Anatomy of the Nose and Olfactory Nerve
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Cranial Nerves
Cranial Nerves (1,5,7,8,9,10,11 and 12) Slides not included 9th and 10th Cranial 11th and 12th Cranial 8th Cranial Nerve 5th and 7th Cranial 1st Cranial Nerve Nerves Nerves Nerves (3,7,11,12,13,21,23,24) - (10,16) (12,23) Slides included: (14 to 17) *Slides that are not included mostly are slides of summaries or pictures. Nouf Alabdulkarim. Med 435 Olfactory Nerve [The 1st Cranial Nerve] Special Sensory Olfactory pathway 1st order neuron Receptors Axons of 1st order Neurons Olfactory receptors are specialized, ciliated nerve cells The axons of these bipolar cells 12 -20 fibers form the that lie in the olfactory epithelium. true olfactory nerve fibers. Which passes through the cribriform plate of ethmoid → They join the olfactory bulb Preliminary processing of olfactory information It is within the olfactory bulb, which contains interneurones and large Mitral cells; axons from the latter leave the bulb to form the olfactory tract. nd 2 order neuron • It is formed by the Mitral cells of olfactory bulb. • The axons of these cells form the olfactory tract. • Each tract divides into 2 roots at the anterior perforated substance: Lateral root Medial root Carries olfactory fibers to end in cortex of the Uncus & • crosses midline through anterior commissure adjacent part of Hippocampal gyrus (center of smell). and joins the uncrossed lateral root of opposite side. • It connects olfactory centers of 2 cerebral hemispheres. • So each olfactory center receives smell sensation from both halves of nasal cavity. NB. Olfactory pathway is the only sensory pathway which reaches the cerebral cortex without passing through the Thalamus . -
Early Aging Effect on the Function of the Human Central Olfactory System
Journals of Gerontology: Biological Sciences cite as: J Gerontol A Biol Sci Med Sci, 2017, Vol. 72, No. 8, 1007–1014 doi:10.1093/gerona/glw104 Advance Access publication June 11, 2016 Original Article Early Aging Effect on the Function of the Human Central Downloaded from https://academic.oup.com/biomedgerontology/article/72/8/1007/2629931 by guest on 27 September 2021 Olfactory System Choice Editor’s Jianli Wang,1 Xiaoyu Sun,1 and Qing X. Yang2 1Department of Radiology, Pennsylvania State University College of Medicine, Hershey. 2Departments of Radiology and Neurosurgery, Pennsylvania State University College of Medicine, Hershey. Address correspondence to Jianli Wang, MD, PhD, Department of Radiology, Pennsylvania State University College of Medicine, Hershey, PA 17033. E-mail: [email protected] Received November 23, 2015; Accepted April 27, 2016 Decision Editor: Rafael de Cabo, PhD Abstract During normal aging process, the smell function declines significantly, starting from the sixth decade of age. While it has been shown that activity in the central olfactory system of seniors responding to odor stimulation is significantly less than that of young people, no information of the aging effect on the functions of this system during normal adulthood and early aging has been gathered. In this study, we used functional magnetic resonance imaging to investigate the olfaction-related brain activity in the central olfactory structures of 43 healthy adult volunteers aged from 22 to 64 years. The participants’ smell identification function was negatively correlated with age (r = −.32, p = .037). Significant negative correlation was observed between age and the olfaction-related activities in the bilateral dorsolateral prefrontal cortex, left insular cortex, and left orbitofrontal cortex (p < .001, corrected with cluster size ≥28 voxels). -
Nerves of the Orbit Optic Nerve the Optic Nerve Enters the Orbit from the Middle Cranial Fossa by Passing Through the Optic Canal
