AI Article Synopsis

  • Imperatorin (IMP) is a furanocoumarin with various pharmacological benefits, and this study investigates its impact on early pig embryo development and underlying mechanisms.* -
  • Results indicated that adding 40 μM IMP to the culture medium improved blastocyst rates, total cell numbers, and reduced apoptosis in embryos, alongside encouraging gene expression related to pluripotency.* -
  • IMP also decreased reactive oxygen species (ROS), enhanced mitochondrial activity, and inhibited autophagy, suggesting it helps promote healthy preimplantation embryo development by minimizing oxidative stress.*

Article Abstract

Imperatorin (IMP), a furanocoumarin derivative with many biological properties and pharmacological activities, is widely used as an antibacterial, anti-inflammatory, antiviral, anticancer, cardiovascular and neuroprotective agent. The purpose of this study was to explore the effects of IMP on early embryo development in pigs as well as the potential mechanisms. Our results showed that IMP can enhance the developmental competence of porcine early embryos. Supplementation of in vitro culture medium with 40 μM IMP significantly increased the blastocyst rate and total cell number. At the same time, apoptosis of blastocysts was also significantly decreased in the supplemented group compared with the control group, in accordance with the subsequent results of FAS and CASP3 gene expression analysis. Furthermore, IMP attenuated intracellular reactive oxygen species (ROS) generation, increased fluorescein diacetate (FDA) and glutathione (GSH) levels. Importantly, IMP not only improved the activity of mitochondria but also inhibited the occurrence of autophagy. In addition, pluripotency-related genes (OCT4, NANOG, and SOX2) and a growth and metabolism regulatory gene (mTOR) were upregulated after IMP supplementation on Day 7. These results demonstrate that IMP exerts a beneficial effect on preimplantation embryo development by reducing oxidative stress and autophagy.

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Source
http://dx.doi.org/10.1016/j.theriogenology.2019.11.029DOI Listing

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