Human Anatomy and Physiology Chapter 12 Nervous Tissue

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Last updated 6:54 AM on 10/13/26
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Primary role of the nervous system

  1. The bodys main control and communication system

  2. Gathers information from internal and external environments, processes it, and transmits signals to trigger responses.


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Three essetnial functions of the nervous sytem

  • Sensory input: sensory receptors detect internal and external stimuli

  • Integration: Processing and interpreting sensory input to determine the appropriate response

  • Motor output: Activating effector organs (muscles or glands) to produce a response


<ul><li><p>Sensory input: sensory receptors detect internal and external stimuli</p></li><li><p>Integration: Processing and interpreting sensory input to determine the appropriate response</p></li><li><p>Motor output: Activating effector organs (muscles or glands) to produce a response</p></li></ul><p></p>
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Anatomical components of the central nervous system (CNS)

  • Brain (occupies cranium) and spinal cord (occupies vertebral canal).

  • Acts as the integrative and control center


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Anatomical components of the peripheral nervous system (PNS)

  • Cranial nerves, spinal nerves, and ganglia (clusters of neuron cell bodies outside the CNS)

  • Communication lines linking all body regions to the CNS


<ul><li><p>Cranial nerves, spinal nerves, and ganglia (clusters of neuron cell bodies outside the CNS)</p></li><li><p>Communication lines linking all body regions to the CNS</p></li></ul><p></p>
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Functional divisions of the PNS

  • Sensory (Afferent) Division: somatic and visceral sensory nerve fibers carrying impulses from receptors to the CNS

  • Motor (Efferent) Division: Motor nerve fibers carrying impulses from the CNS to effectors (muscles, glands, adipose tissue)


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Subdivisions of the Motor (Efferent) Division

  • Somatic Nervous System (SNS): Somatic motor fibers conducting impulses to skeletal muscle (voluntary; also controls involuntary somatic reflexes)

  • Autonomic Nervous system (ANS): Visceral motor fibers regulating smooth muscle, cardiac muscle and glands (involuntary).


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Functional branches of the Autonomic Nervous System (ANS)

  • Sympathetic divisions: Mobilizes body during activity (“fight or flight”)

  • Parasympathetic divisions: conserves energy and promotes housekeeping functions during rest (“rest and digest”)

  • Typically exert antagonistic (opposite) effects


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Structure and autonomy of the Enteric Nervous System (ENS)

  • Third division of the ANS consisting of neuron plexuses (myenteric and submucosal) within the digestive tract walls.

  • Influenced by sympathetic and parasympathetic inputs, but can initiate and coordinate digestive reflexes independently without CNS input


<ul><li><p>Third division of the ANS consisting of neuron plexuses (myenteric and submucosal) within the digestive tract walls.</p></li><li><p>Influenced by sympathetic and parasympathetic inputs, but can initiate and coordinate digestive reflexes independently without CNS input</p></li></ul><p></p>
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Physiological roles of the enteric nervous system

  • Motility: coordinate peristalsis to move substances through the digestive tract

  • Secretion: regulates gastric acid, digestive enzymes, and gut hormones

  • Blood flow: alters local mucosal/wall blood flow to match digestive demands

  • Immune interaction: modulates local mucosal barriers and immune responses



<ul><li><p>Motility: coordinate peristalsis to move substances through the digestive tract</p></li><li><p>Secretion: regulates gastric acid, digestive enzymes, and gut hormones</p></li><li><p>Blood flow: alters local mucosal/wall blood flow to match digestive demands</p></li><li><p>Immune interaction: modulates local mucosal barriers and immune responses</p></li></ul><p></p><p></p>
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Peripheral sensory receptors: Somatic vs visceral vs special

  • Somatic: Monitor skeletal muscles, joints and skin surface

  • Visceral: Monitor internal organs and cardiovascular/digestive status

  • Special: Specialized organs monitoring vision, hearing, balance, taste, and smell


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Structural regions of a typical neuron

  1. Soma

  2. Dendrites

  3. Axon

  4. Telodentria (terminal axonal arborizations)


<ol><li><p>Soma</p></li><li><p>Dendrites</p></li><li><p>Axon</p></li><li><p>Telodentria (terminal axonal arborizations)</p></li></ol><p></p>
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Cytoplasm and cytoskeleton of the neuronal cell body (soma)

  • Cytoplasm surrounding the nucleus is called perikaryon.

