Muscle Vasoconstrictor Neurons Research Articles

Responses of lumbar vasoconstrictor neurons supplying different vascular beds to graded baroreceptor stimuli in the cat

Lumbar sympathetic vasoconstrictor neurons supplying skeletal muscle, hairy skin and pelvic organs were tested for their responses to carotid baroreceptor stimulation in chlorase-anaesthetized cats. Using single- and few-fibre recordings, the responses of the different types of vasoconstrictor neuron to graded steps of non-pulsatile pressure from 110 to 260 mmHg in a vascularly isolated carotid sinus were analyzed quantitatively during the first 10 s of stimulation. The activity in all postganglionic muscle vasoconstrictor (MVC) neurons, preganglionic visceral vasoconstrictor (VVC) neurons and one third of the postganglionic cutaneous vasoconstrictor (CVC 1) neurons was strongly depressed by maximal by baroreceptor stimulation. Moreover, quantitative analysis revealed no significant differences of the baroreceptor sensitivity of MVC and CVC 1 neurons as compared with VVC neurons at all levels of carotid sinus pressure. In contrast, two-thirds of the postganglionic cutaneous vasoconstrictor (CVC 2) neurons exhibited a significantly weaker barosensitivity. The functional implications are discussed.

Viscero-sympathetic reflex responses to mechanical stimulation of pelvic viscera in the cat

Viscero-sympathetic reflex responses to mechanical stimulation of urinary bladder and colon were studied in cutaneous vasoconstrictor (CVC) neurones supplying hairy skin, in muscle vasoconstrictor (MVC) neurones supplying skeletal muscle and in sudomotor (SM) neurones supplying the sweat glands of the central paw pad of the cat hindlimb. The cats were anaesthetized, paralysed and artificially ventilated. The vasoconstrictor activity was recorded from the axons of the postganglionic fibres that were isolated in filaments from the respective peripheral hindlimb nerves. The activity in the sudomotor neurones was monitored by recording the fast skin potential changes occurring on the surface of the central paw pad. Afferents from the urinary bladder and from the colon were stimulated by isotonic distension and isovolumetric contraction of the organs. Most CVC neurones with ongoing activity were inhibited by these stimuli; only a few CVC neurones were excited. The MVC and SM neurones were generally excited by the visceral stimuli, yet the size of the evoked skin potential changes was variable. The reflex responses elicited in the sympathetic outflow to the cat hindlimb by stimulation of visceral afferents from the pelvic organs are uniform with respect to the different types of afferent input system but differentiated with respect to the efferent output systems. Graded stimulation of the visceral afferents from the urinary bladder by isotonic pressure steps elicited graded reflex responses in CVC (threshold < 30 mmHg) and MVC neurones (threshold < 20 mmHg) and a graded increase of the arterial blood pressure (threshold < 20 mmHg). These graded reflex responses are closely related to the quantitative activation of sacral afferent neurones with thin myelinated axons innervating the urinary bladder that are also responsible for eliciting the micturition reflex, but not to the quantitative activation of sacral afferent neurones with unmyelinated axons. The latter have thresholds of 40–50 mmHg intravesical pressure at which the size of the vesico-sympathetic reflexes in the vasoconstrictor neurones was about 50% of maximal size. This does not exclude the fact that activation of unmyelinated vesical afferents contributes to the vesico-sympathetic reflexes.

Respiratory modulation of the activity in sympathetic neurones supplying muscle, skin and pelvic organs in the cat.

1. The respiratory-related modulation of activity in neurones of the lumbar sympathetic outflow to skeletal muscle, skin and pelvic organs was investigated in anaesthetized, paralysed and artificially ventilated cats, using single- and multi-unit recordings. The activity of the neurones was analysed with respect to the phrenic nerve discharge under various experimental conditions. 2. Neurones tentatively classified as muscle vasoconstrictor and visceral vasoconstrictor neurones exhibited two activity peaks, one caused by baroreceptor unloading during the declining phase of the second order blood pressure waves and a respiratory drive-dependent peak in parallel with inspiration. The two peaks were separated by depressions of activity in early inspiration and post-inspiration. After cutting vagus and buffer nerves the activity peak during inspiration remained and was followed and sometimes preceded by a depression of activity. 3. The majority of the neurones tentatively classified as cutaneous vasoconstrictor neurones exhibited no respiratory modulation in their activity. Others exhibited an activity peak in expiration, an activity peak in inspiration, or a respiratory profile similar to that in muscle vasoconstrictor neurones. During increased respiratory drive (induced by hypercapnia) some neurones with unmodulated activity changed to an inspiratory or an expiratory pattern. Neurones discharging predominantly in inspiration projected preferentially to hairless skin. 4. Neurones which were tentatively classified as sudomotor neurones discharged predominantly in early expiration. 5. Some preganglionic neurones which were tentatively classified as motility-regulating neurones discharged during expiration. The majority of these neurones disclosed no respiratory modulation of their activity. 6. The study shows that different types of neurone of the lumbar sympathetic system exhibit distinct patterns of respiratory modulation in their activity. We conclude that the type and degree of central coupling between respiratory system and sympathetic nervous system may vary according to the destination of the sympathetic neurones.

