ABBREV LONG NAME of STRUCTURE PLATE 10N Dorsal
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
The Connexions of the Amygdala
J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.28.2.137 on 1 April 1965. Downloaded from J. Neurol. Neurosurg. Psychiat., 1965, 28, 137 The connexions of the amygdala W. M. COWAN, G. RAISMAN, AND T. P. S. POWELL From the Department of Human Anatomy, University of Oxford The amygdaloid nuclei have been the subject of con- to what is known of the efferent connexions of the siderable interest in recent years and have been amygdala. studied with a variety of experimental techniques (cf. Gloor, 1960). From the anatomical point of view MATERIAL AND METHODS attention has been paid mainly to the efferent connexions of these nuclei (Adey and Meyer, 1952; The brains of 26 rats in which a variety of stereotactic or Lammers and Lohman, 1957; Hall, 1960; Nauta, surgical lesions had been placed in the diencephalon and and it is now that there basal forebrain areas were used in this study. Following 1961), generally accepted survival periods of five to seven days the animals were are two main efferent pathways from the amygdala, perfused with 10 % formol-saline and after further the well-known stria terminalis and a more diffuse fixation the brains were either embedded in paraffin wax ventral pathway, a component of the longitudinal or sectioned on a freezing microtome. All the brains were association bundle of the amygdala. It has not cut in the coronal plane, and from each a regularly spaced generally been recognized, however, that in studying series was stained, the paraffin sections according to the Protected by copyright. the efferent connexions of the amygdala it is essential original Nauta and Gygax (1951) technique and the frozen first to exclude a contribution to these pathways sections with the conventional Nauta (1957) method. -
The Interpeduncular Fossa Approach for Resection of Ventromedial Midbrain Lesions
TECHNICAL NOTE J Neurosurg 128:834–839, 2018 The interpeduncular fossa approach for resection of ventromedial midbrain lesions *M. Yashar S. Kalani, MD, PhD, Kaan Yağmurlu, MD, and Robert F. Spetzler, MD Department of Neurosurgery, Barrow Neurological Institute, St. Joseph’s Hospital and Medical Center, Phoenix, Arizona The authors describe the interpeduncular fossa safe entry zone as a route for resection of ventromedial midbrain le- sions. To illustrate the utility of this novel safe entry zone, the authors provide clinical data from 2 patients who under- went contralateral orbitozygomatic transinterpeduncular fossa approaches to deep cavernous malformations located medial to the oculomotor nerve (cranial nerve [CN] III). These cases are supplemented by anatomical information from 6 formalin-fixed adult human brainstems and 4 silicone-injected adult human cadaveric heads on which the fiber dissection technique was used. The interpeduncular fossa may be incised to resect anteriorly located lesions that are medial to the oculomotor nerve and can serve as an alternative to the anterior mesencephalic safe entry zone (i.e., perioculomotor safe entry zone) for resection of ventromedial midbrain lesions. The interpeduncular fossa safe entry zone is best approached using a modi- fied orbitozygomatic craniotomy and uses the space between the mammillary bodies and the top of the basilar artery to gain access to ventromedial lesions located in the ventral mesencephalon and medial to the oculomotor nerve. https://thejns.org/doi/abs/10.3171/2016.9.JNS161680 KEY WORDS brainstem surgery; interpeduncular fossa; mesencephalon; safe entry zone; surgical technique; ventromedial midbrain HE human brainstem serves as a relay center for the pyramidal tract, which is located in the middle three- ascending and descending fiber tracts that are es- fifths of the cerebral peduncle, to remove ventral lesions sential for motor and sensory control. -
Reorganization of Neural Peptidergic Eminence After Hypophysectomy
