Gaseous transmitters in the brain of the masu salmon, <Emphasis Type="Italic">Oncorhynchus masou</Emphasis> (Salmoniformes,Salmonidae)

Distribution of nitroxidergic and H₂S-producing neurons in the brain of the masu salmon Oncorhynchus masou was studied by methods of histochemical labeling of NADPH-diaphorase and by immunohistochemical labeling of the neuronal nitric oxide synthase and cystathionine β-synthase (CBS). The established distribution of CBS and nNOS/NADPH-d of neurons and fibers in the masu salmon telencephalon, optic tectum, and cerebellum allows suggesting that the NO- and H₂S-producing systems represent individual, non-overlapping neuronal complexes performing specialized functions in the activity of local neuronal networks. In the medullar part, the nNOS-ir and NADPH-d-positive neurons were detected in the composition of viscerosensory (V, VII, and IX–X) and visceromotor (III, IV, and VI) nuclei of craniocerebral nerves, octavolateral afferent complex, reticulospinal neurons, and medial reticular formation. CBS in the masu salmon medulla was revealed in neurons of the nerve X nucleus, reticulospinal neurons, and ventrolateral reticular formation. Distribution of NO-ergic and H₂S-producing neurons in the masu salmon medullar nuclei indicates that NO in masu salmon is the predominant neuromodulator of the medullar viscerosensory systems, while H₂S seems to modulate only the descending motor systems. The results of the performed study allow suggesting that NO in the masu salmon medulla periventricular area can act as a regulator of postnatal ontogenesis.     

Response of NADPH-Diaphorase-Exhibiting Neurons in the Medullar Reticular Formation to High Spinal Cord Injury

1. The effect of hemisection of the cervical spinal cord on NADPH-diaphorase staining in the reticular nuclei of the rabbit medulla was investigated using histochemical technique.2. A quantitative assessment of somal and neuropil NADPH-diaphorase staining was made by an image analyzer in a selected area of each reticular nucleus of the rabbit medulla.3. On the 7th postsurgery day, the highest up-regulation of somatic NADPH-diapho- rase staining was observed in regions regulating cardiorespiratory processes; however, the highest increase of neuropil NADPH-diaphorase staining was found in the reticular nuclei modulating the tonus of postural muscles.4. The degeneration of non-NADPH-diaphorase-stained neurons was detected throughout the reticular formation of the medulla, but the extent of neuronal death did not correlate with the up-regulation of the NADPH-diaphorase staining in the reticular nuclei of the medulla.5. The findings provide evidence that NADPH-diaphorase-exhibiting neurons are refractory to the hemisection of the cervical spinal cord and that the neuronal up-regulation of NADPH-diaphorase at the medullar level is probably not a causative factor leading to the death of the reticulospinal neurons.     

Cytoarchitectonic and neurochemical properties of spinal cord in teleost fishes

Traditional neuromorphological and NADPH-diaphorase methods were used to study the topography, morphology and neurochemical organization properties of spinal cord in teleosts fishes. The heterogeneous population of NO-producing motoneurons was revealed in the motor column of spinal cords from studied species. Dendrites of primary motoneurons formed rich plexus at the spinal segment periphery. This morphological pattern is determined by translational motion of the fishes in the water (trunk-tail movement), and has no connection with the origin of upper and lower extremities. The NO-producing capacity of spinal motoneurons shows their connection with premotor NO-ergic brain system, including over situated motor centers of reticular formation and descending projections of giant steam neurons (Mauthner and Muller cells). The NO-producing Rohon-Berd neurons were found in the dorso-medial part of spinal cord from studied fishes. These cells with the ascending propriospinal targets form spinal nociceptive system. Thus, the sense Rohon-Berd cells and most motor neurons of studied bony fishes are nitric oxide synthesizing ones. Spinal cord NO-synthesizing territories are situated in concordance with dorso-ventral histochemical gradient. Spinal cord interneurons of these fishes produce nitric oxide selectively. The quantity of NO-synthesizing reticular cells is determined by two main factors: the connection with the specialized neurochemical complexes, where NO is a specific neuromodulator, and individual properties of spinal cord structure directed by conditions of morphoadaptation.     

