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To date, three groups of iGluRs classified according to the affinity of their specific agonists are known: N-methyl-D-aspartate (NMDA), -amino-3-hydroxy-5-methyl-4-isoxazole (AMPA), and kainic acid receptors [16] (Fig
R.MagerS
& Bryant, S
10.3390/ijms25073985 62 KnaussH
doi: 10.1152/ajpregu.00565.2004
The peptide's reduced binding to IGFBPs allows greater bioavailability and more sustained receptor activation, making it particularly effective for accelerating cell growth in laboratory applications
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