The document discusses the different types of neuroglia, or non-neuronal cells, in the central and peripheral nervous systems. It describes six main types of neuroglia: oligodendrocytes that produce myelin in the CNS, astrocytes that support neurons structurally and metabolically, ependymal cells that line ventricles, microglia that perform immune functions, Schwann cells that myelinate nerves in the PNS, and satellite cells that cover neuronal cell bodies in ganglia. Neuroglia outnumber neurons 10:1 and play crucial roles in insulation, support, repair and immune defense of the nervous system.
about nerve fibers
It is the structural and the functional unit of nervous system.
The human nervous system contains approximate 1012 neurons.
A nerve fiber is a thread like extension of a nerve cell and consists of an axon and myelin sheath (if present) in the nervous system.
In peripheral nervous system it is formed by
schwann’s cell. While in case of central nervous system it is formed by oligodendroglia.
The places ,where myelin sheath is absent are called node of ranvier(2-3µm) and these are present once about 1-3 mm distance along the myelin sheath.
IT PREVENTS LEAKAGE OF IONS BY 5000 FOLDS.
IT INCREASES VELOCITY OF CONDUCTION BY 5-50 FOLDS DUE TO
SALTATORY CONDUCTION i.e. ABOUT 100 m/s IN CASE OF
MYELINATED NERVE FIBERS WHILE IN NONMYELINATED
IT IS ABOUT 0.25 m/s.
SALTATORY CONDUCTION CONSERVES ENERGY BECAUSE ONLY NODES OF RANVIER GET DEPOLARISED.
These are α type motor nerve fibers.
The neurotransmitter released at the neuron endings is acetylcholine(Ach).
It always leads to muscles excitation . Inhibition takes place centrally due to participation of interneurons.
they innervate smooth muscles , cardiac muscles and glands.
Their main work is to maintain homeostasis with the help of autonomic nervous system.
they can lead to either excitation or inhibition of effector organs
Erlanger and Grasser studied the action potential of mixed nerve trunk by means of cathode ray oscilloscope and they obtained the compounded spike. So they divided nerve fibers into 3 groups. They observed that the main cause of difference in nerve fibers is diameter
AS Diameter increases
Velocity of conduction increases.
Magnitude of electrical response increases.
Threshold of excitation decreases.
Duration of response decreases.
Refractory period decreases.
about nerve fibers
It is the structural and the functional unit of nervous system.
The human nervous system contains approximate 1012 neurons.
A nerve fiber is a thread like extension of a nerve cell and consists of an axon and myelin sheath (if present) in the nervous system.
In peripheral nervous system it is formed by
schwann’s cell. While in case of central nervous system it is formed by oligodendroglia.
The places ,where myelin sheath is absent are called node of ranvier(2-3µm) and these are present once about 1-3 mm distance along the myelin sheath.
IT PREVENTS LEAKAGE OF IONS BY 5000 FOLDS.
IT INCREASES VELOCITY OF CONDUCTION BY 5-50 FOLDS DUE TO
SALTATORY CONDUCTION i.e. ABOUT 100 m/s IN CASE OF
MYELINATED NERVE FIBERS WHILE IN NONMYELINATED
IT IS ABOUT 0.25 m/s.
SALTATORY CONDUCTION CONSERVES ENERGY BECAUSE ONLY NODES OF RANVIER GET DEPOLARISED.
These are α type motor nerve fibers.
The neurotransmitter released at the neuron endings is acetylcholine(Ach).
It always leads to muscles excitation . Inhibition takes place centrally due to participation of interneurons.
they innervate smooth muscles , cardiac muscles and glands.
Their main work is to maintain homeostasis with the help of autonomic nervous system.
they can lead to either excitation or inhibition of effector organs
Erlanger and Grasser studied the action potential of mixed nerve trunk by means of cathode ray oscilloscope and they obtained the compounded spike. So they divided nerve fibers into 3 groups. They observed that the main cause of difference in nerve fibers is diameter
AS Diameter increases
Velocity of conduction increases.
Magnitude of electrical response increases.
Threshold of excitation decreases.
Duration of response decreases.
Refractory period decreases.
09.22.08: Histology of the Peripheral Nervous SystemOpen.Michigan
Slideshow is from the University of Michigan Medical School's M1 Cells and Tissues Sequence
View additional course materials on Open.Michigan:
openmi.ch/med-M1CellsTissues
Slideshow is from the University of Michigan Medical School's M1 Cells and Tissues Sequence
View additional course materials from Open.Michigan:
openmi.ch/med-M1CellsTissues
A brief overview of the physiology of the neuromuscular junction.It includes a video towards the end sourced from the internet with the copyright watermarks intact.