human anatomy 2016 lecture fourteen Dr meethak ali ahmed neurosurgeon Nerves of the Orbit Optic Nerve The optic nerve enters the orbit from the middle cranial fossa by passing through the optic canal . It is accompanied by the ophthalmic artery, which lies on its lower lateral side. The nerve is surrounded by sheath of pia mater, arachnoid mater, and dura mater. It runs forward and laterally within the cone of the recti muscles and pierces the sclera at a point medial to the posterior pole of the eyeball. Here, the meninges fuse with the sclera so that the subarachnoid space with its contained cerebrospinal fluid extends forward from the middle cranial fossa, around the optic nerve, and through the optic canal, as far as the eyeball. A rise in pressure of the cerebrospinal fluid within the cranial cavity therefore is transmitted to theback of the eyeball. Lacrimal Nerve The lacrimal nerve arises from the ophthalmic division of the trigeminal nerve. It enters the orbit through the upper part of the superior orbital fissure and passes forward along the upper border of the lateral rectus muscle . It is joined by a branch of the zygomaticotemporal nerve, whi(parasympathetic secretomotor fibers). The lacrimal nerve ends by supplying the skin of the lateral part of the upper lid. Frontal Nerve The frontal nerve arises from the ophthalmic division of the trigeminal nerve. It enters the orbit through the upper part of the superior orbital fissure and passes forward on the upper surface of the levator palpebrae superioris beneath the roof of the orbit . -
Maxillary Nerve-Mediated Postseptoplasty Nasal Allodynia: a Case Report
E CASE REPORT Maxillary Nerve-Mediated Postseptoplasty Nasal Allodynia: A Case Report Shikha Sharma, MD, PhD,* Wilson Ly, MD, PharmD,* and Xiaobing Yu, MD*† Endoscopic nasal septoplasty is a commonly performed otolaryngology procedure, not known to cause persistent postsurgical pain or hypersensitivity. Here, we discuss a unique case of persis- tent nasal pain that developed after a primary endoscopic septoplasty, which then progressed to marked mechanical and thermal allodynia following a revision septoplasty. Pain symptoms were found to be mediated by the maxillary division of the trigeminal nerve and resolved after percuta- neous radiofrequency ablation (RFA) of bilateral maxillary nerves. To the best of our knowledge, this is the first report of maxillary nerve–mediated nasal allodynia after septoplasty. (A&A Practice. 2020;14:e01356.) GLOSSARY CT = computed tomography; FR = foramen rotundum; HIPAA = Health Insurance Portability and Accountability Act; ION = infraorbital nerve; LPP = lateral pterygoid plate; MRI = magnetic reso- nance imaging; RFA = radiofrequency ablation; SPG = sphenopalatine ganglion; US = ultrasound ndoscopic nasal septoplasty is a common otolaryn- septoplasty for chronic nasal obstruction with resection of gology procedure with rare incidence of postsurgical the cartilage inferiorly and posteriorly in 2010. Before this Ecomplications. Minor complications include epistaxis, surgery, the patient only occasionally experienced mild septal hematoma, septal perforation, cerebrospinal fluid leak, headaches. However, his postoperative course was compli- and persistent obstruction.1 Numbness or hypoesthesia of the cated by significant pain requiring high-dose opioids. After anterior palate, secondary to injury to the nasopalatine nerve, discharge, patient continued to have persistent deep, “ach- has been reported, but is usually rare and temporary, resolv- ing” nasal pain which radiated toward bilateral forehead ing over weeks to months.2 Acute postoperative pain is also and incisors. -
Quantitative Analysis of Axon Collaterals of Single Pyramidal Cells
Yang et al. BMC Neurosci (2017) 18:25 DOI 10.1186/s12868-017-0342-7 BMC Neuroscience RESEARCH ARTICLE Open Access Quantitative analysis of axon collaterals of single pyramidal cells of the anterior piriform cortex of the guinea pig Junli Yang1,2*, Gerhard Litscher1,3* , Zhongren Sun1*, Qiang Tang1, Kiyoshi Kishi2, Satoko Oda2, Masaaki Takayanagi2, Zemin Sheng1,4, Yang Liu1, Wenhai Guo1, Ting Zhang1, Lu Wang1,3, Ingrid Gaischek3, Daniela Litscher3, Irmgard Th. Lippe5 and Masaru Kuroda2 Abstract Background: The role of the piriform cortex (PC) in olfactory information processing remains largely unknown. The anterior part of the piriform cortex (APC) has been the focus of cortical-level studies of olfactory coding, and asso- ciative processes have attracted considerable attention as an important part in odor discrimination and olfactory information processing. Associational connections of pyramidal cells in the guinea pig APC were studied by direct visualization of axons stained and quantitatively analyzed by intracellular biocytin injection in vivo. Results: The observations illustrated that axon collaterals of the individual cells were widely and spatially distrib- uted within the PC, and sometimes also showed a long associational projection to the olfactory bulb (OB). The data showed that long associational axons were both rostrally and caudally directed throughout the PC, and the intrinsic associational fibers of pyramidal cells in the APC are omnidirectional connections in the PC. Within the PC, associa- tional axons typically followed rather linear trajectories and irregular bouton distributions. Quantitative data of the axon collaterals of two pyramidal cells in the APC showed that the average length of axonal collaterals was 101 mm, out of which 79 mm (78% of total length) were distributed in the PC. -
