D2. Cardiorespiratory exercise- full Flashcards

(46 cards)

1
Q

Headings pneumonic

A

FCRNPCBLC

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2
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Headings (list)

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Introduction

Feed-forward control - central command of respiration

Cardiovascular function

Redundancy in the response to central command

Neural circuitry in central command

Peripheral feedback in exercise

Chemoreceptors

Baroreflex

Local vascular changes

Cardiovascular responses to training

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3
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Introduction subheadings (list)

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Exercise

Arterial pressure

Central command

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4
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(Intro) Exercise

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● Skeletal muscle oxygen demand can increase 40-fold during exercise, from 75ml/min to 3000ml/min.
● Exercise is a form of physical activity that involves voluntary contraction of skeletal muscles, leading to an increased metabolic rate which needs to be supported by cardiorespiratory changes.
● Exercise in which skeletal muscle contraction causes principally a change in length with little change in tension is termed dynamic or isotonic, and that in which the contraction causes principally a change in tension with little change in length is termed static or isometric.
● In light static exercise the heart rate and blood pressure increase much more than during dynamic exercise at the same oxygen uptake level.
● Heavy static exercise is characterized by a failure of the local blood flow to adjust to the oxygen demands of the exercising muscles.

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5
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(Intro) Arterial pressure

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● Cardiac output increases during exercise, whereas total peripheral resistance decreases due to vasodilation in skeletal and coronary vascular beds.
● Therefore, there is only a mild increase in mean arterial pressure during exercise.
● The changes which occur in arterial pH, PO2 and PCO2 values during exercise are usually small. ● Arterial PO2 often rises slightly because of hyperventilation although it may eventually fall at high work rates.

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6
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(Intro) Central command

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● The central nervous system is important in increasing both CV and respiratory response both prior to, and at the very beginning of exercise.
● Once exercise has begun, there is peripheral feedback from chemoreceptors and the exercise pressor reflex, that maintains the equilibrium established during exercise.
● The relative importance of central command and exercise pressor reflex components in determining responses to exercise is dependent upon the type of exercise (static or dynamic), the intensity of exercise, the time after onset of exercise (immediate, steady state, exhaustion, etc.) and the effectiveness of blood flow in meeting the metabolic needs of the contracting muscles.
● Figure 1

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7
Q

Feed-forward control- central command of respiration subheadings (list)

A

Krogh & Lindhart 1913

Central-command mechanism

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8
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(Feed-forward) Krogh & Lindhart 1913

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● Central command of cardiorespiratory homeostasis is largely responsible for the initial response to exercise.
● This can often occur prior to exercise due to anticipation, and is typically most prominent, before feedback mechanisms begin to function.
● Krogh & Lindhart in collaboration with Miss Florence Buchanan 1913 performed a seminal study defining the contribution of central command to the control of ventilation and cardiac output.
● The authors used six subjects, three of which were trained to sudden exertions. The authors observed immediate and rapid increases in ventilation and pulse rate on the start of bicycle ergometer exercise.
● Notably, in one of the subjects used (JL)m the subject was told to work at a rapid rate with a heavy load, but the load was not raised on the ergometer. During the first few seconds the ventilatory response was virtually the same as if there had been a heavy load.
● The authors attributed this to an absence of central command, and instead determined these findings as the result of cortical irradiation to the respiratory muscles and the heart. In other words the spreading of excitation of motor areas instead of the international targeting of neuronal signals.

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9
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(Feed-forward) Central-command mechanism

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● Feed-forward control of the respiratory system can be initiated in the hypothalamic locomotor regions, which then feeds on to brainstem respiratory control neurons.
● The sympathetic nervous system, via circulating catecholamines from the adrenal medulla, which act on beta 2 adrenoreceptors, causing bronchodilation, leading to increased ventilation.
● Figure 2

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10
Q

Cardiovascular function subheadings (list)

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Sympathetic activation

Donald 1968

Vinogradova 2002

D’Souza 2014 and HCN

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11
Q

(Cardiovascular) Sympathetic activation

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● The cardiovascular (CV) changes during exercise are largely mediated by the autonomic nervous system.
● Specifically, sympathetic activation, as is seen in the diagram above, is responsible for the increase in cardiac output.
● Catecholamines act on beta 1 adrenergic receptors in the heart having positive chronotropic and inotropic effects, on the pacemaker cells in the sinoatrial node and ventricular myocytes respectively.
● This increase in cardiac contractility is augmented by the increased venous return in exercise, in line with the Starling effect, caused by peripheral muscular contraction, leading to further increases in cardiac output.

