Daily and seasonal rhythms in endocrine, physiological, and behavioral processes arc a fundamental feature of all living organisms reflecting a need to ensure that, biological functions occur at a given time of the day or year. The most obvious example is the fact, that many animals arc active only during the hours of daylight (diurnal species; human belong to this group) or the hours of darkness

(nocturnal species), and are inactive during the other part of the day (sleep-wake cycle). Other rhythms, like hibernation, fur color changes, and migration, can also be given as examples. In human, disruptions of rhythmicity are characteristic Inhibitors,research,lifescience,medical of, and may underlie, a variety of disorders. For example, sleep and circadian Inhibitors,research,lifescience,medical rhythms are often disrupted in neurological disorders, and increasing evidence indicates that alterations in the sleep-wake cycle accompany such neurological disorders. Moreover, delayed synchronization to local

time (jet lag) or with rotation of shift work is associated with general malaise (especially insomnia), a reduction in productivity at work, and an increase in numbers of accidents. The challenge for GABA Receptor inhibitor scientists is to understand the functional mechanisms involved and to develop strategies to control or treat such disorders (eg, to accelerate resynchronization to new work schedules or to treat endogenous depression or sleep disorders). Inhibitors,research,lifescience,medical The mechanism used for the daily or seasonal organization of functions is far from being well understood. Today, however, we know that this mechanism is built around three key components: (i) photoreceptors registering and transmitting environmental Inhibitors,research,lifescience,medical light cues; (ii) “clocks” that generate rhythms with a period of about 24 h and are capable of being entrained to exactly 24 h, especially by the light-dark (LD) cycle; and (iii) endocrine and neuroendocrine effectors receiving signals from the clock and translating them into Inhibitors,research,lifescience,medical a hormonal or neurohormonal response. Over the past, few years, the huge surge in molecular biology has led to the identification of several clock genes

(Perl, Perl, Per3, Clock, BMAL1, Cry1, Cry2, and Caseine kinase ε). These findings led to a molecular model of circadian oscillations based on two interlocking transcriptional/translational feedback loops.1,2 The timing information built into the clock, via nervous and endocrine pathways, is forwarded Urease to specialized structures. Among these structures is the pineal gland, which secretes the hormone melatonin (MEL), whose role and mechanisms of action will be analyzed in this review. Synthesis and production of melatonin In 1917, McCord and Allen reported that bovine pineal extracts were potent frog skin lightening factors.3 In 1958, Lerner et al isolated the agent responsible for the observed aggregation of melanophores, N-acetyl-5-methoxytryptamine, and termed it. melatonin.