Anatomy of Spinal Cord
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Nuclear Expression of PG-21, SRC-1, and Pcreb in Regions of the Lumbosacral Spinal Cord Involved in Pelvic Innervation in Young Adult and Aged Rats
Original Article http://dx.doi.org/10.5115/acb.2012.45.4.241 pISSN 2093-3665 eISSN 2093-3673 Nuclear expression of PG-21, SRC-1, and pCREB in regions of the lumbosacral spinal cord involved in pelvic innervation in young adult and aged rats Richard N. Ranson1,2, Jennifer H. Connelly1, Robert M. Santer1, Alan H. D. Watson1 1Cardiff School of Biosciences, Cardiff University, Cardiff,2 School of Applied Sciences, Northumbria University, Newcastle upon Tyne, UK Abstract: In rats, ageing results in dysfunctional patterns of micturition and diminished sexual reflexes that may reflect degenerative changes within spinal circuitry. In both sexes the dorsal lateral nucleus and the spinal nucleus of the bulbospongiosus, which lie in the L5-S1 spinal segments, contain motor neurons that innervate perineal muscles, and the external anal and urethral sphincters. Neurons in the sacral parasympathetic nucleus of these segments provide autonomic control of the bladder, cervix and penis and other lower urinary tract structures. Interneurons in the dorsal gray commissure and dorsal horn have also been implicated in lower urinary tract function. This study investigates the cellular localisation of PG-21 androgen receptors, steroid receptor co-activator one (SRC-1) and the phosphorylated form of c-AMP response element binding protein (pCREB) within these spinal nuclei. These are components of signalling pathways that mediate cellular responses to steroid hormones and neurotrophins. Nuclear expression of PG-21 androgen receptors, SRC-1 and pCREB in young and aged rats was quantified using immunohistochemistry. There was a reduction in the number of spinal neurons expressing these molecules in the aged males while in aged females, SRC-1 and pCREB expression was largely unchanged. -
Motor Tracts
Motor tracts There are two major descending tracts Pyramidal tracts (Corticospinal ) : Conscious control of skeletal muscles Extrapyramidal: Upper motor Subconscious neurons. regulation of balance, muscle tone, eye, hand, and upper limb position: Vestibulospinal tracts Lower motor neurons. Reticulospinal tracts Rubrospinal tracts Tectospinal tracts Extrapyramidal tracts arise in the brainstem, but are under the influence of the cerebral cortex Rexed laminae • Lamina 8: motor interneurons, Commissural nucleus • Lamina 9: ventral horn, LMN, divided into nuclei: Ventromedial : all segements (extensors of vertebral coloumn) Dorsomedial : (T1-L2) intercostals and abdominal muscles Ventrolateral: C5-C8 (arm) L2-S2 (thigh) Dorsolateral: C5-C8 (Forearm), L3-S3 (Leg) Reterodorsolateral: C8-T1 (Hand), S1-S2 (foot) Central: Phrenic nerve (C3-C5) • Lamina X : Surrounds the central canal – the grey commissure Motor neurons of anterior horn Medial group: (All segments) Lateral group: only enlargements Muscle spindles are sensory receptors within the belly of a muscle that primarily detect changes in the length of this muscle. Each muscle spindle consists of an encapsulated cluster of small striated muscle fibers (" intrafusal muscle fibers ") with somewhat unusual structure (e.g., nuclei may be concentrated in a cluster near the middle of the fiber's length). The skeletal muscle is composed of: Extrafusal fibers (99%): innervated by alpha motor neurons . Intrafusal fibers (1%): innervated by gamma motor neurons . depend on the muscle spindle receptors Activating alpha motor neurons Directly through supraspinal centers: Descending motor pathways (UMN) Indirectly through Muscle spindles Stretch reflex: skeletal muscles are shorter than the distance between its origin and insertion Gamma loop Gamma fibers activate the muscle fibers indirectly, while alpha fibers do it directly. -
Split Spinal Cord Malformations in Children