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12
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(Cardiovascular) Donald 1968

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● This was demonstrated by Donald et al. in 1968 who showed the importance of the sympathetic nervous system in initiating the cardiovascular system’s responses to exercise.
● Using 9 greyhounds, 6 with normal hearts, and 3 denervated hearts, the dogs ran around the race course with their heart rate being recorded.
● Those with denervated hearts had a slower onset and magnitude of heart rate increase.
● In order to determine that the sympathetic nervous system was mediating these effects, experimenters added propranolol, a non-specific beta blocker.
● In dogs with denervated hearts the heart rate increase did not occur when propranolol was present, indicating that circulating adrenaline had been the causative agent in the heart rate increase.
● Future experiments could use a more cardio-selective inhibitor, and look at the heart rate in comparison with the ventilation rate, to determine the relative importance of the sympathetic nervous system in controlling C.V and respiratory systems.

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13
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(Cardiovascular) Vinogradova 2002

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● Method; Used confocal imaging and fluo-3AM to measure CaT in isolated rabbit SANCs
● Results; Demonstrated that 0.1micromol/L isoproterenol induces 3-fold increase in no of Ca release events during diastolic depolarisation [CRDDs] per cycle, a shift to higher CRDD amplitudes and increase in spatial width
● This resulted in acceleration of diastolic depolarisation rate and increased SANC firing rate
● However, application of ryanodine = able to abolish effect of beta-AR stimulation
● Conclusion: Suggests that beta-AR stimulation increases firing rate in rabbit SANCs via recruiting additional local RyR Ca release and synchronising its occurrence
● These Ca sparks can then activate NCX, producing an inward current that can contribute to decay of the pacemaker potential – this = Ca clock hypothesis [Maltsev and Lakatta, 2008]
● Limitation; Did not provide mechanistic insight as to how beta-AR stimulation achieves this – now know that this = through activation of the kinase PKA, which phosphorylates RyR2 tetrameric monomers, LTCCs and phospholamban, resulting in dissociation of RyR2 accessory proteins [e.g. FKBP12.6] thus increasing intracellular Ca release

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14
Q

(Cardiovascular) D’Souza 2014 and HCN

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● Exercise dysregulates the coupled clock
● D’Souza et al in 2014 evaluated this possibility by first demonstrating that exercise in rats by training with uphill running was sufficient to generate bradycardia
● The authors concluded this was attributable to electrophysiological remodelling of SAN cells as the bradycardia persisted in the presence of autonomic nervous blockade with propranolol and atropine in vivo.
● The authors then patch-clamped isolated rat cells from trained and untrained animals in the whole cell configuration.
● Administration of rapid hyperpolarising pulses showed that there was a reduction in whole-cell If conductance in trained mice.
● Therefore, the authors examined expression of the HCN4 mRNA in sinus node cells using qPCR.
● It was observed there was a reduction in HCN4 expression in trained rats compared with sedentary, and the authors showed that this correlated with reduced levels of Tbx3 and increased expression of miR1, which have all previously been shown to affect HCN4 expression in other studies.
● These findings show that the membrane clock dominates in causing bradycardia after training.
● Although it is important to note that the authors did not examine calcium release in trained SAN cells, which may have also been important in the response to training.

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15
Q

Redundancy in the response to central command subheadings (list)

A

Denervated dogs can still exercise

Boulton 2016

Amman 2011 and peripheral feedback

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16
Q

(Redundancy) Denervated dogs can still exercise

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● However, denervated heart dogs were still able to exercise effectively. This is similar to cardiac transplant patients who are still able to exercise.
● However, the heart rate of these patients during exercise remains relatively constant, but the stroke volume increases.
● This suggests there may be some redundancy in the response to central command.
● There is debate as to whether peripheral feedback or central command is more important in cardiovascular control during exercise.

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17
Q

(Redundancy) Boulton 2016

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● Boulton et al in 2016 attempted to investigate this by measuring muscle sympathetic nerve activity with microneurography in the left peroneal nerve.
● The authors compared MSNA activity after electrically stimulated contractions or isometric dorsiflexion, using the presumption that electrically stimulated contractions would not activate central command.
● The authors thus showed that MSNA was significantly elevated with pre-contraction levels, whereas electrically-evoked contractions did not.
● The authors therefore concluded that central command was most important in MSNA activity which controls muscle perfusion.
● However, this assumes that there was not elevated SNS activity in the electrically-evoked contraction group due to stress imposed by the experimental conditions.

