GROUP MEMBERS
y TERRENCE ISACCS y LATISA CUDJOE y PATRICEE DOUGLAS y WAVENEY CHARLES y NIKITA BOWMAN y OLVA BESS y OLYNSIE MORRIS y CORESSA HENRY y NIKETA BARKER
(Leader)
The Nervous System is one of the body s organ systems that contains a network of neurones which coordinate actions and transmit signals around the body. It comprises of two parts 1.The Central Nervous System (CNS) 2.The Peripheral Nervous System (PNS)
yThe CNS comprising of the Brain and spinal cord, serves to integrate and coordinate all activities of the body. yThe Brain is divided into three parts , the cerebrum (the seat of consciousness),the cerebellum and the medulla oblongata
spinal cord to the rest of the body, and nerve relay stations called ganglia.
Ref 2
functional parts,
1. The Autonomic nervous system (ANS) which controls
Ref 6
Ref
deveoplment The Central nervous system is formed The neural plate consisting of the neuroectoderm becomes the neural tube, which forms the brain and the spinal cord
from three main sources 1. The Neural crest Cells 2. The Neural Tube 3. Mesoderm Layer
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Reference 2
A Typical Neurone
Glia Cells
A typical Neurone
Ref
Reference 3
Multipolar neuron
Unipolar neuron
Bipolar neuron
Ref 7
Ref
Reference 1
y The Nerves that are associated with the nervous system are divided into two categories these are; 1. The Spinal Nerves, which arise from the spinal cord (approximately 31 in all found on either side of the vertebral column). They have both motor and sensory aspects. These nerves provide innervation to areas of the body that are below the neck. 2. The Cranial Nerves, (12 in all), emerge directly from the brain and carry impulses mainly to the head and neck
Ref
EMBRYOLOGY
Ref 22,23
Neurulation
y refers to the formation and closure of the neural tube. y (BMP-4), noggin, chordin, (FGF-8), and (N-CAM)
Ref 22, 23
The neural plate folds and give rise to the neural tube which: is open at both ends as the anterior and posterior neuropores the anterior and posterior neuropores connect the lumen of the neural tube to the amniotic cavity.
Ref 22,24
1. anterior neuropore: - closes on day 25 - becomes the lamina terminalis - failure to close results in upper neural tube defects (anencephaly). 2. posterior neuropore: - closes two days later (27th) - failure to close results in lower NTDs (spina bifida with myeloschisis).
Ref 22
C. As the neural plate folds, some cells differentiate into neural crest cells. D. The rostral part of the neural tube becomes the adult brain. E. The neural tube caudal to the fourth somite becomes the spinal cord. F. The lumen of the neural tube gives rise to the ventricular system of the brain and central canal of the spinal cord.
Ref 22,24
the marginal layer: The outermost layer of the spinal cord Contains myelinated fibres of the mantle zone This forms the white matter of the spinal cord
Ref 22, 25
Prosencephalon
y Telencephalon - Cerebral hemispheres, caudate, putamen, amygdaloid, claustrum, lamina terminalis, olfactory bulbs, hippocampus. y Diencephalon - Epithalamus, subthalamus, thalamus,
hypothalamus, mamillary bodies, neurohypophysis, pineal gland, globus pallidus, retina, iris, ciliary body, optic nerve (CN II), optic chiasm, optic tract
Ref 22
Rhombencephalon:
y Metencephalon - Pons, cerebellum y Myelencephalon - Medulla
Mesencephalon: y Midbrain
Ref 22
HISTOLOGY
y Consists of the brain and spinal cord y Composed of neurones, glial cells (supporting cells)
and blood vessels y Macroscopically, parts of CNS are made up of: Grey matter neurone cell bodies White matter axons of neurones
Ref 3
SPINAL CORD
is composed of grey and white matter: y The grey matter - composed of nerve cell bodies and - in a cross-sectional cut appears as a darker stained "H"-like central area
y The white matter
Meninges
y The brain and spinal cord are invested by three layers of supporting tissue collectively called the meninges - the outer most dura mater consists of dense connective tissue. - Middle layer the arachnoid made of dense connective tissue. Spaces within the arachnoid are filled with cerebrospinal fluid. - the inner most layer, the pia mater, consists of loose connective tissue on the surface of the brain and lining channels which penetrate the brain carrying the vascular system
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Neuroglia
y Are support cells which comprise all the non-neural cells of the CNS. y forms almost half the total mass of the CNS y are highly branched cells that occupy the spaces between neurones; the CNS contains little extracellular material. y They have intimate functional relationships with neurones providing both mechanical and metabolic support.
Ref 3
and are responsible for myelination y Astrocytes - highly branched cells that pack the interstices between the neurons, their processes and oligodendrocytes; provide mechanical support as well as mediate the exchange of metabolites between neurons and the vascular system; also form part of the blood-brain barrier and play an important role in repair of CNS tissue after injury or damage by disease
y Microglia - CNS representatives of the monocyte-macrophage system
ventricles and spinal canal. Some are ciliated, which facilitates the movement of cerebrospinal fluid.
Ref 3
Cerebellar cortex
y This portion of the brain's gray matter is arranged into three layers: y the superficial molecular layer containing mostly unmyelinated axons and few cell bodies y a deeper layer of large flask-shaped cells called Purkinje cells that send long dendritic projections into the molecular layer y an inner granular layer containing many small cell bodies
Ref 3
Cerebral cortex
y Consists of a convoluted cortex of grey matter overlying the central
medullary mass of white matter, which conveys fibres between different parts of the cortex and to and from other parts of the CNS.
y Starting at the surface of the cortex and moving inward, you can
identify the first three layers of cell bodies: - superficial molecular layer, containing only a few small cell bodies - outer granular layer, containing small round cell bodies - pyramidal cell layer, containing cell bodies triangular in shape.
y In total, the cerebral cortex consists of six layers with the inner most
three represented by an inner granular layer, internal pyramidal layer, and polymorphic cell layer, the innermost layer containing cell bodies of many shapes.
