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1.
Summary Retinopetal neurons were visualised in the telencephalon and diencephalon of an air-breathing teleost fish, Channa punctata, following administration of cobaltous lysine to the optic nerve. The labelled perikarya (n=45–50) were always located on the side contralateral to the optic nerve that had received the neuronal tracer. The rostral-most back-filled cell bodies were located in the nucleus olfactoretinalis at the junction between the olfactory bulb and the telencephalon. In the area ventralis telencephali, two groups of telencephaloretinopetal neurons were identified near the ventral margin of the telencephalon. The rostral hypothalamus exhibited retrogradely labelled cells in three discrete areas of the lateral preoptic area, which was bordered medially by the nucleus praeopticus periventricularis and nucleus praeopticus, and laterally by the lateral forebrain bundle. In addition to a dorsal and a ventral group, a third population of neurons was located ventral to the lateral forebrain bundle adjacent to the optic tract. The dorsal group of neurons exhibited extensive collaterals; a few extended laterally towards the lateral forebrain bundle, whereas others ran into the dorsocentral area of the area dorsalis telencephali. A few processes extended via the anterior commissure into the telencephalon ipsilateral to the optic nerve that had been exposed to cobaltous lysine. However, the ventral cell group did not possess collaterals. In the diencephalon, retinopetal cells were visualised in the nucleus opticus dorsolateralis located in the pretectal area; these were the largest retinopetal perikarya of the brain. The caudal-most nucleus that possessed labelled somata was the retinothalamic nucleus; it contained the largest number of retinopetal cells. The limited number of widely distributed neurons in the forebrain, some with extensive collaterals, might participate in functional integration of different brain areas involved in feeding, which in this species is influenced largely by taste, not solely by vision. 相似文献
2.
Medaka (Oryzias latipes) is one of the few vertebrate experimental animals in which inbred lines have been established. It is also a species that has advanced in genetic studies in a manner comparable to zebrafish. This fish is therefore a good model for studying functional organization of the nervous system, but anatomical analysis of its nervous system has been limited to embryonic stages. In the present study, we investigated anatomy of cranial nerves in adult fish focusing on the visual function, using an inbred strain of medaka. Cranial nerves of medaka were labeled using biocytin, revealing a central distribution of retinofugal terminals, retinopetal neurons, and oculomotor, trochlear and abducens motor neurons. The optic nerve of the adult medaka was of a complete decussation type. Retinofugal terminals were located in 8 brain nuclei, the suprachiasmatic nucleus, nucleus pretectalis superficialis, nucleus dorsolateralis thalami, area pretectalis pars dorsalis (APd), area pretectalis pars ventralis (APv), nucleus of the posterior commissure (NPC), accessory optic nucleus, and the tectum opticum. Retinopetal neurons were identified in 6 brain nuclei, the ganglion of the terminal nerve, preoptic retinopetal nucleus, nucleus dorsolateralis thalami, APd, APv, and NPC. The oculomotor neurons were mostly labeled ipsilaterally and were located dorsomedially, abutting the fasciculus longitudinalis medialis in the mesencephalon. The trochlear nucleus was located contralaterally and dorsolaterally adjacent to the fasciculus longitudinalis medialis in the mesencephalon. The abducens nucleus was located ipsilaterally in a ventrolateral part of the rhombencephalic reticular formation. These results, generally similar to those in other teleosts, provide the basis for future behavioral and genetic studies in medaka. 相似文献
3.
Carassius RFamide (C-RFa) is a novel peptide found in the brain of the Japanese crucian carp. It has been demonstrated that mRNA of C-RFa is present in the telencephalon, optic tectum, medulla oblongata, and proximal half of the eyeball in abundance. Immunohistochemical methods were employed to elucidate the distribution of the peptide in the brain of the goldfish (Carassius auratus) in detail. C-RFaimmunoreactive perikarya were observed in the olfactory bulb, the area ventralis telencephali pars dorsalis and lateralis, nucleus preopticus, nucleus preopticus periventricularis, nucleus lateralis tuberis pars posterioris, nucleus posterioris periventricularis, nucleus ventromedialis thalami, nucleus posterioris thalami, nucleus anterior tuberis, the oculomotor nucleus, nucleus reticularis superior and inferior, facial lobe, and vagal lobe. C-RFa immunoreactive fibers and nerve endings were present in the olfactory bulb, olfactory tract, area dorsalis telencephali pars centralis and medialis, area ventralis telencephali, midbrain tegmentum, diencephalon, medulla oblongata and pituitary. However, in the optic tectum the immunopositive perikarya and fibers were less abundant. Based on these results, some possible functions of C-RFa in the nervous system were discussed. 相似文献
4.
