Crowding pregnant mice affects attack and threat behavior of male offspring

1985 ◽  
Vol 19 (1) ◽  
pp. 86-97 ◽  
Author(s):  
Philip W. Harvey ◽  
Peter F.D. Chevins
Endocrinology ◽  
2017 ◽  
Vol 158 (8) ◽  
pp. 2533-2542 ◽  
Author(s):  
Martha Susiarjo ◽  
Frances Xin ◽  
Martha Stefaniak ◽  
Clementina Mesaros ◽  
Rebecca A Simmons ◽  
...  

2020 ◽  
Author(s):  
Qiting Qing ◽  
Lili Huang ◽  
Mei Zhao

Abstract Maternal lipopolysaccharide(LPS)exposure during pregnancy induced metabolic abnormalities in male offspring, but the underlying mechanisms are still unclear. The aims of this study were to elucidate the underlying etiologies by characterizing the metabolic alterations in maternal serum and male fetal liver. Pregnant mice were intraperitoneally injected with LPS (50ug/kg/d) from gestational period (GD 15 to GD 17). In the GD18, maternal serum and male fetal liver were collected. The metabolic profiles were analyzed using liquid Chromatograph Mass Spectrometer (LC-MS) techniques. After LPS exposure, glycerophospholipids containing saturated fatty acids were up-regulated, and glycerophospholipids containing polyunsaturated fatty acids were down-regulated in both pregnant mice and male offspring. In addition, we observed that LPS-exposed dams also had increased saturated fatty acids levels and decreased polyunsaturated fatty acids levels. Because these abnormal glycerophospholipids and fatty acid metabolism have been identified as possibly associated with the risk of type 2 diabetes, our study has therefore identified two pathways (glycerophospholipids and fatty acid metabolism) that potentially underlie LPS induced fetal metabolic disease.


2018 ◽  
Vol 106 ◽  
pp. 35-43 ◽  
Author(s):  
Monika Ogrizek ◽  
Neža Grgurevič ◽  
Tomaž Snoj ◽  
Gregor Majdič

2017 ◽  
Vol 595 (5) ◽  
pp. 1547-1562 ◽  
Author(s):  
Tiande Zou ◽  
Daiwen Chen ◽  
Qiyuan Yang ◽  
Bo Wang ◽  
Mei-Jun Zhu ◽  
...  

PLoS ONE ◽  
2017 ◽  
Vol 12 (1) ◽  
pp. e0169889 ◽  
Author(s):  
Qian Zhang ◽  
Xiaofang Sun ◽  
Xinhua Xiao ◽  
Jia Zheng ◽  
Ming Li ◽  
...  

2018 ◽  
Vol 34 (8) ◽  
pp. 507-524 ◽  
Author(s):  
Nisha Bara ◽  
M Eshwarmoorthy ◽  
Kesavan Subaharan ◽  
Gautam Kaul

The increasing use of nanomaterials has naturally caused heightened concerns about their potential risks to human and animal health. We investigated the effect of zinc oxide nanoparticles (ZnO NPs) and mesoporous silica nanoparticles (MSN) on steroidogenesis in the corpus luteum (CL) of pregnant mice and testis of male offspring. Pregnant albino mice were exposed to ZnO NPs and MSN for 2 days on alternate days, gestation days 15–19. Hepatic injury marker enzymes increased in the higher concentration of NM-exposed mother mice, but histological examination revealed no changes in the placenta of pregnant mice, whereas testis of male offspring showed gross pathological changes. The expression pattern of progesterone biosynthesis-related genes was also altered in the CL of NP-exposed pregnant mice. In utero exposure of ZnO NPs increased the relative expression of StAR in 100 mg/kg body weight (BW) ZnO NP-treated and bulk ZnO-treated groups and P450 side-chain cleavage enzyme (P450scc) in 50 mg/kg BW ZnO NP-treated and 100 mg/kg of bulk ZnO-treated male offspring. Serum testosterone concentration significantly increased in the 100 mg/kg of bulk ZnO-treated group and decreased in the 250 mg/kg of MSN-treated group and a single dose of 300 mg/Kg BW of ZnO NPs caused miscarriages and adversely affected the developing foetus in mice.


2014 ◽  
Vol 145 (3) ◽  
pp. 640-646 ◽  
Author(s):  
Astrid Hogenkamp ◽  
Suzan Thijssen ◽  
Naomi van Vlies ◽  
Johan Garssen

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