Rapid phasic baroreceptor inhibition of the activity in sympathetic preganglionic neurones does not change throughout the respiratory cycle

We tested the hypothesis that the inhibitory influence of rapid phasic arterial baroreceptor stimulation on activity in sympathetic preganglionic neurones is weaker in inspiration than in expiration. Using neurophysiological techniques, 59 single preganglionic neurones with typical reflex pattern of muscle vasoconstrictor neurones that projected in the cervical sympathetic trunk were analysed. The inhibitory modulation of the ongoing activity in these neurones by the pulsatile activation of the arterial baroreceptors was determined by constructing post-R-wave histograms separately for both respiratory phases (as indicated by the discharge in the phrenic nerve). Quantitative measurements showed that the inhibition of the activity in the preganglionic neurones following phasic stimulation of arterial baroreceptors by the pulse pressure wave was not statistically different in both respiratory phases, even with increased respiratory drive.

Changes of reflexes in vasoconstrictor neurons supplying the cat hindlimb following chronic nerve lesions: a model for studying mechanisms of reflex sympathetic dystrophy?

The generic term ·reflex sympathetic dystrophy’ describes a clinical syndrome which sometimes develops after traumata at the extremities with lesions of nerves or — more rarely — after other events. The syndrome consists of the following components: pain (hyperpathia, allodynia), trophic changes of skin and deep tissues, dysregulation of sweating and cutaneous blood flow of the extremity concerned. It is assumed that all symptoms are produced by abnormal sympathetic activity. Interruption of the sympathetic activity to the affected extremity abolishes most of the pain and may lead to remission of the trophic changes. The hypothesis is that the trauma with lesion of the primary afferent axons leads subsequently to an abnormal state of the primary afferent neurons and to distorted processing of information in the spinal cord. As a consequence of this abnormal central state the activity in the sympathetic (vasomotor and sudomotor) supply to the affected extremity is distorted. The results are pain, trophic changes and dysregulations of autonomic effector organs. In some yet unknown way a vicious circle between periphery and spinal cord is established (afferent → spinal cord → sympathetic → afferent). This hypothesis was the starting point for analysis of the reflex pattern in postganglionic vasoconstrictor neurons supplying the cat hindlimb after chronic nerve lesions performed in the same limb (cutting and ligating a skin nerve; suturing the central stump of a skin nerve to the peripheral stump of a muscle nerve). The results obtained show that the reciprocity of the reflex pattern which is normally observed between cutaneous and muscle vasoconstrictor neurons is lost in many animals. Cutaneous vasoconstrictor neurons are very similar to muscle vasoconstrictor neurons in their reactions to stimulation of arterial baroreceptors and chemoreceptors. If the same sequence of events also occurs in patients with reflex sympathetic dystrophy, it could explain the dysregulation of blood flow through skin and also the occurrence of trophic changes in the limb.

Discharge patterns of sympathetic neurons supplying skeletal muscle and skin in man and cat

Skeletal muscle and skin of humans and cats are supplied by various sympathetic systems: vasoconstrictor neurons, sudomotor neurons, vasodilator neurons and pilomotor neurons. Only vasoconstrictor and sudomotor neurons have resting activity in both species. Discharge patterns of spontaneous activity in postganglionic neurons with resting activity as well as their reflex responses to various stimuli have been compared for both species: (1) muscle vasoconstrictor neurons react similarly in both species; they are under dominant control of arterial baroreceptors; (2) in both species cutaneous vasoconstrictor neurons are under no or weak control of arterial baroreceptors and they are influenced in similar ways by thermal stimuli. In contrast, other (somatic and visceral) stimuli elicit largely inhibition in these neurons in cats but excitation in humans. This may be due to the different experimental situations (anesthesia, etc.); (3) sudomotor neurons in humans are involved in thermoregulation, in cats they are not. The differences in the reflexes may also be due to the different experimental situations and to species differences; (4) the implications of studies on sympathetic neurons in humans and animals for the progress of research in this field have been discussed.

