RESUMEN
Blocking or impairment of the sphenopalatine ganglia (SPG) is an effective therapy of cluster headache and other pain syndromes. Contrarily, unilateral SPG-stimulation reduces infarction size in the rat permanent suture model. Well, what are the effects of the SPG damage on the following brain ischemia? This study was aimed to investigate the effects of resection of the nerves bundle from the SPG of rat on the brain lesions following middle cerebral artery occlusion (MCAO), and evaluated the roles of the nitric oxygen synthase (NOS) immunoreactive perivascular nerves of cerebral arteries in MCAO. We found that 7 days after bilateral resections of the nerves bundle from the SPG, the NOS activity perivascular nerves in the middle cerebral arteries disappeared, and the infarction volume and the TUNEL positive cells increased significantly after 24 h MCAO, which implicated that the NOS contained nerves from the SPG maybe have an important role in the MCAO.
Asunto(s)
Ganglios Parasimpáticos/cirugía , Infarto de la Arteria Cerebral Media/patología , Arteria Cerebral Media/inervación , Arteria Cerebral Media/patología , Animales , Isquemia Encefálica/patología , Recuento de Células , Ganglios Parasimpáticos/enzimología , Inmunohistoquímica , Etiquetado Corte-Fin in Situ , Infarto de la Arteria Cerebral Media/enzimología , Ligadura , Arteria Cerebral Media/enzimología , NADPH Deshidrogenasa/metabolismo , Fibras Nerviosas/enzimología , Óxido Nítrico Sintasa/metabolismo , Ratas , Ratas Sprague-DawleyRESUMEN
Nitric oxide and carbon monoxide are diffusible gas messengers, synthesized by nitric oxide synthase or heme oxygenase 2, respectively, that can activate soluble guanylyl cyclase in adjacent cells. Nitric oxide and carbon monoxide neuromodulation in cardiac ganglia has been demonstrated. However, identification of nitric oxide or carbon monoxide in human cardiac ganglia needs to be confirmed as suggested from animal model studies. Immunohistochemistry was used to demonstrate neuronal nitric oxide synthase, heme oxygenase 2, and soluble guanylyl cyclase immunoreactivity within neurons of adult human cardiac ganglia. Nitric oxide synthase immunoreactivity was present in 37% of neurons within cardiac ganglia, heme oxygenase 2 immunoreactivity in 79%, and soluble guanylyl cyclase in 53%. Our findings support the hypothesis that nitric oxide and carbon monoxide are modulators of neurotransmission in cardiac ganglia and in neural control of the adult human heart.
Asunto(s)
Monóxido de Carbono/metabolismo , Ganglios Parasimpáticos/enzimología , Guanilato Ciclasa/biosíntesis , Neuronas/enzimología , Óxido Nítrico/biosíntesis , Receptores Citoplasmáticos y Nucleares/biosíntesis , Adulto , Anciano , Nodo Atrioventricular/enzimología , Nodo Atrioventricular/metabolismo , Monóxido de Carbono/análisis , Células Cultivadas , Femenino , Ganglios Parasimpáticos/metabolismo , Guanilato Ciclasa/análisis , Hemo Oxigenasa (Desciclizante)/análisis , Hemo Oxigenasa (Desciclizante)/biosíntesis , Humanos , Masculino , Persona de Mediana Edad , Neuronas/metabolismo , Óxido Nítrico/análisis , Óxido Nítrico Sintasa de Tipo I/análisis , Óxido Nítrico Sintasa de Tipo I/biosíntesis , Receptores Citoplasmáticos y Nucleares/análisis , Nodo Sinoatrial/enzimología , Nodo Sinoatrial/metabolismo , Guanilil Ciclasa Soluble , Adulto JovenRESUMEN
Recent studies showed that Eph/Ephrin tyrosine kinase family plays an important role in the development and functional maintenance of the nervous system, but its function in the sympathetic nervous system is still obscure. In the present study, we examined the effect of Eph/Ephrin-B1 signaling on the whole-cell currents mediated by either alpha7 or alpha3-nicotinic acetylcholine receptors (nAChRs) in acutly dissociated ciliary ganglion (CG) neurons. Firstly, we detected the effect of Ephrin-B1 on nAChRs currents. The neurons were randomly divided into control group, Ephrin-B1Fc-treated group that was stimulated by recombinant Ephrin-B1Fc, IgG-treated group, and Ephrin-B1-treated group. Secondly, we studied the regulatory mechanism of Ephrin-B1Fc on nAChRs currents. The neurons were randomly divided into control group, Ephrin-B1Fc-treated group, PP2 (inhibitor of Src tyrosine kinase) or PD98095 (antagonist of mitogen-activated protein kinase)-treated group, Ephrin-B1Fc + PP2 or PD98095-treated group. The results showed that there was no significant difference between the currents in control group, IgG-treated group and Ephrin-B1-treated group, but Ephrin-B1Fc significantly suppressed both alpha3-nAChRs and alpha7-nAChRs-mediated currents (P=0.002, P=0.003). Pretreatment with PP2 or PD98095 could partially rescue the Ephrin-B1Fc-induced suppression of currents mediated by alpha3-nAChRs or alpha7-nAChRs respectively. These results suggest that the Eph/Ephrin-B1 signaling may inhibit alpha3-nAChRs and alpha7-nAChRs-mediated currents on CG neurons, involving Src tyrosine kinase and mitogen-activated protein kinase signaling in the regulation of sympathetic nervous system.
