The distribution of neuropeptide Y-immunoreactive neurons and nerve fibers in the forebrain of the carp Cyprinus carpio L

The present study reports the distribution of Neuropeptide Y (NPY)-immunoreactive neurons and fibers in the forebrain of the adult carp Cyprinus carpio L. Serial Nissl-stained sections were used for cytoarchitecture and identification of anatomical structures. Immunostaining of NPY-containing neurons and fibers was used as neurochemical marker and tool for comparison with other species, including the goldfish.The general outline of the cytoarchitecture of the carp forebrain is similar to that of other Cypriniformes. However, using NPY immunohistochemistry, we found several specific differences with the goldfish, especially in the diencephalon. In the hypothalamus of the carp NPY-immunoreactive (NPYir) neurons were identified in the n. dorsolateralis thalami, and in the n. ventralis lateralis thalami. In the same location, we observed the n. anterior hypothalami and the n. preglomerulosus pars lateralis, described in the goldfish, as parts of n. prerotundus. However, in the carp we were not able to identify a n. preglomerulosus pars medialis, a n. preglomerulosus pars medialis commissuralis and a n. glomerulosus. We describe a n. rotundus, in which we did not find substructures typical of the goldfish.Further differences with the goldfish, trout and salmon were also noted.     

Analysis of lymphocyte heterogeneity in carp, Cyprinus carpio L., using monoclonal antibodies

Several in vivo and in vitro studies on functional aspects of fish lymphocytes have led to the assumption that lymphoid cell populations analogous to T- and B-cells in higher vertebrates are also present in teleosts. However, formal proof of such heterogeneity based on structure-function correlations is lacking. In this report, data on the reactivity of a number of monoclonal antibodies made against thymocytes or serum immunoglobulin of carp (Cyprinus carpio L.) are reviewed. The data suggest that the use of monoclonal antibodies will provide powerful tools with which to identify and separate structurally heterogeneous populations of fish lymphocytes so that their relative roles in the defense system of these vertebrates can be explored and exploited.     

Investigation of Van Gogh-like 2 mRNA regulation and localisation in response to nociception in the brain of adult common carp (Cyprinus carpio)

The Van Gogh-like 2 (vangl2) gene is typically associated with planar cell polarity pathways, which is essential for correct orientation of epithelial cells during development. The encoded protein of this gene is a transmembrane protein and is highly conserved through evolution. Van Gogh-like 2 was selected for further study on the basis of consistent regulation after a nociceptive stimulus in adult common carp and rainbow trout in a microarray study. An in situ hybridisation was conducted in the brain of mature common carp (Cyprinus carpio), 1.5 and 3 h after a nociceptive stimulus comprising of an acetic acid injection to the lips of the fish and compared with a saline-injected control. The vangl2 gene was expressed in all brain regions, and particularly intensely in neurons of the telencephalon and in ependymal cells. In the cerebellum, a greater number (P = 0.018) of Purkinje cells expressed vangl2 after nociception (n = 7) compared with controls (n = 5). This regulation opens the possibility that vangl2 is involved in nociceptive processing in the adult fish brain and may be a novel target for central nociception in vertebrates.     

Distribution of somatostatin- and neuropeptide Y-immunoreactive nerve fibers in the porcine female reproductive system.

The localization and distribution of somatostatin and neuropeptide Y were studied in the porcine female reproductive system with the indirect immunofluorescence technique. Somatostatin-immunoreactive nerve fibers were observed in different parts of the ovary and in the muscular membrane of the uterus as well as in the mesosalphinx. Somatostatin-immunoreactive neurons were detected in the inferior mesenteric ganglion. Neuropeptide Y immunoreactivity was present in a large number of nerve fibers distributed in different regions of the uterus, oviduct and ovary. The present results suggest that the porcine female genital organs receive innervation by somatostatin- and neuropeptide Y-containing nerve fibers, but their exact functional role remains to be established.     

