The aim of this diploma thesis is to compare quality of northern pike sperm collected by different methods. First method is collection of stripped sperm by abdominal massage of the belly. Second method is collection of stripped sperm with special catheter to eliminate sperm contamination by urine. The last method is collection of testicular sperm. Differently collected sperm was evaluated and compared its quality. The main observed parameters were sperm volume, spermatozoa concentration, spermatozoa motility and velocity and osmolality of seminal fluid. Sperm samples were used for eggs fertilization. In fertilized eggs, the fertility of eggs and larvae hatching rate were observed.

Thesis (MScMedSc)-- Stellenbosch University, 2013. / ENGLISH ABSTRACT: Much has been documented about the detrimental effects of adverse lifestyle factor exposure on the body. Exposure to factors, such as cigarette smoke, have proved to not only be a burden on global health and economy, but have also led to growing concerns about effects on systemic functions such as reproduction. The aim of the present study was to determine the effects of in utero and in vitro nicotine exposure on spermatozoal function and the antioxidant enzyme activity and lipid peroxidation (LPO) status of the male reproductive system. A better understanding of this process is necessary to combat the respective burdens of smoking and male infertility and for the prospective development of treatment strategies. Two experimental models were employed: Wistar rats were exposed to nicotine in utero while human and rat spermatozoa were exposed to nicotine in vitro. In utero studies were achieved by selecting healthy pregnant rats and treating them with 1 mg/kg-bodyweight/day nicotine or 1 ml/kg-bodyweight/day 0.85% physiologic saline throughout gestation and lactation. Male rat pups were selected and sacrificed at each of the following age groups (n=6): 42 days, 84 days and 168 days old. The pups were only exposed to the treatment/saline via placental uptake or lactation. Biochemical analyses of the tissue comprised of measurement of LPO and antioxidant enzyme activity. Results indicated a significant association of maternal nicotine exposure to decreased levels of primary antioxidant enzymes in rat testes. Of particular note was the observation that the treatment group, of which each of the respective antioxidant enzyme levels were significantly less than the control group, was the oldest (d168) rat group. In vitro studies were achieved by collecting sperm samples from healthy human donors (n=12), healthy rats (n=6) and obese rats (n=6). Samples were washed and exposed to different concentrations of high levels of nicotine (Control, 0.1mM, 1mM, 5mM, 10mM) in vitro. Semen parameters such as motility, viability and acrosome reaction were monitored at different time points (30min, 60min, 120min, 180min). Results revealed increasing in vitro nicotine concentrations were associated with decreased viability and acrosomal status of human spermatozoa and decreased progressive motility and viability of rat spermatozoa. Obesity was also associated with decreases in progressive motility and viability of rat spermatozoa. These results indicate that the acute in vitro exposure of spermatozoa to high levels of nicotine could adversely affect semen quality and may be an additive factor to the impediment of male fertility. In utero results reveal maternal nicotine exposure adversely affects male fertility in later life and seems to elicit more detrimental effects on the reproductive system than that of direct nicotine exposure to spermatozoa. Obesity also inhibits parameters of male fertility and these effects are exacerbated by nicotine exposure. The authors believe these adverse effects on the reproductive system to be related to an increased activation of leukocytes, excess production in reactive oxygen species (ROS) and consequent onset of oxidative stress (OS). Nevertheless this study agrees with other studies that nicotine exposure may be an additive factor to the impediment of male fertility. / AFRIKAANSE OPSOMMING: Daar is reeds