[Musculi longus capitis et splenius of the rat and innervating motoneurons (author's transl)].

Abstract:

:The nuclei for the nerves of a dorsal (m. splenius) and a ventral (m. longus capitis) neck muscle of the rat were retrogradely labeled by applying horseradish peroxidase (HRP) to the respective cut muscle nerves. Motoneurons of both muscles were analyzed for their localization, diameter of perikarya, and area of dendritic arborization. The nucleus of m. longus capitis is situated dorsomedially, the nucleus of m. splenius ventromedially within the ventral horn. Thus, the relative positions of the two nuclei are inverse to those of their muscles, with the more ventral nucleus innervating the more dorsal muscle. In both nuclei the areas of dendritic arborization are very large, extending into the nuclei of other neck muscles, and also into the ipsilateral anterior funiculus. In addition, m. longus capitis motoneurons were found to send dendrites into the contralateral ventral horn, reaching the nucleus of the contralateral muscle. The size distribution of perikarya is bimodal for m. longus capitis motoneurons, but only unimodal in the case of m. splenius.

journal_name

Acta Neuropathol

journal_title

Acta neuropathologica

authors

Stillhard G

doi

10.1007/BF00690368

subject

Has Abstract

pub_date

1981-01-01 00:00:00

pages

267-74

issue

4

eissn

0001-6322

issn

1432-0533

journal_volume

53

pub_type

杂志文章
  • Intravenous injection of horseradish peroxidase in the rat stimulates corticosterone and adrenocorticotropic hormone release.

    abstract::Wistar rats were given intravenous (i.v.) horseradish peroxidase (HRP) in saline in doses commonly used to study vascular permeability and the blood-brain barrier. Samples of blood were taken from conscious animals via indwelling catheters at intervals up to 6 h after the HRP injection. Plasma concentrations of adreno...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00687945

    authors: Jezová D,Olsson Y

    更新日期:1986-01-01 00:00:00

  • Cholinesterases colocalize with sites of neurofibrillary degeneration in aged and Alzheimer's brains.

    abstract::Acetylcholinesterase and butyrylcholinesterase have been associated with structures undergoing neurofibrillary degeneration, as well as with all types of senile plaques, in non-demented aged and Alzheimer's brains. At the electron microscope level, the reaction product of both enzymes, appeared to decorate paired heli...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00296744

    authors: Morán MA,Mufson EJ,Gómez-Ramos P

    更新日期:1994-01-01 00:00:00

  • Expression pattern of apoptosis-related markers in Huntington's disease.

    abstract::Inappropriate apoptosis has been implicated in the mechanism of neuronal death in Huntington's disease (HD). In this study, we report the expression of apoptotic markers in HD caudate nucleus (grades 1-4) and compare this with controls without neurological disease. Terminal transferase-mediated biotinylated-UTP nick e...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-004-0957-5

    authors: Vis JC,Schipper E,de Boer-van Huizen RT,Verbeek MM,de Waal RM,Wesseling P,ten Donkelaar HJ,Kremer B

    更新日期:2005-03-01 00:00:00

  • Cystic leukomalacia in the cerebellar folia of premature infants.

    abstract::Cystic necrosis in the cerebellar white matter was found in three premature infants. The necrosis was characteristically localized in the center of the white matter of the superficial cerebellar folia, sparing the overlying cortex. The patients were aged between 28 and 34 gestational weeks, and had a clinical history ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00315013

    authors: Tsuru A,Mizuguchi M,Takashima S

    更新日期:1995-01-01 00:00:00

  • Reverse pinocytosis induced in cerebral endothelial cells by injection of histamine into the cerebral ventricle.

    abstract::Histamine dihydrochloride (10 micrograms of 500 micrograms/ml) was infused during 1 min into the lateral cerebral ventricle of rats, which resulted in a significant stimulation of pinocytosis in the endothelial cells. Systemic injections of mepyramine or metiamide could not prevent this activation. In contrast, raniti...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00686387

    authors: Dux E,Dóczi T,Joó F,Szerdahelyi P,Siklós L

    更新日期:1988-01-01 00:00:00

  • Pursuit of the origin of the large myelinated fibers of the anterolateral funiculus in the spinal cord in humans in relation to the pathomechanism in amyotrophic lateral sclerosis.

    abstract::To determine the origin of the large myelinated fibers in the anterolateral funiculus (ALF) in the spinal cord of humans, myelinated fibers in the ALF of the mid-cervical spinal cord were examined quantitatively. Five groups of subjects were examined, consisting of control subjects, patients with cerebral lesions and ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s004010051129

    authors: Oyanagi K,Kawakami E,Morita T,Takahashi H

    更新日期:1999-12-01 00:00:00

  • Overexpression of human wild-type FUS causes progressive motor neuron degeneration in an age- and dose-dependent fashion.

