Properties of postganglionic sympathetic neurons with axons in the right thoracic vagus.

The resting and reflex-evoked activities of single postganglionic sympathetic neurons with axons in the right thoracic vagus were tested in chloralose-anaesthetized cats. The properties of a majority of neurons were found to be similar. Cardiac- and inspiration-related rhythmicities were present in the resting activity of sympathetic neurons. Their resting activity was not affected by hyperventilation which abolished phrenic nerve discharges. Systemic hypoxia (2 min; 8% O2 in N2) increased the activity of the neurons more effectively in the deafferented state than when both sinus nerves remained intact. Injection of 0.1 ml 1 M sodium bicarbonate saturated with CO2, which activates peripheral chemoreceptors in the right or left carotid sinus, usually evoked a decrease in sympathetic activity in animals with both sinus nerves intact. We concluded that activation of peripheral chemoreceptors may inhibit the activity of the sympathetic neurons with axons in the right thoracic vagus. We suggest that the described sympathetic neurons may be a functionally homogeneous population which may innervate the conducting system of the heart. The close localization of sympathetic and parasympathetic axons in the vagus nerve may facilitate sympathetic-parasympathetic interaction at the level of their endings in the heart.     

Glicentin-immunoreactive perikarya and varicosities in the guinea pig central nervous system

Glicentin-immunoreactive (GLI-IR) neurons and nerves were studied in the central nervous system of guinea pig. GLI-IR perikarya were found in the medulla oblongata located in the nucleus tractus solitarii, in the nucleus commissuralis, in the nucleus reticularis lateralis and the formatio reticularis. Immunoreactive varicosities, however, were seen in many other areas of the central nervous system such as in the hypothalamus, in the nucleus proprius striae terminalis, in the nuclei thalami mediani, in the substantia grisea centralis, in the nuclei raphe, in the formatio reticularis and in the vagus nucleus tractus solitarii-system. Some of the described GLI-IR varicosities may therefore be extensions of the neurons located in the medulla oblongata. Furthermore, the role of GLI as a putative neurotransmitter is discussed.     

Properties of solitary tract neurons receiving inputs from the sub-diaphragmatic vagus nerve

Vagal afferents ascending from the gastrointestinal tract synapse on neurons in the nucleus of the solitary tract. Although these neurons constitute a significant proportion of solitary tract cells their firing behaviour and synaptic properties are not documented. Since gastrointestinal tract afferent termination sites overlap with regions mediating cardiorespiratory reflexes the possibility of convergence with afferents mediating cardiovascular and respiratory reflexes was proposed. Here we describe some electrophysiological and morphological properties of solitary tract neurons orthodromically driven from the subdiaphragmatic vagus nerves and assess possible convergent inputs from cardiorespiratory afferents. Whole-cell recordings of solitary tract neurons responding to electrical stimulation of the sub-diaphragmatic vagus nerves (0.1-1 ms; 1-10 V; 2-20 Hz) were made in a working heart-brainstem preparation of rat. Baroreceptors were stimulated by raising pressure in the aorta or carotid sinus, whereas aortic injection of sodium cyanide (0.05% solution 25-50 microl) was used to activate peripheral chemoreceptors. Phrenic nerve activity and heart rate were monitored continuously. Of 88 solitary tract neurons tested, 39 responded with an evoked excitatory synaptic potential following stimulation of the sub-diaphragmatic vagus nerves. Resting membrane potential and input resistance of sub-diaphragmatic vagus nerve driven solitary tract neurons were 53.2 +/- 0.5 mV and 291 +/- 17 Mohms, respectively (mean +/- S.E.M.). Response latencies to sub-diaphragmatic vagus nerve stimulation were divided into two groups: <20 ms (16.0 +/- 2 ms, n = 7; mean +/- S.E.M.) and >20 ms (77.3 +/- 5 ms, n = 32). One additional neuron displayed an evoked inhibitory postsynaptic potential (latency 175 ms). Nineteen neurons showed ongoing activity which consisted of either irregular single action potential firing (0.5-10 Hz; n = 12) or burst discharge (n = 7). Of 33 neurons tested, 17 showed spike frequency adaptation during injection of positive current, whereas 19 of 38 cells displayed rebound excitation following release from hyperpolarized potentials. There was no correlation between these properties and synaptic latencies. Ninety-one per cent of neurons tested displayed synaptic depression following paired pulse stimulation of the sub-diaphragmatic vagus nerve over intervals up to 500 ms. Stimulation of either baroreceptors (n = 31) or chemoreceptors (n = 36) failed to elicit a synaptic response in all sub-diaphragmatic vagus nerve-driven solitary tract neurons. Neurobiotin-labelled solitary tract neurons (n = 10) were from both latency groups and were located medial to the solitary tract at the level of area postrema, -0.3 mm to +1 mm from the obex. One cell was located in commissural subnucleus at midline, seven cells dorsal to the tractus solitarius and three ventral and medial to it. Soma sizes were 23 +/- 9.6 x 14 +/- 4.9 microm (range: 50 x 16 microm to 15 x 7 microm). The number of primary dendrites varied from three to five, secondary from one to eight and tertiary zero to four. Labelled axons were found in seven cells which ramified extensively in the solitary tract nucleus (n = 3) and/or branched extensively in the dorsal vagal motonucleus (n = 3) and/or projected towards the ventrolateral medulla (n = 3). We conclude that solitary tract neurons receiving signals from the sub-diaphragmatic vagus nerves (most likely from gastrointestinal tract structures) appear to be a distinct pool of neurons. There was a heterogeneity in terms of both their ongoing activity and projection targets but despite this, there were three consistent properties. First, sub-diaphragmatic vagus nerve evoked predominantly excitatory synaptic responses in solitary tract neurons; second, neurons exhibited lasting paired pulse depression following activation of sub-diaphragmatic vagus nerves; and third, sub-diaphragmatic vagus nerve-driven solitary tract neurons were     

