Abstract
Appreciation of the evolution of IVF culture media, highlighting salient discoveries that have led to the tremendous improvement over just a few short years ago, is instrumental in gaining insight into the complexities of gamete and embryo function. In turn, this knowledge brings understanding to the rationale behind current laboratory practices and aids in the ability to make informed decisions in regard to culture methods. Furthermore, discussion of impact of culture media on homeostatic regulation of gametes and embryos, focusing on key decisions made within the laboratory such as media type, macromolecule selection, and pH, further highlights their delicate nature, the need to minimize stressors, and ultimately provides insight into areas where future improvement can be made as we continue to strive for improvement in IVF success rates.
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References
Steptoe PC, Edwards RG, et al. Human blastocysts grown in culture. Nature. 1971;229(5280):132–3.
Steptoe PC, Edwards RG. Reimplantation of a human embryo with subsequent tubal pregnancy. Lancet. 1976;1(7965):880–2.
Pool T, Atiee S, et al. Oocyte and embryo culture: basic concepts and recent advances. Infert Reprod Med Clin North Am. 1998;9(2):181–203.
Menezo Y, Testart J, et al. Serum is not necessary in human in vitro fertilization, early embryo culture, and transfer. Fertil Steril. 1984;42(5):750–5.
Quinn P, Kerin J, et al. Improved pregnancy rate in human in vitro fertilization with the use of a medium based on the composition of human tubal fluid. Fertil Steril. 1985;44:493–8.
Gardner DK, Pool TB, et al. Embryo nutrition and energy metabolism and its relationship to embryo growth, differentiation, and viability. Semin Reprod Med. 2000;18(2):205–18.
Pool TB. Recent advances in the production of viable human embryos in vitro. Reprod Biomed Online. 2002;4(3):294–302.
Gardner DK, Lane M, et al. Environment of the preimplantation human embryo in vivo: metabolite analysis of oviduct and uterine fluids and metabolism of cumulus cells. Fertil Steril. 1996;65(2):349–53.
Biggers JD, Summers MC. Choosing a culture medium: making informed choices. Fertil Steril. 2008;90(3):473–83.
Macklon NS, Pieters MH, et al. A prospective randomized comparison of sequential versus monoculture systems for in-vitro human blastocyst development. Hum Reprod. 2002;17(10):2700–5.
Biggers JD, McGinnis LK, et al. One-step versus two-step culture of mouse preimplantation embryos: is there a difference? Hum Reprod. 2005;20(12):3376–84.
Reed ML, Hamic A, et al. Continuous uninterrupted single medium culture without medium renewal versus sequential media culture: a sibling embryo study. Fertil Steril. 2009;92(5):1783–6.
Leese HJ. Quiet please, do not disturb: a hypothesis of embryo metabolism and viability. Bioessays. 2002;24(9):845–9.
Leese HJ, Baumann CG, et al. Metabolism of the viable mammalian embryo: quietness revisited. Mol Hum Reprod. 2008;14(12):667–72.
Gardner DK. Dissection of culture media for embryos: the most important and less important components and characteristics. Reprod Fertil Dev. 2008;20(1):9–18.
Hardy K, Hooper M, et al. Non-invasive measurement of glucose and pyruvate uptake by individual human oocytes and preimplantation embryos. Hum Reprod. 1989;4(2):188–91.
Gott A, Hardy K, et al. Non-invasive measurement of pyruvate and glucose uptake and lactate production by single human preimplantation embryos. Hum Reprod. 1990;5(1):104–8.
Gardner D, Lane M, et al. Uptake and metabolism of pyruvate and glucose by individual sheep preattachment embryos developed in vivo. Mol Reprod Dev. 1993;36(3):313–9.
Devreker F, Hardy K, et al. Noninvasive assessment of glucose and pyruvate uptake by human embryos after intracytoplasmic sperm injection and during the formation of pronuclei. Fertil Steril. 2000;73(5):947–54.
Lane M, Gardner DK. Inhibiting 3-phosphoglycerate kinase by EDTA stimulates the development of the cleavage stage mouse embryo. Mol Reprod Dev. 2001;60(2):233–40.