Electrical self-stimulation deficits in the anterior and posterior parts of the medial forebrain bundle after ibotenic acid lesion of the middle lateral hypothalamus

The aim of the present study was to analyse the involvement of the intrinsic neurons located in the middle lateral hypothalamus in electrical self-stimulation measured with electrodes in the anterior and posterior parts of the medial forebrain bundle. In rats without hypothalamic lesions, self-stimulation rates from both anterior and posterior electrodes were similar on either side of the brain. For all rats with ibotenic acid-induced lesions in the lateral hypothalamus, self-stimulation rates were lower with electrodes in the area of the lesion, while self-stimulation on the contralateral side was normal. In rats with electrodes in the anterior hypothalamus, the lesion produced a large deficit when stimulation was applied to the anterior electrode ipsilateral to the lesion. Only three rats showed a decrease in self-stimulation with stimulation of the posterior hypothalamic electrode ipsilateral to the lesion; self-stimulation of the other three rats was normal. These results suggest that self-stimulation in the anterior part of the medial forebrain bundle is supported by long fibers originating in the middle part of the lateral hypothalamus, while self-stimulation in the posterior part of the lateral hypothalamus can be influenced by another system not involved in reward processes observed in the rostral part of the medial forebrain bundle.     

Astroglial architecture of the carp ( Cyprinus carpio ) brain as revealed by immunohistochemical staining against glial fibrillary acidic protein (GFAP)

 The present paper is the first comprehensive study on the astroglia of a teleost fish that is based on the immunohistochemical staining of GFAP (glial fibrillary acidic protein, an immunohistochemical marker of astroglia). The ray-finned fishes (Actinopterygii) and their largest group, the Teleostei, represent a separate pathway of vertebrate evolution. Their brain has a very complex macroscopic structure; several parts either have no equivalents in tetrapods or have a very different shape, e.g., the telencephalon. The results show that the teleost brain has a varied and highly specialized astroglial architecture. The primary system is made up of radial glia, which are of ependymal origin and cover the pial surface with endfeet. The tendency is, however, that the more caudal a brain area is, the less regular is the radial arrangement. A typical radial glia dominates some parts of the diencephalon (median eminence, lobus inferior and habenula) and the telencephalon. In the rest of the diencephalon and in the mesencephalon, the course of the glial fibers is modified by brain tracts. The most specialized areas of the teleost brain, the optic tectum and the cerebellum, display elaborate variations of the original radial system, which is adapted to their layered organization. In the cerebellum, an equivalent of the Bergmann-glia can be found, although its fiber arrangement shows meaningful differences from that of mammals or birds. In the lower brain stem radial glia are confined to fibers separating the brain tracts and forming the midline raphe. A dense ependymoglial plexus covers the inner surface of the tectum and the bottom of the rhombencephalic ventricle, intruding into the vagal and facial lobes. The structure and the position of the rhombencephalic plexus suggest that it corresponds to a circumventricular organ that entirely occupies the bottom of the ventricle. Perivascular glia show an unusual form as they consist of long fibers running along the blood vessels. In the large brain tracts long glial fibers run parallel with the course of the neural fibers. At least in the diencephalon, these glial fibers seem to be modified radial fibers. Real astrocytes (i.e., stellate-shaped cells) can be found only in the brain stem and even there only rarely. The glial specialization in the various areas of the teleost brain seems to be more elaborate than that found either in amphibia or in reptiles. Accepted: 15 May 1998     

Ontogeny of GABA-immunoreactive neurons in the central nervous system in a teleost, Gasterosteus aculeatus L.

The inhibitory neurotransmitter γ-aminobutyric acid (GABA) is known to exert various neurotrophic actions in the developing nervous system, but little is known about its distribution in the central nervous system during early development. We have studied the development of GABA-immunoreactive (GABAir) neurons during embryogenesis of a teleost fish, the three-spined stickleback. As early as 51 h postfertilization (PF; hatching occurs 144–168 h PF, and the first monoaminergic neurons appear around 72 h PF) GABAir neurons appear in the ventral prosencephalon caudal to the optic recess, in the ventral meencephalon, and in the spinal cord. Then, there is a gradual addition of GABAir cell groups in the rostral prosencephalon and ventral rhombencephalon (66 h PF), dorsal and caudal hypothalamus and pretecturn (72 h PF), ventral hypothalamus (78 h PF), preoptic region, thalamus, and in the meencephalon and rhombencephalon (96 h PF). GABAir axons appear in the spinal cord already at 51 h PF, and then gradually appear in the various tracts of the early axonal scaffold of pathfinding fibers, so that by 96 h PF the entire axonal scaffold contains GABAir fibers. It appears likely that GABAergic axons contribute a major population to the formation of the axonal scaffold. Moreover, in the prosencephalon GABAir neurons are arranged in clusters that may reflect a neuromerec organization with six prosencephalic neuromeres.     

