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Systematic (IUPAC) name
CAS number 57-27-2
ATC code N02AA01
PubChem 5288826
DrugBank APRD00215
Chemical data
Formula C17H19NO3 
Mol. mass 285.4
Pharmacokinetic data
Bioavailability ~25% (oral); 100% (IV);
Protein binding 30–40%
Metabolism Hepatic 90%
Half life 2–3 hours
Excretion Renal 90%, biliary 10%
Therapeutic considerations
Pregnancy cat.


Legal status

Controlled (S8)(AU) Schedule I(CA) Class A(UK) Schedule II(US)

Dependence Liability Extremely High
Routes smoked/inhaled, insufflated, Oral, SC, IM, IV
Indicated for:
  • Relief of severe pain

Recreational uses:

  • Euphoria
  • Relaxation
  • Sedation

Other uses:

Side effects:


  • Coma
  • Hypoventilation
  • Spontaneous abortion
  • Respiratory arrest
  • Cardiac arrest
  • Death

Atypical sensations:

  • ?


  • Bradycardia
  • Palpitation
  • Faintness
  • Flushing of the face

Ear, nose, and throat:

  • Dry mouth


  • Eugonadism


  • Pupil constriction
  • Intermittent blurring
  • Visual distortions


  • Nausea
  • Constipation
  • Biliary tract spasm


  • Renal failure


  • ?


  • Muscle twitch




  • Slow and shallow respiration


  • Itchiness
  • Flushing

Morphine (INN) (pronounced /ˈmɔrfiːn/) is a highly-potent opiate analgesic drug and is the principal active agent in opium and the prototypical opioid. Like other opiates, e.g., diacetylmorphine (heroin), morphine acts directly on the central nervous system (CNS) to relieve pain, and at synapses of the nucleus accumbens in particular. Studies done on the efficacy of various opioids have indicated that, in the management of severe pain, no other narcotic analgesic is more effective or superior to morphine. Morphine is highly addictive when compared to other substances; tolerance, physical and psychological dependences develop very rapidly. The word "morphine" is derived from Morpheus, the Greek god of dreams.

Additional recommended knowledge


Medical uses

Morphine is used legally:

  • as an analgesic in hospital settings to relieve
    • pain in myocardial infarction
    • pain in sickle cell crisis
    • pain after surgery
    • pain associated with trauma
  • in the relief of severe chronic pain, e.g.,
    • cancer
    • pain from kidney stones
    • severe back pain
  • as an adjunct to general anesthesia
  • in epidural anesthesia or intrathecal analgesia
  • for palliative care (i.e., to alleviate pain without curing the underlying reason for it, usually because the latter is found impossible)
  • as an antitussive for severe cough
  • in nebulised form, for treatment of dyspnea, although the evidence for efficacy is slim.[1] Evidence is better for other routes. [2]
  • as an antidiarrheal in chronic conditions (e.g., for diarrhea associated with AIDS), although loperamide (a non-absorbed opioid acting only on the gut) is the most commonly-used opioid for diarrhea.


The following conditions are contraindications for morphine:

  • acute respiratory depression
  • acute pancreatitis (this may be a result of morphine use as well) because morphine may cause spasm of the sphincter of Oddi and worsen the pain
  • renal failure (due to accumulation of the metabolite morphine-6-glucuronide)
  • chemical toxicity (potentially lethal in low tolerance subjects)
  • raised intracranial pressure, including head injury (exacerbation due pCO2 increases from respiratory depression)


Main article: Opioid receptor

Morphine is the prototype narcotic drug and is the gold standard against which all other opioids are tested. It interacts predominantly with the μ-opioid receptor. These μ-binding sites are discretely distributed in the human brain, with high densities in the posterior amygdala, hypothalamus, thalamus, nucleus caudatus, putamen, and certain cortical areas. They are also found on the terminal axons of primary afferents within laminae I and II (substantia gelatinosa) of the spinal cord and in the spinal nucleus of the trigeminal nerve.[3]