Comparative immunocytochemical localization of putative opioid ligands in the central nervous system
Summary We report a detailed comparative immunocytochemical mapping of enkephalin, CCK and ACTH/gb-endorphin immunoreactive nerves in the central nervous system of rat and guinea pig. Enkephalin immunoreactivity was detected in many groups of nerve cell bodies, fibers and terminals in the limbic system, basal ganglia, hypothalamus, thalamus, brain stem and spinal cord. -endorphin and ACTH immunoreactivity was limited to a single group of nerve cell bodies in and around the arcuate nucleus and in fibers and terminals in the midline areas of the hypothalamus, thalamus and mesencephalic periaqueductal gray with lateral extensions to the amygdaloid area. Cholecystokinin immunoreactive nerve fibers and terminals displayed a distribution similar to that of enkephalin in many regions; but striking differences were also found. An immunocytochemical doublestaining technique, which allowed simultaneous detection of two different peptides in the same tissue section, showed that enkephalin-, CCK- and ACTH/-endorphin-immunoreactive nerves although closely intermingled in many brain areas, occurred separately. The distributions of nerve terminals containing these neuropeptides showed striking overlaps and also paralleled the distribution of opiate receptors. This may suggest that enkephalin, CCK, ACTH and -endorphin may interact with each other and with opiate receptors.Index of Abbreviations CA
Commissura anterior
- CAI
Capsula interna
- CO
Chiasma opticum
- CPF
Cortex piriformis
- CSDD
Commissura supraoptica dorsalis, pars dorsalis (Ganser)
- CSDV
Commissura supraoptica dorsalis, pars ventralis (Meynert)
- FMP
Fasciculus medialis prosencephali
- FOR
Formatio reticularis
- GD
Gyrus dentatus
- GP
Glubus pallidus
- H
Habenula
- HI
Hippocampus
- S
Subiculum
- SGCD
Substantia grisea centralis, pars dorsalis
- SGCL
Substantia grisea centralis, pars lateralis
- SGPV
Substantia grisea periventricularis
- SNC
Substantia nigra, zona compacta
- SNL
Substantia nigra, pars lateralis
- ST
Stria terminalis
- STP
Stria terminalis, pars precommissuralis
- TD
Tractus diagonalis (Broca)
- TO
Tractus opticus
- TSHT
Tractus septohypothalamicus
- TUOP
Tuberculum olfactorium, pars corticalis
- SUM
Decussatio supramamillaris
- a
Nucleus accumbens
- ac
Nucleus amygdaloideus centralis
- aco
Nucleus amygdaloideus corticalis
- am
Nucleus amygdaloideus medialis
- ar
Nucleus arcuatus
- cp
Nucleus caudatus putamen
- dcgl
Nucleus dorsalis corporis geniculati lateralis
- em
Eminentia mediana
- fm
Nucleus paraventricularis, pars magnocellularis
- fp
Nucleus paraventricularis, pars parvocellularis
- ha
Nucleus anterior (hypothalami)
- hd
Nucleus dorsomedialis (hypothalami)
- hl
Nucleus lateralis (hypothalami)
- hp
Nucleus posterior (hypothalami)
- hpv
Nucleus periventricularis (hypothalami)
- hv
Nucleus ventromedialis (hypothalami)
- ip
Nucleus interpeduncularis
- mcgm
Nucleus marginalis corporis geniculatic medialis
- mm
Nucleus mammillaris medialis
- ml
Nucleus mammillaris lateralis
- mh
Nucleus medialis habenulae
- p
Nucleus pretectalis
- pf
Nucleus parafascicularis
- pom
Nucleus preopticus medialis
- pop
Nucleus preopticus periventricularis
- posc
Nucleus preopticus, pars suprachiasmatica
- pt
Nucleus paratenialis
- pvs
Nucleus periventricularis stellatocellularis
- re
Nucleus reuniens
- sc
Nucleus suprachiasmaticus
- sl
Nucleus septi lateralis
- so
Nucleus supraopticus
- st
Nucleus interstitialis striae terminalis
- tad
Nucleus anterior dorsalis thalami
- tam
Nucleus anterior medialis thalami
- tav
Nucleus anterior ventralis thalami
- td
Nucleus tractus diagonalis (Broca)
- th
Nuclei thalami
- tl
Nucleus lateralis thalami
- tlp
Nucleus lateralis thalami, pars posterior
- tm
Nucleus medialis thalami
- tml
Nucleus medialis thalami, pars lateralis
- tmm
Nucleus medialis thalami, pars medialis
- tpo
Nucleus posterior thalami
- tr
Nucleus reticularis thalami
- tv
Nucleus ventralis thalami
- tvd
Nucleus ventralis thalami, pars dorsomedialis
- tvm
Nucleus ventralis medialis thalami, pars magnocellularis 相似文献
5.