Split spinal cord malformations in children Yusuf Ersahin, M.D., Saffet Mutluer, M.D., Sevgül Kocaman, R.N., and Eren Demirtas, M.D. Division of Pediatric Neurosurgery, Department of Neurosurgery, and Department of Pathology, Ege University Faculty of Medicine, Izmir, Turkey The authors reviewed and analyzed information on 74 patients with split spinal cord malformations (SSCMs) treated between January 1, 1980 and December 31, 1996 at their institution with the aim of defining and classifying the malformations according to the method of Pang, et al. Computerized tomography myelography was superior to other radiological tools in defining the type of SSCM. There were 46 girls (62%) and 28 boys (38%) ranging in age from less than 1 day to 12 years (mean 33.08 months). The mean age (43.2 months) of the patients who exhibited neurological deficits and orthopedic deformities was significantly older than those (8.2 months) without deficits (p = 0.003). Fifty-two patients had a single Type I and 18 patients a single Type II SSCM; four patients had composite SSCMs. Sixty-two patients had at least one associated spinal lesion that could lead to spinal cord tethering. After surgery, the majority of the patients remained stable and clinical improvement was observed in 18 patients. The classification of SSCMs proposed by Pang, et al., will eliminate the current chaos in terminology. In all SSCMs, either a rigid or a fibrous septum was found to transfix the spinal cord. There was at least one unrelated lesion that caused tethering of the spinal cord in 85% of the patients. -
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. -
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 -
Spinal Cord Organization
Lecture 4 Spinal Cord Organization The spinal cord . Afferent tract • connects with spinal nerves, through afferent BRAIN neuron & efferent axons in spinal roots; reflex receptor interneuron • communicates with the brain, by means of cell ascending and descending pathways that body form tracts in spinal white matter; and white matter muscle • gives rise to spinal reflexes, pre-determined gray matter Efferent neuron by interneuronal circuits. Spinal Cord Section Gross anatomy of the spinal cord: The spinal cord is a cylinder of CNS. The spinal cord exhibits subtle cervical and lumbar (lumbosacral) enlargements produced by extra neurons in segments that innervate limbs. The region of spinal cord caudal to the lumbar enlargement is conus medullaris. Caudal to this, a terminal filament of (nonfunctional) glial tissue extends into the tail. terminal filament lumbar enlargement conus medullaris cervical enlargement A spinal cord segment = a portion of spinal cord that spinal ganglion gives rise to a pair (right & left) of spinal nerves. Each spinal dorsal nerve is attached to the spinal cord by means of dorsal and spinal ventral roots composed of rootlets. Spinal segments, spinal root (rootlets) nerve roots, and spinal nerves are all identified numerically by th region, e.g., 6 cervical (C6) spinal segment. ventral Sacral and caudal spinal roots (surrounding the conus root medullaris and terminal filament and streaming caudally to (rootlets) reach corresponding intervertebral foramina) collectively constitute the cauda equina. Both the spinal cord (CNS) and spinal roots (PNS) are enveloped by meninges within the vertebral canal. Spinal nerves (which are formed in intervertebral foramina) are covered by connective tissue (epineurium, perineurium, & endoneurium) rather than meninges. -
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. -
Structure and Junctional Complexes of Endothelial, Epithelial and Glial Brain Barriers
International Journal of Molecular Sciences Review Structure and Junctional Complexes of Endothelial, Epithelial and Glial Brain Barriers Mariana Castro Dias *, Josephine A. Mapunda, Mykhailo Vladymyrov and Britta Engelhardt * Theodor Kocher Institute, University of Bern, 3012 Bern, Switzerland; [email protected] (J.A.M.); [email protected] (M.V.) * Correspondence: [email protected] (M.C.D.); [email protected] (B.E.) Received: 14 October 2019; Accepted: 26 October 2019; Published: 29 October 2019 Abstract: The homeostasis of the central nervous system (CNS) is ensured by the endothelial, epithelial, mesothelial and glial brain barriers, which strictly control the