Morphine is a phenanthrene opioid receptor agonist – its main effect is binding to and activating the μ-opioid receptors in the central nervous system. In clinical settings, morphine exerts its principal pharmacological effect on the central nervous system and gastrointestinal tract. Its primary actions of therapeutic value are analgesia and sedation. Activation of the μ-opioid receptors is associated with analgesia, sedation, euphoria, physical dependence, and respiratory depression. Morphine is a rapid-acting narcotic, and it is known to bind very strongly to the μ-opioid receptors, and for this reason, it often has a higher incidence of euphoria/dysphoria, respiratory depression, sedation, pruritus, tolerance, and physical and psychological dependence when compared to other opioids at equianalgesic doses. Morphine is also a κ-opioid and δ-opioid receptor agonist, κ-opioid's action is associated with spinal analgesia, miosis (pinpoint pupils) and psychotomimetic effects. δ-opioid is thought to play a role in analgesia.[4]

The effects of morphine can be countered with opioid antagonists such as naloxone, naltrexone and NMDA antagonists such as ketamine or dextromethorphan (NOTE: NMDA receptor antagonists can actually INCREASE the actions of opioids by reducing tolerance - see Herman et al, Neuropsychopharmacology. 1995 Dec;13(4):269-93.[citation needed].

Morphine is primarily metabolized into morphine-3-glucuronide (M3G) and morphine-6-glucuronide (M6G)[5] via glucuronidation by phase II metabolism enzyme UDP-glucuronosyl transferase-2B7 (UGT2B7). The phase I metabolism cytochrome P450 (CYP) family of enzymes has a role in the metabolism to a lesser extent. Not only does the metabolism occur in the liver but it may also take place in the brain and the kidneys. M6G has been found to be a far more potent analgesic than morphine when dosed to rodents, but crosses the blood-brain barrier with difficulty. M6G has been shown to be relatively more selective for mu-receptors than for delta- and kappa-receptors, whereas M3G does not appear to compete for opioid receptor binding. The significance of M6G formation on the observed effect of a dose of morphine is the subject of extensive debate among pharmacologists.


Like loperamide and other opioids, morphine acts on the myenteric plexus in the intestinal tract, reducing gut motility, causing constipation. The gastrointestinal effects of morphine are mediated primarily by μ-opioid receptors in the bowel. By inhibiting gastric emptying and reducing propulsive peristalsis of the intestine, morphine decreases the rate of intestinal transit. Reduction in gut secretion and increases in intestinal fluid absorption also contribute to the constipating effect. Opioids also may act on the gut indirectly through tonic gut spasms after inhibition of nitric oxide generation. This effect was shown in animals when a nitric oxide precursor reversed morphine-induced changes in gut motility.

Gene expression

Studies have shown that morphine can alter the expression of certain genes in human DNA. A single injection of morphine has been shown to alter the expression of two major groups of genes, for proteins involved in mitochondrial respiration and for cytoskeleton-related proteins.[6]

Effects on the immune system

Morphine has long been known to act on receptors expressed on cells of the central nervous system resulting in pain relief and analgesia. In the 1970s and '80s, evidence suggesting that opiate drug addicts show increased risk of infection (such as increased pneumonia, tuberculosis, and HIV) led scientists to believe that morphine may also affect the immune system. This possibility increased interest in the effect of chronic morphine use on the immune system.

The first step of determining that morphine may affect the immune system was to establish that the opiate receptors known to be expressed on cells of the central nervous system are also expressed on cells of the immune system. One study successfully showed that dendritic cells, part of the innate immune system, display opiate receptors. Dendritic cells are responsible for producing cytokines, which are the tools for communication in the immune system. This same study showed that dendritic cells chronically treated with morphine during their differentiation produce more interleukin-12 (IL-12), a cytokine responsible for promoting the proliferation, growth, and differentiation of T-cells (another cell of the adaptive immune system) and less interleukin-10 (IL-10), a cytokine responsible for promoting a B-cell immune response (B cells produce antibodies to fight off infection).