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18
Q

(Redundancy) Amman 2011 and peripheral feedback

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● Central command is also subject to regulation from peripheral feedback. ● Therefore, the prolonged effects of the central command during exercise undergo some form of regulation.
● Amman et al in 2011 examined this modulatory affect by using intrathecal fentanyl to block Group III/IV afferent muscle fibres.
● The authors were able to estimate central motor drive using an electromyogram. The authors then observed that fentanyl increased central motor command, but depressed cardiovascular functioning as determined by arterial pressure and heartrate measurement.
● However, the time to exhaustion in the constant-load cycling experiment was decreased by fentanyl. ● Thus, central command functioning without adequate feedback from peripheral muscles seems to operate unsatisfactorily. ● A limitation of these studies is that central motor drive was estimated from integrated electromyogram, for which the signal depends not only on the central motor drive but also on the depression or facilitation of corticospinal synapses on motoneurons and muscle membrane excitability.

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19
Q

Neural circuitry in central command subheadings (list)

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Thornton 2002

Eldridge 1981- deep brain structures

Koba 2022 and DBS

Periaqueductal grey

20
Q

(Neural) Thornton 2002

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● Given the importance of central command in the cardiovascular and respiratory response to exercise there is an understandable interest in deciphering the brain regions involved.
● In an attempt to uncouple ‘central command’ from movement feedback, Thornton et al. in 2002 used hypnotic suggestion of exercise during concurrent positron emission tomography scanning.
● Three cognitive conditions were used, involving the imagination of: (i) free-wheeling downhill on a bicycle; (ii) cycling up a hill; and (iii) volitional hyperventilation with the CO2 clamped to match the breathing observed in (ii).
significant activation was seen in the supplementary motor area (SMA) and premotor area (PMA).
● In addition, the thalamus, bilateral cerebellum and right dorsal lateral prefrontal cortex (DLPFC Brodmann area 9) were also activated.
● However, when breathing was driven voluntarily, only the SMA and sensorimotor cortex were activated.
● These findings thus suggest the dorsolateral prefrontal cortex is important in central command.
● However, there are concerns as to whether hypnosis actively replicates exercise or whether these areas that show up on PET scans are significant. However, further investigation is limited by the ability to perform exercise within PET scanners.

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(Neural) Eldridge 1981- deep brain structures

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● There is also interest in the deep brain structures that mediate the cardiovascular responses to exercise.
● Eldridge et al. in 1981 advanced the findings from studies in humans, via experiments in cats.
● Preparations included anesthetized cats with intact brains, unanesthetized with decortication at the level of the hypothalamus, and unanesthetized with decerebration at level of the mesencephalon.
● Spontaneous actual locomotion and attempts to move (fictive locomotion; motor electrical activity in peripheral nerves after pharmacological-induced paralysis) occurred in all preparations, except the mesencephalic cats.
● In addition, electrical stimulation or injection of a GABA antagonist (picrotoxin) into a subthalamic region of the hypothalamus caused locomotion.
● In all cases when locomotion occurred, respiration and arterial pressure increased in proportion to the level of locomotor activity despite control or absence of respiratory and muscle feedback mechanisms and lack of change of metabolic rate.

22
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(Neural) Koba 2022 and DBS

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● Later work in Parkinsonian patients receiving Deep brain stimulation has shown that high frequency stimulation of the STN thus blocking inhibitory neurons increased heart rate and systolic blood pressure.
● Koba et al. (2022) used optogenetics in rats to study a monosynaptic pathway from the mesencephalic locomotor region (MLR) to the rostral ventrolateral medulla (RVLM).
● Voluntary running increased Fos expression in this circuit, indicating neural activation.
● Exciting the pathway optogenetically raised heart rate and blood pressure, mimicking exercise responses.
● Conversely, inhibiting the same pathway during spontaneous exercise reduced arterial pressure, suggesting that the MLR-RVLM circuit centrally regulates cardiovascular responses to exercise.

