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Pioglitazone Mediated Reduction in Oxidative Stress and Alteration in Level of PPARI3, NRF2 and Antioxidant Enzyme Genes in Mouse Preimplantation Embryo during Maternal to Zygotic Transition.

Byline: Xu Lijie, Obaid Ullah, Liu Haixing, Ihsan Ali, Zhongshu Li and Nan-Zhu Fang

Keywords: Peroxisome proliferator-activated receptor gamma (PPARI3), Nuclear regulatory factor 2 (NRF2), Oxidative stress, Developmental block, Maternal-to-zygotic transition.


Embryo cultures are valuable in the study of preimplantation embryonic development, and they are often used to produce transferable embryos, although culture conditions are not optimal (Rizos et al., 2008). The maternal-to-zygotic transition (MZT) is an important period of mammalian embryonic development. Concomitant with this cellular event, zygotic genome activation (ZGA) is triggered, and oocyte-specific components degrading by ubiquitin-mediated proteasomal pathway (Roest et al., 2004), and modulating control of maternal transcripts is switched to zygotic transcripts ultimately (Lee et al., 2014). These changes are crucial to ensure a successful transition from the early embryonic stage to the late embryonic stage. If there is a delay in ZGA, embryos will arrest during development (Qiu et al., 2003).

Mouse embryos generally arrest at the 2-cell stage during the G2 phase, a phenomenon referred to as the 2-cell block (Flach et al., 1982). During the 2-cell stage, there is an increase in the hydrogen peroxide (H2O2) level in cultured mouse embryos at metaphase, which remains elevated until they enter the early 4-cell stage (Naser-Esfahani et al., 1990). An elevated reactive oxygen species (ROS) level can lead to oxidative stress, which damages DNA, lipids, and proteins. Therefore, the 2-cell block is believed to associate with oxidative stress in mouse embryos.

Peroxisome Proliferator-activated receptor gamma (PPARI3), a nuclear receptor of the ligand-activated transcription factor family, can regulate gene transcription. PPARI3 binds the retinoid X receptor (RXR) (Varga et al., 2011), and the heterodimer binds PPARI3 response elements (PPREs), which are located in the promoter region of target genes. A previous study reported that PPARI3 can induce the expression of antioxidant enzymes and suppress the expression and activity of nicotinamide adenine dinucleotide phosphate hydrogen (NADPH) oxidase through PPARI3. PPARI3 then regulates oxidative stress by acting as a ROS scavenger and ROS generator (Jung et al., 2007). It is believed that PPARI3 is a novel antioxidant stress factor (Polvani et al., 2012).

Pioglitazone, a derivative of thiazolidinedione, is a PPARI3 agonist used in the treatment of individuals with type 2 diabetes (Kota et al., 2005). Accumulating evidence indicates that pioglitazone can also protect cells from oxidative stress (Chen et al., 2004).

Currently, the 2-cell block is the main barrier to the mass production of embryos in vitro. Although studies show that supplementing media with antioxidants can reduce the rate of the developmental block (Goto et al., 1992), the effect of pioglitazone as an antioxidant in mouse embryo development is not yet known. To our knowledge, this is the first study to elucidate the mechanism of action of pioglitazone in mouse preimplantation embryos at cellular and molecular levels.

Materials and methods

All chemicals and reagents used in this study were purchased from Sigma-Aldrich Chemical Company (St. Louis, MO, USA) unless otherwise indicated.

Superovulation and zygote collection

Kunming mice were purchased from the Experimental Animal Center of Yanbian University. Female mice 8-10 weeks old were housed under conditions of 12 h light: 12 h dark at approximately 24AdegC. Each female mouse received an intraperitoneal injection of 10 IU pregnant mare serum gonadotropin (PMSG; Ninbo Hormone Co., Ltd., Ninbo China), followed by 10 IU human chorionic gonadotropin (hCG; Ninbo Hormone Co., Ltd.) 48 h later. Immediately after the administration of hCG, each female mouse was mated with a male mouse. Mating was confirmed after 12 h by the presence of vaginal plugs. Approximately 22 h after the administration of hCG, the mice with vaginal plugs were sacrificed. Their oviducts were harvested and placed in the M2 medium. Zygotes were released from the oviducts under a stereo microscope. Cumulus cells were removed with 0.03%. The embryos were washed and then cultured at 37AdegC in a humidified atmosphere of 5% CO2 in the air.

