Pain, Anaesthesia & Inflammation

local anaesthetic

A local anaesthetic numbs one part of the body without touching consciousness — the injection your dentist gives, the gel before stitches, the spinal block for a caesarean section. It works like pulling the plug on a single telephone line: the nerves carrying sensation from that region simply stop sending messages, so you feel nothing there while staying fully awake everywhere else.

Mechanistically these drugs block voltage-gated sodium channels in nerve membranes. A nerve fires by letting sodium rush in to create an electrical impulse; if the sodium gate is plugged, no impulse can form and no signal travels. Local anaesthetics enter the nerve and bind these channels from the inside, preferentially blocking the small, thin pain-carrying fibres first, which is why pain disappears before touch and movement. Lidocaine and bupivacaine are the classic examples.

The art and the danger both lie in keeping the drug local. Adding a vasoconstrictor such as adrenaline keeps the anaesthetic at the injection site, prolonging the block and reducing the amount that reaches the bloodstream. If too much is absorbed systemically, the same sodium-channel blockade that silences a nerve can silence the heart and brain, causing seizures and cardiac arrest — so dose limits and careful injection technique are not optional.

Before a skin biopsy the doctor injects lidocaine with adrenaline; within minutes the patient feels pressure but no pain as the lesion is removed.

Thin pain fibres are blocked before thicker touch and motor fibres.

Inflamed, infected tissue is acidic, which keeps more of the local anaesthetic in its charged form that cannot cross the nerve membrane — one reason dental anaesthesia works poorly in an abscessed tooth.

Also called
local anesthetic局麻药局麻藥