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Revista Brasileira de Zootecnia

On-line version ISSN 1806-9290

R. Bras. Zootec. vol.41 no.12 Viçosa Dec. 2012

http://dx.doi.org/10.1590/S1516-35982012001200006 

BREEDING, GENETICS AND REPRODUCTION

 

Effects of green tea polyphenols, insulin-like growth factor I and glucose on developmental competence of bovine oocytes

 

 

Zhengguang WangI; Chunquan FuII; Songdong YuI

ICollege of Animal Science of Zhejiang University; Key Laboratory for Molecular Animal Nutrition, Ministry of Education, Hang Zhou, 310029, P. R. China
IIJinhua College of Vocation and Technology

 

 


ABSTRACT

The present study examined the effects of green tea polyphenols (GTP), insulin-like growth factor-I (IGF-I) and glucose on oocyte in vitro maturation, subsequent embryo development and blastocyst quality in bovine. Cumulus-oocyte complexes (COC) were aspirated from the ovaries and cultured in synthetic oviduct fluid supplemented with MEM amino acids (SOFaa) media supplemented with one of the following supplements: GTP (0, 10, 15 and 20 µM), IGF-I (0, 50, 100 and 150 ng/mL) or glucose (0, 1.5, 5.6 and 20 mM) for 24 h. The results showed that oocytes cultured in media supplemented with 15 µM GTP, 100 ng/mL IGF-I and 5.6 mM glucose, in separate experiments, have higher cleavage and blastocyst rates compared with oocytes cultured in media without or with other concentration of GTP, IGF-I and glucose. Then these three substances with the concentration above were added together into SOFaa media and constituted a modified medium (Modified SOFaa). The COC were cultured in control SOFaa media and modified SOFaa media, respectively. The results showed that modified SOFaa media increased the intracellular glutathione concentration of matured oocytes, blastocyst rates and total cell numbers and cell numbers of inner cell mass per blastocyst compared with the control. Supplementing of GTP, IGF-I and glucose synchronously to maturation media can increase the intracellular GSH concentration of oocytes after in vitro maturation, and improve the embryo development and blastocyst quality in bovine.

Key words: blastocyst quality, embryo development, in vitro culture, in vitro maturation


 

 

Introduction

In vitro maturation (IVM) of bovine oocytes, followed by in vitro fertilization (IVF) and subsequent embryo culture, is an important tool used for both research and commercial purposes. However, rates of blastocyst formation for oocytes matured and fertilized in vitro are lower than those obtained with in vivo production systems (Lonergan & Fair, 2008). Low blastocyst formation by in vitro matured oocytes indicates that current oocyte maturation systems do not adequately support either nuclear and/or cytoplasmic maturation. Therefore, the improvement of oocyte maturation system by defining IVM conditions more similar to the in vivo environment is very important for increasing the blastocyst formation. Glucose is an essential energy substrate for mammalian cells and has been reported to improve the nuclear maturation of cow, mouse and pig oocytes (Hashimoto et al., 2000a; Herrick et al., 2006; Wongsrikeao et al., 2006). Several previous studies have shown that addition of IGF-I to in vitro media promotes oocytes maturation and also affects their subsequent in vitro development (Quetglas et al., 2001; Stefanello et al., 2006). Recently, researchers have demonstrated that in vitro bovine embryo productions are improved by treatments with GTP during IVM of oocytes (Wang et al., 2007).

However, the effects of GTP, IGF-I and glucose combined supplementation on the nuclear and cytoplasmic maturation of bovine oocytes, subsequent embryo development and blastocyst quality have not been studied. Therefore, the objective of the present study was to evaluate the effects of GTP, IGF-I and glucose for IVM of bovine oocytes on the oocyte glutathione content, oocyte nuclear and cytoplasmic maturation (measured as the capacity of subsequent embryo development), embryonic development (cleavage and blastocyst rates) and blastocyst quality.

 

Material and Methods

All chemicals and media were purchased from Sigma Chemical Co. (St. Louis, MO, USA), unless otherwise indicated. The GTP used in this study contained 99% catechin derivatives, among which the major components were 50% (-)-epigallocatechin gallate (EGCG), 22% (-)-epicatechin gallate, 18% (-)-epigallocatechin and 10% (-)-epicatechin. The average molecular weight of the GTP was calculated according to the percentage of the major component.