Different distributions of nitric oxide synthase-containing neurons in the mouse and rat hypothalamus.

The distribution of nitric oxide synthase-containing neurons was studied in the rat and mouse hypothalamus by immunohistochemistry and NADPH-diaphorase histochemistry. Immunostaining and NADPH-diaphorase staining of hypothalamic neurons were comparable in all hypothalamic nuclei of either species except in the arcuate nucleus that stained positive for nitric oxide synthase immunoreactivity but negative for NADPH-diaphorase reactivity. The presence of nitric oxide synthase-immunopositive neurons in the arcuate nucleus was confirmed by nitric oxide synthase immunofluorescence viewed under the confocal microscope at 1 microm thickness. Cross-species comparison showed that, in general, the number and intensity of nitric oxide synthase-containing neurons were much higher in the rat than in the mouse hypothalamus. Differences in the distribution of nitric oxide synthase-containing neurons between these two rodents were found in most hypothalamic nuclei. In particular, two dense clusters of nitric oxide synthase-containing neurons were found in the paraventricular and supraoptic nuclei of the rat hypothalamus in contrast to their scarcity in the same nuclei of the mouse hypothalamus.     

NADPH-diaphorase-positive nerve fibers associated with motor endplates in the rat esophagus: new evidence for co-innervation of striated muscle by enteric neurons

NADPH-diaphorase histochemistry was combined with demonstration of acetylcholinesterase and immunocytochemistry for calcitonin gene-related peptide to study esophageal innervation in the rat. Most of the myenteric neurons stained positively for NADPH-diaphorase, as did numerous varicose nerve fibers in the myenteric plexus, among striated muscle fibers, around arterial blood vessels, and in the muscularis mucosae. A majority of motor endplates (as demonstrated by acetylcholinesterase histochemistry or calcitonin gene-related peptide immunocytochemistry) were associated with fine varicose NADPH-diaphorase-positive nerve fibers. Analysis of brainstem nuclei, sensory vagal, spinal, and sympathetic ganglia in normal and neonatally capsaicin-treated rats, and comparison with anterogradely labeled vagal branchiomotor, preganglionic and sensory fibers led to the conclusion that NADPH-diaphorase-positive fibers on motor endplates originate in esophageal myenteric neurons. No association of NADPH-diaphorasepositive nerve fibers with motor endplates was found in other organs containing striated muscle. These results suggest extensive, presumably nitrergic, co-innervation of esophageal striated muscle fibers by enteric neurons. Thus, control of peristalsis in the esophagus of the rat may be more complex than hitherto assumed.     

Coexistence of NADPH-diaphorase with vasopressin and oxytocin in the hypothalamic magnocellular neurosecretory nuclei of the rat

Coexistence of NADPH-diaphorase with vasopressin and oxytocin was studied in the magnocellular neurosecretory nuclei of the rat hypothalamus by use of sequential histochemical and immunocytochemical techniques in the same sections. Coexistence was found in all the nuclei examined (supraoptic, paraventricular, circular, fornical, and in some isolated neurons located in the hypothalamic area between the paraventricular and supraoptic nuclei). The ratios of neurons expressing both markers (NADPH-diaphorase and vasopressin, NADPH-diaphorase and oxytocin) in each of the nuclei were very similar. Although further studies must be carried out, the partial coexistence found in all nuclei suggests that NADPH-diaphorase is probably not related to general mechanisms involving vasopressin and oxytocin, but rather in specific functions shared by certain hypothalamic neuronal cell populations.     