    abstract::Amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) are relentlessly progressive neurodegenerative disorders with overlapping clinical, genetic and pathological features. Cytoplasmic inclusions of fused in sarcoma (FUS) are the hallmark of several forms of FTLD and ALS patients with mutati...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-012-1043-z

    authors: Mitchell JC,McGoldrick P,Vance C,Hortobagyi T,Sreedharan J,Rogelj B,Tudor EL,Smith BN,Klasen C,Miller CC,Cooper JD,Greensmith L,Shaw CE

    更新日期:2013-02-01 00:00:00

  • Dysferlin expression in tubular aggregates: their possible relationship to endoplasmic reticulum stress.

    abstract::Dysferlin is a newly identified sarcolemmal protein related to Miyoshi myopathy and limb-girdle muscular dystrophy. Although its function is still unknown, it is inferred from the presence of C2 domains and a transmembrane domain in its sequence that dysferlin may be expressed or located not only at the sarcolemma but...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-003-0686-1

    authors: Ikezoe K,Furuya H,Ohyagi Y,Osoegawa M,Nishino I,Nonaka I,Kira J

    更新日期:2003-06-01 00:00:00

  • Evaluation of CD33 as a genetic risk factor for Alzheimer's disease.

    abstract::In 2011, genome-wide association studies implicated a polymorphism near CD33 as a genetic risk factor for Alzheimer's disease. This finding sparked interest in this member of the sialic acid-binding immunoglobulin-type lectin family which is linked to innate immunity. Subsequent studies found that CD33 is expressed in...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章,评审

    doi:10.1007/s00401-019-02000-4

    authors: Estus S,Shaw BC,Devanney N,Katsumata Y,Press EE,Fardo DW

    更新日期:2019-08-01 00:00:00

  • Neurofibromatosis tumor and skin cells in culture. II. Structural proteins with special reference to the cytoskeletal and cell surface components.

    abstract::Structural proteins of cultured neurofibromatosis (NF) tumor and skin cells were studied with reference to control skin fibroblasts. In polyacrylamide gel electrophoresis (PAGE)/fluorography the banding patterns of the cell lysates were markedly similar. NF tumor cells, however, produced a 60 kD band with a stronger a...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00687332

    authors: Peltonen J,Näntö-Salonen K,Aho HJ,Kouri T,Virtanen I,Penttinen R

    更新日期:1984-01-01 00:00:00

  • Fragmentation of Golgi apparatus of nigral neurons with alpha-synuclein-positive inclusions in patients with Parkinson's disease.

    abstract::We examined whether the Golgi apparatus (GA) is fragmented in nigral neurons in 18 cases with Parkinson's disease (PD) and in 8 control cases. The nigral neurons in cases with PD showed various degrees of Lewy pathology with alpha-synuclein immunohistochemistry, and we divided the neurons into three subtypes according...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-006-0114-4

    authors: Fujita Y,Ohama E,Takatama M,Al-Sarraj S,Okamoto K

    更新日期:2006-09-01 00:00:00

  • Polyneuropathy with minifascicle formation in a patient with 46XY mixed gonadal dysgenesis.

    abstract::A patient with mixed gonadal dysgenesis showed glove and stocking-type sensory impairment and slowing of motor and sensory nerve conduction. Sural nerve biopsy revealed minifascicular formation with decreased density of myelinated fibers. As far as we are aware, this is the first report of polyneuropathy with minifasc...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s004010051085

    authors: Umehara F,Yamaguchi N,Kodama D,Takenaga S,Kiwaki T,Sonoda Y,Arimura Y,Yamada H,Arimura K,Osame M

    更新日期:1999-09-01 00:00:00

  • Protracted form of Canavan's disease: case history and protein kinase activity of membrane fractions.

    abstract::Clinical and morphological findings in an 8-year-old Jewish girl with spongy leukodystrophy are presented. Ultrastructural changes indicated that this may be a form of Canavan's disease with some atypical features. Biochemical measurements indicated that synaptosomal membranes prepared from the striatum but not from t...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00691321

    authors: Boehme DH,Marks N

    更新日期:1981-01-01 00:00:00

  • MELAS: clinical phenotype and morphological brain abnormalities.

    abstract::We describe the clinical and neuropathological findings of three unrelated autopsy cases of MELAS harboring the A3243G transition in the mitochondrial DNA (mtDNA). Using immunohistochemical techniques, we studied the expression of several subunits of the respiratory chain in various brain regions from the same cases. ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-003-0716-z

    authors: Sparaco M,Simonati A,Cavallaro T,Bartolomei L,Grauso M,Piscioli F,Morelli L,Rizzuto N

