Effects of melatonin on oocyte developmental competence and the role of melatonin receptor 1 in juvenile goats

Melatonin enhances in vitro embryo development in several species by improving the oocyte developmental competence during in vitro maturation (IVM). Melatonin has a wide range of actions, from scavenging reactive oxygen species (ROS) to regulating gene expression, and it can also act by way of melatonin receptors. The aim of this study was to determine the mechanism of action of melatonin during the IVM of juvenile goat oocytes and the role of the membrane receptors. Melatonin receptor 1 was immunolocalized in cumulus cells and oocytes before and after 24 hr of IVM. The effect of melatonin on oocyte developmental competence was tested in three experimental IVM groups: (a) control, (b) 10^?7 M melatonin, and (c) 10^?7 M melatonin +10^?7 M luzindole (an inhibitor of both melatonin receptors). After IVM oocytes were assessed for ROS levels, mitochondrial activity, adenosine 5′‐triphosphate (ATP) concentration and relative gene expression (ACTB, SLC1A1, SOD1, GPx1, BAX, DNMT1, GCLC and GDF9). IVM‐oocytes were in vitro fertilized and cultured under conventional conditions. Blastocyst rate and quality (differential cell count) were assessed at 8 days post‐fertilization. Melatonin decreased ROS levels, increased mitochondrial activity and ATP content and increased blastocyst quality compared to control group (55.8 vs. 30.4 inner cell mass ICM, p < 0.05). There was no effect on the relative gene expression due to treatment with melatonin. In conclusion, we have showed that melatonin improves oocyte developmental competence in juvenile goats by reducing ROS levels and improving mitochondrial activity.     

抗氧化剂对家畜胚胎体外发育影响的研究进展

现在研究普遍认为活性氧自由基是导致胚胎体外发育阻滞的主要原因。本文主要综述了不同抗氧化剂对牛胚胎体外发育的影响,并分析其作用机制。     

All‐trans retinoic acid improves goat oocyte nuclear maturation and reduces apoptotic cumulus cells during in vitro maturation

All‐trans retinoic acid (t‐RA) is a natural component and representative physiologically active metabolite of vitamin A, having multiple physiologic functions. The objective of this study was to evaluate the effect of t‐RA on goat oocyte maturation and cumulus cell apoptosis during in vitro maturation (IVM). Immature goat cumulus‐oocyte complexes (COCs) were matured in vitro in the absence or presence of t‐RA at concentrations of 10 nmol/L, 100 nmol/L and 1000 nmol/L. Oocyte maturation and embryo development were assessed by polar body formation and parthenogenetic activation, respectively. Oocyte survival was checked by Trypan blue staining. Apoptosis of cumulus cells was analyzed by terminal deoxynucleotidyl transferase nick end labeling staining and quantitative real‐time PCR. In comparison with the control group, 100 nmol/L and 10 nmol/L t‐RA significantly improved goat nuclear oocyte maturation and survival (P < 0.05). Addition of 1000 nmol/L t‐RA improved nuclear maturation (P < 0.05), but had no effect on survival of goat oocytes. t‐RA had no positive effect on goat parthenogenetic embryonic cleavage, blastocyst formation or total cell numbers. However, t‐RA inhibits the apoptosis of cumulus cells (P < 0.01). t‐RA treatment up‐regulated the expression of B‐cell lymphoma 2 (BCL‐2), catalase (CAT) (P < 0.05) and down‐regulated the expression of Caspase‐8 (P < 0.05). In conclusion, t‐RA has positive effects on goat oocyte nuclear maturation and reduces apoptotic cumulus cells during IVM.     

The Effect of Melatonin on the Secretion of Progesterone in Sheep and on the Development of Ovine Embryos In Vitro

