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Imipramine
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| Systematic (IUPAC) name | |
| 3-(5,6-dihydrobenzo[b][1]benzazepin-11-yl)-N,N-dimethylpropan-1-amine | |
| Identifiers | |
| CAS number | |
| ATC code | N06 |
| PubChem | |
| DrugBank | |
| Chemical data | |
| Formula | C19H24N2 |
| Mol. mass | 280. IUPAC Nomenclature is a system of naming Chemical compounds and of describing the science of Chemistry in general CAS registry numbers are unique numerical identifiers for Chemical compounds Polymers biological sequences mixtures and Alloys They are also referred to The Anatomical Therapeutic Chemical Classification System is used for the classification of drugs It is controlled by the WHO Collaborating Centre for Drug A section of the Anatomical Therapeutic Chemical Classification System containing Psychoanaleptics. PubChem is a Database of chemical Molecules The system is maintained by the National Center for Biotechnology Information (NCBI a component The DrugBank database available at the University of Alberta is a unique Bioinformatics and Cheminformatics resource that combines detailed drug (i A chemical formula is a way of expressing information about the Atoms that constitute a particular Chemical compound, and how the relationship between those atoms changes Carbon (kɑɹbən is a Chemical element with the symbol C and its Atomic number is 6 Hydrogen (ˈhaɪdrədʒən is the Chemical element with Atomic number 1 Nitrogen (ˈnaɪtɹəʤɪn is a Chemical element that has the symbol N and Atomic number 7 and Atomic weight 14 The molecular mass (abbreviated m of a substance, more commonly referred to as molecular weight and abbreviated as MW, is the Mass of one 407 |
| Pharmacokinetic data | |
| Bioavailability | ? |
| Metabolism | Hepatic Main active metabolite desipramine |
| Half life | 11-25 hours |
| Excretion | Renal |
| Therapeutic considerations | |
| Pregnancy cat. |
D(US) |
| Legal status |
℞ Prescription only |
| Routes | Oral |
Imipramine (sold as Antideprin, Deprenil, Deprimin, Deprinol, Depsonil, Dynaprin, Eupramin, Imipramil, Irmin, Janimine, Melipramin, Surplix, Tofranil) is an antidepressant medication, a tricyclic antidepressant of the dibenzazepine group. The regulation of therapeutic goods, that is drugs and therapeutic devices, varies by jurisdiction In Pharmacology and Toxicology, a route An antidepressant is a Psychiatric medication used for alleviating major depression or Dysthymia ('milder' depression Medication, also referred to as medicine, can be loosely defined as any substance intended for use in the diagnosis cure mitigation treatment or prevention of disease Tricyclic antidepressants (abbreviation TCAs) are a class of Antidepressant drugs first used in the 1950s Benzazepines are Heterocyclic compounds consisting of a Benzene ring fused to an Azepine ring Imipramine is mainly used in the treatment of clinical depression and enuresis. Major depressive disorder, also known as major depression, unipolar depression, unipolar disorder, clinical depression, or simply depression Urinary incontinence ( UI) is any involuntary leakage of Urine.
Imipramine was, in the late 1950s, the first tricyclic antidepressant to be developed (by Ciba-Geigy). Initially, it was tried against psychotic disorders (e. g. schizophrenia), but proved insufficient. Imipramine is in fact well known to induce and exacerbate psychosis. During the clinical studies its antidepressant qualities were unsurpassed by other antidepressants. To this day, Imipramine is often considered the "Gold Standard" antidepressant as its ability to lift even the most severe depressive episodes is unsurpassed. Not surprisingly, Imipramine is also known to cause a high rate of manic and hypomanic reactions, especially in patients with preexisting bipolar disease. It is in fact estimated that up to 25% of such patients maintained on Imipramine will switch into mania or hypomania. (http://www.springerlink.com/content/616mb0cndr4ddb42/) Such powerful antidepressant properties have made it favorable in the treatment of TRD, or "Treatment Resistant Depression" and many sufferers have seen positive results from Imipramine.