Ref 3
Choroid Plexus
y The choroid plexus produces the cerebrospinal fluid y It consists of a small tuft of capillaries surrounded by
cuboidal epithelium, the ependymal cells, which also surround the ventricular space and made of ion transporting cells
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ANATOMY
and spinal cord, which are composed of neurones, glial cells and blood vessels. . The brain can be further divided into: 1. The cerebrum 2. The diencephalon 3. The cerebelum 4. The brainstem
Ref 2
The Brain
reasoning, planning, parts of speech, It is the largest portion movement, emotions, and problem solving the mass)
The Cerebrum
of the brain in humans
associated with movement, orientation, recognition, perception of stimuli (accounts for 2/3
occupies the anterior and middle cranial fossae in the skull and
extending backwards over the tentorium cerebelli Divided into left and right hemispheres by a longitudinal fissure associated with visual and connected by the corpus callosum processing Each cerebral hemisphere is divided into 4 lobes by sulci or fissures: The frontal lobe-most ventral The parietal lobe-dorsal to the frontal The occipital lobe- dorsal to the parietal associated with The temporal lobe- lies inferior to the frontal and parietal (at the perception and temple and ears) recognition of auditory
stimuli, memory, and speech
Ref 2, 11
The Cerebellum
Is the large brain mass lying posterior to the pons and
medulla and inferior to the posterior part of the cerebrum. It lies beneath the tentorium cerebelli in the posterior cranial fossa and is separated from the cerebrum by tentorium cerebelli and the transverse fissure It consists of two lateral hemispheres that are united by a narrow middle part, the vermis.
Ref 2
The Diencephalon
y The Diencephalon - located within the cerebrum
between the cerebral hemispheres, and above the brain stem y Composed of : -the thalmus -the hypothalmus -the subthalmus -the epithalmus
Consists of :
The Brainstem
1.
THE MIDBRAIN
most rostral part of the brainstem, lies at the junction of the middle and posterior cranial fossae Acts as relay station for tracts passing between cerebrum and spinal cord or cerebellum Contains reflex centers for visual, auditory and tactile responses THE PONS the part of the brainstem between the midbrain rostrally and the medulla oblongata caudally; it lies in the anterior part of the posterior cranial fossa. Connects the cerebrum to the medulla and the cerebellum to the rest of the CNS via bundles of axons Also functions in conjunction with centres in the medulla to regulate breathing. THE MEDULLA OBLONGATA is the most caudal subdivision of the brainstem; is continuous with the spinal cord; lies in the posterior cranial fossa. Contains automatic centres for regulating breathing and vasoconstriction (blood pressure) Also contains centres for vomitting, coughing, sneezing, hiccuping, and swallowing. Ref 2,4
2.
3.
Ref 2,12
information to the spinal cord from the periphery via dorsal root and cranial nerve ganglia. Motor nerves carry information from the spinal cord to the periphery and include somatic motor nerves and motor nerves of the autonomic nervous system
Ref 13
sensory input form both the internal and external environments, process this information and effect an appropriate motor response.
Ref 4
y Comprised of the sensory receptors which receive the sensory information y The information can either cause: I.
immediate reaction from the brain II. memory of the experience can be stored in the brain y The sensory information enters the CNS and is conducted to sensory areas in :
1. 2. 3. 4. 5.
The spinal cord at all levels the reticular substance of the medulla, pons, and mesencephalon of the brain the cerebellum the thalamus areas of the cerebral cortex
Somatosensory axis of the nervous system. Ref 1
contraction of appropriate skeletal muscles throughout the body II. contraction of smooth muscle in the internal organs III. secretion of active chemical substances by both exocrine and endocrine glands INVOLUNTARYANS CONTROL y Effectors= muscles and glands
I.
Ref 1
Ref 1
1. The spinal cord level- the cord is capable of carrying out its own motor functions (eg walking movements, reflexes that withdraw portions of the body from painful objects reflexes that control local blood vessels etc.) 2. The subcortical level(lower brain)- the medulla, pons, mesencephalon, hypothalamus, thalamus, cerebellum, and basal ganglia. Most subconscious activities of the body occur at this level.(eg. Control of arterial pressure and respiration by the pons and medulla, control of equilibrium) 3. The cortical level(higher brain)- Cerebral cortex is an extremely large memory storehouse that functions in association with lower centers of the brain.
Ref 1
system mainly in the form of nerve action potentials, called simply nerve impulses, through a succession of neurons, one after another. y Nerve impulses are transmitted from one neurone to the next via synapses.
Ref 1
Ref
Anatomy of a Synapse
Ref 2
RELEASE OF NEUROTRANSMITTERS
y Impulses arriving at the terminal end of the
presynaptic neuron cause an increase in the membrane s permeability to Ca y Voltage gated Ca ion channels open leading to influx of Ca ions y Ca ions bind to releasing sites causing neurotransmitter release y These neurotransmitters act on the receptor proteins of the post synaptic neuron
Ref 1
y I. II. y
y y y y y y y y
Neurotransmitter substances are divided into two types: Small molecule, Rapidly- acting transmitters Neuropeptide, Slowly-acting transmitters The small molecule transmitters cause the most acute responses of the nervous system. The most important ones are:
Acetylecholine Norepinephrine Dopamine Glycine GABA (gamma-aminobutyric acid) Glutamate Serotonin Nitric oxide
The neuropeptides usually cause more prolonged actions such as longterm changes in numbers of neuronal receptors, long-term opening or closure of certain ion channels etc. Include ACTH, leutinising hormone, ADH, insulin, glucagon, calcitonin etc.