Asunto(s)
Efrina-B1/metabolismo , Ganglios Parasimpáticos/enzimología , Proteínas Quinasas Activadas por Mitógenos/metabolismo , Neuronas/enzimología , Transducción de Señal , Receptor Nicotínico de Acetilcolina alfa 7/metabolismo , Familia-src Quinasas/metabolismo , Receptores Nicotínicos/metabolismoRESUMEN
OBJECTIVES: The goal of this study was to determine the alterations of glial cell line-derived neurotrophic factor family receptor alpha-2 (GFRalpha2) mRNA expression in the major pelvic ganglia (MPG) and their relationship to the marker for the neural plasticity (growth-associated protein 43: GAP-43) and neuronal nitric oxide synthase (nNOS)-positive neurons following cavernous nerve injury. METHODS: Cavernous nerves were transected unilaterally in 24 Sprague-Dawley rats aged 8 weeks. We used nine sham operated same animals as controls. Bilateral MPGs were harvested at 1, 3, and 6 months following nerve injury. The GFRalpha2 and GAP-43 mRNA expressions of the sham group and the injury group (3 months after surgery) were investigated by reverse transcription-polymerase chain reaction. We also investigated the expression profile of GFRalpha2 mRNA by in situ hybridization combined with nNOS immunostaining. RESULTS: It was revealed semi-quantitatively that the GAP43 mRNA expression moderately increased in the intact MPG, and GFRalpha2 mRNA was maintained in the intact MPG but not in the injured one. A histological double-labeling study showed that the number of GFRalpha2 mRNA- and nNOS-positive neurons increased in the intact MPG and most GFRalpha2 mRNA expressions were colocalized with nNOS immunostaining. CONCLUSIONS: The current study suggested that the GFRalpha2 mRNA alteration closely related to the nNOS expression following the cavernous nerve injury, which would be involved in the maintenance and recovery of erectile function.
Asunto(s)
Proteína GAP-43/genética , Ganglios Parasimpáticos/enzimología , Receptores del Factor Neurotrófico Derivado de la Línea Celular Glial/metabolismo , Regeneración Nerviosa/genética , Óxido Nítrico Sintasa de Tipo I/genética , ARN Mensajero/metabolismo , Traumatismos del Sistema Nervioso/enzimología , Animales , Ganglios Parasimpáticos/patología , Expresión Génica , Masculino , Erección Peniana/fisiología , Pene/inervación , Distribución Aleatoria , Ratas , Ratas Sprague-Dawley , Valores de Referencia , Traumatismos del Sistema Nervioso/patologíaRESUMEN
This is the first study to report presence of nitric oxide synthase (NOS) in the human intracardiac nervous cells. By applying immunohistochemical technique it was shown that majority of neuronal perikaryons contain NOS 1 (neuronal NOS). We conclude that in human heart about half of neurons have NO-ergic phenotype. These cells are also cholinergic and related to parasympathetic part of autonomic nervous system. Moreover in human heart NOS contains pericellular baskets that surround intramural neurons. This points to the presence of the enzyme in parasympathetic preganglionic fibers. A substantial differences of patterns of NOS expression in cardiac neural ganglia between humans and experimental animals are discussed.
Asunto(s)
Ganglios Parasimpáticos/enzimología , Corazón/inervación , Miocardio/citología , Óxido Nítrico Sintasa/biosíntesis , Adulto , Biomarcadores/metabolismo , Ganglios Parasimpáticos/citología , Humanos , Inmunohistoquímica , Técnicas In Vitro , Persona de Mediana EdadRESUMEN
3',5'-Cyclic nucleotide phosphodiesterase 11 (PDE11) is the most recently discovered family of human 3',5'-cyclic nucleotide phosphodiesterases (PDEs). This family contains one gene, PDE11A, with four splice variants (PDE11A1-PDE11A4). The physiological role of PDE11A has not been determined. Tadalafil (Cialis), a PDE5A inhibitor used for the treatment of male erectile dysfunction, has been reported to partially inhibit PDE11. It was therefore of interest to consider the pattern of expression of PDE11 in human tissues. Although four PDE11A mRNA transcripts have been reported, we detected protein corresponding to only one of them, PDE11A4, in human prostate, pituitary, heart and liver. Using immunohistochemistry, there was strong PDE11A antibody staining in the glandular epithelium of the prostate and weak staining of neuronal cells within parasympathetic ganglia in the heart. No PDE11A protein was detected in blood vessels or cardiac myocytes. None of the four potential PDE11A proteins were detected in human skeletal muscle, testis, or penis.
