Nutrients, Vol. 18, Pages 1558: Blueberry Bagasse-Enriched Whey Fermented Formulations: Effect of Incorporation Timing on Functional Properties and Neurobiological Evaluation in a Murine Model Using a Selected Formulation

Nutrients, Vol. 18, Pages 1558: Blueberry Bagasse-Enriched Whey Fermented Formulations: Effect of Incorporation Timing on Functional Properties and Neurobiological Evaluation in a Murine Model Using a Selected Formulation

Nutrients doi: 10.3390/nu18101558

Authors:
Tlalli Uribe-Velázquez
Alejandra Hurtado-Romero
Juliana Marisol Godínez-Rubí
Oscar Kurt Bitzer-Quintero
Javier Ramírez-Jirano
Félix Tadeo Ortiz-Sánchez
Jhonathan Cárdenas-Bedoya
Pablo Quintero-Gutiérrez
Iván Luzardo-Ocampo
Angélica Lizeth Sánchez-López
Luis Eduardo García-Amezquita
Danay Carrillo-Nieves
Tomás García-Cayuela

Background: Mental health disorders are a major global public health challenge. Psychobiotics have emerged as a promising strategy to modulate the microbiota–gut–brain axis. Whey and blueberry bagasse are agro-industrial by-products with potential for functional fermented matrices. Objective: To develop whey biotic blend (WBB) formulations enriched with blueberry bagasse and evaluate the impact of incorporation timing on functional properties, and to explore the neurobiological effects of a selected formulation. Methods: Three WBB formulations were prepared with Lactiplantibacillus plantarum 299v and PS128, differing in the timing of blueberry bagasse incorporation: Control, WBB-Before, and WBB-After. Physicochemical properties, microbial viability, composition, γ-aminobutyric acid (GABA), phenolic profile, and antioxidant and anti-inflammatory capacities were evaluated. Based on these results, WBB-After was selected as the sole formulation and advanced for testing in a lipopolysaccharide (LPS)-induced murine model. Results: All formulations supported probiotic growth (>8.6 log CFU/mL). Blueberry bagasse incorporation significantly influenced functional properties. WBB-After showed ~2.1-fold higher total phenolic content than WBB-Before and enrichment in anthocyanins and hydroxycinnamic acids, with higher antioxidant (≈24% by DPPH) and anti-inflammatory potential (≈19%), whereas WBB-Before exhibited ~20% higher GABA levels. In vivo, WBB-After showed improved recognition performance under baseline conditions (Control vs. WBB), although the overall group effect was marginal. No significant differences were observed in hippocampal cytokines or neuronal integrity markers under LPS-induced inflammation. Conclusions: The timing of blueberry bagasse incorporation shapes WBB functional properties. The selected formulation showed limited neurobiological effects under the evaluated in vivo conditions, highlighting the need for further studies.

​Background: Mental health disorders are a major global public health challenge. Psychobiotics have emerged as a promising strategy to modulate the microbiota–gut–brain axis. Whey and blueberry bagasse are agro-industrial by-products with potential for functional fermented matrices. Objective: To develop whey biotic blend (WBB) formulations enriched with blueberry bagasse and evaluate the impact of incorporation timing on functional properties, and to explore the neurobiological effects of a selected formulation. Methods: Three WBB formulations were prepared with Lactiplantibacillus plantarum 299v and PS128, differing in the timing of blueberry bagasse incorporation: Control, WBB-Before, and WBB-After. Physicochemical properties, microbial viability, composition, γ-aminobutyric acid (GABA), phenolic profile, and antioxidant and anti-inflammatory capacities were evaluated. Based on these results, WBB-After was selected as the sole formulation and advanced for testing in a lipopolysaccharide (LPS)-induced murine model. Results: All formulations supported probiotic growth (>8.6 log CFU/mL). Blueberry bagasse incorporation significantly influenced functional properties. WBB-After showed ~2.1-fold higher total phenolic content than WBB-Before and enrichment in anthocyanins and hydroxycinnamic acids, with higher antioxidant (≈24% by DPPH) and anti-inflammatory potential (≈19%), whereas WBB-Before exhibited ~20% higher GABA levels. In vivo, WBB-After showed improved recognition performance under baseline conditions (Control vs. WBB), although the overall group effect was marginal. No significant differences were observed in hippocampal cytokines or neuronal integrity markers under LPS-induced inflammation. Conclusions: The timing of blueberry bagasse incorporation shapes WBB functional properties. The selected formulation showed limited neurobiological effects under the evaluated in vivo conditions, highlighting the need for further studies. Read More

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