Simple Ways to Dissect Ciliary Ganglion for Orbital Anatomical Education
OkajimasDetection Folia Anat. of ciliary Jpn., ganglion94(3): 119–124, for orbit November, anatomy 2017119 Simple ways to dissect ciliary ganglion for orbital anatomical education By Ming ZHOU, Ryoji SUZUKI, Hideo AKASHI, Akimitsu ISHIZAWA, Yoshinori KANATSU, Kodai FUNAKOSHI, Hiroshi ABE Department of Anatomy, Akita University Graduate School of Medicine, Akita, 010-8543 Japan –Received for Publication, September 21, 2017– Key Words: ciliary ganglion, orbit, human anatomy, anatomical education Summary: In the case of anatomical dissection as part of medical education, it is difficult for medical students to find the ciliary ganglion (CG) since it is small and located deeply in the orbit between the optic nerve and the lateral rectus muscle and embedded in the orbital fat. Here, we would like to introduce simple ways to find the CG by 1): tracing the sensory and parasympathetic roots to find the CG from the superior direction above the orbit, 2): transecting and retracting the lateral rectus muscle to visualize the CG from the lateral direction of the orbit, and 3): taking out whole orbital structures first and dissecting to observe the CG. The advantages and disadvantages of these methods are discussed from the standpoint of decreased laboratory time and students as beginners at orbital anatomy. Introduction dissection course for the first time and with limited time. In addition, there are few clear pictures in anatomical The ciliary ganglion (CG) is one of the four para- textbooks showing the morphology of the CG. There are sympathetic ganglia in the head and neck region located some scientific articles concerning how to visualize the behind the eyeball between the optic nerve and the lateral CG, but they are mostly based on the clinical approaches rectus muscle in the apex of the orbit (Siessere et al., rather than based on the anatomical procedure for medical 2008). -
Odour Discrimination Learning in the Indian Greater Short-Nosed Fruit Bat
© 2018. Published by The Company of Biologists Ltd | Journal of Experimental Biology (2018) 221, jeb175364. doi:10.1242/jeb.175364 RESEARCH ARTICLE Odour discrimination learning in the Indian greater short-nosed fruit bat (Cynopterus sphinx): differential expression of Egr-1, C-fos and PP-1 in the olfactory bulb, amygdala and hippocampus Murugan Mukilan1, Wieslaw Bogdanowicz2, Ganapathy Marimuthu3 and Koilmani Emmanuvel Rajan1,* ABSTRACT transferred directly from the olfactory bulb to the amygdala and Activity-dependent expression of immediate-early genes (IEGs) is then to the hippocampus (Wilson et al., 2004; Mouly and induced by exposure to odour. The present study was designed to Sullivan, 2010). Depending on the context, the learning investigate whether there is differential expression of IEGs (Egr-1, experience triggers neurotransmitter release (Lovinger, 2010) and C-fos) in the brain region mediating olfactory memory in the Indian activates a signalling cascade through protein kinase A (PKA), greater short-nosed fruit bat, Cynopterus sphinx. We assumed extracellular signal-regulated kinase-1/2 (ERK-1/2) (English and that differential expression of IEGs in different brain regions may Sweatt, 1997; Yoon and Seger, 2006; García-Pardo et al., 2016) and orchestrate a preference odour (PO) and aversive odour (AO) cyclic AMP-responsive element binding protein-1 (CREB-1), memory in C. sphinx. We used preferred (0.8% w/w cinnamon which is phosphorylated by ERK-1/2 (Peng et al., 2010). powder) and aversive (0.4% w/v citral) odour substances, with freshly Activated CREB-1 induces expression of immediate-early genes prepared chopped apple, to assess the behavioural response and (IEGs), such as early growth response gene-1 (Egr-1) (Cheval et al., induction of IEGs in the olfactory bulb, hippocampus and amygdala. -
Cranial Nerves 1, 5, 7-12
