Abstract. Accumulating evidence suggests that leptin may play important roles in preimplantation embryonic development, although this remain controversial, and little is known about whether leptin has a stage-dependent regulatory effect on development of porcine embryos derived by parthenogenetic activation (PA) and somatic cell nuclear transfer (SCNT). The objective of this study was to investigate the effects of addition of leptin to in vitro culture (IVC) medium on development of porcine embryos derived by PA and SCNT. We found that addition of 50 ng/ml human recombinant leptin improved the rate of PA embryos reaching the blastocyst stage and increased the total cell number of blastocysts compared with the control group. The maximal blastocyst rate of SCNT embryos was achieved at 50 ng/ml, and the total cell number of blasocysts was increased significantly at 500 ng/ml leptin concentration. However, the ratio of the inner cell mass (ICM) to total cell number was not affected in any of the groups. Supplementation of leptin (50 ng/ml) from day 3, approximately the 4-8-cell stage, as in the case of the positive control, significantly increased the blatocyst rate of PA embryos compared with the negative control and inhibited cell apoptosis. There were no beneficial effects on embryonic development when 50 ng/ml leptin was added to the culture medium from day1 to day 3 or from day 4 to day 6. These results indicate that leptin could improve the development and the quality of PA and SCNT embryos; and 50 ng/ml leptin performs its primary stimulatory effect at 4-8-cell stage and that leptin may have no effect on the maternal-zygote transition (MZT) of porcine PA and SCNT embryos. Key words: Embryo development, Leptin, Parthenogenetic activation, Pig, Somatic cell nuclear transfer (SCNT) (J. Reprod. Dev. 55: [99][100][101][102][103][104] 2009) uccessful production of cloned pigs and many other mammalian species by SCNT not only strongly establishes that differentiated somatic cells still contain complete genetic information which thereby can be dedifferentiated and redifferentiated, but also provides a revolutionary tool for studies on embryonic stem cells, transgenesis or gene targeting and artificial reproductive technologies in such species [1,2]. Although SCNT is of great significance in agriculture, medicine and basic research, widespread application of SCNT is still very limited due to its poor efficiency. It is believed that its lower efficiency is the result of errors in reprogramming, especially incomplete epigenetic reprogramming [1], which could be improved, to some extent, by modifications of donor preparation, oocyte maturation, activation and embryo culture systems. It has been shown that alteration of oxygen tension, basic culture media or supplementation of certain kinds of growth factors, cytokines, vitamins or amino acids can enhance preimplantational development or quality of cloned embryos [3][4][5][6]. Leptin, a 16KD reproductive hormone and product of the obese gene (ob), which is synthesized ...