Opiate

Opiate is a term classically used in pharmacology to mean a substance derived from opium. Opioid, a more modern term, is used to designate all substances, both natural and synthetic, that bind to opioid receptors in the brain (including antagonists).[1] Opiates are alkaloid compounds naturally found in the opium poppy plant Papaver somniferum.[2] The psychoactive compounds found in the opium plant include morphine, codeine, and thebaine. Opiates have long been used for a variety of medical conditions with evidence of opiate trade and use for pain relief as early as the eighth century AD.[3] Opiates are considered drugs with moderate to high abuse potential and are listed on various "Substance-Control Schedules" under the Uniform Controlled Substances Act of the United States of America.

For the class of drugs, see Opioid. For other uses, see Opiate (disambiguation).
Harvesting the poppy pod.

In 2014, between 13 and 20 million people used opiates recreationally (0.3% to 0.4% of the global population between the ages of 15 and 65).[4] According to the CDC, from this population, there has been a recorded 47,000 deaths with a total of a half a million deaths from 2000–2014.[5] In 2016, the World Health Organization reported that 27 million people suffer from opioid abuse disorder. They also reported that in 2015, 450,000 people died as a result of drug use, with between a third and a half of that number being attributed to opioids.[6]

Overview
Codeine
Chemical structure of morphine

Opiates belong to the large biosynthetic group of benzylisoquinoline alkaloids, and are so named because they are naturally occurring alkaloids found in the opium poppy. The major psychoactive opiates are morphine, codeine, and thebaine. Papaverine, noscapine, and approximately 24 other alkaloids are also present in opium but have little to no effect on the human central nervous system. Alkaloids that have no effect on the central nervous system are not considered to be opiates. Very small quantities of hydrocodone and hydromorphone are detected in assays of opium on rare occasions; it appears to be produced by the plant under circumstances and by processes which are not understood at this time and may include the action of bacteria. Dihydrocodeine, oxymorphol, oxycodone, oxymorphone, metopon and possibly other derivatives of morphine and/or hydromorphone also are found in trace amounts in opium.

Despite morphine being the most medically significant opiate, larger quantities of codeine are consumed medically, most of it synthesized from morphine. Codeine has greater and more predictable oral bioavailability, making it easier to titrate the dose. Codeine also has less abuse potential than morphine, and because it is milder, larger doses of codeine are required.[7]

Morphine addiction cure advertisement in the year 1900

Opiate withdrawal syndrome effects are associated with the abrupt cessation or reduction of prolonged opiate usage.

The manifestation of opiate dependence and abuse relies on a variety of factors, including the opiate's pharmacokinetic properties and the user's predisposition for addiction.[8]

Synthesis

While the full synthesis of opioids from naphthoquinone (Gates synthesis) or other simple organic starting materials is possible, they are tedious and uneconomical processes. Therefore, most of the opiate-type analgesics in use today are either extracted from Papaver somniferum or synthesized from those opiates, especially thebaine.[9]

In 2015 researches reported successful biosynthesis of thebaine and hydrocodone using genetically modified yeast. Once scaled for commercial use the process would cut production time from a year to several days and could reduce costs by 90%.[10][11]

Pharmacokinetics

Codeine

Codeine is a prodrug which is converted to morphine and acts on μ-opiate receptors. It is converted to morphine by metabolism of CYP2D6 enzymes. Individuals who have lower CYP2D6 activity may not metabolize codeine efficiently enough to experience its analgesic effects. Conversely, individuals with higher CYP2D6 activity may metabolize the drug too quickly and experience dose-related side effects such as sedation and respiratory depression.[12]

Fentanyl

Fentanyl is a synthetic opioid structurally similar arylpiperidines. It is a strong μ-receptor agonist that is 80–100 times more potent to morphine, and has a fast onset with a shorter duration of action than morphine. It is metabolized in the liver by CYP3A4 enzymes to norfentanyl, an inactive drug.[13]