S. D. Schlussman M. A. Kobylack A. A. Dunn-Meynell S. C. Sharma 《Cell and tissue research》1990,262(3):531-541
Summary Horseradish peroxidase was injected unilaterally into the optic tectum of the channel catfish, Ictalurus punctatus. The sources of tectal afferents were thereby revealed by retrogradely labeled neurons in various brain centers. Retrogradely labeled cells were seen in both the ipsilateral and contralateral telencephalon. The superficial pretectal area was labeled on both sides of the brain. Ipsilateral projections were also observed coming from the entopeduncular nucleus. Both the anterior thalamic nucleus and the ventro-medial thalamic nucleus projected to the ipsilateral optic tectum. Cells in the ipsilateral nucleus of the posterior commissure were seen to project to the tectum. Labeled fibers were visualized in the lateral geniculate nucleus ipsilateral to the injected tectum, however, no labeled cell bodies were observed. Therefore, tectal cells project to the lateral geniculate nucleus, but this projection is not reciprocal. No labeled cells were found in the cerebellum. Labeled cells occurred in both the ipsilateral and contralateral medial reticular formation; they were also observed in the ipsilateral nucleus isthmi. A projection was seen coming from the dorsal funicular nucleus. Furthermore, labeled cells were shown in the inferior raphe nucleus.Abbreviations
AP
Area pretectalis
-
C
Cerebellum
-
DPTN
Dorsal posterior tegmental nucleus
-
H
Habenula
-
IRF
Inferior reticular formation
-
LI
Inferior lobe
-
LGN
Lateral geniculate nucleus
-
LR
Lateral recess
-
MB
Mammillary body
-
MRF
Medial reticular formation
-
MZ
Medial zone of the telencephalon
-
NC
Nucleus corticalis
-
NDL-M
Nucleus opticus dorsolateralis/pars medialis
-
NI
Nucleus isthmi
-
NPC
Nucleus of the posterior commissure
-
OPT
Optic tectum
-
OT
Optic tract
-
PC
Posterior commissure
-
PN
Pineal organ
-
PrOP
Preoptic nucleus
-
PT
Pretectum
-
TBt
Tectobulbar tract
-
TEL
Telencephalon
-
TL
Torus longitudinalis
-
TS
Torus semicircularis
-
VC
Valvula cerebelli
-
VLTN
Ventrolateral thalamic nucleus
-
VMTN
Ventromedial thalamic nucleus 相似文献
6.
The distribution of neurotensin, neurokinin A, dynorphin A, galanin, somatostatin-28 (1-12), neuropeptide Y, vasoactive intestinal polypeptide, gastrin-releasing peptide, gamma-melanocyte stimulating hormone, alpha-neo-endorphin, angiotensin H, cholecystokinin-8, serotonin and tyrosine hydroxylase has been studied in the pretectal nuclei of the Cyprinus carpio: nuclei pretectalis superficialis parvicellularis and magnocellularis, pretectalis centralis, pretectalis, and pretectalis periventricularis dorsalis and ventralis using an indirect immunoperoxidase technique. We have found neuropeptide Y and serotonin immunoreactive fibres in all pretectal nuclei, whereas gastrin-releasing peptide immunoreactive fibres were visualized in the nuclei pretectalis superficialis parvicellularis and magnocellularis, pretectalis centralis. pretectalis and pretectalis periventricularis dorsalis; neurokinin A immunoreactive fibres in the nuclei pretectalis superficialis parvicellularis and magnocellularis and pretectalis periventricularis dorsalis; galanin immunoreactive fibres in the nuclei pretectalis superficialis parvicellularis, pretectalis centralis and pretectalis periventricularis dorsalis; and neurotensin immunoreactive fibres in the nucleus pretectalis periventricularis dorsalis. Additionally, immunoreactive cell bodies containing neuropeptide Y were observed in the nuclei pretectalis superficialis parvicellularis and pretectalis periventricularis dorsalis, and serotonin and tyrosine hydroxylase cell bodies were found in the nuclei pretectalis periventricularis dorsalis and ventralis respectively. The presence of the neuroactive substances found in the carp pretectal nuclei suggest that they might be involved in the regulation of certain functions within the visual system. 相似文献
7.
Summary The septal region represents an important telencephalic center integrating neuronal activity of cortical areas with autonomous processes. To support the functional analysis of this brain area in the guinea pig, the afferent connections to the lateral septal nucleus were investigated by the use of iontophoretically applied horseradish peroxidase (HRP). Retrogradely labeled perikarya were located in telencephalic, diencephalic, mesencephalic and metencephalic sites. The subnuclei of the lateral septum (pars dorsalis, intermedia, ventralis, posterior) receive afferents from the (i) medial septal nucleus, diagonal band of Broca (pars horizontalis and pars ventralis), and the principal nucleus of the stria terminalis, the hippocampus, and amygdala (nucleus medialis); (ii) the medial habenular nucleus, and the para- (peri-) ventricular, parataenial and reuniens nuclei of the thalamus; the anterior, lateral and posterior hypothalamic areas in particular, the medial and lateral preoptic, suprachiasmatic, periventricular, paraventricular, arcuate, premammillary, and supramammillary nuclei; (iii) the periaquaeductal grey, ventral tegmental area, nucleus interfascicularis, nucleus reticularis linearis, central linear nucleus, interpeduncular nucleus; (iv) dorsal and medial raphe complex, and locus coeruleus. Each subnucleus of the lateral septum displays an individual, differing pattern of afferents from the above-described regions. Based on a double-labeling method, the vasopressinergic and serotonergic afferents to the lateral septum were found to originate in the nucleus paraventricularis hypothalami and the raphe nuclei, respectively.Abbreviations
ARC
arcuate nucleus
-
BNST
bed nucleus of the stria terminalis
-
CL
central linear nucleus
-
DBBh
diagonal band of Broca (pars horizontalis)
-
DBBv
diagonal band of Broca (pars ventralis)
-
DR
dorsal raphe nucleus
-
HC
hippocampus
-
IF
interfascicular nucleus
-
IP
interpeduncular nucleus
-
LC
locus coeruleus
-
LDT
laterodorsal tegmental nucleus
-
LHA
lateral hypothalamic area
-
LPO
lateral preoptic area
-
LSN
lateral septal nucleus
-
MA
medial amygdaloid nucleus
-
MH
medial habenular nucleus
-
MPO
medial preoptic region
-
MR
medial raphe nucleus
-
MSN
medial septal nucleus
-
PAG
periaquaeductal grey
-
PEN
periventricular nucleus
-
PHA
posterior hypothalamic area
-
PMd
premammillary region (pars dorsalis)
-
PMv
premammillary region (pars ventralis)
-
PT
parataenial nucleus
-
PVN
paraventricular hypothalamic nucleus
-
PVT
paraventricular thalamic nucleus
-
RE
nucl. reuniens
-
RL
nucl. reticularis linearis
-
SCN
suprachiasmatic nucleus
-
SMl
supramammillary region (pars lateralis)
-
SMm
supramammillary region (pars medialis)
-
SUB
subiculum
-
TS
triangular septal nucleus
-
VTA
ventral tegmental area
-
ac
anterior commissure
-
bc
brachium conjunctivum
-
bp
brachium pontis
-
cc
corpus callosum
-
fr
fasciculus retroflexus
-
fx
fornix
-
ml
medial lemniscus
-
mlf
fasciculus longitudinalis medialis
-
mp
mammillary peduncle
-
mt
mammillary tract
-
oc
optic chiasm
-
on
optic nerve
-
pc
posterior commissure
-
pt
pyramidal tract
-
sm
stria medullaris
-
st
stria terminalis
-
vhc
ventral hippocampal commissure
Supported by the Deutsche Forschungsgemeinschaft (Nu 36/2-1) 相似文献
8.