The Journal of Neuroscience, October 1994, 14(10): 59966012 Reorganization of Neural Peptidergic Systems Median Eminence after Hypophysectomy Marcel0 J. Villar, Bjiirn Meister, and Tomas Hiikfelt Department of Neuroscience, The Berzelius Laboratory, Karolinska Institutet, Stockholm, 171 77 Sweden Earlier studies have shown the formation of a novel neural crease to a final stage of a few, strongly immunoreactive lobe after hypophysectomy, an experimental manipulation fibers in the external layer at longer survival times. Vaso- that causes transection of neurohypophyseal nerve fibers active intestinal polypeptide (VIP)- and peptide histidine- and removal of pituitary hormones. The mechanisms that isoleucine (PHI)-IR fibers in hypophysectomized animals had underly this regenerative process are poorly understood. already contacted portal vessels 5 d after hypophysectomy, The localization and number of peptide-immunoreactive and from then on progressively increased in numbers. Fi- (-IR) fibers in the median eminence were studied in normal nally, most of the peptide fibers described above formed rats and in rats at different times of survival after hypophy- dense innervation patterns around the large blood vessels sectomy using indirect immunofluorescence histochemistry. along the lateral borders of the median eminence. The number of vasopressin (VP)-IR fibers increased in the The present results show that hypophysectomy induces external layer of the median eminence in 5 d hypophysec- a wide variety of changes in hypothalamic neurosecretory tomized rats. Oxytocin (OXY)-IR fibers decreased in the in- fibers. Not only is the expression of several peptides in these ternal layer and progressively extended into the external fibers modified following different survival times, but a re- layer. -
University International
INFORMATION TO USERS This was produced from a copy of a document sent to us for microfilming. While the most advanced technological means to photograph and reproduce this document have been used, the quality is heavily dependent upon the quality of the material submitted. The following explanation of techniques is provided to help you understand markings or notations which may appear on this reproduction. 1. The sign or “target” for pages apparently lacking from the document photographed is “Missing Page(s)”. If it was possible to obtain the missing page(s) or section, they are spliced into the film along with adjacent pages. This may have necessitated cutting through an image and duplicating adjacent pages to assure you of complete continuity. 2. When an image on the film is obliterated with a round black mark it is an indication that the film inspector noticed either blurred copy because of movement during exposure, or duplicate copy. Unless we meant to delete copyrighted materials that should not have been filmed, you will find a good image of the page in the adjacent frame. 3. When a map, drawing or chart, etc., is part of the material being photo graphed the photographer has followed a definite method in “sectioning” the material. It is customary to begin filming at the upper left hand corner of a large sheet and to continue from left to right in equal sections with small overlaps. If necescary, sectioning is continued again—beginning below the first row and continuing on until complete. 4. For any illustrations that cannot be reproduced satisfactorily by xerography, photographic prints can be purchased at additional cost and tipped into your xerographic copy. -
Selective Association with Enkephalin-Containing Neurons (Peptide Processing/Carboxypeptidase/Magnoceliular Hypothalamus/Hippocampus/Proenkephalin) DAVID R
Proc. Natl. Acad. Sci. USA Vol. 81, pp. 6543-6547, October 1984 Neurobiology Enkephalin convertase localization by [3H]guanidinoethylmercaptosuccinic acid autoradiography: Selective association with enkephalin-containing neurons (peptide processing/carboxypeptidase/magnoceliular hypothalamus/hippocampus/proenkephalin) DAVID R. LYNCH, STEPHEN M. STRITTMATTER, AND SOLOMON H. SNYDER* Departments of Neuroscience, Pharmacology and Experimental Therapeutics, Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205 Contributed by Solomon H. Snyder, July 6, 1984 ABSTRACT Enkephalin convertase, an enkephalin-form- tioned by the method of Young and Kuhar (14) as modified ing carboxypeptidase, is potently inhibited by guanidinoethyl- by Strittmatter et al. (15). For autoradiography, sections mercaptosuccinic acid (GEMSA). We have localized enkepha- were incubated at 40C in 0.05 M sodium acetate (pH 5.6) for lin convertase in rat brain by in vitro autoradiography with 5 min and then in the same buffer with 4 nM [3H]GEMSA [3H]GEMSA. [3H]GEMSA-associated silver grains are highly and any inhibitors for 30 min. Nonspecific binding was de- concentrated in the median eminence, bed nucleus of the stria termined in the presence of 10 ,uM unlabeled GEMSA. The terminalis, lateral septum, dentate gyrus, hippocampus, cen- slides were washed twice for 1 min in sodium acetate (pH tral nucleus of the amygdala, preoptic hypothalamus, magno- 5.6) at 40C, dipped in water, and dried rapidly under a stream cellular nuclei of the hypothalamus, interpeduncular nucleus, of air. The slides were dessicated overnight and applied to dorsal parabrachial nucleus, locus coeruleus, nucleus of the LKB Ultrafilm or photographic emulsion.coated coverslips solitary tract, and the substantia gelatinosa of the spinal tri- for 12 days at 40C. -