Asunto(s)
Hidrolasas Diéster Fosfóricas/genética , Hidrolasas Diéster Fosfóricas/metabolismo , Próstata/enzimología , 3',5'-GMP Cíclico Fosfodiesterasas , Adolescente , Adulto , Anciano , Western Blotting , Femenino , Ganglios Parasimpáticos/enzimología , Humanos , Inmunohistoquímica , Hígado/enzimología , Masculino , Persona de Mediana Edad , Músculo Esquelético/enzimología , Miocardio/enzimología , Pene/enzimología , Hipófisis/enzimología , ARN Mensajero/análisis , Testículo/enzimologíaRESUMEN
The present study was aimed at disclosing the chemical coding of nerve structures in the porcine ciliary ganglion (CG) using immunohistochemical methods. The substances under investigation included markers of "classical" neurotransmitters, choline acetyltransferase (ChAT), vesicular acetylcholine transporter (VAChT), tyrosine hydroxylase (TH) and dopamine beta-hydroxylase (DbetaH) as well as neuropeptides, somatostatin (SOM), galanin (GAL), substance P (SP), calcitonin gene-related peptide (CGRP), vasoactive intestinal polypeptide (VIP) and neuropeptide Y (NPY). Immunoreactivity to ChAT and VAChT was found virtually in all the neuronal somata and in numerous intraganglionic, varicose nerve fibres which often formed basket-like formations around the nerve cell bodies. Many CG neurons contained immunoreactivity for SOM (46%) or GAL (29%). Interestingly, a small number (approx. 1%) of the cholinergic somata stained for TH but not for DbetaH; nevertheless, some extra- and intraganglionic nerve fibres displayed immunoreactivity for DbetaH or TH. The CG perikarya stained neither for vasoactive intestinal polypeptide (VIP) nor for neuropeptide Y (NPY), but some NPY- or VIP-positive nerve terminals were observed within nerve bundles distributed outside the ganglion. SP- and CGRP-immunoreactivity was found in some intraganglionic nerve fibres only. The present study revealed that the porcine CG consists of cholinergic neurons many of which contain SOM and GAL. Thus, it can be assumed that in the pig, these neuropeptides are involved, complementary to acetylocholine, in the parasympathetic postganglionic nerve pathway to structures of the eye including the ciliary and iris sphincter muscles.
Asunto(s)
Ganglios Parasimpáticos/química , Neuronas/química , Neurotransmisores/análisis , Porcinos/metabolismo , Animales , Femenino , Ganglios Parasimpáticos/enzimología , Inmunohistoquímica/veterinaria , Neuronas/enzimologíaRESUMEN
Choline acetyltransferase (ChAT), the synthesizing enzyme for acetylcholine, has been implicated to involve multiple isoforms of ChAT mRNA in several animals. Since these isoforms are mostly non-coding splice variants, only a homologous ChAT protein of about 68 kDa has been shown to be produced in vivo. Recent evidence indicates the existence of a protein coding splice variant of ChAT mRNA, which lacks exons 6-9 of the rat ChAT gene. The encoded protein was designated ChAT of a peripheral type (pChAT), because of its preferential expression in the peripheral nervous system as confirmed by Western blot and immunohistochemistry. However, functional significance of pChAT is unknown. To obtain a clue to this question, we examined a possible difference in intracellular trafficking between pChAT and the well-known ChAT of the common type (cChAT) using green fluorescent protein (GFP) in living human embryonic kidney cells. Confocal laser scanning microscopy revealed that pChAT-GFP was detectable in the cytoplasm but not in the nucleus, whereas cChAT-GFP was found in both cytoplasm and nucleus. Following treatment with leptomycin B, a nuclear export pathway inhibitor, pChAT-GFP became detectable in both cytoplasm and nucleus, indicating that pChAT can be translocated to the nucleus. In contrast, the leptomycin B treatment did not seem to affect the content of intranuclear cChAT-GFP. After incubation with protein kinase C inhibitors, enhanced accumulation of pChAT-GFP but not cChAT-GFP occurred in the nucleus. These results clearly indicate that pChAT varies from cChAT in intracellular transportation, probably reflecting the difference in physiological roles between pChAT and cChAT.
Asunto(s)
Acetilcolina/biosíntesis , Empalme Alternativo/fisiología , Sistema Nervioso Central/enzimología , Colina O-Acetiltransferasa/metabolismo , Sistema Nervioso Periférico/enzimología , Transporte Activo de Núcleo Celular/efectos de los fármacos , Transporte Activo de Núcleo Celular/fisiología , Animales , Núcleo Celular/enzimología , Células Cultivadas , Colina O-Acetiltransferasa/genética , Cuerpo Estriado/enzimología , Citoplasma/enzimología , Inhibidores Enzimáticos/farmacología , Ácidos Grasos Insaturados/farmacología , Ganglios Parasimpáticos/enzimología , Proteínas Fluorescentes Verdes , Humanos , Masculino , Isoformas de Proteínas/genética , Isoformas de Proteínas/metabolismo , Proteína Quinasa C/antagonistas & inhibidores , Proteína Quinasa C/metabolismo , Transporte de Proteínas/efectos de los fármacos , Transporte de Proteínas/fisiología , RatasRESUMEN
The juxtamembrane domain (JMD) of N-cadherin cytoplasmic tail is an important regulatory region of the clustering and adhesion activities of the protein. In addition, the JMD binds a diversity of proteins capable of modifying intracellular processes including cytoskeletal rearrangement mediated by Rho GTPases. These GTPases also function as regulators of voltage-activated calcium channels, which in turn modulate neuronal excitability. The present study was designed to determine whether there is a direct functional link, via Rho GTPase, between the N-cadherin JMD and these voltage-activated channels. It was found that the infusion of the soluble JMD into chick ciliary neurons causes a substantial decrease in the amplitude of the high-threshold voltage-activated (HVA) calcium current. The activation time is increased while the inactivation process is reduced, suggesting that the decreased current amplitude reflects a reduction in the number of channels available to open. This effect was reversed by inhibition of RhoA or its downstream effector, Rho-associated kinase (ROCK). Because ROCK determines the active state of myosin, these results suggest that the modulation of HVA by the JMD could be mediated by changes in the status of the actin-myosin cytoskeleton.
