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[PMID: 38663923]

Purpose-built for physicians Human, exendin-based GLP-1 receptor agonists similarly reduce CV, renal risk in diabetes A pooled study assessing trials of eight GLP-1 receptor agonists showed all reduce risk for a combined endpoint of major adverse cardiovascular events, regardless of structural homology to human GLP-1, as well as individual CV components

Administered at a dose of 360 mg/kg for 14 days, the extract markedly reduced IBA-1, IL-1, A1-42, and phosphorylated tau (p-tau) levels, highlighting its anti-inflammatory and neuroprotective properties (Wang Y

Fourthly, the profile of gene expression is different in NCs and CLCs, which also opposes the progenitor function status of NCs [72]