J. W. Resink P. K. Voorthuis R. Van den Hurk H. G. B. Vullings Dr. P. G. W. J. Van Oordt 《Cell and tissue research》1989,256(2):337-345
Summary The olfactory tract of the African catfish, Clarias gariepinus, consists of two tracts, the medial and lateral olfactory tract. Ovulated female catfish are attracted by male steroidal pheromones. Attraction tests with catfish in which the medial and lateral olfactory tract have been selectively lesioned show that the effects of these pheromones are mediated by the medial olfactory tract. The central connections of the medial and lateral olfactory tract have been studied by retro- and anterograde transport techniques using horseradish peroxidase as a tracer. Upon entering the forebrain, the medial olfactory tract innervates the posterior pars ventralis and pars supracommissuralis of the area ventralis telencephali and the nucleus preopticus periventricularis, the nucleus preopticus and the nucleus recessus posterioris. Application of horseradish peroxidase to the olfactory epithelium shows that part of the innervation of the area ventralis telencephali and the nucleus preopticus periventricularis can be attributed to the nervus terminalis, which appears to be embedded in the medial olfactory tract. The lateral olfactory tract sends projections to the same brain areas but also innervates the nucleus habenularis and a large terminal field in the area dorsalis telencephali pars lateralis ventralis. Furthermore, the medial olfactory tract carries numerous axons from groups of perikarya localized in the area dorsalis telencephali. Contralateral connections have been observed in the olfactory bulb, telencephalon, diencephalon and mesencephalon. It is suggested that processes of the medial olfactory tract innervating the preoptic region may influence the gonadotropin-releasing hormone system and in doing so may lead to behavioral and physiological changes related to spawning. 相似文献
9.
Summary Mapping of monoaminergic systems in the brain of the newt Triturus alpestris was achieved with antisera against (1) thyrosine hydroxylase (TH), (2) formaldehyde-conjugated dopamine (DA), and (3) formaldehyde-conjugated serotonin (5-HT). In the telencephalon, the striatum was densely innervated by a large number of 5-HT-, DA-and TH-immunoreactive (IR) fibers; IR fibers were more scattered in the amygdala, the medial and lateral forebrain bundles, and the anterior commissure. In the anterior and medial diencephalon, TH-IR perikarya contacting the cerebrospinal fluid (CSF-C perikarya) were located in the preoptic recess organ (PRO), the organum vasculosum laminae terminalis and the suprachiasmatic nucleus. Numerous TH-IR perikarya, not contacting the CSF, were present in the posterior preoptic nucleus and the ventral thalamus. At this level, DA-IR CSF-C neurons were only located in the PRO. In the posterior diencephalon, large populations of 5-HT-IR and DA-IR CSF-C perikarya were found in the paraventricular organ (PVO) and the nucleus infundibularis dorsalis (NID); the dorsal part of the NID additionally presented TH-IR CSF-C perikarya. Most regions of the diencephalon showed an intense monoaminergic innervation. In addition, numerous TH-IR, DA-IR and 5-HT-IR fibers, orginating from the anterior and posterior hypothalamic nuclei, extended ventrally and reached the median eminence and the pars intermedia of the pituitary gland. In the midbrain, TH-IR perikarya were located dorsally in the pretectal area. Ventrally, a large group of TH-IR cell bodies and some weakly stained DA-IR and 5-HT-IR neurons were observed in the posterior tuberculum. No dopaminergic system equivalent to the substantia nigra was revealed. The possible significance of the differences in the distribution of TH-IR and DA-IR neurons is discussed, with special reference to the CSF-C neurons.Abbreviations
AM
amygdala
-
CAnt
commissura anterior
-
CH
commissura hippocampi
-
CP
commissura posterior
-
Ctm
commissura tecti mesencephali
-
DH
dorsal hypothalamus
-
DTh
dorsal thalamus
-
FLM
fasciculus longitudinalis medialis
-
Fsol
fasciculus solitarius
-
H
habenula
-
LFB
lateral forebrain bundle
-
ME
median eminence
-
MFB
medial forebrain bundle
-
NID
nucleus infundibularis dorsalis
-
nIP
neuropil of nucleus interpeduncularis
-
NPOP
nucleus preopticus posterior
-
NS
nucleus septi
-
OVLT
organum vasculosum laminae terminalis
-
PD
pars distalis
-
Pdo
dorsal pallium
-
PHi
primordium hippocampi
-
PI
pars intermedia
-
Pl
lateral pallium
-
PN
pars nervosa
-
PRO
preoptic recess organ
-
Ptec
pretectal area
-
PVO
paraventricular organ
-
Ra
nucleus raphe
-
Rm
nucleus reticularis medius
-
SCO
subcommisural organ
-
ST
striatum; strm stria medullaris thalami
-
strt
stria terminalis thalami
-
TM
tegmentum mesencephali
-
TO
tectum opticum
-
TP
tuberculum posterius
-
trch
tractus cortico-habenularis
-
trmp
tractus mamillopeduncularis
-
VH
ventral hypothalamus
-
Vm
nucleus motorius nervi trigemini
-
VTh
ventral thalamus
-
II
optic nerve 相似文献
10.