Asunto(s)
Cadherinas/fisiología , Canales de Calcio/fisiología , Señalización del Calcio/fisiología , Calcio/metabolismo , Ganglios Parasimpáticos/fisiología , Proteínas Serina-Treonina Quinasas/fisiología , Proteína de Unión al GTP rhoA/fisiología , ADP Ribosa Transferasas/farmacología , Amidas/farmacología , Animales , Toxinas Botulínicas/farmacología , Cadherinas/química , Adhesión Celular , Embrión de Pollo , Pollos , Ganglios Parasimpáticos/citología , Ganglios Parasimpáticos/enzimología , Péptidos y Proteínas de Señalización Intracelular , Activación del Canal Iónico/fisiología , Transporte Iónico , Neuronas/efectos de los fármacos , Neuronas/enzimología , Neuronas/fisiología , Técnicas de Placa-Clamp , Fosforilación/efectos de los fármacos , Procesamiento Proteico-Postraduccional/efectos de los fármacos , Proteínas Serina-Treonina Quinasas/antagonistas & inhibidores , Estructura Terciaria de Proteína , Piridinas/farmacología , Proteínas Recombinantes de Fusión/química , Proteínas Recombinantes de Fusión/fisiología , Quinasas Asociadas a rho , Proteína de Unión al GTP rhoA/antagonistas & inhibidoresRESUMEN
The tracheal and bronchial parasympathetic ganglia in the cat were studied using the histochemical-tiocholine method of Koelle and Friedenwald and histological techniques. Intensively stained AChE-positive nerve structures, i.e., ganglia and nerve fibres on the wall of the trachea and bronchi, were observed. The ganglia were situated mainly on the dorso-lateral surface of these organs, but they were also present on the ventral surface. The largest ganglia were found in the vicinity of the vagus nerve branches and on the surface of the tracheal smooth muscle. Numerous ganglia (95-210) of different sizes (40 x 230 microm to 260 x 520 microm) and shapes (spindle, longitudinal, oval, elliptical and multiform) were interconnected by nerve fibres and formed a dense ganglionated plexus. The ganglia forming this nerve structure were located mainly on the level of intercartilaginous spaces. They received the nerve branches from the cervical and the upper thoracic branches of vagus nerve and cervical and upper thoracic segments of the sympathetic trunk. Similar AChE-positive ganglionated plexus containing 28-33 ganglia connected by nerve fibres was observed on the posterior wall of the bronchi. Histological investigations confirmed the presence of fascicles of nerve fibers and nerve cells aggregations in the external membrane of the trachea and bronchi. The ganglia consisted of 2-25 cells on the cross-section. They were located mainly on the level of intercartilaginous spaces and contained (except ganglionic neurocytes, nerve fibres) satellite cells and small blood vessels. All the ganglia had thin connective capsule.
Asunto(s)
Acetilcolinesterasa/metabolismo , Bronquios/inervación , Ganglios Parasimpáticos/anatomía & histología , Tráquea/inervación , Acetilcolinesterasa/análisis , Animales , Gatos , Femenino , Ganglios Parasimpáticos/citología , Ganglios Parasimpáticos/enzimología , Histocitoquímica , Masculino , Nervio Vago/citologíaRESUMEN
Tachykinins depolarize guinea pig intracardiac neurons by activating nonselective cationic channels. Recently, members of the transient receptor potential family of membrane channels (TRPC) have been implicated in the generation of G protein-coupled receptor-activated nonselective cationic currents. We have investigated whether guinea pig cardiac neurons exhibit immunoreactivity to TRPC. Our results showed that nerve fibers within guinea pig intrinsic cardiac ganglia exhibited immunoreactivity to TRPC6. After culture of cardiac ganglia whole-mount explants for 72 hours, the TRPC6-IR fiber networks were absent. Therefore, the TRPC6-IR fibers were derived from sources extrinsic to the heart. A small percentage ( approximately 3%) of intracardiac neurons also exhibited TRPC6 immunoreactivity in control preparations, and the percentage of cells exhibiting TRPC6 immunoreactivity was not changed following explant culture for 72 hours. The few intrinsic TRPC6-IR neurons also exhibited nitric oxide synthase (NOS) immunoreactivity, indicating that they were nitrergic as well. We compared the immunohistochemical staining patterns of TRPC6-IR fibers with the staining patterns of a number of other neurotransmitters or neurotransmitter synthetic enzymes that mark specific extrinsic inputs to the intrinsic cardiac ganglia. The TRPC6-IR fibers were not immunoreactive for choline acetyltransferase, tyrosine hydroxylase, or substance P. However, the TRPC6-IR fibers exhibited immunoreactivity to neuronal NOS. Therefore, we propose that the TRPC6-IR fibers within the guinea pig intrinsic cardiac ganglia are vagal sensory fibers that also contain NOS. We found, in support of this conclusion, that TRPC6-IR cells were also present in sections of nodose ganglia.
