Make a short on neurons

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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

Structure of the neuron — cell body, axon hillock, spike initiation zone, myelin sheath, nodes of Ranvier, and presynaptic terminals
Fig. 3.3 — Structure of the neuron. (Costanzo Physiology, 7th Ed.)
Every neuron has four main compartments:
PartDescription
Soma (cell body)The metabolic center — houses the nucleus, endoplasmic reticulum, and Golgi apparatus; responsible for protein synthesis
DendritesShort, tapering, branching processes that receive incoming signals and carry receptors for neurotransmitters
AxonA single, long projection (up to 1 m) arising from the axon hillock; carries action potentials away from the soma toward target cells
Presynaptic terminalsBulb-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:
  1. Depolarization — voltage-gated Na⁺ channels open; Na⁺ rushes in → membrane rapidly swings positive (~+30 mV)
  2. Repolarization — Na⁺ channels inactivate; voltage-gated K⁺ channels open → K⁺ flows out, restoring negative potential
  3. 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:
  1. Voltage-gated Ca²⁺ channels open → Ca²⁺ influx
  2. Synaptic vesicles fuse with the membrane → neurotransmitter release into the cleft
  3. Transmitter diffuses across and binds postsynaptic receptors
  4. Binding generates either an EPSP (excitatory postsynaptic potential) or IPSP (inhibitory), depending on the ion channels opened
  5. 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:
CellFunction
AstrocytesSupply metabolic fuel (lactate), modulate blood flow, buffer extracellular K⁺, secrete neurotrophic factors
OligodendrocytesSynthesize myelin in the CNS
Schwann cellsSynthesize myelin in the PNS
MicrogliaCNS-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
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