Conaghan J, Handyside AH, et al. Effects of pyruvate and glucose on the development of human preimplantation embryos in vitro. J Reprod Fertil. 1993;99(1):87–95.
Carrillo AJ, Lane B, et al. Improved clinical outcomes for in vitro fertilization with delay of embryo transfer from 48 to 72 hours after oocyte retrieval: use of glucose- and phosphate-free media. Fertil Steril. 1998;69(2):329–34.
Coates A, Rutherford AJ, et al. Glucose-free medium in human in vitro fertilization and embryo transfer: a large-scale, prospective, randomized clinical trial. Fertil Steril. 1999;72(2):229–32.
Ben-Yosef D, Amit A, et al. Prospective randomized comparison of two embryo culture systems: P1 medium by Irvine Scientific and the Cook IVF Medium. J Assist Reprod Genet. 2004;21(8):291–5.
Whitten WK. Culture of tubal ova. Nature. 1957;179(4569):1081–2.
Brinster R. Studies on the development of mouse embryos in vitro. II. The effect of energy source. J Exp Zool. 1965;158:59–68.
Biggers JD, Whittingham DG, et al. The pattern of energy metabolism in the mouse oocyte and zygote. Proc Natl Acad Sci U S A. 1967;58(2):560–7.
Gardner DK, Leese HJ. Non-invasive measurement of nutrient uptake by single cultured pre-implantation mouse embryos. Hum Reprod. 1986;1(1):25–7.
Leese HJ, Hooper MA, et al. Uptake of pyruvate by early human embryos determined by a non-invasive technique. Hum Reprod. 1986;1(3):181–2.
Hardy K, Hooper MA, et al. Non-invasive measurement of glucose and pyruvate uptake by individual human oocytes and preimplantation embryos. Hum Reprod. 1989;4(2):188–91.
Wales RG, Whittingham DG. The metabolism of specifically labelled lactate and pyruvate by two-cell mouse embryos. J Reprod Fertil. 1973;33(2):207–22.
Lane M, Gardner DK. Lactate regulates pyruvate uptake and metabolism in the preimplantation mouse embryo. Biol Reprod. 2000;62(1):16–22.
Gibb CA, Poronnik P, et al. Control of cytosolic pH in two-cell mouse embryos: roles of H(+)-lactate cotransport and Na+/H+ exchange. Am J Physiol. 1997;273(2 Pt 1):C404–19.
Edwards LJ, Williams DA, et al. Intracellular pH of the preimplantation mouse embryo: effects of extracellular pH and weak acids. Mol Reprod Dev. 1998;50(4):434–42.
Lane M, Gardner DK. Regulation of ionic homeostasis by mammalian embryos. Semin Reprod Med. 2000;18(2):195–204.
Gardner DK, Lane M. Culture systems for human embryos. In: Gardner DK, Weissman A, Howles C, Zeev S, editors. Textbook of assisted reproductive technologies. Boca Raton: Informa UK Ltd; 2009. p. 219–40.
McKiernan SH, Clayton MK, et al. Analysis of stimulatory and inhibitory amino acids for development of hamster one-cell embryos in vitro. Mol Reprod Dev. 1995;42(2):188–99.
Lane M, Gardner DK. Differential regulation of mouse embryo development and viability by amino acids. J Reprod Fertil. 1997;109(1):153–64.
Ho Y, Wigglesworth K, et al. Preimplantation development of mouse embryos in KSOM: augmentation by amino acids and analysis of gene expression. Mol Reprod Dev. 1995;41(2):232–8.
Biggers JD, McGinnis LK, et al. Amino acids and preimplantation development of the mouse in protein-free potassium simplex optimized medium. Biol Reprod. 2000;63(1):281–93.
Summers MC, McGinnis LK, et al. IVF of mouse ova in a simplex optimized medium supplemented with amino acids. Hum Reprod. 2000;15(8):1791–801.
Gardner DK, Lane M. Alleviation of the ‘2-cell block’ and development to the blastocyst of CF1 mouse embryos: role of amino acids, EDTA and physical parameters. Hum Reprod. 1996;11(12):2703–12.
