2023
DOI: 10.5187/jast.2022.e124
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Molecular characterization and functionality of rumen-derived extracellular vesicles using a Caenorhabditis elegans animal model

Abstract: Molecular characterization and functionality of rumen-derived extracellular vesicles using a Caenorhabditis elegans animal model Running

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Cited by 7 publications
(5 citation statements)
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“…The C. elegans strain fer-15;ferm-1 mutant was used, and they were routinely maintained on Nematode Growth Medium (NGM) agar plates. Eggs were extracted in sodium hypochlorite–sodium hydroxide solution and synchronized L1 worms were grown on NGM agar plates seeded with Escherichia coli OP50 at 25 °C to obtain sterile L4/young adult worms [ 57 ]. To perform a lifespan assay with series of methionine samples, the L1 or L4 stage of C. elegans strain fer-15;fem-1 were individually transferred with a platinum wire onto 35-mm-diameter NGM agar plates.…”
Section: Methodsmentioning
confidence: 99%
“…The C. elegans strain fer-15;ferm-1 mutant was used, and they were routinely maintained on Nematode Growth Medium (NGM) agar plates. Eggs were extracted in sodium hypochlorite–sodium hydroxide solution and synchronized L1 worms were grown on NGM agar plates seeded with Escherichia coli OP50 at 25 °C to obtain sterile L4/young adult worms [ 57 ]. To perform a lifespan assay with series of methionine samples, the L1 or L4 stage of C. elegans strain fer-15;fem-1 were individually transferred with a platinum wire onto 35-mm-diameter NGM agar plates.…”
Section: Methodsmentioning
confidence: 99%
“…The live bacterial lawn was prepared for C. elegans feeding by centrifuging the bacterial pellet at 13,000 rpm for 1 minute, washing it twice with sterile M9 buffer (3 g KH 2 PO 4 , 6 g Na 2 HPO 4 , and 5 g NaCl mixed in 1 L distilled water, autoclaved), and then adding 1 mL of 1 M MgSO 4 (Sigma‒Aldrich, St. Louis, MO, USA). The bacterial pellet was then concentrated to a final concentration of 2.5 mg/L (wet weight) in M9 buffer and suspended on NGM plates [3.5 g Bacto Peptone (BD Difco), 3 g NaCl (Sigma‒Aldrich), and 20 g agar (BD Difco)] ( 11 ).…”
Section: Methodsmentioning
confidence: 99%
“…The transparency of C. elegans ’ body provides a distinct advantage, allowing for easy observation of lipid droplets and other potentially hazardous accumulations. This characteristic makes C. elegans a preferred model for investigating various aspects of health, including obesity, feeding behaviors, satiety, and metabolic disorders ( 11 , 12 ). The combination of these attributes positions C. elegans as a practical and informative model for the initial screening of potential probiotics.…”
Section: Introductionmentioning
confidence: 99%
“…C. elegans, an extensively utilized genetic model organism capable of mimicking numerous human diseases, holds considerable value for in vivo studies at both metabolic and genetic levels [25,26]. This study employed the C. elegans lifespan assay to scrutinize the toxicity of distinct antler velvet extracts, including FAV, FFA, DAV, and CFA.…”
Section: Antler Velvet Extract Increases the Lifespan Of C Elegansmentioning
confidence: 99%