The main object of this study was to establish the basic porcine COCs IVM system fitting for our Lab.，and evaluate the effect of N,2-O-Dibutyryladenosine 3:5-Cyclic Monophosphate (dbcAMP) on porcine oocytes maturation and development in vitro in order to control the in vitro maturation of pig oocytes.Pig oocytes were matured for different maturation durations，with or without exogenous hormone supplements after the first 20h of in vitro maturation，treated with CB or 6-DMAP after electronic activation and were fused with somatic cell used different voltage. Rates of reached to MII stage，development to blastocyst and the rate of fusion and lysis were checked.Use the basic IVM system established above，effect of dbcAMP on pig oocytes at GV stage and development ability of pig PA and SCNT embryo were investigated.Oocytes reached to MII stage cultured for 33h significant lower than 41，49 and 57h(52.54％vs. 79.19%，93.25%and 93.75%，respectively p<0.05)，there is no significant difference among 41，49 and 57h，while oocytes matured for 41h reached to normal 2-4 cells significant higher than them at 57h group(92.26% vs. 56.17%，p <0.05) and the blastocyst rate was also higher than 33h，49h and 57h(41.16%vs. 11.96，21.20 and 26.92%，respectively p < 0.05). Hormone free after the 1st 20h of IVM culture didn’t improve the cleavage(hormone free vs. hormone not free: 86.71% vs. 81.77%，p >0.05) and blastocyst formation(hormone free vs. hormone not free: 30.06% vs. 26.60%，p >0.05). Treat pig PA embryos with CB of 6-DMAP after electric activation，there were no significant difference in cleavage(CB vs. 6-DMAP:70.44%vs. 79.01%) and blastocyst(CB vs. 6-DMAP:28.57%vs. 34.89%).Effect of different fusion voltages on rate of fusion and lysis in somatic cell oo-plasm complex after electronic fusion were also been investigated. Results show that when somatic cell oo-plasm complex fused with voltage at 150V/mm，the fused rate significantly lower than that used 180V/mm (66.38% vs. 86.88%，p <0.05)，while the lysis rate of 150V/mm group(4.26%) was also significantly lower than 180V/mm(19.24%) group but higher than control group(2.49%).Oocytes treated with 1mM dbcAMP for 22，34，37，39，and 72h respectively. Results show that in each group，most oocytes were synchronized at GVII stage. At the check point of 39h，we found that there were 23.50%oocytes reached to GVIV stage，significantly higher than others. And at 72h，about 35.47%oocytes reached to MII stage，and just 29.62%oocytes still arrested at GVII stage. COCs were matured in IVM-III at the first 0，22，24，26，28h of the culture and then released the dbcAMP and hormone，after time released the dbcAMP and hormone，rate of oocyte reached MII were recorded and compared at 11-18h after dbcAMP released. Results shows that at 13h after dbcAMP and hormone free，oocytes in 26 and 28h (28.97%and 31.11%) reached MII stage were higher than that which at 22h matured (0.00%，p<0.05). While there were no significant difference among each group at 11，15，16，17，18h，respectively.At 22h，24h and 26h groups(46.93，61.90 and 57.09%)，oocytes reached MII stage at 15h were significant higher than that at 13h (0.00%，10.98%，28.97%，respectively p<0.05). At 26h group，oocytes at 13h after dbcAMP release reached MII stage were significant higher than 11h(28.97%vs. 1.59%p<0.05). While there were no significant difference between two adjacent check point in 28h group.In conclusion oocytes being treated with dbcAMP for 22，24，26，and 28h were used in SCNT and PA. Our results suggested that there were no significant difference at rates of fusion，cleavage，lysis，fragment and blastocyst in SCNT group，and in parthenogenetic activation group，there were also no any statistic difference between 22 and 28h group in rates of cleavage，lysis，fragment and blastocyst.