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(Neural) Periaqueductal grey

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● The periaqueductal grey is a midbrain region that has a well-established role in the modulation of pain and sympathetic nervous system outflow. ● The neural architectural of the PAG is very heterogeneous where it is divided into four distinct longitudinal columns.
● The PAG, in particular the lPAG and aspects of the dlPAG, appears to be a key communicating circuit for ‘central command’.
● Moreover, the PAG also fulfils many requirements of a command centre.
● It has functional connectivity to higher centres (DLPFC) and the basal ganglia (in particular, the STN), and receives a sensory input from contracting muscle, but, importantly, it sends efferent information to brainstem nuclei involved in cardiorespiratory control.

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Peripheral feedback in exercise subheadings (list)

A

Alam & Smirk 1937

Exercise-pressor reflex

McCloskey & Mitchell 1983

Afferent signals and cardiovascular adjustment

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(Peripheral feedback) Alam & Smirk 1937
● Alam & Smirk in 1937 first provided evidence for a peripheral feedback system now termed the exercise pressor reflex. ● The authors measured blood pressure in the arm of subjects who had sphygmomanometer cuffs around their thighs to occlude blood flow. ● The authors then asked the subjects to exercise, observing an increase in both systolic and diastolic blood pressure. ● After exercise cessation the blood pressure increase was maintained until such time as the circulation was restored by deflation of the sphygmomanometer cuffs. ● These findings were then validated in the arm as well, thus confirming the presence of a metabolic factor in the blood that stimulated peripheral nerve fibres.
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(Peripheral feedback) Exercise-pressor reflex
● The EPR represents a negative feedback mechanism located in the skeletal muscle, which is sensitive to mechanical and metabolic stimuli during muscle work. ● Nerve fibers which are activated by metabolites accumulation (i.e., the “metaboreceptors”), they are thought to be sensitive to several substances such as lactic acid, potassium, bradykinin, arachidonic acid products, ATP, diprotonated phosphate, and adenosine.
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(Peripheral feedback) McCloskey & Mitchell 1983
● McCloskey & Mitchell in 1983 were able to advance our understanding of the reflex cardiovascular responses from muscle. ● The authors used anaesthetised and decerebrate cats, stimulating isometric exercise by electrical excitation of the ventral root nerve fibres. ● The authors performed similar occlusion experiments to Alam & Smirk, and showed this response was mimicked by injection of isotonic injection of KCl or dorsal root sectioning. ● To investigate the nerve fibres involved the authors used direct local anaesthetic block of the dorsal roots to determine the nerve fibres involved. ● It was shown that anaesthetics abolished the cardiovascular responses observed. Given LAs preferentially block small, unmyelinated fibres the authors concluded the reflex response was mediated by Groups III and IV fibres. ● However, it would have been more accurate if the authors could have performed electrophysiology on individual nerve fibres.
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(Peripheral feedback) Afferent signals and cardiovascular adjustment
● Afferent signals from group III/IV fibers are known to project to several brain stem nuclei including the NTS (thought to be the primary centre for EPR signal processing), which in turn promotes a reflex decrease in parasympathetic activity to the heart and an increase in sympathetic outflow to the heart and blood vessels. ● It is now also thought that the PAG may act as an important coordinator of muscle afferent impulses. ● The typical hemodynamic response to metaboreflex activation is an increase in arterial blood pressure. ● This cardiovascular adjustment is thought to be primarily achieved by increasing SVR because of peripheral sympathetic vasoconstriction. ● It has also been proposed that muscle metaboreflex is capable of increasing cardiac filling pressure through splanchnic vasoconstriction and venoconstriction which expel blood volume into the central circulation. ● The exercise pressor reflex is thought to be particularly important in mediating increases in sympathetic activity in static exercise, as opposed to dynamic exercise.
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Chemoreceptors subheadings (list)
Central vs peripheral Wasserman 1975 PaCO2
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(Chemoreceptors) Central vs peripheral
● Both central and peripheral chemoreceptors are important in increasing the respiratory drive during exercise. ● These two chemoreceptors are traditionally thought to be sensitive, either directly or indirectly to plasma carbon dioxide content. ● Recent experimental approaches have changed the understating of the carotid chemoreflex contribution to the autonomic responses during exercise in normoxia and normocapnia. ● Recent data suggest that carotid chemoreceptors are sensitized during exercise and so mediate about one-third of the increase in sympathetic activity during exercise in healthy humans.
