Agonist

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(Redirected from Selective agonist)

  • An agonist is a substance or molecule that activates specific receptors in the body, resulting in a physiological response.
  • Agonists can be naturally occurring compounds or synthetic drugs designed to mimic the effects of endogenous substances. Understanding agonists is important in the field of pharmacology as they play a significant role in the development of therapeutic agents.
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Agonists
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Mechanism of Action[edit | edit source]

GPCR Clipart
Co-agonist Simple
  • Agonists exert their effects by binding to specific receptors on cells, initiating a cascade of events that leads to a physiological response.
  • When an agonist binds to a receptor, it triggers a conformational change in the receptor, activating its signaling pathway.
  • This activation can result in various cellular responses, such as changes in gene expression, enzyme activity, ion channel opening, or neurotransmitter release.
  • The overall effect depends on the specific receptor and signaling pathways involved.

Classification of Agonists[edit | edit source]

  • Agonists can be classified based on their interaction with receptors and their efficacy in producing a response.

The following classifications are commonly used:

Full Agonists[edit | edit source]

  • Full agonists are substances that bind to a receptor and fully activate it, producing a maximal response.
  • They have high affinity for the receptor and induce a robust physiological effect.
  • Examples of full agonists include morphine (opioid receptor agonist) and adrenaline (adrenergic receptor agonist).

Partial Agonists[edit | edit source]

  • Partial agonists are substances that bind to a receptor but only activate it partially, resulting in a submaximal response.
  • They have moderate affinity for the receptor and exhibit a lower efficacy compared to full agonists.
  • Partial agonists can act as agonists in the absence of other agonists or as antagonists in the presence of full agonists.
  • An example of a partial agonist is buprenorphine (opioid receptor agonist/partial agonist).

Inverse Agonists[edit | edit source]

  • Inverse agonists are substances that bind to a receptor and produce the opposite effect of an agonist.
  • Instead of activating the receptor, inverse agonists stabilize the receptor in its inactive state, reducing basal receptor activity.
  • Inverse agonists have negative efficacy and can be useful in cases where excessive receptor activity is present.
  • An example of an inverse agonist is rimonabant (cannabinoid receptor inverse agonist).

Applications in Medical Treatments[edit | edit source]

  • Agonists have numerous applications in medical treatments. Some examples include:

Pain Management[edit | edit source]

  • Opioid receptor agonists, such as morphine and oxycodone, are used for pain relief in moderate to severe pain conditions.
  • These agonists bind to opioid receptors in the central nervous system, inhibiting pain signals and producing analgesia.

Bronchodilators[edit | edit source]

Hormone Replacement Therapy[edit | edit source]

  • In hormone replacement therapy, agonists are used to mimic the effects of endogenous hormones.
  • For example, estrogen agonists are prescribed for menopausal women to alleviate symptoms and prevent complications associated with estrogen deficiency.

Neurotransmitter Modulation[edit | edit source]

See Also[edit | edit source]

Antagonist Partial Agonist Receptor (biochemistry) Drug Discovery Pharmacodynamics

Agonist Resources
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