The subdiaphragmatic vagus nerves mediate activation of locus coeruleus neurons by peripherally administered microbial substances

Our earlier studies demonstrated that representative microbial substances--lipopolysaccharide, peptidoglycan, and poly-inosine: poly-cytosine (poly(I):(C))--increased the spontaneous discharge rates and sensory-evoked responses of isolated locus coeruleus (LC) neurons in a dose- and time-related manner after i.p. injection into rats. We then turned our attention to the mechanism by which microbial substances administered into the peritoneal cavity affect the LC neurons. The involvement of the subdiaphragmatic vagus nerves was examined in this regard since several brain responses to peripherally administered lipopolysaccharide have been found to depend upon the integrity of these nerves. The experiments reported here show that lipopolysaccharide, peptidoglycan, and poly(I):(C) all failed to excite LC neurons after i.p. injection into rats that had previously been subjected to complete transection of the subdiaphragmatic vagus nerves. Furthermore, selective transection of the subdiaphragmatic vagus nerve trunks indicated that the dorsal trunk, and not the ventral trunk, was necessary to excite LC neurons in response to i.p. lipopolysaccharide. The inability of LC neurons to respond to i.p. lipopolysaccharide in vagotomized rats is unlikely to be attributed to a desensitization of the neurons to lipopolysaccharide since i.c.v. injection of lipopolysaccharide excited LC neurons in vagotomized rats as it did in vagus-intact rats. These findings suggest that a variety of microbial substances excited LC neurons after administration into the peritoneal cavity in a manner involving the subdiaphragmatic vagus nerves.     

