I now have rich, well-sourced content. Here is the short explainer on neurons:
Neurons: The Cellular Basis of the Nervous System
What Is a Neuron?
A neuron is the fundamental signaling unit of the nervous system — electrically excitable cells specialized to receive, integrate, and transmit information. The human brain contains roughly 86 billion neurons, each forming thousands of connections with others.
Structure
Fig. 3.3 — Structure of the neuron. (Costanzo Physiology, 7th Ed.)
Every neuron has four main compartments:
| Part | Description |
|---|
| Soma (cell body) | The metabolic center — houses the nucleus, endoplasmic reticulum, and Golgi apparatus; responsible for protein synthesis |
| Dendrites | Short, tapering, branching processes that receive incoming signals and carry receptors for neurotransmitters |
| Axon | A single, long projection (up to 1 m) arising from the axon hillock; carries action potentials away from the soma toward target cells |
| Presynaptic terminals | Bulb-like endings of the axon that release neurotransmitter into the synapse when an action potential arrives |
The junction between two neurons is the synapse — composed of the presynaptic terminal, a ~20 nm synaptic cleft, and the postsynaptic membrane bearing receptors. Synapses can be axodendritic, axosomatic, or axoaxonic.
The Resting Membrane Potential
At rest, a neuron's membrane potential is approximately −70 mV — close to the K⁺ equilibrium potential. This negative charge is maintained by:
- Differential permeability of the membrane (K⁺ leaks out; Na⁺ is mostly excluded)
- The Na⁺/K⁺-ATPase pump (3 Na⁺ out : 2 K⁺ in per cycle)
Clinically, this matters: in hyperkalemia, the resting potential moves toward threshold → the neuron is more excitable. In hypokalemia, it hyperpolarizes → less excitable.
The Action Potential
An action potential (AP) is an all-or-none electrical impulse generated when the membrane depolarizes past threshold (~−55 mV). The sequence:
- Depolarization — voltage-gated Na⁺ channels open; Na⁺ rushes in → membrane rapidly swings positive (~+30 mV)
- Repolarization — Na⁺ channels inactivate; voltage-gated K⁺ channels open → K⁺ flows out, restoring negative potential
- After-hyperpolarization — slow closure of K⁺ channels briefly takes the membrane below resting potential before returning to −70 mV
The spike initiation zone (initial segment of the axon, just past the axon hillock) is where the threshold is lowest and APs are reliably triggered.
"The propensity of a neuron to generate and propagate action potentials from the cell body to its nerve terminals is called its excitability." — Barash's Clinical Anesthesia, 9e
Conduction & Myelination
Axons can be myelinated or unmyelinated:
- Myelinated axons: Wrapped in myelin (a protein-lipid insulator made by oligodendrocytes in the CNS, Schwann cells in the PNS). Gaps in the myelin — nodes of Ranvier — are the only sites where ion exchange occurs.
- Saltatory conduction: The AP "jumps" from node to node, dramatically increasing speed. Conduction velocity depends on both myelin thickness and axon diameter.
- Unmyelinated axons: Continuous conduction along the entire membrane surface — slower.
Fiber classification:
- A fibers (large, myelinated): fast conduction — motor, proprioception, touch
- B fibers (small, myelinated): autonomic preganglionic
- C fibers (unmyelinated): slow — pain, temperature
Demyelination (e.g., multiple sclerosis — CNS; Guillain-Barré syndrome — PNS) slows or blocks conduction, producing the characteristic deficits seen in these diseases.
Synaptic Transmission
When an AP reaches the presynaptic terminal:
- Voltage-gated Ca²⁺ channels open → Ca²⁺ influx
- Synaptic vesicles fuse with the membrane → neurotransmitter release into the cleft
- Transmitter diffuses across and binds postsynaptic receptors
- Binding generates either an EPSP (excitatory postsynaptic potential) or IPSP (inhibitory), depending on the ion channels opened
- The soma integrates all incoming EPSPs and IPSPs — if the net depolarization reaches threshold, a new AP fires
This is the basis for how all psychopharmacological drugs work — they target specific molecules involved in neurotransmission, modifying release, reuptake, or receptor binding.
Supporting Cells: Glia
Neurons do not work in isolation. Glial cells occupy >50% of brain volume:
| Cell | Function |
|---|
| Astrocytes | Supply metabolic fuel (lactate), modulate blood flow, buffer extracellular K⁺, secrete neurotrophic factors |
| Oligodendrocytes | Synthesize myelin in the CNS |
| Schwann cells | Synthesize myelin in the PNS |
| Microglia | CNS-resident immune cells; scavenge debris after injury |
Axonal Transport
The axon can be up to a meter long, so proteins synthesized in the soma must be actively transported:
- Anterograde (soma → terminal): via kinesin along microtubules; fast component (~400 mm/day), slow component (~0.5–10 mm/day)
- Retrograde (terminal → soma): via dynein (~200 mm/day) — also the route hijacked by neurotropic viruses (e.g., herpes simplex, rabies) and tetanus toxin
Sources: Costanzo Physiology 7th Ed. | Ganong's Review of Medical Physiology 26th Ed. | Stahl's Essential Psychopharmacology | Neuroscience: Exploring the Brain 5th Ed. | Guyton & Hall Textbook of Medical Physiology