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Related Concept Videos

Opioid Receptors: Overview01:22

Opioid Receptors: Overview

Opioid receptors, including the mu (μ, MOR), delta (δ, DOR), and kappa (κ, KOR) types, belong to the rhodopsin family of G protein-coupled receptors. These receptors are located throughout the central and peripheral nervous systems and in non-neuronal tissues such as macrophages and astrocytes. Opioid receptor ligands can be categorized into agonists or antagonists. Highly selective agonists include [d-Ala2, MePhe4, Gly(ol)5]-enkephalin or DAMGO for MOR, [D-Pen2, D-Pen5]-enkephalin or DPDPE for...
Analgesia and Pain Management01:25

Analgesia and Pain Management

Pain is critical to various clinical pathologies, provoking an urgent need for effective management. Pain, whether acute or chronic, is a complex neurochemical process. Its alleviation depends on the type, with nonopioid analgesics effective for mild to moderate pain, such as musculoskeletal or inflammatory pain, while neuropathic pain responds best to anticonvulsants, tricyclic antidepressants, or serotonin/norepinephrine reuptake inhibitors. For severe acute or chronic pain, opioids may be...
Drug Abuse and Addiction: Pharmacological Phenomena01:15

Drug Abuse and Addiction: Pharmacological Phenomena

Drug dependence, abuse, and addiction are complex phenomena that can precipitate various abnormal states. Physical dependence refers to a state of pharmacological adaptation to a drug. This adaptation often results in tolerance—a reduced response to the drug after repeated administrations. When the drug use is abruptly stopped, withdrawal symptoms occur due to the body's need to readjust from the pharmacologically induced imbalance. However, tolerance and withdrawal symptoms do not necessarily...
Opioid Analgesics: Synthetic and Semisynthetic Opioids01:15

Opioid Analgesics: Synthetic and Semisynthetic Opioids

Synthetic and semisynthetic opioids are pivotal in pain management and tackling opioid addiction. Semisynthetic opioids, including morphinans (morphine derivatives), oxycodone, oxymorphone, hydrocodone, and hydromorphone, have improved pharmacokinetic profiles compared to morphine. Additionally, heroin and 6-MAM (6-Monoacetylmorphine) show better CNS penetration than morphine due to heightened lipid solubility. Hydromorphone, a potent opioid, undergoes hepatic metabolism to form the active...
Opioid Analgesics: Morphine and Other Natural Cogeners01:20

Opioid Analgesics: Morphine and Other Natural Cogeners

Opioids are a class of drugs that mimic endogenous opioid peptides and act on opioid receptors, and help in pain relief. These compounds are classified as natural, synthetic, or semi-synthetic. Natural opioids, like morphine, codeine, and thebaine, are derived from the opium poppy plant (Papaver somniferum or Papaver album) and are termed opiates. Synthetic opioids are artificial, while semi-synthetic opioids combine natural and synthetic compounds. Morphine, a prototypical opioid, possesses a...
Drug-Receptor Interaction: Agonist01:25

Drug-Receptor Interaction: Agonist

Agonists are drugs that interact with specific receptors in the body to produce a biological response. When an agonist binds to a receptor, it activates or enhances the receptor's function, leading to physiological effects. The interaction between agonist drugs and receptors is crucial for their therapeutic action in various medical treatments.
Agonists can bind to receptors in different ways. Some agonists bind directly to the receptor's active site, mimicking the endogenous ligand's action.

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Tracking Drug-induced Changes in Receptor Post-internalization Trafficking by Colocalizational Analysis
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The multiple facets of opioid receptor function: implications for addiction.

Pierre-Eric Lutz1, Brigitte L Kieffer

  • 1McGill Group for Suicide Studies, Douglas Mental Health University Institute, McGill University, Montreal, QC, Canada.

Current Opinion in Neurobiology
|March 5, 2013
PubMed
Summary

Opioid receptors, including mu, kappa, and delta, significantly influence addiction by affecting reward, emotion, and decision-making. Understanding their distinct roles is crucial for developing effective addiction treatments.

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Area of Science:

  • Neuroscience
  • Psychiatry
  • Pharmacology

Background:

  • Addiction involves altered reward processing, emotional regulation, and decision-making.
  • Opioid receptors are increasingly recognized for their broad involvement in these addictive processes.

Purpose of the Study:

  • To explore the multifaceted roles of mu, kappa, and delta opioid receptors in addiction.
  • To highlight the implications of opioid receptor function in social reward, relapse prevention, mood enhancement, and cognitive deficits.

Main Methods:

  • Review of recent scientific literature on opioid receptors and addiction.
  • Analysis of evidence implicating specific opioid receptor subtypes (mu, kappa, delta) in various aspects of addiction.

Main Results:

  • Mu opioid receptor is central to social reward processes.
  • Kappa opioid receptor antagonism shows promise for preventing relapse and managing withdrawal.
  • Delta opioid receptor acts as a mood enhancer, with its addiction role still under investigation.
  • All three receptors are implicated in addiction-depression comorbidity and cognitive impairments.

Conclusions:

  • Opioid receptors are key targets for understanding and treating addiction.
  • Further research into delta opioid receptor's role and the collective impact on cognitive function is warranted.