Two experiments were carried out in order to determine whether melatonin can improve secretion of progesterone in vivo, and its effect on embryonic development in vitro. In the first experiment, blood samples were collected from 5 ewes at 15 min intervals for 2 h at 7 and 10 days after withdrawal of progestagen pessaries. The first hour constituted a control period, which ended with an intravenous administration of 3 g/(kg bw)^0.75 melatonin. All the ewes on day 7 and three of the ewes on day 10 showed a progesterone response to melatonin challenge, defined as an increase in the plasma progesterone concentration in at least two consecutive samples during the post-treatment period above the mean+2SD of the values in the pre-treatment period. A paired t-test revealed a significant effect of melatonin on the overall plasma progesterone concentrations before and after the challenge, both on day 7 (pre, 0.61±0.11; post, 0.73±0.13 ng/ml; p<0.01) and day 10 (pre, 1.16±0.19; post, 1.30±0.20 ng/ml; p<0.05). Ninety-one thawed embryos (46 morulae and 45 blastocysts) were used in the second experiment, being cultured with or without 1 g/ml melatonin. If the embryos were blastocysts when the culture started, melatonin increased the percentage that had hatched after 24 h of culture (p<0.01), and there was a lower percentage of degenerated embryos at the end of the incubation period (p<0.05). It may be concluded that melatonin treatment in sheep can increase both fertility and prolificacy by improving luteal function and embryonic survival.     

Melatonin improves testicular haemodynamics,echotexture and testosterone production in Ossimi rams during the breeding season

The objective was to determine effects of a single parenteral dose of melatonin on testicular blood flow indices, testicular echogenicity and plasma testosterone concentrations in rams during the physiological breeding season. We hypothesized that melatonin enhances testicular blood flow, echogenicity and plasma testosterone concentrations during the breeding season in rams. During the breeding season, 12 sexually mature Ossimi rams were randomly allocated to either a melatonin group (n = 8) that received 18 mg of melatonin in 1 ml of corn oil (injected SC) or a control group (n = 4) that received 1 ml corn oil only. Blood collection and ultrasonographic assessment of the testes and supratesticular arteries were conducted immediately before treatment (W0) and once weekly for 6 weeks after melatonin injection (W1-W6). Mean plasma testosterone concentrations were greater (p < .05; at least 1 ng/ml) in the melatonin-treated group compared to the control group from W4 to W6 after treatment. A decrease (p < .05) in both resistive index (RI) and pulsatility index (PI) began 1 week after melatonin injection (W1) and persisted until the end of the experiment, with mean RI and PI values in the melatonin group lower (p < .05) than those in the control group on W3 and W4. Furthermore, plasma testosterone concentrations in melatonin-treated rams were inversely correlated to both RI and PI (r = −.7 and −.6, respectively, p < .01). Testicular echogenicity decreased (p < .05) 1 week after melatonin injection (W1) and remained lower (p < .05) in the melatonin-treated group compared to the control group until the end of the study (W6). In conclusion, melatonin administration significantly altered testicular blood flow and echogenicity and increased plasma testosterone concentrations in Ossimi rams during the breeding season.     

Impact of incubator type on the yield of in vitro produced bovine blastocysts.

Because of suboptimal in vitro production of bovine blastocysts a new incubator model (Mini) was tested against the traditional (Heraeus). The difference between their properties seemed only to be the volume of the incubator space. No difference was noted between the CO2 or the temperature, but the data clearly showed a highly significant increase of the blastocyst rates, 6% versus 51% in the Heraeus and the Mini incubator, respectively, calculated as blastocysts per cleaved embryos. It was concluded that the incubator type or model may be a very important part of the in vitro production of bovine embryos, although we were not able to pin point specific causes for this difference.     

Aflatoxin B1 impairs mitochondrial functions,activates ROS generation,induces apoptosis and involves Nrf2 signal pathway in primary broiler hepatocytes

Aflatoxin B1 (AFB1) is known as a mycotoxin that causes various health problems in animals, but the precise mechanism of AFB1 on mitochondrial functions and apoptosis in primary broiler hepatocytes (PBHs) is not clear. The objective of this study was to investigate the effects of AFB1 on the mitochondrial functions, reactive oxygen species (ROS) generation, apoptosis and nuclear factor erythroid 2‐like factor 2 (Nrf2)‐related signal pathway in PBHs. Here, the mitochondrial membrane potential (MMP), ROS generation, antioxidative genes and apoptosis in PBHs induced by AFB1 were investigated. The results showed that AFB1 evoked mitochondrial ROS generation, decreased MMP and induced apoptosis in PBHs. AFB1 increased the percentage of apoptotic cells, and expression of caspase‐9 and caspase‐3, upregulated messenger RNA (mRNA) expression of Nrf2 and downregulated mRNA expressions of NAD(P)H: quinine oxidoreductase 1, superoxide dismutase and Heme oxygenase 1 in PBHs. The expression of Bax was also observed in cytoplasm. These findings suggested AFB1 results in a significant impairment of mitochondrial functions, activates ROS generation, induces apoptosis, and is involved in Nrf2 signal pathway through mitochondria ROS‐dependent signal pathways in PBHs.     