baie bekend oor die moontlik newe effekte vir die liggaam wat met ‘n ongesonde lewenstyl gepaard gaan. Menslike blootstelling aan sulke faktore, soos sigaret rook, is wêreldwyd ‘n las vir gesondheid en ekonomie en het gelei tot geweldige kommer onder navorsers oor die moontlike komplikasies vir liggaamlike funksies soos voortplanting. Die doel van die betrokke projek was om die effekte van in utero en in vivo nikotien blootstelling op die antioksiderende ensiem aktiwiteit en lipied peroksidasie status van reproduktiewe weefsel en die funksionele parameters van spermatozoa te bepaal. ‘n Beter begrip van hierdie proses is noodsaaklik om die las van rook en vetsug teen te werk en vir die moontlike ontwikkeling van behandelingsstrategieë. Twee eksperimentele modelle is ontwerp: Wistar rotte is in utero blootgestel aan nikotien terwyl mens- en rot- spermatosoë ook in vitro aan nikotien blootgestel is. Vir die in utero studie is gesonde dragtige rotte gedurende swangerskap en laktasie met 1 mg/kgliggaamsgewig/ dag nikotien of 1 ml/kg-liggaamsgewig/dag 0.85% fisiologiese soutoplossing behandel. Manlike welpies is gekies en geoffer op elk van die volgende ouderdomme (n=6): 42 dae, 84 dae en 168 dae. Die welpies is slegs aan nikotien blootgestel deur plasentale opname en laktasie. Biochemiese analise van die testikulêre weefsel het ‘n beduidende assosiasie getoon tussen maternale nikotien blootstelling en verminderde vlakke van die primêre antioksiderende ensieme. Die 168 dag oue groep het ‘n merkbare vermindering getoon tussen kontrole en nikotien weefsel vir elk van die antioksiderende ensieme. Vir die in vitro studie is sperm monsters verkry vanaf gesonde mans (n=12), gesonde rotte (n=6) en vet rotte (n=6). Monsters is gewas en in vitro blootgestel aan verskeie hoë vlakke van nikotien (kontrole, 0.1mM, 1mM, 5mM, 10mM). Seminale parameters soos motiliteit, lewensvatbaarheid en akrosoom status is by verskei tydpunte gemeet (30min, 60min, 120min, 180min). Dit blyk dat verhoging in in vitro nikotien konsentrasies verband hou met verlaagde lewensvatbaarheid en akrosoom status van menslike spermatosoë en verlaagde progressiewe motilteit en lewensvatbaarheid van rot spermatosoë. Vetsug is ook geassosieer met verlagings in progressiewe beweeglikheid en lewensvatbaarheid van rot spermatosoë. In utero resultate openbaar dat maternale nikotien blootstelling manlike vrugbaarheid nadelig beïnvloed in latere lewe en blyk dat dit meer van ‘n nadelige uitwerking op die voortplantingstelsel het as dié van direkte nikotien blootstelling aan spermatosoë. In vitro blootstelling van spermatosoë aan hoë vlakke van nikotien, het wel ook semen kwaliteit nadelig beïnvloed. Vetsug inhibeer ook manlike vrugbaarheids parameters en hierdie effek word vererger deur nikotien blootstelling. Die outeure glo dat hierdie nadelige uitwerking op die voortplantingstelsel verband hou met 'n verhoogde aktivering van leukosiete, oortollige produksie van reaktiewe suurstof spesies en die gevolglike aanvang van oksidatiewe stres bevorder. Hierdie studie stem wel ooreen met ander studies wat nikotien blootstelling bestempel as ‘n bydraende faktor tot die struikelblok van manlike onvrugbaarheid. / Harry Crossley Foundation (South Africa)

Thesis (PhD)--Stellenbosch Uni versity, 2000. / ENGLISH ABSTRACT: Intracytoplasmic sperm injection (ICSI) introduced a revolutionary way of treatment for male factor infertility. With the exception of some cases of non-obstructive azoospermia, all other male factor infertility cases have the potential to be successfully treated with ICS!. The only prerequisite seems to be the presence of a motile or viable immotile sperm cell for each oocyte. In this study we report on our own experience with the development and implementation of the ICSI method in the Reproductive Biology Unit at Tygerberg Hospita!. An analysis of 5 years of ICSI experience showed that semen parameters, sperm morphology, motility and concentration did not influence fertilization and pregnancy rates adversely. In most cases, patients who could not be treated with in vitro fertilization (IVF) and gamete intrafallopian