Human umbilical cord mesenchymal stem cells (hUC-MSCs) have shown very attractive potential in clinical applications for the treatment of various diseases. However, the data about the reproductive and developmental toxicity of hUC-MSCs remains insufficient. Thus, we assessed the potential effects of intravenous injection of hUC-MSCs on reproduction and development in Sprague-Dawley rats. In the fertility and early embryonic development study, hUC-MSCs were administered at dose levels of 0, 6.0 × 10, 8.5 × 10, and 1.2 × 10/kg to male and female rats during the pre-mating, mating and gestation period. In the embryo-fetal development study, the pregnant female rats received 0, 6.0 × 10, 1.2 × 10, and 2.4 × 10/kg of hUC-MSCs from gestation days (GD) 6-15. Assessments made included mortality, clinical observations, body weight, food consumption, fertility parameters of male and female, litter, and fetus parameters, etc. No hUC-MSCs-related toxicity was observed on the fertility of male and female rats, and no teratogenic effect on fetuses. hUC-MSCs at 1.2 × 10/kg caused a mildly decrease in body weight gain of male rats, transient listlessness, tachypnea, and hematuria symptoms in pregnant female rats. Death was observed in part of the pregnant females at a dose of 2.4 × 10/kg, which could be due to pulmonary embolism. Based on the results of the studies, the no-observed-adverse-effect levels (NOAELs) are 8.5 × 10/kg for fertility and early embryonic development, 1.2 × 10/kg for maternal toxicity and 2.4 × 10/kg for embryo-fetal development in rats intravenous injected with hUC-MSCs, which are equivalent to 8.5-fold, 12-fold, and 24-fold respectively of its clinical dosage in humans. These findings may provide a rational basis for human health risk assessment of hUC-MSCs.
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http://dx.doi.org/10.3389/fcell.2022.883996 | DOI Listing |
Alzheimers Dement
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B.S.A. College of Engineering and Technology, Mathura, Uttar Pradesh, India.
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December 2024
Keck School of Medicine at University of Southern California, Los Angeles, CA, USA.
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View Article and Find Full Text PDFAlzheimers Dement
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University of Ibadan, Ibadan, Oyo, Nigeria.
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Discov Med (Cham)
January 2025
Institute of Biomedical Engineering, University of Toronto, Toronto, ON Canada.
Background: Microvascular dysfunction (MVD) is a recognized sign of disease in heart failure progression. Intact blood vessels exhibit abnormal vasoreactivity in early stage, subsequently deteriorating to rarefaction and reduced perfusion. In managing heart failure with preserved ejection fraction (HFpEF), earlier diagnosis is key to improving management.
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