内脏伤害性传入信息向三叉神经脊束间质核的投射

舌咽、迷走神经向三叉神经脊束间质核的投射纤维除传递非伤害性内脏信息者外是否也含内脏伤害性传入？尚未见报道。本文综合应用：（1）福尔马林刺激舌咽、迷走神经支配的一些内脏诱导FOS蛋白表达；（2）抽除外周神经节观察三叉神经脊束间质核内一些与伤害性信息传递有关的神经递质的变化；（3）运用荧光金逆行追踪与免疫组化相结合的双重反应等方法，对大鼠投射至三叉神经脊束间质核的舌烟、迷走神经初级传入纤维中是否含传递伤害性刺激信息的成分进行了研究。结果证明：(1)2％福尔马林刺激大鼠软腭、咽、食道和胃后，三叉神经脊束间质核内有大量FOS阳性神经元表达，这些阳性神经元与舌咽、迷走神经初级传入分布区基本一致。（2）抽除一侧舌咽、谈走神经报及其神经节后，术侧三叉神经脊束间质核内SP、CGRP等和痛传递有关的神经肽及BSI-B_4阳性终末与对侧比较明显减少。（3）荧光金微量注入三叉神经脊束间质核后，在舌咽、迷走神经节的下节内发现被荧光金逆标的细胞中分别有10％和12％呈SP、CGRP阳性，此两种双重阳性细胞分别占SP、CGRP阳性细胞的33．3%和278％。以上结果提示，三叉神经脊束间质核接受舌咽、迷走神经的传入纤维中有一部分传递内脏伤害性信息。     

Gastric afferents to the paraventricular nucleus in the rat

Summary Extracellular recordings were made from vasopressin (AVP) and oxytocin (OXT)-secreting cells in the paraventricular nucleus (PVN) of the hypothalamus in rats anesthetized with urethane-chloralose to determine the effects of electrical stimulation of vagal gastric nerves and gastric distension on their activity. Electrical stimulation of gastric branches of the vagus nerves inhibited 5 and excited 10 of 32 phasically firing neurosecretory cells. Approximately one third of the phasically firing neuro-secretory cells (9 out of 29 cells) were transiently inhibited by gastric distension; an effect which was completely abolished by bilateral cervical vagotomy. In contrast, gastric nerve stimulation excited 45 of 72 non-phasically firing paraventricular cells. Thirteen of 77 non-phasically firing cells tested were excited by gastric distension. We conclude that there are some sensory afferent inputs originating from gastric receptors and transmitted by gastric vagal afferents which inhibit the activity of AVP- secreting neurons in the PVN although other inputs excite the cells. Similar inputs also excite some of the putative OXT-secreting neurons in the PVN.     

Participation of the parasympathetic and sympathetic nerves in regulation of gallbladder motility in the dog

The participation of the parasympathetic and sympathetic nerves in the canine gallbladder motility was examined. Efferent stimulation of the parasympathetic (vagus) and sympathetic (celiac) nerves caused contraction or inhibition of the neck, body and fundus of the gallbladder. The contractile response induced by vagus nerve stimulation was reduced by subthreshold efferent stimulation of the celiac nerve, while the inhibitory response was neither reduced nor enhanced by subthreshold efferent stimulation of the celiac nerve. The contractile and inhibitory response induced by celiac nerve stimulation was not reduced in the neck, body and fundus by subthreshold efferent stimulation of the vagus nerve. The contractile response to vagus nerve stimulation was reversed to a relaxant response by atropine administration, which was reduced or abolished by hexamethonium. It is suggested that the vagus nerve-induced contractile response in the canine gallbladder is modulated by sympathetic nerves presynaptically at the vagus nerve endings in the enteric ganglion, but the vagus nerve-induced relaxant response, which probably was induced by non-adrenergic non-cholinergic inhibitory neurons, is not modulated by the sympathetic nerves.     

Role of σ-opiate receptors in development of ischemic arrhythmias

In acute experiments on anesthetized cats, the selective σ-opiate receptor agonist DSLET has a pronounced antiarrhythmic effect on ischemic heart rhythm disturbances. This effect is probably related to inhibition of the sympathetic heart rhythm regulation, because the antifibrillation effect of DSLET is not mediated via the vagus nerves, but on the other hand DSLET considerably modulates cardiac adrenoreactivity. Translated fromByulleten' Eksperimental'noi Biologii i Meditsiny, Vol. 127, No. 2, pp. 164–167, February, 1999.     

