2022
DOI: 10.1007/s13105-021-00862-5
|View full text |Cite
|
Sign up to set email alerts
|

Dietary interventions in mice affect oxidative stress and gene expression of the Prlr and Esr1 in the adipose tissue and hypothalamus of dams and their offspring

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 7 publications
(2 citation statements)
references
References 39 publications
0
2
0
Order By: Relevance
“…S-PRLR differs from L-PRLR in that it has a 39-base pair inserted at the beginning of the cytoplasmic domain and two consecutive intra-frame terminating codons at its 3 end [15]. Oxidative stress in offspring mice was found to be associated with an increased expression of PRLR in the hypothalamus and adipose tissue due to the restrictive or hypercaloric diets of maternal mice [49]. Dandawate et al found that penfluridol could block the expression of PRLR in pancreatic cancer cells leads to a reduction in cell proliferation, induction of autophagy, and deceleration of xenograft tumour growth in mice [50].…”
Section: Prl Regulated Oxidative Stress Autophagy and Apoptosis By Bi...mentioning
confidence: 97%
“…S-PRLR differs from L-PRLR in that it has a 39-base pair inserted at the beginning of the cytoplasmic domain and two consecutive intra-frame terminating codons at its 3 end [15]. Oxidative stress in offspring mice was found to be associated with an increased expression of PRLR in the hypothalamus and adipose tissue due to the restrictive or hypercaloric diets of maternal mice [49]. Dandawate et al found that penfluridol could block the expression of PRLR in pancreatic cancer cells leads to a reduction in cell proliferation, induction of autophagy, and deceleration of xenograft tumour growth in mice [50].…”
Section: Prl Regulated Oxidative Stress Autophagy and Apoptosis By Bi...mentioning
confidence: 97%
“…Bisphenol A exposure can promote ovarian ROS/RNS synthesis and lipid peroxidation and then changes the expression of the estrogen receptor gene, ultimately affecting ovarian and reproductive health in organisms [12]. Dietary interventions in mice affect oxidative stress and gene expression of Esr1 in the adipose tissue and hypothalamus of dams and their offspring [13]. The testis is vulnerable to free radical damage and becomes an easy target organ.…”
Section: Introductionmentioning
confidence: 99%