Evaluation of epididymis storage temperature and cryopreservation conditions for improved mitochondrial membrane potential,membrane integrity,sperm motility and in vitro fertilization in bovine epididymal sperm

The maintaining of the epididymis at lower temperatures during storage and transport improves sperm quality. Our study aimed to test whether epididymis storage temperature (post‐mortem) and sperm cryopreservation affect sperm kinetics, membrane integrity, mitochondrial potential and fertility capacity. Thirty‐six epididymides were collected from 18 bulls after slaughter and divided into two groups: at 4 or 34°C for 2–3 hr. The sperm was collected from the epididymis cauda. The evaluation consisted of computer‐assisted sperm analysis (CASA), SYBR14/PI/JC1 to evaluate membrane integrity, mitochondrial membrane potential (MMP) and measurement of lipid peroxidation (TBARS). The sperm was then frozen using an automatic device. After thawing, sperm samples were evaluated by the same variables and further in vitro fertilization rates. Cryopreservation negatively affected sperm motility in samples stored at 4 and 34°C. Nevertheless, the 4°C samples yielded higher rates of blastocyst formation. Pre‐freeze sperm motility, progressive motility and velocity were higher in sperm from epididymis stored at 4°C while post‐thaw sperm motility, progressive motility and velocity remained the same among samples from epididymis stored at 4 or 34°C. However, with regard to the kinetic patterns, samples collected from epididymis stored at 34°C had lower values when compared to those stored at 4°C prior the cryopreservation process. Our results indicate that epididymis handling conditions after cryopreservation may affect sperm quality after thawing, especially due to compromised MMP in sperm collected from epididymis stored at higher temperatures.     

Addition of erythrocytes to in vitro culture medium attenuates the detrimental effects of reactive oxygen species on bovine preimplantation embryo development

Erythrocytes were recently found to improve the early development of mice embryos by their antioxidant effect. The purpose of the present study was to examine the effect of erythrocytes on the in vitro development of bovine in vitro fertilized (IVF) embryos in medium supplemented with reactive oxygen species (ROS). IVF embryos were cultured in CR1aa medium supplemented with oxidizing agents, 0.5 mmol/L hypoxanthine and 0.01 U/mL xanthine oxidase (HX/XOD), in the presence and absence of erythrocytes (5 × 10⁴, 5 × 10⁵, 5 × 10⁶ and 5 × 10⁷ erythrocytes/mL). After 8 days, blastocysts were examined with a stereomicroscope. HX/XOD blocked development to the blastocyst stage (HX/XOD: 0%, control: 33%), but in the presence of both erythrocytes and HX/XOD, blastocyst development was restored to about one‐third to two‐thirds the normal rate (5 × 10⁵ to 5 × 10⁷ erythrocytes/mL: 12 to 23%). Furthermore, adding erythrocytes or erythrocyte hemolysate to medium without HX/XOD increased the blastocyst rate. These results suggest that the addition of erythrocytes can attenuate the detrimental effects of ROS on embryo development in bovine species as well as in mice.     

Effects of aflatoxin B1 on mitochondrial respiration,ROS generation and apoptosis in broiler cardiomyocytes

Aflatoxin B1 (AFB1) develops various toxic effects in the liver by impairing mitochondrial function, inducing cell apoptosis. However, little is focused on its toxicity to broiler cardiomyocytes (BCMs). Here, the mitochondrial membrane potential (MMP), reactive oxygen species (ROS) generation, cardiac troponin T (cTnT) location, apoptosis induced by AFB1, and antioxidative genes were investigated in BCMs. It was found that AFB1 evoked intracellular ROS generation, and induced apoptosis in BCMs. AFB1 treatment resulted in increased percentage of apoptotic cells, increased location range of cTnT in cytoplasm, upregulated messenger RNA (mRNA) expression of nuclear factor erythroid 2‐related factor 2 (Nrf2) and downregulated mRNA expressions of Mn‐superoxide dismutase in BCMs. These findings suggested AFB1 treatment caused significant cardiomyocyte damage and cardiotoxicity, impairment of mitochondrial functions, activated ROS generation, and induced apoptosis, and probably was involved in the Nrf2 signal pathway in BCMs.     

