Traditional methods of oocyte selection for in vitro studies have proven inefficient with respect to achieving a level of predictability for competency. In this study, a novel method of oocyte selection was implemented that identified a relationship between oocyte morphological parameters (as defined by a ratio of a shape factor (SF) to average fluorescence intensity (AFI) and AFI, followed by in vitro fertilization (IVF) and in vitro culture (IVC) using the Well of Well (WOW) method to evaluate oocyte competency. Specifically, we used non-cytotoxic fluorescent molecular probes and multiphoton microscopy to non-invasively characterize spatial localization and functional activity of mitochondria, mitochondrial membrane potential (Δψm), and intracellular calcium activity ([Ca2+]i) using rhodamine 123, JC-1 and Fluo-4, AM, respectively in bovine and canine in vitro matured (IVM) oocytes. Comparison of morphological grading with fluorescence intensity yielded similar trends between all grades of oocytes for both species with no visually obvious, distinct characteristic staining that would permit classification of each oocyte as a specific morphological grade. Our studies confirmed that oocyte mitochondria were homogeneously distributed but primarily localized to the peri- and sub-cortical regions of the oocyte at MII stage for both species. Further, heterogeneously polarized mitochondria were localized to the peri- and sub- cortical regions of the oocyte for both species. In bovine oocytes labeled with Fluo-4, AM, levels of [Ca2+]i were either unremarkable, or very low and limited to the peri-cortical areas, just beneath the oolema. For canine MII stage oocytes, levels of [Ca2+]i were within the same range of AFI as bovine. Ranges of fluorescence intensity compatible for optimal embryo development for bovine and optimal fertilization for canine oocytes were 30-300 and 20-35, and 20-30 and 20-25.5 for rhodamine 123 and Fluo-4, AM, respectively. The optimal range for bovine oocytes imaged with JC-1 was 1.25-2.25 and <6 for canine.

Traditional methods of oocyte selection for in vitro studies have proven inefficient with respect to achieving a level of predictability for competency. In this study, a novel method of oocyte selection was implemented that identified a relationship between oocyte morphological parameters (as defined by a ratio of a shape factor (SF) to average fluorescence intensity (AFI) and AFI, followed by in vitro fertilization (IVF) and in vitro culture (IVC) using the Well of Well (WOW) method to evaluate oocyte competency. Specifically, we used non-cytotoxic fluorescent molecular probes and multiphoton microscopy to non-invasively characterize spatial localization and functional activity of mitochondria, mitochondrial membrane potential (Δψm), and intracellular calcium activity ([Ca2+]i) using rhodamine 123, JC-1 and Fluo-4, AM, respectively in bovine and canine in vitro matured (IVM) oocytes. Comparison of morphological grading with fluorescence intensity yielded similar trends between all grades of oocytes for both species with no visually obvious, distinct characteristic staining that would permit classification of each oocyte as a specific morphological grade. Our studies confirmed that oocyte mitochondria were homogeneously distributed but primarily localized to the peri- and sub-cortical regions of the oocyte at MII stage for both species. Further, heterogeneously polarized mitochondria were localized to the peri- and sub- cortical regions of the oocyte for both species. In bovine oocytes labeled with Fluo-4, AM, levels of [Ca2+]i were either unremarkable, or very low and limited to the peri-cortical areas, just beneath the oolema. For canine MII stage oocytes, levels of [Ca2+]i were within the same range of AFI as bovine. Ranges of fluorescence intensity compatible for optimal embryo development for bovine and optimal fertilization for canine oocytes were 30-300 and 20-35, and 20-30 and 20-25.5 for rhodamine 123 and Fluo-4, AM, respectively. The optimal range for bovine oocytes imaged with JC-1 was 1.25-2.25 and <6 for canine.