Somatostatin is contained in and released from cholinergic nerves in the heart of the toad Bufo marinus

The heart of the toad Bufo marinus contained a substance with somatostatin-like immunoreactivity which eluted with somatostatin on reverse phase high pressure liquid chromatography. Immunoreactivity to somatostatin was localised histochemically to nerve fibers in muscle bundles of the sinus venosus, atria and ventricles and to nerve cell bodies in the sinus venosus and inter-atrial septum. Nerve cell bodies were localised both by interference contrast microscopy and immunohistochemistry; all detectable intracardiac neurons were immunoreactive. Synthetic somatostatin inhibited the rate and force of beat of atrial preparations, but did not affect the driven ventricle. Vagal stimulation caused inhibition of all cardiac chambers. After muscarinic blockade with hyoscine, vagal stimulation with 3 Hz or more still caused inhibition of the pacemaker and atrium, but not of the ventricle. The hyoscine-resistant vagal effects were diminished by about 60% after induction of tachyphylaxis to somatostatin. When when the vagus nerves were stimulated intermittently for 1 h at 10 Hz, in the presence or absence of hyoscine, the effect of somatostatin was reduced by about 60%. It is concluded that the cholinergic postganglionic neurons of the cardiac vagus contain somatostatin. When the vagus is stimulated at 3 Hz or more, the neurons release sufficient somatostatin to inhibit the pacemaker and atrial muscle.     

Analysis of the humoral basis underlying periodic alternation of cardiac inhibition and stimulation on prolonged stimulation of the vagus

Summary Prolonged stimulation of the vagus nerves (up to 40 uninutes) evoked periodic changes in the activity of the heart muscle. It is manifested by the interchange of phases of inhibition and recovery of heart activity (Sechenov-Mecimikov phenomenon).Experiments were performed on hearts of frogs (Rana temporaria). It was established that the functional periodicity in the activity of the heart, which was observed under conditions of prolonged stimulation of the vagus nerves is associated with periodic appearance of chemically active substances of different origin in the heart. Thus, the periodic appearance of phases of inhibition is connected with periodic secretion of acetylcholine, while the periodic apperance of phases of recovery-with periodical secretion of adrenaline-like substances.It is probable that acetylcholine plays a regulating role in cardiac activity, promoting liberation of adrenaline-like substances under conditions of prolonged stimulation of the vagus nerve.Submitted by Active Member of the AMS USSR Professor N. I. Grashchenkov     

Inhibition of epibranchial placode-derived ganglia in the developing rat by bisdiamine

Although bisdiamine has been shown to affect the development of mammals, its effect on the nervous system has gone largely unrecognized. In the present study, rats were given bisdiamine by gavage on days 9 and 10 of pregnancy. They were sacrificed at intervals and the fetuses were prepared for study of serial sections stained with hematoxylin and eosin, or by immunohistochemical reaction with HNK-1 monoclonal antibody. HNK-1 reacted strongly with the nervous system, allowing precise analysis of the components and their relationships. Controls receiving no bisdiamine were prepared and studied in parallel with the experimental fetuses. Administration of bisdiamine inhibited development of the petrosal and nodose ganglia, altered associations of the glossopharyngeal, vagus, and hypoglossal nerves, and inhibited contributions of vagal nerve fibers to the developing enteric system. The proximal ganglia of the glossopharyngeal and vagus nerves developed normally. It is concluded that bisdiamine affects, directly or indirectly, the differentiation of nervous components derived from the epibranchial placodes. It seems likely that these placode-derived components serve as pioneer neurons in establishing the pathway for the posteriorly extending trunks of the glossopharyngeal and vagus nerves. The early changes in congenital conditions such as the DiGeorge syndrome may not be limited to alterations in neural crest derivatives. It may be worthwhile to investigate more closely whether there are alterations in the nervous system associated with these syndromes. © 1992 Wiley-Liss, Inc.     

Convergence of excitatory inputs from the chorda tympani, glossopharyngeal and vagus nerves onto superior salivatory nucleus neurons in the cat

Superior salivatory nucleus (SSN) neurons were identified by antidromic spike responses to stimulation of the chorda tympani nerve, and were tested to stimulation of the ipsilateral chorda tympani, glossopharyngeal, vagus and lingual nerves in urethane-chloralose anesthetized cats. In 48 SSN neurons identified, 33 (69%) responded with spikes to stimulation of at least one of these nerves, and 24 (50%) were excited with inputs from more than one stimulated nerve. The mean latencies of the reflex responses to stimulation of the chorda tympani, glossopharyngeal, vagus or lingual nerve were 13.2, 18.9, 24.6 or 11.4 ms, respectively.     