Gardner DK, Lane M. Amino acids and ammonium regulate mouse embryo development in culture. Biol Reprod. 1993;48(2):377–85.
Lane M, Gardner DK. Increase in postimplantation development of cultured mouse embryos by amino acids and induction of fetal retardation and exencephaly by ammonium ions. J Reprod Fertil. 1994;102(2):305–12.
Lane M, Hooper K, et al. Effect of essential amino acids on mouse embryo viability and ammonium production. J Assist Reprod Genet. 2001;18(9):519–25.
Lane M, Gardner DK. Ammonium induces aberrant blastocyst differentiation, metabolism, pH regulation, gene expression and subsequently alters fetal development in the mouse. Biol Reprod. 2003;69(4):1109–17.
Zander DL, Thompson JG, et al. Perturbations in mouse embryo development and viability caused by ammonium are more severe after exposure at the cleavage stages. Biol Reprod. 2006;74(2):288–94.
Biggers JD, McGinnis LK, et al. Discrepancies between the effects of glutamine in cultures of preimplantation mouse embryos. Reprod Biomed Online. 2004;9(1):70–3.
Biggers JD, McGinnis LK, et al. Enhanced effect of glycyl-L-glutamine on mouse preimplantation embryos in vitro. Reprod Biomed Online. 2004;9(1):59–69.
Summers MC, McGinnis LK, et al. Mouse embryo development following IVF in media containing either L-glutamine or glycyl-L-glutamine. Hum Reprod. 2005;20(5):1364–71.
Baltz JM, Tartia AP. Cell volume regulation in oocytes and early embryos: connecting physiology to successful culture media. Hum Reprod. 2010;15(2):166–76.
Richards T, Wang F, et al. Rescue of postcompaction stage mouse embryo development from hypertonicity by amino acid transporter substrates that may function as organic osmolytes. Biol Reprod. 2010;82(4):769–77.
Van Winkle LJ, Haghighat N, et al. Glycine protects preimplantation mouse conceptuses from a detrimental effect on development of the inorganic ions in oviductal fluid. J Exp Zool. 1990;253(2):215–9.
Lawitts JA, Biggers JD. Joint effects of sodium chloride, glutamine, and glucose in mouse preimplantation embryo culture media. Mol Reprod Dev. 1992;31(3):189–94.
Pool T. Blastocyst development in culture: the role of macromolecules. In: Gardner DK, Lane M, editors. ART and the human blastocyst. New York: Springer; 2001. p. 105–17.
McKiernan SH, Bavister BD. Different lots of bovine serum albumin inhibit or stimulate in vitro development of hamster embryos. In Vitro Cell Dev Biol. 1992;28A(3 Pt 1):154–6.
Bavister BD, Kinsey DL, et al. Recombinant human albumin supports hamster in-vitro fertilization. Hum Reprod. 2003;18(1):113–6.
Bungum M, Humaidan P, et al. Recombinant human albumin as protein source in culture media used for IVF: a prospective randomized study. Reprod Biomed Online. 2002;4(3):233–6.
Pool TB, Martin JE. High continuing pregnancy rates after in vitro fertilization-embryo transfer using medium supplemented with a plasma protein fraction containing alpha- and beta-globulins. Fertil Steril. 1994;61(4):714–9.
Meintjes M, Chantilis SJ, et al. A randomized controlled study of human serum albumin and serum substitute supplement as protein supplements for IVF culture and the effect on live birth rates. Hum Reprod. 2009;24(4):782–9.
Ben-Yosef D, Yovel I, et al. Increasing synthetic serum substitute (SSS) concentrations in P1 glucose/phosphate-free medium improves implantation rate: a comparative study. J Assist Reprod Genet. 2001;18(11):588–92.
Lane M, Maybach JM, et al. Cryo-survival and development of bovine blastocysts are enhanced by culture with recombinant albumin and hyaluronan. Mol Reprod Dev. 2003;64(1):70–8.