Opposite modulating effects of the hypothalamic region on cardiac reflexes of Gadus morhua cod and Rana temporaria frogs

The effects of hypothalamic stimulation on cardiac reflexes have been investigated in the cod Gadus morhua and frog Rana temporaria. Cardiac reflexes were elicited by electrical stimulation of the medullar vagal lobes in fishes and central end of cardiac vagal branch in frogs. During simultaneous or successive stimulation of the hypothalamic region and vagal structures, modulation of the reflexes was observed. Reflex bradycardia was either augmented or inhibited, indicating the corresponding pattern of hypothalamic influences. No correlation was found between the parameters of stimulation, reflex intensity, hypothalamic region and the pattern of modulating influences. The data obtained suggest the existence of opposite modulating influences of the hypotalamic region upon parasympathetic reflexes in the heart of fishes and frogs.     

Nitroxidergic elements in the digestive system of Mactra chinensis and Spisula sachalinensis (Mollusca: Bivalvia: Mactridae)

Localization and morphology of NO-ergic elements in the digestive system of bivalve molluscs Mactra chinensis and Spisula sachalinensis were studied using histochemical technique [1] for detection of NADPH-diaphorase (EC 1.6.99.1) [1]. The NO-producing elements were revealed in all parts of the digestive system of the studied animals. NADPH-diaphorase was found in cells of several morphological types as well as in nerve plexuses. The most abundant in the digestive tract parts of the studied molluscs were intraepithelial nerve cells of the “open” type, whose thin apical process is directed towards the gut lumen. Subepithelial NO-ergic neurons were revealed in stomach and crystalline style sac of Mactra chinensis. Besides, diformazan granules are present in brush-border epitheliocytes of the major and secondary ducts of the digestive gland as well as in cells of digestive tubules of this gland. All studied parts were found to contain basiepithelial and subepithelial NO-ergic nerve fibers forming networks of various densities from, most commonly, loose to dense plexuses particularly developed in labia, esophagus, and gut of the studied molluscs.     

Septal nuclei in the regulation of vago-sensitive neurons activity of the solitary nucleus in cats

The descending influences of the septal nuclei (lateral nucleus--LSN and bed nucleus stria terminalis--BNST) on activity of viscero-sensory neurons of the nucleus of tractus solitarius (NTS) identified by stimulation of cervical part of the n. vagus were investigated in the cat anaesthetised by chloraloze-nembutal combination. It was found that out of 70 units recorded in the NTS area 50 were identified as those of primary and secondary input vagal neurons. Influence of single, paired and frequency stimulation on the septal structures was studied on these neurons. It was revealed that 30% (15 un) reacted by phase-specific response to the single stimulation of the septal nuclei. The latent period of initial excitation was in the range 5-25 ms. During the paired stimulation these neurons were not able to react to the second stimulus for the equal 10-300 ms. It was revealed that 34% (17 un) of the identified vagal neurons reacted by a tonic change of their spontaneous activity. The increase of frequency stimulation to 20 Hz evoked different changes of the rhythmical activity of the vagal neurons (increase, diminishing or inhibition). The study of interaction between central and peripheral signals in the solitary neurons induced blocking influence of descending septal discharge on the vagal test response. It is possible that the septal downward impulses reach the vago-sensitive solitary neurons indirectly through other structures of the limbic brain (amygdala, hypothalamus) and participate in modulation of the spontaneous activity of these neurons.     

Nitroxidergic Cells in the Intestine of the Bivalve Mollusk Modiolus kurilensis

The distribution of nitroxidergic (NO-ergic) cells in the direct and recurrent loops of the midgut and in the hindgut of the bivalve mollusk Modiolus kurilensis was studied using a NADPH-diaphorase (NADPH-d) histochemistry [13]. Intraepithelial NO-ergic cells were found in the intestinal groove, in the major typhlosole of the direct loop, in the recurrent loop of the midgut, as well as in the hindgut. The apical processes of these cells are directed to the intestinal lumen, whereas the basal processes connect to the basiepithelial NO-ergic plexus. The latter, in turn, have separate fibers that are in contactswith the subepithelial NO-ergic plexus. Both plexuses are well developed in the intestinal groove of the direct loop and in the recurrent loop of the midgut, as well as in the hindgut. In the major typhlosole and crystalline style sac of the direct loop, both basi- and subepithelial NO-ergic plexuses are less developed. In the minor typhlosole, the basiepithelial NO-ergic plexus is absent and only single fibers of the subepithelial plexus occur. In the connective tissue and muscular layers of the recurrent loop of the midgut, subepithelial NO-ergic nerve cells were found.     

