The influence of tocotrienol on the development of preimplantation embryos and pregnancy outcome in corticosterone-treated mice

• Main Author: Nasibah Azme (Author)
• Format: Thesis Book
• Language: English
• Published: Sungai Buloh, Selangor Universiti Teknologi MARA. Faculty of Medicine 2013
• Subjects: Tocotrienols; Tocotrienols > adverse effects; Antioxidants; Pregnancy, Animal > physiology; Corticosterone > administration and dosage; Corticosterone > adverse effects
• Online Access: Click Here to View Status and Holdings.
• Item Description: UiTM Digitized
• Physical Description: xviii, 224 pages illustrations, charts, 16 numbered leaves of plates 30 cm 1 computer optical disc (4 ¾ inch)
• Format: System requirements: Mac OS X 10.7.5+ and Safari 6.0+, Windows Vista+ and Firefox 22+; DVD-ROM drive
• Bibliography: Includes bibliographical references (page 151-178)

Tocotrienol (TCT), a component of vitamin E is a powerful antioxidant whereas corticosterone (CORT), a known prooxidant has been shown to impair the development of embryo and pregnancy outcome. This study aims to determine the effect of TCT supplementation on the quality and in vitro development of embryos and the pregnancy outcome in CORT-treated mice. In embryonic experiment, 5- to 6 weeks old female mice were divided into four groups of eight animals. They received CORT (10 mg/kg) intraperitoneal (ip) concurrently with TCT at the dose of 30, 60 and 90 mg/kg orally and the control group had 0.1 ml com oil (ip) and orally for seven consecutive days. On Day 7, after superovulation and mating, animals were euthanized and embryos were flushed out from the fallopian tubes. The morphology and in vitro development of embryos were recorded. In pregnancy outcome experiment, 7- to 8 weeks old female mice were divided into similar groups and treatment for the first seven days of pregnancy were conducted as above with using TCT at 60, 90 and 120 mg/kg. On Day 7 of pregnancy, laparotomy was done to determine the number of implantation sites; to observe any resorption signs while litter sizes were measured at birth. It was found that TCT (90 mg/kg) improved the quality of embryo whereas TCT (60 mg/kg) increased the number of embryos that reached hatched blastocyst stage in CORT-treated groups. In addition to that, TCT (60 mg/kg) increased the implantation sites, whereas TCT (120 mg/kg) decreased the resorption percentage and increased the level of progesterone hormone towards control in CORT-treated pregnant mice. Tocotrienol supplementation in our study is able to reverse the CORT-induced adverse impact on all reproductive outcomes as mentioned above. The effect of TCT alludes further exploration to ascertain their mechanism