transfer (GIFT), due to poor semen parameters or fertilization failure, were treated successfully with ICS!. Even a case of globozoospermia was treated successfully with ICS!. Testicular spermatozoa, fresh or frozen-thawed, also resulted in excellent fertilization and pregnancy rates. Cryopreservation of testicular samples facilitated the management of the infertile couple, aiding the coordination of the recovery of vital gametes from both partners and also limiting the repetition of testicular biopsies. Incubation (maturation) of testicular spermatozoa also induced an enhancement in pregnancy rates. It can be concluded that ICSI proved to be a treatment method with success similar to that of in vitro fertilization (IVF) and gamete intrafallopian transfer (GIFT), in spite of a severe male factor. The study also indicated transfer route and embryo quality (viability) to be very important factors in the success of ICS!. The tubal transfer route was shown to be a significant contributor to the pregnancy success (compared to uterine transfer) as was the transfer of embryos that showed early division to the 2-cell stage, 26 hours post injection. The transfer of early dividing embryos into the fallopian tube resulted in a pregnancy rate of almost 40%, a result similar to that of GIFT with a mild male factor. The role of the oocyte in fertilization and pregnancy success was also revealed indirectly by the introduction of ICS!. Visual observation of denuded oocytes was possible and many morphological features, normal and abnormal, can be observed. Immature oocytes can also be identified and it was shown that they could be successfully matured in vitro before injection. In this study transmission electron microscopy (TEM) was used to study abnormalities in oocyte morphology. The standard method was adapted and modified for single cell TEM. The abnormalities observed included lysosomal and non-lysosomal degeneration (yellowish or darkly coloured oocytes), degeneration and vacuole formation (vacuolated oocytes), large secondary lysosomes filled with multiple small lipid droplets - lipofuscin body (refractile body) and a fragmented oocyte. It was also possible to study at ultrastructural level, possible reasons for fertilization failure in ICS!. Different stages of oocyte activation failure, cytoplasmic immaturity, sperm cell extrusion, abnormal sperm cell decondensation, female spindle abnormalities and technique related factors were observed. TEM was also successfully implemented to elucidate the reason for infertility in a patient with a longstanding, unexplained history of infertility. TEM evaluation of two of the patient's unfertilized oocytes revealed a spindle abnormality with contributing cytoskeletal anomalies at ultrastructural level. The modified TEM technique offers a valuable tool to study this small, but important group of patients with unexplained infertility. ThisTEM study opened up a new, valuable and interesting avenue of research with both diagnostic and prognostic value for patients with unexplained infertility. ICSI is therefore a valuable method in the treatment of especially male factor infertility. It is the most advanced fertilization technique developed in the last decade in this field. Not only can almost all male factor patients be treated, but unexplained female infertility can also be exposed, studied and hopefully in future also be treated with micromanipulation methods. / AFRIKAANSE OPSOMMING: Die ontwikkeling van die mikromanipulasie tegniek "Intracytoplasmic sperm injection" (ICSI) het die behandeling van die manlike faktor in infertiliteit, revolusionêr verander. Met die uitsondering van sommige gevalle van nie-obstruktiewe asoospermia, kan potensieel alle ander manlike infertiliteits faktore suksesvol met ICSI behandel word. Die enigste voorvereiste blyk "n bewegende of "n nie-bewegende, maar bewese lewende spermsel te wees. In hierdie studie word verslag gedoen oor die ontwikkeling en toepassing van die ICSI metode in die Eenhed vir Reproduktiewe Biologie by Tygerberg Hospitaal. 