Localization of NO-Ergic Structures in Oral Lobes, Labia, and Esophagus of the Bivalve Mollusc Crenomytilus grayanus

Localization of NO-ergic elements in oral lobes, labia, and esophagus in the bivalve mollusc, mussel Crenomytilus grayanus was studied using histochemical technique [1] for detection of NADPH-diaphorase (EC 1.6.99.1). The NO-producing elements were revealed in all studied parts of the digestive system. NADPH-diaphorase was found in nerve and secretory cells as well as in nerve plexuses. Numerous NO-ergic nerve cells were observed in the basal part of epithelium of labia and of the initial part of esophagus as well as in the subepithelial area of these organs. In the middle and posterior parts of esophagus, only subepithelially located NO-ergic nerve cell are present. Basiepithelial NO-producing secretory cells are found in all the parts, but most of these cells are observed in labia and the initial part of esophagus. Subepithelial secretory cells labeled with diformazan granules are spread from the folded surface of oral lobes to the initial part of esophagus; no such cells were found on the smooth surface of the lobes. The deposit labeled basi- and subepithelial nerve plexuses in all studied organs except for oral lobes. These plexuses are the most developed in labia and the initial part of esophagus of the studied mollusc.     

NO-Ergic Innervation of the Intestine of the Snow Sculpin Myoxocephalus brandti

Distribution, localization, and morphological peculiarities of NO-ergic nerve cells in the intestine of the snow sculpin Myoxocephalus brandti (Cottidae family) were studied using histochemical staining for NADPH-diaphorase ( NADPH-d). These cells were shown to be present in the pyloric appendages, middle and posterior parts of the intestine and in its rectal part. The NO-ergic cells are the most numerous in the myenteric plexus and circular muscle layer of all studied parts of the intestine. Single NO-ergic nerve cells are revealed in the submucosal plexus of pyloric appendages, middle and posterior parts of the intestine. No NO-ergic neural cells were found in subserosal and subepithelial plexuses, longitudinal layer of smooth muscle in all studied parts, and in the submucosal plexus of the rectal part of the intestine.     

NADPH-diaphorase, nitric oxide synthase, and tyrosine hydroxylase in the diencephalon of the Rhodeus sericeus (Cyprynidae:Teleostei)

The presence and distribution of nitric oxide synthase (NOS)-like neurons as well as tyrosine hydroxylase-immunoreactive (TH) neurons was studied in the diencephalon of the cypriniform teleost Rhodeus sericeus. The anatomical relationships between tyrosine hydroxylase (TH)- and nitric oxide synthase (NOS)-containing cells were visualized both by NOS-immunohistochemistry and NADPH-histochemistry. Immunohistochemical labeling and morphological studies were performed on the same sections. The results reported in this paper show that both a NOS and TH activity are present in the preoptic region, posterior tuberculum, paraventricular organ and hypothalamus of R. sericeus. Putative nitrergic neurons were identified in all major hypophysiotrophic nuclei of the R. sericeus brain using both NADPH-d histochemistry and nNOS immunohistochemistry. In the preoptic region, nitrergic neurons were found in both the parvocellular and the magnocellular nuclei. Within these nuclei, the distribution of NADPH-d reactivity was similar to that of nNOS immunoreactivity. However, we found no evidence of colocalization of NADPH-d and nNOS in consecutive sections. NOS- and TH-containing neurons were observed in all the nuclei under study (hypothalamus, posterior tuberculum, ventral thalamus) and telencephalon (preoptic region), although most neurons showing the coexistence of both substances were mainly located in the preoptic nucleus and hypothalamus, some labelled neurons were found in the posterior tuberculum. Most of the cerebrospinalliquor-contacting cells (LCNs) in diencephalic periventricular area of R. sericeus were TH-immunoreactive. Also, a large number ofnitrergic small LCNs distributed throughout the third ventricle were observed in these regions. The data obtained supports the existence of a nitrergic circumventricular system in teleost. LCNs in R. sericeus are thought to be involved in osmoregulatory functions as osmosensitive neurons. Due to their chemical properties, NO produced by these cells might play an important role in the maintenance and regulation of CSF homeostasis through the modulation of cerebral blood flow.     

