167 Basal and maximal oxygen consumption of oocytes from young and old mares
G. Catandi A , Y. Obeidat B , A. Chicco A , T. Chen B C and E. Carnevale AA College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, CO, USA;
B Department of Electrical and Computer Engineering, Colorado State University, Fort Collins, CO, USA;
C School of Biomedical Engineering, Colorado State University, Fort Collins, CO, USA
Reproduction, Fertility and Development 31(1) 208-208 https://doi.org/10.1071/RDv31n1Ab167
Published online: 3 December 2018
Abstract
Mitochondria play a critical role in oocyte developmental competence by providing energy to the oocyte through oxidative phosphorylation. We hypothesised that oxygen consumption, a measure of mitochondrial function, would be lower in the oocytes of old versus young mares as a potential mechanism of reduced developmental competence associated with equine aging. To test this hypothesis, we used a novel electrochemical sensor device to compare basal and maximal oxygen consumption rates of oocytes obtained from mares aged 6 to 12 years (Young, n = 8 from 7 mares) and = 20 years (Old, n = 12 from 8 mares). Cumulus-oocyte complexes (COC) were collected by transvaginal, ultrasound-guided follicular aspirations of dominant follicles (35 mm) during oestrus and at 16 ± 2 h after induction of follicular maturation (2000 IU of hCG and 0.75 mg of deslorelin acetate). Recovered COC were incubated in medium [TCM-199; Life Technologies, Grand Island, NY, USA) with 10% fetal calf serum, 25 mg mL−1 gentamicin, and 0.2 mM pyruvate] at 38.5°C in 5% CO2 and air for 26 ± 2 h. After maturation, COC were stripped of cumulus cells and checked for the presence of an extruded polar body before electrochemical measurements using amperometry. A microchamber with a 3-electrode system (working, counter, and reference electrodes) was filled with 120 µL of medium (G-MOPS™, Vitrolife, Englewood, CO, USA) and overlaid with 120 µL of paraffin oil (OVOIL™, Vitrolife). The baseline current was measured before adding the oocyte through the oil layer and over the centre of the working electrode. Oxygen consumption was monitored as the linear decrease in the oxygen reduction current over time, which was converted to femtomoles of O2 consumed per second (fmol s−1) using a calibration curve for the sensor. Basal (nonstimulated) oxygen consumption was measured for 5 min, followed by assessment of maximal noncoupled respiratory capacity obtained by titrating 1 µM carbonyl cyanide m-chlorophenyl hydrazone (CCCP) at 8-min intervals. The highest value observed during CCCP titrations was considered the maximal oxygen consumption. Two-tailed Student’s t-tests were used to analyse data. Oocytes from young mares had higher basal oxygen consumption compared with old mares, respectively (mean ± s.e.m., 1.74 ± 0.18 and 1.27 ± 0.09 fmol s−1; P = 0.04) as well as higher maximal oxygen consumption (2.67 ± 0.19 and 2.05 ± 0.12 fmol s−1; P = 0.016). Mitochondrial efficiency (maximal/basal oxygen consumption) was not different for Young and Old, respectively (1.62 ± 0.13 and 1.65 ± 0.07; P = 0.9). In summary, we used a novel electrochemical sensor device to measure basal and maximal oxygen consumption of oocytes and to confirm our hypothesis that aging impairs mitochondrial respiratory capacity in equine oocytes, which may contribute to age-associated changes in equine fertility.