'n Analise van 5 jaar se resultate na die implementering van die ICSI metode het gewys dat die semen parameters, sperm morfologie, motiliteit en konsentrasie, nie "n effek op bevrugting- en swangerskapsyfers gehad het nie. Pasiënte wat, as gevolg van ontoereikende semen parameters, nie met die klassieke metodes, in vitro bevrugting (IVB) of gameet intrafallopiusbuis terugplasing (GIFT) behandel kon word nie, kon suksesvol met ICSI behandel word. Daar was selfs "n geval van manlike infertiliteit as gevolg van globosoospermie, wat suksesvol met ICS behandel is. Die ICSI metode het dit ook moontlik gemaak om uitstekende bevrugting- en swangerskap resultate met testikulêre spermatosoa .(vars en gevries) te bereik. Die bevriesing van testisweefsel het ook bygedra tot beter hantering van sulke pasiënte. Herhaalde testisbiopsies word uitgeskakel en die koórdinasie van die verkryging van die manlike en vroulike gamete, word ook vergemaklik wanneer testisweefsel in gevriesde vorm beskikbaar is. Die studie het verder getoon dat wanneer testikulêre weefsel geïnkubeer word (om spermatosoa te laat matureer), die swangerskapsyfers verhoog was. Dit is dus duidelik dat die ICSI metode net so suksesvol soos die IVB en GIFT metodes toegepas kan word, selfs en veral in gevalle van erge manlike faktor infertiliteit. Die studie het ook verder getoon dat die plek waar embrios teruggeplaas word, asook die embriokwalitiet van teruggeplaasde embrios, belangrike bydraende faktore in die ICSI swangerskapsukses was. Embrioterugplasing in die buis van fallopius en terugplasing van embrios wat vroeë 2-sel deling, 26 uur na ICSI getoon het, is uitgewys as faktore wat ICSI swangerskap betekenisvol verbeter het. Dit was moontlik om "n swangerskapsyfer van ongeveer 40%, sootgelyk aan die van GIFT sonder "n erge manlike faktor, te bereik met die terugplasing van ten minste een vroeë deler embrio in die fallopiese buis. Die ICSI tegniek het ook indirek bygedra tot nuwe insigte met betrekking tot die rol wat die vroulike eiersel (oësief in ICSI bevrugting speel. Oósiete word gestroop van hulomringende selle vir die ICSI proses en kan dan maklik vir hul normale en abnormale morfologiese eienskappe evalueer word. Oësiete wat immatuur is kan ook so geïdentifiseer word en dit is moontlik om hulle suksesvol te matureer voor mikro-inspuiting. Transmissie-elektronmikroskopie (TEM) is in die studie gebruik om die ultrastruktuur van onbevrugde en abnormale oësiete te bestudeer. Hiervoor is "n bestaande tegniek gemodifiseer vir die hantering van "n enkele sel, in hierdie geval die oosiet. Lisasomale en nie-lisosomale degenerasie (oósiete wat geelof donker van kleur voorkom), degeneratiewe tekens en vakuole (oësiete met vakuole), groot sekondêre lisosome gevul met klein lipieddruppels ('refractile body') en 'n gefragmenteerde oosiet was van die morfologies abnormale eienskappe wat ultrastruktureel geïdentifiseer is. Moontlike faktore wat 'n rol kan speel in nie-bevrugting na ICSI kon ook op ultrastrukturele vlak met die tegniek geïdentifiseer word. Hierdie faktore het die volgende ingesluit: die onvermoë van verskillende stadiums van oosiet aktivering, sitoplasmatiese immaturiteit, uitwerping van die spermsel na die periviteliene spasie, abnormale spermsel dekondensasie, vroulike spoelvormings abnormaliteite en tegniekgekoppelde faktore. Die TEM tegniek is ook suksesvol aangewend om die infertiliteitsprobleem van 'n pasiënt wat vir etlike jare aan onverklaarbare infertiliteit gely het, te identifiseer. TEM het op die ultrastrukturele vlak gewys dat daar 'n spoel abnormaliteit in twee van haar onbevrugde oëslete was. TEM kan dus baie vrugbaar gebruik word in hierdie groep pasiënte om onverklaarbare infertiliteit, wat andersins ongeïdentifiseerd sou bly, te verklaar. Die ICSI metode is die mees revolusionêre tegniek wat die afgelope dekade vir die behandeling van veral manlike infertiliteit ontwikkel en baie suksesvol toegepas is. Die metode ook kan 'n bydraende rol speel in die hantering van onverklaarbare infertiliteit veral ten opsigte van die vroulike gameet. In die toekoms is dit moontlik dat selfs hierdie probleem met nuwe mikromanipulasietegnieke opgelos sal kan word.