  • Cytoskeleton contains neurofilaments (intermediate filaments) and neurotubules (microtubules)

  • Bundles called neurofibrils extend into processes, resistig tensile (pulling) forces.


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Structure and microscopic significance of Nissl bodies

  • Dense clusters of rough endoplasmic reticulum (RER) and free ribosomes in the perikaryon

  • Stan darkly with cresyl violet and give gross gray matter its dusky gray hue


<ul><li><p>Dense clusters of rough endoplasmic reticulum (RER) and free ribosomes in the perikaryon</p></li><li><p>Stan darkly with cresyl violet and give gross gray matter its dusky gray hue</p></li></ul><p></p>
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Centriole deficiency and neurogenesis limitations in mature neurons

  • Most mature neurons lack centrioles and cannot undergo mitotic division

  • Neural stem cells remail largely inactive in adults, except in the olfactory epithelium (smell receptor renewal) and the hippocampus


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Metabolic characteristics and longevity of neurons

  • Extreme longevity (can function over 100 years).

  • Exceptionally high metabolic rate requiring constant glucose and oxygen; vulnerable to irreversible damage within minutes of hypoxia


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Receptive morphology and specializations of dendrites

  • Short, tapering, highly branched processes serving as input regions

  • Contain dendritic spines (bulbous projections for synaptic contact) and house most organelles found in the cell body


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Axon hillock and initial segment

  • The axon hillock is the cone-shaped junction where the axon originates from the soma

  • The initial segment lie immediately distal to the hillock and functions as the trigger zone containing high densities of voltage-gated ion channels


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Organelle composition of the axon vs. the cell body

  • Contains mitochondria, neurotubules, and neurofilaments, but completely lacks rough endoplasmic reticulum and golgi apparatus

  • Entirely dependent on axonal transport from the cell body for protein synthesis and membrane renewal


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Anterograde axonal transport mechanism and cargo

  • Movement away from the soma toward axon terminals

  • Powered by the ATP-dependent motor protein kinesin along microtubules (speeds up to 40cm/day)

  • Transports mitochondria, cytoskeletal components, membrane lipids, and neurotransmitter synthesis enzymes.


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Retrograde axonal transport mechanism and cargo

  • Movement from axon terminals back toward the cell body

  • Powered by the ATP-dependent motor protein dynein along microtubules.

  • Returns degraded organelles for recycling and delivers intracellular communication molecules (signaling vesicles, neurotrophic factors).


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Anaxonic neuron: Structure and location

  • Small with numerous dendritic processes but no distinguishable, visible axon

  • Found in the brain and special sense organs; functions remain poorly understood.


<ul><li><p>Small with numerous dendritic processes but no distinguishable, visible axon</p></li><li><p>Found in the brain and special sense organs; functions remain poorly understood.</p></li></ul><p></p>
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Bipolar neuron: Structure and location

  • Two distinct processes: one fused dendrite branching distally and one axon, with the cell body positioned between them.

  • Rare; specialized sensory neurons for vision (retina), olfaction (nasal mucosa), and hearing/inner ear.


<ul><li><p>Two distinct processes: one fused dendrite branching distally and one axon, with the cell body positioned between them.</p></li><li><p>Rare; specialized sensory neurons for vision (retina), olfaction (nasal mucosa), and hearing/inner ear.</p></li></ul><p></p>
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Unipolar (Pseudounipolar) neuron: structure and location

  • Single short process emerging from soma that branches T-shaped into a peripheral process (axon with distal receptive endings) and a central process entering the CNS.