雌激素撤退大鼠海马和基底前脑神经元线粒体超微结构的观察

目的观察在去卵巢后海马CA1区锥体细胞和基底前脑外侧隔核神经元线粒体超微结构的变化情况。方法雌性SD大鼠8只,随机分为正常对照组(4只)和OVX组(4只)。采用去卵巢(ovariectomized,OVX)SD大鼠模型,OVX组行双侧卵巢切除术,术后第12天,常规固定、包埋,透射电镜观察海马CA1区锥体细胞和基底前脑外侧隔核神经元线粒体结构。结果与正常对照组相比,OVX组海马CA1区锥体细胞部分线粒体肿胀较明显,嵴出现断裂和脱落,部分线粒体空泡化;但基底前脑线粒体基本正常。结论大鼠去势12d后,其海马易感区神经元线粒体超微结构发生改变,并可能引起神经元退变,为女性更年期后老年性痴呆易感性增加提供了有益的线索。     

Transient and prolonged facilitation of tone-evoked responses induced by basal forebrain stimulations in the rat auditory cortex

We investigated the relationships between cortical arousal and cholinergic facilitation of evoked responses in the auditory cortex. The basal forebrain (BF) was stimulated unilaterally, while cluster recordings were obtained simultaneously from both auditory cortices in urethane-anesthetized rats. The global electroencephalogram (EEG; large frontoparietal derivation) and the local EEG (from the auditory cortex) were recorded. The BF was stimulated at two intensities, a lower one which did not desynchronize the EEG and a higher one which did. Twenty pairing trials were delivered, during which a tone was presented 50 ms after the end of the BF stimulation. At low intensity, the pairing procedure led to a transient increase in the ipsilateral tone-evoked responses. At high intensity, the pairing increased the ipsilateral evoked responses up to 15 min after pairing. Such effects were not observed for the contralateral recordings. Systemic atropine injection prevented the facilitations observed ipsilaterally. BF stimulations alone did not induce any increased evoked response either at low or at high intensity. These results show (1) that a tone, presented while the cortex is activated by cholinergic neurons of the BF, evokes enhanced cortical responses, and (2) that the duration of this facilitation is dependent on the stimulation intensity. These results are discussed in the context of neural mechanisms involved in general arousal and cortical plasticity.     

Seasonal sexually dimorphic distribution of neuropeptide Y-like immunoreactive neurons in the forebrain of the lizard Podarcis hispanica

Since neuropeptide Y (NPY) is involved in several sex-specific physiological and behavioral processes, a sexual dimorphic distribution is expected in forebrain areas that take part in the control of reproduction physiology and sexual behavior. This question has been studied in the lizard Podarcis hispanica by comparing the distribution of NPY-like immunoreactive cells in several forebrain areas of males and females during the season of active (spring/summer) and inactive (fall/winter) reproductive activity. Both qualitative observations and statistical analysis (analysis of variance) indicate that the number of reactive cells within two forebrain areas, the lateral septum and the periventricular preoptic nucleus, depends on the sex (P = 0.02) and season (P = 0.03) and that, in fact, intersexual differences depend on the season of the reproductive annual cycle (P = 0.046). Other areas, such as the amygdaloid nucleus sphericus, show neither sexual dimorphism (P = 0.67), nor seasonal variation in the number of reactive cells (P = 0.18), nor seasonal variation of the intersexual differences (P = 0.75). When analyzed independently, the lateral septum shows a clear sexual dimorphism in favour of females (P = 0.003) whereas the number of reactive cells in the periventricular preoptic nucleus is significantly higher (P = 0.006) in males than in females. In the case of the preoptic nucleus, this sexual dimorphism is clearly accentuated during the season of reproductive activity (P = 0.007), but this dependence is not so clear for the lateral septum (P = 0.059). In the light of these findings the possible roles of NPY on the regulatory mechanisms of sexual behavior and other aspects of the physiology of reproduction are discussed.     