Speciation, the formation of new species, is an essential evolutionary process that causes species diversity on the Earth. At the beginning of this process is the separation of two populations by a reproductive barrier that prevents gene flow between these populations. One of the mechanisms, which enable reproductive isolation, is hybrid sterility (HS). It is a mechanism of postzygotic isolation that is described in a number of eukaryotes. The first discovered gene of hybrid sterility in vertebrates is the mice gene Hst1, later identified as gene Prdm9. By genetic and molecular analysis the locus on the X chromosome was determined, whose interaction with Prdm9 causes sterility or reduced fitness in male hybrids. This locus contains two genetic factors: Hstx1, causing an abnormal morphology of spermatozoa, and Hstx2, causing an arrest in spermatogenesis in pachytene spermatocytes and sterility. In my thesis I focus on the effect of deletion of a candidate hybrid sterility gene Fmr1nb on the X chromosome. The analysis of males B6N.Fmr1nbmut with deletion variants of the Fmr1nb gene showed that Fmr1nb is one of the factors influencing spermatogenesis. An increase in morphologic abnormalities in spermatozoa occurred in males with Fmr1nb gene deletion. This phenotype is identical with Hstx1. The effect...

Orientador: Luiz Claudio Nogueira Mendes / Coorientador: Sergio Moraes Aoki / Banca: Flavia Lombardi Lopes / Banca:Gisele Zoccal Mingotti / Banca:Maria denise Lopes / Banca: Eduardo Harry Birgel Junior / Resumo: Novas metodologias para a sexagem de sêmen são buscadas devido à citometria de fluxo apresentar limitações e desvantagens e os aptâmeros surgem como potenciais candidatos para a identificação de espermatozoides conforme a presença do cromossomo X ou Y. Os objetivos foram avaliar o uso de três aptâmeros desenvolvidos para se ligarem especificamente ao espermatozoide Y na separação magnética por sexo de espermatozoides de touro, e desenvolver uma técnica de qPCR que permita realizar facilmente o diagnóstico da proporção sexual em amostras de sêmen. Protocolos de separação por magnetismo utilizando aptâmeros biotinilados foram utilizados em sêmen comercial, e duas frações de espermatozoides foram obtidas para cada aptâmero testado (livre e retida). A proporção relativa de espermatozoides Y foi analisada em reações de qPCR desenvolvidas para este objetivo. A curva padrão utilizada na qPCR foi eficiente para a quantificação da proporção sexual relativa em amostras de sêmen convencional e sexado. Diferença significativa da proporção relativa de Y foi encontrada na fração de espermatozoides livres do aptâmero C12 em relação ao controle (47,7% vs. 51,3%, respectivamente; P = 0,009); as demais separações não apresentaram diferença significativa. Os aptâmeros selecionados não produziram o efeito desejado de separação do sêmen conforme a presença do cromossomo X ou Y, nestas condições utilizadas, mas a diminuição da proporção relativa de Y em uma das frações não retidas indica ser possí... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: Sex preselection of livestock offspring represents a big potential for genetic improvement. There are a search for new methods to sex-sort bull semen in order to avoid the limitations of flow cytometry/cell sorting technique. Aptamers emerge as potential candidates for sperm identification relative the presence of chromosome X or Y. In this work, the objectives were 1, to evaluate three aptamers developed to specifically binding to the Y-bearing sperm in magnetic separation by sex of bovine sperm and 2, to develop a SYBR Green Real-Time PCR method to determinate sex ratio in bovine semen in semen samples. Separation protocols by magnetism using biotinylated aptamers were used in commercial semen, and two fractions of sperm were obtained for each tested aptamer (free and trapped). The relative ratio of Y-bearing spermatozoa was analyzed in qPCR reactions developed for this purpose. The standard curve for qPCR was efficiently