Effects of β-endorphin on cardiac afferent systems

Studies performed on cats have shown that the antifibrillatory effect of β-endorphin under acute myocardial ischemia is mediated by afferent pathways of the vagus nerves and sympathetic components of arrhythmogenesis. This effect is associated with the ability of β-endorphin to change the impulse activity of cardiovascular and integrative neurons of the nodose ganglion. Translated fromByulleten' Eksperimental'noi Biologii i Meditsiny, Vol. 126, No. 9, pp. 294–298, September, 1998     

Inhibition of epibranchial placode-derived ganglia in the developing rat by bisdiamine.

Although bisdiamine has been shown to affect the development of mammals, its effect on the nervous system has gone largely unrecognized. In the present study, rats were given bisdiamine by gavage on days 9 and 10 of pregnancy. They were sacrificed at intervals and the fetuses were prepared for study of serial sections stained with hematoxylin and eosin, or by immunohistochemical reaction with HNK-1 monoclonal antibody. HNK-1 reacted strongly with the nervous system, allowing precise analysis of the components and their relationships. Controls receiving no bisdiamine were prepared and studied in parallel with the experimental fetuses. Administration of bisdiamine inhibited development of the petrosal and nodose ganglia, altered associations of the glossopharyngeal, vagus, and hypoglossal nerves, and inhibited contributions of vagal nerve fibers to the developing enteric system. The proximal ganglia of the glossopharyngeal and vagus nerves developed normally. It is concluded that bisdiamine affects, directly or indirectly, the differentiation of nervous components derived from the epibranchial placodes. It seems likely that these placode-derived components serve as pioneer neurons in establishing the pathway for the posteriorly extending trunks of the glossopharyngeal and vagus nerves. The early changes in congenital conditions such as the DiGeorge syndrome may not be limited to alterations in neural crest derivatives. It may be worthwhile to investigate more closely whether there are alterations in the nervous system associated with these syndromes.     

The distribution of somatomedins in the nervous system of the cat and their release following neural stimulation

Recent evidence suggests a regulatory role in the nervous system for somatomedins. The present study, using a somatomedin radioreceptorassay which primarily detects insulin-like growth factors 1 and 2, shows that somatomedins are widely distributed throughout the nervous system of the cat. Whilst somatomedins were present in all CNS regions, the highest concentration occurred in the hypothalamus followed by cerebral cortex. In the spinal cord, the dorsal roots contained twice the concentration found in the ventral roots. Activity was also present in the sympathetic ganglia, vagus nerve and sciatic nerves. Following electrical stimulation of the brachial and sciatic nerves somatomedins were released into perfusates from extirpated cut limbs. These findings suggest that somatomedins may be neuroregulatory hormones.     

Projections of calcitonin gene-related peptide immunoreactive neurons in the vagal ganglia of the rat

We have studied the connections of calcitonin gene-related peptide immunoreactive (CGRP-ir) sensory neurons in the ganglia of the vagus nerve. Many CGRP-ir neurons were identified in the jugular ganglion located in the cranial cavity, while fewer CGRP-ir neurons were found in the nodose ganglion located at the level of the jugular foramen. Application of Fluorogold to the cut end of the cervical vagus nerve resulted in many Fluorogold-labeled neurons in both the jugular and the nodose ganglia. Application of Fluorogold to the cut end of the subdiaphragmatic vagus nerve resulted in Fluorogold-labeled neurons mostly in the nodose ganglion with only a few labeled neurons in the jugular ganglion. Injection of Fluorogold into the heart resulted in Fluorogold-labeled neurons in both the jugular and the nodose ganglia. Double labeling combining CGRP immunohistochemistry and Fluorogold retrograde tracing showed that in cases of both the application of Fluorogold to the cut end of the cervical vagus nerve and the injection of Fluorogold into the heart, about 40% of the Fluorogold-labeled neurons in the jugular ganglion expressed CGRP-like immunoreactivity. These results indicate that many CGRP-ir neurons in the jugular ganglion innervate the cervical and thoracic visceral organs, including the heart, but only a few CGRP-ir neurons project to the abdominal visceral organs.     

