Production ofin vitrobovine embryos supplemented withl-carnitine in different oxygen tensions and the relation to nitric oxide

Summary The aim of this study was to evaluate the production of bovine embryos in vitro when supplemented with l -carnitine for 24 h beginning on day 5 (d 5) under two different oxygen tensions (20% or 5%) and the relationship of nitric oxide (NO) in in vitro culture (IVC) medium to embryo development. Cumulus–oocyte complexes (COC; n = 837) were matured in vitro for 24 h and fertilization was performed for 18 h. Zygotes were cultured in vitro for 9 days after in vitro fertilization in synthetic oviductal fluid (SOF) medium with 5% fetal calf serum. At d 5 the plates were assigned to one of four treatment groups: high (20%) or low (5%) O 2 tension either with or without the addition of 3.03 mM l -carnitine (High-Cont, High-Lcar, Low-Cont, Low-Lcar). The concentration of NO in the culture medium was evaluated on d 5, d 6 and d 9. On d 7, parts of the embryos were submitted for evaluation of intracellular lipid droplets. The cleavage rate was similar ( P > 0.05) between high and low O 2 tension and the blastocyst rate was similar in all conditions evaluated. The hatching rate was higher ( P < 0.05) for Low-Cont. The NO concentration was higher at d 9 under low O 2 tension ( P < 0.1). The addition of 3.03 mM l -carnitine between d 5 and d 6 of IVC was not efficient in reducing cytoplasmic lipid content of bovine embryos. Additionally, IVC at a low oxygen tension without l -carnitine promoted better conditions for embryo development. A higher concentration of NO in medium was observed under low O 2 tension.