Localization of Luteinizing Hormone-Releasing Hormone (LHRH) Neurons That Project to the Median Eminence
The Journal of Neuroscience, August 1987, 7(8): 2312-2319 Localization of Luteinizing Hormone-Releasing Hormone (LHRH) Neurons That Project to the Median Eminence Ann-Judith Silverman,’ Jack Jhamandas, and Leo P. Renaud ‘Department of Anatomy and Cell Biology, Columbia University, New York, New York 10032, and Neurosciences Unit, Montreal General Hospital and McGill University, Montreal H3G lA4, Canada The neuropeptide, luteinizing hormone-releasing hormone septal, preoptic, and hypothalamic regions,forming a loosecon- (LHRH), is released from nerve terminals in the median em- tinuum from the level of the diagonal band of Broca, including inence and carried via the hypophysial portal system to the both its vertical and horizontal limbs, the medial and triangular anterior pituitary, where it stimulates the release of gonad- septal nuclei, and periventricular, medial, and lateral preoptic otropins. LHRH-containing neurons are located in many dif- and anterior hypothalamic areas. Some LHRH cells are found ferent regions of the rodent brain, including olfactory, septal, rostra1 to the supraoptic nucleus, others in the retrochiasmatic preoptic, and hypothalamic structures. Since those LHRH zone, just medial to the optic tract. A few LHRH neuronsare neurons that project to the median eminence form the final seenwithin the circumventricular organs, i.e., the organum vas- common pathway for the regulation of the pituitary/gonadal culosum of the lamina terminalis (OVLT) and the subfomical axis, we wished to determine which of these cell groups are organ. Finally, LHRH neuronsare associatedwith the accessory afferent to this structure. A retrograde tracer, the lectin wheat olfactory bulb and other olfactory-related structures, including germ agglutinin (WGA), was placed directly on the exposed the nervus terminalis. -
Thalamus and Hypothalamus
DIENCEPHALON: THALAMUS AND HYPOTHALAMUS M. O. BUKHARI 1 DIENCEPHALON: General Introduction • Relay & integrative centers between the brainstem & cerebral cortex • Dorsal-posterior structures • Epithalamus • Anterior & posterior paraventricular nuclei • Habenular nuclei – integrate smell & emotions • Pineal gland – monitors diurnal / nocturnal rhythm • Habenular Commissure • Post. Commissure • Stria Medullaris Thalami • Thalamus(Dorsal thalamus) • Metathalamus • Medial geniculate body – auditory relay • Lateral geniculate body – visual relay Hypothalamic sulcus • Ventral-anterior structure • Sub-thalums (Ventral Thalamus) • Sub-thalamic Nucleus • Zona Inserta • Fields of Forel • Hypothalamus M. O. BUKHARI 2 Introduction THE THALAMUS Location Function External features Size Interthalamic 3 cms length x 1.5 cms breadth adhesion Two ends Anterior end– Tubercle of Thalamus Posterior end– Pulvinar – Overhangs Med & Lat.Gen.Bodies, Sup.Colliculi & their brachia Surfaces Sup. Surface – Lat. Part forms central part of lat. Vent. Med. Part is covered by tela choroidea of 3rd vent. Inf. Surface - Ant. part fused with subthalamus - Post. part free – inf. part of Pulvinar Med. Surface – Greater part of Lat. wall of 3rd ventricle Lat. Surface - Med.boundary of Post. Limb of internal capsule M. O. BUKHARI 3 Function of the Thalamus • Sensory relay • ALL sensory information (except smell) • Motor integration • Input from cortex, cerebellum and basal ganglia • Arousal • Part of reticular activating system • Pain modulation • All nociceptive information • Memory & behavior • Lesions are disruptive M. O. BUKHARI 4 SUBDIVISION OF THALAMUS M. O. BUKHARI 5 SUBDIVISION OF THALAMUS: WHITE MATTER OF THE THALAMUS Internal Medullary Stratum Zonale Lamina External Medullary Lamina M. O. BUKHARI 6 LATERAL MEDIAL Nuclei of Thalamus Stratum Zonale Anterior Nucleus Medial Dorsal Lateral Dorsal (Large) EXT.Med.Lam ILN Ret.N CMN VPL MGB VPM PVN Lateral Ventral Medial Ventral LGB (Small) LD, LP, Pulvinar – Dorsal Tier nuclei Hypothalamus VA, VL, VPL, VPM – Ventral Tier nuclei M. -
