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CNS Pharmacology

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Question:

Ramelteon

Author: Suzuki



Answer:

Ramelteon is a selective agonist at the MT1 and MT2 subtypes of melatonin receptors. Normally, light stimulating the retina transmits a signal to the suprachiasmatic nucleus (SCN) of the hypothalamus that, in turn, relays a signal via a lengthy nerve pathway to the pineal gland that inhibits the release of melatonin from the gland. As darkness falls and light ceases to strike the retina, melatonin release from the pineal gland is no longer inhibited, and the gland begins to secrete melatonin. Stimulation of MT1 and MT2 receptors by melatonin in the SCN is able to induce and promote sleep and is thought to maintain the circadian rhythm underlying the normal sleep–wake cycle. Ramelteon is indicated for the treatment of insomnia in which falling asleep (increased sleep latency) is the primary complaint.


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Suzuki
Suzuki