The distribution of zinc in the forebrain and midbrain of the lizard Gekko gecko

Summary The distribution of zinc in the forebrain and midbrain of the lizard Gekko gecko was studied with the recently modified Timm method. Areas with a high intensity of staining are almost exclusively found in the telencephalon, although also some structures in the diencephalon display notable staining. Cortical areas that stain heavily are the deep zone of the subcortical layer of the small-celled medial cortex, the longitudinal association bundle that encompasses the large-celled medial cortex, and the dorsal cortex. Of the subcortical areas, particularly the anterior septal nucleus shows a high intensity of staining. Moderate to dense Timm staining is further observed in the ventral part of the anterior lateral cortex, the lateral septal nucleus, the striatum, the amygdaloid complex, and the dorsal ventricular ridge. Staining in the diencephalon is primarily confined to the stria terminalis and the ventromedial hypothalamic nucleus, whereas in the midbrain weak staining is observed in the ventral tegmental area and the periventricular layers of the tectum and the tegmentum. The presence of zinc in the gekkonid brain is discussed in relation to connections and neurotransmitters as studied in the same species. Moreover, similarities in pattern of staining for zinc in mammals and reptiles and possible evolutionary implications are mentioned.Abbreviations Acc nucleus accumbens - Alh area lateralis hypothalami - Amc nucleus centralis amygdalae - Ame nucleus externus amygdalae - Aml nucleus lateralis amygdalae - Anm nucleus marginalis amygdalae - Bmfb bed nucleus of the medial forebrain bundle - Cgld corpus geniculatum laterale pars dorsalis - Cglv corpus geniculatum laterale, pars ventralis - Cgp corpus geniculatum pretectale - cpa commissura pallii anterior - cso commissura supraoptica - Cxd cortex dorsalis - Cxla cortex lateralis, pars anterior - Cxlp cortex lateralis, pars posterior - Cxml cortex medialis, large-celled part - Cxms cortex medialis, small-celled part - Dlh nucleus dorsolateralis hypothalami - Dll nucleus dorsolateralis thalami, large-celled part - Dls nucleus dorsolateralis thalami, small-celled part - Dm nucleus dorsomedialis thalami - DVR dorsal ventricular ridge - Ent nucleus entopeduncularis - Hab ganglion habenulae - lfb lateral forebrain bundle - lfbv lateral forebrain bundle, ventral peduncle - Lte nucleus lentiformis thalami, pars extensa - Ltp nucleus lentiformis thalami, pars plicata - Mp nucleus medialis posterior - Mt nucleus medialis thalami - NdB nucleus of the diagonal band of Broca - Nsa nucleus septalis anterior - Nsd nucleus septalis dorsalis - Nsl nucleus septalis lateralis - Nsm nucleus septalis medialis - Nsph nucleus sphericus - oph organon periventriculare hypothalami - Ph nucleus periventricularis hypothalami - Ppo periventricular preoptic area - Rot nucleus rotundus - Rub nucleus ruber - Sped nucleus suprapeduncularis - st stria terminalis - Str striatum - tect tectum - topt tractus opticus - Torc nucleus centralis of the torus semicircularis - Torl nucleus laminaris of the torus semicircularis - tsh tractus septohypothalamicus - Vltv nucleus ventrolateralis thalami, pars ventralis - Vmh nucleus ventromedialis hypothalami - Vmt nucleus ventromedialis thalami - VTA ventral tegmental area - III nucleus nervi oculomotorii     

Immunohistochemical demonstration of serotonin nerve fibers in the subthalamic nucleus of the rat, cat and monkey

Distribution of serotonin-immunoreactive nerve fibers (5-HT fibers) in the subthalamic nucleus (STN) of the rat, cat and monkey was examined with a modified peroxidase-anti-peroxidase method using 5-HT antiserum without pretreatment. Fine varicose 5-HT fibers formed a fine network in the STN. Overall density of 5-HT fibers in the STN was highest in the monkey, and lowest in the rat. In the rat and cat, these fibers were distributed almost diffusely in the STN, whereas in the monkey they were particularly abundant in the ventral and medial parts of the STN. Many thick 5-HT fibers ran through the monkey STN.     