Asunto(s)
Canales de Calcio/metabolismo , Ganglios Parasimpáticos/enzimología , Cobayas/metabolismo , Corazón/inervación , Miocardio/enzimología , Neuronas Nitrérgicas/enzimología , Óxido Nítrico Sintasa/metabolismo , Nervio Vago/enzimología , Aferentes Viscerales/enzimología , Animales , Axones/enzimología , Axones/ultraestructura , Células Cultivadas , Colina O-Acetiltransferasa/metabolismo , Femenino , Ganglios Parasimpáticos/citología , Inmunohistoquímica , Masculino , Miocardio/citología , Neuronas Aferentes/enzimología , Neuronas Aferentes/ultraestructura , Neuronas Nitrérgicas/citología , Óxido Nítrico/metabolismo , Ganglio Nudoso/citología , Ganglio Nudoso/enzimología , Fibras Simpáticas Posganglionares/citología , Fibras Simpáticas Posganglionares/enzimología , Tirosina 3-Monooxigenasa/metabolismo , Nervio Vago/citología , Aferentes Viscerales/citologíaRESUMEN
The naris muscles control the aperature of the external naris in tiger salamanders, Ambystoma tigrinum, and may contribute to glandular secretion. Autonomic neurons of the palatine ganglion and possibly neurons associated with the nervus terminalis innervate these muscles. To elucidate the neural control of the naris muscles, neurotransmitters in nerve fibers supplying the naris muscles and in neurons of the palatine ganglion were examined using acetylcholinesterase enzyme histochemistry and immunocytochemistry to visualize possible peptide candidates for muscle innervation. The naris muscles, autonomic neurons, and associated nerve fascicles demonstrated strong acetylcholinesterase labeling, and the muscles were innervated by substance P fibers passing through the palatine ganglion from the trigeminal ganglion. Gonadotropin-releasing hormone and molluscan cardioexcitatory peptide-like immunoreactivities were found in secretory cell bodies and/or fibers in the palatine ganglion, and gonadotropin-releasing hormone was found in fiber projection pathways into the muscles. Vasoactive intestinal peptide was found in cell bodies and fibers of the palatine ganglion but appeared to provide a sparse innervation to the naris dilator muscle only. These findings suggest a typical autonomic cholinergic and sensory innervation of the naris muscles with some variations in peptide innervation. The presence of gonadotropin-releasing hormone in palatine ganglion and naris constrictor muscle suggests a potential modulation of autonomic neurons and perhaps even muscle fibers by this neuropeptide. We hypothesize that this reproductive hormone may modulate the activity of the naris constrictor muscle during reproductively appropriate events in order to provide access of pheromones to the vomeronasal organ.
Asunto(s)
Acetilcolinesterasa/metabolismo , Ambystoma , Músculo Esquelético/enzimología , Músculo Esquelético/inervación , Cavidad Nasal/anatomía & histología , Neuropéptidos/metabolismo , Animales , Ganglios Parasimpáticos/citología , Ganglios Parasimpáticos/enzimología , Hormona Liberadora de Gonadotropina/metabolismo , Imagenología Tridimensional , Inmunohistoquímica , Fibras Nerviosas/enzimología , Hueso Paladar/inervación , Coloración y Etiquetado , Sustancia P/metabolismo , Péptido Intestinal Vasoactivo/metabolismoAsunto(s)
Ganglios Parasimpáticos/enzimología , Aparato Lagrimal/enzimología , Proteínas de Transporte de Membrana , Neuronas/enzimología , Óxido Nítrico Sintasa/metabolismo , Proteínas de Transporte Vesicular , Animales , Proteínas Portadoras/metabolismo , Femenino , Ganglios Parasimpáticos/metabolismo , Técnicas Inmunológicas , Aparato Lagrimal/metabolismo , Ratones , Ratones Endogámicos , Neuronas/metabolismo , Óxido Nítrico Sintasa de Tipo I , Valores de Referencia , Distribución Tisular , Proteínas de Transporte Vesicular de AcetilcolinaRESUMEN
It is generally considered that parasympathetic postganglionic nerve fibers innervating the lacrimal gland (LG) arise from the pterygopalatine ganglion (PPG), while sympathetic and sensory innervations arise from the superior cervical ganglion (SCG) and trigeminal ganglion (TG), respectively. Recently, we reported for the first time that the parasympathetic innervation of the cat LG was also provided by the otic ganglion (OG) and ciliary ganglion (CG), and that the sensory innervation was also provided by the superior vagal ganglion (SVG) and superior glossopharyngeal ganglion (SGG). To determine if nitric oxide (NO) is a neurotransmitter of the autonomic and sensory neurons innervating the LG, we injected the cholera toxin B subunit (CTB) as a retrograde tracer into the cat LG, and used double-labeling fluorescent immunohistochemistry for CTB and nitric oxide synthase (NOS). We found that NOS-/CTB-immunofluorescent double-labeled perikarya were localized in the PPG, OG, TG, SVG and SGG, but not in the CG and SCG. The highest numbers of NOS-/CTB-immunofluorescent double-labeled neurons were found in the PPG and TG. In addition, we examined the presence of nitrergic nerve fibers in the LG using NADPH-d histochemistry and found that a large amount of NADPH-d-stained nerve fibers were distributed around the glandular acini and in the walls of glandular ducts and blood vessels. This study provides the first direct evidence showing that NO may act as a neurotransmitter or modulator involved in the parasympathetic and sensory regulation of lacrimal secretion and blood circulation, but may not be implicated in the sympathetic control of LG activities, and that nitrergic nerve fibers in the LG arise mainly from parasympathetic postganglionic neurons in the PPG and sensory neurons in the TG. The present results suggest that NO plays an important role in the regulation of LG activities.
