Ovaries from apparently normal reproductive organs of heifers and cattle of unknown age and breeding history were collected within 30 minutes after slaughter and evisceration of animals at the private EL-Bagor abattoir. The ovaries were kept in a thermos flask containing warm normal saline and gentamycin. Then transported to the lab within 1-2 h after slaughtering according to the previous literatures 5614.The ovaries were further washed as soon as we arrived to the lab in warm normal saline to remove the blood, debris and then kept in water bath at 37°C during oocyte collection. Before COCs selection by at least 1h, the maturation dish(s) is prepared by putting 100µl maturation media drops in sterile disposable petri dish then covered with mineral oil and incubated at 38.5 C^◦ under 5% CO₂ and 90% humidity 515.

Using of 18-gauge needle attached to 10 ml syringe, medium sized follicles (3: 8 mm in diameter) were aspirated and pooled in a 15-ml conical tube16. After the end of aspiration, the tubes were left 10:15 minutes to allow follicular cells settlement. After sedimentation, about 5ml of sediment was recovered by dropper pipette and placed in 80 mm diameter sterile petri dish. COCs were selected using a stereomicroscope and transferred into another dish containing fresh pre-warmed TCM199 614.

The retrieved COCs were classified according to817 into 4 grades based on their morphological appearance.

Grade A (good), COCs with six layers of dense compact cumulus cells investment and evenly granular homogenous ooplasm. Grade B (fair), similar to grade A, but with 2-4 layers cumulus cells. Grade C (poor), partially or completely denuded oocytes. Grade D (very poor), characterized by highly scattered cumulus cells and dark irregular ooplasm.

Grade A and Grade B COCs were washed three times in TCM199, followed by incubation under mineral oil in the same medium (10:15 oocytes/100 µl) for 22 h at 38.5 C^◦ under 5% of CO₂ in air with 90% humidity18.

Bovine frozen semen was obtained from Animal Reproduction Research Institute and prepared according to previous literatures 58.

Preparation of media and stock solution requests a sterile technique with exact and careful weighting of components. The use of a laminar flow cabinet is indispensable to evade any contamination that may alter and spoil the prepared media. An analytical balance with readability of at least 10 μg and accuracy of ± 0.1μg was used. All media were filtered using 0.2 μm (Millipore, USA) syringe filter and incubated for at least 2 h in a humidified atmosphere, 5% CO2 at 38.5°C before culturing the oocytes and spermatozoa58. The medium used for oocyte IVM was tissue culture media 199 (TCM-199) supplemented with 10% heat inactivated Fetal Calf Serum (FCS), 5 μg/ml Luteinizing hormone (LH) 19, 0.5 μg/ml Follicle-stimulating hormone (FSH)2021 and 1 μg/ml estradiol-17β 22.The pH was adjusted to 7.458. The basic media used for IVF was sperm Tyrode’s Albumin medium with Lactate and Pyruvate (sperm -TALP)23, and 20 µg/ml heparin sulfate is added to the media before filtration. The pH of the media is adjusted to 7.4. The medium used for culture is Modified synthetic oviductal fluid (MSOF) supplemented with 1 mM glutamine, 1% MEM (Eagle′s Minimum Essential Medium) essential amino acids, 0.5% MEM essential amino acids and 10% FCS was the In vitro culture medium (24). The pH was adjusted to 7.4. The selected COCs were randomly allocated to 4 maturation medium groups with different l carnitine concentration (0, 1.25mM, 2.5mM and 5mM). All COCs groups were matured, fixed and stained. Cumulus expansion rate was assessed.

Fixative, stain and stain removing agents are prepared according to25. Acetic acid- ethanol fixative (1:3 v/v)., Aceto-orcein stain: 1% (w/v) orcein stain in 45% acetic acid. Stain differentiation solution is acetic acid, distal water and glycerol (1:3:1 v/v/v).

Three straws of frozen semen were thawed for 30 sec. in 37C^◦ water bath, evacuated in test tube. Swim-up technique, in modified-sperm TALP medium, was used for separation of motile sperm(26). Dilution of the final pellet of spermatozoa is made to obtain a sperm concentration of 2 million/ml as a final sperm cell concentration 27. 100 µl drops of sperm-TALP media containing spermatozoa is deposited in sterile disposable petri dish, and then covered with mineral oil incubated at 38.5 C^◦ under 5% CO₂ and 90% humidity.

