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Amorphinism refers to the mental and physical symptoms arising when a morphine-addict is deprived of morphine. Morphine is a potent opioid agonist derived from poppy plants and was originally used as a painkiller before being abused for euphoric and relieving purposes. It gave rise to morphine dependence, which caused the development of morphine withdrawal symptoms when morphine is reduced or stopped.
| Amorphinism | |
|---|---|
| |
| Morphine | |
| Pronunciation |
|
| Symptoms | Tremors, insomnia, anxiety, gastrointestinal disturbances |
| Treatment | Withdrawal Management |
| Medication | Buprenorphine, Methadone, Clonidine |
 | It has been suggested that this article be merged into Opioid withdrawal. (Discuss) Proposed since August 2024. |
Two of many possible mechanisms that give rise to morphine addiction and withdrawal symptoms include changes to the dopaminergic pathway, which gives drug craving behaviours and withdrawal symptoms, and neuronal adaptations, which gives withdrawal symptoms as well.
Symptoms of morphine withdrawal may include tremors, insomnia, anxiety, gastrointestinal disorders and more. While no diagnostic tests are done specifically for morphine withdrawal, urine toxicology tests, electrocardiogram, complete blood count, basic metabolic panel, and blood alcohol level tests are conducted for differential diagnosis.
To treat morphine withdrawal, the severity of morphine dependence is measured, via scales, to determine the appropriate withdrawal management. Examples of scales used include the Short Opiate Withdrawal Scale (SOWS) and the Clinical Opiate Withdrawal Scale (COWS). Patients with mild severity of dependence are given medications for symptomatic relief, while more patients of more severe dependence are give opioid agonists like methadone, opioid partial agonists like buprenorphine, or alpha-2 adrenergic agonists like clonidine. Psychosocial therapy may also be conducted in addition to drug therapy, where interventions differ based on lower or greater severity of morphine dependence.
Morphine, a morphian-framed alkaloid, is a potent opioid agonist (stimulates the opioid receptors) found naturally in poppy plants.[1][2] It was discovered in 1806 by German pharmacist Friedrich Wilhelm Sertürner when he isolated a pure alkaloid base from opium.[3] He then named it "morphinum", which we now call morphine, in 1817 in honour of the god of dreams.[3]
While morphine is primarily indicated as an analgesic (painkiller), morphine and other opioids are also abused due to the euphoric feeling and mental relaxation experienced when taken.[4] Prolonged use of morphine leads to morphine dependence, and people with morphine dependence experience amorphinism when the amount of morphine is reduced or stopped completely.[4]
The dopaminergic pathway and neuron adaptations are two possible mechanisms that lead to the development of morphine dependence and withdrawal symptoms.
Addiction to opioids such as morphine occur due to the changes in the dopaminergic signalling of the mesocorticolimbic system as a result of chronic opioid use.[5] Changes to the dopaminergic signalling gives rise to drug craving behavior.[5] Changes to the dopaminergic signalling leads to signs and symptoms of morphine withdrawal when amount of morphine is reduced or discontinued.[5] The impairment of the dopaminergic signalling also leads to a decrease in dopamine (a neurotransmitter used to transmit signals across nerve cells in the central nervous system) in the mesocorticolimbic system, otherwise known as the reward system, which is suggested to have a critical role in morphine withdrawal.[6][7][8] It can lead to morphine sensitization, or tolerance, such that more morphine is needed to achieve the same pharmacological effect.[6]
Addiction to morphine may also arise due to various adaptations of the neurons, including the desensitization of the μ-opioid receptor (MOR) (MOR has less response to stimuli), the impairment of the cell communication of MOR, the changes in brain systems that interact with neurons sensitive to μ-opioid, and the activation of supporting cells in the brain known as glial cells.[9][10]
In the sudden discontinuation or reduced dose of opioids like morphine, physiological responses occur in response to the decreased occupancy of the μ-opioid receptor (MOR), thus producing signs and symptoms of morphine withdrawal.[9]
The withdrawal from various opioid medications, including morphine, causes similar effects, most of which is caused by stimulation and over-stimulation of the central nervous system.[11][4] The effects of morphine withdrawal can range from gastrointestinal disturbances to symptoms like tremors (involuntary shaking, most commonly in hands), opioid cravings, anxiety and insomnia.[12][13] While morphine withdrawal is not fatal, patients in withdrawal may experience anxiousness, fear and become difficult to manage.[14]
The onset of withdrawal symptoms varies with the duration of action of the medication. For short-acting morphine (morphine with short duration of action), withdrawal symptoms begin 8 to 24 hours after the last dose and persist for 4 to 10 days. For long-acting morphine (morphine with long duration of action), withdrawal symptoms begin 12 to 48 hours after the last dose and persist for 10 to 20 days.[14]
Withdrawal from opioids such as morphine also leads to a extended withdrawal phase.[14] It persists for up to half a year, and is categorised by a strong craving for opioids and a decline in well-being.[14]
There is no test to diagnose for morphine withdrawal.[4] However, a toxicology test using urine is conducted to determine if withdrawal symptoms are caused by other non-opioid drugs or a combination of both.[4] In addition, heart tests such as an electrocardiography (ECG), or blood tests such as complete blood count (CBCs) are also conducted.[4]
The severity of a patient in withdrawal can be estimated based on scales such as the Short Opioid Withdrawal Scale and the Clinical Opiate Withdrawal Scale (COWS) . Patients with mild withdrawal are given medicine for symptomatic relief, while patients suffering from more severe withdrawal are given medications against opioids dependence.