Walter Heiligenberg Clifford H. Keller Walter Metzner Masashi Kawasaki 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1991,169(2):151-164
Summary The complex of the diencephalic nucleus electrosensorius (nE) provides an interface between the electrosensory processing performed by the torus semicircularis and the control of specific behavioral responses. The rostral portion of the nE comprises two subdivisions that differ in the response properties and projection patterns of their neurons. First, the nEb (Fig. 1 B), which contains neurons that are driven almost exclusively by beat patterns generated by the interference of electric organ discharges (EODs) of similar frequencies. Second, the area medial to the nEb, comprising the lateral pretectum (PT) and the nE-acusticolateralis region (nEar, Fig. 1 B-D), which contains neurons excited predominantly by EOD interruptions, signals associated with aggression and courtship. Neurons in the second area commonly receive convergent inputs originating from ampullary and tuberous electroreceptors, which respond to the low-frequency and high-frequency components of EOD interruptions, respectively. Projections of these neurons to hypothalamic areas linked to the pituitary may mediate modulations of a fish's endocrine state that are caused by exposure to EOD interruptions of its mate.Abbreviations
a
axon
-
ATh
anterior thalamic nucleus
-
CCb
corpus cerebelli
-
CE
central nucleus of the inferior lobe
-
CP
central posterior thalamic nucleus
-
Df
frequency difference between neighbor's EOD and fish's own
-
DFl
nucleus diffusus lateralis of the inferior lobe
-
DFm
nucleus diffusus medialis of the inferior lobe
-
DTn
dorsal tegmental nucleus
-
EOD
electric organ discharge
-
G
glomerular nucleus
-
Hc
caudal hypothalamus
-
Hd
dorsal hypothalamus
-
Hl
lateral hypothalamus
-
Hv
ventral hypothalamus
-
JAR
jamming avoidance response
-
LL
lateral lemniscus
-
MGT
magnocellular tegmental nucleus
-
MLF
medial longitudinal fasciculus
-
nB
nucleus at the base of the optic tract
-
nE
nucleus electrosensorius
-
nEar
nucleus electrosensorius-acusticolateral region
-
nEb
nucleus electrosensorius-beat related area
-
nE
nucleus electrosensorius, area causing rise of EOD frequency
-
nE
nucleus electrosensorius, area causing fall of EOD frequency
-
nLT
nucleus tuberis lateralis
-
nLV
nucleus lateralis valvulae
-
PC
posterior commissure
-
Pd
nucleus praeeminentialis, pars dorsalis
-
PeG
periglomerular complex
-
PG
preglomerular nucleus
-
PLm
medial division of the perilemniscal nucleus
-
Pn
pacemaker nucleus
-
PPn
prepacemaker nucleus
-
PT
pretectal nucleus
-
PTh
prethalamic nucleus
-
R
red nucleus
-
Sc
suprachiasmatic nucleus
-
SE
nucleus subelectrosensorius
-
TAd
nucleus tuberis anterior-dorsal subdivision
-
TAv
nucleus tuberis anterior-ventral subdivision
-
TeO
optic tectum
-
TL
torus longitudinalis
-
TSd
dorsal (electrosensory) torus semicircularis
-
TSv
ventral (mechanosensory and auditory) torus semicircularis
-
tTB
tecto-bulbar tract
-
VCb
cerebellar valvula
-
VP
valvular peduncle
-
VPn
nucleus of the valvular peduncle 相似文献
11.
