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It has not been linked to any notable side effects or toxicity, whether applied topically or via subcutaneous injection
after reconstitution store at 2-8C and protect from light
Oral research-planning ranges are usually higher than the subcutaneous ranges to account for lower absorption across the gut lining
The proposed mechanism involves controlling glutamate release in the synaptic cleft, modulating NMDA receptor stimulation, affecting excitatory amino acid transporter (EAAT)-mediated reuptake, and maintaining the glutamate/glutamine cycle within astrocytes
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