Ref 1
An excitatory transmitter increaes membrane pemeability to Na ions y Influx of Na causes depolarisation, changing the resting potential to a less negative excitatory postsynaptic potential y The EPSP rises to a point at which it is capable of initiating an action potential in the postsynaptic neuron y Inhibition y Inhibitory neurotransmitters cause Cl ion channels to oprn causing influx of Cl ions y They cause K ion channels to open causng efflux of these ions y These two actions lead to hyperpolarisation of the membrane- a more negative potential than the resting potential is established ( an Inhibitory Postsynaptic Potential) y The neuron is inhibited
y
Ref 1
SUMMATION
y Spatial Summation y Temporal Summation
Ref 1
y y
(hind brain) into the pharyngeal arches. The rhombencephalon is divided into eight segments called rhombomeres (R1-R8) Cranial neural crest cells from R1 and R2 migrate into pharyngeal arch 1 (which also receives neural crest cells from the midbrain area). R4 migrate into pharyngeal arch 2. R6 and R7 migrate into pharyngeal arch 3. This pattern is controlled by the expression of the Hoxb gene complex and OTX2.
The cranial nerves are classified into three groups, according to their embryologic origins: y Somatic Efferent Cranial Nerves y Nerves of Pharyngeal Arches y Special Sensory Nerves
Ref 22
CRANIAL NERVES
Olfactory nerve CN I y Olfactory nerve is derived from the nasal (olfactory) placode . CN I is capable of regeneration. y Olfactory neurosensory cells - olfactory epithelium in the superior part of the lateral and septal walls of the nasal cavity. y axons from these cells pass - foramina in the cribriform plate of the ethmoid bone, pierce the dura and arachnoid mater, and y enter the olfactory bulbs in the anterior cranial fossa. y During breathing air molecules attach to the olfactory mucosa and stimulate the olfactory and electrical activity is transduced into the olfactory bulb. y Olfactory bulb cells then transmit electrical activity to other parts of the central nervous system via the olfactory tract.
Ref 20
CRANIAL NERVES
Ref 20
CRANIAL NERVES
CN II. Optic Nerve
is derived from the ganglion cells of the retina (which is a diverticulum of the diencephalon) .
y The optic nerve originates from the bipolar cells of the retina which are connected to the specialized receptors in the retina (rod and cone cells). y The optic nerve passes poster medially through the orbit, runs through the optic canal to the middle cranial fossa and joins the optic chiasm. y Posterior to the optic chiasm the optic nerves are instead called optic tracts. Most fibers in the optic tracts terminate in the lateral geniculate bodies of the thalamus. y Visual information enters the eye in the form of photons of light which are converted to electrical signals in the retina. These signals are carried via the optic nerves, chiasm, and tract to the lateral geniculate nucleus of each thalamus and then to the visual centers of the brain for interpretation.
Ref 20
CRANIAL NERVES
Ref 9
CRANIAL NERVES
Oculomotor nerve (CN III)
y is derived from the basal plate of the rostral midbrain. y Emerges from the midbrain, pierces the dura, runs in the lateral wall of y y
the cavernous sinus. Exits the skull through the superior orbital fissure and enters the orbit. From here it splits into a superior division (which supplies the superior rectus m.) and an inferior division (which supplies the inferior and medial rectus and inferior oblique m. and also carries autonomic fibers to the ciliary ganglion). The somatic motor component of CN III plays a major role in controlling the muscles responsible for the precise movement of the eyes for visual tracking or fixation on an object. The visceral motor component is involved in the pupillary light and accomodation reflexes
Ref 9
CRANIAL NERVES
Ref 9
CRANIAL NERVES
CN IV. Trochlear Nerve y is derived from the basal plate of the caudal midbrain. y emerges from the dorsal surface of the midbrain , winds around the brainstem, pierces the dura and passes anteriorly in the lateral wall of the cavernous sinus. y Exits the cavernous sinus and passes through the superior orbital fissure into the orbit to supply the superior oblique muscle.
Ref 21
CRANIAL NERVES
y CN V. Trigeminal Nerve y The motor division of CN V is derived from the basal plate of the rostral pons. The
y Emerges from the pons by a small motor root and a large sensory root. The ophthalmic
y through the superior orbital fissure. The maxillary division (V2) is exclusively sensory
and exits through the foramen rotundum. The and a branchial motor component (SVE).
y mandibular division (V3) exits through the foramen ovale; it has a sensory component y In the sensory innervation:
1.Ophthalamic branch (word root = 'eye') Innervates upper face including conjunctiva, cornea, forehead, eyelid,bridge of nose Maxillary branch (word root = 'upper jaw') Innervates upper jaw, cheeks, nasal cavity Mandibular branch (word root = 'lower jaw') Innervates lower jaw, teeth gums, anterior 2/3 of tongue.
y
Ref 21
CRANIAL NERVES
y The motor component includes innervations of :
1. muscles of mastication, which aid in biting 2. tensor tympani, which adjusts the tension of the eardrum, which allows us to increase our sensitivity to really quiet sounds
Ref 21
CRANIAL NERVES
y CN VI. Abducent Nerve y Abducent nerve (CN VI) is derived from the basal plate of the caudal pons y Exits brainstem at medullopontine junction between the pyramids and pons. It then pierces the dura and passes through the y cavernous sinus. Enters the orbit through the superior orbital fissure and runs anteriorly to supply the lateral rectus muscle. y The function of the abducent nerve is to contract the lateral rectus which results in abduction of the eye. The abducens nerve in humans is solely and somatomotor nerve.
Ref 21
Cranial nerve VII: Facial nerve y Emerges from the brainstem between the pons and medulla and passes through the internal acoustic meatus. y the motor division of this nerve derived from the basal plate of the pons while its sensory division is from the cranial neural crest cells. y Both divisions are innervations of pharyngeal arch 2 derivatives eg. Stapes, stapedius muscle y The facial nerve carries somatic motor innervation to the many muscles for facial expression. y This nerve has five branches: temporal, zygomatic, buccal, mandibular and submandibular(cervical). y The fibers are of 4 types
I. II. III. IV.
y It carries sensory information form the face (deep pressure sensation) and taste
information from the anterior two thirds of the tongue. y It arises at the pons in the brainstem and it emerges through openings in the temporal bone and stylomastoid foramen and has many branches. Ref 23, 26 y It is composed of both sensory and motor axons.
