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CONCLUSIONS Our findings suggest that the BK-dependent activation of mTORC1 may represent a promising mechanism underlying antidepressant pharmacology. Deciding on their affordability and access, ACEIs may emerge as a novel fast-onset antidepressant, particularly for patients with comorbid depression and hypertension. Is designed to synthesize the evidence of the effectation of small amounts (≤30-g/meal) of fructose and its own epimers (allulose, tagatose, and sorbose) on the postprandial glucose

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