Heroin
Global estimates of drug users in 2016
(in millions of users)[14]
SubstanceBest
estimate		Low
estimate		High
estimate
Amphetamine-
type stimulants		34.1613.4255.24
Cannabis192.15165.76234.06
Cocaine18.2013.8722.85
Ecstasy20.578.9932.34
Opiates19.3813.8026.15
Opioids34.2627.0144.54

Heroin, the brand name for diacetylmorphine, is the first of several semi-synthetic opioids to be derived from morphine, a component of natural opium.[15] Although it is derived from, rather than directly found in, natural opium, it is commonly referred to as an opiate. Heroin (diacetylmorphine) is a morphine prodrug; it is metabolized by the liver into morphine after administration. One of the major metabolites of heroin, 6-monoacetylmorphine (6-MAM), is also a morphine prodrug.

Hydromorphone

Hydromorphone is used as an alternative to morphine. It has a high first-pass metabolism, and is primarily glucuronidated in the liver to hydromorphone-3-glucoronide (H3G). 75% of hydromorphone is renally excreted, with 7% excreted as the parent opiate.[13]

Meperidine

Meperidine is a synthetic opiate part of the arylpiperidine class. It is a strong μ-receptor agonist with 1/10th the potency of morphine. It is used to treat rigors, and has a half-life of three to four hours. It is hepatically metabolized to the active metabolites of normeperidine, normepiridinic acid, and medperidinic acid. Normeperidine at toxic levels can cause CNS excitation and seizures.[13]

Methadone

Methadone has a higher bioavailability and half life compared to morphine.[16] It is metabolized to an inactive product by N-demethylation by CYP3A4 enzymes in the liver. It has high person to person variability because of varying levels of CYP3A4 in individuals.[17] It is approved for treatment of moderate to severe pain as well as opioid dependence.[18] Because of its high risk of drug interactions, liver toxicity, and patient variability, patients have to be monitored closely at methadone clinics.[19]

Morphine

Nicomorphine (morphine dinicotinate), dipropanoylmorphine (morphine dipropionate), desomorphine (di-hydro-desoxy-morphine), methyldesorphine, acetylpropionylmorphine, dibenzoylmorphine, diacetyldihydromorphine, and several others are also derived from morphine.[20]

Morphine is metabolized in the liver to morphine-3-glucuronide (M3G) and morphine-6-glucuronide (M6G), and are excreted by the kidneys. They are also able to cross into the blood-brain barrier into the cerebrospinal fluid. M6G has potent analgesic activity, binds to opioid receptors, and is a main contributor to the therapeutic benefit of morphine.[21] M3G does not act as an analgesic, has a low affinity for opioid receptors, and may possibly antagonize the therapeutic effects of morphine and M6G. Moreover, high doses of morphine, and thus M3G, is associated with neurotoxic side effects such as hyperalgesia, allodynia and myoclonus.[22]

Oxymorphone

Oxymorphone is a congener of morphine. It is metabolized to 6-hydroxy-oxymorphone and oxymorphone-3-glucuronide, and 40% is excreted as metabolites. 6-hydroxy-oxymorphine is active and exists in a 1:1 ratio with the parent drug. Oxymorphone-3-glucuronide's activity is unknown.[13]

Indication

Opiates are mainly used for pain management with the premise that there will be benefits for both pain & function that will outweigh the risks to the patient.[23]

Opiate dose conversions may be necessary when switching medications given the differing pharmacodynamics between opiates. Generally, morphine is used as the standard for converting between opiates to achieve equivalent analgesic effects. These differences in morphine-equivalents may differ between formulations of the same medication.[24] Calculating total daily dose using morphine milligram equivalents is used to identify patients at risk of overdose.[25]

Complications and side effects

Common side effects associated to opioid use include: sedation, nausea, dizziness, vomiting, constipation, physical dependence, tolerance, and respiratory depression. Of these the most common are constipation & nausea and there are no development of tolerance to these side effects.[26] This is why stool softeners or laxatives (polyethylene glycol, docusate, and senna) are often prescribed with opioids.[27]

Less common side effects include: delayed gastric emptying, hyperalgesia, immunologic and hormonal dysfunction, muscle rigidity, and myoclonus.[28]

Opiate use for pain is widely accepted in the healthcare system. However, long-term treatment for chronic pain is highly controversial as there is a high risk of addiction associated with its use leading to abuse and diversion to others even when taken properly.[29] Those addicted to opiates will prioritize acquiring these drugs over other activities in their lives, negatively impacting their professional and personal relationships.

