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Laxatives !

Medicines that soften stool or speed up the bowel. They work by drawing in water, coating stool, stimulating the gut wall or blocking opioid effects.

Updated 2026-11-01

What they are

A broad group for constipation and bowel preparation: osmotic agents (lactulose, macrogol), stimulants (bisacodyl, senna), stool softeners (docusate), chloride-secretion activators (lubiprostone, linaclotide) and peripheral μ-opioid antagonists (methylnaltrexone).

Mechanism of action

Osmotic laxatives are poorly absorbed molecules that hold water in the lumen. Stimulants act on the enteric nerves and the colonic lining to increase motility and fluid secretion. Softeners let water and fat into the stool. Secretagogues open chloride channels in the gut lining so water follows. Peripheral opioid antagonists block μ receptors in the gut wall without reversing pain relief in the brain.

Target: Several: colonic contents, enteric nervous system, chloride channels (ClC-2, CFTR via guanylate cyclase C) and gut μ-opioid receptors

Drugs in this class

Others in the class

  • Psyllium
  • Lactitol
  • Sorbitol
  • Magnesium hydroxide
  • Sodium picosulfate
  • Prucalopride
  • Plecanatide
  • Naloxegol
  • Naldemedine

Test yourself

Think of the answer, then tap the question to see it.

Which laxative is also used to lower blood ammonia in hepatic encephalopathy?

Lactulose: colonic bacteria turn it into acids that trap ammonia as ammonium, which then leaves in the stool.

How do lubiprostone and linaclotide differ in mechanism?

Lubiprostone activates the ClC-2 chloride channel directly; linaclotide activates guanylate cyclase C, and the rise in cGMP opens CFTR. Both increase chloride-rich fluid secretion.

What brown discoloration of the colon is linked to chronic senna use?

Melanosis coli, a pigment in the colonic lining after long-term anthraquinone laxatives.

Why can methylnaltrexone relieve opioid constipation without causing pain to return?

It is a quaternary amine that barely crosses the blood-brain barrier, so it blocks μ receptors in the gut but not in the brain.

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← All of pharmacology

Educational content on how drugs work; not a prescribing guide and no substitute for a health professional's advice. No doses are given.

Sources: ATCDDD - ATC/DDD Index (WHO Collaborating Centre for Drug Statistics Methodology, 2026); Farmacología básica y clínica (Katzung), 16.ª ed., cap. 62 (McGraw Hill, 2025); Polyethylene Glycol 3350: MedlinePlus Drug Information (MedlinePlus (U.S. National Library of Medicine), 2016); Bisacodyl: MedlinePlus Drug Information (MedlinePlus (U.S. National Library of Medicine), 2018).

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Representative model, for educational purposes only.