    更新日期:2003-09-01 00:00:00

  • Pericapillary rosettes in the human spinal cord.

    abstract::We have found large eosinophilic bodies in the pericapillary regions of the gray and white matter in the human spinal cord. These are entirely different from the previously reported pericapillary inclusion bodies (PIB). We have designated them pericapillary rosettes (PR), since they consist of clusters of round or ovo...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00299408

    authors: Sasaki S,Maruyama S

    更新日期:1992-01-01 00:00:00

  • The temporal evolution of hypoglycemic brain damage. III. Light and electron microscopic findings in the rat caudoputamen.

    abstract::The caudate nucleus and putamen belong to the selectively vulnerable brain regions which incur neuronal damage in clinical and experimental settings of both hypoglycemia and ischemia. We have previously documented the density and distribution of the hypoglycemic damage in rat caudoputamen, but the evolution of the inj...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00688122

    authors: Kalimo H,Auer RN,Siesjö BK

    更新日期:1985-01-01 00:00:00

  • Neuropathology of mice with targeted disruption of Hexa gene, a model of Tay-Sachs disease.

    abstract::A murine model of Tay-Sachs disease, the prototype of the GM2 gangliosidoses, was produced through the targeted disruption of the Hexa gene encoding the subunit of alpha-hexosaminidase A. The mice were completely devoid of beta-hexosaminidase A activity and accumulated GM2 ganglioside in the CNS in an age-dependent ma...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00309622

    authors: Taniike M,Yamanaka S,Proia RL,Langaman C,Bone-Turrentine T,Suzuki K

    更新日期:1995-01-01 00:00:00

  • Medulloblastoma subgroups remain stable across primary and metastatic compartments.

    abstract::Medulloblastoma comprises four distinct molecular variants with distinct genetics, transcriptomes, and outcomes. Subgroup affiliation has been previously shown to remain stable at the time of recurrence, which likely reflects their distinct cells of origin. However, a therapeutically relevant question that remains una...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-015-1389-0

    authors: Wang X,Dubuc AM,Ramaswamy V,Mack S,Gendoo DM,Remke M,Wu X,Garzia L,Luu B,Cavalli F,Peacock J,López B,Skowron P,Zagzag D,Lyden D,Hoffman C,Cho YJ,Eberhart C,MacDonald T,Li XN,Van Meter T,Northcott PA,Haibe-Kain

    更新日期:2015-03-01 00:00:00

  • Ultrastructural pathology in emetine-induced myopathy.

    abstract::Progressive myopathy developed in two women who consumed ipecac syrup containing emetine hydrochloride to induce vomiting as part of their anorexia nervosa. Muscle biopsy specimens were characterized by severe disruption of the sarcomeres. The ultrastructural spectrum extended from "Z-band streaming" to the formation ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00686202

    authors: Halbig L,Gutmann L,Goebel HH,Brick JF,Schochet S

    更新日期:1988-01-01 00:00:00

  • Analysis of BRAF V600E mutation in 1,320 nervous system tumors reveals high mutation frequencies in pleomorphic xanthoastrocytoma, ganglioglioma and extra-cerebellar pilocytic astrocytoma.

    abstract::Missense mutations of the V600E type constitute the vast majority of tumor-associated somatic alterations in the v-RAF murine sarcoma viral oncogene homolog B1 (BRAF) gene. Initially described in melanoma, colon and papillary thyroid carcinoma, these alterations have also been observed in primary nervous system tumors...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-011-0802-6

    authors: Schindler G,Capper D,Meyer J,Janzarik W,Omran H,Herold-Mende C,Schmieder K,Wesseling P,Mawrin C,Hasselblatt M,Louis DN,Korshunov A,Pfister S,Hartmann C,Paulus W,Reifenberger G,von Deimling A

    更新日期:2011-03-01 00:00:00

  • Spheroids and altered axons in the spinal gray matter of the normal cat. An electron-microscopic study.

    abstract::In our recent ultrastructural studies on synapses of the nucleus dorsalis, central cervical nucleus, and anterior horn of the spinal cord of the normal cat we happened to find spheroids and several types of axonal alterations. These spheroids were up to 39 micrometer in diameter. They were found in myelinated and unmy...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00705809

    authors: Saito K

    更新日期:1980-01-01 00:00:00

  • Granulovacuolar degeneration in the hippocampal cortex of aging and demented patients--a quantitative study.

