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Melatonin and Melatonin Receptors in Neuroprotection

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Melatonin, Neuroprotective Agents and Antidepressant Therapy

Abstract

Melatonin (Mel) is a neurohormone which is synthesized from tryptophan with the activation of beta-adrenergic receptors of the pineal gland [2, 11, 36]. It is chemically known as N-acetyl-5-methoxytryptamine [1]. The main task of this hormone is adjusting the rhythm of the body and protecting the biological clock of the body. Also, it has a role in many biological and physiological processes in the body [11, 34, 58]. At this point, apart from the protection of the tissues by preventing the lipid peroxidation [8, 33], Mel is directly a free radical scavenger, and it is stronger than all known antioxidants by this effect [1, 55] as having a neuroprotective effect mechanism [2, 69]. Also, Mel shows tissue protective effect by increasing antioxidant enzyme levels or inhibiting pro-oxidative enzymes through receptors [49]. With this perspective, this chapter of the book reviews the therapeutic effects of Mel and Mel receptors in neuroprotection.

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Deniz, O.G., Turkmen, A.P., Onger, M.E., Altunkaynak, B.Z., Kaplan, S. (2016). Melatonin and Melatonin Receptors in Neuroprotection. In: López-Muñoz, F., Srinivasan, V., de Berardis, D., Álamo, C., Kato, T. (eds) Melatonin, Neuroprotective Agents and Antidepressant Therapy. Springer, New Delhi. https://doi.org/10.1007/978-81-322-2803-5_5

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