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(Chemoreceptors) Wasserman 1975
● The significance of the chemoreceptor response during exercise was highlighted by Wasserman et al in 1975. ● Subjects in this experiment had previously been treated for asthma using carotid body denervation thus eliminating part of the peripheral chemoreceptor response. ● The denervated patients had reduced hyperpnoea in exercise above the anaerobic threshold (where lactic acid in the blood begins to rise rapidly), indicating that the chemoreceptor reflex is key in increasing ventilation during intense exercise. ● However, the researchers used a control group of patients without underlying asthma, so it is difficult to interpret whether or not the changes in ventilation increase are due to the asthma or the absence of chemoreceptor functioning. ● Furthermore, it would have been interesting if the authors had measured heart rate in response to exercise to observe whether the carotid bodies are also important in cardiovascular control.
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(Chemoreceptors) PaCO2
● There has been some debate as to what is the trigger for the activation of chemoreceptors, given that the mean PaCO2 remains roughly constant. ● However, there has been suggestions that given PaCO2 fluctuates, this may activate the chemoreceptors. ● Alternatively, other soluble factors such as H+, K+ and lactic acid have been proposed.
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Baroreflex subheadings (list)
Resetting through muscle afferents or central command Potts 2003 Controlling muscle vasodilation and cardiac chronotropism
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(Baroreflex) Resetting through muscle afferents or central command
● As mean and pulsatile pressure increase, baroreceptors should respond to increase parasympathetic and decrease sympathetic outflows, a pattern designed to counter the rise in arterial pressure. ● However, during exercise the baroceptor needs to be reset to permit rises in arterial pressure. ● This baroreflex resetting is thought to occur through either muscle afferents or central command.
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(Baroreflex) Potts 2003
● Potts et al in 2003 proposed one mechanism of this arterial baroreceptor resetting by using an arterially perfused decerebrate rat. ● The authors used electrically evoked forelimb contraction and measured the baroreceptor responsiveness. ● The authors measured this responsiveness by assessing the heart rate changes to transient increases in arterial perfusion pressure and rate. ● The authors were thus able to show that evoking forelimb contraction activated forelimb skeletal afferent muscle fibres, which in turn significantly reduced baroreflex responsiveness. ● The authors then provided some mechanistic detail by inhibiting this baroreflex reset with the GABA A antagonist, bicuculline, when injected with a micropipette into the caudal NTS. ● The authors therefore concluded that GROUP III/IV afferents synapse onto inhibitory GABA interneurons in the NTS which depress afferent signalling from baroreceptors. ● To confirm the role of these GABAergic neurons in the NTS, it would be interesting to repeat these experiments using optogenetic approaches.
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(Baroreflex) Controlling muscle vasodilation and cardiac chronotropism
● Resetting of the arterial baroreflex may occur from stimulation of skeletal muscle afferents and/or activation of central command. ● The baroreflexes during exercise therefore oppose any mismatch between vascular resistance and CO by controlling muscle vasodilatation and cardiac chronotropism in order to avoid any excessive variation in blood pressure.
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Local vascular changes subheadings (list)
Metabolic substances Groucher 1990 Zhao 2020
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(Local) Metabolic substances
● The metabolic control of skeletal muscle arterioles is important to match perfusion to skeletal muscle metabolism. ● During enhanced metabolic demand, and depending on the actual conditions, tissue cells release several substances that apparently act as vasodilatory mediators, including increased pCO2, lactate, K+, adenosine, H+, inorganic phosphate and reactive oxygen species. ● Adenosine is mainly generated from AMP that is released from the skeletal muscle fibres and dephosphorylated by ecto 5′nucleotidase bound to the sarcolemma. ● This adenosine is a potent vasodilator in both the coronary and skeletal muscle vasculature by acting on extraluminal A2A receptors on the vascular smooth muscle.
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(Local) Groucher 1990
● In a seminal study in 1990, Groucher et al used the adenosine receptor antagonist, 8-phenyltheophylline, which had lower phosphodiesterase interactions than its predecessors. ● The authors exposed the right gracilis muscle in anaesthetised cats and stimulated contraction with electrical impulses to the obturator nerve. ● The authors measured blood flow with an electromagnetic flow probe and measured the blood flow for 30 minutes following exercise. ● It was shown that gracilis muscle blood flow increased during exercise. However, this increase in blood flow was decreased over 40%, suggesting adenosine is a significant in metabolic regulation of vascular tone. ● However, the use of anaesthetised cats is a significant limitation as the sodium pentobarbitone used is associated with cardiovascular depression.