designed to quantify the sex relative ratio of sorted and unsorted semen samples. Significant difference in the relative proportion of Y-bearing sperm was found in the fraction of free sperm samples from aptamer C12 compared to the control samples (47.7% vs. 51.3%, respectively; P = 0.009); other separations showed no significant difference. Selected aptamers did not produce the wanted effect of sperm separation by the presence of chromosome X or Y, in these conditions used, but decreased relative proportion of Y-bearing sperm in one of the free fractions ... (Complete abstract click electronic access below) / Doutor

Orientador: Wilma De Grava Kempinas / Resumo: A infertilidade afeta aproximadamente 15% dos casais em idade reprodutiva, sendo o homem responsável por cerca da metade dos casos. A diminuição da fertilidade masculina é devido a uma variedade de condições que incluem malformações congênitas, distúrbios genéticos e endócrinos, doenças infecciosas e inflamatórias, disfunção sexual e estilo de vida. A proteína espermática SP22 (sperm protein, 22kDa) tem demonstrado ser um biomarcador de fertilidade masculina, visto que, em ratos, está bem estabelecido que sua concentração, em extratos de espermatozoides da cauda epididimária, se correlaciona com a fertilidade desses gametas. No entanto, para incorporar essa proteína como um biomarcador em estudos epidemiológicos e clínicos são necessários dados quantitativos em humanos. Assim, o presente estudo teve por objetivos padronizar a técnica de quantificação e imunolocalização da proteína espermática SP22, investigar possíveis correlações entre parâmetros seminais convencionais e funcionais, de homens férteis e inférteis, com a concentração dessa proteína e avaliar o seu potencial preditivo como um biomarcador, não invasivo, de fertilidade. Para tanto foram realizados dois estudos observacionais: um do tipo caso-controle e outro do tipo seccional. O estudo caso-controle foi desenvolvido em amostras seminais de 44 voluntários da cidade de Botucatu e região, com idade entre 20 a 50 anos, que foram agrupados de acordo com a fertilidade: férteis (um ou mais filhos) e inférteis. Já o estu... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: Infertility affects approximately 15% of couples in reproductive age and 50% of the cases are directly related to man. The decrease in male fertility is due to several conditions including congenital malformations, genetic and endocrine disorders, infectious and inflammatory diseases, sexual dysfunction and lifestyle. Sperm protein SP22 (22kDa) has been shown to be a male fertility biomarker since, in rats, it is well established that its concentration, in sperm extractions from the epididymal tail, correlates with the fertility of these gametes. However, to incorporate this protein as a fertility biomarker in epidemiological and clinical studies, quantitative data are required in humans. Thus, the present study aimed to standardize the SP22 quantification and immunolocalization technique, investigate possible correlations among conventional and functional seminal parameters of fertile and infertile men with the concentration of this protein and to evaluate its predictive potential as a non-invasive fertility biomarker. Therefore, two observational studies were performed: one case-control type and the other sectional type. The case-control study was carried out on 44 volunteers’s seminal samples from Botucatu city and region, aged between 20 and 50 years, who were placed according to fertility: fertile (one or more children) and infertile. The sectional study was carried out on 12 patients’s attendend by the Human Reproduction Center of the Botucatu Medical School – UNESP, al... (Complete abstract click electronic access below) / Doutor

"April 2004." / Thesis (Ph.D.)--Chinese University of Hong Kong, 2004. / Includes bibliographical references (p. 158-181). / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Mode of access: World Wide Web. / Abstracts in English and Chinese.