A prolonged growth phase of the ovulatory follicle results in follicular aging. Whether follicular aging is detrimental or beneficial to oocyte competence is not fully known. The objective of this thesis is to investigate the effects of follicular aging on oocyte competence and granulosa cell gene expression in cattle. Four sets of experiments were designed to address the objective. The following hypotheses were tested during the course of these studies: 1) oocyte competence will improve by the longer growing phase but will be adversely affected by FSH starvation, 2) follicles that undergo superstimulation will have different gene expression than dominant follicles from a natural cycle, 3) extending the superstimulation protocol by 3 days will allow follicles to mature better and 4) markers of maturity, cellular health and survival will be turned off by FSH starvation. The objective of the first study (Chapter 3) was to determine the effects of extending the length of superstimulation and follicular aging on oocyte competence by in vitro embryo production. Multiple follicles were allowed to grow for 4 (Short FSH) or 7 days (Long FSH) under the treatment of 8 or 14 injections of FSH (at 12-hour intervals), respectively. Multiple follicles in the FSH starvation group were allowed to grow for 7 days but FSH was provided for only the first 4 days of superstimulation. Extending the duration of follicular growth by superstimulation resulted in a greater number of ≥9 mm follicles and in 2.5 more transferable embryos per animal (morulae+blastocysts) at Day 9 of in vitro embryo culture. The FSH starvation resulted in a greater proportion of poor quality oocytes lower cleavage rate and lower embryonic development. Microarray analysis was used to assess the effect of superstimulation (Chapter 4), follicular aging (Chapter 5) and FSH starvation (Chapter 6) on the gene expression profile of superstimulated granulosa cells. Gene expression of granulosa cells from the post-LH preovulatory dominant follicle was compared (Chapter 4) with those from follicles of the same status after a standard 4-day superstimulation (same protocol as Short FSH group from Chapter 3). A total of 190 genes were down-regulated and 280 genes were upregulated in the superstimulated group when compared with the reference (non-superstimulated control). Data analysis showed that superstimulated follicles are still in a growing phase compared to untreated dominant follicles (most of the upregulated genes are related to matrix remodeling due to tissue proliferation) and did not respond to LH properly (down regulation of LH gene markers). Four-day superstimulation also disturbed genes related to angiogenesis and activated oxidative stress response genes. Extending the superstimulation protocol (7 days; same protocol as Long FSH from Chapter 3) allowed more time for follicles to leave the growing stage and properly respond to LH surge (most of the upregulated genes in the Long FSH group are markers of post LH surge) when compared to the standard 4 day superstimulation protocol (Short FSH; reference group) (Chapter 5). Moreover, the follicles from Long FSH show proximity to ovulation. The continuous FSH support during the extended superstimulation protocol is crucial for follicular health since FSH starvation disturbed genes markers of oocyte quality and embryo development (Chapter 6). Granulosa cells that underwent FSH starvation do not respond to LH surge, which could be detrimental to ovulation (Chapter 6). Therefore, follicles from Short FSH are delayed in maturation and differentiation but the oocyte competence is not compromised. Extending superstimulation protocol by 3 d enhanced the ovarian response to FSH treatment and allowed more time for follicles to mature and properly respond to the LH stimulus. A period of FSH starvation after superstimulatory treatment compromised follicular health, ability to respond to LH and ovulate, oocyte quality and the fertilization process.

The wave-like developmental pattern of follicles ≥1 mm in temporal relationship with follicle stimulating hormone (FSH) and the existence of 2- and 3-waves of follicular development during an interovulatory interval (IOI) have been clearly defined in cattle. However, information about the developmental pattern of antral follicles <1 mm and the repeatability of the wave pattern (2- or 3-wave IOI) is lacking. Using approaches such as immunization against GnRH (to suppress circulating concentrations of FSH) and histomorphometric study of ovarian tissues collected from cyclic heifers on different days after ovulation, the developmental pattern of antral follicles <1 mm and the role of FSH in their development were studied in heifers. Ultrasonographically acquired follicular data were used to determine the repeatability of 2- and 3-wave patterns and the effect of season on the wave patterns. The ovulatory follicle in 3-wave IOI is exposed to a shorter term high-progesterone environment than that of 2-wave IOI, and it has been argued that the less-aged ovulatory follicle of 3-wave IOI yields a more fertile oocyte than the 2-wave IOI. The developmental competence of oocytes in preovulatory follicles of 2- versus 3-wave IOI was compared using in vivo environments created to mimic short-term low- and high-progesterone environments similar to 2- and 3-wave IOI, respectively. The developmental competence of oocytes in persistent dominant-type follicles was also determined.<p>The vaccination against GnRH attenuated FSH surges but did not suppress the basal circulating concentrations of FSH. The attenuation of FSH surges suppressed the wave-like emergence of follicles ≥4 mm but not of the antral follicles <4 mm. The study revealed an inverse relationship between the mean and peak circulating concentrations of FSH and the number of follicles recruited into ≥1 mm size category. Histomorphometric study revealed that antral follicles <1 mm developed in a wave-like fashion in response to a rise in the circulating concentrations of FSH. After treatment with exogenous FSH, the growth rate of follicles in GnRH-immunized heifers was similar to controls. <p>The duration of IOI was predictive of the wave pattern (i.e., 2- or 3-wave IOI), and the pattern was repeatable within individuals throughout the year. The dominant follicle of Wave 1 in 2-wave IOI had a longer duration of dominance than in 3-wave IOI. Hence, the dominant follicle of Wave 1 may have a primary role in the regulation of 2- and 3-wave patterns. Greater attrition of follicles in 3-wave IOI, due to the emergence of an extra wave compared to 2-wave IOI, may contribute to earlier follicular depletion and onset of reproductive senescence in heifers with primarily a 3-wave pattern. The fertilization capacity of oocytes that were exposed to the short-term low-progesterone environment (i.e., similar to the early growing phase of the ovulatory follicle of 3-wave IOI) was increased, but the developmental competence post-fertilization was not different from oocytes that were exposed to a short-term high-progesterone environment (i.e., similar to the early growing phase of preovulatory follicle of 2-wave IOI). Multiple follicles developed under the prolonged-low progesterone environment, but failed to ovulate.

