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1.
Neurourol Urodyn ; 35(3): 382-9, 2016 Mar.
Article in English | MEDLINE | ID: mdl-25597596

ABSTRACT

AIMS: The urethral sphincter and urethral muscle innervation are critically involved in maintaining continence, especially in the female. However, the urethral muscle type and distribution, as well as the urethral nerves are far from being well documented. Our aim was to clearly identify the distribution of urethral striated muscle, smooth muscle, and urethral nerves. METHODS: In a cohort analysis of 3-month-old female Sprague-Dawley rats, cross and longitudinal sections of female rat urethra were extensively investigated using morphological techniques. Urethras were harvested to the sections, in order to provide both global and detailed visions of the urethra. H&E, Masson's Trichrome, phalloidin and immunoflourence stains were used. The cytoarchitecture, nitrergic, and cholinergic innervations were mainly investigated. Different layers of the segments of urethra were traced to draw curve graphs that represent the thickness of each muscle layer of urethral wall. RESULTS: The results showed that the primary peak of striated muscle is in the middle urethra. The inner layer close to mucosa was found to contain longitudinal smooth muscle. Near the bladder orifice, the circular smooth muscle dominates, which becomes thinner distally throughout the rest of urethra. In the middle urethra the vast majority of the urethral muscle are circularly oriented striated muscle cells. Typical nerve endings were present in high power images to show the different characteristic features of nerve innervation. CONCLUSIONS: This study has illustrated the detailed morphological structure and innervations of the normal female rat urethra and can serve as a basis for further study of stress urinary incontinence (SUI).


Subject(s)
Adrenergic Neurons , Cholinergic Neurons , Muscle, Skeletal/innervation , Muscle, Smooth/innervation , Nerve Endings , Nitrergic Neurons , Urethra/innervation , Adrenergic Neurons/chemistry , Animals , Cholinergic Neurons/chemistry , Female , Muscle, Skeletal/cytology , Muscle, Smooth/cytology , Nitrergic Neurons/chemistry , Rats, Sprague-Dawley , Urethra/cytology
2.
J Chem Neuroanat ; 116: 101989, 2021 10.
Article in English | MEDLINE | ID: mdl-34126223

ABSTRACT

In a recent paper, we described the distribution of Nitric oxide (NO) in the diencephalon of the rock cavy (Kerodon rupestris). This present paper follows this work, showing the distribution of NO synthesizing neurons in the rock cavy's brainstem. For this, we used immunohistochemistry against the neuronal form of nitric oxide synthase (NOS) and NADPH diaphorase histochemistry. In contrast to the diencephalon in the rock cavy, where the NOS neurons were seen to be limited to some nuclei in the thalamus and hypothalamus, the distribution of NOS in the brainstem is widespread. Neurons immunoreactive to NOS (NOS-ir) were seen as rostral as the precommissural nuclei and as caudal as the caudal and gelatinous parts of the spinal trigeminal nucleus. Places such as the raphe nuclei, trigeminal complex, superior and inferior colliculus, oculomotor complex, periaqueductal grey matter, solitary tract nucleus, laterodorsal tegmental nucleus, pedunculopontine tegmental, and other nuclei of the reticular formation are among the locations with the most NOS-ir neurons. This distribution is similar, but with some differences, to those described for other rodents, indicating that NO also has an important role in rock cavy's physiology.


Subject(s)
Brain Stem/metabolism , Nitrergic Neurons/metabolism , Nitric Oxide Synthase/metabolism , Nitric Oxide/metabolism , Animals , Brain Stem/chemistry , Brain Stem/cytology , Female , Guinea Pigs , Male , Nitrergic Neurons/chemistry , Nitric Oxide/analysis , Nitric Oxide Synthase/analysis , Species Specificity
3.
J Comp Neurol ; 529(13): 3321-3335, 2021 09.
Article in English | MEDLINE | ID: mdl-34008863

ABSTRACT

Nitrergic neurons (NNs) are inhibitory neurons capable of releasing nitric oxide (NO) that are labeled with nicotinamide adenine dinucleotide phosphate diaphorase histochemistry. The rat primary somatosensory (S1) and motor (M1) cortices are a favorable model to investigate NN populations by comparing their morphology, since these areas share the border of forepaw representation. The distribution of the Type I NN of the forepaw representation in the S1 and M1 cortices of the rat in different laminar compartments and the morphological parameters related to the cell body and dendritic arborization were measured and compared. We observed that the neuronal density in the S1 (130 NN/mm3 ) was higher than the neuronal density in the M1 (119 NN/mm3 ). Most NN neurons were multipolar (S1 with 58%; M1 with 69%), and a minority of the NN neurons were horizontal (S1 with 6%; M1 with 12%). NN found in S1 had a higher verticality index than NN found in M1, and no significant differences were observed for the other morphological parameters. We also demonstrated significant differences in most of the morphological parameters of the NN between different cortical compartments of S1 and M1. Our results indicate that the NN of the forepaw in S1 and M1 corresponds to a neuronal population, where the functionality is independent of the different types of sensory and motor processing. However, the morphological differences found between the cortical compartments of S1 and M1, as well as the higher density of NNs found in S1, indicate that the release of NO varies between the areas.