bFGF对3-硝基丙酸处理的小鼠受精卵体外发育能力的影响

【目的】研究在体外培养液中添加碱性成纤维细胞生长因子(bFGF)对3-硝基丙酸(3-NPA)处理的小鼠受精卵体外发育能力的影响,为提高氧化应激早期胚胎体外发育质量提供参考。【方法】在小鼠受精卵体外培养液中添加0、20、50、100和150 ng/mL bFGF,培养24、48和96 h,统计2-细胞率、4-细胞率和囊胚率,筛选最佳bFGF处理浓度。经腹腔注射12.5 mg/kg 3-NPA生产氧化应激体内受精卵,正常组小鼠腹腔注射等体积生理盐水,将获得的受精卵分为添加或不添加bFGF组,即3-NPA和3-NPA+bFGF组及对照组(C)和bFGF组,培养到囊胚后,用DCFH-DA检测胚胎内活性氧(reactive oxygen species, ROS)水平,CMF2HC检测谷胱甘肽(glutathione, GSH)水平,JC-1检测早期胚胎线粒体膜电位强度。【结果】0、20、50、100和150 ng/mL bFGF组2-细胞率均无显著差异(P>0.05),100 ng/mL bFGF组囊胚率显著高于其他各组(P<0.05),150 ng/mL bFGF组4-细胞率和囊...     

Melatonin protects the integrity of granulosa cells by reducing oxidative stress in nuclei,mitochondria, and plasma membranes in mice

Melatonin protects luteinized granulosa cells (GCs) from oxidative stress in the follicle during ovulation. However, it is unclear in which cellular components (e.g., nuclei, mitochondria, or plasma membranes) melatonin works as an antioxidant. GCs from immature (3 wks) ICR mice were incubated with hydrogen peroxide (H2O2; 0.01, 0.1, 1, 10 mM) in the presence or absence of melatonin (100 μg/ml) for 2 h. DNA damage was assessed by fluorescence-based immunocytochemistry using specific antibodies for 8-hydroxydeoxyguanosine (8-OHdG), an indicator of oxidative guanine base damage in DNA, and for histone H2AX phosphorylation (γH2AX), a marker of double-strand breaks of DNA. Mitochondrial function was assessed by the fluorescence intensity of MitoTracker Red probes, which diffuse across the membrane and accumulate in mitochondria with active membrane potentials. Lipid peroxidation of plasma membranes was analyzed by measuring hexanoyl-lysine (HEL), a oxidative stress marker for lipid peroxidation. Apoptosis of GCs was assessed by nuclear fragmentation using DAPI staining, and apoptotic activities were evaluated by caspase-3/7 activities. H2O2 treatment significantly increased the fluorescence intensities of 8-OHdG and γH2AX, reduced the intensity of MitoTracker Red in the mitochondria, increased HEL concentrations in GCs, and enhanced the number of apoptotic cells and caspase-3/7 activities. All these changes were significantly decreased by melatonin treatment. Melatonin reduced oxidative stress-induced DNA damage, mitochondrial dysfunction, lipid peroxidation, and apoptosis in GCs, suggesting that melatonin protects GCs by reducing oxidative stress of cellular components including nuclei, mitochondria, and plasma membranes. Melatonin helps to maintain the integrity of GCs as an antioxidant in the preovulatory follicle.     

Lipid-rich bovine serum albumin improves the viability and hatching ability of porcine blastocysts produced in vitro