Gardner DK, Rodriegez-Martinez H, et al. Fetal development after transfer is increased by replacing protein with the glycosaminoglycan hyaluronan for mouse embryo culture and transfer. Hum Reprod. 1999;14(10):2575–80.
Palasz AT, Rodriguez-Martinez H, et al. Effects of hyaluronan, BSA, and serum on bovine embryo in vitro development, ultrastructure, and gene expression patterns. Mol Reprod Dev. 2006;73(12):1503–11.
Swain J, Smith G. Cryoprotectants. In: Chian R, Quinn P, editors.Cryopreservation in female fertility preservation. Cambridge:Cambridge Publishing; 2010.
Dale B, Menezo Y, Cohen J, et al. Intracellular pH regulation in the human oocyte. Hum Reprod 1998; 13(4): 964–970.
Phillips KP, Petrunewich MA, et al. The intracellular pH-regulatory HCO −3 /Cl− exchanger in the mouse oocyte is inactivated during first meiotic metaphase and reactivated after egg Âactivation via the MAP kinase pathway. Mol Biol Cell. 2002;13(11):3800–10.
Erdogan S, FitzHarris G, et al. Mechanisms regulating intracellular pH are activated during growth of the mouse oocyte coincident with acquisition of meiotic competence. Dev Biol. 2005;286(1):352–60.
Fitzharris G, Baltz J. Regulation of intracellular pH during oocyte growth and maturation in mammals. Reproduction. 2009;138(4):619–27.
Squirrell JM, Lane M, et al. Altering intracellular pH disrupts development and cellular organization in preimplantation hamster embryos. Biol Reprod. 2001;64(6):1845–54.
Lane M, Lyons EA, et al. Cryopreservation reduces the ability of hamster 2-cell embryos to regulate intracellular pH. Hum Reprod. 2000;15(2):389–94.
Zander-Fox DL, Mitchell M, Thompson JG, Lane M. Alterations in mouse embryo intracellular pH by DMO during culture impair implantation and fetal growth. Reprod Biomed Online. 2010;21(2):219–29.
Fitzharris G, Baltz JM. Granulosa cells regulate intracellular pH of the murine growing oocyte via gap junctions: development of independent homeostasis during oocyte growth. Development. 2006;133(4):591–9.
FitzHarris G, Siyanov V, et al. Granulosa cells regulate oocyte intracellular pH against acidosis in preantral follicles by multiple mechanisms. Development. 2007;134(23):4283–95.
Lane M, Baltz JM, et al. Na+/H+ antiporter activity in hamster embryos is activated during fertilization. Dev Biol. 1999;208(1):244–52.
Phillips KP, Baltz JM. Intracellular pH regulation by HCO −3 /Cl− exchange is activated during early mouse zygote development. Dev Biol. 1999;208(2):392–405.
Zhu ZY, Chen DY, et al. Rotation of meiotic spindle is controlled by microfilaments in mouse oocytes. Biol Reprod. 2003;68(3):943–6.
Lenart P, Bacher CP, et al. A contractile nuclear actin network drives chromosome congression in oocytes. Nature. 2005;436(7052):812–8.
Regula CS, Pfeiffer JR, et al. Microtubule assembly and disassembly at alkaline pH. J Cell Biol. 1981;89(1):45–53.
Bavister BD, Squirrell JM. Mitochondrial distribution and function in oocytes and early embryos. Hum Reprod. 2000;15 Suppl 2:189–98.
Nagai S, Mabuchi T, et al. Correlation of abnormal mitochondrial distribution in mouse oocytes with reduced developmental competence. Tohoku J Exp Med. 2006;210(2):137–44.
Krisher RL, Bavister BD. Enhanced glycolysis after maturation of bovine oocytes in vitro is associated with increased developmental competence. Mol Reprod Dev. 1999;53(1):19–26.
Spindler RE, Pukazhenthi BS, et al. Oocyte metabolism predicts the development of cat embryos to blastocyst in vitro. Mol Reprod Dev. 2000;56(2):163–71.