The pathway through which this regulation of cytokines occurs is via the p38 MAPK (mitogen activated protein kinase) dependent pathway. Usually, the p38 within the dendritic cell expresses TLR4 (toll-like receptor 4), which is activated through the ligand LPS (lipopolysaccharide). This causes the p38 MAPK to be phosphorylated. This phosphorylation activates the p38 MAPK to begin producing IL-10 and IL-12. When the dendritic cell is chronically exposed to morphine during their differentiation process then treated with LPS, the production of cytokines is different. Once treated with morphine, the p38 MAPK does not produce IL-10, Dr. George B. Stefano discovered all of this instead favoring production of IL-12. The exact mechanism through which the production of one cytokine is increased in favor over another is not known. Most likely, the morphine causes increased phosphorylation of the p38 MAPK. Transcriptional level interactions between IL-10 and IL-12 may further increase the production of IL-12 once IL-10 is not being produced. Future research may target the exact mechanism that increases the production of IL-12 in morphine treated dendritic cells. This increased production of sIL-12 causes and increased T-cell immune response. This response is due to the ability of IL-12 to cause T helper cells to differentiate into the Th1 cell, causing a T cell immune response.


Most of the licit morphine produced is used to make codeine by methylation. It is also a precursor for both heroin (diacetylmorphine), hydromorphone, and oxymorphone. Replacement of the N-methyl group of morphine with an N-phenylethyl group results in a product that is 18 times morphine in its opiate agonist potency.[citation needed] Combining this modification with the replacement of the 6-hydroxyl with a 6-methylene produces a compound some 1440 times morphine in potency,[citation needed] stronger than the Bentley compounds such as etorphine. If this compound were cut into regular heroin, it is most unlikely that it would show up on any tests.[citation needed]

Both morphine and its hydrated form, C17H19NO3H2O, are sparingly soluble in water. In five liters of water, only one gram of the hydrate will dissolve. For this reason, pharmaceutical companies produce sulphate and hydrochloride salts of the drug, both of which are over 300 times more water-soluble than its parent molecule. Whereas the pH of a saturated morphine hydrate solution is 8.5, the salts are acidic. Since they derive from a strong acid but weak base, they are both at about pH = 5; as a consequence, the morphine salts are mixed with small amounts of NaOH to make them suitable for injection.[7]

It is interesting to note that morphine has recently been found to be endogenously produced by humans, made by cells in the heart, pancreas and brain.[8] It has also been isolated from a range of other mammals, as well as toads and some invertebrates. It is unclear, however, what the normal endogenous role of morphine is.


A Hungarian chemist, Janos Kabay found and internationally patented a method to extract morphine from 'poppy-straw': dried poppy pods and stem, and other parts of the dry plant, except for seeds and root. In natural form, in poppy plant, the alkaloids are bound to meconic acid. The method is to extract from the crushed plant with diluted sulphuroic-acid, which is a stronger acid than meconic acid, but not so strong to react with alkaloid molecules. The extraction is performed in many steps (one amount of crushed plant is at least six to ten times extracted, so practically every alkaloid goes into the solution). From the solution obtained at the last extraction step, the alkaloids precipitated by either ammonium-hydroxide or sodium-carbonate. The last step is purifying and separating morphine from other opium alkaloids (Opium poppy contains at least 15-20 different alkaloids, but most of them are of very low concentration). They found the company 'Alkaloida'. For several years in 1950s and 1960s, Hungary gave near 60% of Europe's total legal, medication-purpose morphine production. To this very day, plantation poppy in Europe is legal in Hungary, only the plantation area is limited by law to 2 acres. It is also legal to sell dried poppy in flowershops to decorate with other dried flowers and plants.

Legal classification

  • In the United Kingdom, morphine is listed as a Class A drug under the Misuse of Drugs Act 1971.
  • In the United States, morphine is classified as a Schedule II drug under the Controlled Substances Act.
  • In Canada, morphine is classified as a Schedule I drug under the Controlled Drugs and Substances Act.
  • In Australia, morphine is classified as a Schedule 8 drug under the variously titled State and Territory Poisons Acts.
  • In the Netherlands, morphine is classified as a List 1 drug under the Opium Law.
  • Internationally, morphine is a Schedule I drug under the Single Convention on Narcotic Drugs.[9]

History and non-medical use

  Morphine was first isolated in 1804 in Paderborn, Germany[10] by the German pharmacist Friedrich Wilhelm Adam Sertürner, who named it "morphium" after Morpheus, the Greek god of dreams. But it was not until the development of the hypodermic needle in 1853 that its use spread.[11] It was used for pain relief, and as a "cure" for opium and alcohol addiction. Later it was found out that morphine was even more addictive than either alcohol or opium, and its extensive use during the American Civil War allegedly resulted in over 400,000[12] sufferers from the "soldier's disease" of morphine addiction.[13] [14] This statement has been subjected to controversy, as there have been suggestions that such a disease was in fact a hoax and soldier's disease never occurred after the Civil War.[15][16]

