Ornithine aspartate effects on bacterial composition and metabolic pathways in a rat model of steatotic liver disease

• Published in: World journal of hepatology Vol. 16; no. 5; pp. 832 - 842
• Main Authors: Lange, Elisa Carolina, Rampelotto, Pabulo Henrique, Longo, Larisse, de Freitas, Laura Bainy Rodrigues, Uribe-Cruz, Carolina, Alvares-da-Silva, Mario Reis
• Format: Journal Article
• Language: English
• Published: United States Baishideng Publishing Group Inc 27-05-2024
• Subjects: Basic Study; Gut microbiota; Animal model; Metabolic-associated steatotic liver disease; Ornithine aspartate; Metabolic prediction
• ISSN: 1948-5182; 1948-5182
• DOI: 10.4254/wjh.v16.i5.832

Metabolic-dysfunction associated steatotic liver disease (MASLD) is a hepatic manifestation of metabolic syndrome. Studies suggest ornithine aspartate (LOLA) as drug therapy.
To analyze the influence of LOLA intake on gut microbiota using a nutritional model of MASLD.
Adult male Sprague Dawley rats were randomized into three groups: Control (10 rats fed with a standard diet), MASLD (10 rats fed with a high-fat and choline-deficient diet), and LOLA (10 rats receiving 200 mg/kg/d LOLA, after the 16
week receiving high-fat and choline-deficient diet). After 28 wk of the experiment, animals were euthanized, and feces present in the intestine were collected. Following fecal DNA extraction, the V4 region of the 16S rRNA gene was amplified followed by sequencing in an Ion S5™ system.
Alpha and beta diversity metrics were comparable between MASLD and LOLA. 3 OTUs were differentially abundant between MASLD and LOLA, which belong to the species
,
, and
. The functional prediction provided two different metabolic profiles between MASLD and LOLA. The 9 pathways differentially abundant in MASLD are related to a change in energy source, adenosine/purine nucleotides degradation as well as guanosine and adenosine deoxyribonucleotides biosynthesis. The 14 pathways differentially abundant in LOLA are associated with four major metabolic functions primarily influenced by L-aspartate, including tricarboxylic acid cycle pathways, purine/guanosine nucleotides biosynthesis, pyrimidine ribonucleotides biosynthesis and salvage as well as lipid IVA biosynthesis.
Although LOLA had no influence on alpha and beta diversity in this nutritional model of MASLD, it was associated with changes in specific gut microbes and their related metabolic pathways.