Response of medial telencephalic neurons to stimulation in reinforcing sites in the medial forebrain bundle and ventral tegmental area.

Responses of 361 single units recorded extracellularly in various medial telencephalic loci (?2.5 mm from midline) to stimulation in behaviorally-verified, intracranial self-stimulation (ICSS) sites were studied in rats lightly anesthetized with halothane. Trains of 100 Hz stimulation in ICSS sites at behaviorally effective intensities produced widespread effects on telencephalic neurons; 78% showed a short-term response (duration <1.5 sec), a long-term response (duration several sec), or both. Most areas had no single predominant type of response and showed a mixture of ON and OFF short-term responses. Exceptional regions were the superficial layers of cortex, predominantly ON responses, and the lateral septal region, predominantly OFF responses. The responses in most regions were similar to barpressing ICSS in that they directly depended on pulse frequency, i.e., 100 Hz stimulation produced a stronger response than 50 or 25 Hz. The septal region was high in frequency dependent response whereas the globus pallidus and olfactory nuclei were low. Short-term OFF responses were more often frequency dependent than ON responses, particularly those associated with short-latency (?20 msec) spike discharges. Stimulation in two ICSS sites tested on the same neuron produced more mutual OFF responses than mutual ON responses. The results indicate that ICSS has pervasive influences in the telencephalon. Of these influences, the inhibitory types appear to be most consistently related to ICSS behavior.     

Evidence for the occurrence of an enkephalin-like peptide in adrenaline and noradrenaline neurons of the rat medulla oblongata

Summary The indirect immunofluorescence technique was used to analyze the catecholaminergic neurons in the medulla oblongata of the rat for the presence of enkephalin (ENK) — and neuropeptide Y (NPY)-like immunoreactivity (LI). In colchicine pretreated animals, using a double staining technique with mouse and rabbit antibodies against ENK and tyrosine hydroxylase (TH) or phenylethanolamine N-methyltransferase (PNMT), it was demonstrated that both TH-and ENK-LI occurred in the same neurons, particularly in many neurons of the A1 noradrenaline cell group. In the transition zone to the C1 adrenaline cell group, a proportion of PNMT-positive cells also contained ENK-LI. In the rostral and mid portion of the C1 group only few TH/PNMT-positive cells were found to be ENK-positive. In the noradrenergic A2 region, a moderate number of cell bodies also contained TH plus ENK-LI, whereas only a few of the adrenaline cells of the C2 and C3 groups showed ENK-LI. In addition, with an elution restaining technique it was possible to demonstrate that several of the cells containing TH-and ENK-LI were also positive for NPY-LI. The present findings demonstrate that a subpopulation of the catecholaminergic neurons in the medulla oblongata of the rat is ENK positive, thereby indicating a possible co-release of the two compounds in their projection areas, for example the paraventricular nucleus and the spinal cord.     

The relationship between ventral striatal efferent fibers and the distribution of peptide-positive woolly fibers in the forebrain of the rhesus monkey.