    abstract::The occurrence and topographic analysis of granulovacuolar degeneration (GVD) in the hippocampal cortex of mentally normal controls (75 cases) and patients with Alzheimer's dementia (AD; 17 cases which included Alzheimer's disease and senile dementia of Alzheimer type), multi-infarct dementia (MID; 16 cases), Pick's d...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00304627

    authors: Xu M,Shibayama H,Kobayashi H,Yamada K,Ishihara R,Zhao P,Takeuchi T,Yoshida K,Inagaki T,Nokura K

    更新日期:1992-01-01 00:00:00

  • Fine structure of intercellular junctions and blood vessels in medulloblastomas.

    abstract::Six medulloblastomas were studied by electron microscopy. Two features were found which seem to be constant and essential characteristics of medulloblastoma. First, cell junctions are abundant between tumor cells. These are mostly desmosome-like but other, closer junctions, were also seen. Second, the capillary endoth...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00685966

    authors: Hassoun J,Hirano A,Zimmerman HM

    更新日期:1975-10-27 00:00:00

  • An autopsy case of the "demyelinating type" of Wilson's disease.

    abstract::A 17 year-old male, who was mentally and bodily retarded from the age of 7 years. At the age of 16 years, several neurological signs appeared. Pathologically, there was widespread myelin loss and tissue sponginess in the white matter of the cerebrum and cerebellum, bilaterally and symmetrically. A great many Alzheimer...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:

    authors: Miyakawa T,Murayama E

    更新日期:1976-01-01 00:00:00

  • Organic lead and histological parameters of brain development.

    abstract::Relatively little work has been done on the structural effects of organic lead in the central nervous system (CNS), although this form of lead may be a significant fraction of total brain lead. We tested a number of easily measured light-histological parameters of neuronal development in rats for sensitivity to (a) no...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00687338

    authors: Ferris NJ,Cragg BG

    更新日期:1984-01-01 00:00:00

  • Ultrastructural study of aggregates in the spinal cord of transgenic mice with a G93A mutant SOD1 gene.

    abstract::The ultrastructural features of SOD1-positive aggregates were determined to clarify whether these aggregates are associated with the pathogenesis of SOD1 mutant mice. We examined the spinal cord of transgenic mice expressing a G93A mutant human SOD1 gene with fewer copies (gene copy 10). At the early presymptomatic st...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-004-0939-7

    authors: Sasaki S,Warita H,Murakami T,Shibata N,Komori T,Abe K,Kobayashi M,Iwata M

    更新日期:2005-03-01 00:00:00

  • Expression of glial fibrillary acidic protein in human glioma cell lines as detected by molecular hybridization.

    abstract::The expression of glial fibrillary acidic protein (GFAP) in continuous glioma and non-glioma cell lines was evaluated by molecular hybridization and immunocytochemistry. RNA transcripts from the GFAP gene were detected in two of six cell lines by Northern blot analysis of cellular RNAs using a cloned mouse GFAP cDNA p...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00688264

    authors: Dewhurst S,Stevenson M,McComb RD,Volsky DJ

    更新日期:1987-01-01 00:00:00

  • Artificial intelligence in neurodegenerative disease research: use of IBM Watson to identify additional RNA-binding proteins altered in amyotrophic lateral sclerosis.

    abstract::Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease with no effective treatments. Numerous RNA-binding proteins (RBPs) have been shown to be altered in ALS, with mutations in 11 RBPs causing familial forms of the disease, and 6 more RBPs showing abnormal expression/distribution in ALS albeit...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-017-1785-8

    authors: Bakkar N,Kovalik T,Lorenzini I,Spangler S,Lacoste A,Sponaugle K,Ferrante P,Argentinis E,Sattler R,Bowser R

    更新日期:2018-02-01 00:00:00

  • Reversibility of neurofilamentous inclusion formation following repeated sublethal intracisternal inoculums of AlCl3 in New Zealand white rabbits.

    abstract::In this report, we describe the clinical, topographical and immunohistochemical characteristics of neurofilament (NF) inclusion formation induced by the intracisternal inoculation of young adult New Zealand white rabbits at 28-day intervals with 100 micrograms AlCl3 over the course of 267 days. The ability to recover ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00294460

    authors: Strong MJ,Gaytan-Garcia S,Jakowec DM

    更新日期:1995-01-01 00:00:00

  • Progressive supranuclear palsy with palatal myoclonus.

    abstract::We present a case of progressive supranuclear palsy (PSP) with palatal myoclonus occurred in a 64-year-old man. The nucleus olivaris of the medulla oblongata showed high signal intensity on T2-weighted MR images, indicating brainstem tegmental atrophy, which were confirmed as hypertrophy of the nucleus inferior olivar...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s004010050706

    authors: Suyama N,Kobayashi S,Isino H,Iijima M,Imaoka K

    更新日期:1997-09-01 00:00:00