D2. Cardiorespiratory exercise- full Flashcards
(46 cards)
Headings pneumonic
FCRNPCBLC
Headings (list)
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
Introduction subheadings (list)
Exercise
Arterial pressure
Central command
(Intro) Exercise
● 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.
(Intro) Arterial pressure
● 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.
(Intro) Central command
● 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
Feed-forward control- central command of respiration subheadings (list)
Krogh & Lindhart 1913
Central-command mechanism
(Feed-forward) Krogh & Lindhart 1913
● 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.
(Feed-forward) Central-command mechanism
● 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
Cardiovascular function subheadings (list)
Sympathetic activation
Donald 1968
Vinogradova 2002
D’Souza 2014 and HCN
(Cardiovascular) Sympathetic activation
● 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.
(Cardiovascular) Donald 1968
● 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.
(Cardiovascular) Vinogradova 2002
● 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
(Cardiovascular) D’Souza 2014 and HCN
● 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.
Redundancy in the response to central command subheadings (list)
Denervated dogs can still exercise
Boulton 2016
Amman 2011 and peripheral feedback
(Redundancy) Denervated dogs can still exercise
● 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.
(Redundancy) Boulton 2016
● 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.
(Redundancy) Amman 2011 and peripheral feedback
● 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.
Neural circuitry in central command subheadings (list)
Thornton 2002
Eldridge 1981- deep brain structures
Koba 2022 and DBS
Periaqueductal grey
(Neural) Thornton 2002
● 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.
(Neural) Eldridge 1981- deep brain structures
● 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.
(Neural) Koba 2022 and DBS
● 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.
(Neural) Periaqueductal grey
● 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.
Peripheral feedback in exercise subheadings (list)
Alam & Smirk 1937
Exercise-pressor reflex
McCloskey & Mitchell 1983
Afferent signals and cardiovascular adjustment