Asunto(s)
Ganglios Parasimpáticos/enzimología , Ganglios Sensoriales/enzimología , Aparato Lagrimal/enzimología , Aparato Lagrimal/inervación , Neuronas/enzimología , Óxido Nítrico Sintasa/metabolismo , Fibras Parasimpáticas Posganglionares/enzimología , Animales , Gatos , Recuento de Células , Toxina del Cólera/farmacocinética , Femenino , Técnica del Anticuerpo Fluorescente , Ganglios Parasimpáticos/citología , Ganglios Sensoriales/citología , Ganglios Simpáticos/citología , Ganglios Simpáticos/enzimología , Nervio Glosofaríngeo/citología , Nervio Glosofaríngeo/enzimología , Aparato Lagrimal/citología , Masculino , NADPH Deshidrogenasa/metabolismo , Neuronas/citología , Óxido Nítrico/metabolismo , Fibras Parasimpáticas Posganglionares/citología , Fibras Simpáticas Posganglionares/citología , Fibras Simpáticas Posganglionares/enzimología , Ganglio del Trigémino/citología , Ganglio del Trigémino/enzimología , Nervio Vago/citología , Nervio Vago/enzimologíaRESUMEN
This study was conducted to determine the origin(s) of neuronal nitric oxide synthase-immunoreactive (NOS-IR) fibers within guinea pig atrial whole-mount preparations containing the cardiac ganglia. Intrinsic NOS-IR cardiac neurons exhibited choline acetyltransferase (ChAT) immunoreactivity, indicating that they were cholinergic as well as nitrergic. Comparison of control versus 72-hour explant culture preparations indicated that most of the nitrergic fibers within cardiac ganglia were extrinsic. The extrinsic NOS-IR fibers were not IR for ChAT (marker of preganglionic parasympathetic neurons), tyrosine hydroxylase (marker of catecholaminergic sympathetic postganglionic axons), or calcitonin gene-related peptide (CGRP) (marker of afferent fibers). Separate NOS-IR and ChAT-IR neurons were present within medullary regions containing the cardiovascular regulatory nuclei (nucleus ambiguus and dorsal motor nucleus of the vagus), but no cells were found that exhibited both NOS immunoreactivity and ChAT immunoreactivity. The small size and location of the medullary NOS-IR neurons suggested they were probably interneurons. Only an occasional sympathetic postganglionic cell in the stellate ganglion complex exhibited NOS immunoreactivity. NOS-IR cells were present in dorsal root ganglia (thoracic 1-5), but these typically also exhibited CGRP immunoreactivity. NOS-IR cells were also present in the nodose ganglia, but only some exhibited CGRP immunoreactivity. We concluded that virtually all the extrinsic NOS-IR nerve fibers represented an afferent fiber input that was separate from the substance P (SP)/CGRP-containing population of sensory fibers. Furthermore, much of this NOS innervation is probably derived from the nodose ganglia.
Asunto(s)
Ganglios Parasimpáticos/enzimología , Cobayas/metabolismo , Sistema de Conducción Cardíaco/enzimología , Bulbo Raquídeo/enzimología , Fibras Nerviosas/metabolismo , Óxido Nítrico Sintasa/metabolismo , Vías Aferentes/enzimología , Animales , Colina O-Acetiltransferasa/metabolismo , Femenino , Ganglios Parasimpáticos/citología , Ganglios Parasimpáticos/fisiología , Ganglios Espinales/citología , Ganglios Espinales/enzimología , Ganglios Espinales/fisiología , Ganglios Simpáticos/citología , Ganglios Simpáticos/enzimología , Ganglios Simpáticos/fisiología , Sistema de Conducción Cardíaco/citología , Sistema de Conducción Cardíaco/fisiología , Inmunohistoquímica , Masculino , Neuronas/enzimología , Óxido Nítrico Sintasa de Tipo I , Valores de Referencia , Transmisión Sináptica/fisiología , Distribución Tisular , Nervio Vago/citología , Nervio Vago/enzimología , Nervio Vago/fisiologíaRESUMEN
Central cholinergic systems have been visualized by immunohistochemistry using antibodies to choline acetyltransferase (ChAT). Peripheral cholinergic cells and fibers, however, have been hardly detectable with most of these antibodies. This phenomenon suggests that a different form of ChAT may exist in peripheral tissues. Here we report two types of mRNA for ChAT expressed by alternative splicing in rat pterygopalatine ganglion. One is exactly identical with ChAT mRNA reported in the central nervous system (ChAT of a common type; cChAT). The other lacks exons 6, 7, 8 and 9, which was detected only in the pterygopalatine ganglion (ChAT of a peripheral type; pChAT). The peculiarity of pChAT in chemical structure, possessing a splice joint of the exons 5 and 10, led us to produce rabbit antisera against a recombinant peptide of 41 amino acids which spans over the splice joint. On Western blots using a successfully obtained antiserum, an intense band of about 50 kDa, corresponding to the expected molecular weight of pChAT, was detected in the pterygopalatine ganglion but not in the brain. Immunohistochemistry using the antiserum failed to reveal positive staining of known brain cholinergic structures, while it permitted us to observe peripheral, probably cholinergic, nerve cells and fibers including those in the pterygopalatine ganglion and enteric nervous system.