Mature oocytes were washed three times in sperm-TALP then added to the fertilization drops, 10 oocytes in each drop. Gametes were co-incubated at 38.5 C◦ under 5% of CO2 and 90% humidity for 21 hrs. 27.

The culture dish is prepared by putting 50µl culture media drops in sterile disposable petri dish then covered with mineral oil and incubated at 38.5 C◦ under 5% of CO₂ and 90% humidity. After 21hrs of gametes co-incubation, presumptive zygotes were removed from fertilization droplets. These zygotes washed three times in the culture medium. The presumptive zygotes (10 zygote/50 μl droplets) were cultured at 38.5 C^◦ under 5% of CO₂ and 90% humidity18. Semi replacement of the culture medium by fresh medium is done every 48 hrs. 24.

Matured oocytes were fixed and stained with aceto-orcein stain 1%. Maturation was indicated by germinal vesicle break down1525.

Presumptive zygotes were fixed and stained with aceto-orcein stain 1%. Normal fertilization was indicated by presence of two pronuclei 25.

Embryos were assessed for cleavage 48 hours from the beginning of culture and further stages (morula and blastocyst) were checked approximately every 48 hours for up to 7 days. The embryo development rates were calculated according to 28 as follows:

Cleavage rate = no. of cleaved zygotes ×100/total no. of zygotes.

Morula rate = no. of morula ×100/total no. of zygotes.

Blastocyst rate = no. of blastocysts ×100/total no. of zygotes.

Mature oocyte and fertilized oocytes were fixed and stained according to Mehmood et al. 201125.

Each experiment was at least three times replicated. According to Elmetwally et al.2018 and 2019 (29,30), the normality of quantitative parameters was tested using normal probability plots and the Kolmogorov-Smirnov test created with SAS's UNIVARIATE technique. All experimental results are shown as mean SEM. The recovery rate, cleavage and maturation rate, and blastocyst rate are all represented as percentages. SAS® (version 9.2, SAS Institute, Cary, NC, USA) will be used for statistical analyses. Differences will be judged significant when they reach (P ≤ 0.05).

The data of the present study the supplementation of the maturation media with 2.5 and 5 mM of LC induced a higher rate of cumulus expansion than the lower LC concentration as well as the control oocytes.

In previous studies indicating the beneficial effects of LC on maintenance of intracellular lipid droplets and the different microtubular structure. Accordingly, LC was proven to improve the process of cryopreservation of certain mammalian embryos and so far used as a repetitive procedure, the substantial differences of efficiency of this method depend on stage, species and origin of cells either produced in vivo or in vitro 531. Factors that are supposed to cause most of these differences are the amount of intracellular lipid droplets and the different microtubular structure which leads to chilling injury in addition to the volume/surface ratio plays a crucial role for the cryoprotectant penetration32. The important impact of LC results from the mitigation of the harmful effects of vitrification on mitochondrial function, which lowers the competence of vitrified oocytes and results in ATP loss 3334. Animal cells produced more ATP when supplemented with LC 3536. LC regarded as a major beta-oxidation agent, facilitates the transfer of fatty acids from the cytosol to the mitochondria, hence promoting lipid metabolism within mammalian cells 3738.

So far, the metabolic activity plays a critical role in the developing embryo, preimplantation embryo development in mammals can be split into two phases: 1 the phase that is regulated by the proteins and mRNAs that accumulate in the oocyte and is marked by low metabolic activity, and 2 the phase that occurs after the embryonic genome is activated and is marked by a marked increase in metabolism concurrent with the formation and expansion of the blastocoel cavity. The transition of the embryo from the oviduct to the uterus is also linked to this alteration in the metabolic activity of the embryo 39. The success rate of in vitro embryo production (IVEP) has been significantly impacted by the study of these mechanisms, which has led to the development of culture media that take into account the metabolic needs of the embryo and the makeup of oviductal and uterine fluids 40.

