This chapter is vaguely relevant toSectionG5(i) of the2017CICM Primary Syllabus, whichexpects the exam candidate to describe the role of the vasomotor centre and the autonomic nervous system in the regulation of cardiac output and venous return". The vasomotor centre is the starof this show, and any discussion of the autonomic nervous system inevitably leads to this central control organ. Fortunately, nobody has ever been asked for an in-depth exploration of this matter in any of the past papers, which means the time-poor exam candidate can easily ignore this section. Adetailed understanding of central vasomotor control is not requiredto write "nucleus tractus solitarius" and "rostral ventrolateral medulla" in exam answers, invokingthese names asmagical incantationsto ward against failure.
- Medullary centres which control sinoatrial node rate and thetone of peripheral smooth muscle are described as "vasomotor" centres
- These central processor and relay organs are involved in the majority of cardiac reflex arcs, i.e. cardiac reflex afferent inputs are received by these centres, and the efferent outputs originate from them.
Parasympathetic regulation of cardiovascular function
- Afferents include:
- carotid sinus and aortic arch baroreceptors
- "low pressure" baroreceptors in the atria
- Cerebral hemispheres, thalami and hypothalamus
- Efferents release acetylcholine at the pacemaker cells, which opens a ligand-gatedpotassium channel and hyperpolarises the pacemaker cells
- These effects aremore rapid than those of sympathetic regulation
Main parasympathetic structures include:See AlsoNeuroanatomy, Nucleus AmbiguusNeuroanatomy, Area PostremaDangerous Causes of Nausea/Vomiting Beyond the GI System - CohaiTungChi Tech
- Nucleus of the solitary tract:integrates cardiovascular afferent input and regulate parasympathetic and sympathetic responses
- Complex arc: regulation of sympathetic tone via CVLM
- Short quick reflex arc: vagal baroreflex
- Nucleus ambiguus, cardiac ganglia, vagus nerve
- NA contains preganglionic vagal neurons
- Sends efferent fibres to the cardiac ganglia via the vagus nerve
- Cardiac ganglia are near the SA node, AV node, and in the atria
- Caudal ventrolateral medulla (CLVM)
- Stimulated by the solitary tract nucleus
- Sends inhibitory GABA-ergic projections to the rostral medulla
Sympathetic regulation of cardiovascular function
- Rostral ventrolateral medulla (RVLM)
- Glutamate-secreting presympathetic neurons which act as the tonic "pacemarker" of sympathetic cardiovascular control
- Tonic activity here dictates baseline vascular smooth muscle tone
- RVLM sends descending projections to sympathetic preganglionic neurosn in the intermediolateral spinal cord
- Efferent sympathetic pathways:
- Sympathetic fibres which innervate the cardiac pacemakers, myocardium and vascular smooth muscle
- α1receptors mediate peripheral vasoconstriction
- β1 receptors mediate the cardiac rate and contractility effects
Neural Mechanisms of Cardiovascular Integration by Chapleau et al (2004) is probably the definitive peer-reviewed source for this chapter, but considering that it is over 400 pages and the material has zero exam relevance, recommending it to the reader would be preposterous. The next best resource which rolls everything up into a neat peer-reviewed package is Gordan et al (2015), which also happens to be free to read on PubMed. The approach is enviably systematic, and where possible the ensuing summary draws on this structure, keeping the detailwhile trying to maintain respect for exam relevance.
"Vasomotor centre" is not a term we like to use anymore.
Because it is a rather archaic description for a collection of brainstem structures which cooperate and conspire to produce some sort of a net balance between sympathetic and parasympathetic autonomic activity. The term itself originates in the dark age of physiology, when well-heeled gentlemen of independent means dissected animals for fun and made reference to the "bulbar vasomotor centre" to explain the origins of haemodynamic embarrassment which they observed when they crudely probed those animal's brainstem structures. For example, Shore (1891)exposed the floor of the fourth ventricle in rabbits, and poured chloroform directly into the hole. The observed "vasomotor excitation" was attributed to stimulation of central vasomotor structures, though it was short-lived as "one or two drops so applied were sufficient to kill the animal".