Cranial nerve VIII: Vestibulocochlear nerve y Emerges from the internal acoustic meatus y derived from the otic placode. y innervates the hair cell receptors of the inner ear. It carries vestibular information to the brain from the semicircular canals, utricle, and saccule providing the sense of balance and equilibrium. It also carries information from the cochlea providing the sense of hearing. y branches into the Vestibular branch (balance) and the cochlear branch (hearing). The cochlear fibers originate from the spiral ganglion. It is pure sensory nerve fiber.
Ref 5, 23
Cranial nerve IX: Glossopharyngeal nerve y Emerges from the jugular foramen. y Has 2 divisions.
y y
The motor division is derived from the basal plate of the medulla. The sensory division is derived from the cranial neural crest cells.
y It is composed of both sensory and motor axons and originates from the
derivatives. innervates the pharynx (upper part of the throat), the soft palate and the posterior one-third of the tongue. It carries sensory information (touch, temperature, and pressure) from the pharynx and soft palate. It carries taste sensation from the taste buds on the posterior one third of the tongue. It provides somatic motor innervation to the throat muscles involved in swallowing. It provides visceral motor innervation to the salivary glands. This cranial nerve also supplies the carotid sinus and reflex control to the heart.
Ref 23
Cranial nerve X: Vagus nerve . emerges from the jugular foramen. y The motor division of CN X is derived from the basal plate of the medulla. The
y y
y y y y y
sensory division of CN X is derived from the cranial neural crest cells. Mediates the sensory and motor innervation of pharyngeal arches 4 and 6 derivatives. The vagus nerve consists of many rootlets that come off of the brainstem just behind the glossopharyngeal nerve. The branchial motor component originates from the nucleus ambiguous in the reticular formation of the medulla. The visceral component originates from the dorsal motor nucleus of the vagus located in the floor of the fourth ventricle in the rostral medulla and in the central grey matter of the caudal medulla. It is the longest cranial nerve innervating many structures in the throat, thorax and abdominal cavity. It provides sensory information (touch, temperature and pressure) from the external auditory meatus and a portion of the external ear It carries taste sensation from taste buds in the pharynx. It also provides sensory information from the esophagus, respiratory tract, and abdominal viscera (stomach, intestines, liver, etc.). It provides visceral motor innervation to the heart, stomach, intestines, and gallbladder. It is part of the ANS, the parasympathetic branch. Other parasympathetic ganglia include CN III , CN VII and CN IX . Ref 5, 23
Cranial nerve XI: Spinal Accessory nerve y Emerges from the jugular foramen y is derived from the basal plate of the spinal segments C-1 to C-6. y The spinal accessory nerve has two branches. The cranial branch provides somatic motor innervation to some of the muscles in the throat involved in swallowing. This cranial branch is accessory to CN X, originating in the caudal nucleus ambiguous, with the fibers of the cranial root traveling the same extracranial path as the branchial motor component of the vagus nerve. The spinal branch provides somatic motor innervation to the trapezius muscles, providing muscle movement for the upper shoulders head and neck. It is pure motor nerve fiber. Cranial nerve XII: Hypoglossal nerve y Emerges from the hypoglossal canal. y is derived from the basal plate of the medulla. y CN XIII innervates the intrinsic and extrinsic muscles of the tongue. The hypoglossal nerve provides somatic motor innervation to the muscles of the tongue. This pure motor nerve originates from the hypoglossal nucleus located in the tegmentum of the medulla.
Ref 23, 27
Ref 27
lateral ventricles and the midline 3rd and 4th ventricles connected by the cerebral aqueduct y CSF, largely secreted by the choroid plexuses of the ventricles, fills these brain cavities and the subarachnoid space of the brain and spinal cord.
Ref 2,14
The Lateral Ventricles: - are the largest cavities of the ventricular system; occupy large -
areas of the cerebral hemispheres. Each opens through an interventricular foramen into the 3rd ventricle. The Third Ventricle: a slit-like cavity between the right and the left halves of the diencephalon;continuous posteroinferiorly with the cerebral aqueduct, which connects the 3rd and 4th ventricles The Fourth Ventricle: pyramid-shaped; posterior to the pons and medulla and it extends inferoposteriorly. Inferiorly, it tapers to a narrow channel that continues into the cervical region of the spinal cord as the central canal
Ref 2
SUBARACHNOID CISTERNS
CFS fills the subarachnoid cisterns of the brain. They are:
- The Cerebellomedullary Cistern: largest of the subarachnoid cisterns, located between the cerebellum and the medulla - The Pontocerebellar Cistern : ventral to the pons, continuous inferiorly with the spinal subarachnoid space. - The Interpeduncular Cistern: located in the interpeduncular fossa - The Chiasmatic Cistern: Inferior and anterior to optic chiasm - The Quadrigeminal Cistern : located between the posterior part of the corpus callosum and the superior surface of the cerebellum. - The Ambient Cistern :located on the lateral aspect of the midbrain and continuous posteriorly with the quadrigeminal
Ref 2
choroidal epithelial cells of the choroid plexuses in the ventricles The choroid plexuses : -are vascular structures arising from the walls of each of the four ventricles of the brain -They are invaginated into the roofs of the 3rd and 4th ventricles and on the floors of the bodies and inferior horns of the lateral ventricles
Ref 2
subarachnoid space over brain and spinal cord reabsorption into venous sinus blood via arachnoid granulations. Ref 2
Ref 2
LEAKAGE OF CEREBROSPINAL FLUID y CSF Otorrhea- fractures in the floor of the middle cranial fossa may result in CSF leakage from the external acoustic meatus if the meninges superior to the middle ear are torn and the tympanic membrane is ruptured
y CSF rhinorrhea- fractures in the floor of the anterior cranial fossa may involve the cribriform plate of the ethmoid, resulting in CSF leakage through the nose
Both CSF otorrhea and CSF rhinorrhea may be the primary indications of a cranial base fracture
Ref 2
and quadrigeminal cisterns. C y CSF also passes into the extensions of the subarachnoid space around the cranial nerves, the most important of which are those surrounding the optic nerves.
