08 Sympathetic Nervous System and Renin Angiotensin System Flashcards
Describe the processes of the biochemical synthesis of noradrenaline
Tyrosine -> DOPA (by tyrosine hydroxylase)
DOPA -> dopamine (by DOPA decarboxylase)
Dopamine -> noradrenaline (dopamine B-hydroxylase in vesicle)
Describe how is noradrenaline broken down after release
Neuronal breakdown: MAO-A (monoamine oxidase A)
Peripheral breakdown: COMT (catechol-O methyltransferase)
What are the subdivision of adrenoreceptors
a1: located on the post-synaptic neurone and elicit vasoconstriction
a2: located on pre-synaptic neurone and inhibit effect
B1: stimulatory to the heart and inhibitory to GIT and kidneys
B2: on bronchial, uterine
*a1 uses Gq, a2 uses Gi, beta uses Gs
List both natural and synthetic adrenoceptor agonists and their target receptors. Describe their effects
Noradrenaline (a1, a2, B1): potent vasoconstrictor and increase BP, but reduce HR
Adrenaline (a1, a2, B1, B2): increase HR and decrease DBP
Dopamine (weak on a1 and B1)
Isoprenaline (B1 and B2): increase HR significantly and no effect on MBP
Phenyleprhine (a1)
Describe the effect of binding to adrenoceptors on some vascular beds
Skin: a receptors - NA, AD cause vasoconstriction
Visceral: a receptors - same as skin
Renal: a receptor and B1 - same as skin
Coronary: a and B1 - NA, AD and isoprenaline cause vasodilation
Skeletal muscle: a and B2: NA causes vasoconstriction and AD and isoprenaline cause vasodilation
Name the drug that inhibit ACE and Ang II Type 1 receptor
Captopril
Losartan
List the stimuli that cause the release of renin
B1 receptor activation on juxtaglomerular cells
Reduced renal prefusion
Low NaCl sensed by macula densa
List potential pharmacological targets to manipulate renin release
ACE inhibitor (Captopril) Angiotensin Type 1 receptor inhibitor (Losartan) Renin receptor blockers Beta blocker Loop diuretics NSAID
Describe the effects of angiotensin in terms of peripheral resistance, renal function and cardiovascular structure
TPR:
1) direct vasoconstriction
2) increase release and reduce reuptake of NA
3) increase sympathetic activity
4) release catecholamine from adrenal gland
Renal function:
1) increase NaCl reabsorption
2) altered renal haemodynamics: renal artery vasoconstriction and enhanced effect of NA on kidneys
3) aldosterone release
CV structure
1) increase wall stress and increase preload and afterload
2) increase expressions of proto-oncogenes, growth factors and increase ECM proteins
What are the stimuli for the release of aldosterone
Angiotensin II
ACTH
Increase in K+ concentration - most important trigger
How do you distinguish between primary and secondary hyperaldosteronism
Primary: high BP and no oedema
Secondary: low/normal BP and high oedema
What is the body’s reflex to stress such as fluid loss
Activation of both sympathetic nervous system and renin-angiotensin system
1) increase CO and stroke volume
2) increase BP
3) increase salt and water retention
4) coagulation (with decreased fibrinolysis)
5) Platelet activation