A criopreservação de sêmen humano tem sido amplamente utilizada como método de preservação da fertilidade. A fim de reduzir os danos causados pelo processo de congelamento, diversos estudos utilizaram substâncias antioxidantes e estimulantes, porém, sua eficácia, bem como seu papel no controle funcional dos espermatozoides, não está bem estabelecida na literatura. Assim, o objetivo do estudo foi avaliar o efeito da suplementação de melatonina e cafeína nas características estruturais e funcionais de espermatozoides pré-criopreservação e pós-descongelamento. Para isso, este estudo prospectivo utilizou 30 amostras seminais de pacientes entre 19 e 45 anos de idade da rotina do Laboratório Androscience entre maio de 2013 e maio de 2017. Todas as amostras foram classificadas como normozoospérmicas, segundo análise seminal inicial de acordo com os critérios da Organização Mundial da Saúde (OMS). Em seguida, as amostras foram criopreservadas com Human Tubal Fluid modificado sem suplemento ou com 2mM de melatonina. Após o descongelamento, as amostras foram analisadas ou suplementadas com 2 mM de cafeína, incubadas por 15 minutos. Ao final dos experimentos, obtivemos 4 grupos: Amostras pós-descongelamento sem suplementação (CONT), amostras suplementadas com cafeína (CAF), melatonina (MEL) e cafeína + melatonina (CM). Parâmetros seminais de contagem, motilidade e cinética, analisados pelos critérios da OMS e pelo software SCA®, a atividade mitocondrial, pela coloração por diaminobenzidina, avaliação da taxa de fragmentação de DNA, pelo método SCSA® e a dosagem dos níveis de radicais livres de oxigênio (ROS), pelo método de luminescência, foram realizados pré-criopreservação e pós-descongelamento com ou sem suplementação. Os dados foram analisados pelo teste T de Student pareado e pela análise de variâncias de uma via com medidas repetidas, seguida pelo pós-teste de Holm-Sidak, e adotado um alfa de 5%. Observamos redução significativa concentração espermática (p < 0,001), motilidade total (p < 0,001) e progressiva (p < 0,001), parâmetros cinéticos (p < 0,009) e atividade mitocondrial (p < 0,001) e aumento das taxas de fragmentação de DNA (p=0,046) e ROS (p=0,052) nas amostras CONT quando comparadas com as amostras a fresco. Quando suplementadas com cafeína e melatonina, observamos aumento da motilidade progressiva nos grupos CAF (p=0,005) e CM (p=0,048) e aumento da atividade mitocondrial no grupo CM (p < 0,05). Podemos concluir que a associação da suplementação com cafeína e melatonina nas amostras pré-criopreservação e pós-descongelamento demonstrou ser uma ferramenta importante para ser aplicada em amostras criopreservadas para atuarem como substâncias estimuladoras de motilidade espermática / Human semen cryopreservation has been widely used as a method of preserving fertility. In order to reduce the damages caused by the freezing process, several studies used antioxidant and stimulant substances, however, their efficiency as well as their role in the functional control of spermatozoa have not been well established in literature. Thus, the goal of this study was to investigate the effect of melatonin and caffeine supplementation on the structural and functional characteristics of pre-cryopreservation and post-thaw spermatozoa. For this, this prospective study used 30 seminal samples from patients aged from 19 to 45 years in the routine of the Androscience Laboratory between May 2013 and May 2017. All samples were classified as normozoospermic, according to the initial seminal analysis following criteria of the World Health Organization (WHO). Then, the samples were cryopreserved with modified Human Tubal Fluid without supplement or with 2 mM of melatonin. After thawing, the samples were analyzed or supplemented with 2 mM of caffeine, and incubated for 15 minutes. At the end of the experiments, we obtained 4 groups: Post-thaw samples without supplementation (CONT), samples supplemented with caffeine (CAF), melatonin (MEL) and caffeine + melatonin (CM). Seminal parameters for count, motility and kinetics, analyzed by WHO criteria and by the SCA® software, mitochondrial activity, by diaminobenzidine staining, evaluation of DNA fragmentation rate, by the SCSA® method, and dosage of radical oxygen species (ROS) levels, by the luminescence method, pre-cryopreservation and post-thaw were carried out with or without supplementation. The data were analyzed by the paired Student\'s t-test and by one-way analysis of variance with repeated measurements, followed by the Holm-Sidak post-test, adopting an alpha of 5%. We observed a significant reduction in sperm concentration (p < 0.001), total (p < 0.001) and progressive (p < 0.001) motility, kinetic parameters (p < 0.009) and mitochondrial activity (p < 0.001), and increased rates of DNA fragmentation (p=0.046) and ROS (p=0.052) production in the CONT samples when compared with fresh sample. When supplemented with caffeine and melatonin, we observed an increase in progressive motility in the CAF (p=0.005) and CM (p=0.048) groups, and an increase in mitochondrial activity in CM group (p < 0.05). We can conclude that that the combination of caffeine and melatonin supplementation in pre-cryopreservation and post-thaw samples proved to be an important tool to be applied in cryopreserved samples to act as substances that stimulate sperm motility