Diacetylmorphine (better known as heroin) was derived from morphine in 1874 and brought to market by Bayer in 1898. Heroin is approximately 1.5-2 times more potent than morphine on a milligram-for-milligram basis. Using a variety of subjective and objective measures, the relative potency of heroin to morphine administered intravenously to post-addicts found 1.80 mg of morphine sulfate equals to 1 mg of diamorphine hydrochloride (heroin).[17] The pharmacology of heroin and morphine is identical except the two acetyl groups increase the lipid solubility of the heroin molecule, and thus the molecule enters the brain a bit more rapidly. The additional groups are then detached, yielding morphine, which is what causes the subjective effects of heroin. Therefore, the effects of morphine and heroin are identical except that heroin is slightly more potent and acts slightly faster.[18] Morphine, along with heroin and cocaine were outlawed and their possession without a prescription was criminalized in the U.S. by the Harrison Narcotics Tax Act of 1914.

In 1952, Dr. Marshall D. Gates, Jr. was the first person to chemically synthesize morphine at the University of Rochester. This breakthrough is well renowned in the field of organic chemistry. [19]

Morphine is routinely carried by soldiers on operations in an autoinjector.

Morphine was the most commonly abused narcotic analgesic in the world up until heroin was synthesized and came into use. Even today, morphine is the most sought after prescription narcotic by heroin addicts when heroin is scarce.


  Morphine is a highly addictive substance, both psychologically and physically, with an addiction potential comparable to that of heroin. In a study comparing the physiological and subjective effects of heroin and morphine administered intravenously in post-addicts, the post-addicts showed no preference for one or the other of these drugs when administered on a single injection basis. Equipotent doses of these drugs had quite comparable action time courses when administered intravenously, and on this basis there was no difference in their ability to produce feelings of "euphoria," ambition, nervousness, relaxation, drowsiness, or sleepiness.[20] Although the heroin abstinence syndrome was of shorter duration than that of morphine, the peak intensity was quite comparable for the two drugs. Data acquired during short-term addiction studies did not support the statement that tolerance develops more rapidly to heroin than to morphine. These findings have been discussed in relation to the physiochemical properties of heroin and morphine and the metabolism of heroin. When compared to other opioids — hydromorphone, fentanyl, oxycodone, and meperidine — post-addicts showed a strong preference for heroin and morphine over the others, suggesting that heroin and morphine are more liable to abuse and addiction. Morphine and heroin were also much more likely to produce feelings of euphoria and other such subjective effects when compared to most other opioid analgesics.[21][22]

Withdrawal syndrome

The withdrawal symptoms associated with morphine addiction are usually experienced shortly before the time of the next scheduled dose, sometimes within as early as a few hours (usually between 6-12 hours) after the last administration. Early symptoms include watery eyes, insomnia, diarrhea, runny nose, yawning, dysphoria, and sweating and in some cases a strong drug craving. Restlessness, irritability, loss of appetite, body aches, severe abdominal pain, nausea and vomiting, tremors, and even stronger and more intense drug craving appear as the syndrome progresses. Severe depression and vomiting are very common. The heart rate and blood pressure are elevated and can lead to a heart attack, blot clot or stroke. Chills or cold flashes with goose bumps ("cold turkey") alternating with flushing (hot flashes), kicking movements of the legs ("kicking the habit" - similar to restless leg syndrome) and excessive sweating are also characteristic symptoms.[23] Severe pains in the bones and muscles of the back and extremities occur, as do muscle spasms. At any point during this process, a suitable narcotic can be administered that will dramatically reverse the withdrawal symptoms. Major withdrawal symptoms peak between 48 and 96 hours after the last dose and subside after about 8 to 12 days. Sudden withdrawal by heavily dependent users who are in poor health is very rarely fatal. Morphine withdrawal is considered less dangerous than alcohol, barbiturate, or benzodiazepine withdrawal.[24]