Effects of Electrical Stimulation of the Hunger Center in the Lateral Hypothalamus and Food Reinforcement on Impulse Activity of the Proper Masticatory Muscle in Rabbits under Conditions of Hunger and Satiation

Threshold stimulation of the lateral hypothalamus in starving and preliminary fed (satiated) rabbits in the absence of feed induces searching behavior associated with burst-like impulse activity of proper masticatory muscle with a bimodal distribution of interpulse intervals, what represents an anticipatory type of reaction. The increase in the level of food motivation during threshold stimulation of the lateral hypothalamus in starving and satiated rabbits with the food offered led to successful food-procuring behavior, during which the frequency and amplitude of spike bursts in the proper masticatory muscle become comparable with those under conditions of natural foraging behavior stimulated by the need in nutrients. Motivational excitation and backward afferentation from food reward are addressed to the same neurons of the masticatory center in the medulla oblongata.     

Substance P and somatostatin content and transport in the vagus and sciatic nerves of the aging Fischer 344 rat

The two widely distributed neuropeptides, substance P (SP) and somatostatin (SS), are synthesized in cell bodies of the sensory ganglia of the vagus and sciatic nerves and transported bidirectionally toward the central nervous system and sites of sensory innervation. In this study, the content of both peptides was measured in the vagus and sciatic nerves of Fischer 344 rats aged 4, 12 and 25 months. In addition, as an indicator of biosynthesis within the sensory ganglia, the quantity of neuropeptide transported during 22 hours in a peripheral orthograde direction was measured using the ligation technique in animals age 12, 18 and 25 months. The content and transported quantity of SP was unchanged or slightly increased in both nerves as a function of age. Somatostatin content was unchanged and transport increased in the vagus of older rats. In contrast, in the sciatic nerve, SS content was reduced by more than 30% in older rats (p less than 0.01); transported somatostatin was proportionately reduced (p less than 0.05). These findings demonstrate that neuropeptide levels in the sensory vagus are not reduced as a function of age. Somatostatinergic dorsal root ganglion neurons may be selectively vulnerable in the aging Fischer rat.     

The reflex regulation of the activity of the heart in fishes

Summary The author studied the reflex control of the fish heart which has only one path of effector innervation, viz., the vagus nerves. Literature and personal data show that inhibitory tone in the heart is absent in fish. In stimulating intestinal receptors there appears, depending upon the strength of the afferent stimulation, inhibition or accleration of the cardiac activity.Hence both effects may be considered as the result of an active impulse of the vagus nerve on the heart.Presented by Active Member AMN SSSR S. E. Severin     

Neurons in the nucleus of the solitary tract mediating inputs from emetic vagal afferents and the area postrema to the pattern generator for the emetic act in dogs.

Roles of neurons in the nucleus of the solitary tract corresponding to the area subpostrema (mNST) for the retching reflex were investigated in decerebrate, paralyzed dogs. Retching was defined as rhythmic coactivation of the phrenic and abdominal muscle nerves. Retching which had been induced by stimulation of the left and right abdominal vagus nerves was impaired by cooling the left and right mNSTs, respectively. This result indicates that the mNST neurons mediate activities of emetic vagal afferents. All 40 non-respiratory neurons in the mNST, which had excitatory response to pulse train stimulation of the vagus nerve, were also activated by continuous stimulation of the vagus nerve to provoke retching. During provoked retching, however, these neurons did not exhibit any activities modulated in association with retching. The average latency of responses of these neurons to the pulse train stimulation (306.5 ms) was significantly shorter than that of the inspiratory neurons in the lateral NST and the adjacent reticular formation. Discharge frequencies of these neurons in the mNST gradually increased after administration of apomorphine (6/10) and glutamate (14/14) to the 4th ventricle. Antidromic responses to stimulation of the B?tzinger complex were observed in some (20/289) of the mNST neurons. These findings suggest that neurons in the mNST mediate the information from both the abdominal vagal afferents and the area postrema and drive the pattern generator for retching and vomiting, which is assumed to be located in the B?tzinger complex.