Ref 2
blood sugar level) CSF cell count: 0 - 5 white blood cells (all mononuclear), and no red blood cells Chloride: 110 - 125 mEq/L
Ref 2
the cerbrospinal fluid delivers nutrients to the structures of the nervous system y the cerebrospinal fluid removes wastes from the brain and spinal cord, detoxifying the environment of the nervous system y shock absorption y the cerbrospinal fluid protects the brain and spinal cord from trauma brought upon by movement, falls, blows, etc.
y
prevents the weight of the brain from compressing the cranial nerve roots and blood vessels
Ref 2
y The peripheral nervous system(PNS) is the portion on the nervous system which lies outside the CNS and is composed of:
-Nerves that carry sensory messages to CNS and motor commands from CNS to muscles and glands. Nerves are bundles of axons(axons that occur in nerve fibers are called nerve fibers) -ganglia, swellings associated with nerves that contain collections of cell bodies.
Ref 4
PERIPHERAL NERVES
y These nerves include cranial and spinal nerves. y Some nerves contain sensory input(afferent) fibers, while some contain motor output(efferent) fibers. y Some cranial nerves, however, contain both sensory and motor fibers(mixed nerves) y The afferent fibers have sensory receptors which detect internal and external stimuli(which is sent to the CNS and interpreted) y The motor fibers conduct impulses to the effectors(muscles and glands) which respond to the stimuli detected by the sensory receptors. y In the PNS, cranial nerves take impulses to and from the brain, and the spinal nerve take impulses to and from the spinal cord.
Ref 4
Ref 19
the neural plate. The neural plate(consisting of neuroectoderm) becomes the neural tube. This gives rise to the brain and spinal cord. y The PNS is derived from 3 sources: -neural crest cells -neural tube(gives rise to all preganglionic autonomic fibers and all fibers that innervate skeletal muscles. -mesoderm(gives rise to the dura mater and connective tissue investments of peripheral nerve fibers(endoneurium, perineurium, epineurium)
Ref 22
basal plate of the neural tube and neural crest cells y The basal plate gives rise to the preganglionic sympathetic neurons y The neural crest cells give rise to postganglionic sympathetic neurons within the sympathetic chain ganglia
Ref 22
Ref 22
receptors that detect stimuli are of two types: -unencapsulated nerve endings(free nerve endings) -encapsulated nerve endings
Ref 19
FREE NERVE ENDINGS- These are responsible for detecting pain and temperature and are of two types: -hair follicle receptors(located in and around hair follicles) -Merkel discs(basal layer of epidermis) ENCAPSULATED NERVE ENDINGS-These consist of one or more end fibers of sensory neurons and are enclosed in connective tissue. y There are three types: -Meissner s corpuscles(nipples, eyelids, external genitalia, fingertips) -Pacinian corpuscles(subcutaneous:tendons, ligaments, joint capsules) -Ruffini s corpuscles(deep in the dermis, hypodermis, joint capsules)
Ref 19
muscles and glands via secreting neurotransmitters at neuromuscular junctions. y They also secrete these neurotransmitters at varicosities at smooth muscle and glands.
Ref 19
Ref 4
y The first neuron has a cell body within the CNS and its axon is called the preganglionic fiber. The second neuron has a cell body within the ganglion and its axon is called the postganglionic fiber. y However, in the sympathetic nervous system, the preganglionic fiber is shorter than the postganglionic fiber. y This is the opposite in the parasympathetic nervous system: the preganglionic fiber is longer than the postganglionic fiber.
Ref 4
pressure(degree of stretch in blood vessel walls) and breathing rate(abnormal CO2 and O2 levels) are very important to the maintenance of homeostasis. y The reflexes begin when sensory neurons in contact with the internal organs send messages to the CNS. Motor neurons within the autonomic system effect the response
Ref 4
Ref
impulse after which it becomes depolarised providing that the stimulus is great enough for the neuron to meet the threshold value. This information is then relayed to the motor neuron by a relay neuron. This motor neuron is associated directly with the muscle a the neuromuscular junction. When the action potential reaches the terminal bouton of the neuromuscular junction its simulates the opening of gated Ca2+ channels which facilitates the movement of Ca2+ into the terminal bouton. y This influx of Ca2+ allows or the binding of synaptic vesicles containing ACETYLCHOLINE (a neurotransmitter) to the membrane of the bouton. Hence the contents of the vesicles are released into the synaptic clef.
Ref 18
Ref 18
NEUROMUSCULAR JUNCTION
Ref17
CRANIAL NERVES
y There are 12 crainal nerves total, numbered I through XII. y Cranial nerves I and II attach to the forebrain y All others attach to the brain stem y Primarily serve head and neck structures y However the vagus nerve (X) extends into the abdomen
Ref 17
CRANIAL NERVES
Ref17
SPINAL NERVES
They are named from the point of issue from the
spinal cord.
8 pairs of cervical nerves (C1-C8) 12 pairs of thoracic nerves (T1-T12) 5 pairs of lumbar nerves (L1-L5) 5 pairs of sacral nerves (S1-S5) 1 pair of coccygeal nerves (Co1)
Ref 19
Ref
Ref 19
y y y y y y
cord There are more than 100 kinds of peripheral nerve disorders. They can affect one nerve or many nerves. Some are the result of other diseases, like diabetic nerve problems. Others, like Guillain-Barre syndrome, happen after a virus infection. Still others are from nerve compression, like carpal tunnel syndrome or thoracic outlet syndrome. In some cases, like complex regional pain syndrome, the problem begins after an injury. Some people are born with peripheral nerve disorders. Symptoms often start gradually, and then get worse. They include Numbness Pain Burning or tingling Muscle weakness Sensitivity to touch
Ref 18
y is a painful, blistering skin rash. y caused by the varicella-zoster virus, the same virus that causes
chickenpox. y Symptoms manifest years after one would have had chickenpox.
y Guillian Barre Syndrome REF. 2 y An autoimmune disorder. y Occurs with viral infections such as HIV, herpes simplex and mononucleosis. y Results n damage to myelinated nerve fibres. y Myasthenia Gravis REF. 2 y An autoimmune neuromuscular disorder. y The body s antibodies invade the neuromuscular junctions and block the acetylcholine receptors preventing the binding of it. y Results in disruption of nerve impulse transmitting.