Asunto(s)
Empalme Alternativo , Colina O-Acetiltransferasa/genética , Ganglios Parasimpáticos/enzimología , Variación Genética , Fibras Nerviosas/enzimología , Neuronas/enzimología , ARN Mensajero/genética , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Colina O-Acetiltransferasa/análisis , Colina O-Acetiltransferasa/química , Cartilla de ADN , Dihidrolipoamida Deshidrogenasa/análisis , Exones , Sueros Inmunes , Inmunohistoquímica , Masculino , Datos de Secuencia Molecular , Fragmentos de Péptidos/química , Reacción en Cadena de la Polimerasa , Conejos , Ratas , Ratas WistarRESUMEN
The expression of inducible and constitutive heme oxygenase and biliverdin reductase was studied in normal and cultured peripheral ganglia from adult rats, using immunocytochemistry and in situ hybridization. Dramatic changes were induced by one to two days' culturing of dorsal root ganglia, nodose ganglia, otic ganglia, sphenopalatine ganglia and superior cervical ganglia. An up-regulation of inducible heme oxygenase was found in satellite cells of the cultured nodose ganglia, dorsal root ganglia, sphenopalatine ganglia and otic ganglia, whereas only a few satellite cells in the superior cervical ganglia responded with an increase in inducible heme oxygenase immunoreactivity. In the superior cervical ganglia inducible heme oxygenase also appeared in a subpopulation of macrophages. During culturing, expression of inducible heme oxygenase immunoreactivity also increased in axons and in nerve cell bodies. In situ hybridization corroborated the immunocytochemical findings, revealing a strong up-regulation of inducible heme oxygenase messenger RNA in satellite cells, and less pronounced up-regulation in nerve cell bodies. Constitutive heme oxygenase immunoreactivity was found in most neurons in all of the ganglia studied. No significant changes in constitutive heme oxygenase immunoreactivity could be observed in cultured ganglia. Biliverdin reductase immunoreactivity was barely detectable in any of the normal ganglia; however, after culturing it appeared in axons, single nerve cell bodies and nerve cell nuclei. The results show that inducible heme oxygenase is up-regulated in peripheral ganglia after axonal injury, and suggest a role for carbon monoxide in cellular signaling and a requirement for the antioxidant (bilirubin) during the regeneration process.
Asunto(s)
Ganglios/enzimología , Hemo Oxigenasa (Desciclizante)/metabolismo , Plasticidad Neuronal/fisiología , Oxidorreductasas actuantes sobre Donantes de Grupo CH-CH , Oxidorreductasas/metabolismo , Animales , Femenino , Ganglios Parasimpáticos/enzimología , Ganglios Sensoriales/enzimología , Ganglios Espinales/enzimología , Hemo-Oxigenasa 1 , Ratas , Ratas Sprague-Dawley , Ganglio Cervical Superior/enzimologíaRESUMEN
The avian ciliary ganglion (CG) controls choroidal blood flow by its choroidal neurons, and pupil constriction and accommodation by its ciliary neurons. It was previously reported that both choroidal and ciliary neurons label positively for NADPH diaphorase (NADPHd), a marker for nitric oxide synthase (NOS). To assess if this labeling is preganglionic or postganglionic and to determine if it is attributable to neuronal NOS (nNOS), we studied pigeon CG using NADPHd histochemistry and nNOS immunohistochemistry (IHC). Short-duration staining times by NADPHd histochemistry yielded intense labeling of structures that appeared to be the cap-like endings on ciliary neurons and the boutonal endings on choroidal neurons that arise from the nucleus of Edinger-Westphal (EW), and light or no postganglionic perikaryal staining. The light postganglionic staining that was observed tended to be localized to ciliary neurons. Consistent with this, NADPHd+ nerve fibers were observed in the postganglionic ciliary nerves but rarely in the postganglionic choroidal nerves. These same staining times yielded robust staining of neurons in the orbital pterygopalatine microganglia network, which are known to be nNOS+. Diffuse staining of CG perikarya was observed with longer staining durations, and this staining tended to mask the preganglionic labeling. Preganglionic NADPHd+ staining in CG with short staining times was blocked by the NOS inhibitors iodonium diphenyl (IDP) and dichlorophenol-indophenol (DPIP), but the diffuse postganglionic staining observed with the longer staining times was not completely blocked. Labeling of CG sections for substance P (SP) by IHC (which labels EW-originating preganglionic endings in CG) and subsequently for NADPHd confirmed that NADPHd was localized to preganglionic endings on CG neurons. Immunohistochemical double labeling for nNOS and SP or enkephalin further confirmed that nNOS is found in boutonal and cap-like endings in the CG. Two studies were then carried out to demonstrate that the nNOS+ preganglionic endings in CG arise from EW. First, NADPHd+ and nNOS+ neurons were observed in EW in pigeons treated with colchicine to enhance perikaryal labeling. Second, NADPHd+ and nNOS+ preganglionic endings were eliminated from CG ipsilateral to an EW lesion. These various results indicate that NOS is present in EW-arising preganglionic endings on choroidal and ciliary neurons in avian CG. NOS also appears to be found in some ciliary neurons, but its presence in choroidal neurons is currently uncertain.