Chronic opioid use can lead to tolerance. This often causes the patient to need higher and/or more frequent doses of the drug to get the desired effects.[30]

Concentration-dependence adverse effects may vary based on the user's genetic polymorphisms which can alter drug metabolism. Cytochrome P450 (notably CYP2D6) is responsible for the metabolism of various opiates to active metabolites and variations in CYP450 activity lead to varying serum drug levels.[31]

Pharmacology in pain

Pain is an unpleasant sensory and emotional experience associated with actual or potential tissue damage. It is an essential defensive function where pain works as an alarm to avoid or limit tissue damage. Opiates act upon opioid receptors that are coupled to inhibitor G protein coupled receptors (GPCR). These receptors fall into 3 classes: μ (mu), δ (delta), and κ (kappa) receptors.[32]

More than 70% of opioid receptors are μ receptors, predominantly located on the central terminals of nociceptors in the dorsal horn of the spinal cord. The remaining 30% of opioid receptors are located post-synaptically on dendrites of second-order spinothalamic neurons & interneurons.[32]

When an opiate binds as an agonist to the GPCR, there will be a signaling cascade resulting in the inhibition of adenylate cyclase and calcium ion channels with the stimulation of potassium ion channels. The net effect of these changes is a reduced intracellular cAMP and hyperpolarization of the neuronal cell reducing neurotransmitter release.[33] Through this pathway, when opiates bind to and activate the mu receptor, there is a decrease transmission of pain signalling. This pathway targeted for the analgesia properties that opiates are known and used for. Other clinically important roles of mu are its involvement in respiratory and cardiovascular functions, gastrointestinal peristalsis, feeding, and mood.[34] These other pathways are important because they explain the side effects of opiate use like respiratory depression at high doses, constipation with chronic use, and addicting properties.[28]

Absolute contraindications

Those with the following conditions should not be using opioids:[35]

  • severe respiratory instability
  • acute psychiatric instability
  • uncontrolled suicide risk
  • diagnosed non-nicotine substance abuse
  • QTc intervals longer than 500 milliseconds if prescribed methadone
  • acute diversion of controlled substances
  • intolerance from previous trial use with specific opioids
  • serious adverse effects or lack of efficacy.

Risk factors for prescription abuse

The following are risk factors for opiate prescription abuse:[36]

  • past or current history of substance abuse
  • psychiatric disorders that haven't been treated
  • patients of a young age
  • family history of substance abuse
  • social environments that encourage substance use
  • prolonged use or treatment with opioids.

Statistically, middle-aged patients with substance use history and psychiatric comorbidities are seen with higher mortality risks such as suicide.

