Nervous Tissue – Detailed Study Notes
Introduction
- Purpose of Chapter 12 (Nervous Tissue)
- Show how the nervous system maintains controlled conditions in support of health & homeostasis
- Survey the major anatomical/functional divisions (CNS vs. PNS; sensory vs. motor vs. integrative)
- Identify every cell type present in nervous tissue and describe its role
Gross Organization of the Nervous System
- Two master divisions
- Central Nervous System (CNS)
- Brain & spinal cord; integrative and higher‐order centers
- Peripheral Nervous System (PNS)
- Cranial nerves, spinal nerves, ganglia, enteric plexuses & sensory receptors outside the CNS
- PNS functional subdivisions
- Sensory (Afferent) Division
- Somatic senses (touch, pain, proprioception, temperature)
- Special senses (vision, taste, smell, hearing, equilibrium)
- Motor (Efferent) Division
- Somatic Nervous System (SNS): voluntary output to skeletal muscle
- Autonomic Nervous System (ANS): involuntary output to smooth & cardiac muscle, glands
- Sympathetic division | Parasympathetic division (antagonistic but cooperative)
- Enteric Nervous System (ENS): intrinsic neural plexuses that govern the GI tract
Core Functions of the Nervous System
- Sensory
- Detect internal & external changes via specialized receptors → relay information to CNS
- Integrative
- Analyze sensory input, store portions, make decisions → formulate appropriate response
- Motor
- Send commands through effectors (muscle fibers, glands) to restore/maintain homeostasis
Overview of Nervous Tissue
- Two broad cell classes
- Neurons (nerve cells)
- Electrically excitable; propagate action potentials
- Possess distinct morphological regions (dendrites, soma, axon, terminals)
- Neuroglia (glial cells, “nerve glue”)
- Roughly one‐half the volume of the nervous system
- Fill spaces, support, insulate & protect neurons; can divide mitotically; do NOT conduct impulses
Neurons in Detail
- Electrophysiological hallmark: ability to generate & conduct the nerve impulse (action potential)
- Structural classification – based on number of processes
- Multipolar: many dendrites, one axon (most CNS neurons, all motor neurons)
- Bipolar: one dendrite & one axon (retina, inner ear, olfactory epithelium)
- Pseudounipolar (Unipolar): fused dendrite–axon with soma off to side (most sensory neurons)
- Functional classification – based on impulse direction
- Sensory / Afferent → convey information to CNS
- Motor / Efferent → convey commands from CNS to effectors
- Interneurons / Association → integrate sensory data, decide motor output (vast majority of neurons)
Neuroglia of the CNS (4 types)
- Astrocytes
- Most abundant; contact neurons & capillaries; regulate extracellular ion composition, help form blood–brain barrier, guide neuron migration, influence synaptic activity, store glycogen, react to injury (scar)
- Oligodendrocytes
- Myelinate multiple CNS axons → form insulating myelin sheaths; increase conduction velocity
- Microglia
- Small, mobile phagocytes; remove microbes, debris; secrete cytokines; form scar tissue after injury
- Ependymal cells
- Ciliated epithelial lining of ventricles & central canal; produce and circulate cerebrospinal fluid (CSF)
Neuroglia of the PNS (2 types)
- Schwann Cells
- Myelinate single axons (or envelop several unmyelinated) in PNS; aid axonal regeneration
- Satellite Cells
- Surround neuronal cell bodies in ganglia; regulate micro-environment; electrical insulation & protection
Myelination
- Myelin sheath produced by Schwann cells (PNS) & oligodendrocytes (CNS)
- Functions: electrical insulation, increased conduction speed, axonal maintenance
Electrical Signals in Neurons
- Two major signal types
- Graded Potentials (GP)
- Small, localized voltage changes; occur in dendrites/soma; amplitude varies with stimulus; decremental (die out with distance); may summate
- Action Potentials (AP)
- Large, propagated voltage spikes along axon; all-or-none; constant amplitude (≈100 mV); capable of long-distance transmission
- Requirements for either signal