Cranial Nerve I Olfactory Nerve Nerve fiber modality: Special sensory afferent Cranial Nerves 1, 5, 7-12 Function: Olfaction Remarkable features: – Peripheral processes act as sensory receptors (the other special sensory nerves have separate Warren L Felton III, MD receptors) Professor and Associate Chair of Clinical – Primary afferent neurons undergo continuous Activities, Department of Neurology replacement throughout life Associate Professor of Ophthalmology – Primary afferent neurons synapse with secondary neurons in the olfactory bulb without synapsing Chair, Division of Neuro-Ophthalmology first in the thalamus (as do all other sensory VCU School of Medicine neurons) – Pathways to cortical areas are entirely ipsilateral 1 2 Crania Nerve I Cranial Nerve I Clinical Testing Pathology Anosmia, hyposmia: loss of or impaired Frequently overlooked in neurologic olfaction examination – 1% of population, 50% of population >60 years Aromatic stimulus placed under each – Note: patients with bilateral anosmia often report nostril with the other nostril occluded, eg impaired taste (ageusia, hypogeusia), though coffee, cloves, or soap taste is normal when tested Note that noxious stimuli such as Dysosmia: disordered olfaction ammonia are not used due to concomitant – Parosmia: distorted olfaction stimulation of CN V – Olfactory hallucination: presence of perceived odor in the absence of odor Quantitative clinical tests are available: • Aura preceding complex partial seizures of eg, University of Pennsylvania Smell temporal lobe origin -
Synaptic Organization of Anterior Olfactory Nucleus Inputs to Piriform Cortex
9414 • The Journal of Neuroscience, December 2, 2020 • 40(49):9414–9425 Systems/Circuits Synaptic Organization of Anterior Olfactory Nucleus Inputs to Piriform Cortex Marco J. Russo,1 Kevin M. Franks,1 Roxanne Oghaz,1 Richard Axel,2 and Steven A. Siegelbaum3 1Department of Neuroscience, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York, 2Mortimer B. Zuckerman Mind Brain Behavior Institute, Department of Neuroscience, Department of Biochemistry and Molecular Biophysics, Howard Hughes Medical Institute, Vagelos College of Physicians & Surgeons, Columbia University, New York, New York, and 3Department of Neuroscience, Kavli Institute for Brain Science, Mortimer B. Zuckerman Mind Brain Behavior Institute, Department of Pharmacology, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York Odors activate distributed ensembles of neurons within the piriform cortex, forming cortical representations of odor thought to be essential to olfactory learning and behaviors. This odor response is driven by direct input from the olfactory bulb, but is also shaped by a dense network of associative or intracortical inputs to piriform, which may enhance or constrain the cort- ical odor representation. With optogenetic techniques, it is possible to functionally isolate defined inputs to piriform cortex and assess their potential to activate or inhibit piriform pyramidal neurons. The anterior olfactory nucleus (AON) receives direct input from the olfactory bulb and sends an associative projection to piriform cortex that has potential roles in the state-dependent processing of olfactory behaviors. Here, we provide a detailed functional assessment of the AON afferents to piriform in male and female C57Bl/6J mice. We confirm that the AON forms glutamatergic excitatory synapses onto piriform pyramidal neurons; and while these inputs are not as strong as piriform recurrent collaterals, they are less constrained by disynaptic inhibition. -
On the Scent of Human Olfactory Orbitofrontal Cortex: Meta-Analysis and Comparison to Non-Human Primates
Brain Research Reviews 50 (2005) 287 – 304 www.elsevier.com/locate/brainresrev Review On the scent of human olfactory orbitofrontal cortex: Meta-analysis and comparison to non-human primates Jay A. Gottfrieda,*, David H. Zaldb aDepartment of Neurology and the Cognitive Neurology and Alzheimer’s Disease Center, Northwestern University Feinberg School of Medicine, 320 E. Superior St., Searle 11-453, Chicago, IL 60611, USA bDepartment of Psychology, Vanderbilt University, Nashville, TN 37240, USA Accepted 25 August 2005 Available online 6 October 2005 Abstract It is widely accepted that the orbitofrontal cortex (OFC) represents the main neocortical target of primary olfactory cortex. In non-human primates, the olfactory neocortex is situated along the basal surface of the caudal frontal lobes, encompassing agranular and dysgranular OFC