Opioid receptors

From WikiMD.org
Jump to navigation Jump to search

Opioid Receptors

Opioid receptors (/oʊˈpiːɔɪd rɪˈsɛptərz/) are a group of G protein-coupled receptors with opioids as ligands. The endogenous opioids are dynorphins, enkephalins, endorphins, endomorphins and nociceptin. The opioid receptors are ~40% identical to somatostatin receptors (SSTRs).

Etymology

The term "opioid" originates from the Greek words "opion" meaning "poppy juice" and "eidos" meaning "like". The term "receptor" is derived from the Latin "recipere" meaning "to receive". Thus, "opioid receptor" refers to a receptor that receives opioids.

Types of Opioid Receptors

There are four major types of opioid receptors in the body: mu-opioid receptor (MOR), delta-opioid receptor (DOR), kappa-opioid receptor (KOR), and nociceptin receptor (NOP). Each receptor type has a different function and is activated by different types of opioids.

Mu-Opioid Receptor

The mu-opioid receptor (MOR) is the primary site of action for the most commonly used opioids, including morphine, heroin, fentanyl, and methadone.

Delta-Opioid Receptor

The delta-opioid receptor (DOR) is thought to play a role in analgesia, depression, anxiety, and epilepsy.

Kappa-Opioid Receptor

The kappa-opioid receptor (KOR) is involved in pain control, stress response, and addictive behavior.

Nociceptin Receptor

The nociceptin receptor (NOP), also known as the ORL1 receptor, is involved in pain control, anxiety, and depression.

Related Terms

External links

Esculaap.svg

This WikiMD dictionary article is a stub. You can help make it a full article.


Languages: - East Asian 中文, 日本, 한국어, South Asian हिन्दी, Urdu, বাংলা, తెలుగు, தமிழ், ಕನ್ನಡ,
Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, European español, Deutsch, français, русский, português do Brasil, Italian, polski