Synthetic melatonin is a dietary supplement. The FDA does not regulate supplements. Therefore, melatonin is not officially FDA-approved for any indication. However, there are several melatonin receptor agonists on the market, such as ramelteon and tasimelteon, which are FDA-approved for treatment of insomnia.
Non-FDA Approved Indications for Melatonin
Despite the lack of FDA approval, melatonin is considered first-line pharmacologic therapy for the treatment of insomnia by the American Academy of Family Physicians (AAFP). It is relatively safe with a low risk of side effects.
Studies on the efficacy of melatonin supplementation for treatment of insomnia have varied, but one metanalysis by Ferracioli-Oda showed that subjects taking melatonin fell asleep an average of 7 minutes faster, stayed asleep about 8 minutes longer, and reported better sleep quality than subjects receiving a placebo. Doses used, results, and study quality varied considerably between trials.
Other Ongoing Research
Although there are no formal recommendations at this time, research is also being conducted on the role of melatonin treatment for other conditions, such as:
Synthesis of Endogenous Melatonin
Endogenous melatonin is a hormone produced naturally by the body, synthesized and secreted primarily in the pineal gland. Melatonin production begins with tryptophan, which is converted via a several-step pathway to serotonin in other parts of the brain. Some of the serotonin produced makes its way to the pineal gland, where it is converted to melatonin in a cyclic, light-dependent process.
The conversion of serotonin to melatonin is controlled by the suprachiasmatic nucleus (SCN) of the hypothalamus, the coordinator of the circadian rhythms of the body. Information about low light to dark condition travels from the retina along the retinohypothalamic tract to the SCN. The SCN, in turn, sends signals through the sympathetic nervous system to the superior cervical ganglia, which innervates the pineal gland.
Sympathetic stimulation of the pineal gland upregulates the production of the enzyme arylalkylamine N-acetyltransferase (AA-NAT). AA-NAT functions to convert serotonin to N-acetyl-serotonin, the rate-limiting step in melatonin formation. This intermediate is then converted to melatonin. Studies have shown that bilateral surgical removal of the superior cervical ganglia or SCN in rats stops the activation of AA-NAT and eliminates the rhythmic pattern of melatonin secretion, which disrupts the sleep-wake cycle.
Functions of Endogenous Melatonin
The best-known purpose of melatonin is its role in the promotion of sleep. Melatonin is released from the pineal gland into the third ventricle, and from there into circulation. Melatonin is involved in the regulation of the body’s sleep-wake cycles through its interactions with the suprachiasmatic nucleus of the hypothalamus and the retina, both promoting sleep and inhibiting wake-promoting signals via interactions with its MT1 and MT2 receptors.
Other Biological Functions of Melatonin Under Study
Melatonin Content of Supplements
Supplements are generally presumed safe and are not regulated by the FDA. However, this can lead to concerns about the actual concentrations of supplements, including melatonin. One study analyzed 31 melatonin supplements and found that actual melatonin content ranged from -83% to +478% of the labeled content. Variable tablet content can make accurate dosing difficult and may be responsible for some of the wide ranges of efficacy reported in various trials. One way to assure correct dosing is to look for supplements with approval from the United States Pharmacopeia, an independent non-profit organization. Searching for supplements marked “USP verified” can help assure quality and dosing of supplements.
Routes of Administration
As the FDA does not regulate melatonin as a drug, effective dosing is not well-defined. Dosing used in studies varied from 0.1 to 10 mg, administered up to two hours before bedtime.
Not defined in trials
One to 2 hours, depending on the formulation
Highly variable, 1% to 74%, likely dependent on formulation and dose
Ninety percent of melatonin is metabolized in the liver primarily by the enzyme CYP1A2. It is metabolized by hydroxylation to 6-Hydroxymelatonin, conjugated to sulfuric or glucuronic acid, and excreted in the urine. A smaller amount is excreted in feces.
Melatonin is relatively non-toxic, although some mild side-effects have been reported with higher doses and extended-release formulations, including:
No evidence suggests that people develop tolerance to melatonin.
Pregnancy and Breastfeeding
Melatonin is not recommended for pregnant or breastfeeding women due to insufficient evidence of safety although this is under study.
Caution is advised for dialysis patients due to the risk of increased adverse effects due to the inability to adequately clear melatonin.
Caution is advised for patients with impaired liver functioning due to decreased ability to metabolize melatonin. Further studies into possible effects versus benefits are pending.
Caution is advised for patients with some autoimmune diseases such as rheumatoid arthritis or post-organ transplant. Melatonin has been shown to stimulate the function of the immune system via the production of interleukins IL-1, IL-2, IL-6, and IL-12, interferon gamma, helper T cells, cytotoxic T cells, B-cell precursors, and T-cell precursors. The clinical significance of this effect is not yet certain.
Insomnia is one of the more frequent complaints seen in both the outpatient and inpatient setting. Melatonin is a safe first-line sleep aid which may help promote a regular sleep cycle. Melatonin is one of the few over the counter supplements that can be recommended for insomnia.
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