d-morphine, but not l-morphine, has low micromolar affinity for the non-competitive N-methyl-D-aspartate site in rat forebrain. Possible clinical implications for the management of neuropathic pain.

Author: MakinM K, MilesJ, MorleyJ S, StringerM

Paper Details 
Original Abstract of the Article :
A diverse range of opioids and enantiomers were examined for their ability to displace binding at the [(3)H] MK-801-labelled site of the N-methyl-D-aspartate (NMDA) receptor in rat forebrain, displacement which is equitable with non-competitive NMDA receptor antagonist activity. Surprisingly, d-morp...See full text at original site
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引用元:
https://doi.org/10.1016/s0304-3940(00)01573-1

データ提供:米国国立医学図書館(NLM)

d-Morphine: A Potential Game-Changer in Neuropathic Pain Management

Neuropathic pain is a debilitating condition often resistant to traditional pain relief methods. This study explores the potential of d-morphine, an enantiomer of morphine, as a novel treatment option for neuropathic pain.

d-Morphine: A Unique Approach to Pain Relief

The researchers found that d-morphine, but not l-morphine, has a low micromolar affinity for the NMDA receptor, a key player in the regulation of pain perception. This suggests that d-morphine might offer a unique approach to pain management, potentially reducing tolerance development. The study also examined the effects of other opioid mu-receptor agonists, such as levorphanol and methadone, on the NMDA receptor.

Health Implications and Everyday Applications

This research provides a glimmer of hope for individuals struggling with neuropathic pain. The potential of d-morphine to effectively manage pain while minimizing tolerance development is significant. However, further research is necessary to fully understand its efficacy and safety in humans. Like a camel seeking a hidden oasis in the desert, researchers are diligently searching for new solutions to alleviate neuropathic pain.

Dr.Camel's Conclusion

d-Morphine holds promising potential as a novel treatment for neuropathic pain. Its unique mechanism of action could lead to a significant improvement in pain management and potentially reduce tolerance development. However, further research is crucial to confirm its effectiveness and safety in humans. Like a camel navigating a challenging landscape, it’s essential to approach this topic with a discerning eye and a thirst for knowledge.

Date :
  1. Date Completed 2001-01-09
  2. Date Revised 2019-07-01
Further Info :

Pubmed ID

11078927

DOI: Digital Object Identifier

10.1016/s0304-3940(00)01573-1

Related Literature

SNS
PICO Info
in preparation
Languages

English

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