Pioglitazone antioxidant capacity assay

Zygotes without cumulus cells were washed in M16 medium containing 25mM H2O2 three times and then cultured in the same medium at 37AdegC in a humidified atmosphere of 5% CO2 in air for 30 min. After H2O2 treatment, the zygotes were randomly divided into two groups; one group was cultured in an M16 medium, while the other group was cultured in M16 medium containing 5uM pioglitazone. Pioglitazone was removed after 48 h, and the embryos were cultured until day 4. Embryo development up to the blastocyst stage was assessed. Non-treated embryos served as the control.

Measurement of the ROS level

Mouse embryos from control and treated groups were washed twice in poly vinyl alcohol (PVA) (1 mg/ml) and then placed in a 50 ul drop of 2', 7'-dichlorodihydro-fluoroscein diacetate (DCHFDA) (10 mol/L). The embryos were incubated for 15 min in dark at 37AdegC in a humidified atmosphere of 5% CO2. Embryos were then washed twice with phosphate-buffered saline (PBS) and examined under an epifluorescent microscope (Leica DM IRM, Leica, Wetzlar, Germany) equipped with blue-light (535 nm) excitation. The images were analyzed by ImageJ 1.49 software-(Pro plus 6.0) (National Institutes of Health, Bethesda, MD, USA). The experiment was performed three times.

RNA isolation and cDNA synthesis

For PCR analysis, 200 embryos at the 2-cell stage were harvested at 42 h after hCG injection as described previously (Zhang et al., 2015). Total RNA was isolated from whole embryos using the Qiagen RNeasy Mini Kit (Qiagen, Hiden, Germany) according to the manufacturer's instructions. cDNA was synthesized by reverse transcription using the Prime Script(tm) RT Reagent Kit with gDNA Eraser (Takara Biotechnology Co., Ltd., Dalian, China) according to the manufacturer's instructions. PCR was carried out in 25 ul reaction volumes containing 13 ul of 2x Taq PCR Master Mix (Tiangen Biotech Co., Ltd., Beijing, China), 2 ul of cDNA, 0.5 ul of forward and reverse primers (5 mM) (Table I), and 9 ul of sterile H2O (Tiangen Biotech Co., Ltd.). Following the initial preincubation step at 95AdegC for 3 min, the reaction consisted of 35 cycles of denaturation at 95AdegC for 30 sec, annealing at 56-62AdegC for 30 sec, and extension at 72AdegC for 30 sec.

The final extension was performed at 72AdegC for 5 min. The PCR products were separated by electrophoresis on 2% agarose gels (Wenmin et al., 2017). The band intensities were analyzed by Lane 1D Analysis Software (Beijing Sage Creation Science Co., Ltd., Beijing, China). Three biological replicates were performed.

Statistical analysis

Statistical analysis was carried out using SPSS 17.0 software (IBM Corp., New York, USA). Data are expressed as percentages (mean +- SEM). P 0.05). By contrast, the 4-cell stage and the blastocyst rate of embryos exposed to H2O2 were significantly lower (P < 0.05) than in the control and those treated with H2O2 and pioglitazone.

Effects of H2O2 and pioglitazone on the ROS level in mouse embryos

The intracellular ROS level plays an important role in the development of embryos (Ali et al., 2017). To quantify the ROS level by fluorescent microscopy, embryos were collected at the blastocyst stage and stained with DCHFDA (Fig. 1A). The ROS level in embryos treated with H2O2was significantly higher (P < 0.05) than the control and those treated with H2O2 and pioglitazone (Fig. 1B).