The psychological dependence associated with morphine addiction is complex and protracted. Long after the physical need for morphine has passed, the addict will usually continue to think and talk about the use of morphine (or other drugs) and feel strange or overwhelmed coping with daily activities without being under the influence of morphine. Psychological withdrawal from morphine is a very long and painful process.[25] Addicts often suffer severe depression, anxiety, insomnia, mood swings, amnesia (forgetfulness), low self-esteem, confusion, paranoia, and other psychological disorders. The psychological dependence on morphine can, and usually does, last a lifetime.[26] There is a high probability that relapse will occur after morphine withdrawal when neither the physical environment nor the behavioral motivators that contributed to the abuse have been altered. Testimony to morphine's addictive and reinforcing nature is its relapse rate. Abusers of morphine (and heroin), have the highest relapse rates among all drug users, including abusers of other opioids, cocaine, and methamphetamine.[citation needed] A complication that may arise from long term morphine use or abuse is neurotoxicity. Morphine is more often associated with nightmares where oxycodone is not. It is not fully understood yet exactly how morphine may cause neurotoxicity. Morphine neurotoxicity, such as delirium, resolves when rotating from morphine to oxycodone. Oxycodone neurological side effects are more cognitive than motor (myoclonus) and hallucinations are reported less frequently with oxycodone than with morphine. [1] [27]

Hepatitis C and morphine withdrawal

Researchers at the University of Pennsylvania have demonstrated that morphine withdrawal complicates hepatitis C by suppressing IFN-alpha-mediated immunity and enhancing virus replication. Heptatitis C virus (HCV) is common among intravenous drug users, with 70 to 80% of abusers infected in the United States.[citation needed] This high association has piqued interest in determining the effects of drug abuse, specifically morphine and heroin, on progression of the disease. The discovery of such an association would impact treatment of both HCV infection and drug abuse.[28]

Access to morphine in poor countries

Although morphine is cheap, people in poorer countries often do not have access to it. According to a 2005 estimate by the International Narcotics Control Board, six countries consume 79 percent of the world’s morphine. The less affluent countries, accounting for 80 percent of the world's population, consumed only about 6 percent of the global morphine supply. Some countries import virtually no morphine, and in others the drug is rarely available even for relieving severe pain while dying. Experts in pain management attribute the under-distribution of morphine to an unwarranted fear of the drug's potential for addiction and abuse. While morphine is clearly addictive, western doctors believe it is worthwhile to use the drug and then ween the patient off when the treatment is over.[29]

Additional images

See also

Wikinews has related news:
2005 Afghan opium harvest begins


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  5. ^ Kilpatrick G.J. and Smith T.W. (2005). "Morphine-6-glucuronide: actions and mechanisms". Med. Res. Rev. 25 (5): 521-544. PMID 15952175.
  6. ^ Loguinov A, Anderson L, Crosby G, Yukhananov R (2001). "Gene expression following acute morphine administration". Physiol Genomics 6 (3): 169-81. PMID 11526201.
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  8. ^ Chotima Boettcher, Monika Fellermeier, Christian Boettcher, Birgit Drager, and Meinhart H. Zenk. How human neuroblastoma cells make morphine. Proceedings of the National Academy of Sciences. June 14, 2005. 102(24): 8495–8500
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  20. ^ W. R. Martin 1 and H. F. Fraser 1
  21. ^ 1 National Institute of Mental Health, Addiction Research Center, U. S. Public Health Service Hospital, Lexington, Kentucky
  22. ^ Journal of Pharmacology And Experimental Therapeutics, Vol. 133, Issue 3, 388-399, 1961
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  26. ^ O'Neal, Maryadele J. Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals. Merck. October 18, 2006.
  27. ^ Opioids in Cancer Pain By Mellar P. Davis, Paul Glare, Janet Hardy Page 135
  28. ^ Wang C-Q, Li Y, Douglas SD, Wang X, Metzger DS, Zhang T, Ho W-Z: Morphine withdrawal enhances hepatitis C virus (HCV) replicon expression. Am J Pathol 2005, 167:1333-1340
  29. ^ Donald G. McNeil Jr.. "Drugs Banned, Many of World’s Poor Suffer in Pain", New York Times, 2007-09-10. Retrieved on 2007-09-11. 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Morphine". A list of authors is available in Wikipedia.
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