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Nortriptyline chemical structure
Nortriptyline

3-(10,11-dihydro-5H-dibenzo[a,d] cyclohepten-5-ylidene)- N-methyl-1-propanamine
IUPAC name
CAS number
72-69-5
ATC code

N06AA10

PubChem
4543
DrugBank
APRD00602
Chemical formula {{{chemical_formula}}}
Molecular weight 263.377 g/mol
Bioavailability well absorbed
Metabolism Hepatic
Elimination half-life 16 and 90 hours
Excretion Renal
Pregnancy category C
Legal status Rx-only
Routes of administration oral

Nortriptyline is a second generation tricyclic antidepressant marketed as the hydrochloride under the tradenames Aventyl®, Pamelor® and Nortrilen®. It is used in the treatment of depression and childhood nocturnal enuresis (bedwetting). In addition it is sometimes used for chronic pain modification and labile affect in some neurological conditions.

Clinical pharmacology[]

Nortriptyline inhibits the reuptake of serotonin, and, to a lesser extent, norepinephrine (noradrenalin) (Basic & Clinical Pharmacology, 10th Edition, Bertram G. Katzung, MD, PhD). Operant conditioning techniques in rats and pigeons suggest that nortriptyline has a combination of stimulant and depressant properties.

Indications[]

FDA-approved for treatment of depressive disorders. In the United Kingdom also may be used for treating nocturnal enuresis with courses of treatment lasting no more than three months. Also used off-label for the treatment of panic disorder, irritable bowel disease, prevention of migraine headaches and chronic pain or neuralgia modification (particularly Temporomandibular joint disorder).[1] It can also aid in quitting smoking with one study showing a six-month abstinence rate of 14% for subjects receiving nortriptyline compared to 3% for subjects not undergoing pharmacological treatment.[2]

Metabolism[]

Nortriptyline is metabolised in the liver by hepatic enzyme CYP2D6. Approximately 7 to 10 percent of Caucasians are poor metabolisers and might experience more adverse effects, so a lower dosage is often necessary in these individuals.[How to reference and link to summary or text] Blood levels of nortriptyline should be obtained during long term treatment to avoid toxicity and optimise response.

Dosage[]

For depression: low starting doses are used, increasing as necessary to 75–100mg (0–50mg for adolescents and the elderly). Maximum daily dosage is 150mg.[3]

For the management of noctiral enuresis: lower dosages are used with the maximum period of treatment, including gradual withdrawal, being three months and a full examination including electrocardiogram (ECG or EKG) required before further courses.[3]

For its off-label use for migraine and headache prophylaxis and treating chronic pain: treatment is started at very low 10mg once at night to minimise side-effects. The dose is then increased every two weeks if required to a maximum of 50mg.

Side effects[]

Dry mouth, drowsiness, orthostatic hypotension, urinary retention, constipation, and rapid or irregular heartbeat. Some sexual side effects may be a problem as well. Less commonly, seizures and ECG/EKG changes have been reported, especially in overdose.

Alcohol may exacerbate some of its side effects and should be avoided.

However, the incidence of side effects with nortriptyline is somewhat lower than with the first generation tricyclics (e.g. imipramine (Tofranil®), amitriptyline (Elavil®)).

Warnings[]

Closer monitoring is required for those with a history of cardiovascular disease, stroke, glaucoma and/or seizures as well as those who have hyperthyroidism or are receiving thyroid medication.

Contraindications[]

In the acute recovery phase after myocardial infarction (e.g. heart attack). As for all tricyclic antidepressants concurrent use, or failure to allow a two week gap, with monoamine oxidase inhibitors (MAO inhibitors, e.g. phenelzine, tranylcypromine, etc.) may precipitate hyperpyretic crises and/or severe convulsions; fatalities have occurred.

Overdose[]

Main article: Tricyclic antidepressant

The symptoms and the treatment of an overdose are largely the same as for the other tricyclic antidepressants.

References[]

  1. (2002) Sweetman SC Martindale. The complete drug reference, 33, Pharmaceutical Press. ISBN 0-85369-499-0.
  2. Prochazka A, Weaver M, Keller R, Fryer G, Licari P, Lofaso D (1998). A randomized trial of nortriptyline for smoking cessation.. Arch Intern Med 158 (18): 2035-9. PMID 9778204.
  3. 3.0 3.1 British National Formulary 45 March 2003

Further reading[]