Reflex activation of postganglionic vasoconstrictor neurones supplying skeletal muscle by stimulation of arterial chemoreceptors via non-nicotinic synaptic mechanisms in sympathetic ganglia.

Postganglionic sympathetic neurones supplying skeletal muscle and skin can be activated from the preganglionic site via cholinergic nicotinic, muscarinic and noncholinergic synaptic mechanisms. The experiments described in this paper were designed in order to show that postganglionic vasoconstrictor neurones supplying skeletal muscle can be activated by the naturally occurring discharge pattern in preganglionic axons when the nicotinic transmission is blocked. For this purpose, the activity was recorded simultaneously from postganglionic vasoconstrictor axons supplying skeletal muscle and vasoconstrictor axons supplying hairy skin. The preganglionic neurones were driven reflexly by stimulation of the arterial chemoreceptors. 1) During blockade of nicotinic transmission muscle vasoconstrictor neurones were activated via the CNS during stimulation of arterial chemoreceptors. This activation is either generated by muscarinic action of released acetylcholine or by a noncholinergic synaptic mechanism. 2) Postganglionic cutaneous vasoconstrictor neurones were inhibited during stimulation of arterial chemoreceptors. During blockade of cholinergic nicotinic transmission these neurones were not activated reflexly by stimulation of arterial chemoreceptors although they received inputs via cholinergic muscarinic and noncholinergic synaptic mechanisms. 3) The results illustrate that postganglionic vasoconstrictor neurones supplying skeletal muscle can not only be activated via non-nicotinic synaptic mechanisms through synchronous repetitive electrical stimulation of preganglionic axons but also by the discharge pattern produced in preganglionic neurones during stimulation of arterial chemoreceptors.

Transmission of impulses from pre- to postganglionic vasoconstrictor and sudomotor neurons

Transmission of impulses from pre- to postganglionic neurons supplying skeletal muscle and skin of the cat's hindlimb and tail was investigated. The objective of the study was to determine whether these postganglionic neurons can be influenced from the preganglionic side by non-nicotinic synaptic mechanisms in the lumbar sympathetic chain ganglia. The activity of the postganglionic neurons was recorded from their axons being isolated from peripheral skin and muscle nerves. 1. (1) Vasoconstrictor neurons can be activated by muscarinic action of released acetylcholine and by a non-cholinergic synaptic mechanism. This type of non-nicotinic excitation of postganglionic vasoconstrictor neurons requires the activation of thin, probably unmyelinated preganglionic axons and considerable summation. Postganglionic sudomotor and pilomotor neurons cannot be activated in this way. 2. (2) Ongoing activity in postganglionic vasoconstrictor neurons, but not in sudomotor neurons, can be enhanced for up to 60 min by brief trains of stimuli applied to the preganglionic site. Also this enhancement requires the activation of thin preganglionic axons. 3. (3) Stimulation of thin preganglionic axons leads to an activation of muscle vasoconstrictor neurons via non-nicotinic synaptic mechanisms in the ganglia after complete block of nicotinic transmission. 4. (4) Postganglionic vasoconstrictor neurons and sudomotor neurons may be inhibited by a catecholaminergic autogenic mechanism in the ganglia. 5. (5) The results indicate that integration may take place in the sympathetic chain ganglia by other than divergent and convergent processes. In this integration muscarinic actions of released acetylcholine and non-cholinergic synaptic mechanisms may be involved.

