page 32: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/32.jpg)
All adrenerg receptors are heterotrimeric G protein-coupled
7 transmembrane segment receptors
BETA2-adrenerg receptor:
![Page 33: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/33.jpg)
β1,2,3 receptors activate,
α2 receptors inhibit
adenylyl cyclase
α1-receptor increases [Ca2+] intracellularly
![Page 34: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/34.jpg)
α1D
![Page 35: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/35.jpg)
Stimulatory effects of adrenalin/noradrenalin in cardiomyocytes, inhibitory effect of Ach
RyR = ryanodine receptor Ca2+ channel = Ca2+-csatorna
PLB = phospholambane = foszfolambán = Ca2+-ATP-áz reguláló fehérje/ regulating protein
AKAP = A kinase anchoring protein = PKA-horgonyzó fehérje
VOCC = voltage-operated Ca2+ channel = feszültségfüggő Ca2+-csatorna
VOCC
![Page 36: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/36.jpg)
Adrenalin activates gluconeogenesis and glycogenolysis,
it inhibits glycolysis and glycogen synthesis in liver
![Page 37: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/37.jpg)
Adrenalin activates gluconeogenesis and glycogenolysis,
it inhibits glycolysis and glycogen synthesis in liver
![Page 38: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/38.jpg)
Control of lypolysis in white adipocytes
ATGL
AC and PKA are inhibited,
PDE is activated
FFA-albumin
liver
![Page 39: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/39.jpg)
Alfa1-adrenerg receptor
α1-receptors are found in arteriols,
blood vessels contract
by the effect of adrenalin and noradrenalin
to increase blood pressure,
so α1-receptor antagonist drugs
can decrease the blood pressure.
![Page 40: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/40.jpg)
1.) In different organs different ARs are dominated, mainly only these are mentioned:
α 1: arteriols, GI and GU sphincters contract
liver glycogenolysis
kidney Na+ reabsorption, skin sweating
adipocyte lipolysis and glycogenolysis
α2: GI longitudinal muscles relax, sphincters contract,
pancreas insulin secretion↑, glucagon secretion↓
β1: all the heart function increase, (β1: β2 = 80:20, also β3 and α1)
adipocyte lipolysis, glycogenolysis
kidney renin secretion from juxtaglomerular cells,
ghrelin secretion from stomach
β2 : bronchi, GI and GU smoothe muscles relax
liver: glycogenolysis, glyconeogenesis,
adipocyte lipolysis,
kidney renin secretion
β3: white adipocyte lipolysis ↑, brown adipocyte thermogenesis
![Page 41: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/41.jpg)
2.) adrenerg receptor type in organs depends on species
e.g. human adipocytes β1 > β2 > β3 and also α1 and α2,
but rat β3 > β2 > β1 and also α1 and α2
3.) receptor types have different signal transduction and different effect
e.g. β 1,2,3 and α1 receptors activate, but α2 inhibit HSL
(hormonsensitive lipase) enzyme in adipocyte
4.) adrenerg receptor type depends on age, differentiation stage
e.g. in neonatal heart α1 receptors’ overproduction make growth,
heart hypertrophy
5.) altered metabolic state changes receptor types
e.g. in obesity α2/β1,2,3 ratio increases, consequently lipolysis decreases
e.g. in heart failure β1 receptor number ↓, while β2 and α1 receptors
non cAMP-dependent signal transduction↑
![Page 42: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/42.jpg)
K+ channel opens,
Ca2+ channel closes
everything contracts
and moves
Different signal transduction routes of adrenergic receptors
![Page 43: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/43.jpg)
• Speed of the synthesis e.g. testosteron, TNF-α → adipocyte β2-AR mRNA↑
• Desensitization happens due to repeated or continuous stimulus: a) AR-P (phosphorylated adrenergic receptor) → internalization → degradation translocation back e.g. β-AR → PKA → NA or A-bound AR-P → internalization α1-AR → PKC → NA or A- not bound AR-P → internalization b) AR mRNA and/or AR proteins are degraded
Quantity and sensitivity of adrenal receptors depends on:
Figure 15-51 Molecular Biology of the Cell
(© Garland Science 2008)
Localization and trafficking of
α2-adrenergic receptor subtypes
in cells and tissues (1999)
![Page 44: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/44.jpg)
It depends on the target cell protein content, which proteins are phosphorylated, by this way the activity or amount of proteins are changed
PKA (cyclic AMP-dependent protein-kinase) substrates that are phosphorylated: adipocyte: HSL activated (perilipin also) TAG → 3 FA + glycerol → FFA ↑ heart muscle: L-VOCC opens→ Ca2+↑ → + inotropic effect phospholamban SER-ben → Ca2+-pump act. → during relaxation Ca2+ enters to SER ↑ → faster reuptake of Ca2+ → faster heart beat = tachycardia PFK-2/FBP → F2,6P2 ↑ → PFK-1 act. → glycolysis ↑ smooth muscle: MLCK → Ca2+ sensitivity↓ → relaxation liver: GS inact. → glycogen synthesis ↓ PFK-2/FBP → F2,6P2 ↓ → PFK-1 not act. and F1,6P2-ase not inact. → gluconeogenesis ↑ and glycolysis ↓ CREBP → in nucleus it induces: PC, PEPCK, F1,6P2-ase, G6P → gluconeogenesis ↑ PK inact. → glucose sparing PDHC inact. → from pyruvate AcCoA ↓ → glucose sparing ACC α inact. → malonyl-CoA ↓→ FA synthesis ↓ skeletal muscle: GPK act. → GP act. → glycogen degradation ↑ CREB → PGC -1α induction → mt. DNS replication ↑ → mt. number↑ → longer aerobic metabolism during excercise
![Page 45: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/45.jpg)
The A-kinase anchoring proteins (AKAPs) are an important family of
scaffold molecules that are involved in the organization of multiprotein,
multivalent G-protein-signalling complexes. The example shown is that
of the AKAP gravin (also known as AKAP250), which associates
reversibly with the cell membrane in response to the activation of
protein kinase A (PKA) and the phosphorylation of gravin and the G-
protein-coupled receptor (GPCR; in this case, the 2-adrenergic
receptor) on its C-terminal cytoplasmic tail. The scaffold functions as a
'toolbox' of interacting molecules that affect the overall signalling of the
G-protein-based signalling complex. Molecules organized by gravin
include adenylyl cyclase (AC), the regulatory (R) and catalytic (C)
subunits of PKA, protein kinase C (PKC), Ca2+/calmodulin-dependent
protein kinase II (CaMKII), the GPCR, the receptor tyrosine kinase Src,
the phosphoprotein phosphatase PP2B, and the adaptor protein -
arrestin ( -arr). The G-protein subunits as well as the scaffold can bind
various cytoskeletal elements, such as microtubules and filamentous
actin networks. Other G-protein-interacting proteins include the
regulators of G-protein signalling (RGS), the activators of G-protein
signalling (AGS), and Partners of Inscuteable (Pins), which functions in
spindle formation. cAMP, cyclic AMP; P, phosphate.
![Page 46: Dr. Erzsébet Tóth - Semmelweis Egyetemsemmelweis.hu/biokemia/files/2015/10/EN_lec_g0202_MaE_CHOLIN_ADRENER… · - one binding site for quaterner N - at the active site carbonyl](https://reader033.vdocument.in/reader033/viewer/2022050717/5e16234975927f70f453f064/html5/thumbnails/46.jpg)
Figure 15-36 Molecular Biology of the Cell (© Garland Science 2008)
Effect on gene
expression