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Agonists: full, partial, inverse and biased

Explains drugs that activate receptors: how much they can activate them (full vs partial), drugs that push activity below baseline (inverse), and drugs that activate only some of a receptor's signals (biased).

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Orient

Agonist – drug binds to receptor and acts similarly to (mimics) endogenous neurotransmitter. Agonists can be full, partial, or inverse. Endogenous neurotransmitters can be thought of as “balanced” agonists; some drugs can be “biased” agonists – selectively altering a certain signaling pathway of a metabotropic receptor (functional selectivity).

Course terms

Your professor's wording, word for word from the slides. Learn the term and this definition — the explanation underneath is only there to help it make sense.

Agonist
“Drug binds to receptor and acts similarly to (mimics) endogenous neurotransmitter”Slides 05, p. 9

Examples: opioid drugs (μ-opioid agonism), classical psychedelics (5-HT2A agonism).

Full / partial / inverse agonist
“Can be full, partial, or inverse”Slides 05, p. 9

Full reaches maximum, partial reaches only part of it, inverse pushes activity below baseline.

Partial agonist
“Buprenorphine is partial agonist – use in treatment”Slides 05, p. 9

Aripiprazole partially agonizes D2; ropinirole fully agonizes D2.

Balanced agonist
“Endogenous neurotransmitters can be thought of as “balanced” agonists”Slides 05, p. 12

Normal activation of all the receptor's signaling pathways.

Biased agonist
“Some drugs can be “biased” agonists – selectively altering a certain signaling pathway of a metabotropic receptor”Slides 05, p. 12

Also called functional selectivity (Rankovic et al., 2016).

From your course: Course slides 05, pp. 9–12, 15

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Full lesson: Reversible receptor binding

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