Summary Retinofugal and retinopetal projections were investigated in the teleost fish Channa micropeltes (Channiformes) by means of the cobaltous lysine and horseradish peroxidase (HRP) tracing techniques. Retinofugal fibers cross completely in the optic chiasma. A conspicious lamination is present in those parts of the optic tract that give rise to the marginal branches of the optic tract. This layering of optic fibers continues in the marginal branches to mesencephalic levels. Retinal projections to the preoptic and hypothalamic regions are sparse; they are more pronounced in the area of pretectal nuclei. The medial pretectal complex and the cortical pretectal nucleus are more fully differentiated than in other teleostean species. Further targets include the thalamus and the optic tectum. The course of major optic sub-tracts and smaller fascicles is described. Retinopetal neurons are located contralaterally in a rostral and a caudal part of the nucleus olfactoretinalis, and in a circumscribed nucleus thalamoretinalis. The present findings are compared with reports on other teleost species. 相似文献
12.
Summary Cells immunoreactive with an anti-LHRH serum were visualized in the brain of the three-spined stickleback, Gasterosteus aculeatus, by means of the PAP technique. Positive cells were found in a periventricular position in the nucleus praeopticus pars magnocellularis, the nucleus dorsomedialis thalami, the nucleus ventromedialis thalami, the nucleus periventricularis posterior, and in the periventricular dorsomedian tegmentum. These cells were frequently observed to contact the CSF. 相似文献
13.
Summary The retinal efferents of the catfish, Mystus vittatus, were investigated with the use of the horseradish peroxidase (HRP) technique. Most retinal fibres extended contralateral to the eye that had received HRP label, while a few fascicles projected to the ipsilateral side without decussation in the optic chiasma. The contralateral fibres projected to the suprachiasmatic nucleus, the nucleus opticus dorsolateralis, the nucleus of the posterior commissure, the nucleus geniculatus lateralis, pretectal nuclear complex, and to two layers of the optic tectum, i.e., stratum fibrosum et griseum superficiale and stratum griseum centrale. The accessory optic tract arose from the inner area of the optic tract and extended ventromedially to the accessory optic nucleus. The ipsilateral fascicles projected to almost all the above mentioned nuclei, but these projections were comparatively sparse. The ipsilateral retinal projection was restricted to the rostral tectum. 相似文献
14.
N. Aste C. Viglietti-Panzica A. Fasolo C. Andreone H. Vaudry G. Pelletier G. C. Panzica 《Cell and tissue research》1991,265(2):219-230
Summary In the present study, we have demonstrated, by means of the biotin-avidin method, the widespread distribution of neuropeptide Y (NPY)-immunoreactive structures throughout the whole brain of the Japanese quail (Coturnix coturnix japonica). The prosencephalic region contained the highest concentration of both NPY-containing fibres and perikarya. Immunoreactive fibres were observed throughout, particularly within the paraolfactory lobe, the lateral septum, the nucleus taeniae, the preoptic area, the periventricular hypothalamic regions, the tuberal complex, and the ventrolateral thalamus. NPY-immunoreactive cells were represented by: a) small scattered perikarya in the telencephalic portion (i.e. archistriatal, neostriatal and hyperstriatal regions, hippocampus, piriform cortex); b) medium-sized cell bodies located around the nucleus rotundus, ventrolateral, and lateral anterior thalamic nuclei; c) small clustered cells within the periventricular and medial preoptic nuclei. The brainstem showed a less diffuse innervation, although a dense network of immunopositive fibres was observed within the optic tectum, the periaqueductal region, and the Edinger-Westphal, linearis caudalis and raphes nuclei. Two populations of large NPY-containing perikarya were detected: one located in the isthmic region, the other at the boundaries of the pons with the medulla. The wide distribution of NPY-immunoreactive structures within regions that have been demonstrated to play a role in the control of vegetative, endocrine and sensory activities suggests that, in birds, this neuropeptide is involved in the regulation of several aspects of cerebral functions.Abbreviations
AA
archistriatum anterius
-
AC
nucleus accumbens
-
AM
nucleus anterior medialis
-
APP
avian pancreatic polypeptide
-
CNS
centrai nervous system
-
CO
chiasma opticum
-
CP
commissura posterior
-
CPi
cortex piriformis
-
DIC
differential interferential contrast
-
DLAl
nucleus dorsolateralis anterior thalami, pars lateralis
-
DLAm
nucleus dorsolateralis anterior thalami, pars medialis
-
E
ectostriatum
-
EW
nucleus of Edinger-Westphal
-
FLM
fasciculus longitudinalis medialis
-
GCt
substantia grisea centralis
-
GLv
nucleus geniculatus lateralis, pars ventralis
-
HA
hyperstriatum accessorium
-
Hp
hippocampus
-
HPLC
high performance liquid chromatography
-
HV
hyperstriatum ventrale
-
IF
nucleus infundibularis
-
IO
nucleus isthmo-opticus
-
IP
nucleus interpeduncularis
-
IR
immunoreactive
-
LA