passage of molecules, solutes and immune cells. While the endothelial blood-brain barrier (BBB) and the epithelial blood-cerebrospinal fluid barrier (BCSFB) have been extensively investigated, less is known about the epithelial and mesothelial arachnoid barrier and the glia limitans. Here, we summarize current knowledge of the cellular composition of the brain barriers with a specific focus on describing the molecular constituents of their junctional complexes. We propose that the brain barriers maintain CNS immune privilege by dividing the CNS into compartments that differ with regard to their role in immune surveillance of the CNS. We close by providing a brief overview on experimental tools allowing for reliable in vivo visualization of the brain barriers and their junctional complexes and thus the respective CNS compartments. Keywords: brain barriers; blood-brain barrier; neurovascular unit; blood-cerebrospinal fluid barrier; arachnoid barrier; glia limitans; tight junctions; adherens junctions 1. Introduction The brain barriers established by the endothelial blood-brain barrier (BBB), the epithelial blood-cerebrospinal fluid barrier (BCSFB), the meningeal brain barriers and the blood spinal cord barrier are essential for maintaining central nervous system (CNS) homeostasis [1]. -
Lecture 4: the Meninges And
1/1/2016 Introduction • Protection of the brain – Bone (skull) The Nervous System – Membranes (meninges) – Watery cushion (cerebrospinal fluid) – Blood-brain barrier (astrocytes) Meninges CSF The Meninges The Meninges • Series of membranes • Three layers • Cover and protect the CNS – Dura mater • Anchor and cushion the brain – Arachnoid mater – • Contain cerebrospinal fluid (CSF) Pia mater The Meninges • Dura mater – “Tough mother” Skin of scalp Periosteum – Strongest meninx Bone of skull Periosteal Dura – Fibrous connective tissue Meningeal mater Superior Arachnoid mater – sagittal sinus Pia mater Limit excessive movement of the brain Subdural Arachnoid villus – space Blood vessel Forms partitions in the skull Subarachnoid Falx cerebri space (in longitudinal fissure only) Figure 12.24 1 1/1/2016 Superior The Meninges sagittal sinus Falx cerebri • Arachnoid mater – “Spider mother” Straight sinus – Middle layer with weblike extensions Crista galli – Separated from the dura mater by the subdural space of the Tentorium ethmoid cerebelli – Subarachnoid space contains CSF and blood vessels bone Falx Pituitary cerebelli gland (a) Dural septa Figure 12.25a The Meninges • Pia mater – “Gentle mother” – Connected to the dura mater by projections from the arachnoid mater – Layer of delicate vascularized connective tissue – Clings tightly to the brain T Meningitis TT121212 Ligamentum flavumflavumflavum L • LL555 Lumbar puncture Inflammation of meninges needle entering subarachnoid • May be bacterial or viral spacespacespace LLL444 • Diagnosed by -
The Degenerations Kesulting from Lesions of Posterior
THE DEGENERATIONS KESULTING FROM Downloaded from LESIONS OF POSTERIOR NERVE ROOTS AND FROM TRANSVERSE LESIONS OF THE SPINAL CORD IN MAN. A STUDY OF TWENTY CASES. http://brain.oxfordjournals.org/ BY JAMES COLLIEB, M.D., B.Sc, F.E.C.P. Assistant Physician to the National Hospital, E. FARQUHAR BUZZARD, M.D., M.R.C.P. Pathologist to the National Hospital, and Assistant Physician to the Royal Free Hospital. HAVING held successively the post of pathologist to the at Florida Atlantic University on March 21, 2016 National Hospital we have had the opportunity of examin- ing (1) two cases in which there were isolated lesions of the posterior roots in the cervical or lumbo-sacral region, and (2) twelve cases of transverse lesion of the spinal cord, at various levels. In all of these cases the method of Marchi was applicable. In connection with the descending systems of the pos- terior columns we have also made use of several cases of transverse lesion of the spinal cord, which we have examined by the Weigert-Pal method. For the Marchi method we have invariably used Busch's sodium-iodate process. Inasmuch as the literature of the subject is very extensive, we have deemed it convenient to refer only to the more recent investigations concerning such anatomical and physiological points as have been but lately brought to light, or as are still debatable, and to which our observations may add some further information. A bibliography of the more recent literature upon these subjects is appended. 560 ORIGINAL ARTICLES AND CLINICAL CASES The subject matter of this paper is arranged as follows : — The posterior roots.—(1) The descending intraspinal pro- longations and their relations to the coma tract, to the septo-marginal system, and to other posterior descending systems. -