Nitroxidergic neurons in nuclei of rat and human medulla oblongata

Four types of neurons distinguished by NADPH-diaphorase reaction have been identified in seven nuclei of human and rat medulla oblongata. It was found that nitrogen oxide (NO)-positive neurons had similar distributions; neurons with high NO-synthase activity predominated in vasomotor nuclei and, in sensitive nuclei, most neurons had low NO-syntase activity.     

Appearance and differentiation of NADPH-D-neurons in ontogeny of the cerebral cortex in rats

The appearance of presumptive NO-ergic nerve cells and their differentiation in the rat neocortex were studied. For this purpose, a comparative analysis of the development and differentiation of NADPH-D-positive neurons in the neocortex transplants taken from the embryos of different ages and transplanted in the occipital cortex of adult rats and in the normally developing cerebral cortex. The nervous tissue was stained histochemically for NADPH-D. The results we obtained suggest that no NADPH-D-containing neurons were found in the transplants from 15-day embryos, while they developed in those from 18-day embryos. Hence, precursors of NO-ergic neurons were still absent in the presumptive neocortex of 15-day embryos and appeared only on day 16-18 of embryogenesis. Expression of NADPH-D begins in them only within four to five days, but the neurons are differentiated during a relatively short period of time. Most NADPH-D-positive neurons reach their structural-functional maturity already by the end of the first week of postnatal development, while their complete maturation takes place by the end of the second week of postnatal development.     

Difference of pericentral NADPH-d positive neurons in the rabbit spinal cord segments

The purpose of the present investigation was to characterize and determine the number of NADPH-diaphorase positive neurons around the central canal in the rabbit spinal cord. These neurons are known to function as interneurons and are present in all spinal cord segments. They differ in shape of their bodies and in length and branching of their processes. The main differentiation was observed in their number, depending on the place of their localization. The highest number of these NADPH-diaphorase positive neurons was in sacral part (6 in average), the lowest one was noticeable in thoracic spinal cord (1-2 in average). It can be concluded that pericentral neurons of the rabbit spinal cord are capable of synthesizing nitric oxide and that they differ in number, depending on the place of their localization in each spinal cord segment.     

A developmental study of the localization of NADPH-diaphorase in the ganglionated plexus of the guinea-pig gallbladder

A histochemical investigation of age-related changes that occur with respect to the localization of NADPH-diaphorase in the ganglionated plexus of the guinea-pig gallbladder was carried out. In all age groups examined (embryonic stages day 34 and 52, 2 to 4-day old, 6-month old and 2-year old), the mean percentage of NADPH-diaphorase-positive neurons per ganglion was obtained by taking the number of neurons that were immunoreactive to protein gene product 9.5 (a general neuronal marker) as 100%. In addition, the possible co-existence of NADPH-diaphorase and nitric oxide synthase in the ganglionated plexus of 2 to 4-day old and 6-month old guinea-pig gallbladder was investigated. NADPH-diaphorase was not present in the ganglionated plexus of the gallbladder at embryonic day 34. At embryonic day 52, all the protein gene product 9.5-immunoreactive neurons showed positive staining to NADPH-diaphorase; this dropped to a minimum at 2–4 days (26.7%), rose slightly at 6 months (33.6%), and finally returned close to the 100% value at 2 years. In the gallbladders of 2-year old guinea-pigs, some (3 out of 10) ganglia were devoid of protein gene product 9.5-immunoreactive neurons, but NADPH-diaphorase-stained granules were found within the ganglia. However, all those neurons that were immunopositive to protein gene product 9.5 also expressed NADPH-diaphorase. Moreover, NADPH-diaphorase-positive neurons in the gallbladder of 2 to 4-day-old and 6-month-old guinea-pigs were found to express nitric oxide synthase.     

