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Lee, J., Lee, A., Kim, J
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Importantly, Retatrutide monotherapy in non-diabetic rats (R group) produced a significant up-regulation of both BDNF and CREB at the mRNA level, while Retatrutide-treated diabetic rats (STZR) showed an intermediate pattern without significant changes relative to either C or STZ.This profile suggests that Retatrutide can actively modulate BDNF-CREB signalling at the transcriptional level under nondiabetic conditions and may partially counteract diabetesrelated vulnerability, even when clear normalisation is not achieved, consistent with clinical evidence that GLP1 receptor agonists improve cognitive outcomes in patients with type 2 diabetes [31] and with preclinical data demonstrating that GLP[1[based and multi-receptor agonists, including tirzepatide, strengthen the BDNF-TrkB-CREB axis and protect against neurodegeneration [39,40]
