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Skeletal muscle circulation
 Enormous range of blood flow in skeletal
muscle: 2.7 ml/100g/min at rest (15.6% of CO)
 During exercise: 100 ml/100g/min (80-85% of
CO)
 Resistance vessels have high resting tone
(myogenic)
 Neural
 neural control dominates at rest
 tonic sympathetic nervous system vasoconstrictor activity (1
Hz) alpha 1 adrenergic receptor mediated
 an increase in sympathetic nervous system activity (4-5 Hz)
can decrease flow by 70%
 – vasodilatation at rest is passive due to withdrawal of
sympathetic nervous system activity
 sympathetic-cholinergic fibers are anatomically present -
physiological role is uncertain
 with increased activity there is an increase in
 the production of vasodilator metabolites
 n vasodilator metabolites are dominant during
 exercise although sympathetic nervous system
 activity to the working muscle is also enhanced
 Mediators of Vasodilation
 – increased interstitial [K+] stimulates
 Na+/K+ATPase hyperpolarizes membrane
 – interstitial acidosis/hypoxia hyperpolarizes
 membrane
 – interstitial hyperosmolarity
 – adenosine?
Physical factors
 Cyclical contraction and
relaxation of active skeletal
muscle vessels
 vessels are compressed
during the contraction phase
blood flow becomes
intermittent
 muscle perfusion is
enhanced by the muscle
pump
 during activity muscle pump
lowers the venous pressure
which increases the
pressure gradient driving
flow
 Autoregulation
 blood flow is relatively constant from 60 to 120
mmHg (mainly myogenic)
 Reactive Hyperemia
 brief occlusion of blood flow is followed by a
transient increase in flow
Role of Skeletal Muscle Circulation in
Blood Pressure Control
 large mass of tissue: 40 - 45% of body weight
 major site of resistance vessels
 Peripheral resistance regulated by controlling muscle
resistance
 resistance influenced by
 tonic vasoconstrictor activity
 metabolic vasodilators
 regulation by reflex mechanisms (baroreceptors,
cardiopulmonary receptors, etc.)
Splanchnic circulation
 Blood supply of
 Intestines
 Pancreas
 Spleen
 Liver
Mesenteric arteries ->
intestines -> portal vein ->
liver -> hepatic vein
Liver is supplied by hepatic
artery
 Blood flow 25% of resting CO - can increase by
30 -100% after a meal
 blood flow is closely coupled to absorption of
water, electrolytes and nutrients
 Series/parallel configuration: the venous
drainage from the capillary bed of the
gastrointestinal tract, spleen and pancreas
flows into the portal vein, which provides most
of the blood flow to the hepatic circulation
 Hepatic artery provides the remainder of the
blood flow into the liver
 High compliance venous system (25
ml/mmHg/kg) acts as a reservoir (especially
the liver)
 Contains 20% of the blood volume at rest
 Sympathetic nervous system
 innervation of arterioles, precapillary sphincters and
venous capacitance vessels
 little or no basal sympathetic nervous system tone
 sympathetic nervous system activity strong vaso-
and venoconstriction
 redistributes BF, and increases functional
circulating blood volume (“mobilization”)
Parasympathetic
 no innervation of blood vessels
 Increased activity, increased motility, increased
metabolism
 functional hyperemia due to local vasodilator
metabolites (NO?)
Hormones
 Gastrin, cholecystokinin functional hyperemia
 Angiotensin II, vasopressin vasoconstriction
 Autoregulation
 – poorly developed metabolic mechanism
dominates
 Autoregulatory escape
 increased sympathetic nervous system activity
causes a transient decrease in BF
 after 2 -4 minutes blood flow returns towards
normal due to accumulation of metabolites
(adenosine) and vasodilation of arterioles
 veins remain constricted
 Hypotension
 – vasoconstriction due to sympathetic nervous
system, angiotensin II and vasopressin -> increased
TPR
 – venoconstriction displaces blood centrally
increased central venous pressure
Reservoir function
 Spleen pumps blood & ability to plasma into
lymphatics
 Sympathetic stimulation causes spleen to contract
strongly and discharges blood into circulation
 Liver is a large expandable organ
 Act as a reservoir when there is excess of blood
 Releases extra blood into the circulation
Renal circulation
 At rest 420.0 ml100g/min (1260 ml/min) 23.3 % CO
 Pressure drop across the glomerulus is only 1-3 mmHg
 Further drop at the efferent arteriole
 Regulation
 Norepinephrine, Angiotensin II – vasoconstriction
 Dopamine – vasodilatation
 – Sympathetic activity (alpha receptor) – vasoconstriction
 – Stimulation of renal nerves - increases renin secretion
 Autoregulation is present
 – Myogenic effect, NO may be involved
 Renal cortex high blood flow poor O2 extraction but in medulla
low blood flow but high O2 extraction
Points to remember
 Blood flow ml/min or ml/10g/min
 % cardiac output
 Autoregulation
 Metabolic hyperaemia
 Reactive hyperaemia
 Local factors eg. Nitric oxide
 Neural and hormonal factors
 Other factors
 Effects of ischemia

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Circulation through special regions 3

  • 1. Skeletal muscle circulation  Enormous range of blood flow in skeletal muscle: 2.7 ml/100g/min at rest (15.6% of CO)  During exercise: 100 ml/100g/min (80-85% of CO)  Resistance vessels have high resting tone (myogenic)
  • 2.  Neural  neural control dominates at rest  tonic sympathetic nervous system vasoconstrictor activity (1 Hz) alpha 1 adrenergic receptor mediated  an increase in sympathetic nervous system activity (4-5 Hz) can decrease flow by 70%  – vasodilatation at rest is passive due to withdrawal of sympathetic nervous system activity  sympathetic-cholinergic fibers are anatomically present - physiological role is uncertain
  • 3.  with increased activity there is an increase in  the production of vasodilator metabolites  n vasodilator metabolites are dominant during  exercise although sympathetic nervous system  activity to the working muscle is also enhanced
  • 4.  Mediators of Vasodilation  – increased interstitial [K+] stimulates  Na+/K+ATPase hyperpolarizes membrane  – interstitial acidosis/hypoxia hyperpolarizes  membrane  – interstitial hyperosmolarity  – adenosine?