Peptidergic fibers in the globus pallidus of the monkey appear in the morphological form referred to as woolly fibers. These fibers are composed of a dense plexus of thin beaded axons which ensheath an unstained central core. Such structures are not confined to the globus pallidus, but are also present in the bed nucleus of the stria terminalis, the hypothalamus, the dorsal part of the amygdala, and ventrally in the basal forebrain. The present study describes the relationship between projections from the rostral and ventral striatum and the enkephalin- and substance P-positive woolly fibers. Following injections of either tritiated amino acids or the lectin Phaseolus vulgaris-leucoagglutinin in the ventral striatum, anterogradely labeled fibers and terminals in the forebrain were visualized simultaneously with enkephalin- or substance P immunoreactivity in the same tissue section in order to determine: (i) the extent to which the woolly fiber distribution represents striatal output systems; (ii) whether woolly fibers can be considered as a marker for the entire striatal forebrain projection; and (iii) whether enkephalin and substance P are involved differentially in distinct ventral striatopallidal pathways. Phaseolus vulgaris-leucoagglutinin labeling is seen in the globus pallidus and adjacent structures either as single, beaded fibers or in a profile strikingly similar to that of woolly fibers. In tissue sections treated for a double immunohistochemical protocol, following which the Phaseolus vulgaris-leucoagglutinin-immunoreactive fibers turn black and the peptidergic woolly fibers brown; many of the lectin-positive fibers are seen to enter the peptide-positive woolly fiber plexus. Likewise, following the injections with tritiated amino acids in the ventral striatum, coarse structures that have dimensions resembling those of the woolly fibers are identified. In sections immunohistochemically stained and subsequently treated for autoradiography, peptide-positive woolly fibers can be identified underlying the silver grains. In sections stained for both peptide immunoreactivity and tracer substances, enkephalin or substance P-positive woolly fibers are present in all pallidal regions that receive ventral striatal input. However, the ventral striatum also sends fibers to the hypothalamus, bed nucleus of the stria terminalis, the dorsal part of the amygdala, the septum, the preoptic area, and other areas of the basal forebrain. In these nuclei the peptide-positive woolly fiber distribution is less extensive than the terminal labeling. The distribution of substance P-positive fibers in the subcommissural pallidal region is more limited than the distribution of enkephalinergic fibers.(ABSTRACT TRUNCATED AT 400 WORDS)     

The distribution of GABA-immunoreactive neurons in the brain of the silver eel (Anguilla anguilla L.)

The distribution of GABA-immunoreactivity was studied in the brain of the silver eel (Anguilla anguilla) by means of antibodies directed against GABA. Immunoreactive neuronal somata were distributed throughout the brain. Positive perikarya were detected in the internal cellular layer of the olfactory bulb, and in all divisions of the telencephalon, the highest density being observed along the midline. Numerous GABA-reactive cell bodies were found in the diencephalon, particularly in the preoptic and tuberal regions of the hypothalamus, and the dorsolateral, dorsomedial and ventromedial thalamic nuclei. In the optic tectum, the majority of GABApositive cell bodies were located in the periventricular layer. A number of immunolabelled cell bodies were observed in different tegmental structures, notably the torus semicircularis. In the cerebellum, the Purkinje cells were either very intensely or very weakly immunoreactive. In the rhombencephalon, reactive cell bodies were observed in the eminentia granularis, the valvula cerebellaris, the octavolateral nucleus, the lobus vagus and in the vagal and glossopharyngeal motor nuclei. Intensely immunoreactive axons and terminals were observed in the external granular layer and internal cellular layer of the olfactory bulb. In the telencephalon, the highest density of reactive fibres and boutons was found in the fields of the medial wall. Many immunolabelled fibres were seen in the medial and lateral forebrain bundles. In the diencephalon, intense labelling of fibres and terminals were observed in the nuclei situated close to the midline. In the optic tectum the highest density of reactive fibres was seen in the sfgs, the layer to which the retina projects massively. Finally, in the rhombencephalon the strongest labelling of neurites was observed in the nuclei of the raphé, the nucleus octavocellularis magnocellularis and the nuclei of the IXth and Xth cranial nerves. The GABAergic system of the eel, which is well developed, appears to be generally comparable to that described in tetrapod vertebrates.     

The distribution of nitric oxide synthase-, adenosine deaminase- and neuropeptide Y-immunoreactivity through the entire rat nucleus tractus solitarius: Effect of unilateral nodose ganglionectomy