Ref 16,19
The sympathetic nervous system (SNS) is composed of a network of:y Short efferent CNS axons that extend to ganglia located near the spine and y Long efferent neurons extending from the ganglia directly to each target organ.
Ref1
Ref1
components of the ANS will be subject to the effects of the two opposing neurotransmitters. If the sympathetic nerve ending excites a particular organ, the parasympathetic synapse usually inhibits it.
the heart and inhibits gastrointestinal motility and secretion, inhibiting digestion, whereas the parasympathetic system slows up the heart rate and increases gastrointestinal activity.
Ref1
opposition to each other. This natural opposition is better understood as complementary in nature rather than antagonistic. We can think of the sympathetic division as the accelerator and the parasympathetic division as the brake. The sympathetic division typically functions in actions that require quick responses. The parasympathetic division functions with actions that do not require immediate reaction.
y The afferent fibers of the ANS, which transmit sensory information
from the internal organs of the body back to the central nervous system, are not divided into parasympathetic and sympathetic fibers as the efferent fibers are. Instead, autonomic sensory information is conducted by general visceral afferent fibers. Ref1
Ref1
threshold (and the threshold can vary enormously), including feelings, and by noise, light, drugs and chemicals (e.g. caffeine). y In response to the stimulus an immediate anticipatory state is generated by the release of adrenaline. This causes the heart to beat more quickly and strongly, increases blood supply to the muscles, raises blood pressure, dilates the bronchii and increases the breathing rate, raises the blood sugar level for increased energy, speeds up mental activity, increases tension in the muscles, dilates pupils and increases sweating. y Non-emergency functions, such as digestion are lessened or suspended. the fight or flight to describe the function of the rapid mobilisation of resources.
Ref1
Organization
y Sympathetic nerves originate inside the vertebral column,
toward the middle of the spinal cord in the intermediolateral cell column (or lateral horn), beginning at the first thoracic segment of the spinal cord and are thought to extend to the second or third lumbar segments. Because its cells begin in the thoracic and lumbar regions of the spinal cord, the SNS is said to have a thoraco-lumbar outflow. Axons of these nerves leave the spinal cord through the anterior rootlet/root. They pass near the spinal (sensory) ganglion, where they enter the anterior rami of the spinal nerves. out through white rami connectors (so called from the shiny white sheaths of myelin around each axon) that connect to either the paravertebral (which lie near the vertebral column) or prevertebral (which lie near the aortic bifurcation) ganglia extending alongside the spinal column.
Ref1
must travel long distances in the body, and, to accomplish this, many axons relay their message to a second cell through synaptic transmission. The ends of the axons link across a space, the synapse, to the dendrites of the second cell.
y The first cell (the pre-synaptic cell) sends a
neurotransmitter across the synaptic cleft where it activates the second cell (the postsynaptic cell). The message is then carried to the final destination.
Ref1
signal through the sympathetic system; pre- and post- ganglionic. The shorter preganglionic neurons originate from the thoracolumbar region of the spinal cord (levels T1 - L2, specifically) and travel to a ganglion, often one of the paravertebral ganglia, where they synapse with a postganglionic neuron. From there, the long postganglionic neurons extend across most of the body. In the SNS and other components of the peripheral nervous system, these synapses are made at sites called ganglia. The cell that sends its fiber is called a preganglionic cell, while the cell whose fiber leaves the ganglion is called a postganglionic cell.
The ganglia include not just the sympathetic trunks but also the cervical ganglia (superior, middle and inferior), which sends sympathetic nerve fibers to the head and thorax organs, and the celiac and mesenteric ganglia (which send sympathetic fibers to the gut). Ref1
ganglia or prevertebral ganglia. This can occur through one of four methods:
originating spinal nerve, and then ascends to a more superior paravertebral ganglion, where it synapses with the postsynaptic cell. y 2. The nerve enters the paravertebral ganglion at the level of its originating spinal nerve and synapses with the postsynaptic cell at that level. y 3. The nerve enters the paravertebral ganglion at the level of its originating spinal nerve, and then descends to a more inferior paravertebral ganglion, where it synapses with the postsynaptic cell. y 4. The nerve enters the paravertebral ganglion at the level of its originating spinal nerve and then descends to a prevertebral ganglion, where it synapses with the postsynaptic cell.
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messages can trigger changes in different parts of the body simultaneously. For example, the sympathetic nervous system can accelerate heart rate; widen bronchial passages; decrease motility (movement) of the large intestine; constrict blood vessels; increase peristalsis in the esophagus; cause pupillary dilation, piloerection (goose bumps) and perspiration (sweating); and raise blood pressure. Afferent messages carry sensations such as heat, cold, or pain.
y The first synapse (in the sympathetic chain) is mediated by
nicotinic receptors physiologically activated by acetylcholine, and the target synapse is mediated by adrenergic receptors physiologically activated by either noradrenaline (norepinephrine) or adrenaline (epinephrine).
Ref1
innervation but have muscarinic acetylcholine receptors, which are normally characteristic of the parasympathetic nervous system.
y Another exception is the adrenal medulla, which develops in
tandem with the sympathetic nervous system, and acts as a modified sympathetic ganglion: synapses occur between preand post- ganglionic neurons within it, but the post ganglionic neurons do not leave the medulla; instead they directly release norepinephrine and epinephrine into the blood.