See also

References
  1. Hemmings, Hugh C.; Egan, Talmage D. (2014). Pharmacology and Physiology for Anesthesia: Foundations and Clinical Application: Expert Consult - Online and Print. Elsevier Health Sciences. p. 253. ISBN 978-1437716795. Opiate is the older term classically used in pharmacology to mean a drug derived from opium. Opioid, a more modern term, is used to designate all substances, both natural and synthetic, that bind to opioid receptors (including antagonists).
  2. "Opiate - Definitions from Dictionary.com". dictionary.reference.com. Retrieved 2008-07-04.
  3. Brownstein, M J (1993-06-15). "A brief history of opiates, opioid peptides, and opioid receptors". Proceedings of the National Academy of Sciences of the United States of America. 90 (12): 5391–5393. doi:10.1073/pnas.90.12.5391. ISSN 0027-8424. PMC 46725. PMID 8390660.
  4. "Status and Trend Analysis of Illict [sic] Drug Markets" (PDF). World Drug Report 2015. Retrieved 26 June 2015.
  5. "CDC Press Releases". CDC. 2016-01-01. Retrieved 2019-10-17.
  6. "WHO | Information sheet on opioid overdose". WHO. Retrieved 2019-10-21.
  7. "Canadian Guideline for Opioid Use for Pain — Appendix B-8: Opioid Conversion and Brand Availability in Canada". nationalpaincentre.mcmaster.ca. Retrieved 2016-04-18.
  8. Gruber, Staci A.; Silveri, Marisa M.; Yurgelun-Todd, Deborah A. (2007-09-01). "Neuropsychological Consequences of Opiate Use". Neuropsychology Review. 17 (3): 299–315. doi:10.1007/s11065-007-9041-y. ISSN 1573-6660. PMID 17690984. S2CID 22057898.
  9. Synthesis of morphine alkaloids Presentation School of Chemical Sciences, University of Illinois at Urbana-Champaign Archived 2013-02-28 at the Wayback Machine retrieved 12-02-2010
  10. Galanie, Stephanie; Thodey, Kate; Trenchard, Isis J.; Interrante, Maria Filsinger; Smolke, Christina D. (2015-09-04). "Complete biosynthesis of opioids in yeast". Science. 349 (6252): 1095–1100. doi:10.1126/science.aac9373. ISSN 0036-8075. PMC 4924617. PMID 26272907.
  11. Mobley, Emily (2015-08-13). "Yeast cells genetically modified to create morphine-like painkiller". The Guardian. ISSN 0261-3077. Retrieved 2016-04-17.
  12. Kirchheiner, J.; Schmidt, H.; Tzvetkov, M.; Keulen, J.-Tha; Lötsch, J.; Roots, I.; Brockmöller, J. (August 2007). "Pharmacokinetics of codeine and its metabolite morphine in ultra-rapid metabolizers due to CYP2D6 duplication". The Pharmacogenomics Journal. 7 (4): 257–265. doi:10.1038/sj.tpj.6500406. ISSN 1473-1150. PMID 16819548.
  13. Inturrisi, Charles E. (July 2002). "Clinical pharmacology of opioids for pain". The Clinical Journal of Pain. 18 (4 Suppl): S3–13. doi:10.1097/00002508-200207001-00002. ISSN 0749-8047. PMID 12479250. S2CID 17984040.
  14. "Annual prevalence of use of drugs, by region and globally, 2016". World Drug Report 2018. United Nations Office on Drugs and Crime. 2018. Retrieved 7 July 2018.
  15. Copeland, CS (Jul–Aug 2014). "The Human Side of the Heroin Epidemic" (PDF). Healthcare Journal of New Orleans.
  16. Grissinger, Matthew (August 2011). "Keeping Patients Safe From Methadone Overdoses". Pharmacy and Therapeutics. 36 (8): 462–466. ISSN 1052-1372. PMC 3171821. PMID 21935293.
  17. Ferrari, Anna; Coccia, Ciro Pio Rosario; Bertolini, Alfio; Sternieri, Emilio (December 2004). "Methadone--metabolism, pharmacokinetics and interactions". Pharmacological Research. 50 (6): 551–559. doi:10.1016/j.phrs.2004.05.002. ISSN 1043-6618. PMID 15501692.