NO-Synthase in the Central Nervous System of Freshwater Bivalve Mollusc Nodularia vladivostokensis in Norm and in Hypoxia

Using light- and electron microscopic methods, localization and activity of NO-synthase were studied in the CNS of the freshwater bivalve mollusc Nodularia vladivostokensis in norm and in acute hypoxia. Distribution peculiarities and the relative content of NO-ergic neurons were revealed in nervous ganglia. A rise of the NO-synthase activity was found in perikarya of medium-size neurons and in processes of small neurons in hypoxia. Ultrastructural localization of NO-synthase was established in cytoplasmic granules, cytosomes. In acute hypoxia an increase of the number of cytosomes and of their NO-synthase activity was revealed.     

Differential control over postganglionic neurons in rat cardiac ganglia by NA and DmnX neurons: anatomical evidence

In previous single-labeling experiments, we showed that neurons in the nucleus ambiguous (NA) and the dorsal moto nucleus of the vagus (DmnX) project to intrinsic cardiac ganglia. Neurons in these two motor nuclei differ significantly in the size of their projection fields, axon caliber, and endings in cardiac ganglia. These differences in NA and DmnX axon cardiac projections raise the question as to whether they target the same, distinct, or overlapping populations of cardiac principal neurons. To address this issue, we examined vagal terminals in cardiac ganglia and trace injection sites in the brain stem using two different anterograde t ace s 1,1-dioleyl-3,3,3,3-tetramethylindocarbocyanine methanesulfonate and 4-[4-(dihexadecylamino)-styryl]-N-methylpyridinium iodide] and confocal microscopy in male Sprague-Dawley rats. We found that 1) NA and DmnX neurons innervate the same cardiac ganglia, but these axons target separate subpopulations of principal neurons and 2) axons arising from neurons in the NA and DmnX in the contralateral sides of the brain stem enter the cardiac ganglionic plexus through separate bundles and preferentially innervate principal neurons near their entry regions, providing topographic mapping of vagal motor neurons in left and right brain stem vagal nuclei. Because the NA and DmnX project to distinct populations of cardiac principal neurons, we propose that they may play different roles in controlling cardiac function.     

Androgen receptors in cranial nerve motor nuclei of male and female rats

This study compared AR proteins in four cranial nerve motor nuclei among male and female rats that were intact, gonadectomized, or gonadectomized and given TP by immunohistochemistry. AR-immunoreactive (ir) neurons were found, in descending order of abundance, in the nucleus ambiguus, hypoglossal nucleus, and the facial and trigeminal motor nuclei of both males and females of intact and gonadectomized plus TP rats. Virtually every neuron of the nucleus ambiguus was AR-ir. In contrast, AR-ir neurons were either restricted to a specific area of the hypoglossal nucleus, or randomly distributed in the facial and trigeminal motor nuclei. The predominant AR-ir site shifted from cell nuclei to the cytoplasm, depending upon the presence or absence of ligand. Sex differences in the amount and staining intensity of AR-ir neurons were discernable in all four motor nuclei of intact rats, and these differences were maintained in gonadectomized plus TP rats, with the exception of the nucleus ambiguus. The immunostaining results were complemented by results from AR binding studies. Cytosolic AR binding values for the hypoglossal and facial motor nuclei of females were only approximately 50% of those of males despite the absence of a sex difference in neuron number. These results indicate that intrinsic sex differences in AR levels and androgenic regulation of AR exist in cranial nerve motor nuclei, and that there are differences in the abundance and distribution pattern of AR responsive neurons in cranial nerve motor nuclei. These results are consistent with the idea that sex differences in AR could account for sex differences observed in nerve regeneration and neuron loss following cranial nerve injury.