T image was converted to TIFF files by using Adobe Photoshop
T image was converted to TIFF files by using Adobe Photoshop 7.0 (Adobe Systems Inc., San Jose, CA), then analyzed using Scion Image Beta 4.02 PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/25957400 (Scion Co., Maryland, USA). The fluorescent image of the embryos was measured by counting the number of pixels after inversion of the color.Experiment 3: Measurement of intracellular GSH content Intracellular GSH content was measured as described by previous studies [27,28]. For each replicate, we placed pools of 10?5 Day 1 embryos or 20?5 Day 2 embryos in 5 of 0.2 M sodium order Procyanidin B1 phosphate buffer containing 10 mM Na2-EDTA (pH 7.2) and 5 of 1.25 M phosphoric acid in microtubes and then all the embryos were frozen at -80 . The concentrations of GSH in the embryos were determined by dithionitrobenzoic acid ?glutathione disulphide (DTNB-GSSG) reductase recycling assay [29]. Briefly, the samples were thawed, and then 175 sodium phosphate buffer containing 0.33 mg/ml nicotinamide adenine dinucleotide phosphate (NADPH) (Sigma), 25 of 6 mM DTNB (Wako Pure Chemical Industries, Ltd., Osaka, Japan), and 40 of water were added to each sample tube. The samples were warmed at room temperature for 15 min, and then the assay was initiated with the addition of 5 of 125 IU glutathione disulphide reductase (Wako). Absorbance was measured five times by spectrophotometer (DU7500; Beckman Coulter, Inc., CA, USA) at 30-s intervals at a wavelength of 412 nm. A GSH standard and a sample blank lacking GSH was also assayed. Standards were prepared for each assay, and the total GSH content per sample was determined from a standard curve of GSH. The GSH concentration per embryo was calculated by dividing the total concentration per sample by the number of embryos present in the sample. Experiment 4: TUNEL assay DNA fragmentation of blastocyst was analyzed by using a combined technique for simultaneous nuclear staining and TUNEL (in situ cell death detection system; Roche Diagnostic Corporation, Indianapolis, IN, USA) by amodification of the procedures previously described by Karja et al. [30]. Blastocysts on Day 6 in each group were fixed overnight at 4 in 3.7 (w/v) paraformaldehyde diluted in phosphate buffer saline (PBS). After overnight fixation, embryos were washed thrice in PBS containing 3 (w/v) polyvinyl alcohol (PVA) and permeabilized in 0.5 (v/v) Triton X-100 for 60 min, and then incubated in a blocking solution (PBS containing 10 mg/ml BSA) overnight at 4 . As positive controls, one or two embryos per TUNEL analysis were incubated in 1000 U/ ml deoxyribonuclease I (DNase I; Sigma) for 20 min. After washing in PBS-PVA, the positive controls and all experimental embryos were incubated in TUNEL reaction cocktail at 37 for 1 h in the dark. The embryos were then counterstained with 50 /ml propidium iodide (PI) for 20 min to label all nuclei. The embryos were washed extensively and mounted with slight coverslip compression in an anti-bleaching solution (Slow-Fade; Molecular Probes, Eugene, OR, USA). The embryos were examined under a confocal laser-scanning microscope (IX-71, Olympus) fitted with 25/40 ?PL Fluotar/0.75 oil objectives, and an argon/krypton laser was used for excitation at wavelengths of 488 and 568 nm for detection of the TUNEL reaction and PI, respectively. A complete Z series of 20?7 optical sections at 3- to 4- intervals was acquired from each embryo. The images were reconstructed using Fluoview software (Olympus). Each optical section of the blastocyst was analyzed for total number of nucl.
