Lannoo, M.J. Neuro Manual
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Distance Learning Program Anatomy of the Human Brain/Sheep Brain Dissection
Distance Learning Program Anatomy of the Human Brain/Sheep Brain Dissection This guide is for middle and high school students participating in AIMS Anatomy of the Human Brain and Sheep Brain Dissections. Programs will be presented by an AIMS Anatomy Specialist. In this activity students will become more familiar with the anatomical structures of the human brain by observing, studying, and examining human specimens. The primary focus is on the anatomy, function, and pathology. Those students participating in Sheep Brain Dissections will have the opportunity to dissect and compare anatomical structures. At the end of this document, you will find anatomical diagrams, vocabulary review, and pre/post tests for your students. The following topics will be covered: 1. The neurons and supporting cells of the nervous system 2. Organization of the nervous system (the central and peripheral nervous systems) 4. Protective coverings of the brain 5. Brain Anatomy, including cerebral hemispheres, cerebellum and brain stem 6. Spinal Cord Anatomy 7. Cranial and spinal nerves Objectives: The student will be able to: 1. Define the selected terms associated with the human brain and spinal cord; 2. Identify the protective structures of the brain; 3. Identify the four lobes of the brain; 4. Explain the correlation between brain surface area, structure and brain function. 5. Discuss common neurological disorders and treatments. 6. Describe the effects of drug and alcohol on the brain. 7. Correctly label a diagram of the human brain National Science Education -
Review Article Meninges: from Protective Membrane to Stem Cell Niche
Am J Stem Cell 2012;1(2):92-105 www.AJSC.us /ISSN: 2160-4150/AJSC1205003 Review Article Meninges: from protective membrane to stem cell niche Ilaria Decimo1, Guido Fumagalli1, Valeria Berton1, Mauro Krampera2, Francesco Bifari2 1Department of Public Health and Community Medicine, Section of Pharmacology, University of Verona, Italy; 2De- partment of Medicine, Stem Cell Laboratory, Section of Hematology, University of Verona, Italy Received May 16, 2012; accepted May 23, 2012; Epub 28, 2012; Published June 30, 2012 Abstract: Meninges are a three tissue membrane primarily known as coverings of the brain. More in depth studies on meningeal function and ultrastructure have recently changed the view of meninges as a merely protective mem- brane. Accurate evaluation of the anatomical distribution in the CNS reveals that meninges largely penetrate inside the neural tissue. Meninges enter the CNS by projecting between structures, in the stroma of choroid plexus and form the perivascular space (Virchow-Robin) of every parenchymal vessel. Thus, meninges may modulate most of the physiological and pathological events of the CNS throughout the life. Meninges are present since the very early em- bryonic stages of cortical development and appear to be necessary for normal corticogenesis and brain structures formation. In adulthood meninges contribute to neural tissue homeostasis by secreting several trophic factors includ- ing FGF2 and SDF-1. Recently, for the first time, we have identified the presence of a stem cell population with neural differentiation potential in meninges. In addition, we and other groups have further described the presence in men- inges of injury responsive neural precursors. In this review we will give a comprehensive view of meninges and their multiple roles in the context of a functional network with the neural tissue. -
Endoscopic Anatomical Study of the Arachnoid Architecture on the Base of the Skull
DOI 10.1515/ins-2012-0005 Innovative Neurosurgery 2013; 1(1): 55–66 Original Research Article Peter Kurucz* , Gabor Baksa , Lajos Patonay and Nikolai J. Hopf Endoscopic anatomical study of the arachnoid architecture on the base of the skull. Part I: The anterior and middle cranial fossa Abstract: Minimally invasive neurosurgery requires a Introduction detailed knowledge of microstructures, such as the arach- noid membranes. In spite of many articles addressing The arachnoid was discovered and named by Gerardus arachnoid membranes, its detailed organization is still not Blasius in 1664 [ 22 ]. Key and Retzius were the first who well described. The aim of this study is to investigate the studied its detailed anatomy in 1875 [ 11 ]. This description