John DP, Kiessling AA. Improved pronuclear mouse embryo development over an extended pH range in Ham’s F-10 medium without protein. Fertil Steril. 1988;49(1):150–5.
Lane M, Baltz JM, et al. Regulation of intracellular pH in hamster preimplantation embryos by the sodium hydrogen (Na+/H+) antiporter. Biol Reprod. 1998;59(6):1483–90.
Leclerc C, Becker D, et al. Low intracellular pH is involved in the early embryonic death of DDK mouse eggs fertilized by alien sperm. Dev Dyn. 1994;200(3):257–67.
Zhao Y, Chauvet PJ, et al. Expression and function of bicarbonate/chloride exchangers in the preimplantation mouse embryo. J Biol Chem. 1995;270(41):24428–34.
Zhao Y, Baltz JM. Bicarbonate/chloride exchange and intracellular pH throughout preimplantation mouse embryo development. Am J Physiol. 1996;271(5 Pt 1):C1512–20.
Lane M, Bavister BD. Regulation of intracellular pH in bovine oocytes and cleavage stage embryos. Mol Reprod Dev. 1999;54(4):396–401.
Brinster RL. Studies on the development of mouse embryos in vitro. I. The effect of osmolarity and hydrogen ion concentration. J Exp Zool. 1965;158:49–57.
Hershlag A, Feng H. The effect of CO2 concentration and pH on the in vitro development of mouse embryos. Fertil Mag. 2001;4:21–2.
Summers MC, Biggers JD. Chemically defined media and the culture of mammalian preimplantation embryos: historical perspective and current issues. Hum Reprod Update. 2003;9(6):557–82.
Steel T, Conaghan J. pH equilibration dynamics of culture medium under oil. Fertil Steril. 2008;89 suppl 2:s27.
Swain JE, Pool TB. Supplementation of culture media with zwitterinoic buffers supports sperm function and embryo development within the elevated CO2 levels of the laboratory incubator. J Clinic Embryol. 2008;11(2):24.
Barnett DK, Bavister BD. Inhibitory effect of glucose and phosphate on the second cleavage division of hamster embryos: is it linked to metabolism? Hum Reprod. 1996;11(1):177–83.
Barnett DK, Clayton MK, et al. Glucose and phosphate toxicity in hamster preimplantation embryos involves disruption of cellular organization, including distribution of active mitochondria. Mol Reprod Dev. 1997;48(2):227–37.
Lane M, Ludwig TE, et al. Phosphate induced developmental arrest of hamster two-cell embryos is associated with disrupted ionic homeostasis. Mol Reprod Dev. 1999;54(4):410–7.
Farrell PS, Bavister BD. Short-term exposure of two-cell hamster embryos to collection media is detrimental to viability. Biol Reprod. 1984;31(1):109–14.
Escriba MJ, Silvestre MA, et al. Comparison of the effect of two different handling media on rabbit zygote developmental ability. Reprod Nutr Dev. 2001;41(2):181–6.
Palasz AT, Brena PB, et al. The effect of different zwitterionic buffers and PBS used for out-of-incubator procedures during standard in vitro embryo production on development, morphology and gene expression of bovine embryos. Theriogenology. 2008;70(9):1461–70.
Good NE, Winget GD, et al. Hydrogen ion buffers for biological research. Biochemistry. 1966;5(2):467–77.
Good NE, Izawa S. Hydrogen ion buffers. Methods Enzymol. 1972;24:53–68.
Ferguson WJ, Braunschweiger KI, et al. Hydrogen ion buffers for biological research. Anal Biochem. 1980;104(2):300–10.
Iwasaki T, Kimura E, et al. Studies on a chemically defined medium for in vitro culture of in vitro matured and fertilized porcine oocytes. Theriogenology. 1999;51(4):709–20.
Morgia F, Torti M, et al. Use of a medium buffered with N-hydroxyethylpiperazine-N-ethanesulfonate (HEPES) in intracytoplasmic sperm injection procedures is detrimental to the outcome of in vitro fertilization. Fertil Steril. 2006;85(5):1415–9.