All mammalian eggs are surrounded by a relatively thick glycoprotein layer called the zona pellucida which plays an important role during oogenesis, fertilization and preimplantation development 41. The mouse zona pellucida consists of three glycoproteins that are synthesized solely by growing oocytes and assembled into long fibrils. that constitutes a matrix. Zona pellucida glycoproteins are responsible for species-restricted binding of sperm to unfertilized eggs, inducing sperm to undergo acrosomal exocytosis, and preventing sperm from binding to fertilized eggs. Increasing maternal age and embryo culture conditions were adversely affected by the ZP elasticity and thinning which are essential for the hatching process 424344. A thick ZP may be associated with low quality embryos 454647.

Basically, the rate of glucose, pyruvate, lipid, and amino acid ingestion influences the synthesis of adenosine triphosphate (ATP) in embryo metabolism 48. Additionally, pyruvate and glucose are the main supplements added to culture media. But bovine embryos also contain stores of fat and glycogen. Though lipids, especially fatty acids, are the most abundant energy reserve in bovine embryos, the concentration of glycogen appears to be nearly nonexistent and is not well documented in the literature 6. In addition, when creating culture media for in vitro embryo formation, lipids as an energy source have not been considered. Triacylglycerol (TG) or free fatty acids are lipid chain macromolecules that are found in cells and act as energy storage. They are made up of long-chain hydrocarbons with a terminal carboxyl group 540.

The beneficial effects of L carnitine supplementation to the IVM medium on the present study on the improvement of the oocyte expansion rate may be attributed to the ability of LC as well as the antioxidants, such as β-mercaptoethanol, cysteine, and cysteamine to stimulate the synthesis of intracellular GSH, which in turn has a crucial an antioxidative role and enhances viability of IVF produced embryos 4950. LC (β-hydroxy-γ-trimethylammoniumbutyric acid), an antioxidative agent, is known to have a beneficial role in cellular metabolism and embryonic development in mammalian species. LC protects cell membranes and DNA from damage induced by oxygen free radicals 51. In the same line, previous researches showed that the lower concentration from LC is associated with a significant improvement of immature bovine oocyte vitrification 52. Meanwhile, excessive LC concentration may result in reduction of lipid density which may be unfavorable to in vitro bovine embryo development 40.

In the current study, the supplementation of the maturation media with LC has a great impact on the cleavage rate of the immature bovine oocytes. The higher cleavage rate was investigated with the supplementation of the maturation media by 5 mM of LC when compared to the other concentrations of LC and control group. Furthermore, the other supplementation of the maturation media with other LC concentrations showed a significant rise in the cleavage rate of the immature bovine oocytes than the control group.

A possible explanation for this is that LC is a cofactor for lipid metabolism in animal cells, helping to move fatty acids from the cytosol to the mitochondria for firewood beta-oxidation. Previous studies have shown that using LC improved recovery and survival rates, as well as minimal abnormalities in the cytoplasm and zona pellucida when compared to controls 3738. Consequently, LC improved ATP production in animal cells 53. Similar results were investigated after adding LC to the IVM prior to vitrification on in vitro-matured calf oocytes52. On the other side, we published before that the supplementation of IVM with 1.2 mg LC increased the rate of zona pellucida abnormalities and cytoplasmic abnormalities and this may be attributed that excessive LC concentration may result in reduction of lipid density which may be unfavorable to in vitro bovine embryo development 40.

Further, the use of the basic media alone in vitrification of oocytes lead to decrease in maturation rate and developmental competence of vitrified oocytes as vitrification damages certain cytoplasmic components. Also, the vitrification of GV oocytes causes damage to the surrounding cumulus cells which consequently disrupts their communication with enclosed oocytes54. This communication is very important for successful completion of invitro maturation and subsequent embryonic development 6, so supplementation of the basic media of vitrification with LC avoided this damage55. The oxidative activity of mitochondria was mildly decreased by vitrification and drastically increased by LC adding to vitrification media in both mouse strains 56.

Similar to the current results, In vitro maturation (IVM) of pig oocytes causes active mitochondria to translocate from the cytoplasm's periphery to the cytoplasm's interior, or medullary area, according to previous observations 52. This process promotes embryonic development. Similar to this, the oocyte accelerated nuclear maturation, increased the number of active mitochondria, and lowered the levels of lipid droplets when the medium was supplemented with LC during in vitro maturation 525758. Similarly, the inclusion of LC raised the percentage of embryos that hatched; this result was ascribed to an increase in the quality of the embryos and their capacity for development as a result of the lipid content being reduced 5758.