  18. Anderson, Ilene B; Kearney, Thomas E (January 2000). "Use of methadone". Western Journal of Medicine. 172 (1): 43–46. doi:10.1136/ewjm.172.1.43. ISSN 0093-0415. PMC 1070723. PMID 10695444.
  19. Lugo, Ralph A.; Satterfield, Kristin L.; Kern, Steven E. (2005). "Pharmacokinetics of methadone". Journal of Pain & Palliative Care Pharmacotherapy. 19 (4): 13–24. doi:10.1080/J354v19n04_05. ISSN 1536-0288. PMID 16431829. S2CID 29509469.
  20. "Esters of Morphine". www.unodc.org. United Nations Office on Drugs and Crime. Retrieved 10 March 2012.
  21. Christrup, L. L. (January 1997). "Morphine metabolites". Acta Anaesthesiologica Scandinavica. 41 (1): 116–122. doi:10.1111/j.1399-6576.1997.tb04625.x. PMID 9061094. S2CID 9858042.
  22. Andersen, Gertrud; Christrup, Lona; Sjøgren, Per (January 2003). "Relationships among morphine metabolism, pain and side effects during long-term treatment: an update". Journal of Pain and Symptom Management. 25 (1): 74–91. doi:10.1016/s0885-3924(02)00531-6. ISSN 0885-3924. PMID 12565191.
  23. Cohen, Brandon; Preuss, Charles V. (2019), "Opioid Analgesics", StatPearls, StatPearls Publishing, PMID 29083658, retrieved 2019-10-31
  24. Patanwala, Asad E; Duby, Jeremiah; Waters, Dustin; Erstad, Brian L (2007-02-01). "Opioid Conversions in Acute Care". Annals of Pharmacotherapy. 41 (2): 255–267. doi:10.1345/aph.1H421. ISSN 1060-0280. PMID 17299011. S2CID 2684749.
  25. "Morphine Equivalent Units/Morphine Milligram Equivalents". www.asam.org. Retrieved 2019-11-10.
  26. Benyamin, Ramsin; Trescot, Andrea M.; Datta, Sukdeb; Buenaventura, Ricardo; Adlaka, Rajive; Sehgal, Nalini; Glaser, Scott E.; Vallejo, Ricardo (2008). "Opioid complications and side effects". Pain Physician. 11 (2 Suppl): S105–120. ISSN 1533-3159. PMID 18443635.
  27. Publishing, Harvard Health. "Pain relief, opioids, and constipation". Harvard Health. Retrieved 2019-10-24.
  28. Benyamin, Ramsin; Trescot, Andrea M.; Datta, Sukdeb; Buenaventura, Ricardo; Adlaka, Rajive; Sehgal, Nalini; Glaser, Scott E.; Vallejo, Ricardo (March 2008). "Opioid complications and side effects". Pain Physician. 11 (2 Suppl): S105–120. ISSN 1533-3159. PMID 18443635.
  29. Reference, Genetics Home. "Opioid addiction". Genetics Home Reference. Retrieved 2019-10-24.
  30. Abuse, National Institute on Drug. "Prescription Opioids". www.drugabuse.gov. Retrieved 2019-10-24.
  31. Foster, Adriana; Mobley, Elizabeth; Wang, Zixuan (2007). "Complicated Pain Management in a CYP450 2D6 Poor Metabolizer". Pain Practice. 7 (4): 352–356. doi:10.1111/j.1533-2500.2007.00153.x. ISSN 1533-2500. PMID 17986163. S2CID 30624022.
  32. Fornasari, Diego (2014). "Pain pharmacology: focus on opioids". Clinical Cases in Mineral and Bone Metabolism. 11 (3): 165–168. ISSN 1724-8914. PMC 4269136. PMID 25568646.
  33. Pathan, Hasan; Williams, John (2012). "Basic opioid pharmacology: an update". British Journal of Pain. 6 (1): 11–16. doi:10.1177/2049463712438493. ISSN 2049-4637. PMC 4590096. PMID 26516461.
  34. Pasternak, Gavril W.; Pan, Ying-Xian (October 2013). "Mu Opioids and Their Receptors: Evolution of a Concept". Pharmacological Reviews. 65 (4): 1257–1317. doi:10.1124/pr.112.007138. ISSN 0031-6997. PMC 3799236. PMID 24076545.
  35. "Appendix C – Opioid Pharmacology". ICSI. Retrieved 2019-10-24.
  36. Webster, Lynn R. (2017). "Risk Factors for Opioid-Use Disorder and Overdose". Anesthesia and Analgesia. 125 (5): 1741–1748. doi:10.1213/ANE.0000000000002496. ISSN 1526-7598. PMID 29049118.
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