The Conus Medullaris: a Comprehensive Review
THE SPINE SCHOLAR VOLUME 1, NUMBER 2, 2017 SEATTLE SCIENCE FOUNDATION REVIEW The Conus Medullaris: A Comprehensive Review Garrett Ng1, Anthony V. D’Antoni1, R. Shane Tubbs2 1 The CUNY School of Medicine, New York, NY 10031, USA 2 Department of Anatomical Sciences, St. George’s University, Grenada http:thespinescholar.com https:doi.org/10.26632/ss.10.2017.1.2 Key Words: anatomy, embryology, spinal cord, spine ABSTRACT The position of the conus medullaris within the vertebral canal varies. Given its role in sensory and motor function, a comprehensive understanding of the conus medullaris is necessary. PubMed and Google Scholar were used to review the literature on the conus medullaris. Pathological states and traumatic injury relating to the conus medullaris should be studied further. Spine Scholar 1:93-96, 2017 INTRODUCTION The conus medullaris (Fig. 1), also known as the medullary cone, is the distal end of the spinal cord. Its location varies, and in adults it tapers at approximately the first or second lumbar vertebra, ranging from T11 and L3 (Neel, 2016). Derived from the neural tube, the structure ascends in the vertebral canal because the growth rates of the spinal cord and the vertebral column differ during development (Salbacak et al., 2000). Figure 1: Schematic drawing of the conus medullaris and distal nerve roots in relation to the sacrum. The conus contains the sacral and coccygeal segments of the spinal cord (Taylor and Coolican, 1988). Criteria for recognizing the conus on computed tomography (CT) scans have been published by Grogan et al. (1984). The radiological properties of the structure have been studied through magnetic resonance imaging (MRI) (Saifuddin et al., 1997). -
Meningioma ACKNOWLEDGEMENTS
AMERICAN BRAIN TUMOR ASSOCIATION Meningioma ACKNOWLEDGEMENTS ABOUT THE AMERICAN BRAIN TUMOR ASSOCIATION Meningioma Founded in 1973, the American Brain Tumor Association (ABTA) was the first national nonprofit advocacy organization dedicated solely to brain tumor research. For nearly 45 years, the ABTA has been providing comprehensive resources that support the complex needs of brain tumor patients and caregivers, as well as the critical funding of research in the pursuit of breakthroughs in brain tumor diagnosis, treatment and care. To learn more about the ABTA, visit www.abta.org. We gratefully acknowledge Santosh Kesari, MD, PhD, FANA, FAAN chair of department of translational neuro- oncology and neurotherapeutics, and Marlon Saria, MSN, RN, AOCNS®, FAAN clinical nurse specialist, John Wayne Cancer Institute at Providence Saint John’s Health Center, Santa Monica, CA; and Albert Lai, MD, PhD, assistant clinical professor, Adult Brain Tumors, UCLA Neuro-Oncology Program, for their review of this edition of this publication. This publication is not intended as a substitute for professional medical advice and does not provide advice on treatments or conditions for individual patients. All health and treatment decisions must be made in consultation with your physician(s), utilizing your specific medical information. Inclusion in this publication is not a recommendation of any product, treatment, physician or hospital. COPYRIGHT © 2017 ABTA REPRODUCTION WITHOUT PRIOR WRITTEN PERMISSION IS PROHIBITED AMERICAN BRAIN TUMOR ASSOCIATION Meningioma INTRODUCTION Although meningiomas are considered a type of primary brain tumor, they do not grow from brain tissue itself, but instead arise from the meninges, three thin layers of tissue covering the brain and spinal cord.