At the advent of SSRIs, its sometimes intolerable side effect profile became evident. Selective serotonin reuptake inhibitors ( SSRIs) are a class of Antidepressants used in the treatment of depression, Anxiety disorders Subsequently, it was extensively used as a standard antidepressant and later served as a prototypical drug for the development of the later released tricyclics. It is not as commonly used today, but is sometimes used to treat major depression as a second-line treatment. It has also seen limited use in the treatment of migraines, ADD and post concussive syndrome. Migraine is a neurological Syndrome characterized by altered bodily experiences painful headaches and nausea Attention-Deficit Hyperactivity Disorder (ADHD is a neurobehavioral developmental disorder affecting about 3-5% of the world's population Post-concussion syndrome, also known as postconcussive syndrome or PCS, is a set of symptoms that a person may experience for weeks months or occasionally years Imipramine has additional indications for the treatment of panic attacks, chronic pain, and Kleine-Levin syndrome. Panic attacks are sudden discrete periods of intense anxiety mounting Physiological arousal fear stomach problems and discomfort that are associated with a variety of Chronic pain is defined as Pain that persists longer than the temporal course of natural healing associated with a particular type of injury or disease process Kleine-Levin Syndrome, or KLS is a rare disorder characterized by the need for excessive amounts of sleep ( Hypersomnia) (e In pediatric patients it is relatively frequently used to treat pavor nocturnus and nocturnal enuresis. A night terror, also known as pavor nocturnus, is a Parasomnia disorder characterized by extreme terror and a temporary inability to regain full consciousness Bedwetting is involuntary Urination while asleep after the age at which bladder control would normally be anticipated
Imipramine, a tertiary amine, affects numerous neurotransmitter systems know to be involved in the etiology of depression, anxiety , ADD/ADHD, enuresis and numerous other mental and physical conditions. Amines are Organic compounds and Functional groups that contain a basic Nitrogen Atom with a Lone pair. Imipramine is similar in structure to some muscle relaxants, and has a significant analgesic effect and thus is very useful in some pain conditions.
The mechanisms of Imipramine's medicinal action all include, but are not limited to effects on; norepinephrine, serotonin, dopamine, epinephrine, opiates, enkephalinase, histamine, muscarine, and acetylcholine. Norepinephrine ( INN) (abbreviated norepi or NE) or noradrenaline ( BAN) (abbreviated NA or NAd) is a Serotonin (ˌsɛrəˈtoʊnən ( 5-hydroxytryptamine, or 5-HT) is a Monoamine Neurotransmitter synthesized in serotonergic Neurons Dopamine is a Hormone and Neurotransmitter occurring in a wide variety of animals including both vertebrates and invertebrates For other uses see Opiate (disambiguation, or for the class of drugs see Opioid. Histamine is a Biogenic amine involved in local immune responses as well as regulating physiological function in the gut and acting as a Neurotransmitter Muscarine, L-(+-muscarine, or muscarin is a natural product found in certain Mushrooms particularly in Inocybe The Chemical compound acetylcholine (often abbreviated ACh) is a Neurotransmitter in both the Peripheral nervous system (PNS and Central
Effects on;
Norepinephrine(NE) -Reuptake inhibition (strong).
Serotonin(SE) -Reuptake inhibition (moderate to strong). The reuptake inhibition is almost comparable but still less than Imipramine's potency of reuptake inhibition on norepinephrine. Stronger SERT inhibition than most other tricyclic antidepressants, making it more akin to the SSRI class of antidepressents (e. g. Prozac(fluoxetine), Zoloft (sertraline)) than its metabolite desipramine, which has almost purely noradrenergic effects.
Acetylcholine(ACe) Imipramine is an anticholinergic. An anticholinergic agent is a substance that blocks the Neurotransmitter acetylcholine in the central and the Peripheral nervous system. Thus, it is prescribed with caution to the elderly and with extreme caution to those with pyschosis, as the general brain activity enhancement in combination with the "dementing" effects of anti-cholinergices increases the potential of Imipramine to cause hallucinations, confusion and delirium in this population. Imipramine is an antagonist at M2 muscarinic acetylcholine receptors (see external links). The blockade of (cholinergic) muscarine receptors is known to cause euphoria, potentially contributing to the mood lifting effects of Imipramine as well.
Epinephrine Imipramine antagonizes adreno-receptors (II), thus sometimes causing increased heart rate (contributed to by other effects as well), orthostatic hypotentsion, and a general decrease in the responsiveness of the central nervous system (hence, a contribution to its potent anti-anxiety properties).
Dopamine - reuptake and release at D1 and D2 receptors. similar to but less potent than the psychostimulants, dopamine agonists and atypical antidepressant buproprion on dopaminergic mechanisms. (increase in release and blockade of reutpake inhibition). While this effect is much less than the primary effects on NE, SE and ACe, it is non-the-less significant and is partially responsible for the therapeutic benefits of treatment with Imipramine. Enhancement of brain dopamine activity has been implicated in Imipramine's ability to stimulate motor activity and prolong time spent in escape in mice.
Opiates and Enkephalinase - Opiate activity enhancement is thought to contribute to Imiprapmine's analgesic and antidepressant effect, primarily at the sigma receptors. - Imipramine also inhibits the break down of Enkephalinase, an effect lending towards enhanced opiate activity.