The present study has employed immunocytochemistry on free-floating sections of adult rat medulla oblongata to characterise the distribution of nitric oxide synthase- (NOS), adenosine deaminase- (ADA) and neuropeptide Y- (NPY) immunoreactivity (IR) throughout the entire rostro–caudal axis of the nucleus tractus solitarius (NTS). In addition, unilateral nodose ganglionectomy was performed in a group of rats to determine whether any observed immunoreactivity was associated with central vagal afferent terminals. NOS-IR was found throughout the entire NTS, in cells, and both varicose and non-varicose fibres. Furthermore, unilateral nodose ganglionectomy resulted in a clear reduction in NOS-IR (visualised with diaminobenzidine) in a highly restricted portion of the ipsilateral medial NTS. Similarly, ADA- and NPY-containing cells, fibres and terminals were also found throughout the adult rat NTS. However, following unilateral nodose ganglionectomy, there was no apparent reduction in either ADA-IR or NPY-IR on the denervated side of the NTS. These data indicate a role for nitric oxide, purines and neuropeptide Y as neuromodulators within the rat NTS, although only nitric oxide appears to be primarily associated with vagal afferent input. Adenosine deaminase and neuropeptide Y-containing neurons appear to be predominantly postsynaptic to vagal input, although their possible association with vagal afferents cannot be completely excluded.     

雌激素对去卵巢大鼠基底前脑NOS及Nestin阳性神经元的影响

目的 观察雌激素替代对去卵巢大鼠基底前脑一氧化氮合酶(NOS)及巢蛋白(Nestin)阳性神经元的影响。方法 将28只健康成年雄性SD大鼠随机分为4个处理组:去势24 h雌激素替代组、去势2周雌激素替代组、去势植物油替代组及假手术组。用组织化学及免疫组织化学染色方法观察基底前脑的内侧隔核(MS)、斜角带垂直支(vDB)及水平支(hDB)的NOS和Nestin阳性神经元数的变化。结果 去势行植物油替代可使MS、vDB的NOS阳性神经元数明显下降(P<0.01);去势24 h或2周行雌激素替代均可使以上亚区的NOS阳性神经元数明显升高至正常水平(P<0.01)。去势行植物油替代或雌激素替代对hDB的:Nestin阳性神经元数的影响趋势与NOS阳性神经元的相似(P<0.01),但对MS及vDB的Nestin阳性神经元数影响不大(P>0.05)。结论 去卵巢行雌激素替代可选择性地使基底前脑不同亚区NOS、Nestin阳性神经元数升高,这可能与雌激素高调了NOS和Nestin的表达有关。     

Localization of enkephalinergic neurons in the central nervous system of the salmon (Salmo salar L.) by in situ hybridization and immunocytochemistry

The distribution of neurons expressing preproenkephalin (PPE) mRNA in the brain of the salmon was investigated by means of non-radioactive in situ hybridization, and directly compared with the distribution of enkephalin-immunoreactive (ENKir) neurons. This approach, utilized here for the first time in a non-mammalian vertebrate for the identification of neurons containing opioid peptides, permitted a detailed analysis of the distribution of putative enkephalinergic neurons in the salmon brain. Several cell groups containing neurons that express PPE mRNA also contain ENKir neurons. Such cell groups are located in the ventral telencephalic area, the nucleus of the rostral mesencephalic tegmentum and another nucleus immediately dorsal to it, the torus semicircularis, the valvula cerebelli and the corpus cerebelli. These cell groups consistently contain larger numbers of PPE mRNA expressing cells than ENKir ones. Some cell groups express PPE mRNA, but do not contain ENKir neurons. These cell groups are located in the dorsal telencephalic area, the inferior lobes of the hypothalamus, the pretectal area, the magnocellular superficial pretectal nucleus, the optic tectum, the oculomotor nucleus, the trochlear nucleus, the magnocellular vestibular nucleus, the secondary gustatory nucleus, the superior and medial reticular nuclei, the motor nucleus of the vagus and the ventral horn of the spinal cord. Moreover, some cell groups contain ENKir neurons, but no PPE mRNA expressing neurons. These cell groups are located in the ventromedial thalamic nucleus, the lateral tuberal nucleus, the nucleus of the lateral recess and the nucleus of the posterior recess. The majority of these periventricular ENKir neurons were of the cerebrospinal fluid-contacting type. ENKir neurons were also located in the dorsal lateral tegmental nucleus and in area B9. The results also permitted a tentative identification of enkephalinergic neurons afferent to the optic tectum, that have previously not been identified with immunocytochemistry, located in the dorsal telencephalic area, as well as enkephalinergic neurons intrinsic to the tectum that may contribute to the laminar arrangement of ENKir fibers in the optic tectum.