Ref1
Ref1
When large portions of the sympathetic nervous system discharge at the same time, that is a mass discharge, this increases in many ways the ability of the body to perform vigorous muscle exercises. Some of these ways are:
y Increased arterial pressure y Increased blood flow to active muscles concurrent with
y y y y y y
decreased blood flow to organs such as the gastrointestinal tract and the kidneys that are not needed for rapid motor activity Increased rates of cellular metabolism throughout the body Increased blood glucose concentration Increased glycolysis in the liver and in muscle Increased muscle strength Increased mental activity Increased rate of blood coagulation
Ref1
strenuous physical activity than would otherwise be possible. Because either mental or physical stress can excite the sympathetic system, it is frequently said that the purpose of the sympathetic system is to provide extra activation of the body in states of stress: this is called the sympathetic stress response.
many emotional states. For instance, in the state of rage, which is elicited to a great extent by stimulating the hypothalamus, signals are transmitted downward through the reticular formation of the brain stem and into the spinal cord to cause massive sympathetic discharge; most aforementioned sympathetic events ensue immediately. This is called the sympathetic alarm reaction.
Ref1
Presynaptic neurons synthesize and package their neurotransmitter in vesicles for release (by exocytosis) at the synapse and often have "reuptake" transporters that reclaim the transmitter back into the cell when it has done its job. Postsynaptic neurons display receptors to which the neurotransmitter binds. All of this machinery provides many targets for alteration by exogenous chemicals; that is, psychoactive chemicals introduced into the body. These drugs fall into several distinct families. (stimulants, sedatives, local anesthetics, opiates, anti-depressants, etc.) Stimulants The most widely used stimulants are: y caffeine (in coffee, tea, and cola beverages) y nicotine (in cigarettes) y amphetamines y cocaine All of these drugs mimic the stimulation provided by the sympathetic nervous system. Ref
Nicotine binds to a subset of acetylcholine (ACh) receptors. ACh is a neurotransmitter at synapses early in the pathways of sympathetic stimulation. Although a weak drug in one sense, nicotine is strongly addictive. The use of chewing gum and skin patches containing nicotine is designed to satisfy the craving for nicotine while avoiding the serious health effects of other ingredients in cigarette smoke. Amphetamines and cocaine bind to thus blocking transporters used for the reuptake of dopamine (and noradrenaline) into presynaptic neurons. This causes the level of dopamine to rise in the synapses. High levels of dopamine in an area of the brain called the nucleus accumbens appear to mediate the pleasurable effects associated with these (as well as other) psychoactive drugs. Some amphetamines:
y y
The chief medical uses for amphetamines and amphetamine-like drugs areto help people lose weight (because they suppress appetite); to help children with attention deficit/hyperactivity disorder (ADHD) to perform better in school. At first glance, this second use seems counterproductive. This controversial procedure seems to work by increasing the alertness of the child so that it can focus its energies more effectively on the tasks in front of it.
Ref
Fen-Phen y Fen-Phen refers to a mixture of two amphetamine-like drugs: fenfluramine and phentermine y These were prescribed for losing weight. Because of reports of occasional very serious side effects, the mixture is no longer available and fenfluramine has been removed from the U.S. market. Cocaine y Cocaine has been used for thousands of years by certain tribes in the Andes of South America. Cocaine and some of its relatives have legitimate medical uses as local anesthetics (e.g., lidocaine). However, the widespread recreational use of cocaine has created serious social problems.
y Immunity to cocaine addiction? In order to achieve its effects, cocaine must cross the so-called bloodbrain barrier. If antibodies are bound to the cocaine molecule, it cannot cross. This has raised the possibility of immunizing people against cocaine. It works in mice.
Ref
to 2 minutes, whereas the actions of some other commonly used sympathomimetic drugs last for 30 minutes to 2 hours.
Ref
Important drugs that stimulate specific adrenergic receptors but not others are:
y phenylephrine (alpha receptors) y isoproterenol (beta receptors)
Ref
1. The synthesis and storage of norepinephrine in the sympathetic nerve endings can be prevented. The best known drug that causes this effect is reserpine. 2. Release of norepinephrine from the sympathetic endings can be blocked. This is caused by guanethidine. 3. The sympathetic alpha receptors can be blocked. Two drugs that cause this effect are: phenoxybenzamine and phentolamine. 4. The sympathetic beta receptors can be blocked. A drug that blocks beta1 and beta 2 receptors is propranolol. One that blocks mainly beta1receptors is metoprolol. 5. Sympathetic activity can be blocked by drugs that block transmission of nerve impulses through the autonomic ganglia. An important drug for blockade of both sympathetic and parasympathetic transmission through the ganglia is hexamethonium.
Ref
stimulation of "rest-and-digest" activities that occur when the body is at rest, including (SLUDD): salivation, lacrimation (tears), urination, digestion and defecation. It s also involve in sexual arousal.
Ref
y All preganglionic neurons are cholinergic. y Either all or most of the postganglionic neurons of the parasympathetic nervous system
are cholinergic.
y The terminal nerve endings of the parasympathetic system all or virtually all secrete
acetylcholine.
y Therefore, acetylcholine is called a parasympathetic transmitter.
Ref 1
Synthesis of Acetylcholine, Its Destruction After Secretion, and Its Duration of Action.
y Acetylcholine is synthesized in the terminal endings and varicosities of the cholinergic
nerve fibers where it is stored in vesicles in highly concentrated form until it is released.
y Acetyl-CoA + Choline (Acetylcholine acetyltransferase) gives acetylcholine. y When acetylcholine is secreted into a tissue by a cholinergic nerve ending, it persists in
the tissue for a few seconds while it performs its nerve signal transmitter function.
y Then it is split into an acetate ion and choline, catalyzed by the enzyme
acetylcholinesterase that is bound with collagen and glycosaminoglycans in the local connective tissue.
y This is the same mechanism for acetylcholine signal transmission and subsequent
acetylcholine destruction that occurs at the neuromuscular junctions of skeletal nerve fibers.
y The choline that is formed is then transported back into the terminal nerve ending,
Ref 1
STRUCTURE OF ACETYLCHOLINE
Ref 1
protein molecule that penetrates all the way through the cell membrane.
y When the transmitter substance binds with the receptor, this causes a conformational
causing a change in cell membrane permeability to one or more ions or (2) activating or inactivating an enzyme attached to the other end of the receptor protein where it protrudes into the interior of the cell.