Variations in Number of Dopamine Neurons and Tyrosine Hydroxylase Activity in Hypothalamus of Two Mouse Strains
0270.6474/83/0304-0832$02.00/O The Journal of Neuroscience Copyright 0 Society for Neuroscience Vol. 3, No. 4, pp. 832-843 Printed in U.S.A. April 1983 VARIATIONS IN NUMBER OF DOPAMINE NEURONS AND TYROSINE HYDROXYLASE ACTIVITY IN HYPOTHALAMUS OF TWO MOUSE STRAINS HARRIET BAKER,2 TONG H. JOH, DAVID A. RUGGIERO, AND DONALD J. REIS Laboratory of Neurobiology, Cornell University Medical College, New York, New York 10021 Received May 3, 1982; Revised August 23, 1982; Accepted October 8, 1982 Abstract Mice of the BALB/cJ strain have more neurons and greater tyrosine hydroxylase (TH) activity in the midbrain than mice of the CBA/J strain (Baker, H., T. H. Joh, and D. J. Reis (1980) Proc. Natl. Acad. Sci. U. S. A. 77: 4369-4373). To determine whether the strain differences in dopamine (DA) neuron number and regional TH activity are more generalized, regional TH activity was measured and counts of neurons containing the enzyme were made in the hypothalamus of male mice of the BALB/cJ and CBA/J strains. TH activity was measured in dissections of whole hypothalamus (excluding the preoptic area), the preoptic area containing a rostral extension of the Al4 group, the mediobasal hypothalamus containing the A12 group, and the mediodorsal hypothal- amus containing neurons of the Al3 and Al4 groups. Serial sections were taken and the number of DA neurons was established by counting at 50- to 60-pm intervals all cells stained for TH through each area. In conjunction with data obtained biochemically, the average amount of TH per neuron was determined. -
Brainstem and Its Associated Cranial Nerves
Brainstem and its Associated Cranial Nerves Anatomical and Physiological Review By Sara Alenezy With appreciation to Noura AlTawil’s significant efforts Midbrain (Mesencephalon) External Anatomy of Midbrain 1. Crus Cerebri (Also known as Basis Pedunculi or Cerebral Peduncles): Large column of descending “Upper Motor Neuron” fibers that is responsible for movement coordination, which are: a. Frontopontine fibers b. Corticospinal fibers Ventral Surface c. Corticobulbar fibers d. Temporo-pontine fibers 2. Interpeduncular Fossa: Separates the Crus Cerebri from the middle. 3. Nerve: 3rd Cranial Nerve (Oculomotor) emerges from the Interpeduncular fossa. 1. Superior Colliculus: Involved with visual reflexes. Dorsal Surface 2. Inferior Colliculus: Involved with auditory reflexes. 3. Nerve: 4th Cranial Nerve (Trochlear) emerges caudally to the Inferior Colliculus after decussating in the superior medullary velum. Internal Anatomy of Midbrain 1. Superior Colliculus: Nucleus of grey matter that is associated with the Tectospinal Tract (descending) and the Spinotectal Tract (ascending). a. Tectospinal Pathway: turning the head, neck and eyeballs in response to a visual stimuli.1 Level of b. Spinotectal Pathway: turning the head, neck and eyeballs in response to a cutaneous stimuli.2 Superior 2. Oculomotor Nucleus: Situated in the periaqueductal grey matter. Colliculus 3. Red Nucleus: Red mass3 of grey matter situated centrally in the Tegmentum. Involved in motor control (Rubrospinal Tract). 1. Inferior Colliculus: Nucleus of grey matter that is associated with the Tectospinal Tract (descending) and the Spinotectal Tract (ascending). Tectospinal Pathway: turning the head, neck and eyeballs in response to a auditory stimuli. 2. Trochlear Nucleus: Situated in the periaqueductal grey matter. Level of Inferior 3. -
Characterization of the Human Habenula In-Vivo and Ex-Vivo at 7T
Characterization of the Human Habenula in-vivo and ex-vivo at 7T B. Strotmann1, M. Weiss1, C. Kögler1, A. Schäfer1, R. Trampel1, S. Geyer1, A. Villringer1, and R. Turner1 1Max-Planck-Institute for Human Cognitive and Brain Sciences, Leipzig, Germany Introduction: The habenula has an important controlling role within the human reward system [1,2]: positive reward is signaled by the dopamine system, whereas disappointment is linked to habenular activation. Overactivation of the lateral habenula is associated with depression [3,4]. The habenula is positioned next to the third ventricle in front of the pineal body. It is divided into a medial and lateral part, which receive input from frontal parts of the brain via the stria medullaris and