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. 2021 Jun 22;26(11):6394–6410. doi: 10.1038/s41380-021-01166-2

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© The Author(s) 2021

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 8 — BACE1 inhibition or deficiency causes reduction in distributed of synaptic vesicles to the active zone. This causes less number of glutamate (Glu) released from these exocytosis, and weaker activation of NMDA and AMPA receptors on the postsynaptic membranes. mGluR1 PAM counteracts such a reduction by inducing more calcium (Ca²⁺) release through G-coupled receptor G_q-PLC-IPs pathway.