medially and agranular insula laterally, where this latter structure wraps onto the posterior orbital surface. Direct afferent inputs arrive from most primary olfactory areas, including piriform cortex, amygdala, and entorhinal cortex, in the absence of an obligatory thalamic relay. While such findings are almost exclusively derived from animal data, recent cytoarchitectonic studies indicate a close anatomical correspondence between non-human primate and human OFC. Given this cross-species conservation of structure, it has generally been presumed that the olfactory projection area in human OFC occupies the same posterior portions of OFC as seen in non-human primates. This review questions this assumption by providing a critical survey of the localization of primate and human olfactory neocortex. Based on a meta-analysis of human functional neuroimaging studies, the region of human OFC showing the greatest olfactory responsivity appears substantially rostral and in a different cytoarchitectural area than the orbital olfactory regions as defined in the monkey. -
A Cortical Pathway Modulates Sensory Input Into the Olfactory Striatum 3 4 5 Kate A
bioRxiv preprint doi: https://doi.org/10.1101/235291; this version posted December 16, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 2 A cortical pathway modulates sensory input into the olfactory striatum 3 4 5 Kate A. White1,2,3, Yun-Feng Zhang4, Zhijian Zhang5, Janardhan P. Bhattarai4, Andrew 6 H. Moberly4, Estelle in ‘t Zandt1,2, Huijie Mi6, Xianglian Jia7, Marc V. Fuccillo4, Fuqiang 7 Xu5, Minghong Ma4, Daniel W. Wesson1,2,3* 8 9 1Department of Pharmacology & Therapeutics 10 2Center for Smell and Taste 11 University of Florida 12 1200 Newell Dr.; Gainesville, FL, 32610. U.S.A. 13 3Department of Neurosciences 14 Case Western Reserve University 15 2109 Adelbert Rd.; Cleveland, OH, 44106. U.S.A. 16 4Department of Neuroscience 17 University of Pennsylvania Perelman School of Medicine 18 211 CRB, 415 Curie Blvd; Philadelphia, PA, 19104. U.S.A 19 5Center for Brain Science 20 Wuhan Institute of Physics and Mathematics 21 Chinese Academy of Sciences 22 Wuhan 430071, China 23 6College of Life Sciences 24 Wuhan University 25 Wuhan 430072, China 26 7Shenzhen Institutes of Advanced Technology 27 Chinese Academy of Sciences 28 Shenzhen 518055, China 29 30 *corresponding author; [email protected] 31 RUNNING HEAD: Olfactory striatum input 32 33 Author Contributions: Conceptualization: K.A.W. and D.W.W.; Methodology: K.A.W., Z.Z., F.X., 34 M.M., and D.W.W.; Investigation: K.A.W., Y-F.Z., Z.Z., J.P.B., A.H.M., E.I.Z., H.M., and X.J.; 35 Resources: M.V.F.; Writing – Original Draft: K.A.W., Z.Z., M.M., and D.W.W.; Writing – Review & 36 Editing: all authors; Visualization: K.A.W., Z.Z., Y-F.Z., J.P.B., D.W.W.; Supervision: F.X., M.M., 37 and D.W.W.; Funding Acquisition: K.A.W., F.X., M.M., and D.W.W. -
Sheep Brain Dissection Sheep Brain External Anatomy Procedure
Sheep Brain Dissection Sheep Brain External Anatomy Procedure 1. Set the brain down so the flatter side, with the white spinal cord at one end, rests on the dissection pan. 2. Notice that the brain has two halves, or hemispheres. 3. Identify the cerebrum (frontal , temporal, parietal, and occipital lobes) and the cerebellum 4. Turn the brain over. 5. Identify the medulla, pons, midbrain, and olfactory bulbs. 6. Find the olfactory bulb on each hemisphere. These will be slightly smoother and a different shade than the tissue around them. The olfactory bulbs control the sense of smell. The nerves to the nose are no longer connected, but you can see nubby ends where they were. The nerves to your mouth and lower body are attached to the medulla; the nerves to your eyes are connected to the optic chiasm. Sheep Brain Dissection: Internal Anatomy 1. Place the brain with the cerebrum facing up. 2. Use a scalpel to slice through the brain along the center line, starting at the cerebrum and going down through the cerebellum, spinal cord, medulla, and pons. 3. Separate the two halves of the brain and lay them with the inside facing up. 4. Identify the corpus callosum, medulla, pons, midbrain, and the place where pituitary gland attaches to the brain. (In many preserved specimens the pituitary gland is no longer present.) 5. Use your fingers or a teasing needle to gently probe the parts and see how they are connected to each other. Sheep Brain Dissection: 1. Frontal Lobe 2. Temporal Lobe Internal Anatomy 3.