project down the brainstem via the fasciculus retroflexus[5]. The habenular commissure connecting the nuclei on both hemispheres forms the habenular trigone. However, the visualization of this structure is difficult because of its rather small size of approximately 5-9 mm in diameter. Therefore, we made use of a high field strength of 7T to obtain high resolution and high contrast T1, T2* und proton density maps to visualize and determine structural subdivisions of the habenula in-vivo and ex-vivo. Methods: All experiments were performed on a 7 Tesla whole-body MR scanner (MAGNETOM 7T, Siemens Healthcare, Erlangen, Germany) using a 24 channel phased-array head coil (Nova Medical Inc, Wilmington MA, USA) for in-vivo scans, and a custom-built single channel square coil (120mm side) with the post mortem brain tissue centred inside. The study was approved by the ethics committee of the local university and informed consent was obtained. -
The Oculomotor Cistern: Anatomy and High- ORIGINAL RESEARCH Resolution Imaging
The Oculomotor Cistern: Anatomy and High- ORIGINAL RESEARCH Resolution Imaging K.L. Everton BACKGROUND AND PURPOSE: The oculomotor cistern (OMC) is a small CSF-filled dural cuff that U.A. Rassner invaginates into the cavernous sinus, surrounding the third cranial nerve (CNIII). It is used by neuro- surgeons to mobilize CNIII during cavernous sinus surgery. In this article, we present the OMC imaging A.G. Osborn spectrum as delineated on 1.5T and 3T MR images and demonstrate its involvement in cavernous H.R. Harnsberger sinus pathology. MATERIALS AND METHODS: We examined 78 high-resolution screening MR images of the internal auditory canals (IAC) obtained for sensorineural hearing loss. Cistern length and diameter were measured. Fifty randomly selected whole-brain MR images were evaluated to determine how often the OMC can be visualized on routine scans. Three volunteers underwent dedicated noncontrast high-resolution MR imaging for optimal OMC visualization. RESULTS: One or both OMCs were visualized on 75% of IAC screening studies. The right cistern length averaged 4.2 Ϯ 3.2 mm; the opening diameter (the porus) averaged 2.2 Ϯ 0.8 mm. The maximal length observed was 13.1 mm. The left cistern length averaged 3.0 Ϯ 1.7 mm; the porus diameter averaged 2.1 Ϯ1.0 mm, with a maximal length of 5.9 mm. The OMC was visualized on 64% of routine axial T2-weighted brain scans. CONCLUSION: The OMC is an important neuroradiologic and surgical landmark, which can be routinely identified on dedicated thin-section high-resolution MR images. It can also be identified on nearly two thirds of standard whole-brain MR images. -
The Nuclear Pattern of the Non-Tectal Portions of the Midbrain and Isthmus in Primates
THE NUCLEAR PATTERN OF THE NON-TECTAL PORTIONS OF THE MIDBRAIN AND ISTHMUS IN PRIMATES ELIZABETH C. CROSBY AND RUSSELL T. WOODBURNE Department of Anatomy, University of Michigan FOURTEEN PLATES (TWENTY-THREE FIGURES) INTRODUCTION The various nuclear groups in the midbrain of primates show marked resemblances to their homologues in subprimate forms, although certain regions are characterized by a marked increase and others by a definite decrease in development. The literature dealing with special regions is considerable in amount and some of it is of relatively early date. That pertinent to the present consideration of these regions has been reviewed under the account of the general literature placed at the end of this series of papers. Attention is called here to a few contributions that have been particularly helpful in the preparation of the primate descriptions. Among such are the studies of Ziehen on various regions of the midbrain, particularly his account of the periventricular regions, and the descriptive analysis of Ingram and Ranson ('35) of the nucleus of Darkschewitsch and the interstitial nucleus of the medial longitudinal fasciculus, which confirmed Stengel's ( '24) earlier account. There are innumerable figures and descrip- tions of various parts of the oculomotor and trochlear gray in primates. Among these may be mentioned the work of Panegrossi ('04), Ram6n y Cajal ('ll), Brouwer ('18, and elsewhere), Le Gros Clark ( '26) and Mingazzini ( '28). The differences in nomenclature with respect to the periventricular gray of caudal midbrain and isthmus regions are indicated 441 442 G. CARL HUBER ET AL. to some extent on the figures of the human brain as well as considered in the general literature.