MRGPRX4

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MRGPRX4 is a gene that encodes the Mas-related G-protein coupled receptor member X4 in humans. This receptor is part of the MRGPR family, which is a group of G protein-coupled receptors with a distinct structure and function, primarily involved in sensory perception and inflammatory pain modulation. The MRGPRX4 receptor is expressed in various tissues but is most notably found in sensory neurons, where it plays a role in the detection of specific pain and itch stimuli.

Function[edit | edit source]

The MRGPRX4 receptor is involved in the detection of non-peptide ligands, which distinguishes it from other members of the MRGPR family that typically respond to peptide ligands. This receptor has been implicated in the sensation of itch, particularly in response to certain pruritogenic (itch-inducing) compounds. It is also thought to play a role in the modulation of inflammatory pain, making it a potential target for the development of new analgesic and anti-pruritic treatments.

Expression[edit | edit source]

MRGPRX4 is expressed predominantly in the dorsal root ganglia (DRG), which contain the cell bodies of sensory neurons that transmit pain, temperature, and touch sensations from the peripheral to the central nervous system. The expression of MRGPRX4 in these sensory neurons suggests its importance in the sensory perception of pain and itch.

Clinical Significance[edit | edit source]

The MRGPRX4 receptor has garnered interest in the field of pain and itch research due to its unique role in sensory perception. Understanding the signaling pathways and ligands that activate MRGPRX4 could lead to novel therapeutic approaches for treating chronic pain and itch, conditions that are often poorly managed with current treatments. Additionally, since MRGPRX4 is involved in the detection of non-peptide ligands, it represents a novel pharmacological target that could be exploited for developing new classes of analgesic and anti-pruritic drugs.

Research[edit | edit source]

Research on MRGPRX4 is ongoing, with studies focusing on identifying specific ligands that activate the receptor, understanding its signaling mechanisms, and exploring its role in pain and itch perception. These studies are crucial for developing targeted therapies that can modulate MRGPRX4 activity to treat pain and itch without the side effects associated with current treatments.


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Contributors: Prab R. Tumpati, MD