The term "vaso-motor" had been used throughout the 19th century to refer to anything vaguely neurological involiving the control of the circulation, but the idea that there was some central regulatory organ was relatively novel.Claude Bernard (1863)demonstrated that high spinal cord lesions produced profound hypotension, which then ledOwsjannikow and Dittmar to look for some sort of medullary control centre in the early 1870s. Careful experiments were performed, where minuscule brainstem regions of various experimental mammals were selectively destroyed, until a tiny 3mm area was discovered which was essential for the maintenance of vascular smooth muscle tone. This was the rostral ventrolateral medulla (RVLM). That's not a very memorable name, and "vasomotor" remained in common use, popularised by textbooks such as Julius Althaus'Nervous Diseases:
"The chief vasomotor centre is situated in the medulla oblongata... Faradisation of this organ causes constriction of all arteries below the seat of irritation, while destruction of it priduces dilatation of the same, likewise below the seat of the lesion".
Animal cruelty notwithstanding, the main objection to the use of this term is that it is inaccurate and vague. Most of the time, when one happens upon an instance of itscolloquial use, the useris referring to either the central control of the sympathetic nervous system, or the central autonomic control of the circulation as a whole. In the event of (god forbid) an exam question or a cross-table viva, it would probably be better to describe the specific structures and to use their real anatomical names. On the other hand, as one can clearly see from what follows, there is a lot about this topic which could be described as "inaccurate and vague", and some might say there is merit in continuing to use a familiar term, as its definition is no less precise than anything else.
Nucleus of the solitary tract
This is a tiny ball of grey matter in the dorsomedial medulla, which receives multiple afferent fibres, most notably from the vagus and glossopharyngeal nerve.In case you ever need to read about it in detail (and in French), Jean (1991) has an excellent review in theArchives Internationales. In short, it is very well connected for its size. Its afferents include cardiovascular baroreceptor input andrespiratory input, as well as gustatory and orotactile information. Efferentprojections extend to wherever the afferents come from(i.e. what projects to the nucleus tends to receive projections fromthe nucleus) as well as the cerebral cortex, the spinal cord, the thalami and the hypothalamus.
For the purpose of this cardiocentric chapter, the mainfocus should probably be the role of the solitary nucleusin the integration of cardiovascular homeostatic control. To paraphraseAndresen (2004), there are two main roles: one, tomediate a short simple baroreflex loop for vagal rate control, and the other, to regulate the tonic activity of medullary sympathetic pathways. That probably sounds really simple, but in fact looking at diagrams of these pathways recallsRenaissance cartography, swarming with mermaids and kraken, blanks filled with placeholder values like" 3rd order interneuron goes here".
At this stage, usually a textbook would molestits readers' eyes with extensively labelled crosssections of a brainstem as if knowing the precise location of the solitary nucleus will somehow give them an edge in the management of clinical problems involving the baroreflex. This alarming delusioninfects much of the neurology and physiology literature. Not to be left behind in the race to be the most confusing and pointless resource on the subject, this authorwill do the same:
All this really does isimpress on the reader that these specks of grey matter have a physiological significance which is vastly out of proportion to their anatomical size, something they probably already knew. For exam purposes, one only needs to know that the NTS receives vagal and glossopharyngeal afferents and projects to numerous locations, most notably the nucleus ambiguus and the sympathetic control organs of the ventrolateral medulla.
Nucleus ambiguus, vagus nerve and cardiac ganglia
An even smaller grey matter focus, the nucleus ambiguus is the site of motor neuron cell bodies which (among other things) innervate the muscles of the pharynx and larynx. Its name apparently means "ambivalent" rather than "vague", as Jacob Augustus Lockhart Clarke, who described it in 1851,thought that it couldn't seem to decide whether to send its efferents along the vagus or the glossopharyngeal nerve(Haines & Olry, 2010).The role of the nucleus ambiguus in the regulation of the cardiovascular reflexes is reviewed thoroughly by Wanget al (2006). For the purpose of this discussion,is a body of preganglionic parasympathetic neurons which projects efferent fibres via the vagus nerve to the cardiac ganglion.