was topography of the arachnoid in the anterior cranial fossa an anatomical one, without mentioning clinical aspects. The and the middle cranial fossa. Rigid endoscopes were intro- first clinically relevant study was provided by Liliequist in duced through defined keyhole craniotomies, to explore 1959 [ 13 ]. He described the radiological anatomy of the sub- the arachnoid structures in 110 fresh human cadavers. We arachnoid cisterns and mentioned a curtain-like membrane describe the topography and relationship to neurovascu- between the supra- and infratentorial cranial space bearing lar structures and suggest an intuitive terminology of the his name still today. Lang gave a similar description of the arachnoid. We demonstrate an “ arachnoid membrane sys- subarachnoid cisterns in 1973 [ 12 ]. With the introduction of tem ” , which consists of the outer arachnoid and 23 inner microtechniques in neurosurgery, the detailed knowledge arachnoid membranes in the anterior fossa and the middle of the surgical anatomy of the cisterns became more impor- fossa. -
The Strain Rates in the Brain, Brainstem, Dura, and Skull Under Dynamic Loadings
Mathematical and Computational Applications Article The Strain Rates in the Brain, Brainstem, Dura, and Skull under Dynamic Loadings Mohammad Hosseini-Farid 1,2,* , MaryamSadat Amiri-Tehrani-Zadeh 3, Mohammadreza Ramzanpour 1, Mariusz Ziejewski 1 and Ghodrat Karami 1 1 Department of Mechanical Engineering, North Dakota State University, Fargo, ND 58104, USA; [email protected] (M.R.); [email protected] (M.Z.); [email protected] (G.K.) 2 Department of Orthopedic Surgery, Mayo Clinic, Rochester, MN 55905, USA 3 Department of Computer Science, North Dakota State University, Fargo, ND 58104, USA; [email protected] * Correspondence: [email protected]; Tel.: +1-7012315859 Received: 7 March 2020; Accepted: 5 April 2020; Published: 7 April 2020 Abstract: Knowing the precise material properties of intracranial head organs is crucial for studying the biomechanics of head injury. It has been shown that these biological tissues are significantly rate-dependent; hence, their material properties should be determined with respect to the range of deformation rate they experience. In this paper, a validated finite element human head model is used to investigate the biomechanics of the head in impact and blast, leading to traumatic brain injuries (TBI). We simulate the head under various directions and velocities of impacts, as well as helmeted and unhelmeted head under blast shock waves. It is demonstrated that the strain rates for the brain 1 are in the range of 36 to 241 s− , approximately 1.9 and 0.86 times the resulting head acceleration under impacts and blast scenarios, respectively. The skull was found to experience a rate in the range 1 of 14 to 182 s− , approximately 0.7 and 0.43 times the head acceleration corresponding to impact and blast cases. -
MR of the Diaphragma Sellae
765 MR of the Diaphragma Sellae David L. Daniels 1 The appearance of the diaphragma sellae is described in cryomicrotomic sections Kathleen W. Pojunas1 and on MR in patients with and without intra- and suprasellar masses. On MR, it appears David P. Kilgore 1 as a thin band of negligible signal that is best shown when adjacent CSF or a mass has Peter Pech 2 greater signal intensity. Its position or absence can be used to differentiate intrasellar Glenn A. Meyer masses with suprasellar components from suprasellar masses. Alan L. Williams 1 1 Victor M. Haughton Differentiating intrasellar masses with suprasellar components from suprasellar masses may be difficult with CT because the pituitary gland, diaphragma sellae, and suprasellar masses may enhance equally after intravenous contrast adminis tration. Theoretically, MR should be able to show the diaphragma sellae because other dural reflections, such as the falx cerebri and walls of the cavernous sinuses, can be differentiated from the adjacent CSF when it has greater signal intensity [1 ]. Materials and Methods Sagittal or coronal anatomic images of the sella were obtained by sectioning four fresh frozen cadaver heads with a horizontally cutting heavy-duty sledge cryomicrotome (LKB 2250) and then serially photographing the surfaces of the specimens [2]. In the anatomic images, the diaphragma sellae and associated blood vessels, the pituitary gland, and the infundibulum were identified using anatomic literature [3-5]. Ten normal volunteers and 22 patients were studied with MR . The patients included 12 with pituitary microadenomas that were verified by surgical findings (four cases) and by CT, clinical , and chemical findings [6]; seven with pituitary macroadenomas and two with tuber culum sellae meningiomas that were verified by CT and surgery; and one with a large suprasellar aneurysm that was verified by CT and angiography. -