PPARI3 and NRF2 expression in mouse embryos during the MZT

Compared to the respective controls, there were no significant changes in PPARI3 and nuclear regulatory factor 2 (NRF2) expression levels in embryos treated with H2O2. However, PPARI3 and NRF2 levels increased significantly (P <0.05) in embryos treated with H2O2 and pioglitazone (Fig. 2B).

Expression of antioxidant genes downstream of NRF2 in mouse embryos during the MZT

To determine the role of pioglitazone in H2O2-induced oxidative damage, the expression levels of several antioxidant enzymes in mouse embryos treated with H2O2 or H2O2 and pioglitazone were measured. Compared to the respective controls, there were no significant changes in the expression levels of GPX4 in embryos treated with H2O2. By contrast, the expression levels of GPX3, SOD1, and SOD3 increased in embryos treated with H2O2, while those of GPX4 and SOD2 decreased compared with the respective controls (Fig. 3B). After the treatment of embryos with H2O2 and pioglitazone, the expression levels of GPX3, GPX4, SOD1, SOD2, and SOD3 increased compared to H2O2 treatment alone.

NADPH oxidase expression in mouse embryos during the MZT transition

To further investigate the role of pioglitazone in H2O2-induced oxidative damage, the NADPH oxidase expression level in mouse embryos treated with H2O2 or H2O2 and pioglitazone was measured. As shown in Figure 4B, the expression levels of NOX2, NOX4, DUOX1, and NOXA1 increased in 2-cell stage embryos treated with H2O2. After the treatment of embryos with H2O2 and pioglitazone, the NOX2, NOX4, DUOX1 and NOXA1 level decreased compared to H2O2 treatment alone.


In vitro, culture conditions create a suboptimal environment for mouse preimplantation embryos (Ecker et al., 2004), which are extremely susceptible to oxidative stress. Cultured embryos, whose defense mechanisms are insufficient, tend to arrest during development (Qiu et al., 2003). Therefore, altering the response of cultured embryos to oxidative stress might prevent their developmental arrest.

Several studies have reported that PPARI3 agonists can activate antioxidant pathways. For instance, the PPARI3 agonist GW1929 stimulated the activity of human dopaminergic neurons and protected them from oxidative stress induced by H2O2 and the mitochondrial toxin rotenone (Makela et al., 2016). Similar results were reported in human umbilical vein endothelial cells; H2O2 decreased the PPARI3 expression level, which was reversed by catalase (CAT) treatment (Blanquicett et al., 2010). However, these findings are inconsistent with the results of this study. We demonstrated that H2O2 had no effect on the PPARI3 expression level in mouse embryos. This discrepancy in results might be due to differences in cell culture conditions, the H2O2 concentration, the length of incubation, and the time of termination after treatment.

Next, we determined whether pioglitazone can affect H2O2-induced oxidative stress and promote development. H2O2 treatment impaired embryo development, while pioglitazone promoted embryo development by partially alleviating the oxidative stress. This effect was independent from that of PPARI3 on oxidative stress, because the Nrf2 antioxidant pathway was activated.

Under physiological conditions, Nrf2 is inactive in the cytosol, where it rapidly degrades, When cells encounter oxidative stress, active Nrf2 shuttles to the nucleus, where it binds to the antioxidant reactive element (ARE) in the promoter of antioxidant genes (Polvani et al., 2012). In this study, oxidative stress failed to induce Nrf2 expression in 2-cell stage embryos. These results agree with those of Amin et al. (2014) who reported that the Nrf2 mRNA level in bovine embryos cultured under high-oxygen conditions (i.e., 20% vs. 5%, the normal) decreased moderately. However, the Nrf2 expression level in late-stage embryos cultured under high-oxygen conditions was higher than in embryos cultured under low-oxygen conditions. It might be because the activation of Nrf2 takes much longer time in oxidative stress environment in embryos development (Nasr-Esfahani et al., 1990).