  • Primary sensory neurons with cell bodies clustered in dorsal root ganglia of the spinal cord and sensory cranial ganglia


<ul><li><p>Single short process emerging from soma that branches T-shaped into a peripheral process (axon with distal receptive endings) and a central process entering the CNS.</p></li><li><p>Primary sensory neurons with cell bodies clustered in dorsal root ganglia of the spinal cord and sensory cranial ganglia</p></li></ul><p></p>
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Multipolar neuron: structure and location

  • Three or more processes: multiple dendrites and a single long axon

  • Most common structural class

  • Examples include: cerebellar Purkinje cells and cerebral pyramidal cells.


<ul><li><p>Three or more processes: multiple dendrites and a single long axon</p></li><li><p>Most common structural class </p></li><li><p>Examples include: <strong>cerebellar Purkinje cells</strong> and <strong>cerebral pyramidal cells.</strong></p></li></ul><p></p>
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Functional definition of sensory (afferent) neurons

  • Transmit sensory impulses from internal or external receptors toward the CNS

  • Most are structurally unipolar with cell bodies in peripheral sensory ganglia


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Functional definition of motor (efferent) neurons

  • Carry impulses away from the CNS to effector organs (muscles, glands).

  • Structurally multipolar; cell bodies reside within the CNS gray matter (except for postganglionic autonomic neurons)


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Functional definition and distribution of interneurons

  • Lie between sensory and motor neurons; integrate inputs and coordinate outputs.

  • Confined entirely to the CNS; make up >99% of all multipolar


<ul><li><p>Lie between sensory and motor neurons; integrate inputs and coordinate outputs.</p></li><li><p>Confined entirely to the CNS; make up &gt;99% of all multipolar</p></li></ul><p></p>
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General characteristics of neuroglial cells vs neurons

  • Smaller, darker-staining nuclei, far outnumber neurons, and make up 50% of total nervous tissue volume

  • Retain the ability to undergo cell division throughout life

  • Do not conduct action potentials; act as a supportive, protective, and homeostatic framework


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Pathogenesis and clinical features of gliomas

  • Primary brain tumors originating from abnormally proliferating glial cells (which retain division capacity, unlike neurons).

  • Account for 60% of primary brain tumors and 2% of all cancers; highly malignant with 1-year survival rates <50%


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Astrocyte morphology and structural connections

  • Star-shaped, largest and most numerous CNS glial cells with radiating cytoplasmic processes ending in expanded perivascular feet

  • Packed with intermediate microfilaments; interconnected to one another via gap junctions to transmit calcium waves


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Metabolic and chemical homeostatic roles of astrocytes

  • Regulate extracellular microenvironment- by absorbing leaked potassium ions (K+) and recapturing released neurotransmitter.

  • Guide the migration of developing neurons and synapse formation during neurogenesis.


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Astrocytes and the Blood-Brain Barrier (BBB)

  • Astrocytes perivascular feet envelop brain capillary endothelial cells.

  • Secrete regulatory chemicals that induce endothelial cells to form tight junctions, restricting capillary permeability and shielding the CNS from circulating fluctuations


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Microglia structure, origin and defense functions

  • Smallest and least abundant CNS neuroglia; possess thorny, branching processes that monitor neuronal health.

  • Differentiate into mobile, macrophage- like phagocytes upon pathogen detection or tissue damage to remove dead neurons and debris.

  • Primary defense since circulating leukocytes have restricted CNS access.


