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E Bustos-Obregon

Publications and source records attributed to E Bustos-Obregon.

At least 19 recordsLinked to original sources

An in vitro model to evaluate the effect of an organophosphoric agropesticide on cell proliferation in mouse seminiferous tubules.

Recently, there has been public concern about the toxic effects of organophosphoric pesticides (OP) upon human and animal populations. Since the seminiferous epithelium is an actively proliferating tissue, it was of interest to study germ cell proliferation in the isolated seminiferous tubules of mice that were cultured in the presence of Parathion or paraoxon, its metabolite. Eighteen 3-month-old CF-1 male mice were used. Paraoxon (PO) and Parathion (PT) were added to cultures of seminiferous tubules in the following groups: (1) Ham F-10 medium pH 7.4 (M) (control); groups 2 to 5, M + decreasing doses of either PO or PT (0.8; 0.4; 0.04; 0.004; 0.0004 mM). Each group consisted of six mice. Incubation of the tubules was carried out for 5 h at 35 degrees C, 5% CO2, 95% air. One hour before the end of incubation 5 microCi of 3H-thymidine was added to the cultures. DNA uptake was measured by scintillation counting. PO and PT at concentrations of 0.8 mM elicited a sharp decrease in testicular DNA synthesis. Recuperation at concentrations under 0.4 mM was different. With PO it was rapid, possibly due to the high detoxificative ability of the testis, which contains high quantities of the enzyme 'type A esterases' that hydrolyses PO. At concentrations lower than PO, PT has an inhibitory effect upon germ cell proliferation, which deserves further research.

Animals↗

Reappraisal of the hypo-osmotic swelling test to improve assessment of seminal fertility status.

The hypo-osmotic swelling (HOS) test has been proposed as a useful assay for evaluation of the functional competence of the human sperm membranes. To assess this further, the HOS-test was evaluated in 187 semen samples collected from fertile men and from male patients consulting for infertility. These samples were classified as normal, oligo-, astheno- or oligoasthenozoospermic on the basis of their standard semen variables. The percentage of total sperm tail swelling and of sperm exhibiting different tail swelling patterns was recorded. In the fertile men and in the group of patients with normal semen variables, significantly more (P less than 0.001) HOS-reactive sperm were observed after hypo-osmotic treatment in comparison with those groups exhibiting abnormal semen parameters. Swelling of the sperm in a hypo-osmotic medium was highly correlated with both progressive motility (r = 0.62, P less than 0.001) and sperm viability (r = 0.65, P less than 0.001). A weak positive correlation was also observed between sperm swelling and sperm morphological features (r = 0.31, P less than 0.005) and between sperm swelling and sperm concentration (r = 0.31, P less than 0.005). No significant correlation was observed between sperm swelling and in-vitro sperm fertilizing capacity as assessed by the zona-free hamster oocyte penetration assay. However the majority of the semen samples (87.3%) showing a normal penetration rate (greater than or equal to 10%) also exhibited a 60% (or higher) reaction in the HOS-test.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Nuclear chromatin decondensation of spermatozoa in vitro: a method for evaluating the fertilizing ability of ovine semen.

Spermatozoa obtained from testes, epididimydes and complete ejaculates of healthy rams during the breeding and non-breeding seasons were induced to show nuclear chromatin decondensation by controlled exposure to dithiotreitol (DTT) and sodium dodecyl sulphate (SDS) in vitro. A gradual resistance to decondensation was shown by sperm during epididymal transit, confirming a progressive increase in the prevalence of chromatinic disulphide bonds during sperm maturation in this species. A high % of stable (non-decondensed) sperm nuclei after treatment (79%) was found in semen from rams with normal fertility (64% non-return rate at first oestrus). Opposite changes were found in the semen from rams having low fertility rates (37%), as these showed only 31% of stable sperm nuclei. There were no differences in the spermiograms of these two groups. When semen from the same rams was tested during the non-breeding season, a similar relationship was found, although in both groups there was a higher % of sperm with stable nuclei than during the breeding season. The possible role of seminal plasma and of some of its constituents (e.g., zinc) on the decondensation of ram sperm nuclear chromatin was also studied. The presence of seminal plasma and the addition of zinc largely or completely inhibited the decondensation of ram sperm nuclear chromatin whilst the reverse situation was seen following the addition of chelating agents (e.g. EDTA) to the semen samples. The present results suggest that the induction of sperm nuclear decondensation by exposure to DTT and SDS under controlled conditions may provide a simple but reliable method for predicting in vitro the fertilizing ability of a ram semen sample.