The wave-like developmental pattern of follicles ≥1 mm in temporal relationship with follicle stimulating hormone (FSH) and the existence of 2- and 3-waves of follicular development during an interovulatory interval (IOI) have been clearly defined in cattle. However, information about the developmental pattern of antral follicles <1 mm and the repeatability of the wave pattern (2- or 3-wave IOI) is lacking. Using approaches such as immunization against GnRH (to suppress circulating concentrations of FSH) and histomorphometric study of ovarian tissues collected from cyclic heifers on different days after ovulation, the developmental pattern of antral follicles <1 mm and the role of FSH in their development were studied in heifers. Ultrasonographically acquired follicular data were used to determine the repeatability of 2- and 3-wave patterns and the effect of season on the wave patterns. The ovulatory follicle in 3-wave IOI is exposed to a shorter term high-progesterone environment than that of 2-wave IOI, and it has been argued that the less-aged ovulatory follicle of 3-wave IOI yields a more fertile oocyte than the 2-wave IOI. The developmental competence of oocytes in preovulatory follicles of 2- versus 3-wave IOI was compared using in vivo environments created to mimic short-term low- and high-progesterone environments similar to 2- and 3-wave IOI, respectively. The developmental competence of oocytes in persistent dominant-type follicles was also determined.<p>The vaccination against GnRH attenuated FSH surges but did not suppress the basal circulating concentrations of FSH. The attenuation of FSH surges suppressed the wave-like emergence of follicles ≥4 mm but not of the antral follicles <4 mm. The study revealed an inverse relationship between the mean and peak circulating concentrations of FSH and the number of follicles recruited into ≥1 mm size category. Histomorphometric study revealed that antral follicles <1 mm developed in a wave-like fashion in response to a rise in the circulating concentrations of FSH. After treatment with exogenous FSH, the growth rate of follicles in GnRH-immunized heifers was similar to controls. <p>The duration of IOI was predictive of the wave pattern (i.e., 2- or 3-wave IOI), and the pattern was repeatable within individuals throughout the year. The dominant follicle of Wave 1 in 2-wave IOI had a longer duration of dominance than in 3-wave IOI. Hence, the dominant follicle of Wave 1 may have a primary role in the regulation of 2- and 3-wave patterns. Greater attrition of follicles in 3-wave IOI, due to the emergence of an extra wave compared to 2-wave IOI, may contribute to earlier follicular depletion and onset of reproductive senescence in heifers with primarily a 3-wave pattern. The fertilization capacity of oocytes that were exposed to the short-term low-progesterone environment (i.e., similar to the early growing phase of the ovulatory follicle of 3-wave IOI) was increased, but the developmental competence post-fertilization was not different from oocytes that were exposed to a short-term high-progesterone environment (i.e., similar to the early growing phase of preovulatory follicle of 2-wave IOI). Multiple follicles developed under the prolonged-low progesterone environment, but failed to ovulate.