Effects of central thermal stimuli on activity in cutaneous and muscle vasoconstrictor neurones supplying the cat hindlimb

Cutaneous (CVC) and muscle vasoconstrictor neurones (MVC) exhibit characteristic reflex patterns upon somatic and visceral stimuli. Central thermal stimuli should be specific for CVC neurones and not affect MVC neurones. In the following the reactions of these sympathetic neurones to warming and cooling of hypothalamus and spinal cord are described. The hypothalamus was warmed and cooled by a water-perfused thermode which was positioned stereotaxically into the rostral part of the third ventricle, the spinal cord by a water-perfused U-shaped tubing positioned epidurally. Vasoconstrictor activity was recorded from postganglionic axons which have been isolated in bundles from peripheral skin and muscle nerves of the cat hindlimb. The following results were obtained: I) Hypothalamic and spinal cord wanning lead to a decrease of activity in CVC neurones in a graded manner. When both brain structures are warmed the decrease of activity is larger than the algebraic sLm~nation of the individual effects. 2) Central cooling leads to an increase of activity in the CVC neurones. This increase was very often transient and comparatively smaller than the effects upon central warming. 3) The activity in MVC neurones was either not influenced by central thermal stimuli or increased due to small decreases of systematic blood pressure (baroreceptor unloading). 4) During hypothalamic warming respiratory rhythmicity in the activity of many CVC neurones was enhanced.

The organization of lumbar preganglionic neurons.

The organization of pre- and postganglionic neurons supplying blood vessels of the skin (vasoconstrictor neurons) and of the skeletal muscle (vasoconstrictor neurons), sweat glands (sudomotor neurons) and erector pilimuscles (pilomotor neurons) of the cat's hind limb and tail is discussed. Each sympathetic subsystem has its own, though as yet unknown, central organization which is reflected in the reaction patterns typically seen. The conduction velocities of the pre- and postganglionic axons of each subsystem have their unique distributions. Postganglionic vasoconstrictor neurons supplying skeletal muscle and skin are influenced via cholinergic muscarinic and non-cholinergic synaptic mechanisms from thin, probably unmyelinated, preganglionic axons; postganglionic sudomotor and pilomotor neurons most likely do not receive this synaptic input. A high proportion of preganglionic neurons projecting with their axons onto postganglionic neurons which supply skin and skeletal muscle are silent and do not exhibit reflex activity. Some of these neurons synapse with postganglionic pilomotor, vasodilatator and sudomotor neurons; part of them may also synapse with vasoconstrictor neurons. However, the high proportion of preganglionic neurons without reflex and resting activity which cannot be classified on the basis of functional properties presents a considerable problem in the analysis of the central organization of the sympathetic nervous system. It is concluded that the 4 types of pre- and postganglionic neurons mentioned constitute 4 largely separate channels which transmit information from the spinal cord to the respective target organs.

Effects of sytemic hypoxia and hypercapnia on cutaneous and muscle vasoconstrictor neurones to the cat's hindlimb.

1. Reactions of cutaneous and muscle vasoconstrictor neurones to the hindlimb on systemic hypoxia and systemic hypercapnia were investigated in chloralose anaesthetized cats. Mainly four types of preparations were used: brain intact and decrebrate (pontomedullary) animals with and without carotid sinus (CSN) and vagal nerves (VN). 2. In brain intact animals with intact CSN and VN most cutaneous vasoconstrictor neurones were depressed and most muscle vasoconstrictor neurones were excited during systemic hypoxia and hypercapnia. The responses to hypercapnia were smaller than those to hypoxia. 3. In brain intact deafferented animals and in decerebrate animals with and without intact CSN and VN systemic hypoxia and hypercapnia induced excitation in both cutaneous and muscle vasoconstrictor neurones. The responses to hypoxia were significantly smaller in deafferented preparations when compared to those in preparations with intact CSN and VN. Furthermore in muscle vasoconstrictor neurones the size of the responses was not significantly different in decerebrate preparations from that in brain intact preparations. 4. These results indicate a distinct neuronal organization of the chemoreceptor reflexes in the vasoconstrictor systems in the brain stem. Suprapontine brain structures are most important for producing the inhibition of the cutaneous vasoconstrictor neurones during hypoxia and hypercapnia.

Cardiac and respiratory rhythmicities in cutaneous and muscle vasoconstrictor neurones to the cat's hindlimb.

Cardiac and respiratory rhythmicities have been investigated quantitatively in postganglionic vasoconstrictor neurones supplying skeletal muscle and skin of the hindlimb in chloralose anesthetized, immobilized cats. Both rhythmicities are largest in muscle vasoconstrictor neurones, smaller in vasoconstrictor neurones supplying hariy skin, and smallest in vasoconstrictor neurones supplying hairless skin. The magnitude of the cardiac rhythmicity in the vasoconstrictor neurones is positively correlated with the quantitative reaction to systemic hypoxia.

Periodicities in efferent discharge of splanchnic nerve of the cat.

Periodicities in efferent discharge of splanchnic nerve of the cat.