Ref
y They are called muscarinic and nicotinic receptors. The reason for these
names is that muscarine, a poison from toadstools, activates only muscarinic receptors and will not activate nicotinic receptors, whereas nicotine activates only nicotinic receptors; acetylcholine activates both of them.
y Muscarinic receptors are found on all effector cells that are stimulated by
the postganglionic cholinergic neurons of either the parasympathetic nervous system or the sympathetic system.
between the preganglionic and postganglionic neurons of both the sympathetic and parasympathetic systems. Ref 1
STIMULATION OF DISCRETE ORGANS AND MASS STIMULATION IN OTHER INSTANCES BY THE PARASYMPATHETIC SYSTEMS
The eyes- when bright light is shone into the eyes, the messages is transmitted to the midbrain giving rise to an appropriate stimulus which travels through the parasympathetic fibers to the oculomotor(third cranial nerve), to the pupils which results in the autonomic contraction of the pupillary muscles, constricting the aperture, thus reducing the amount of light reaching the sensory cells of the retina. The stomach- stimuli of entry of food into the stomach are conveyed by afferent fibers of the vagus nerve to the command station where messages are conveyed through efferent fibers of the vagus nerve back to the stomach. As a result there is secretion of gastric juices and peristaltic contraction to mix food. These food is conveyed to the small intestine where it follows the same parasympathetic nervous pathway. Bladder and rectum- emptying the bladder and rectum is not entirely autonomic but is subjected to parasympathetic impulses that are voluntary controlled. The filling of the urinary bladder stimulates stretch sensitive receptors in its wall whence the message is conveyed to the midbrain where the stimulus to blood contraction and opening of sphincter is voluntary initiated for the discharge of urine.
2.
3.
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stimuli in the dilatation of the cervix and involuntary control of the uterine musculature with delivery of the fetus assisted by voluntary contraction of the abdominal muscles.
Ref 1
Autonomic Reflexes Many visceral functions of the body are regulated by autonomic reflexes.
control especially the arterial blood pressure and the heart rate. y One of these is the baroreceptor reflex, Baroreceptors are located in the walls of several major arteries, including especially the internal carotid arteries and the arch of the aorta. y When these become stretched by high pressure, signals are transmitted to the brain stem, where they inhibit the sympathetic impulses to the heart and blood vessels and excite the parasympathetics; this allows the arterial pressure to fall back toward normal. Ref 1
controlled principally by autonomic reflexes. For instance, the smell of appetizing food or the presence of food in the mouth initiates signals from the nose and mouth to the vagal, glossopharyngeal, and salivatory nuclei of the brain stem. These in turn transmit signals through the parasympathetic nerves to the secretory glands of the mouth and stomach, causing secretion of digestive juices sometimes even before food enters the mouth.
yWhen fecal matter fills the rectum at the other end of the alimentary canal,
sensory impulses initiated by stretching the rectum are sent to the sacral portion of the spinal cord, and a reflex signal is transmitted back through the sacral parasympathetics to the distal parts of the colon; these result in strong peristaltic contractions that cause defecation.
Ref1
emptying the rectum; stretching of the bladder sends impulses to the sacral cord, and this in turn causes reflex contraction of the bladder and relaxation of the urinary sphincters, thereby promoting micturition.
y Also important are the sexual reflexes, which are initiated both by
psychic stimuli from the brain and by stimuli from the sexual organs. Impulses from these sources converge on the sacral cord and, in the male, result first in erection, mainly a parasympathetic function, and then ejaculation, partially a sympathetic function. regulation of pancreatic secretion, gallbladder emptying, kidney excretion of urine, sweating, blood glucose concentration, and many other visceral functions.
Ref 1
REFERENCES
1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13.
Medical Physiology, 11th Clinically Oriented Anatomy Wheather s Functional Histology Madder, Sylvia S.,(2006),Inquiry Into Life, McGraw-Hill Board review Physiology 3rd Edition Lynda S Costanzo, PHD http://www2.estrellamountain.edu/faculty/farabee/biobk/biobooknerv.htm l#The Neuron How the body works- A comprehensive illustrated Enclopedia of Anatomy DR. Peter Abrams http://www.chop.edu/healthinfo/acute-spinal-cord-injury.html http://www.meddean.luc.edu/lumen/MedEd/grossanatomy/h_n/c/cn1/mai nframe.htm http://www.cerebromente.org.br/n02/fundamentos/circulation_i.htm http://www.le.ac.uk/pa/teach/va/anatomy/case3/frmst3.html http://www.chop.edu/healthinfo/acute-spinal-cord-injury.html http://www.southtexascollege.edu/nilsson/4_GB_LectureNotes_f/4_GB_16_ AnimS_Ho_J_Spr2003.html
References
14. 15. 16. 17. 18. 19. 20. 21. 22. 23. 24. 25. 26. 27.
http://www.highlands.edu/academics/divisions/scipe/biology/faculty/harnd en/2121/notes/cns.htm http://www.siumed.edu/~dking2/ssb/muscle.htm http://www.nlm.nih.gov/medlineplus/peripheralnervedisorders.html http://www.ncbi.nlm.nih.gov/pubmedhealth http://www.nlm.nih.gov/medlineplus/peripheralnervedsorders.html Group 4 presentation http://www.med.yale.edu/caim/cnerves/cn1/cn1_4.htm http://www.med.yale.edu/caim/cnerves/cn4/cn4_1.html Dudek, Ronald W., James D. Fix, Embryology 3rd edi.(2005) Lippincott Williams & Wilkins Moore, Keith, 8th Edition, The Developing Embryo, Saunders. Sadler, T. W., Langman s Medical Embryology, 9th ed. Sweeney, Lauren J., (1998), Basic Concepts in Embryology: A Student s Survival Guide, McGraw-Hill Group 3- cranial nerves http://www.juniordentist.com/12-cranial-nerves.html