The effects of lipid-rich bovine serum albumin (LR-BSA) on the development of porcine blastocysts producedin vitro were examined. Addition of 0.5 to 5 mg/ml LR-BSA to porcine blastocyst medium(PBM) from Day 5 (Day 0 = in vitro fertilization) significantly increased the hatching ratesof blastocysts on Day 7 and the total cell numbers in Day-7 blastocysts. When Day-5 blastocysts were culturedwith PBM alone, PBM containing LR-BSA, recombinant human serum albumin or fatty acid-free BSA, addition ofLR-BSA significantly enhanced hatching rates and the cell number in blastocysts that survived compared withother treatments. The diameter, ATP content and numbers of both inner cell mass and total cells in Day-6 andDay-7 blastocysts cultured with PBM containing LR-BSA were significantly higher than in blastocysts culturedwith PBM alone, whereas LR-BSA had no effect on mitochondrial membrane potential. The mRNA levels of enzymesinvolved in fatty acid metabolism and β-oxidation (ACSL1, ACSL3,CPT1, CPT2 and KAT) in Day-7 blastocysts weresignificantly upregulated by the addition of LR-BSA. The results indicated that LR-BSA enhanced hatchingability and quality of porcine blastocysts produced in vitro, as determined by ATP content,blastocyst diameter and expression levels of the specific genes, suggesting that the stimulatory effects ofLR-BSA arise from lipids bound to albumin.     

Alpha-lipoic acid improves the maturation and the developmental potential of goat oocytes in vitro

Oxidative stress inevitably occurs during oocyte maturation in vitro. α-lipoic acid (α-LA) has a strong antioxidant capacity, but the effect of α-LA on parthenogenetic activation of oocytes was rarely reported. This study aims to investigate the effect of supplementing α-LA to in vitro maturation medium on the subsequent developmental ability of goat parthenogenetic embryos during oocytes maturation. In the study, the goat cumulus-oocyte complex was divided into the experimental (with 25 μmol/L α-LA) and the control (without α-LA) groups. Oxidase expression was measured using RT-qPCR. After 18–22 hr of maturation, the oocytes were then parthenogenetic activated. The total antioxidant capacity of embryos was measured after 0, 24, 48, 72 and 96 hr of culture. Rates of oocyte maturation and the rates of development for parthenogenetic embryos in the α-LA group were significantly improved by 7.88% (p < .05) and 5.41% (p < .05) compared with those in the control group, respectively. After 24 hr, the difference in total antioxidant capacity was extremely significant in both groups. An evident decrease in the control group and a minor decrease in the α-LA group were observed (p < .01). The ratio of inner cell mass cells to the total cell number of blastocysts in the α-LA group increased compared with that in the control group (p < .05) on day 8. α-LA significantly promoted the expression of SOD and GPX4 of parthenogenetic blastocysts and maturated oocytes. α-LA (25 μmol/L) improved the maturation rate and the developmental competence of the parthenogenetic activation of oocytes, which might be mediated by maintaining the total antioxidant ability of oocytes during the culture period.     

藏红花素对小鼠卵母细胞体外成熟能力的影响

试验旨在探讨藏红花素（crocin）的抗氧化应激作用对小鼠卵母细胞体外成熟及后续胚胎发育能力的影响。在体外成熟（IVM）培养液中添加不同浓度藏红花素（0、5、10、15、20、25、30 μmol/L）,小鼠卵母细胞在体外成熟培养12 h后,检测卵母细胞第一极排出情况、卵母细胞胞质内活性氧（ROS）和谷胱甘肽（GSH）含量,并进行体外受精（IVF）;体外受精后6 h统计受精率,24 h统计卵裂率,96 h统计囊胚率。结果显示,与对照组相比,10、15 μmol/L藏红花素显著提高了卵母细胞第一极体排出率（P<0.05）;当藏红花素浓度继续增加时,卵母细胞的第一极体排出率下降,30 μmol/L藏红花素显著降低了卵母细胞第一极体排出率（P<0.05）;5、10、15 μmol/L藏红花素均显著降低了卵母细胞ROS含量（P<0.05）,10、15 μmol/L藏红花素均显著提高了卵母细胞GSH含量（P<0.05）。与对照组相比,10 μmol/L藏红花素组受精率、卵裂率、囊胚率差异均不显著（P>0.05）,15、20、25、30 μmol/L藏红花素均显著降低受精率和囊胚率（P<0.05）,对卵裂率影响不显著（P>0.05）。结果表明,在小鼠卵母细胞体外成熟培养液中添加10 μmol/L藏红花素可以显著增加第一极体排出率,显著降低卵母细胞ROS含量、提高卵母细胞GSH含量,但对受精后的胚胎发育无显著影响。     

