Journal of Pineal Research · 1994 · 251 citations · 8 references
Life SciencesBiochemistryPharmacologyHormone BiochemistryNeurochemistryNeuroendocrinologyDrug SolubilityHormone Binding ProteinsCell Membrane BindingHydrophilicityHydrophilicity EffectsMelatonin PhysiologyMembrane HydrophilicityMembrane Receptor RecognitionPineal Gland FunctionPineal Gland Physiology
The pineal hormone melatonin (5-methoxy-N-acetyl-tryptamine) has been reported to participate in important physiological processes. Although some of its biological actions seem to depend on a protein receptor at the membrane surface, melatonin is known to interact with a large variety of tissues and cells, suggesting that the molecule may not necessarily interact through a specific membrane receptor at a specific cell. Most discussions of melatonin activity have assumed that the molecule is highly hydrophobic. Contrary to belief, the present work shows that melatonin is soluble in a purely aqueous medium up to 5 x 10(-3) M and describes a new method of melatonin preparation which shows the high hydrophilicity of the molecule. The results presented will affect the current biological hypothesis on the need of a melatonin carrier in the blood stream or the mechanisms which allow the hormone to cross the cell membrane and interact at the level of the nucleus.
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