Nervous System - PNS and CNS
Nervous System - PNS AND CNS Locate the following structures on the appropriate model or diagram. Understand the function of ea Neuron Spinal nerves Cerebrum axon cervical plexus cerebral hemisphere dendrite phrenic cerebral cortex cell body gray matter Schwann cell brachial plexus white matter node of Ranvier axillary gyrus (convolution) myelin sheath radial longitudinal fissure neurolemma median falx cerebri Nissl bodies ulnar central sulcus synaptic knobs lateral sulcus synaptic vesicles lumbar plexus frontal lobe femoral parietal lobe Spinal Cord obturator occipital lobe central canal temporal lobe posterior column sacral plexus insula lateral column sciatic corpus callosum anterior column tibial olfactory bulb posterior sulcus common fibular olfactory tract anterior fissure superficial fibular posterior horn deep fibular Diencephalon lateral horn thalamus anterior horn intercostal nerves intermediate mass gray commissure hypothalamus conus medularis Autonomic NS infundibulum dorsal nerve root sympathetic trunk pituitary gland dorsal root ganglion ganglia (paravertebral) pineal gland ventral nerve root mammillary bodies spinal nerve Brainstem optic nerve cauda equina = medulla, pons, mid, optic tract filum terminale cranial nerves optic chiasm Meninges Midbrain dura mater cerebral peduncles Cranial Nerves dural sinus superior colliculus I olfactory epidural space inferior colliculus II optic arachnoid mater III oculomotor subarachnoid space Pons IV trochlear arachnoid granulations (villi) V trigeminal pia mater Medulla Oblongata VI abducens choroid plexus pyramids VII facial denticulate ligament olive VIII vestibulocochlear IX glossopharyngeal Cerebellum X vagus Ventricles cerebellar hemisphere XI accessory lateral ventricles vermis XII hypoglossal septum pellucidum transverse fissure third ventricle tentorium cerebelli cerebral aqueduct falx cerebelli fourth ventricle arbor vitae. -
What to Expect After Having a Subarachnoid Hemorrhage (SAH) Information for Patients and Families Table of Contents
What to expect after having a subarachnoid hemorrhage (SAH) Information for patients and families Table of contents What is a subarachnoid hemorrhage (SAH)? .......................................... 3 What are the signs that I may have had an SAH? .................................. 4 How did I get this aneurysm? ..................................................................... 4 Why do aneurysms need to be treated?.................................................... 4 What is an angiogram? .................................................................................. 5 How are aneurysms repaired? ..................................................................... 6 What are common complications after having an SAH? ..................... 8 What is vasospasm? ...................................................................................... 8 What is hydrocephalus? ............................................................................... 10 What is hyponatremia? ................................................................................ 12 What happens as I begin to get better? .................................................... 13 What can I expect after I leave the hospital? .......................................... 13 How will the SAH change my health? ........................................................ 14 Will the SAH cause any long-term effects? ............................................. 14 How will my emotions be affected? .......................................................... 15 When should -
Clones in the Chick Diencephalon Contain Multiple Cell Types and Siblings Are Widely Dispersed