母源基因Gdf9、Zar1、Mater和Dnmt1mRNA在绵羊卵母细胞和早期胚胎中的表达

为探讨母源基因在绵羊卵母细胞和胚胎发育过程中的表达模式,运用Real-time PCR技术研究4种母源基因:Gdf9(生长分化因子9)、Zar1(合子阻泄因子)、Mater(胚胎必要的母体抗原)及Dnmt1(DNA甲基化转移酶1)的mRNAs在绵羊GV期卵母细胞,24h成熟卵母细胞,2-细胞、4-细胞、8-细胞、16-细胞胚胎以及囊胚中的含量变化情况。结果表明:在GV期卵中Zar1、Mater、Gdf9以及Dnmt1m RNA相对含量最高(P<0.05);从2-细胞胚胎开始,4种基因的mRNA相对含量显著降低(P<0.05),各基因mRNA的含量在不同发育阶段的卵母细胞和胚胎中存在动态变化,这对卵子生长和胚胎发育有重要意义。     

沉默信息调节因子2相关酶3调控机制及其在疾病中的作用

沉默信息调节因子2相关酶3（silent information regulator 2-related enzyme 3,SIRT3）是烟酰胺腺嘌呤二核苷酸（nicotinamide adenine dinucleotide,NAD⁺）依赖性组蛋白去乙酰化酶家族成员,参与能量代谢、氧化应激和细胞凋亡等过程并起到关键作用,其调控作用与多种疾病的发生密切相关。综述了SIRT3下游转录因子腺苷酸活化蛋白激酶（AMP-activated protein kinase,AMPK）、线粒体通透性转换孔（mitochondrial permeability transition pore,mPTP）、核因子κB（nuclear factor-κB,NF-κB）等的调控机制,以及SIRT3在心血管疾病、肿瘤、糖尿病中的作用,以期为相关疾病的预防和治疗提供参考。     

Blastocyst production from in vitro-produced day-2 bovine embryos classified by cleavage stage, and cytogenetical evaluation of the resultant day-8 blastocysts

The present study was conducted to determine the criteria for selecting good quality embryos on Day-2 post-insemination and at the blastocyst stage. Bovine oocytes were matured, fertilized and cultured in vitro. First, Day-2 embryos were classified based on the number of blastomeres into 2-cell, 3- to 4-cell, 5- to 8-cell and >8-cell stage embryos; chromosome samples were then prepared. In the second experiment, the Day-2 embryos classified according to the number of blastomeres were cultured separately for an additional 6 days (Day 8). The resultant Day-8 blastocysts from each group of Day-2 embryos were classified into the following 3 grades based on morphology and diameter: Grade A, hatched and hatching blastocysts; Grade B, expanded blastocysts; and Grade C, unexpanded blastocysts. Chromosome samples were then prepared. The 5- to 8-cell stage Day-2 embryos had the lowest incidence of chromosomal abnormalities (13.5%, P<0.05) and the highest development rate to blastocysts (59.2%, P<0.05). Furthermore, the blastocysts derived from the 5- to 8-cell stage embryos had the largest mean number of cells (102.8+/-42.4, P<0.05), largest number of metaphases per blastocyst (9.5+/-4.8, P<0.05) and lowest incidence of chromosomal abnormalities (24.6%, P<0.05). The Grade A blastocysts had the largest mean number of cells (136.6+/-33.4, P<0.05), a large number of metaphases per blastocyst (11.9+/-5.5, P<0.05) and a low incidence of severe chromosomal abnormalities (17.3%). The results showed that, at Day 2, the 5- to 8-cell stage embryos were of better quality since they had the lowest incidence of chromosomal abnormalities and the highest blastocyst rate and the resultant blastocysts had the largest number of cells and lowest incidence of chromosomal abnormalities. In particular, selection of Grade A blastocysts can improve the development rate to term.     

L-精氨酸对热处理MLTC-1细胞氧化、凋亡及睾酮合成相关基因表达的影响

试验旨在研究热处理对睾丸间质细胞的影响及L-精氨酸对热处理睾丸间质细胞抗氧化、抗凋亡及睾酮合成相关基因表达的影响.试验选用小鼠睾丸间质瘤细胞系(MLTC-1)细胞,将细胞分为4组,分别为对照组(C)、热处理组(HT)、5 μg/mL L-精氨酸+热处理组(5H)和10μg/mL L-精氨酸+热处理组(10H),处理结束...