Zigler Jr JS, Lepe-Zuniga JL, et al. Analysis of the cytotoxic effects of light-exposed HEPES-containing culture medium. In Vitro Cell Dev Biol. 1985;21(5):282–7.
Lepe-Zuniga JL, Zigler Jr JS, et al. Toxicity of light-exposed Hepes media. J Immunol Methods. 1987;103(1):145.
Butler JE, Lechene C, et al. Noninvasive measurement of glucose uptake by two populations of murine embryos. Biol Reprod. 1988;39(4):779–86.
Byrd SR, Flores-Foxworth G, et al. In vitro maturation of ovine oocytes in a portable incubator. Theriogenology. 1997;47(4):857–64.
Downs SM, Mastropolo AM. Culture conditions affect meiotic regulation in cumulus cell-enclosed mouse oocytes. Mol Reprod Dev. 1997;46(4):551–66.
Geshi M, Yonai M, et al. Improvement of in vitro co-culture systems for bovine embryos using a low concentration of carbon dioxide and medium supplemented with beta-mercaptoethanol. Theriogenology. 1999;51(3):551–8.
Bhattacharyya A, Yanagimachi R. Synthetic organic pH buffers can support fertilization of guinea pig eggs, but not as efficiently as bicarbonate buffer. Gamete Res. 1988;19(2):123–9.
Behr BR, Stratton CJ, et al. In vitro fertilization (IVF) of mouse ova in HEPES-buffered culture media. J In Vitro Fert Embryo Transf. 1990;7(1):9–15.
Hagen DR, Prather RS, et al. Development of one-cell porcine embryos to the blastocyst stage in simple media. J Anim Sci. 1991;69(3):1147–50.
Lee MA, Storey BT. Bicarbonate is essential for fertilization of mouse eggs: mouse sperm require it to undergo the acrosome reaction. Biol Reprod. 1986;34(2):349–56.
Mahadevan MM, Fleetham J, et al. Growth of mouse embryos in bicarbonate media buffered by carbon dioxide, hepes, or phosphate. J In Vitro Fert Embryo Transf. 1986;3(5):304–8.
Ali J, Whitten WK, et al. Effect of culture systems on mouse early embryo development. Hum Reprod. 1993;8(7):1110–4.
Ozawa M, Nagai T, et al. Successful pig embryonic development in vitro outside a CO2 gas-regulated incubator: effects of pH and osmolality. Theriogenology. 2006;65(4):860–9.
Liu Z, Foote RH, et al. Effect of amino acids and alpha-amanitin on the development of rabbit embryos in modified protein-free KSOM with HEPES. Mol Reprod Dev. 1996;45(2):157–62.
Graves CN, Biggers JD. Carbon dioxide fixation by mouse embryos prior to implantation. Science. 1970;167(924):1506–8.
Quinn P, Wales RG. Fixation of carbon dioxide by pre-implantation mouse embryos in vitro and the activities of enzymes involved in the process. Aust J Biol Sci. 1971;24(6):1277–90.
Quinn P, Wales RG. Fixation of carbon dioxide by preimplantation rabbit embryos in vitro. J Reprod Fertil. 1974;36(1):29–39.
Swain JE, Pool TB. New pH-buffering system for media utilized during gamete and embryo manipulations for assisted reproduction. Reprod Biomed Online. 2009;18(6):799–810.
Phillips KP, Leveille MC, et al. Intracellular pH regulation in human preimplantation embryos. Hum Reprod. 2000;15(4):896–904.
Eagle H. Buffer combinations for mammalian cell culture. Science. 1971;174(8):500–3.
Hashimoto S, Nishihara T, et al. Medium without ammonium accumulation supports the developmental competence of human embryos. J Reprod Dev. 2008;54(5):370–4.
Bunton CA. Oxidation of α-diketones and α-keto acids by hydrogen peroxide. Nature. 1949;163:144.
Morales H, Tilquin P, et al. Pyruvate prevents peroxide-induced injury of in vitro preimplantation bovine embryos. Mol Reprod Dev. 1999;52(2):149–57.