09.22.08: Histology of the Peripheral Nervous SystemOpen.Michigan
Slideshow is from the University of Michigan Medical School's M1 Cells and Tissues Sequence
View additional course materials on Open.Michigan:
openmi.ch/med-M1CellsTissues
Slideshow is from the University of Michigan Medical School's M1 Cells and Tissues Sequence
View additional course materials from Open.Michigan:
openmi.ch/med-M1CellsTissues
A brief overview of the physiology of the neuromuscular junction.It includes a video towards the end sourced from the internet with the copyright watermarks intact.
The dance between Glia and Neurons is critical to the development and maintenance to CNS. Did you know: • up to 90% of the cells in the vertebrate nervous system are “not neurons” • make > 50% of the brain volume. This is a great overview to anyone that wants to learn more.
estas diapositivas te servirán de ayuda, para comprender, mejorar y conocer mas afondo el tejido nervioso, este material es exclusivo para la formación de los estudiantes de medicina
CPG Implementation is “the phase in the guideline lifecycle in which strategies, systems, and tools are created to operationalize the knowledge and recommendations set forth by the guideline developers”, or is “ the part of the guideline lifecycle in which systems are introduced to influence clinicians’ behavior toward guideline adherence”. Implementation barriers and facilitators are defined as factors that actually prevent or enhance, respectively, changes in clinical behavior.
The concept of CPG Implementability was first defined by Shiffman as a set of characteristics that can predict the ease of and/ or obstacles to CPG implementation. Implementability is an abstract concept related to several factors, including intrinsic factors that are specific to the CPG itself and under control of the CPG development group) and extrinsic factors that are often specific to the intended healthcare settings and context of implementation. Also a validated tool for appraisal of implementability of CPGs named “GuideLine Implementability Appraisal (GLIA)” was developed by Schiffman RN et al, from the Yale Center for Medical Informatics, Yale School of Medicine and School of Nursing at Yale University in USA in 2005. A second version was released including a free online platform (electronic or e-GLIA). The GLIA considers only the intrinsic factors in the appraisal and is organized into two parts; part 1, including the global dimension with seven questions that examine the entire CPG document as a whole, and part 2, including the other nine dimensions with twenty-four questions that appraise each recommendation individually regarding the identified nine intrinsic factors or dimensions of implementability. The nine dimensions are decidability, executability, effect on the process of care, presentation and formatting, measurable outcomes, apparent validity, novelty/ innovation, flexibility, and computability.
The nervous system includes the brain, spinal cord, and a complex network of nerves. This system sends messages back and forth between the brain and the body.
The brain is what controls all the body's functions. The spinal cord runs from the brain down through the back. It contains threadlike nerves that branch out to every organ and body part. This network of nerves relays messages back and forth from the brain to different parts of the body.What Are the Parts of the Nervous System?
The nervous system is made up of the central nervous system and the peripheral nervous system:
The central nervous system includes the brain and spinal cord.
The peripheral nervous system includes the nerves that run throughout the whole body.How Does the Nervous System Work?
The nervous system uses tiny cells called neurons (NEW-ronz) to send messages back and forth from the brain, through the spinal cord, to the nerves throughout the body.
Billions of neurons work together to create a communication network. Different neurons have different jobs. For example, sensory neurons send information from the eyes, ears, nose, tongue, and skin to the brain. Motor neurons carry messages away from the brain to the rest of the body to allow muscles to move. These connections make up the way we think, learn, move, and feel. They control how our bodies work — regulating breathing, digestion, and the beating of our hearts.
This slides gives a brief description about the structure of neuron, information flow in neurons and also how transcription takesplace and protein synthesis in the cell. This presentation also explain the types of glia and non glial cells.
The origins of the endoneurial collagen of peripheral nerves and their roots have
not yet been determined. Ochoa (1976) has recently commented upon the presence
of collagen in endoneurial clefts some weeks before the earliest appearance of endoneurial
fibroblasts and consequently attributed collagen production to the immediately
adjacent Schwann cells. The occurrence of collagen in 'pockets' invaginated
into the Schwann cells of unmyelinated fibres (Gamble, 1964) was interpreted as
showing a tendency in such cells to enwrap any suitably sized and orientated structure,
but Thomas (1973) thought the phenomenon more probably indicative of a
capacity of Schwann cells to replace degenerated axons with newly formed collagen.