Development 122, 65-78 (1996) 65 Printed in Great Britain © The Company of Biologists Limited 1996 DEV8292 Clones in the chick diencephalon contain multiple cell types and siblings are widely dispersed Jeffrey A. Golden1,2 and Constance L. Cepko1,3 1Department of Genetics, Harvard Medical School, 2Department of Pathology, Brigham and Women’s Hospital, and 3Howard Hughes Medical Institute, 200 Longwood Avenue, Boston, MA 02115, USA SUMMARY The thalamus, hypothalamus and epithalamus of the ver- clones dispersed in all directions, resulting in sibling cells tebrate central nervous system are derived from the populating multiple nuclei within the diencephalon. In embryonic diencephalon. These regions of the nervous addition, several distinctive patterns of dispersion were system function as major relays between the telencephalon observed. These included clones with siblings distributed and more caudal regions of the brain. Early in develop- bilaterally across the third ventricle, clones that originated ment, the diencephalon morphologically comprises distinct in the lateral ventricle, clones that crossed neuromeric units known as neuromeres or prosomeres. As development boundaries, and clones that crossed major boundaries of proceeds, multiple nuclei, the functional and anatomical the developing nervous system, such as the diencephalon units of the diencephalon, derive from the neuromeres. It and mesencephalon. These findings demonstrate that prog- was of interest to determine whether progenitors in the enitor cells in the diencephalon are multipotent and that diencephalon give rise to daughters that cross nuclear or their daughters can become widely dispersed. neuromeric boundaries. To this end, a highly complex retroviral library was used to infect diencephalic progeni- tors. Retrovirally marked clones were found to contain Key words: cell lineage, central nervous system, diencephalon, neurons, glia and occasionally radial glia. -
Sylvian Aqueduct Syndrome and Global Rostral Midbrain Dysfunction Associated with Shunt Malfunction
Sylvian aqueduct syndrome and global rostral midbrain dysfunction associated with shunt malfunction Giuseppe Cinalli, M.D., Christian Sainte-Rose, M.D., Isabelle Simon, M.D., Guillaume Lot, M.D., and Spiros Sgouros, M.D. Department of Pediatric Neurosurgery and Pediatric Radiology, Hôpital Necker•Enfants Malades, Université René Decartes; and Department of Neurosurgery, Hôpital Lariboisiere, Paris, France Object. This study is a retrospective analysis of clinical data obtained in 28 patients affected by obstructive hydrocephalus who presented with signs of midbrain dysfunction during episodes of shunt malfunction. Methods. All patients presented with an upward gaze palsy, sometimes associated with other signs of oculomotor dysfunction. In seven cases the ocular signs remained isolated and resolved rapidly after shunt revision. In 21 cases the ocular signs were variably associated with other clinical manifestations such as pyramidal and extrapyramidal deficits, memory disturbances, mutism, or alterations in consciousness. Resolution of these symptoms after shunt revision was usually slow. In four cases a transient paradoxical aggravation was observed at the time of shunt revision. In 11 cases ventriculocisternostomy allowed resolution of the symptoms and withdrawal of the shunt. Simultaneous supratentorial and infratentorial intracranial pressure recordings performed in seven of the patients showed a pressure gradient between the supratentorial and infratentorial compartments with a higher supratentorial pressure before shunt revision. Inversion of this pressure gradient was observed after shunt revision and resolution of the gradient was observed in one case after third ventriculostomy. In six recent cases, a focal midbrain hyperintensity was evidenced on T2-weighted magnetic resonance imaging sequences at the time of shunt malfunction. This rapidly resolved after the patient underwent third ventriculostomy. -
Meninges Ventricles And
Meninges ,ventricles & CSF Dr.Sanaa Al-Shaarawy Dr. Essam Eldin Salama OBJECTIVES • By the end of the lecture the student should be able to: • Describe the cerebral meninges & list the main dural folds. • Describe the spinal meninges & locate the level of the termination of each of them. • Describe the importance of the subarachnoid space. • List the Ventricular system of the CNS and locate the site of each of them. • Describe the formation, circulation, drainage, and functions of the CSF. • Know some clinical point about the CSF MENINGES • The brain and spinal cord are invested by three concentric membranes ; • The outermost layer is the dura matter. • The middle layer is the arachnoid matter. • The innermost layer is the pia matter. DURA MATER ▪The cranial dura is a two layered tough, fibrous thick membrane that surrounds