Unusual germ cell organization in the seminiferous epithelium of a murid rodent from southern Asia, the greater bandicoot rat, Bandicota Indica.

In the greater bandicoot rat, Bandicota indica, of south-east Asia, nine cell associations were documented in the testicular seminiferous epithelium. In about 10% of the tubule cross sections two or more cell associations occurred and, furthermore, some of the generations of germ cells within the cell associations were sometimes either out of phase, or missing, in the tubule cross sections. These features, together with the fact that this species has a highly pleiomorphic sperm head shape, are somewhat reminiscent of those of the seminiferous epithelium in humans and some other primates but not of common laboratory rodents. This species could thus be a good model for investigating irregular patterns of spermatogenesis in naturally occurring wild species of rodent.

Histopathological alterations in the edible snail, Babylonia areolata (spotted babylon), in acute and subchronic cadmium poisoning.

Histopathological alterations in 6- to 8-month-old juvenile spotted babylon, Babylonia areolata, from acute and subchronic cadmium exposure were studied by light microscopy. The 96-h LC(50) value of cadmium for B. areolata was found to be 3.35 mg/L, and the maximum acceptable toxicant concentration (MATC) was 1.6 mg/L. Snails were exposed to 3.35 and 0.08 mg/L (5% of MATC) of cadmium for 96 h and 90 days, respectively. After exposure the gill, the organs of the digestive system (proboscis, esophagus, stomach, digestive gland, and rectum), and the foot were analyzed for cadmium accumulation. The results showed that most digestive organs had a high affinity for cadmium. The main target organ was the stomach, which could accumulate on average 1192.18 microg/g dry weight of cadmium. Cadmium was shown to accumulate to a lesser extent in the digestive gland, gill, rectum, esophagus, proboscis, and foot. Histopathological alterations were observed in the gill and digestive organs (proboscis, esophagus, stomach, and rectum). The study showed that the stomach and gill were the primary target organs of both acute and subchronic exposure. Gill alterations included increased size of mucous vacuoles, reduced length of cilia, dilation and pyknosis of nuclei, thickening of basal lamina, and accumulation of hemocytes. The epithelial lining of the digestive tract showed similar alterations such as increased size of mucous vacuoles, reduced length of cilia, and dilation of nuclei. In addition, fragmentation of the muscle sheath was observed.

Opisthorchis viverrini: ultrastructure and cytochemistry of the glycocalyx of the tegument.

The ultrastructure and cytochemistry of the glycocalyx of the tegument of Opisthorchis viverrini during maturation from newly excysted juvenile to adult stages were investigated using colloidal iron, ruthenium red and lectin stainings. The results showed that the glycocalyx was intensely stained by the first two dyes, thus indicating the presence of relatively high amounts of negative charges. However, the thickness and intensity of the staining decreased during the fluke's maturation. Binding studies using lectin probes on the surface of adult parasites showed that binding sites for Canavalia ensiformis (Con A), Triticum vulgaris (WGA) and Ricinus communis I (RCA I) were present in relative large amounts on the glycocalyx of the adult tegument, whereas those for Dolichos biflorus (DBA) were relatively fewer in number, and those for Ulex europaeus I (UEA I) were absent. The binding patterns of Con A, WGA, RCA I and DBA were generally similar, and the reaction product was uniformly distributed over the dorsal and ventral surfaces of the parasite's body. These bindings, therefore, indicate the presence of D-mannose/D-glucose, N-acetyl-D-glucosamine/sialic acid, D-galactose and N-acetyl-D-galactosamine residues on the glycocalyx of the adult tegument.

The developing Xenopus oocyte specifies the type of gonadotropin-stimulated steroidogenesis performed by its associated follicle cells.