  • Alexanderson, B., Evans, D. A., & Sjoqvist, F. (1969). Steady-state plasma levels of nortriptyline in twins: Influence of genetic factors and drug therapy: BMJ: British Medical Journal Vol 4(5686) Dec 1969, 764-768.
  • Alexanderson, B., Price Evans, D. A., & Sjoqvist, F. (1969). Steady-state plasma levels of nortriptyline in twins: Influence of genetic factors and drug therapy: BMJ: British Medical Journal Vol 4(5686) Dec 1969, 764-768.
  • Ambrosini, P. J., Bianchi, M. D., Metz, C., & Rabinovich, H. (1994). Evaluating clinical response of open nortriptyline pharmacotherapy in adolescent major depression: Journal of Child and Adolescent Psychopharmacology Vol 4(4) Win 1994, 233-244.
  • Angelico, P., Ibba, M., Abbiati, G. A., & Testa, R. (1986). Different effects of nortriptyline on electroconvulsive shock and footshock-induced analgesia in rats: IRCS Medical Science: Psychology & Psychiatry Vol 14(1-2) Jan-Feb 1986, 126-127.
  • Appioti, A., & et al. (1974). The combination of nortriptyline and fluphenazine in the treatment of the depression-anxiety syndrome: Rivista di Psichiatria Vol 9(4) Jul-Aug 1974, 346-363.
  • Apter, J. T., Kushner, S. F., & Woolfolk, R. L. (1994). Bupropion/nortriptyline combination for refractory depression: Annals of Clinical Psychiatry Vol 6(4) Dec 1994, 255-258.
  • Atkinson, J. H., Slater, M. A., Williams, R. A., Zisook, S., Patterson, T. L., Grant, I., et al. (1998). A placebo-controlled randomized clinical trial of nortriptyline for chronic low back pain: Pain Vol 76(3) Jun 1998, 287-296.
  • Austin, L. S., Arana, G. W., & Ballenger, J. C. (1990). Rapid response of patients simultaneously treated with lithium and nortriptyline: Journal of Clinical Psychiatry Vol 51(3) Mar 1990, 124-125.
  • Baumann, P., Jonzier-Perey, M., Koeb, L., Le, P. K., & et al. (1986). Amitriptyline pharmacokinetics and clinical response: I. Free and total plasma amitriptyline and nortriptyline: International Clinical Psychopharmacology Vol 1(2) Apr 1986, 89-101.
  • Beaglehole, B., Luty, S. E., Mulder, R. T., Kennedy, M. A., & Joyce, P. R. (2007). Low red cell folate levels are associated with poor response to nortriptyline in major depression: Acta Neuropsychiatrica Vol 19(3) Jun 2007, 204-207.
  • Bebchuk, J. M., & Stewart, D. E. (1991). Drug interaction between rifampin and nortriptyline: A case report: International Journal of Psychiatry in Medicine Vol 21(2) 1991, 183-187.
  • Behnke, K., Mejer-Nielsen, B., Korner, A., Arup, P., & et al. (1992). Rolipram versus nortriptyline in gerontopsychiatric inpatients with major depression: Nordic Journal of Psychiatry Vol 46(6) 1992, 407-411.
  • Benazzi, F. (1997). Venlafaxine-fluoxetine-nortriptyline interaction: Journal of Psychiatry & Neuroscience Vol 22(4) Jul 1997, 278-279.
  • Berger, A., Dukes, E., Edelsberg, J., Stacey, B., & Oster, G. (2007). Use of Tricyclic Antidepressants in Older Patients With Diabetic Peripheral Neuropathy: Clinical Journal of Pain Vol 23(3) Mar-Apr 2007, 251-258.
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External links[]


Antidepressants (ATC N06A) edit
Monoamine oxidase inhibitors (MAOI) Harmaline, Iproclozide, Iproniazid, Isocarboxazid, Nialamide, Phenelzine, Selegiline, Toloxatone, Tranylcypromine
Reversible inhibitor of monoamine oxidase A (RIMA) Brofaromine, Moclobemide
Dopamine reuptake inhibitor (DARI) Amineptine, Phenmetrazine, Vanoxerine, Modafinil
Norepinephrine-dopamine reuptake inhibitors Bupropion
Norepinephrine reuptake inhibitor (NRI) or (NARI) Atomoxetine, Maprotiline, Reboxetine, Viloxazine
Serotonin-norepinephrine reuptake inhibitor (SNRI) Duloxetine, Milnacipran, Venlafaxine
Selective serotonin reuptake inhibitor (SSRI) Alaproclate, Etoperidone, Citalopram, Escitalopram, Fluoxetine, Fluvoxamine, Paroxetine, Sertraline, Zimelidine
Selective serotonin reuptake enhancer (SSRE) Tianeptine
Tricyclic antidepressants (TCA) Amitriptyline, Amoxapine, Butriptyline, Clomipramine, Desipramine, Dibenzepin, Dothiepin, Doxepin, Imipramine, Iprindole, Lofepramine, Melitracen, Nortriptyline, Opipramol, Protriptyline, Trimipramine
Tetracyclic antidepressants Maprotiline, Mianserin, Nefazodone, Trazodone
Noradrenergic and specific serotonergic antidepressant (NaSSA) Mirtazapine
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