Asunto(s)
Fibras Autónomas Preganglionares/enzimología , Columbidae/metabolismo , Ganglios Parasimpáticos/enzimología , Óxido Nítrico Sintasa/análisis , Nervio Oculomotor/enzimología , Animales , Coroides/irrigación sanguínea , Inmunohistoquímica , NADPH Deshidrogenasa/análisis , Proteínas del Tejido Nervioso , Óxido Nítrico Sintasa de Tipo IRESUMEN
The distribution of neuronal-constitutive nitric oxide synthase (ncNOs)-positive nerve fibres was compared immunohistochemically, and the effect of NOs inhibitor and NO scavenger on the secretory response was compared functionally, in the two glands. Numerous ncNOs-positive fibres were distributed around acini in the submandibular gland but scarcely any around acini in the sublingual gland. Within the submandibular ganglion (parasympathetic), the nerve-cell bodies were strongly positive. Within the superior cervical ganglion (sympathetic), the nerve-cell bodies were negative, although some positive nerve fibres were observed. The secretory responses to the electrical stimulation of the chorda were significantly reduced by the NOs inhibitor, N(G)-nitro-L-arginine methyl ester (L-NAME, 10(-9)-10(-3) M) in a dose-dependent manner. The NO scavenger, 2-(4-carboxyphenyl)4,4,5,5-tetramethylimidazoline-1-oxyl 3-oxide (carboxy-PTIO) also reduced the chorda-evoked secretion (10(-9)-10(-6) M). The submandibular secretions evoked by stimulation of the superior cervical ganglion were not affected by L-NAME or carboxy-PTIO. In the sublingual gland, neither L-NAME nor carboxy-PTIO affected chorda-evoked salivary secretion. The histochemical and functional results both suggest that NO plays an excitatory role in the regulation of parasympathetic nerve-induced salivary secretion in the rat submandibular gland, but not in the sublingual gland.
Asunto(s)
Fibras Nerviosas/enzimología , Neuronas/enzimología , Óxido Nítrico Sintasa/metabolismo , Óxido Nítrico/fisiología , Sistemas de Mensajero Secundario/fisiología , Glándula Sublingual/efectos de los fármacos , Glándula Submandibular/efectos de los fármacos , Animales , Benzoatos/farmacología , Nervio de la Cuerda del Tímpano/efectos de los fármacos , Nervio de la Cuerda del Tímpano/fisiología , Relación Dosis-Respuesta a Droga , Estimulación Eléctrica , Inhibidores Enzimáticos/administración & dosificación , Inhibidores Enzimáticos/farmacología , Depuradores de Radicales Libres/farmacología , Ganglios Parasimpáticos/efectos de los fármacos , Ganglios Parasimpáticos/enzimología , Imidazoles/farmacología , Inmunohistoquímica , Masculino , NG-Nitroarginina Metil Éster/administración & dosificación , NG-Nitroarginina Metil Éster/farmacología , Fibras Nerviosas/efectos de los fármacos , Neuronas/efectos de los fármacos , Óxido Nítrico/antagonistas & inhibidores , Óxido Nítrico Sintasa/antagonistas & inhibidores , Ratas , Ratas Wistar , Sistemas de Mensajero Secundario/efectos de los fármacos , Glándula Sublingual/inervación , Glándula Sublingual/metabolismo , Glándula Submandibular/inervación , Glándula Submandibular/metabolismo , Ganglio Cervical Superior/efectos de los fármacos , Ganglio Cervical Superior/enzimologíaRESUMEN
It is known that the vagus nerve contains catecholaminergic fibers. However, the origin of these fibers has not been systematically examined. In this study, we addressed this issue using retrograde tracing from the subdiaphragmatic vagus nerve combined with immunocytochemistry. The cervical and thoracic sympathetic trunk ganglia, the nodose ganglia and the dorsal motor nucleus of the vagus nerve were examined following injection of Fluoro-Gold or cholera toxin horseradish peroxidase conjugate into the trunks of the subdiaphragmatic vagus nerve of rats. Numerous retrogradely labeled neurons were seen in the nodose ganglion and the dorsal motor nucleus of the vagus nerve. Very few labeled neurons were found in the sympathetic ganglia (less than 0.06% of the neurons in either superior cervical ganglion or cervicothoracic ganglion were retrogradely labeled). Double labeling with immunofluoresence for catecholamine synthesizing enzymes revealed that: (1) 92% of all Fluoro-Gold retrogradely labeled tyrosine hydroxylase immunoreactive neurons were found in parasympathetic sources (75% in the dorsal motor nucleus of the vagus nerve and 17% in the nodose ganglia), and only 8% in the cervicothoracic sympathetic ganglia; (2) 12% of the retrogradely labeled catecholaminergic neurons in the dorsal motor nucleus of the vagus nerve were also dopamine-beta-hydroxylase immunopositive neurons; (3) 70% of the retrogradely labeled neurons in the sympathetic ganglia were tyrosine hydroxylase immunopositive and 54% of these catecholaminergic neurons contained dopamine-beta-hydroxylase, while 30% of the retrogradely labeled neurons were non-catecholaminergic neurons. These results indicate that catecholaminergic fibers in the abdominal vagus nerve are primarily dopaminergic and of parasympathetic origin, and that only an extremely small number of these fibers, mostly noradrenergic in nature, arise from postganglionic sympathetic neurons.