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uridine diphosphate/stroke

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Oral administration of circulating precursors for membrane phosphatides can promote the synthesis of new brain synapses.

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Although cognitive performance in humans and experimental animals can be improved by administering omega-3 fatty acid docosahexaenoic acid (DHA), the neurochemical mechanisms underlying this effect remain uncertain. In general, nutrients or drugs that modify brain function or behavior do so by

Synthesis and Ability of New Ligands for G Protein-Coupled Receptors 17 (GPR17).

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GPR17 is believed to be a novel target for the development of new therapeutic approaches to human stroke and multiple sclerosis. Hence, the selection of GPR17 ligands may be a potent way to reduce the progression of ischemic damage. New potential ligands for GPR17, mono-, di-, and triphosphate
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