Animals↗

Testicular specific soluble antigens and spermatogenic onset in the mouse.

Soluble antigens, specific for mouse testis, were detected by immunoelectrophoresis using a rabbit antiserum against a testicular extract (TE; supernatant of a mouse testicular homogenate spun at 105,000 g for 2 hr). At least 18 archs of precipitation were defined for the adult TE, but only three were testis specific. They were found in the epididymal extract, thus suggesting that these may be spermatozoal antigens. In immature mice, the testis-specific antigens start to appear in coincidence with the onset of pachytene spermatocytes. Immunohistochemical observations (peroxidase-antiperoxidase) showed specific reaction over spermatocytes and spermatids. The site of reaction was the surface or the peripheric cytoplasm of these cells.

Animals↗

Ultrastructure and function of the lamina propria of mammalian seminiferous tubules.

The lamina propria of the seminiferous tubules comprises the basement membrane, plus one or more layers of cells, depending on the species, and intercellular material. The myoid (contractile) cells are nearest to the seminiferous tubules. In larger mammals, several layers of contractile cells, surrounding the seminiferous tubules are normally present. They are charaterized by the presence of boundles of 80 A filaments, which are responsible for the contractility. It is supposed, that the myoid cells are renewed from adjacent peripheral fibroblast-like cells.

Animals↗

Ultrastructure of testes and excurrent ducts in the bonnet monkey (Macaca radiata).

The testes and excurrent ducts of four bonnet macaques (Macaca radiata) were examined using scanning and transmission electron microscopy. The three layers of contractile and connective tissue composing the tunica albuginea, and the multilayered tunica propria of the seminiferous tubules were similar to that of man. Spermatids project from the epithelium or are found free in the lumen. The stages of the cycle of the germinal epithelium in the bonnet macaque were similar to that in other macaques. The epithelium of the rete testis consisted of thin brush-bordered cells, whereas the epithelium of the efferent ducts consisted of tall, prismatic or cylindrical cells lined by kinocillia or short stereocilia and basal cells. The height of the epididymal epithelium and lumen diameter was maximal in the caput region and minimal at the cauda. Spermatozoa were found among clusters of stereocilia. The epithelium of the vas deferens showed gradual transition from the stereocilia covering typical of the epididymis to that of a shorter, apical microvilli covering.

Animals↗

Comparative scanning electron microscope study of boar, bull and ram spermatozoa.

The comparative ultrastructure of ejaculated boar, bull and ram spermatozoa is studied by scanning electron microscopy. After washing, the spermatozoa are fixed in glutaraldehyde or im picric acid-formaldehyde-glutaraldehyde mixture. Samples are prepared either by critical point drying (Freon) on Millipore filters or by air drying on glass cover slips. In all the species studied, three regions may be distinguished in the paddle-shaped head of the sperm: an anterior segment (surrounded by the marginal thickening) and an equatorial segment constituting together the acrosome, and the postacrosomal region. Most of the feature of the postacrosomal lamina described in transmission electron microscopy are visible through the plasma membrane, particularly after air drying. The surface morphology of the neck and of the different segments of the flagellum is also evident. Some species differences are encountered, e.g. rough surface of acrosome and absence of serrations in postacrosomal lamina of boar spermatozoa only. The techniques employed result in good general morphology and fine resolution of surface detail of the sperm samples; they also permit analysis of spermatozoa treated by freezing or submitted to acrosomal extraction.

Acrosome↗

Morphological appraisal of gametogenesis. Spermatogenetic process in mammals with particular reference to man.

The process of spermatogenesis in man can be subdivided into prenatal, postnatal and adult phases. Special attention is devoted to the cytomorphology of the germ cells in these phases, with a more detailed description of the proliferation, maturation and differentiation of the germ cells in the adult. Thus, spermatogonial renewal, meiotic division and the morphological transformations of the spermatids into mature spermatozoa are described. An outline of the structures characteristic of the latter is also given. The histological organization of the seminiferous epithelium is considered, whereby the concepts of the cycle, stage of the cycle and wave of the seminiferous epithelium are discussed. The duration of both the cycle and that of spermatogenesis of the adult are considered. The present review on mammalian, and chiefly human spermatogenic processes aims at: surveying of current concepts, and compiling of the more important facts and problems of spermatogenesis. The nomenclature and definitions advanced here arise from the concept of continuity of the processes of spermatogenesis from embryo to adult.

Adolescent↗