Histamine -Imipramine is an antagonist at histamine H1 receptors. This contributes to the acute sedative effect that it has in most people. In turn, its anti-histaminergic and general calming effects take place immediately and thus, Imiparmine is sometimes prescribed as a sleep aid in low doses.
Imipramine is converted to desipramine, another TCA, in the body. Desipramine is a Tricyclic antidepressant (TCA that inhibits the reuptake of Norepinephrine. Tricyclic antidepressants (abbreviation TCAs) are a class of Antidepressant drugs first used in the 1950s
Imipramine should not be given in conjunction with, or within 14 days of treatment with a MAO inhibitor. Tricyclic antidepressants (abbreviation TCAs) are a class of Antidepressant drugs first used in the 1950s Combined therapy of this type could lead to the appearance of serious interactions such as hypertensive crises, hyperactivity, hyperpyrexia, spasticity, severe convulsions or coma and death may occur.
Imipramine is contraindicated in patients with existing severe hepatic or renal damage, and those with a history of blood dyscrasias.
Imipramine is contraindicated in patients who have shown hypersensitivity to the drug or hypersensitivity to tricyclic antidepressants belonging to the dibenzazepine group.
Imipramine is contraindicated for use during the acute recovery phase following a myocardial infarction.
It should not be used in patients with convulsive disorders or glaucoma.
(http://www.mentalhealth.com/drug/p30-t03.html#Head_3)
After taking the medicine this drug may cause some side effects in some patients, particularly with the first few doses.
Isolated cases of pneumonitis (fever, chills, cough, difficulty with breathing, unusual weight loss, feeling sick) have been reported. Pneumonitis is a general term that refers to inflammation of lung tissue A puffy, swollen face, tongue or body has been reported. These reactions may be severe, causing shortness of breath, swelling, shock and collapse. If you develop any allergic symptoms, stop taking the medicine and contact your doctor immediately.
Isolated changes in blood cells. If you notice that you are bruising more frequently or have more nosebleeds or infections you should consult your doctor.
Arrhythmias: Irregular heart rhythms. Dysrhythmia redirects here For the American band see Dysrhythmia (band.
Weight gain has been reported frequently. Disturbances in sexual function have been reported occasionally. Isolated cases of enlarged mammary glands, production or over-production of breast milk, increased or decreased blood sugar levels and weight loss have been reported. Low levels of salt in the blood have been reported, usually in elderly patients, which can be identified by a blood test.
Tremor has been reported frequently. Headache, confusion, orthostatic hypotension (resulting in dizziness upon standing), numbness/tingling, agitation, anxiety, restlessness, mood swings, exaggerated behaviour, delusions and hallucinations have been reported occasionally and are more common in the elderly or in patients on high doses. Aggressiveness, weakness, lack of co-ordination, sudden muscle spasms, difficulty speaking have been reported in isolated cases.
Imipramine also enhances the CNS effects of both stimulants and alcohol, and blocks the parasympathomimetic effects of stimulants while enhancing the cortical excitation. This can be dangerous in some cases and result in seizures and coma.
Ringing or buzzing in the ears have been reported.
Feeling or being sick and loss of appetite have been reported occasionally. Isolated cases of tongue lesions and inflammation of the mucus membranes in the mouth have been reported. Extreme dry mouth or "cotton mouth" has been reported. Mild to severe constipation has also been reported.
Changes in liver function have been reported occasionally. This would be identified by a blood test. Hepatitis and jaundice (yellowing of the skin and/or whites of the eyes) have been reported in isolated cases. Hepatitis (plural hepatitides) implies injury to the Liver characterized by the presence of Inflammatory cells in the tissue of Jaundice, also known as icterus (attributive adjective "icteric" is yellowish discoloration of the Skin, sclerae (whites of the eyes
Allergic reactions such as an itchy skin rash have been reported occasionally. Isolated cases of swelling, sensitivity to the sun or sun lamps, hair loss, small purple red spots and itching have been reported.
If the medicine is stopped too quickly, there is the possibility the user may suffer from feeling or being sick, stomach pains, diarrhea, headache, sleeplessness, nervousness, anxiety, irritability and increased sweating.
The symptoms and the treatment of an overdose are largely the same as for the other tricyclic antidepressants. Tricyclic antidepressants (abbreviation TCAs) are a class of Antidepressant drugs first used in the 1950s Cardinal symptoms are cardiac (tachycardia, widened QRS complex) and neurological disturbances. Any ingestion by children should be considered as serious and potentially fatal.