<ul><li><p>Smallest and least abundant CNS neuroglia; possess thorny, branching processes that monitor neuronal health.</p></li><li><p>Differentiate into mobile, macrophage- like phagocytes upon pathogen detection or tissue damage to remove dead neurons and debris.</p></li><li><p>Primary defense since circulating leukocytes have restricted CNS access.</p></li></ul><p></p>
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Ependymal cells: Histological structure and ventricular lining

  • Simple cuboidal to columnar epithelial layer lining the cerebral ventricles and the spinal cord central canal

  • Apical surfaces possess microvilli and monitoring CSF


<ul><li><p>Simple cuboidal to columnar epithelial layer lining the cerebral ventricles and the spinal cord central canal</p></li><li><p>Apical surfaces possess microvilli and monitoring CSF</p></li></ul><p></p>
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Oligodendrocytes: morphology and myelination mechanism

  • Possess fewer, sheet-like cytoplasmic processes extending from a small soma

  • Each process wraps around an axon segment to produce a multilayered myelin sheath; a single cell myelinates segments of multiple adjacent axons


<ul><li><p>Possess fewer, sheet-like cytoplasmic processes extending from a small soma</p></li><li><p>Each process wraps around an axon segment to produce a multilayered myelin sheath; a single cell myelinates segments of multiple adjacent axons</p></li></ul><p></p>
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Structural distinction between CNS white matter and gray matter

White matter: Regions dominated by lipid-rich, glossy-white myelinated axons (tracts).

Gray matter: regional containing unmyelinated axons, cell bodies, dendrites, and terminal synaptic arborizations.

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Satellite cells in the PNS

  • Flattened glial cells that surround and cushion neuronal cell bodies in peripheral sensory and autonomic ganglia.

  • Functionally analogous to astrocytes: regulate local nutrients, O2, CO2, and the neurotransmitter levels in ganglia.


<ul><li><p>Flattened glial cells that surround and cushion neuronal cell bodies in peripheral sensory and autonomic ganglia.</p></li><li><p>Functionally analogous to astrocytes: regulate local nutrients, O2, CO2, and the neurotransmitter levels in ganglia.</p></li></ul><p></p>
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Schwann cells (Neurolemmocytes): PNS myelination and regeneration

  • Envelop all peripheral nerve fibers

  • Form myelin sheaths around thick peripheral axons (each Schwann cell wraps a single internode segment of one axon, unlike oligodendrocytes)

  • Play a vital role in axonal repair and regeneration following peripheral nerve trauma.


<ul><li><p>Envelop all peripheral nerve fibers</p></li><li><p>Form myelin sheaths around thick peripheral axons (each Schwann cell wraps a single internode segment of one axon, unlike oligodendrocytes)</p></li><li><p>Play a vital role in axonal repair and regeneration following peripheral nerve trauma.</p></li></ul><p></p>
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Resting membrane potential (RMP) polarity and standard value

  • Electrical charge difference across the resting neuronal plasma membrane, typically -70mV

    • Inner cytoplasmic face is net negative relative to the extracellular fluid


<ul><li><p>Electrical charge difference across the resting neuronal plasma membrane, typically <strong>-70mV</strong></p><ul><li><p>Inner cytoplasmic face is net negative relative to the extracellular fluid</p></li></ul></li></ul><p></p>
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Chemical gradient differences across the resting plasma membrane

  • Extracellular fluid (ECF): High concentration of sodium (Na+) and chloride (Cl-)

  • Intracellular cytosol (ICF): High concentration of potassium (K+) and impermeable negative proteins/phosphates


<ul><li><p>Extracellular fluid (ECF): High concentration of <strong>sodium (Na+) and chloride (Cl-)</strong></p></li><li><p>Intracellular cytosol (ICF): High concentration of potassium (K+) and <strong>impermeable negative proteins/phosphates</strong></p></li></ul><p></p>
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Resting membrane permeability to K+ vs Na+

  • The resting membrane is roughly 25 times more permeable to K+ than to Na+ due to abundant open potassium leak channels

  • Large intracellular protein anions cannot pass through the membrane


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Primary mechanism established the resting negative potential

  • Unopposed outward diffusion of K+ down its concentration gradient through open leak channels leaves behind impermeable organic anions

  • This loss of positive charge makes the interior increasingly negative until electrical attraction pulls K+ back, reaching equilibrium.


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