nucleus lateralis anterior thalami
-
LC
nucleus linearis caudalis
-
LFS
lamina frontalis superior
-
LH
lamina hyperstriatica
-
LHRH
luteinizing hormone-releasing hormone
-
LoC
locus coeruleus
-
LPO
lobus paraolfactorius
-
ME
eminentia mediana
-
N
neostriatum
-
NC
neostriatum caudale
-
NPY
neuropeptide Y
-
NIII
nervus oculomotorius
-
NV
nervus trigeminus
-
NVI
nervus facialis
-
NVIIIc
nervus octavus, pars cochlearis
-
nIV
nucleus nervi oculomotorii
-
nIX
nucleus nervi glossopharyngei
-
nBOR
nucleus opticus basalis (ectomamilaris)
-
nCPa
nucleus commissurae pallii
-
nST
nucleus striae terminalis
-
OM
tractus occipitomesencephalicus
-
OS
nucleus olivaris superior
-
PA
palaeostriatum augmentatum
-
PBS
phosphate-buffered saline
-
POA
nucleus praeopticus anterior
-
POM
nucleus praeopticus medialis
-
POP
nucleus praeopticus periventricularis
-
PP
pancreatic polypeptide
-
PYY
polypeptide YY
-
PVN
nucleus paraventricularis magnocellularis
-
PVO
organum paraventriculare
-
R
nucleus raphes
-
ROT
nucleus rotundus
-
RP
nucleus reticularis pontis caudalis
-
Rpc
nucleus reticularis parvocellularis
-
RPgc
nucleus reticularis pontis caudalis, pars gigantocellularis
-
RPO
nucleus reticularis pontis oralis
-
SCd
nucleus subcoeruleus dorsalis
-
SCv
nucleus subcoeruleus ventralis
-
SCNm
nucleus suprachiasmaticus, pars medialis
-
SCNl
nucleus suprachiasmaticus, pars lateralis
-
SL
nucleus septalis lateralis
-
SM
nucleus septalis medialis
-
Ta
nucleus tangentialis
-
TeO
tectum opticum
-
Tn
nucleus taeniae
-
TPc
nucleus tegmenti pedunculo-pontinus, pars compacta
-
TSM
tractus septo-mesencephalicus
-
TV
nueleus tegmenti ventralis
-
VeL
nucleus vestibularis lateralis
-
VLT
nucleus ventrolateralis thalami
-
VMN
nucleus ventromedialis hypothalami
A preliminary report of this study was presented at the 15th Conference of European Comparative Endocrinologists, Leuven, Belgium, September 1990 相似文献
15.
The distribution of noradrenaline and adrenaline in the brain of the urodele amphibian Pleurodeles waltlii has been studied with antibodies raised against noradrenaline and the enzymes dopamine--hydroxylase and phenylethanolamine-N-methyltransferase. Noradrenaline-containing cell bodies were found in the anterior preoptic area, the hypothalamic nucleus of the periventricular organ, the locus coeruleus and in the solitary tract/area postrema complex at the level of the obex. Noradrenergic fibers are widely distributed throughout the brain innervating particularly the ventrolateral forebrain, the medial amygdala, the lateral part of the posterior tubercle, the parabrachial region and the ventrolateral rhombencephalic tegmentum. Putative adrenergic cell bodies were found immediately rostral to the obex, ventral to the solitary tract. Whereas the cell bodies and their dendrites were Golgi-like stained, axons were more difficult to trace. Nevertheless, some weakly immunoreactive fibers could be traced to the basal forebrain. A comparison of these results with data previously obtained in anurans reveals not only several general features, but also some remarkable species differences.Abbreviations
Acc
Nucleus accumbens
-
AP
area postrema
-
Apl
amygdala, pars lateralis
-
Apm
amygdala, pars medialis
-
ca
commissura anterior
-
Cb
cerebellum
-
cc
central canal
-
Dp
dorsal pallium
-
epl
external plexiform layer
-
gl
glomerular layer of the olfactory bulb
-
H
ganglion habenulae
-
igl
internal granular layer
-
Ip
nucleus interpeduncularis
-
Lc
locus coeruleus
-
Ll
lateral line lobe
-
Lp
lateral pallium
-
Ls
lateral septum
-
ml
mitral cell layer
-
Mp
medial pallium
-
Ms
medial septum
-
nPT
nucleus pretectalis
-
NPv
nucleus of the periventricular organ
-
nV
nervus trigeminus
-
oc
optic chiasm
-
Poa
preoptic area
-
Ri
nucleus reticularis inferior
-
SC
nucleus suprachiasmaticus
-
sol
solitary tract
-
Str
striatum
- thd
thalamus dorsalis
-
thv
thalamus ventralis
-
To
tectum opticum
-
TP
tuberculum posterius
-
V
ventricle
-
VH
ventral hypothalamic nucleus
-
III
nucleus nervi oculomotorii
-
IXm
nucleus motorius nervi glossopharyngei
-
Xm
nucleus motorius nervi vagi 相似文献
16.
Summary The central projections of the pineal complex of the silver lamprey Ichthyomyzon unicuspis were studied by injection of horseradish peroxidase. The pineal tract courses caudally along the left side of the habenular commissure, and a few fibers penetrate the brain through the caudalmost portion of this commissure. Most of the fibers, however, continue caudally and enter the brain through the posterior commissure. The pineal tract projects bilaterally to the subcomissural organ, the superficial and periventricular pretectum, the posterior tubercular nucleus, the dorsal and ventral thalamus, the dorsal hypothalamus, the optic tectum, the torus semicircularis, the midbrain tegmentum, and the oculomotor nucleus. A few fibers decussate in the tubercular commissure, but the course of these decussate fibers could not be followed owing to the bilateral nature of the projections. No retrogradely labeled cells were found in the brain. With the exception of the projections to the optic tectum and torus semicircularis, the pineal projections in the silver lamprey are similar to those reported in other anamniote vertebrates. 相似文献
17.
