Abstract. The activities of hydroxysteroid dehydrogenases (HSDs) and adenylate cyclase in parthenogenetic mouse blastocysts derived from the ova activated and diploidized by the treatment of ethanol and cytochalasin B were histochemically examined, and were compared with those in control blastocysts developed from fertilized ova. Although the activities of ∆ 5 -3β-HSD with DHA and 17α-hydroxypregnenolone as the substrates, 17β-HSD with testosterone, 20α-HSD and 20β-HSD did not differ between parthenogenetic and control blastocysts, the activities of ∆ 5 -3β-HSD with pregnenolone as the substrate, 17β-HSD with estradiol-17β and adenylate cyclase were significantly lower in parthenogenetic blastocysts. These results suggest that the metabolism of 17α-hydroxyprogesterone, 20α-hydroxyprogesterone, 20β-hydroxyprogesterone and androgen in parthenogenetic blastocysts is comparable to that in control blastocysts, whereas the metabolism of progesterone, estrogen and cyclic AMP in parthenogenetic blastocysts is low compared with that in control blastocysts. When parthenogenetic blastocysts were treated with hCG, the activities of ∆ 5 -3β-HSD with pregnenolone as the substrate and 17β-HSD with estradiol-17β were stimulated, but were still lower than those of control blastocysts. The low potential of development in parthenogenetic embryos was discussed in relation to their steroid metabolism. [7] have been studied in the mouse, and the metabolism or synthesis of these substances has been found to be low, compared with that of fertilized embryos. It has also been reported histochemically that the ability of digestion and of interconversion between carbohydrate and lipid are lower in parthenogenetic mouse blastocysts than in blastocysts developed from fertilized ova [8]. Thus, such low metabolic activities in parthenogenetic embryos are thought to be a reason for lower potentials of development in these embryos [5][6][7][8]. However, there have been no reports in which the metabolism of substances, other than is stated that the proportion of nucleolonema in the nucleolus in these embryos is higher than that in fertilized embryos, and parthenogenetic embryos have many mitochondria with vacuolated cristae, but very few cytoplasmic organelles, such as Golgi apparatus, lysosomes and ribosomes. It has also been determined in morphological studies of the mouse that the contents of lipid droplets and crystalloids are fewer in parthenogenetic blastocysts than in blastocysts developed from fertilized ova [1,4]. From these results, it has been assumed that the metabolic activity is lower in parthenoge-