The vagus nerve is the vagus nerve, "quia non determinatur ad aliquam specialem partem, sed per omnia viscera vagatur". For the purpose of cardiac reflex control, the most important fibres are obviously those coursing to the myocardium, via thethoracic cardiac branch.Oblivious to his own earlier objections regarding the frivolousness ofarrayinganatomical illustrations forthe non-surgeon, the author takes this opportunity to reproduce a beautifulimage from Cunningham's Text-Book of Anatomy (1914),which is still the best and clearest representation of these structures:
These vagal fibresterminate in the cardiac ganglia, collections of acetylcholinergic neurons which surround the sinoatrial node. In fact they are pretty well distributed in the upper chambers of the heart, around the roots of the venae cava and pulmonary veins, near the AV node, in the interatrial septum,and in the atrialappendages (Baptista & Kirby, 1997). According to most textbooks, there does not seem to be much vagal innervation of the ventricle,though Coote (2013) spends several pages explaining that we might be wrong about this. Anyway: the postganglionic fibres terminate at the pacemaker cells, where the release of acetylcholine activates the IK-Ach channel, which is a ligand-gated potassium channel. An essentially immediate slowing of the heart rate is thereby produced (Tomson & Arora, 2016), as the flux of potassium out of the membrane hyperpolarises the pacemaker cell and delays the rate of its depolarisation:
So, that is therelatively straightforward efferent parasympathetic signalling pathway for the cardiac reflexes. Any of thosethat end up slowing the heart rate generally doso through the solitary nucleus / ambiguus / vagus axis. This includes the baroreflex, the Bainbridge reflex,the Barcroft-Edholm reflex, as well as the mechanisms underlying vasovagal syncope.
Caudal ventrolateral medulla
This structure could easily be grouped with the nucleus ambiguus as a part of the overallparasympathetic efferent process. This little pile of drowsy GABA-secreting interneurons acts as the brakes for the sympathetic nervous system, inhibiting the tonic activity of the sympathetic regulatory centre and therefore acting in synergy with the rest of the vagal efferents. The importance of its role is revealed by the catastrophe in its absence. When Cravo & Morrison (1993)damaged the CVLM regions of rats, their MAP went from 80 to 130mmHg and their splanchnic circulation vasoconstricted by 200%, mainly under the normal tonic output of the sympathetic centre. In short, this vasomotor nucleus maintains some sort of calm restraint in the sympathetic output of the medulla, and acts in coordination with the vagal centres to mediate vasodilation at the same time as the vagus mediates bradycardia, thus decreasing the blood pressure.
Rostral ventrolateral medulla and sympathetic efferents
This, for lack of a better word, isthevasomotor centre. It is thought that clonidine exerts its antihypertensive effect by binding to α2 receptors in this exact region (Ernsberger et al, 1990). Itcontains presympathetic (mainly glutamate-secreting) C1 neurons which project to the spinal cord and which maintain a constant tonic firing rate. In fact to say that this region "projects to the spinal cord" is unfairly vasocentric as it conceals from the reader the true extent of the connections here, and they really stretch in all directions, to multiple central nervous system targets. But yes, in the spinal cordthe targets of descending projections from the RVLM arepreganglionicneurons of the sympathetic nervous system, sitting in the thoracic intermediolateral column.
An extensive discussion, more than is required for any normal person, is offered byGuyenet & Stornetta (2004).Without tediouslyre-grinding all the minor details, it will suffice to say that the constant tonic activity of this brainstem region is responsible for most of the sympathetic contribution to peripheral vascular resistance (the rest being contributed by whatever circulating catecholamines are floating around). At the same time, sympathetic innervation of the heart also exerts a counter-regulatory effect (opposing vagal stimulus), increasing heart rate and contractility. Apart for the inhibitory effects of descending control (eg. the GABA neurons in the caudal ventrolateral medulla), this centre is also affected by numerous circulating mediators, for example, angiotensin.
It will suffice to say that, unlike the rapid effects of vagal acetylcholinergic transmission, sympathetic effects take slightly longer, because they are mediated by a secondary messenger (cAMP) which in turn activates cyclic nucleotide-gated ion channels. Because the synthesis and degradation of cAMP addextra steps into the process of signal transduction, the sympathetic effect is slower. The cardiac effects of the sympathetic nervous system are mainly mediated by β1-receptors, and the vascular effects are mediated byα1receptors.The vascular effectors are the smooth muscle fibres of the small arterioles: noradrenaline release here tends to produce a calcium-mediated contraction.In case anybody needs a detailed reference, Bruno et al (2012)have produced an excellent in-depth review of these vascular regulatoryfunctions. Anyway, thesympathetic nervous system is a large enough topic that the college had allocated whole swaths of their syllabus document to it, and to revisit this here would represent a descent into silliness.