As a response to gonadotropin, amphibian ovarian follicles primarily synthesize and secrete estradiol-17 beta (E2) during vitellogenesis and progesterone (P) when fully grown. Stage IV (vitellogenic) and stage VI (full-grown) ovarian follicles from Xenopus laevis, as well as intermediate sizes, were used to explore this change in steroidogenesis. Optimum steroidogenesis occurred in both stage IV and stage VI follicle exposed for 6 h to 20 IU human chorionic gonadotropin/mL. Although the total amounts of steroid fund were about the same, the E2/P ratios ranged from 26 to 35 for intact stage IV follicles, but only 0.02-0.03 for intact stage VI follicles. Steroid-producing follicle cells were isolated from stage IV and stage VI follicles by non-enzymatic procedures, were washed and were tested for steroidogenic activity in the absence of oocytes. In both cases, P was the predominant steroid produced (E2/P = 0.004-0.04), so the presence of stage IV, but not stage VI, oocytes appears to be necessary for E2 production as a response to gonadotropin. Octanol had no significant effect on the E2/P ratio of intact stage IV follicle. Dissected oocyte/follicle cell preparations from stage IV follicles were also periodically challenged with gonadotropin over 72 h, during which time most follicle cells detached from the oocyte and formed a monolayer over the bottom of the culture dish. The relatively high E2/P ratios for such preparations showed no significant change when stimulated with gonadotropin at various times over the 72 h, as long as the medium was not replaced. We conclude that the estrogenic effect of stage IV oocytes is most likely mediated by a secretory product rather than by gap junctions or by cell contact. Because the X. laevis oocyte has been shown to be a self-differentiating cell, the steroidogenic shift that occurs in developing ovarian follicles appears to be fundamentally regulated by the growing oocyte as if undergoes a physiological change rather than by different gonadotropins.

Inhibition of implantation of hamster embryos by lectins.

In order to test their effects on implantation, lectins (Con A and WGA) were infused into one horn of the uterus of each female hamster aged between 10 and 14 weeks at day 3 of pregnancy (D3). Con A was given to three groups of 10 animals each at dosages of 100, 200 and 400 micrograms/10 microliter normal saline (NS)/animal, and WGA to four groups of animals at dosages of 20, 50, 100 and 200/10 microliter NS/animal. Control groups consisted of untreated animals and animals treated with saline. On D8, laparotomy was performed and the number of fetuses were counted. In untreated and NS-treated groups the number of fetuses were 6.9 and 6.8 per horn, which were not significantly different. In Con A-treated groups, at dosages of 100, 200 and 400 micrograms the number of fetuses were 2.2, 2.5 and 2.1 per horn, respectively. By contrast, in WGA-treated groups no implantation was detected, except at the dosage of 20 micrograms, in which 1.1 fetuses per horn was observed. To study the mechanism of inhibition, another three groups of animals were similarly treated with NS, 100 micrograms Con A and 50 micrograms WGA/10 microliter NS/animal, respectively. On D4 at 1300-1400 h, uterine lumens were flushed to collect unimplanted blastocysts. No blastocyst was found in NS- and Con A-treated groups, whereas 6.2 blastocysts with complete zona pellucida were collected per horn in WGA-treated group. Histologically, Con A caused vacuolization in epithelium and edema in the stromal layer of endometrium. However, such changes were not observed in WGA-treated uteri.

Effect of estradiol treatment on the secretion and structure of gastric H+ and pepsin-secreting cells in the rat.

Gastrin-stimulated secretory rate of gastric H+ and pepsin were markedly inhibited (P less than 0.001) in ovariectomized rat after 7 days of estradiol treatment (80 micrograms/kg/day) in comparison to ovariectomized untreated rat and sham control. In correlation to the secretions, the majority of parietal cells failed to show the typical ultrastructural transformation associated with active secretion. Pyknotic nuclei with dilatation of nuclear envelope and degenerative changes were observed in the parietal cells. Meanwhile, the chief cell showed inactive characteristics in that a large number of pepsinogen granules were retained in the cells. In contrast, in ovariectomized untreated rat, the rate of gastrin-stimulated H+ and pepsin secretion were not significantly different from the sham (P greater than 0.05). Consistent with secretion, after gastrin stimulation, the morphology and ultrastructure of the parietal cell and chief cell showed active secretory features in a pattern similar to changes observed in sham. The results suggest that impairment in the structure of the functional parts of secretory cells by estrogen treatment was a factor contributing to the inhibition of the gastric secretions.