  • 5. Physical factors  Cyclical contraction and relaxation of active skeletal muscle vessels  vessels are compressed during the contraction phase blood flow becomes intermittent  muscle perfusion is enhanced by the muscle pump  during activity muscle pump lowers the venous pressure which increases the pressure gradient driving flow
  • 6.  Autoregulation  blood flow is relatively constant from 60 to 120 mmHg (mainly myogenic)  Reactive Hyperemia  brief occlusion of blood flow is followed by a transient increase in flow
  • 7. Role of Skeletal Muscle Circulation in Blood Pressure Control  large mass of tissue: 40 - 45% of body weight  major site of resistance vessels  Peripheral resistance regulated by controlling muscle resistance  resistance influenced by  tonic vasoconstrictor activity  metabolic vasodilators  regulation by reflex mechanisms (baroreceptors, cardiopulmonary receptors, etc.)
  • 8. Splanchnic circulation  Blood supply of  Intestines  Pancreas  Spleen  Liver Mesenteric arteries -> intestines -> portal vein -> liver -> hepatic vein Liver is supplied by hepatic artery
  • 9.  Blood flow 25% of resting CO - can increase by 30 -100% after a meal  blood flow is closely coupled to absorption of water, electrolytes and nutrients  Series/parallel configuration: the venous drainage from the capillary bed of the gastrointestinal tract, spleen and pancreas flows into the portal vein, which provides most of the blood flow to the hepatic circulation
  • 10.  Hepatic artery provides the remainder of the blood flow into the liver  High compliance venous system (25 ml/mmHg/kg) acts as a reservoir (especially the liver)  Contains 20% of the blood volume at rest
  • 11.  Sympathetic nervous system  innervation of arterioles, precapillary sphincters and venous capacitance vessels  little or no basal sympathetic nervous system tone  sympathetic nervous system activity strong vaso- and venoconstriction  redistributes BF, and increases functional circulating blood volume (“mobilization”)
  • 12. Parasympathetic  no innervation of blood vessels  Increased activity, increased motility, increased metabolism  functional hyperemia due to local vasodilator metabolites (NO?)
  • 13. Hormones  Gastrin, cholecystokinin functional hyperemia  Angiotensin II, vasopressin vasoconstriction
  • 14.  Autoregulation  – poorly developed metabolic mechanism dominates  Autoregulatory escape  increased sympathetic nervous system activity causes a transient decrease in BF  after 2 -4 minutes blood flow returns towards normal due to accumulation of metabolites (adenosine) and vasodilation of arterioles  veins remain constricted
  • 15.  Hypotension  – vasoconstriction due to sympathetic nervous system, angiotensin II and vasopressin -> increased TPR  – venoconstriction displaces blood centrally increased central venous pressure
  • 16.
  • 17. Reservoir function  Spleen pumps blood & ability to plasma into lymphatics  Sympathetic stimulation causes spleen to contract strongly and discharges blood into circulation  Liver is a large expandable organ  Act as a reservoir when there is excess of blood  Releases extra blood into the circulation
  • 18. Renal circulation  At rest 420.0 ml100g/min (1260 ml/min) 23.3 % CO  Pressure drop across the glomerulus is only 1-3 mmHg  Further drop at the efferent arteriole  Regulation  Norepinephrine, Angiotensin II – vasoconstriction  Dopamine – vasodilatation  – Sympathetic activity (alpha receptor) – vasoconstriction  – Stimulation of renal nerves - increases renin secretion  Autoregulation is present  – Myogenic effect, NO may be involved  Renal cortex high blood flow poor O2 extraction but in medulla low blood flow but high O2 extraction
  • 19. Points to remember  Blood flow ml/min or ml/10g/min  % cardiac output  Autoregulation  Metabolic hyperaemia  Reactive hyperaemia  Local factors eg. Nitric oxide  Neural and hormonal factors  Other factors  Effects of ischemia