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(Local) Zhao 2020
● Another adenosine-based molecule, ATP, is also important in metabolic regulation of vascular tone. ● Zhao et al in 2020 showed the importance of ATP-sensitive potassium channels in cardiac myocytes. ● The authors used a mouse papillary muscle preparation where the small septal artery was cannulated and pressurised. ● The authors showed that pinacidil application to this preparation induced vasodilation in the artery through opening of KATP channels. ● In mice with smooth-muscle specific ablation of KATP channels did not reverse these effects, indicating that the KATP channels were on the cardiomyocytes themselves. ● The authors later demonstrated that the inwardly rectifying Kir2.1 channel conductance was augmented by elevated potassium, as released from KATP channels. ● The inwardly rectifying channels were present on coronary smooth muscle cells and induced hyperpolarisation, thus demonstrating the potential for the vasodilatory response to reduced ATP levels, matching energy demand to perfusion. ● To further dissect the role of KATP channels in coronary blood flow regulation, transgenic approaches must be used to specifically manipulate KATP channel activity.
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(Local) Catecholamines
● Furthermore, the sympathetic nervous system helps to redistribute blood flow during exercise. ● Circulating catecholamines promote vasoconstriction in mesenteric and gastric resistance arteries. ● However, adrenaline is capable of dilating coronary blood flow to promote blood flow. Metabo-regulation of skeletal blood vessels is particularly important as well.
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Cardiovascular responses to training subheadings (list)
White 1998 and vascularisation of cardiac muscle Diameter of resistance vessels Serneri 2001 and hypertrophy
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(CVS responses to training) White 1998 and vascularisation of cardiac muscle
● There have been many studies showing there is angiogenesis in skeletal muscle cells, increasing delivery of oxygen to these tissues, although there have been studies, notably by White et al in 1998. ● Researchers trained minipigs for 1, 3, 8 and 16 weeks, compared them with controls, and observed the capillary and arteriolar densities and diameters. ● Capillaries had increased in density at the end of week 3 in the coronary vasculature, and from then there was increased arteriolar formation by week 16. ● Increased blood flow to the cardiac muscle allows more efficient pumping of the heart, leading to greater cardiac output and further muscular contraction. ● However, the researchers didn’t work out the mechanisms behind this, and in the future, could use endothelial cells in culture, along with heart organoids to observe this process.
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(CVS responses to training) Diameter of resistance vessels
● Training can lead to long-term adaptations that facilitate increased exercise intensity. ● One such change is the increased diameter of resistance vessels within tissues that require oxygen during exercise. ● There may also be an increase in vasodilation potential during exercise in response to continued training in some individuals.
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(CVS responses to training) Serneri 2001 and hypertrophy
● Power and strength training, such as power lifting, results in pressure overload and concentric physiological hypertrophy endurance training, such as swimming or running, results in volume overload and eccentric physiological hypertrophy. ● Work by Serneri et al in 2001 led to the hypothesis that insulin-like growth factor 1 (IGF1) signalling was involved in physiological hypertrophy. ● Researchers compared the aortic-coronary sinus gradient for IGF-1 in soccer players and sedentary controls, using radioimmunoassay for IGF-1. ● There was no gradient observed in sedentary controls, but in trained athletes, there was a positive IGF-1 gradient, with more growth factor present in the coronary sinus. ● This was positively correlated with the levels of hypertrophy assessed using echocardiographic measurements. ● However, soccer players are more likely to be subject to volume overload than pressure overload, so further studies were required to see if IGF-1 was involved in both eccentric and concentric hypertrophy. ● There are a number of signalling pathways involved in physiological hypertrophy, most notably the insulin-like growth factor 1 (IGF1) pathway
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Conclusion
● Exercise necessitates cardiovascular and ventilatory adaptations to facilitate increased blood flow and supply sufficient oxygen to skeletal muscles. ● These changes are either mediated by feedforward central command which promotes sympathetic outflow, increasing heart rate and stroke volume. ● Furthermore, there is activation of the motor outflow to respiratory muscles. ● Alternatively, feedback control from the muscle pressor reflex or chemoreceptors which feedback to midbrain regions and also increase sympathetic outflow.