The in vitro production of embryos was carried out as previously described by Rizos et al. (2002) with minor modifications. Briefly, cumulus-oocyte complexes (COC) were obtained by aspirating 2 to 6 mm follicles from the ovaries of cows collected at abattoir. The COC with compact cumulus cells were washed three times in Hepes buffered Tyrode's medium supplemented with 0.3% bovine serum albumin (BSA) and in maturation medium, respectively. Groups of 10 COC were placed in 50 µL maturation medium, covered with mineral oil and then incubated at 38.5 ºC in 5% CO2 in air with saturated humidity for 24 hours. The basic maturation medium was SOFaa, which consisted of modified synthetic oviduct fluid (SOF) supplemented with MEM non-essential amino acids, BME essential amino acids, 1.5 mM glucose, 1 mM glutamine, 1 µg/mL porcine FSH, 5 µg/mL ovine LH and 4 mg/mL BSA. The SOF medium used in this study was based upon the original formulation (Tervit et al., 1972) with subsequent modifications (Gardner et al., 1994). To evaluate the nuclear maturation, after 24 hours of culture, oocytes were completely denuded by vortex shaking and placed on glass slides in small drops. The slides were fixed in methanol:acetic acid fixative (1:3) solution for a minimum of 24 hours. The oocytes were stained with 1% aceto-orcein and examined under a phase contrast microscope. Oocytes at the M II stage with the first polar body were classified as fully matured. Maturation rate is defined as the ratio of oocytes at the M II stage and total oocytes.

The in vitro fertilization was performed with frozen-thawed sperm from one bull at a concentration of 2×106 spermatozoa/mL. Frozen bull semen was thawed and prepared by a swim-up procedure (Parrish et al., 1986). Gametes were co-incubated for 22 hours at 38.5 ºC under an atmosphere of 5% CO2 in air with maximum humidity in dishes with 10 COC and 50 µL of Tyrode's albumin lactate pyruvate medium (TALP). Approximately 20 h post insemination (hpi), presumptive zygotes were denuded by gentle vortexing and washed four times in PBS and once in SOFaa medium. Embryo culture took place in SOFaa under mineral oil in a humidified atmosphere of 5% CO2, 7% O2 at 38.5 ºC. Cleavage and development of embryos to the blastocyst stage were assessed at 48 hpi and 192 hpi, respectively.

For the GSH assay, a sample of matured oocytes was stripped off surrounding cumulus cells by repeated pipetting with a narrow-bore glass pipette in Hepes-TALP and washed three times in Mg2+/Ca2+-free PBS, containing 1 mg/mL polyvinylpyrrolidone. Pools of 50 oocytes in 10 µL of PBS were placed in microtubes, frozen at -20 ºC and thawed at room temperature. This procedure was repeated three times. Complete cell disruption was achieved by repeated aspiration using a narrow- bore pipette. Samples were then mixed with 0.1 M phosphate buffer containing 5 mM EDTA. After rapid mixing with 5 mM 5,5'-dithiobis 2-nitrobenzoic acid, 1 IU of glutathione reductase and 1.1 mM NADPH, the increase in absorbance at 412 nm from 30 s to 5 min was measured using a double-beam spectrophotometer (Beckman Mod. 35, Irvine, CA). Blanks containing 10 µL of PBS without oocytes were similarly processed and no detectable amounts of GSH-GSSG were found. The total GSH content in the oocyte was calculated from a standard curve prepared using GSH (Tietze, 1969; Takahashi et al., 1993). In the conditions at the laboratory where the analyses took place, the assay limit was 25 pmol of GSH-GSSG.