- Establishment of a Resting Membrane Potential (RMP) (non-conducting neuron ≈-70 mV)
- Presence of selective ion channels in membrane
Ion Channels in Neurons
- Leak (Passive) Channels – randomly open/close; set RMP; more K^+ than Na^+ leaks → negative interior
- Ligand-Gated Channels – open when specific chemical (neurotransmitter) binds; typical in dendrites & soma
- Mechanically-Gated Channels – open to vibration, pressure, stretch; e.g., touch receptors
- Voltage-Gated Channels – open when membrane potential reaches threshold; abundant in axons
Resting Membrane Potential (RMP)
- Results from:
- Unequal ion distribution – high extracellular Na^+/Cl^-; high intracellular K^+/anions (phosphates, proteins)
- Selective permeability – membrane more permeable to K^+ (leaks out) than Na^+ (enters)
- Na^+/K^+ ATPase pump – actively exports 3 Na^+, imports 2 K^+ per ATP → maintains gradients & contributes ~-3 mV to RMP
Graded Potentials (GP) in Depth
- Produced by opening of ligand-gated or mechanically-gated channels
- Can be depolarizing (EPSP) or hyperpolarizing (IPSP)
- Stimulus strength ↔ amplitude (larger stimulus → larger GP)
- Summation
- Spatial – simultaneous stimuli at different locations add
- Temporal – rapid succession of stimuli at one site add
- If GP depolarization at axon hillock reaches threshold (≈-55 mV), an AP fires
Action Potentials (AP) in Depth
- Phases
- Depolarization – voltage-gated Na^+ channels open (activation gates), Na^+ influx drives Vm → +30 mV
- Repolarization – Na^+ channels inactivate, voltage-gated K^+ channels open, K^+ efflux returns Vm toward -70 mV
- After-hyperpolarization – K^+ channels remain open briefly; Vm dips ~-90 mV before returning to RMP
- Refractory Periods
- Absolute (≈1 msec) – no AP possible (Na^+ channels either open or inactive)
- Relative – a larger-than-normal stimulus may trigger AP (K^+ channels still open)
- Stimulus encoding – intensity coded by AP frequency, not size (size invariant)
Propagation of Action Potentials
- Continuous Conduction – unmyelinated axons; every adjacent segment depolarizes sequentially
- Saltatory Conduction – myelinated axons; AP “jumps” Node of Ranvier to node; faster & energy-efficient
- Propagation speed influenced by
- Axon diameter – larger caliber → lower resistance → faster
- Myelination – presence increases speed dramatically
- Temperature – higher temperature ↑ conduction velocity (within physiological range)
Synaptic Transmission
- Synapse: junction between neuron–neuron or neuron–effector
- Electrical Synapse
- Gap junctions provide cytoplasmic continuity → direct ionic current; synchronize activity (e.g., cardiac & some smooth muscle, CNS circuits)
- Chemical Synapse (most common)
- AP arrives at presynaptic terminal → depolarizes → opens voltage-gated Ca^{2+} channels
- Ca^{2+} influx triggers exocytosis of neurotransmitter (NT) vesicles into synaptic cleft
- NT diffuses, binds to receptors on postsynaptic membrane
- Ionotropic receptor – ligand-gated ion channel integral to receptor
- Metabotropic receptor – receptor coupled via G protein to separate channel/second messengers
- Postsynaptic membrane generates EPSP (depolarizing) or IPSP (hyperpolarizing) graded potentials
- NT removal terminates signal via diffusion, enzymatic degradation (e.g., AChE), or reuptake (neurons or glia)
- Summation of EPSPs & IPSPs at trigger zone determines whether threshold is reached
Major Neurotransmitters
- Small Molecule NTs
- Acetylcholine (ACh) – neuromuscular junction; excitatory at NMJ, inhibitory in cardiac muscle via muscarinic receptors
- Amino acids: Glutamate (major excitatory CNS; ↑Ca^{2+} → learning; excessive → excitotoxicity); GABA & Glycine (inhibitory via Cl^- channels)
- Biogenic amines: Dopamine (motor control, reward); Norepinephrine, Epinephrine (ANS), Serotonin (mood, sleep); Histamine
- ATP & other purines – co-transmitters; act on purinergic receptors
- Gases: Nitric oxide (NO), Carbon monoxide (CO) – diffuse freely; modulate vasodilation, memory
- Neuropeptides (3–40 amino acids)