The relationship between PPARI3, a protein of the Nrf2 antioxidant pathway, and Nrf2 is direct (Park et al., 2004); in the absence of Nrf2, PPARI3 expression decreases, and vice versa. For example, PPARI3 expression was markedly reduced in Nrf2 null mice compared to wild-type mice (Cho et al., 2010). Furthermore, PPARI3 agonists, such as rosiglitazone and 15d-PGJ2, upregulated Nrf2 expression, PPARI3 might also act together with Nrf2 in the activation of antioxidant genes (Park et al., 2004), such as CAT, glutathione peroxidase (GPx), and superoxide dismutase (SOD). During oxidative stress, PPARI3 regulates the expression of CAT (Girnun et al., 2002; Gray et al., 2012), one of the two most important enzymes involved in the degradation of H2O2. The activation of PPARI3 also markedly increased CAT expression and activity. In rat cortical neurons, for example, pioglitazone activated PPAR, thereby inducing CAT activity (Gray et al., 2012).

Furthermore, the protection of endothelial cells against H2O2-induced oxidative stress by rosiglitazone is dependent on CAT (Girnun et al., 2002).

GPx is the other important enzyme involved in the degradation of H2O2. Studies with PPARI3 agonists report PPARI3 to regulate GPx in different cell lines (Chung et al., 2009; Pei et al., 2013). In human skeletal muscle cells treated with H2O2, the PPARI3 agonist troglitazone upregulated GPx3 mRNA and protein levels (Chung et al., 2009). Similar results were reported by Pei et al. (2013) who showed that rosiglitazone prevented the decrease in GPx expression and activity in rat cardiomyocytes exposed to infrasound, while O2(-) and H2O2 levels decreased. In the same study, rosiglitazone also upregulated SOD1 and SOD2 expression and activity (Pei et al., 2013). Results from transient transfixion assays, promoter analysis, and knockout mice reveal that PPARI3 regulates SOD (Flach et al., 1982; Yu et al., 2008). For example, SOD2 mRNA and protein levels decreased in the heart of PPARI3 knockout mice (Yu et al., 2008).

The PPARI3 agonist pioglitazone also elevated the mRNA levels of all three SOD isoforms. Our finding was in the line with these results.

In addition to up regulating the expression levels of antioxidant enzymes, PPARI3 downregulates NADPH oxidase expression. The different NADPH oxidase isoforms NOX1-NOX5 and DUOX1/2 play important roles in ROS generation because oxidative stress induced by H2O2 can activate NADPH oxidase (Wu et al., 2010). Hwang et al. (2005) reported that PPARI3, a negative regulator of NADPH oxidase, can reduce the production of O2 (-), Similar results were reported in vascular endothelial cells, supporting the concept that PPARI3 agonists decrease p22-phox gene expression in HUVECs. Another study reported that PPARI3 agonist ciglitazone down regulated the NOX regulatory subunit of p47-phox oxidase in phagocytes (Von et al., 2002). We found that pioglitazone inhibits not only the NOX catalytic subunit but also the NOX regulatory subunit of NOXA1, crucial components of NADPH oxidase.

The mechanism responsible for the decrease in NADPH oxidase expression is not clear. Based on the evidence that the PPARI3 agonist rosiglitazone decreased NADPH oxidase expression in endothelial cells via AMPK activation (Ceolott et al., 2007).


In conclusion, pioglitazone functions as an antioxidant in mouse embryos by increasing the PPARI3 level, activating the Nrf2 anti-oxidative pathway, and inhibiting NADPH oxidase. These cellular events led to the suppression of H2O2-induced ROS production, which improved embryonic development. PPARI3, resulting in an increase in antioxidant enzyme activity but a decrease in the NADPH oxidase level, mediated the protective effects of pioglitazone.


This work was funded by the National Natural Science Foundation of China (No. 31360546).

Statement of conflict of interest

The authors report no conflicts of interest. The authors alone are responsible for the content and writing of this article.


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Author:Lijie, Xu; Ullah, Obaid; Haixing, Liu; Ali, Ihsan; Li, Zhongshu; Fang, Nan-Zhu
Publication:Pakistan Journal of Zoology
Article Type:Report
Geographic Code:9CHIN
Date:Jun 30, 2019
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