Cloning older adult rabbits can serve as a model in animal breeding, biodiversity preservation and in human therapeutic cloning. To establish the required exposure time of fibroblasts from these kind of animals to reprogramming factors, in the present study three different time intervals between fusion and activation were tested (30 min, 30-ADF group; 60 min, 60-ADF group; and 90 min, 90-ADF group). Vitrified epithelial fibroblasts derived from four older adult rabbit females (D1, D2, D3 and D4) and cultured from passages 0 to 4 were used as nuclear donors. Nuclear status of reconstructed embryos was not evaluated. No differences were observed in blastocyst rate (30-ADF 21% vs 60-ADF 19% vs 90-ADF 18%). Differences in hatching rates did not reach significance (30-ADF 11% vs 60-ADF 18% vs 90-ADF 18%). However, in the 60- and 90-ADF groups, embryos reached the blastocyst stage earlier than in the 30-ADF group (day 4: 40% and 50% vs 8%; p>0.05). Moreover, the quality of blastocysts (good vs poor) was lower in the 30-ADF group (good: 30-ADF 38% vs 60-ADF 90% vs 90-ADF 90%; p>0.05). Overall, these results suggest an unfavourable effect of the shortest exposure time tested (30 min). Differences between specimen origins were detected (blastocyst and hatching rates: D2 (26%; 25%) and D4 (25%; 27%) vs D1 (10%; 11%) and D3 (12%; 12%)), but significance were not reached. Effect of culture passage was not detected in any parameter studied.