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Selection should reflect the reason for supplementation, product quality, tolerance and route-related risk

[Nephrotoxicity induced by chemotherapy]

In our study, we found that the increased A plaques firstly appeared in the cortex and hippocampus of earlier 8-week ethanol exposed APP/PS1 mice (in both 2BC and IP paradigms), and no A plaque was found even after 10 weeks ethanol exposure in WT mice, suggesting that chronic ethanol exposure did not directly result in A plaques but accelerate the A deposition

D-Ala substitution provided dual benefits: modest intrinsic potency enhancement (3-fold) plus protection against DPP-IV degradation