Monitoring of patients’ symptoms and complications from morphine withdrawal should be done 3 to 4 times a day.[14] Monitoring and subsequent management can be determined via the Short Opiate Withdrawal Scale or the Clinical Opioid Withdrawal Scale.[14][4]
The scores obtained from the scales vary based on the current symptoms a person with morphine withdrawal is suffering from, where different severities of withdrawal are identified based on these scores along with the respective treatment strategies. For the Short Opiate Withdrawal Scale, a score of 0-10 indicates mild withdrawal, while 10-20 indicates moderate withdrawal, and 20-30 indicates severe withdrawal.[14] Patients with mild withdrawal are given medications based on symptoms experienced.[14] Patients with moderate withdrawal are given medications for symptomatic relief or medications against opioid dependence like opioid agonists (buprenorphine, methadone) and clonidine.[14] Patients with severe withdrawal are given medication against opioid dependence.[14][11] Apart from the methods above, patients may also choose to simply stop the opioid (“cold-turkey”).[11]
Buprenorphine is an FDA approved medication that can be prescribed in clinics to treat opioid dependence.[16][14] It is a partial agonist to opioids, which means it can partially activate the opioid receptors, as it mimics the structure of thebaine, another drug in the opium family found in the opium poppy.[17] It is used as a low-potency substitute (comparatively weak) to treat dependency to more-potent opioids such as morphine and heroin, and functions by alleviating withdrawal symptoms and cravings to opioids.[17][16] Naloxone, a drug that blocks the opioid receptors, may be added to the medication regimen to avoid misuse of Buprenorphine.[16] Under the Mainstreaming Addiction Treatment (MAT) Act, Buprenorphine is prescribed in events of Opioid misuse.[4]
Methadone is an opioid agonist also used to treat opioid dependence. Similar to Buprenorphine, methadone reduces cravings to opioids and symptoms of withdrawals.[18] It also has detoxifying effects against morphine.[18] However, as it is a full agonist and not a partial agonist like Buprenorphine, it has addictive properties. While it is addictive, it is an effective treatment to opioid dependency under medical supervision.[18] Methadone is also included in the WHO’s list of essential medicines.[18]
While Opioid agonists and partial agonists are safe and efficacious, they should be used carefully to minimize unwanted side effects.[16][19] For example, buprenorphine should be used in caution if the patient has diabetes, respiratory problems or urethral obstruction, while methadone should be used in caution if the patient has problems such as respiratory problems and severe hepatic impairment.[19][16] Furthermore, the dose and frequency of dosage of both buprenorphine and methadone should be altered based on symptomatic control and degree of morphine use.[14][16][19]
Clonidine is an alpha-2 adrenergic agonist primarily used in the treatment of hypertension.[20] Additionally, it has several off-label uses (use of a drug for purpose different than what it is approved for), one being the management of symptoms due to opioid withdrawal.[20][14] While it can alleviate symptoms mentioned above, it can also lead to drowsiness and low blood pressure.[14] Clonidine is only prescribed if the patient has a measured heart rate greater than 50bpm or a blood pressure greater than 90/50mmHg, and does not show a drop in blood pressure after initial administration of clonidine.[14]
In addition to drug therapy, psychosocial intervention is also used to reduce the relapse of morphine addiction.[14] Some interventions are given below based on the severity of morphine dependence.
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