Guyton 14e
Guyton 14e
Guyton 14e
Guyton 14e
Guyton 14e
Guyton 14e
Guyton 14e
Guyton 14e
Guyton 14e
Guyton 14e
Guyton 14e
Guyton 14e
Guyton 14e
Guyton 14e
Guyton 14e
Guyton 14e
Guyton 14e
Guyton 14e
Guyton 14e
Guyton 14e
Transmission
- The action potential reaches the presynaptic terminal → opens voltage-gated Ca²⁺ channels.
- Ca²⁺ influx triggers exocytosis of neurotransmitter into the synaptic cleft.
- Transmitter binds postsynaptic receptors → a graded potential: EPSP (Na⁺/Ca²⁺ in, depolarizing) or IPSP (Cl⁻ in / K⁺ out, hyperpolarizing).
- The neuron integrates EPSPs − IPSPs; if threshold is reached it fires an action potential.
- Transmitter is removed (enzymatic breakdown, reuptake or diffusion).
Properties
One-way conduction (Dale), synaptic delay (~0.5 ms), temporal and spatial summation, fatigue, and high sensitivity to drugs, hypoxia and pH.
Dorsal column–medial lemniscus (DCML)
- Carries: fine touch, vibration, conscious proprioception.
- Course: ascends ipsilaterally in the dorsal columns and decussates in the medulla.
Spinothalamic (anterolateral)
- Carries: pain, temperature, crude touch.
- Course: decussates in the spinal cord within 1–2 segments of entry, then ascends.
Common features
Both are 3-neuron chains relaying in the thalamus (VPL) → primary somatosensory cortex (postcentral gyrus, somatotopic homunculus).
Clinical value
The different crossing levels let a cord hemisection (Brown-Séquard) be localised: ipsilateral loss of fine touch/proprioception below + contralateral loss of pain/temperature.
The pathway
The UMN (corticospinal tract) runs from the motor cortex, decussates at the medullary pyramids, to the LMN in the anterior horn; the LMN runs to the muscle.
UMN lesion signs
- Increased tone — spasticity; hyper-reflexia and clonus.
- Positive Babinski (up-going toe).
- Little atrophy (disuse only); no fasciculations.
LMN lesion signs
- Decreased tone — flaccid paralysis; hypo-/areflexia.
- Marked muscle atrophy and fasciculations.
- Negative Babinski.
Functions
The cerebellum does not initiate movement; it coordinates movement by comparing the intended with the actual movement and correcting it. It controls timing and smoothness of voluntary movement, balance and posture (via the vestibulocerebellum), and motor learning.
Lesion features (ipsilateral)
- Ataxia — incoordination, broad-based gait.
- Intention tremor — tremor that worsens on approaching a target.
- Dysmetria — past-pointing (finger–nose test).
- Dysdiadochokinesia — impaired rapid alternating movements.
- Nystagmus, scanning speech, hypotonia.
All signs occur on the same side as the lesion.
Origin
Sympathetic = thoracolumbar (T1–L2); parasympathetic = craniosacral (CN III, VII, IX, X and S2–S4).
Fibres/ganglia
Sympathetic: short pre-, long post-ganglionic (ganglia near the cord). Parasympathetic: long pre-, short post-ganglionic (ganglia near the organ).
Transmitters/receptors
All ganglia and the NMJ: ACh on nicotinic receptors. Sympathetic post-ganglionic: noradrenaline on α/β receptors (except sweat glands = ACh). Parasympathetic post-ganglionic: ACh on muscarinic receptors.
Overall effects
Sympathetic = 'fight or flight' (↑HR, pupils dilate, bronchodilate, ↓gut). Parasympathetic = 'rest and digest' (↓HR, pupils constrict, ↑gut). The adrenal medulla is a modified sympathetic ganglion.