The differential staining of inner cell mass (ICM) and trophoectoderm cells (TE) associated with TUNEL was used to assess the Day 8 blastocyst quality and the apoptosis conditions as previously described (Fouladi-Nashta et al., 2005). Briefly, embryos were permeablized using 0.2% (v/v) solution of Triton X-100 in SOF containing 4 mg/mL BSA for 20 s. Embryos were then washed and incubated in 30 µg/mL propidium iodide (stains the TE cells red) for 10 min followed by washing and fixation in 4% paraformaldehyde containing 30 µg/mL Hoescht 33342 (stains all cells blue). Apoptotic cells were then detected by TUNEL labeling using a FITC-conjugated in situ cell death detection kit, fluorescein (Roche, Penzberg, Germany) according to the instructions of the manufacturer. Briefly, embryos were permeabilized by incubating in 0.1% (v/v) Triton X-100 for 5 min and incubated in the kit reagent (1:10 dilution of the terminal deoxynucleotidyl transferase solution in label solution) in a humid chamber for 45 min at 37 ºC. Embryos were washed and immediately mounted on glass slides and examined under an epifluorescent microscope.

In experiment 1, oocytes were matured in SOFaa media supplemented with the different concentrations of GTP (0, 10, 15 and 20 µM), respectively. In experiment 2, IGF-I (0, 50, 100 and 150 ng/mL, respectively) were added in SOFaa media to optimize the supplemental concentration of IGF-I during IVM of bovine oocytes. In experiment 3, oocytes were matured in SOFaa media in the presence of 0, 1.5, 5.6 and 20 mM glucose, respectively. In experiment 4, GTP (15 µM), IGF-I (100 ng/mL) and glucose (5.6 mM) were added together into SOFaa media based on the results of experiment 1-3 and constituted a modified media (Modified SOFaa). Oocytes were cultured in SOFaa (control) and modified SOFaa, respectively. In experiment 4, matured oocytes were fixed to assay the intracellular GSH concentration and then Day 8 blastocysts were used to investigate the effects of modified SOFaa media on the embryo quality and apoptosis conditions.

All experiments were replicated three times. Data were analyzed by analysis of variance (ANOVA) of the software SAS (Statistical Analysis System, version 6.13). Comparisons were considered significantly different if P<0.05.

 

Results

The maturation rates of oocytes were higher in 10 and 15 µM GTP treatments than in the 20 µM GTP treatment (P<0.05; Table 1). Supplementation of media with three GTP concentrations during IVM improved the cleavage rate compared with control (P<0.05). Compared with no addition and supplementation of 10 µM GTP, the inclusion of 15 µM and 20 µM GTP during IVM increased the blastocyst rate (P<0.05).

The inclusion of 100 and 150 ng/mL IGF-I during IVM increased the maturation rates of oocytes compared with control and 50 ng/mL IGF-I (P<0.05; Table 2). The presence of 100 ng/mL IGF-I during IVM increased cleavage and blastocyst rate compared with 50 ng/mL IGF-I and control (P<0.05). No improvements in the cleavage and blastocyst rate were found when 150 ng/mL IGF-I were added to maturation medium in comparison with the 100 ng/mL IGF-I treatment.

Supplementation of media with glucose during IVM improved maturation of bovine oocytes compared with control (Table 3). The oocytes matured in media supplemented with 5.6 mM glucose had higher cleavage and blastocyst rate than oocytes matured with 1.5 mM glucose and control (P<0.05). However, a further increase in glucose concentration from 5.6 to 20 mM resulted in a decrease in cleavage and blastocyst rate (P<0.05).

The modified SOFaa media did not improve the maturation rate and cleavage rate compared with control (Figure 1). The modified media increased the blastocyst rates on day 8 of in vitro insemination compared with the control media (P<0.05). The modified media increased the intracellular GSH concentration within the oocytes when compared to control media (P<0.05; Figure 2). The total cell numbers and ICM cell numbers of blastocysts were significantly higher in the modified SOFaa group than the control (P<0.05; Table 4). However, the apoptosis rates of blastocysts had no difference between the modified SOFaa group and the control (P>0.05).

 

 

 

 

Discussion

The main finding of this study was that GTP, IGF-I and glucose supplemented synchronously during IVM improve the subsequent developmental competence of embryos. This improvement in developmental competence of oocytes may be partly due to increase of intracellular GSH concentration of matured oocytes and improvement of the quality of blastocysts.