The culture conditions for oocyte maturation and embryonic development are critical determinants for the successful development of in vitro-produced embryos in a wide variety of mammalian species. In this study, the effects of an antioxidant (LC) treatment on the blastocyst formation and nuclear maturation during IVM of immature bovine oocytes was investigated 31. Previous studies proved that the LC affects the intracellular levels of GSH and ROS in oocytes and accordingly, improve the developmental competence of the bovine oocytes. In addition, there are expressions of several transcription factors and apoptosis-related genes in embryos that were derived from LC-treated oocytes 31.

The present results indicated that the supplementation of the maturation media with 2.5 and 5 mM of LC has a greater impact on the blastocyst formation as well as the nuclear maturation than the other LC concentrations and control treatment. In mammalian species, the antioxidant LC (β-hydroxy-γ-trimethylammoniumbutyric acid) is so far recognized to play a positive effect in cellular metabolism and embryonic development. DNA and cell membranes are shielded from oxygen free radical destruction by LC 59. The integrity of microtubule and chromosome structural integrity, as well as the amount of apoptosis, were significantly improved and lowered when mouse metaphase II (MII) oocytes and 8-cell embryos were cultured in a medium supplemented with LC (0.6 mg/mL)60.Furthermore, by lowering the levels of DNA damage and the inhibiting effects of actinomycin-D, hydrogen peroxide, and tumor necrosis factor-α on embryonic development, the addition of 0.3 mg/mL LC to culture medium enhanced the formation of blastocysts in mice 51.

In another study, it has been reported that the treatment of immature oocytes with LC during IVM resulted in enhanced preimplantation development of PA and SCNT embryos in pigs. Furthermore, other research reveals the favorable effects of L-carnitine on embryonic development in mice, bovine, and porcine49505161. LC was successful in raising GSH levels in oocytes following IVM, but it had no effect on nuclear maturation 61. This finding suggested that LC advantageous effects were more pronounced on cytoplasmic maturation than on nuclear maturation. After PA and SCNT, this may have helped boost embryonic development even further 31.

The beneficial effects of LC in the current study may be attributed to its effects on the expression of DNMT1, PCNA, FGFR2, and POU5F1 mRNA levels in immature oocytes cultured in the IVM media supplementation with LC. Although the exact mechanism by which LC treatment raised mRNA levels is unknown, it is possible that cytoplasmic modification, including elevated GSH and decreased ROS activity, induced by LC treatment produced favorable microenvironments for donor nuclei's nuclear reprogramming and stimulated gene expression in cloned embryos 6263.

We also hypnotized the beneficial effects of LC may be attributed to its effects on the expression of the apoptotic proteins. Apoptosis is thought to be a normal mechanism that gets rid of cells that have chromosomal or DNA defects 4950. Nonetheless, loss of viability and failure to grow can result from an overabundance of apoptotic cells during embryonic development6465. LC functions as an antioxidant in animal cells or embryos and reduces apoptosis induced by oxidative stress by increasing intracellular GSH level and affecting mitochondrial functions. It has been reported that oxidative stress derived from ROS generation can induce apoptosis when oocytes or embryos are cultured in vitro 52646566.

Previous studies have investigated that, the supplementation of IVM media with LC increased the expression of both pro-and anti-apoptotic genes; however, the pro-apoptotic gene (BAX) showed a greater increase in expression than the anti-apoptotic gene 31. Other studies showed that giving LC during IVM decreased the likelihood that parthenogenetic blastocysts in pigs would experience apoptotic nuclei 61. The cause of the proapoptotic gene's elevated expression was unknown, despite the fact that LC therapy benefited embryonic development and ROS levels were lower in IVM oocytes. Apoptosis is more common in capable oocytes from cycling gilts than in less competent oocytes from prepubertal gilts, according to a recent publication 67.

In summary, our results suggest that IVM treatment of oocytes with LC improves the cleavage, expansion, blastocyst and nuclear maturation and this may be regarding to the effects of LC on increasing intracellular GSH levels, reducing ROS toxicity, and regulating expression of POU5F1 and transcription factor(s) expression, which are necessary for the normal development of embryos.