- Substance P – pain transmission enhancement
- Enkephalins, Endorphins, Dynorphins – endogenous opioids; analgesia, mood, temperature, learning
- Hypothalamic releasing/inhibiting hormones – regulate anterior pituitary
- Angiotensin II – thirst, blood pressure regulation
- Cholecystokinin (CCK) – “stop-eating” signal, GI function
- Neuropeptide Y – stimulates food intake, stress response
Plasticity, Regeneration & Repair
- Plasticity: nervous tissue can reorganize synaptic connections based on experience & learning
- Regeneration potential
- CNS: minimal; inhibited by oligodendrocyte molecules & rapid glial scar formation
- PNS: may regenerate if soma intact, Schwann cells active, limited scar tissue; involves axonal sprouting, Wallerian degeneration, regeneration tube formation
Selected Neurological Disorders
- Multiple Sclerosis (MS)
- Autoimmune demyelination of CNS; variable symptoms—muscle weakness, double vision; genetic/environmental triggers suspected
- Depression
- Types: Major, Dysthymia, Bipolar, Seasonal Affective Disorder
- Symptoms: anhedonia, sadness, helplessness; treated commonly with SSRIs (↑serotonin in synapse)
- Epilepsy
- Recurrent seizures from synchronous neuronal discharges; may be motor, sensory, psychological
- Excitotoxicity
- Neuronal death from excessive excitatory transmission (e.g., glutamate overload after ischemia/stroke)
Neural Integration: Summation & Circuits
- Spatial vs. Temporal Summation – additive effect of multiple EPSPs/IPSPs in space/time
- Neural Circuits (wiring patterns)
- Simple Series – one-to-one relay
- Diverging – one input → many outputs (amplification)
- Converging – many inputs → one output (aggregation)
- Reverberating – feedback loop; prolonged output (rhythm generation, breathing)
- Parallel after-discharge – input via parallel chains reconverging later; bursts of output (high-level problem solving)
Comprehensive Structure–Function Summary (Neuron Parts)
- Dendrites: ligand/mechanically-gated channels; receive stimuli & generate GPs (generator or receptor potentials in sensory neurons; EPSPs/IPSPs in others)
- Cell Body (Soma): integrates inputs; contains organelles
- Axon Hillock / Initial Segment (Trigger Zone): sums EPSPs & IPSPs; if net depolarization ≥ threshold → AP initiation
- Axon: propagates APs (voltage-gated Na^+ / K^+)
- Axon Terminals / Synaptic End Bulbs: voltage-gated Ca^{2+} entry triggers NT release
Key Numerical / Statistical References & Equations
- Typical neuronal RMP V_{rest} \approx -70\,\text{mV}
- AP amplitude \approx 100\,\text{mV} (from -70 to +30 mV)
- Na^+/K^+ ATPase stoichiometry 3\,Na^+{out} : 2\,K^+{in} per ATP
- Threshold potential V_{th} \approx -55\,\text{mV}
- Absolute refractory period \sim 1\,\text{msec}; relative refractory follows
- Propagation speeds: unmyelinated \sim 0.5\text{–}2\,\text{m/s}; myelinated Aα fibers up to 120\,\text{m/s} (diameter & myelination dependent)
Ethical, Philosophical & Practical Implications
- Understanding ion channel pharmacology underlies development of anesthetics, antiepileptics, antidepressants
- Demyelinating diseases (MS) highlight immune–nervous interdependence; prompts exploration of immunomodulatory therapies
- Plasticity emphasizes lifelong learning capability & rehabilitation potential after injury
- Excitotoxicity research guides neuroprotective strategies in stroke/head trauma
Connections to Earlier & Future Content
- Builds on cellular membrane transport (diffusion, active transport)
- Prepares for later chapters: sensory systems (graded potentials), motor control, autonomic physiology, higher brain functions
Real-World Applications & Examples
- EEG measures summed postsynaptic potentials (clinical diagnosis of epilepsy, sleep patterns)
- Local anesthetics (e.g., lidocaine) block voltage-gated Na^+ channels → inhibit APs → analgesia
- Myelin loss in MS visible on MRI; correlates with conduction block & neurological deficits
- SSRIs prolong serotonin presence in synaptic cleft → mood elevation in depression management
End of Notes