It was remarked also (Ochoa, 1971) that although collagen pockets may be quite
numerous in young adult human nerves they had not appeared in the sural nerve of
a human fetus of 18 weeks of intrauterine life, i.e. at a stage of development when Schwann cells are extremely active in the establishment of complex interrelationships with unmyelinated axons. In the course of work directed to the study of the development of the human trochlear nerve some observations have been made which are pertinent to the problem of the origin of the endoneurial collagen. They are reported and discussed below.
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
3. Overview
Glial Cells & Neuronal Activity
Glial cells are 10 times more abundant in the mammalian brain than
neurons.
In the CNS glial cells surround most of the neurons
Glial cells furnish a microenvironment ideal for neuronal activity.
They are six and will be discussed in the following slides.
4. 1) Oligodendrocytes
Oligodendrocytes (Gr. oligos, small,
few + dendron, tree + kytos, cell)
Produce myelin sheath through
their extensive processes
Predominately existent in white
matter.
Their processes is not visible by light
staining microscope.
2) Astrocytes
Astrocytes (Gr. astron, star, + kytos)
fibrous astrocytes relatively few long
processes are located in the white matter.
protoplasmic astrocytes, with many short,
branched processes, are found in the gray
matter.
1) Support neurons
2) Very important in early development
3) They form perivascular feet
4) They form Glial limiting membrane
5) Glial fibrillary acid protein (GFAP) is an
important marker
In detail
5. (a): X500. Gold chloride.
Cytoplasmic processes (P)
cell body or soma (S).
Morphological y:
fibrous (relatively few and straight processes)
protoplasmic (numerous branching processes
(b): X500. Anti-GFAP immunoperoxidase and
hematoxylin counterstain.
fibrous astrocyte (A) and its processes. perivascular
feet (PF) at the ends of numerous astrocytic
processes.
6.
7. 3) Ependymal Cells
low columnar or cuboidal cells.
1. Lining ventricles and spinal cord
2. Cillia for (CSF).
3. Other times microvilli for absorption
4. Joined apically by junctional complexes
like epithelia
5. No basal lamina but extend to neuropil
4) Microglia
are small cells with short irregular
processes
1. Migrate to neuropil to analyse and
the area
2. Major mechanism of defence for CNS.
3. Their origin is not neural tube, but
from circulating monocytes in blood.
8. Ependymal cells
epithelial-like cells that form a single layer lining the fluid-filled ventricles of
(a) the cerebrum (b) the central canal of the spinal cord.
9. 5) Schwann cells
also called neurolemmocytes,
Have trophic interactions with neurons.
One neurolemmocyte forms myelin
around a segment of one axon
6) Satellite Cells of Ganglia
Form a covering layer over the large
neuronal cell bodies in PNS ganglia.
trophic or supportive role, but the
molecular basis of their support is poorly
understood.
10. Big Picture
Glial Cell Type Origin Location Main Functions
Oligodendrocyte Neural tube Central nervous system Myelin production, electric insulation
Neurolemmocyte Neural crest Peripheral nerves Myelin production, electric insulation
Astrocyte Neural tube Central nervous system Structural support, repair processes
Blood-brain barrier, metabolic exchanges
Ependymal cell Neural tube Central nervous system Lining cavities of central nervous system
Microglia Bone marrow Central nervous system Immune-related activity
11. Glial cell in the CNS:
(a): Oligodendrocytes
myelinate parts of several axons.
(b): Astrocytes
have multiple processes and form perivascular
feet that completely enclose all capillaries
(only a few such feet are shown here to allow
their morphology to be seen).
12. (c): Ependymal cells
are epithelial-like cells that line the
ventricles and central canal.
(d): Microglial cells have a protective,
phagocytic, immune-related function. Glial
cells in the PNS.
13. Glial cells in the PNS:
(e): Neurolemmocytes:
commonly called Schwann cells, form a series
enclosing axons.
(f): Satellite cells
are restricted to ganglia where
they cover and support the large neuronal cell
bodies.
14. References
Fundemental Neuroscience for Basic and Clinical Applications, 3rd Ed
Color Textbook of Histology
Janguira’s Basic Histology, 12th Ed
15. शुक्रिया … آپ کا شکریہ ..
謝謝… .. شكرا
Danke Je ..
Thank you …
Merci ...
Gracias …
E se …
ありがとう… Ef̱charistó …̱