Subject(s)
Forelimb/metabolism , Motor Cortex/metabolism , Nitrergic Neurons/metabolism , Somatosensory Cortex/metabolism , Animals , Forelimb/chemistry , Forelimb/innervation , Male , Motor Cortex/chemistry , Motor Cortex/cytology , NADP/analysis , NADP/metabolism , Nitrergic Neurons/chemistry , Rats , Rats, Wistar , Somatosensory Cortex/chemistry , Somatosensory Cortex/cytology
4.
Article in Russian | MEDLINE | ID: mdl-29460906

ABSTRACT

AIM: To obtain the data on the spatial relationships between catecholamine (TH-positive) and nitroxidergic (nNOS-positive) neurons in vasomotor nuclei of the medulla in different periods of hypertension development. MATERIAL AND METHODS: The experiment was performed on male Wistar rats (n=45) with induced renovascular hypertension (RVH). TH and nNOS in neurons of solitary tract nuclei, reticular small-and giant cell nuclei were detected using immunohistochemical methods. RESULTS AND CONCLUSION: The most early and severe changes in the intensity of reaction and amount of nNOS-positive neurons were noted in the solitary tract nucleus. Significant changes in the quantitative parameters of TH-positive neurons in RVH were identified only in the reticular giant cell nucleus but they appeared later and were less expressed compared to nNOS-positive cells. This resulted in the changes of spatial relationships between two types of neurons and remodeling of the bulbar region of the cardiovascular center.


Subject(s)
Brain Stem/pathology , Hypertension/pathology , Nitrergic Neurons/pathology , Animals , Catecholamines/analysis , Male , Medulla Oblongata/chemistry , Medulla Oblongata/pathology , Nitrergic Neurons/chemistry , Nitric Oxide Synthase Type I/analysis , Rats , Rats, Wistar , Solitary Nucleus/chemistry , Solitary Nucleus/pathology
5.
Anat Rec (Hoboken) ; 294(6): 1066-73, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21538934

ABSTRACT

Dorsal root ganglia (DRGs) contain the cell bodies of primary afferent neurons that transmit sensory information from the periphery into the spinal cord. Distinct populations of DRG neurons have been characterized by a variety of different immunohistochemical markers. A subpopulation of ganglionic neurons containing neuronal nitric oxide synthase (nNOS), an enzyme known to generate nitric oxide, has been detected in a number of mammalian species. Despite previous studies, no information is known on the presence and exact distribution of nNOS-immunoreactive neurons in the DRGs of the bottlenose dolphin. In this investigation, immunoperoxidase for nNOS was used to determine the distribution and the perikaryal size of nitrergic neurons in the DRGs of this species. Double immunofluorescence protocol was used to determine the percentage of nNOS-immunoreactive (IR) neurons over the total primary afferent neurons. In addition, double immunostaining was used to verify whether there was colocalization of nNOS with substance P (SP). In all DRGs, a subpopulation of small- and medium-sized neurons (about 9%) exhibited nNOS immunoreactivity. Data analysis revealed that the majority of nNOS-IR neurons (81.3%) expressed SP. The density of nNOS-immunoreactive and nNOS/SP-double immunopositive cells was relatively constant throughout the ganglia. However, as observed in others mammals, the number of nitrergic neurons decreased in the caudalmost DRGs. Our results, in conjunction with previous observations, suggest that nNOS-IR neurons may be involved in the afferent transmission of visceral and nociceptive information as well as in the regulation of the vascular tone.


Subject(s)
Bottle-Nosed Dolphin , Ganglia, Spinal/chemistry , Nitrergic Neurons/chemistry , Nitric Oxide Synthase Type I/metabolism , Nitric Oxide/analysis , Animals , Bottle-Nosed Dolphin/metabolism , Ganglia, Spinal/enzymology , Nitrergic Neurons/enzymology , Nitric Oxide/metabolism
6.
Am J Physiol Regul Integr Comp Physiol ; 290(6): R1626-38, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16682470

ABSTRACT

Stimulation of cardiac mechanoreceptors during volume expansion elicits reflex compensatory changes in sympathetic nerve activity (SNA). The hypothalamic paraventricular nucleus (PVN) and nucleus of the tractus solitarius (NTS) are autonomic regions known to contribute to this reflex. Both of these nuclei project to the rostral ventrolateral medulla (RVLM), critical in the tonic generation of SNA. Recent reports from our laboratory show that these pathways 1) are activated following cardiac mechanoreceptor stimulation, and 2) produce nitric oxide, known to influence SNA. The aims of the present study were to determine whether 1) the activated neurons within the PVN and NTS were nitrergic and 2) these neurons projected to the RVLM. Animals were prepared, under general anesthesia, by microinjection of a retrogradely transported tracer into the pressor region of the RVLM and the placement of a balloon at the right venoatrial junction. In conscious rats, the balloon was inflated to stimulate the cardiac mechanoreceptors or was left uninflated. Balloon inflation elicited a significant increase in Fos-positive neurons in the parvocellular PVN (sevenfold) and NTS (fivefold). In the PVN, 51% of nitrergic neurons and 61% of RVLM-projecting nitrergic neurons were activated. In the NTS, these proportions were 8 and 18%, respectively. The data suggest that nitrergic neurons within the PVN and, to a lesser extent, in the NTS, some of which project to the RVLM, may contribute to the central pathways influencing SNA elicited by cardiac mechanoreceptor stimulation.


Subject(s)
Heart/physiology , Mechanoreceptors/physiology , Medulla Oblongata/physiology , NADPH Dehydrogenase/metabolism , Nitrergic Neurons/physiology , Animals , Consciousness , Heart/innervation , Immunohistochemistry , Male , Medulla Oblongata/cytology , NADPH Dehydrogenase/analysis , Nitrergic Neurons/chemistry , Nitrergic Neurons/cytology , Paraventricular Hypothalamic Nucleus/cytology , Paraventricular Hypothalamic Nucleus/physiology , Physical Stimulation , Proto-Oncogene Proteins c-fos/analysis , Proto-Oncogene Proteins c-fos/metabolism , Rats , Rats, Sprague-Dawley , Solitary Nucleus/cytology , Solitary Nucleus/physiology
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