Oral lipoteichoic and lipoic acids improve insulin resistance and body composition in porphyria mice on a high-carbohydrate diet

Acute intermittent porphyria (AIP) is a genetic metabolic disorder characterized by neurovisceral attacks. Although high-carbohydrate diets or intravenous glucose administration can help alleviate incipient attacks in patients, these interventions may also promote insulin resistance and increase metabolic risk. This study explored targeted dietary interventions to manage hyperinsulinemia and to enhance glucose uptake in insulin-sensitive organs under high-carbohydrate diet. Body composition and fecal microbiota profile were also investigated in a murine model of the disease. Wild-type and AIP mice (n = 6/group) were supplemented with tapioca maltodextrin in drinking water for 12 weeks, alongside heat-treated Bifidobacterium animalis subsp. lactis CECT-8145 (BPL1®HT), its by-product lipoteichoic acid (LTA), or the insulin-sensitizing agent α-lipoic acid (α-LA). Liver-targeted therapies, previously assessed in AIP mice, were also included in this study. AIP mice on a high-carbohydrate diet exhibited hyperinsulinemia and tissue-specific differences in glucose uptake compared to wild-type mice. Dysbiosis, marked by reduced fecal Dorea spp. and Adlercreutzia muris, alongside higher abundance of Escherichia coli, was also showed. Supplementation with α-LA and LTA revealed superior ability to improve glucose tolerance test and skeletal muscle glucose uptake, reduce hyperinsulinemia, and enhance body composition by increasing lean mass relative to fat, compared to gene therapy or liver-targeted insulin administration. Notably, LTA restored fecal microbiota profiles resembling those of wild-type mice. In conclusion, supplementation with LTA from BPL1®HT and α-LA may represent promising dietary interventions to manage glucose tolerance, improve insulin sensitivity in muscle and adipose tissues, and potentially ameliorate body composition in AIP patients under a high-carbohydrate diet.

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Publication Details

Journal
Journal of Physiology and Biochemistry
Published
2025-09-26
DOI
https://doi.org/10.1007/s13105-025-01124-4
Citations
1
Primary Topic
Porphyrin Metabolism and Disorders
Type
article
Field-Weighted Citation Impact
0.81
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article

Oral lipoteichoic and lipoic acids improve insulin resistance and body composition in porphyria mice on a high-carbohydrate diet

Teresa Cortes, Gemma Quincoces, María J. Moreno‐Aliaga, María Collantes et al.
1 citations
Journal of Physiology and Biochemistry
Porphyrin Metabolism and Disorders
0.81
article

Oral lipoteichoic and lipoic acids improve insulin resistance and body composition in porphyria mice on a high-carbohydrate diet

Teresa Cortes, Gemma Quincoces, María J. Moreno‐Aliaga, María Collantes, Iván Peñuelas, Michele Battistin, Matías A. Ávila, José Ignacio Riezu‐Boj, Patricia Martorell, Araceli Lamelas, Stefano Gatti, Juan F. Martínez‐Blanch, Daniel Ramón, Francesco Urigo, Paola Dongiovanni, Marica Meroni, Miriam Longo, Empar Chenoll, Isabel Solares, Fermı́n I. Milagro, Daniel Jericó, Erika Paolini, Antonio Fontanellas, Elena Di Pierro, Ana Sampedro, Andrea Rodenes-Gavidia, Jordi Cervero
article en
1 citations

Abstract

Acute intermittent porphyria (AIP) is a genetic metabolic disorder characterized by neurovisceral attacks. Although high-carbohydrate diets or intravenous glucose administration can help alleviate incipient attacks in patients, these interventions may also promote insulin resistance and increase metabolic risk. This study explored targeted dietary interventions to manage hyperinsulinemia and to enhance glucose uptake in insulin-sensitive organs under high-carbohydrate diet. Body composition and fecal microbiota profile were also investigated in a murine model of the disease. Wild-type and AIP mice (n = 6/group) were supplemented with tapioca maltodextrin in drinking water for 12 weeks, alongside heat-treated Bifidobacterium animalis subsp. lactis CECT-8145 (BPL1®HT), its by-product lipoteichoic acid (LTA), or the insulin-sensitizing agent α-lipoic acid (α-LA). Liver-targeted therapies, previously assessed in AIP mice, were also included in this study. AIP mice on a high-carbohydrate diet exhibited hyperinsulinemia and tissue-specific differences in glucose uptake compared to wild-type mice. Dysbiosis, marked by reduced fecal Dorea spp. and Adlercreutzia muris, alongside higher abundance of Escherichia coli, was also showed. Supplementation with α-LA and LTA revealed superior ability to improve glucose tolerance test and skeletal muscle glucose uptake, reduce hyperinsulinemia, and enhance body composition by increasing lean mass relative to fat, compared to gene therapy or liver-targeted insulin administration. Notably, LTA restored fecal microbiota profiles resembling those of wild-type mice. In conclusion, supplementation with LTA from BPL1®HT and α-LA may represent promising dietary interventions to manage glucose tolerance, improve insulin sensitivity in muscle and adipose tissues, and potentially ameliorate body composition in AIP patients under a high-carbohydrate diet.

Journal of Physiology and BiochemistryVol. 81(4)
University of Milan (IT), Universidad Cardenal Herrera CEU (ES), Parc Científic de la Universitat de València (ES), Instituto de Salud Carlos III (ES), Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico (IT), Navarre Institute of Health Research (ES), Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (ES), Clinica Universidad de Navarra (ES), Universidad de Navarra (ES)
Openalex Percentile: Top 23%
Porphyrin Metabolism and Disorders
0.81
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