Summary Immunoreactive neuropeptide Y and dynorphin have been localized in the brain and pituitary gland of the platyfish, Xiphophorus maculatus, at different ages and stages of development from birth to sexual maturity. Immunoreactive neuropeptide Y was found in perikarya and tracts of the nucleus olfactoretinalis, telencephalon, ventral tegmentum and in the neurohypophysis and in the three regions of the adenohypophysis. Immunoreactive dynorphin was found in nerve tracts in the olfactory bulb and in cells of the pars intermedia and the rostral pars distalis of the pituitary gland. 相似文献
18.
Mario F. Wullimann Michael H. Hofmann Dietrich L. Meyer 《Cell and tissue research》1991,266(2):285-293
Summary In the spiny eel, Macrognathus aculeatus, anterodorsal and (to a lesser degree) anteroventral lateralline nerves project massively to the granular layer of the valvula cerebelli, throughout its rostrocaudal extent. The posterior lateral-line nerve terminates in the corpus cerebelli. Thus, valvula and corpus cerebelli are supplied with mechanosensory input of different peripheral origins. An analysis of the taxonomic distribution of experimentally determined primary lateral-line input to the three parts of the teleostean cerebellum reveals that the eminentia granularis always receives such input, and that the corpus cerebelli is the recipient of primary lateral-line input in many teleosts. The valvula, however, receives primary lateral-line afferents in only two examined species. In M. aculeatus, the massive lateral-line input to the valvula probably originates in mechanoreceptors located in the elongated rostrum of the upper jaw, a characteristic feature of mastacembeloid fishes. This projection to the valvula may therefore represent a unique specialization that arose with the evolution of the peculiar rostrum. 相似文献
19.
Summary About 60 pairs of ascending interneurons are present in the terminal ganglion of the crayfish Procambarus clarkii (Girard). Some of these interneurons have been impaled intracellularly, characterized physiologically, and then labeled with horseradish peroxidase (HRP) to examine the distribution and ultrastructure of synapses. A close relationship between ultrastructure and physiological properties has been found between two types of interneurons, which either have a pre-motor effect upon motor neurons or have no such effect. In one interneuron with a pre-motor effect (6D2), input and output synapses are intermingled on thicker branches, whereas only input synapses are found on small diameter branches. Only input synapses have been observed on the branches in another interneuron with-out a pre-motor effect (6B1). No differences in branch morphology are found in these two interneurons. Interneuron 6D2 contains large numbers of small round agranular vesicles, but the same type of synaptic vesicles is rarely seen in interneuron 6B1, which has no output synapses. Our results indicate a good correlation between the synaptic distribution and pre-motor effects of interneurons in the terminal ganglion.Abbreviations
A6, 7
Sixth and seventh abdominal segment of the terminal ganglion
-
AVC
anterior ventral commissure
-
DC I
dorsal commissure I
-
DIT
dorsal intermediate tract
-
DMT
dorsal medial tract
-
eLG
extra lateral giant interneuron
-
LVT
lateral ventral tract
-
LG
lateral giant interneuron
-
LVT
lateral ventral tract
-
MDT
median dorsal tract
-
MG
medial giant interneuron
-
MoG
motor giant neuron
-
MVT
median ventral tract
-
PVC
posterior ventral commissure
-
R1s
sensory fiber tract of nerve root 1
-
R3m
motor fiber tract of nerve root 3
-
R4–7
nerve roots 4–7
-
SC I,II
sensory commissure I,II
-
VC I,III
ventral commissure I, III
-
VIT
ventral intermediate tract
-
VLT
ventral lateral tract
-
VMT
ventral medial tract 相似文献
20.
Retinal projections were studied experimentally in the Northern water snake using modifications of the Nauta silver impregnation technique. Contralaterally, the retina projects to nucleus geniculatus lateralis pars dorsalis and pars ventralis, nucleus lentiformis mesencephali and nucleus geniculatus pretectalis. A sparse projection was also observed to nucleus ovalis. An additional afferent thalamic projection to nucleus ventrolateralis was found in two cases. The retina projects ipsilaterally to the dorsolateral portion of nucleus geniculatus lateralis pars dorsalis, and sparsely to nucleus lentiformis mesencephali and nucleus geniculatus pretectalis. Nucleus posterodorsalis receives dense bilateral retinal projections. Contralaterally, the retina also projects to the superficial layers of the tectum (layers 8–13 of Ramón) and to nucleus opticus tegmenti. Armstrong's findings that the retinal projections in Natrix are qualittatively similar to those in lizards were confirmed. However there are marked quantitative differences among the various pathways and their corresponding nuclei. These differences are particularly striking in comparing the visual projections to the dorsal thalamus, the retino-tecto-rotundal and the retino-geniculate systems. The first is reduced in volume and the second is markedly increased in volume in comparison with lizards. These data lend support to the theories of Walls that snakes evolved from fossorial lizards and of Underwood that the eyes of these lizards underwent reduction but not complete degeneration. Qualitatively the retinal projections are conservative among lizards and snakes, but a history of reduction of these pathways in ancestral snakes with a selective increase in the retino-geniculate system as a surface niche was reattained is reflected in the anatomy of this ophidian visual system. 相似文献