the brain. ▪It is formed of two layers; periosteal and meningeal. ▪The periosteal layer is attached to the skull. ▪The meningeal layer is folded forming the dural folds : falx cerebri, and tentorium cerebelli. ▪Sensory innervation of the dura is mostly from : meningeal branches of the trigeminal and vagus nerves & C1 to C3(upper cervical Ns.). DURA MATER Folds Two large reflection of dura extend into the cranial cavity : 1.The falx cerebri, In the midline, ▪It is a vertical sickle-shaped sheet of dura, extends from the cranial roof into the great longitudinal fissure between the two cerebral hemispheres. ▪It has an attached border adherent to the skull. ▪And a free border lies above the corpus callosum. DURA MATER Folds 2. A horizontal shelf of dura, The tentorium cerebelli, ▪ It lies between the posterior part of the cerebral hemispheres and the cerebellum. -
Auditory and Vestibular Systems Objective • to Learn the Functional
Auditory and Vestibular Systems Objective • To learn the functional organization of the auditory and vestibular systems • To understand how one can use changes in auditory function following injury to localize the site of a lesion • To begin to learn the vestibular pathways, as a prelude to studying motor pathways controlling balance in a later lab. Ch 7 Key Figs: 7-1; 7-2; 7-4; 7-5 Clinical Case #2 Hearing loss and dizziness; CC4-1 Self evaluation • Be able to identify all structures listed in key terms and describe briefly their principal functions • Use neuroanatomy on the web to test your understanding ************************************************************************************** List of media F-5 Vestibular efferent connections The first order neurons of the vestibular system are bipolar cells whose cell bodies are located in the vestibular ganglion in the internal ear (NTA Fig. 7-3). The distal processes of these cells contact the receptor hair cells located within the ampulae of the semicircular canals and the utricle and saccule. The central processes of the bipolar cells constitute the vestibular portion of the vestibulocochlear (VIIIth cranial) nerve. Most of these primary vestibular afferents enter the ipsilateral brain stem inferior to the inferior cerebellar peduncle to terminate in the vestibular nuclear complex, which is located in the medulla and caudal pons. The vestibular nuclear complex (NTA Figs, 7-2, 7-3), which lies in the floor of the fourth ventricle, contains four nuclei: 1) the superior vestibular nucleus; 2) the inferior vestibular nucleus; 3) the lateral vestibular nucleus; and 4) the medial vestibular nucleus. Vestibular nuclei give rise to secondary fibers that project to the cerebellum, certain motor cranial nerve nuclei, the reticular formation, all spinal levels, and the thalamus. -
Lecture 12 Notes
Somatic regions Limbic regions These functionally distinct regions continue rostrally into the ‘tweenbrain. Fig 11-4 Courtesy of MIT Press. Used with permission. Schneider, G. E. Brain structure and its Origins: In the Development and in Evolution of Behavior and the Mind. MIT Press, 2014. ISBN: 9780262026734. 1 Chapter 11, questions about the somatic regions: 4) There are motor neurons located in the midbrain. What movements do those motor neurons control? (These direct outputs of the midbrain are not a subject of much discussion in the chapter.) 5) At the base of the midbrain (ventral side) one finds a fiber bundle that shows great differences in relative size in different species. Give examples. What are the fibers called and where do they originate? 8) A decussating group of axons called the brachium conjunctivum also varies greatly in size in different species. It is largest in species with the largest neocortex but does not come from the neocortex. From which structure does it come? Where does it terminate? (Try to guess before you look it up.) 2 Motor neurons of the midbrain that control somatic muscles: the oculomotor nuclei of cranial nerves III and IV. At this level, the oculomotor nucleus of nerve III is present. Fibers from retina to Superior Colliculus Brachium of Inferior Colliculus (auditory pathway to thalamus, also to SC) Oculomotor nucleus Spinothalamic tract (somatosensory; some fibers terminate in SC) Medial lemniscus Cerebral peduncle: contains Red corticospinal + corticopontine fibers, + cortex to hindbrain fibers nucleus (n. ruber) Tectospinal tract Rubrospinal tract Courtesy of MIT Press. Used with permission. Schneider, G.