Abstract
Pregnancy is a unique physiological state, in which C60 fullerene is reported to be distributed in both maternal and fetal tissues. Tissue distribution of C60 differs between pregnant and non-pregnant states, presumably due to functional changes in vasculature during pregnancy. We hypothesized that polyvinylpyrrolidone (PVP) formulated C60 (C60/PVP) increases vascular tissue contractility during pregnancy by increasing Rho-kinase activity. C60/PVP was administered intravenously to pregnant and non-pregnant female Sprague Dawley rats. Vascular responses were assessed using wire myography 24. h post-exposure. Increased stress generation was observed in uterine artery, thoracic aorta and umbilical vein. Rho-Rho-kinase mediated force maintenance was increased in arterial segments from C60/PVP exposed pregnant rats when compared to PVP exposed rats. Our findings suggest that intravenous exposure to C60/PVP during pregnancy increases vascular tissue contractility of the uterine artery through elements of Rho-Rho-kinase signaling during late stages of pregnancy.
Original language | English |
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Pages (from-to) | 86-100 |
Number of pages | 15 |
Journal | Reproductive Toxicology |
Volume | 49 |
DOIs | |
Publication status | Published or Issued - Nov 2014 |
Externally published | Yes |
Keywords
- Nanotoxicology
- Polyvinylpyrrolidone
- Pregnancy
- Rho-kinase pathway
- Umbilical vein
- Uterine artery
- Vascular tissue contractility
ASJC Scopus subject areas
- Toxicology