Target Name: Opioid receptor
NCBI ID: P5850
Review Report on Opioid receptor Target / Biomarker Content of Review Report on Opioid receptor Target / Biomarker
Opioid receptor
Other Name(s): None

TRK-1: A Potential Drug Target for Pain and Addiction

The Opioid receptor, also known as TRK-1, TRK-2, or TRK-3, is a family of G protein-coupled receptors that play a crucial role in pain signaling and neurotransmission. The Opioid receptor is a diverse family that contains several subtypes, each with distinct features and functions. One of the subtypes, designated as TRK-1, TRK-2, or TRK-3, is a potential drug target and biomarker for the treatment of opioid addiction and other chronic pain conditions.

The Opioid receptor is a G protein-coupled receptor, which means it is composed of a protein called G protein and a nucleotide that binds to the receptor. The G protein is responsible for transmitting the signal from the receptor to the cell's intracellular signaling pathway. The Opioid receptor is a member of the G protein-coupled receptor subfamily, which includes over 70 different subtypes, including TRK-1, TRK-2, and TRK-3.

TRK-1, TRK-2, and TRK-3 are all involved in the perception and modulation of pain signals. TRK-1 is the most abundant subtype, and it is expressed in the central nervous system (CNS) and the peripheral nervous system (PNS). TRK-2 is expressed in the PNS, and TRK-3 is expressed in both the CNS and the PNS. Each subtype of the Opioid receptor has unique features that make it distinct from the others.

One of the key features of the Opioid receptor is its ability to modulate pain signals. When the body perceives pain, the TRK-1 subtype is activated and causes the release of endogenous opioids, such as delta-opioid and enkeji. These opioids help to alleviate pain by interacting with the endogenous opioid system in the brain. The TRK-1 subtype is also involved in the modulation of pain signals by neurotransmitters, such as GABA and glutamate.

Another important function of the Opioid receptor is its role in the treatment of opioid addiction. The TRK-1 subtype is also involved in the modulation of the brain's reward system, which is often impaired in individuals with opioid addiction. By activating the TRK-1 subtype, endogenous opioids can help to enhance the rewarding effects of drugs and improve the individual's motivation to seek out and use them.

TRK-1 has also been shown to play a role in the development and maintenance of chronic pain conditions, such as fibromyalgia and chronic low back pain. By modulating the pain modulatory systems in the brain, TRK-1 may contribute to the development of chronic pain.

In addition to its role in pain modulation, TRK-1 has also been shown to play a potential drug target in the treatment of addiction. The TRK-1 subtype has been shown to interact with several drugs that are used to treat addiction, including opioids, benzodiazepines, and naltrexones. By modulating the activity of TRK-1, these drugs can enhance their efficacy and help individuals to overcome addiction.

TRK-1 has also been shown to be involved in the regulation of neurotransmitter release in the brain. The TRK-1 subtype has been shown to interact with several neurotransmitters, including GABA, GABA-B, and glutamate. By modulating the activity of these neurotransmitters, TRK-1 can regulate the release of neurotransmitters that are involved in pain modulation and addiction.

In conclusion, the Opioid receptor is a diverse family of G protein-coupled receptors that plays a crucial role in pain signaling and neurotransmission. The TRK-1 subtype, which is expressed in the

Protein Name: Opioid Receptor (nonspecified Subtype)

The "Opioid receptor Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about Opioid receptor comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

More Common Targets

OPLAH | OPN1LW | OPN1MW | OPN1MW3 | OPN1SW | OPN3 | OPN4 | OPN5 | OPRD1 | OPRK1 | OPRL1 | OPRM1 | OPRPN | OPTC | OPTN | OR10A2 | OR10A3 | OR10A4 | OR10A5 | OR10A6 | OR10A7 | OR10AA1P | OR10AB1P | OR10AC1 | OR10AD1 | OR10AF1P | OR10AG1 | OR10AK1P | OR10C1 | OR10D1P | OR10D3 | OR10D4P | OR10G2 | OR10G3 | OR10G4 | OR10G7 | OR10G8 | OR10G9 | OR10H1 | OR10H2 | OR10H3 | OR10H4 | OR10H5 | OR10J1 | OR10J2P | OR10J3 | OR10J5 | OR10K1 | OR10K2 | OR10P1 | OR10Q1 | OR10R2 | OR10S1 | OR10T2 | OR10V1 | OR10W1 | OR10X1 | OR10Z1 | OR11A1 | OR11G2 | OR11H1 | OR11H12 | OR11H13P | OR11H2 | OR11H5P | OR11H6 | OR11H7 | OR11J2P | OR11J5P | OR11K2P | OR11L1 | OR11M1P | OR12D2 | OR12D3 | OR13A1 | OR13C2 | OR13C3 | OR13C4 | OR13C5 | OR13C8 | OR13C9 | OR13D1 | OR13F1 | OR13G1 | OR13H1 | OR13J1 | OR13Z2P | OR14A16 | OR14A2 | OR14C36 | OR14I1 | OR14J1 | OR14L1P | OR1A1 | OR1A2 | OR1B1 | OR1C1 | OR1D2 | OR1D4 | OR1D5