Made available in DSpace on 2014-08-20T13:32:49Z (GMT). No. of bitstreams: 1 tese_elisa_caroline_da_silva_santos.pdf: 986483 bytes, checksum: 66da36a6826c54f5bd79701d8e49d914 (MD5) Previous issue date: 2014-02-18 / The production of swine embryos in vitro requires efficient in vitro maturation (IVM), which can be achieved by selection the most competent cumulus-oocyte complexes COC).The Brilliant Cresyl Blue (BCB) dye allows the selection of COC with complete growth by assessing their levels of the G6PDH enzyme. However, there is a possible negative effect of selection with BCB. This effect may be due to its intrinsic toxicity or to factors related to the composition of the media used during the test. This research had the objectives: to determine potential toxicity after exposure to BCB and to evaluate the effect of different medias for BCB staining on the ability to support oocyte development. On the first research, after BCB staining and after IVM, several tests were performed to evaluate the effects of their potential toxicity on mitochondrial activity and functionality: reactive oxygen species (ROS), ATP, mitochondrial membrane potential and the number of copies of mitochondrial DNA. The results showed that oocytes stained with BCB produced high levels of ROS, compared with control immediately after staining and after the IVM. The ATP and mitochondrial membrane potential showed similar results between groups after staining, however, after IVM oocytes BCB showed lower membrane potential and ATP. There was no difference in the number of copies of mtDNA in the evaluated groups. Already, on test of ATP content in early embryos, ATP was lower in BCB oocytes, however, there was no difference statistical. In second study, the most commonly used media, D-PBS, was compared with a more elaborate media for BCB called here: ReproPEL. The COC s submitted to both media were submitted to nuclear and cytoplasmatic maturation, parthenogenetic activation, and to the comet test. The great rates of nuclear IVM (P<0.05) were obtained for DPBS+ (63.1%), ReproPELc (55.1%) and ReproPEL+ (50.2%). The group with smaller area of CG (P<0.05), showing better migration, were ReproPELc, D-PBS+, D-PBS- and ReproPEL+. The parthenogenetic activation indicated that ReproPEL media presented satisfactory capacity of oocyte maintenance, resulting in acceptable rates of development to blastocyst stage: 13.0% for ReproPEL+; and 12.7% for ReproPELc. So, the ReproPEL media can be used for maintenance of swine oocytes, but it was not the most appropriate media for BCB staining. Moreover, after exposure to BCB and after IVM, BCB oocytes presented high toxicity at mitochondrial level, due to increased production of ROS, decreased membrane potential and compromised ATP production. However, the mitochondrial function was restored in early embryonic development. In conclusion, BCB was responsible for toxicity in immature swine oocytes, nevertheless, further studies must be performed to evaluate the changes caused by BCB in the embryonic level. / Para a obtenção de embriões suínos produzidos in vitro faz-se necessário que a maturação in vitro (MIV) ocorra de forma eficiente, o que exige a seleção dos complexos cumulus-oócitos (CCOs) mais competentes. O corante Brilliant Cresyl Blue (BCB) permite selecionar os CCOs que completaram seu crescimento, mediante a avaliação dos níveis da enzima G6PDH. Entretanto, existe um possível efeito nocivo relacionado ao processo de seleção com BCB, o qual pode ser devido a uma toxicidade intrínseca do corante ou aos vários fatores relacionados à composição dos meios para a realização do teste. Desta forma, esta pesquisa teve como objetivos: averiguar a existência de toxicidade após exposição ao BCB e avaliar o efeito de diferentes meios para a coloração com BCB sobre a capacidade de suporte ao desenvolvimento oocitário. Na primeira pesquisa, após a coloração com BCB e após a MIV, vários testes foram realizados para avaliar os efeitos de sua potencial toxicidade sobre a atividade e a funcionalidade mitocondrial: análises de espécies reativas de oxigênio (ROS), ATP, potencial de membrana mitocondrial e número de cópias de DNA mitocondrial. Como resultados, obteve-se que oócitos corados com BCB produziram altos níveis de ROS quando comparados com o controle imediatamente após a coloração e após a MIV. O ATP e potencial de membrana mitocondrial apresentaram resultado similar entre os grupos após a coloração, porém, após a MIV oócitos BCB apresentaram menor potencial de membrana e ATP. Não ocorreu diferença no número de cópias do DNAmt nos grupos avaliados. Já, no teste do conteúdo de ATP em embriões iniciais, o ATP foi inferior em oócitos BCB, porém, não ocorreu diferença significativa. Na segunda pesquisa, comparou-se o meio mais utilizado, D-PBS, com um meio mais elaborado para o BCB, chamado de ReproPEL. Os CCOs submetidos aos dois meios foram submetidos à MIV e avaliados quanto à maturação nuclear e citoplasmática, ativação partenogenética e ao teste cometa. Na MIV nuclear, as maiores taxas de MII (P<0,05) foram obtidas no DPBS+ (63,1%), ReproPELc (55,1%) e ReproPEL+ (50,2%). Quanto à densidade dos GC, os grupos com menor área (P<0,05), evidenciando melhor migração, foram ReproPELc, D-PBS+, D-PBS- e ReproPEL+. A ativação partenogenética demonstrou que o meio ReproPEL possui boa capacidade de manutenção oocitária, possibilitando taxas aceitáveis de desenvolvimento até o estágio de blastocisto: ReproPEL+ (13,0%); e ReproPELc (12,7%). Desta forma, o meio ReproPEL pode ser indicado para a manutenção oocitária, porém não foi o meio mais indicado para o corante BCB. Com relação à toxicidade, após a exposição ao BCB e após a MIV, os oócitos BCB apresentaram alterações em nível mitocondrial, devido ao aumento na produção de ROS, diminuição do potencial de membrana e ao comprometimento da produção de ATP. Porém, a função mitocondrial foi restaurada no início do desenvolvimento embrionário. Com tudo isso, conclui-se que o BCB foi responsável por toxicidade em oócitos suínos imaturos, sendo necessários novos estudos para avaliar as alterações causadas pelo BCB em nível embrionário.