2023
DOI: 10.3390/ani13071135
|View full text |Cite
|
Sign up to set email alerts
|

LPS Administration during Fertilization Affects Epigenetic Inheritance during Embryonic Development

Abstract: Intrauterine inflammation can cause infertility by disrupting reproductive function. The pathogenesis underlying this process may primarily involve endotoxins from lipopolysaccharides (LPS), which are produced by Gram-negative bacteria. However, the long-term effects of endotoxins in mammalian pregnancy following LPS exposure during fertilization have not been clarified. In this study, we performed experiments to analyze the influence of LPS on early embryonic development and fetal development in mice. Mice ut… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2024
2024
2024
2024

Publication Types

Select...
1

Relationship

1
0

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 41 publications
(46 reference statements)
0
1
0
Order By: Relevance
“…Total RNA was extracted using TRIzol reagent (15596018, Thermo Fisher Scientific, Waltham, MA, USA). For cDNA synthesis and real-time PCR, the methods described by Kim et al (2023) were followed [37]. In brief, the total RNA concentration was determined using a Nanodrop (Thermo Fisher Scientific); 1 µg of total RNA was treated with DNase and converted into cDNA using Random Primers (48190011, Thermo Fisher Scientific) and SuperScriptTM II (18064022, Thermo Fisher Scientific) with a GeneAtlas thermal cycler 482 (4990902, ASTEC, Kasuya, Fukuoka, Japan).…”
Section: Rna Preparation and Real-time Pcrmentioning
confidence: 99%
“…Total RNA was extracted using TRIzol reagent (15596018, Thermo Fisher Scientific, Waltham, MA, USA). For cDNA synthesis and real-time PCR, the methods described by Kim et al (2023) were followed [37]. In brief, the total RNA concentration was determined using a Nanodrop (Thermo Fisher Scientific); 1 µg of total RNA was treated with DNase and converted into cDNA using Random Primers (48190011, Thermo Fisher Scientific) and SuperScriptTM II (18064022, Thermo Fisher Scientific) with a GeneAtlas thermal cycler 482 (4990902, ASTEC, Kasuya, Fukuoka, Japan).…”
Section: Rna Preparation and Real-time Pcrmentioning
confidence: 99%