The GTP have strong antioxidant activity (Higdon & Frei, 2003) and are potent scavengers of ROS (reactive oxygen species), such as superoxide, hydrogen peroxide, hydroxyl radicals and nitric oxide (Schroeder et al., 2003). The results of experiment 1 showed that treatment with 15 µM GTP during IVM culture enhanced the developmental competence of bovine oocytes. However, a further increase in the concentration of GTP from 15 to 20 µM did not improve the blastocyst rate. These findings were consistent with previous reports (Wang et al., 2007). In agreement with thse observations, it has been stated that supplementation of lower EGCG concentration (10 µg/mL) during IVF significantly increased the fertilization rate, while higher EGCG concentration (25 µg/mL) decreased the percentage of fertilized oocytes (Spinaci et al., 2008). Yavari et al. (2010) also demonstrated that the treatment with higher concentrations of EGCG (10 and 50 µM) during IVC is apparently harmful for the in vitro development of porcine parthenotes.

The results of experiment 2 demonstrated that IGF-I at a dose of 100 or 150 ng/mL stimulated nuclear maturation of cumulus-enclosed oocytes. The addition of IGF-I during oocyte maturation not only helped in achieving nuclear maturation but also influenced the cytoplasmic maturation and improved early embryonic development. These findings were consistent with previous reports (Pawshe et al., 1998) showing that IGF-I enhanced embryonic cleavage rate and development in bovine when added to the oocyte maturation medium. Although the reasons for this enhancement were unknown, the previous study suggested that IGF-I increased oestradiol production by the theca granulosa cells in serum-free culture (Shores et al., 2000). Furthermore, it was indicated that IGF-I acts as an anti-apoptotic factor during bovine oocyte maturation (Wasielak & Bogacki, 2007). The biological effects of IGF-I were mediated by its interaction with the IGF type I receptor and modulated by IGF binding proteins (Jones & Clemmons, 1995). Thus, the addition of IGF-I beyond the optimum concentration (100 ng/mL) did not improve the embryo development in this study.

The results of experiment 3 indicated that sufficient glucose is required for oocytes to obtain developmental competence during the maturation period. The beneficial effect of glucose supplementation in the IVM medium may be due to their ability to speed up the progression of nuclear maturation (Iwata et al., 2004). The results from this study also demonstrated that excessive glucose during oocyte maturation impairs the developmental competence. In agreement with the results of experiment 3, Hashimoto et al. (2000b) reported that the COC cultured in substantially high glucose concentrations (10-28 mM glucose) compromised the blastocyst development compared with COC cultured in low to moderate glucose levels (1.5 mM or 5.6 mM glucose).

The present study demonstrated first the effects of GTP, IGF-I and glucose supplementing synchronously to maturation media on improving the development of bovine in vitro embryo. This improvement in the developmental competence of oocytes may be partly due to increase of intracellular GSH concentration after IVM of oocytes. Furthermore, the results of experiment 4 showed that modified SOFaa increase the total cell number and cell number of ICM in Day 8 blastocysts. One approach to evaluate blastocyst quality is to count the cell numbers of the ICM and the TE, as well as total cells of the embryo by differential staining. It is well documented that total cell numbers and numbers of ICM cell can be regarded as valuable indicators of cattle embryo viability (Knijin et al., 2003; Koo et al., 2002). Thus, the current result suggested that supplementing GTP, IGF-I and glucose to maturation media synchronously can improve the quality of bovine blastocysts. In agreement with our observation, it has been suggested that the proportion of ICM cells in blastocysts is crucial for later post-implantation development (Iwasaki et al., 1990) and an increase in total cell number in blastocysts correlates with improved embryo viability (van Soom et al., 1997).

 

Conclusions

Supplementing of green tea polyphenols, insulin-like growth factor I and glucose synchronously to maturation media can increase the intracellular glutathione concentration of oocytes after in vitro maturation, and improve the embryo development and blastocyst quality in bovine.

 

Acknowledgements

This research was supported by grants from Zhejiang Science and Technology Committee (Grant Agreement No.: 2008C02002-2; 2010C34009) and Zhejiang Province Natural Science Foundation (Grant Agreement No.: Y3100076).

 

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Received August 31, 2012 and accepted July 25, 2012.

 

 

Corresponding author: wzhguang68@zju.edu.cn

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