Agonist

(Redirected from Full agonist)
Jump to navigation Jump to search
Agonists

WikiDoc Resources for Agonist

Articles

Most recent articles on Agonist

Most cited articles on Agonist

Review articles on Agonist

Articles on Agonist in N Eng J Med, Lancet, BMJ

Media

Powerpoint slides on Agonist

Images of Agonist

Photos of Agonist

Podcasts & MP3s on Agonist

Videos on Agonist

Evidence Based Medicine

Cochrane Collaboration on Agonist

Bandolier on Agonist

TRIP on Agonist

Clinical Trials

Ongoing Trials on Agonist at Clinical Trials.gov

Trial results on Agonist

Clinical Trials on Agonist at Google

Guidelines / Policies / Govt

US National Guidelines Clearinghouse on Agonist

NICE Guidance on Agonist

NHS PRODIGY Guidance

FDA on Agonist

CDC on Agonist

Books

Books on Agonist

News

Agonist in the news

Be alerted to news on Agonist

News trends on Agonist

Commentary

Blogs on Agonist

Definitions

Definitions of Agonist

Patient Resources / Community

Patient resources on Agonist

Discussion groups on Agonist

Patient Handouts on Agonist

Directions to Hospitals Treating Agonist

Risk calculators and risk factors for Agonist

Healthcare Provider Resources

Symptoms of Agonist

Causes & Risk Factors for Agonist

Diagnostic studies for Agonist

Treatment of Agonist

Continuing Medical Education (CME)

CME Programs on Agonist

International

Agonist en Espanol

Agonist en Francais

Business

Agonist in the Marketplace

Patents on Agonist

Experimental / Informatics

List of terms related to Agonist

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]


In pharmacology an agonist is a substance that binds to a specific receptor and triggers a response in the cell. It mimics the action of an endogenous ligand (such as hormone or neurotransmitter) that binds to the same receptor.

Types

Full agonists bind (have affinity for) and activate a receptor, displaying full efficacy at that receptor.

One example of a drug that acts as a full agonist is isoproterenol which mimics the action of adrenaline at β adrenoreceptors.

Partial agonists (such as buspirone, aripiprazole, buprenorphine, or norclozapine) also bind and activate a given receptor, but have only partial efficacy at the receptor relative to a full agonist. They may also be considered ligands which display both agonistic and antagonistic effects - when both a full agonist and partial agonist are present, the partial agonist actually acts as a competitive antagonist, competing with the full agonist for receptor occupancy and producing a net decrease in the receptor activation observed with the full agonist alone.[1]

A co-agonist works with other co-agonists to produce the desired effect together. NMDA receptor activation requires the binding of both of its glutamate and glycine co-agonists. An antagonist blocks a receptor from activation by agonists. Clinically partial agonists can activate receptors to give a desired submaximal response when inadequate amounts of the endogenous ligand are present, or they can reduce the overstimulation of receptors when excess amounts of the endogenous ligand are present.[2]

A selective agonist is selective for one certain type of receptor. It can additionally be of any of the aforementioned types.

A physiological agonist is a substance that creates the same bodily responses, but does not bind to the same receptor.

Receptors can be activated or inactivated either by endogenous (such as hormones and neurotransmitters) or exogenous (such as drugs) agonists and antagonists, resulting in stimulating or inhibiting a biological response. To see how an agonist may activate a receptor see this link

New findings that broaden the conventional definition of pharmacology demonstrate that ligands can concurrently behave as agonist and antagonists at the same receptor, depending on effector pathways. Terms that describe this phenomenon are "functional selectivity" or "protean agonism".[3][4]

Activity (EC50)

Potency

The potency of an agonist is usually defined by its EC50 value. This can be calculated for a given agonist by determining the concentration of agonist needed to elicit half of the maximum biological response of the agonist. Elucidating an EC50 value is useful for comparing the potency of drugs with similar efficacies producing physiologically similar effects. The lower the EC50, the greater the potency of the agonist the lower the concentration of drug that is required to elicit the maximum biological response

Therapeutic index

When a drug is used therapeutically, it is important to understand the margin of safety that exists between the dose needed for the desired effect and the dose that produces unwanted and possibly dangerous side effects. This relationship, termed the therapeutic index, is defined as the ratio LD50:ED50. In general, the narrower this margin, the more likely it is that the drug will produce unwanted effects. The therapeutic index has many limitations, notably the fact that LD50 cannot be measured in humans and, when measured in animals, is a poor guide to the likelihood of unwanted effects in humans. Nevertheless, the therapeutic index emphasizes the importance of the margin of safety, as distinct from the potency, in determining the usefulness of a drug.

Etymology

From the Greek αγωνιστής (agōnistēs), contestant; champion; rival < αγων (agōn), contest, combat; exertion, struggle < αγω (agō), I lead, lead towards, conduct; drive

See also

References

  1. Principles and Practice of Pharmacology for Anaesthetists By Norton Elwy Williams, Thomas Norman Calvey Published 2001 Blackwell Publishing ISBN 0632056053
  2. Zhu BT (2005). "Mechanistic explanation for the unique pharmacologic properties of receptor partial agonists". Biomed. Pharmacother. 59 (3): 76–89. doi:10.1016/j.biopha.2005.01.010. PMID 15795100.
  3. Kenakin T. (2001). Inverse, protean, and ligand-selective agonism: matters of receptor conformation. FASEB J. 15:598-611. PMID 11259378. Fulltext
  4. Urban J.D. et al. (2007). Functional selectivity and classical concepts of quantitative pharmacology. J. Pharmacol. Exp. Ther. 320:1-13. PMID 16803859.


ar:ناهضة (علم الأدوية) ca:Agonista da:Agonist de:Agonist (Pharmakologie) he:אגוניסט sl:Agonist sr:Агониста fi:Agonisti sv:Agonist th:อะโกนิสต์ it:Agonista


Template:WikiDoc Sources