Spinorphin
Spinorphin is an endogenous heptapeptide with the sequence Leu-Val-Val-Tyr-Pro-Trp-Thr. It is derived from the hemoglobin β-chain and has been identified as an inhibitor of several enzymes and receptors in the nervous system.
Biological Function[edit | edit source]
Spinorphin is known to inhibit the activity of enkephalinase, an enzyme that degrades enkephalins, which are endogenous opioid peptides. By inhibiting enkephalinase, spinorphin increases the levels of enkephalins, thereby enhancing their analgesic effects. Spinorphin also inhibits the activity of neutrophil elastase, an enzyme involved in the inflammatory response, suggesting a potential role in modulating inflammation.
Mechanism of Action[edit | edit source]
Spinorphin exerts its effects primarily through the inhibition of enkephalinase and neutrophil elastase. By preventing the breakdown of enkephalins, spinorphin prolongs their action on opioid receptors, which are involved in pain modulation. Additionally, the inhibition of neutrophil elastase by spinorphin can reduce tissue damage and inflammation, contributing to its potential anti-inflammatory properties.
Potential Therapeutic Applications[edit | edit source]
Due to its ability to modulate pain and inflammation, spinorphin has been studied for its potential therapeutic applications in conditions such as chronic pain, inflammatory diseases, and neuropathic pain. However, further research is needed to fully understand its efficacy and safety in clinical settings.
Research and Development[edit | edit source]
Ongoing research is focused on understanding the detailed mechanisms of spinorphin's action, its potential side effects, and its therapeutic potential in various medical conditions. Studies are also exploring the development of spinorphin analogs with improved stability and efficacy.
See Also[edit | edit source]
References[edit | edit source]
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Contributors: Prab R. Tumpati, MD