2022
DOI: 10.3389/fnut.2022.852012
|View full text |Cite
|
Sign up to set email alerts
|

Preventive Effect of Limosilactobacillus fermentum SCHY34 on Lead Acetate-Induced Neurological Damage in SD Rats

Abstract: Lead poisoning caused by lead pollution seriously affects people's health. Lactic acid bacteria has been shown to be useful for biological scavenging of lead. In this experiment, Sprague-Dawley (SD) rats were treated with 200 mg/L of lead acetate solution daily to induce chronic lead poisoning, and oral Limosilactobacillus fermentum (L. fermentum) SCHY34 to study its mitigation effects and mechanisms on rat neurotoxicity. The L. fermentum SCHY34 showed competent results on in vitro survival rate and the lead i… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
8
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
8
2

Relationship

2
8

Authors

Journals

citations
Cited by 26 publications
(8 citation statements)
references
References 64 publications
0
8
0
Order By: Relevance
“…The thermocycling conditions were: Pre-denaturation at 95˚C for 5 min; followed by 35 cycles of annealing at 58˚C for 50 sec and extension at 72˚C for 90 sec; and a final extension at 72˚C for 10 min. GAPDH was used as an internal reference, and the expression was calculated using the 2 -∆∆Cq method ( 16 , 17 ). The sequences of the primers used for qPCR are listed in Table I .…”
Section: Methodsmentioning
confidence: 99%
“…The thermocycling conditions were: Pre-denaturation at 95˚C for 5 min; followed by 35 cycles of annealing at 58˚C for 50 sec and extension at 72˚C for 90 sec; and a final extension at 72˚C for 10 min. GAPDH was used as an internal reference, and the expression was calculated using the 2 -∆∆Cq method ( 16 , 17 ). The sequences of the primers used for qPCR are listed in Table I .…”
Section: Methodsmentioning
confidence: 99%
“…The PCR reaction was conducted in a fluorescence PCR instrument (Onestep Plus quantitative PCR instrument, Thermo Fisher Scientific) using a reaction volume of 20 μL for each of the eight tubes. The Ct values of each template were determined using GAPDH as the internal reference gene and the 2 −ΔΔCt method was employed to calculate the relative content of the target genes (13,14).…”
Section: Mrna Expression Intensity Of Mrna In Murine Intestinal Tissuesmentioning
confidence: 99%
“…Mouse whole blood was obtained through retro-orbital bleeding. The collected samples were centrifuged at 4000 rpm for 10 min at 4 o C to separate the serum [9]. The levels of IL-6, IL-10, IL-1β, and TNF-α in ammatory markers in the serum were measured using ELISA assay kits (Thermo Fisher, MA, USA).…”
Section: Measurement Of In Ammatory Cytokines In Mouse Serummentioning
confidence: 99%