Orsi NM, Leese HJ. Protection against reactive oxygen species during mouse preimplantation embryo development: role of EDTA, oxygen tension, catalase, superoxide dismutase and pyruvate. Mol Reprod Dev. 2001;59(1):44–53.
O’Fallon JV, Wright RWJ. Pyruvate revisited: a non-metabolic role for pyruvate in preimplantation embryo development. Theriogenology. 1995;43:288.
Montgomery CM, Webb JL. Metabolic studies on heart mitochondria. J Biol Chem. 1955;221:359–68.
Montgomery CM, Webb JL. Metabolic studies on heart mitochondria. II. The inhibitory action of parapyruvate on the tricarboxylic acid cycle. J Biol Chem. 1956;221(1):359–68.
Wales R, Dg W. Decomposition of sodium pyruvate in culture media stored at 5°C and its effects on the development of the preimplantation mouse embryo. J Reprod Fertil. 1971;24:126.
Kim JB, Yu YM, et al. Anti-inflammatory mechanism is involved in ethyl pyruvate-mediated efficacious neuroprotection in the postischemic brain. Brain Res. 2005;1060(1–2):188–92.
Lin RY, Vera JC, et al. Human monocarboxylate transporter 2 (MCT2) is a high affinity pyruvate transporter. J Biol Chem. 1998;273(44):28959–65.
Malaisse WJ, Jijakli H, et al. Insulinotropic action of methyl pyruvate: secretory, cationic, and biosynthetic aspects. Arch Biochem Biophys. 1996;335(2):229–44.
Varma SD, Devamanoharan PS, et al. Prevention of intracellular oxidative stress to lens by pyruvate and its ester. Free Radic Res. 1998;28(2):131–5.
Sims CA, Wattanasirichaigoon S, et al. Ringer’s ethyl pyruvate solution ameliorates ischemia/reperfusion-induced intestinal mucosal injury in rats. Crit Care Med. 2001;29(8):1513–8.
Rocheleau JV, Head WS, et al. Quantitative NAD(P)H/flavoprotein autofluorescence imaging reveals metabolic mechanisms of pancreatic islet pyruvate response. J Biol Chem. 2004;279(30):31780–7.
Zeng J, Liu J, et al. Exogenous ethyl pyruvate versus pyruvate during metabolic recovery after oxidative stress in neonatal rat cerebrocortical slices. Anesthesiology. 2007;107(4):630–40.
Zeng J, Yang GY, et al. Pyruvate improves recovery after PARP-1-associated energy failure induced by oxidative stress in neonatal rat cerebrocortical slices. J Cereb Blood Flow Metab. 2007;27(2):304–15.
Dave SH, Tilstra JS, et al. Ethyl pyruvate decreases HMGB1 release and ameliorates murine colitis. J Leukoc Biol. 2009;86(3):633–43.
Di Paola R, Mazzon E, et al. Ethyl pyruvate reduces the development of zymosan-induced generalized inflammation in mice. Crit Care Med. 2009;37(1):270–82.
Yang R, Shaufl AL, et al. Ethyl pyruvate ameliorates liver injury secondary to severe acute pancreatitis. J Surg Res. 2009;153(2):302–9.
Swain JE, Pool TB. Supplementation of culture media with esterified forms of pyruvate improves mouse embryo development. In Proceedings from the ASRM Annual Meeting, San Francisco, CA; 2008.
Combelles CM, Gupta S, et al. Could oxidative stress influence the in-vitro maturation of oocytes? Reprod Biomed Online. 2009;18(6):864–80.
Wang X, Falcone T, et al. Vitamin C and vitamin E supplementation reduce oxidative stress-induced embryo toxicity and improve the blastocyst development rate. Fertil Steril. 2002;78(6):1272–7.
Angle M. Using two concurrent sequential culture media improves pregnancy outcomes. Clinical Embryologist. 2006;9(1):5–11.
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Swain, J.E., Pool, T.B. (2012). Culture Media in IVF: Decisions for the Laboratory. In: Nagy, Z., Varghese, A., Agarwal, A. (eds) Practical Manual of In Vitro Fertilization. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-1780-5_11
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