eactivation of MPF and MAPK. Newly ovulated oocytes collected 13 h after hCG administration were activated with SrCl2 and MPF and MAPK activities were assayed at different times after IA. Oocytes collected 19 h post hCG were cultured in mR1ECM for different times before assay for kinase activities during SA. Whereas freshly ovulated oocytes show 100% of MPF and MAPK activities, both kinase activities decreased to about 85% in oocytes recovered for SA 19 h post hCG. During IA, the MPF activity decreased 2 MAPK, SAC and Oocyte Spontaneous Activation Time of culture Oocytes observed % MII oocytes % Oocytes at different stages of IA Total AnII 0 a b c e-TelII 0 a a b l-TelII 0 0 0 a a a Int 0a 0a 0a 0a 0a 0a 20.265.9b c d 0 0.5 1 1.5 2 3 6 ad 53 58 60 57 58 58 63 100 a b c 0 34 53 57 58 58 63 42.065.4 11.863.7 0d 0d 0 0 d d 97.462.6 6.363.2a 0a 0 a a 2.662.6 44.8613.6 55.2613.7 93.763.2c 0a 17.2610.1b 38.965.6 67.166.9 82.8610.1c 61.165.6 8.762.9 a b 4.062.1 : Values with a common letter in their superscripts do not differ in the same column. Each treatment was repeated 34 times with 1520 oocytes in each replicate. doi:10.1371/journal.pone.0032044.t001 immediately after Sr2+ treatment and reached the lowest level by 1.5 h, but the MAPK activity did not decline until after 0.75 h and did not reach the lowest level until 2.25 h after Sr2+ treatment. During SA, however, both MPF and MAPK activities declined immediately after culture and reached the lowest level in close succession at 0.75 h and 1.5 h of culture, respectively. After that, while both kinase activities remained constant at the lowest level during IA, they went up significantly during SA to above their level at the onset of culture. Because only about half of the oocytes underwent SA during in vitro aging, while almost all the oocytes underwent IA after Sr2+ treatment, we expected that the difference in MAPK activity between SA and IA oocytes would be more remarkable if the MAPK activity was detected in only those 
oocytes that had actually initiated SA. To test this expectation, rat oocytes collected 19 h post hCG were aged for different times in mR1ECM before examination for p-MAPK expression. At 0.5 h and 1 h PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/22189214 of aging, whereas non-SA oocytes with tidily arranged spindle beta-Mangostin biological activity chromosomes showed marked expression of p-MAPK on their spindles, p-MAPK expression was either faint or undetectable in SA oocytes with dispersed spindle chromosomes. By 6 h of aging, however, p-MAPK expression became marked again in SA oocytes arrested in MIII. The relative p-MAPK contents of SA oocytes were then quantified by measuring fluorescence intensities in confocal images. Oocytes collected 19 h post hCG were aged for 0, 1 and 6 h before p-MAPK quantification. Oocytes aged for 0 h were divided into those destined to undergo SA with less p-MAPK and those not destined with more p-MAPK. Oocytes aged for 1 or 6 h were classified as SA and non-SA according to morphology. The average fluorescence of total 0-h oocytes was set as 89.4% as measured in the MBP kinase assay and the averages of oocytes in other treatments were expressed relative to this value. Whereas the not-destined and non-SA oocytes showed about 100% of p-MAPK at different aging intervals, p-MAPK contents in the destined and SA oocytes first decreased but then increased again. Taken together, the results suggested that during SA of rat oocytes, both MPF and MAPK ran an abortive decline with their activities increasing again before touching the s