<p>Prostasomes are extracellularly occurring organelles which are secreted in human semen by the prostate gland. Prostasomes have several known biological activities, but their physiological function is still unclear. In this thesis some new aspects were studied on the biological role of the prostasomes. </p><p>The motility-stimulatory effect of prostasomes on cryopreserved spermatozoa was further studied by supplementing the swim-up medium with seminal prostasomes, and with prostasomes purified from a PC-3 prostate cancer cell line (PC-3 prostasomes), on fresh spermatozoa. The recovery of motile spermatozoa after swim-up increased by 50% when the swim-up medium was supplemented with prostasomes. The PC-3 prostasomes bore a functional resemblance to seminal prostasomes as regards various expressions of sperm motility promotion. </p><p>Prostasomes proved to have potent antibacterial effects. The effects were not strictly confined to Bacillus megaterium since a few other bacteria were also sensitive. The high percentage of patients with anti-prostasome antibodies showed that prostasomes could be one of the major targets for antisperm antibodies (ASA). The results demonstrate that ASA in serum of infertile men and women recognise prostasomes as antigens, and that polyclonal antibodies raised against prostasomes agglutinate human spermatozoa. This suggests that prostasomes contribute at least partly to immunological infertility. Three types of prostasomes (seminal-, native- and metastasis-derived prostasomes) demonstrated similarities regarding a high cholesterol/phospholipid ratio and some marker enzymes. The conclusion is that prostasomes have a common and exclusive prostatic origin in man and that they are internalised in storage vesicles of the secretory cells and released in toto by an ordinary exocytotic event.</p>

Sexual selection can influence the mating system of an organism through multiple mechanisms. These mechanisms result in variation in reproductive success among individuals, and include scramble competition, endurance rivalries, contests, mate choice and cryptic choice, and sperm competition. Understanding the mating system of a species requires the identification of which processes are occurring, and to what degree. In this thesis, I explored the influence of mate choice mechanisms on the mating system of the terrestrial red-legged salamander, Plethodon shermani. I also documented the potential for post-copulatory processes (such as sperm competition and cryptic choice) to influence mating system dynamics. The evolution of mate choice requires (among other factors) variation in the reproductive value of potential mates. This variation is made apparent to choosy individuals through cues. Most animals use multiples cues incorporating many modalities to assess the reproductive quality of potential mates. In Chapter 2, I tested the contribution of two cues (chemical and visual) to mate choice by female P. shermani. I found that a male visual cue ("foot-dancing") increased courtship success. In contrast, delivery of non-volatile pheromones during courtship did not influence courtship success in the laboratory setting, but did affect the duration of one of the courtship stages. In Chapter 4, I identified a tactile cue that was significantly correlated with male reproductive success. Thus, P. shermani females could use at least three modalities to assess the reproductive quality of potential mates. Mate choice can also evolve in males. In Chapter 3, I tested this possibility in P. shermani. I found that males vary the reproductive effort they invest in a particular courtship based on the reproductive value of their partner, indicating male mate choice is occurring. A male invested most when paired with a female with large, well developed ova, and invested less with females that were non-gravid or had small ova. In addition to documenting male mate choice, I showed that the male visual display ("foot-dancing") that affected female mate choice was correlated with male condition, implying foot-dancing may be an honest indicator of male quality. Finally, in Chapter 5, I explored the potential for post-copulatory processes to influence the P. shermani mating system. The opportunity for sperm from multiple males to overlap in the female reproductive tract (i.e., the opportunity for females to mate multiply) is necessary for post-copulatory processes such as cryptic choice and sperm competition. The capacity for long-term sperm storage by females can increase the likelihood that this overlap in sperm from multiple males will occur. I found that females can store viable sperm for at least 9 months and in some cases beyond oviposition. In addition, I documented one female with sperm in her sperm storage organ from a mating that occurred 17 months earlier. Such lengthy sperm storage allows the possibility of sperm from one breeding season to interact with sperm from a subsequent season. Thus, the potential for post-copulatory sexual selection within this salamander system is high. / Graduation date: 2012