Desmetramadol

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Desmetramadol
Clinical data
Other namesO-Desmethyltramadol; O-DSMT; Omnitram
Pharmacokinetic data
MetabolismCYP3A4 and CYP2B6[1]
Elimination half-life6-8 hours
Identifiers
  • 3-(2-((dimethylamino)methyl)-1-hydroxycyclohexyl)phenol
JSmol)
  • OC2(c1cc(O)ccc1)CCCCC2CN(C)C
  • InChI=1S/C15H23NO2/c1-16(2)11-13-6-3-4-9-15(13,18)12-7-5-8-14(17)10-12/h5,7-8,10,13,17-18H,3-4,6,9,11H2,1-2H3 checkY
  • Key:UWJUQVWARXYRCG-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Desmetramadol (

INNTooltip International Nonproprietary Name), also known as O-desmethyltramadol (O-DSMT), is an opioid analgesic and the main active metabolite of tramadol.[2] Tramadol is demethylated by the liver enzyme CYP2D6[3] to desmetramadol in the same way as codeine
, and so similarly to the variation in effects seen with codeine, individuals who have a less active form of CYP2D6 will tend to have reduced analgesic effects from tramadol. Because desmetramadol itself does not need to be metabolized to induce an analgesic effect, it can be used in individuals with low CYP2D6 activity unlike tramadol.

Pharmacology

Pharmacodynamics

(+)-Desmetramadol is a G-protein biased

δ- and κ-opioid receptors.[5]

The two enantiomers of desmetramadol show quite distinct pharmacological profiles;[6] both (+) and (−)-desmetramadol are inactive as serotonin reuptake inhibitors,[7] but (−)-desmetramadol retains activity as a norepinephrine reuptake inhibitor,[8] and so the mix of both the parent compound and metabolites contributes significantly to the complex pharmacological profile of tramadol. While the multiple receptor targets can be beneficial in the treatment of pain (especially complex pain syndromes such as neuropathic pain), it increases the potential for drug interactions compared to other opioids, and may also contribute to side effects.

Desmetramadol is also an antagonist of the serotonin 5-HT2C receptor, at pharmacologically relevant concentrations, via competitive inhibition.[9] This suggests that the apparent anti-depressant properties of tramadol may be at least partially mediated by desmetramadol, thus prolonging the duration of therapeutic benefit.

Inhibition of the 5-HT2C receptor is a suggested factor in the mechanism of anti-depressant effects of agomelatine and maprotiline. The potential selectivity and favorable side effect profile of desmetramadol compared to its prodrug, tramadol, makes it more suitable for clinical use, although no such large scale controlled trials have been conducted with patients.

Upon inhibition of the receptor, downstream signaling causes dopamine and norepinephrine release, and the receptor is thought to significantly regulate mood, anxiety, feeding, and reproductive behavior. 5-HT2C receptors regulate dopamine release in the striatum, prefrontal cortex, nucleus accumbens, hippocampus, hypothalamus, and amygdala, among others.[10]

Research indicates that some suicide victims have an abnormally high number of 5-HT2C receptors in the prefrontal cortex.[11] There is some mixed evidence that agomelatine, a 5-HT2C antagonist, is an effective antidepressant.[12] Antagonism of 5-HT2C receptors by agomelatine results in an increase of dopamine and norepinephrine activity in the frontal cortex.

Pharmacokinetics

Metabolites

Desmetramadol is metabolized in the liver into the active metabolite N,O-didesmethyltramadol via CYP3A4 and CYP2B6. The inactive tramadol metabolite N-desmethyltramadol is metabolized into the active metabolite N,O-didesmethyltramadol by CYP2D6.

History

The history of desmetramadol is intrinsically linked to its discovery and development within the pharmaceutical industry. This journey begins with its synthesis in the research laboratories of

Grünenthal GmbH
, a prominent pharmaceutical establishment based in Germany, during the late 1970s.

This innovative synthesis marked the inception of desmetramadol as a pharmacological entity. While tramadol, its precursor, was introduced to the global pharmaceutical market in the early 1980s under various brand names and gained adoption as a pain-relieving medication notable for its dual-action characteristics, desmetramadol emerged as a significant metabolite derived from tramadol's metabolism.

In the realm of pharmacology, desmetramadol garnered attention for its unique pharmacological profile. Researchers and healthcare professionals recognized its distinct properties and utility. This recognition proved particularly crucial in cases where tramadol's effectiveness was influenced by individual variations in CYP2D6 enzyme activity. Today, desmetramadol stands as a noteworthy component of the pharmaceutical landscape, offering valuable insights into pain management and pharmacogenetics.

Society and culture

Recreational use

Desmetramadol has been sold in a blend called Krypton and marketed as powdered

kratom leaf (Mitragyna speciosa). Krypton was reportedly linked to at least 9 accidental deaths from overdose in Sweden during 2010–2011.[13][14][15]

Medicinal use

Unusually for a compound that first came to prominence as a recreational designer drug, desmetramadol has recently been reevaluated as a potential novel analgesic drug for use in medicine, with its well studied pharmacology and toxicology as an active metabolite of the widely used analgesic drug tramadol offering advantages over more structurally novel alternatives. Human clinical trials have shown it to offer similar analgesic benefits to drugs such as oxycodone and fentanyl but with reduced respiratory depression and a comparatively favorable safety profile.[16][4]

Legality

United Kingdom

Desmetramadol was made a Class A drug in the United Kingdom on 26 Feb 2013.[17]

See also

References

  1. ^ Tramadol Pharmacokinetics, PharmGKB
  2. PMID 8220877
    .
  3. PMID 14624403
    .
  4. ^
    PMID 32116679
    .
  5. PMID 10991912
    .
  6. PMID 10992001
    .
  7. PMID 9389855
    .
  8. PMID 8467366
    .
  9. S2CID 23775035
    .
  10. S2CID 143950479
    .
  11. PMID 11282248
    .
  12. PMID 20694073
    .
  13. PMID 21112167
    .
  14. PMID 21294331
    .
  15. PMID 21513619
    .
  16. PMID 31005596
    .
  17. ^ "The Misuse of Drugs (Designation) (Amendment) (England, Wales and Scotland) Order 2013". UK Home Office. 31 January 2013.
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