29,573 research outputs found
Postprandial morphological response of the intestinal epithelium of the Burmese python (Python molurus)
The postprandial morphological changes of the intestinal epithelium of
Burmese pythons were examined using fasting pythons and at eight time points
after feeding. In fasting pythons, tightly packed enterocytes possess very
short microvilli and are arranged in a pseudostratified fashion. Enterocyte
width increases by 23% within 24 h postfeeding, inducing significant increases
in villus length and intestinal mass. By 6 days postfeeding, enterocyte volume
had peaked, following as much as an 80% increase. Contributing to enterocyte
hypertrophy is the cellular accumulation of lipid droplets at the tips and
edges of the villi of the proximal and middle small intestine, but which were
absent in the distal small intestine. At 3 days postfeeding, conventional and
environmental scanning electron microscopy revealed cracks and lipid extrusion
along the narrow edges of the villi and at the villus tips. Transmission
electron microscopy demonstrated the rapid postprandial lengthening of
enterocyte microvilli, increasing 4.8-fold in length within 24 h, and the
maintaining of that length through digestion. Beginning at 24 h postfeeding,
spherical particles were found embedded apically within enterocytes of the
proximal and middle small intestine. These particles possessed an annular-like
construction and were stained with the calcium-stain Alizarine red S suggesting
that they were bone in origin. Following the completion of digestion, many of
the postprandial responses were reversed, as observed by the atrophy of
enterocytes, the shortening of villi, and the retraction of the microvilli.
Further exploration of the python intestine will reveal the underlying
mechanisms of these trophic responses and the origin and fate of the engulfed
particles
Light and scanning electron microscopy of the intestine of the young red jungle fowl (Gallus gallus)
Thirty males of Red Jungle Fowl (RJF) were divided into 3 equal groups, euthanized at day 1, 10 and 20 days after hatching. The morphometric analyses were performed at three different magnification levels. Different segments (duodenum, jejunum and ileum) and cecum were weighted and length of each small intestinal segments and cecum were determined at a macroscopic level. The mucosa of the intestinal segments was compared and contrasted using both, light and scanning electron microscopy. The villi height, villi surface area, crypt depth and muscularis externa were measured. The body weight was doubled at 10th day and again doubled at 20th day. The weight and length of intestinal segments were significantly higher throughout the experiment except the constant rate of the duodenal and jejunal lengths after 10th days. Relative to body weight, the organs weight and length were declined after 10th days. The duodenal villi height and surface area were greater than the jejunum followed by the ileum. The muscularis externa and crypt depth increased significantly at 10th day. However, the latter showed retardation thereafter. Day one intestinal villi appeared finger-like shape with zigzag arrangement, tongue-like and leaf-like shaped in 10 and 20th days, respectively. The villi distribution and patterns in the middle region of cecum were characteristic. The epithelial cells of the duodenal villi showed more activities and development than those on the jejunum and the ileum throughout the age. The body growth in RJF progresses very slowly while the relative intestinal segment weight and length failed to follow the body weight after 10th days. The duodenal mucosa shows better developmental features than the jejunum and the ileum
Effects of supplemental glutamine and glutamate on growth performance, gastrointestinal development, jejunum morphology and Clostridium perfringens count in caecum of broilers
Optimal villi density for maximal oxygen uptake in the human placenta
We present a stream-tube model of oxygen exchange inside a human placenta
functional unit (a placentone). The effect of villi density on oxygen transfer
efficiency is assessed by numerically solving the diffusion-convection equation
in a 2D+1D geometry for a wide range of villi densities. For each set of
physiological parameters, we observe the existence of an optimal villi density
providing a maximal oxygen uptake as a trade-off between the incoming oxygen
flow and the absorbing villus surface. The predicted optimal villi density
is compatible to previous experimental measurements. Several
other ways to experimentally validate the model are also proposed. The proposed
stream-tube model can serve as a basis for analyzing the efficiency of human
placentas, detecting possible pathologies and diagnosing placental health risks
for newborns by using routine histology sections collected after birth
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Placental Structure in Preterm Birth Among HIV-Positive Versus HIV-Negative Women in Kenya.
BackgroundPreterm birth (PTB) is a major cause of infant morbidity and mortality in developing countries. Recent data suggest that in addition to Human Immunodeficiency Virus (HIV) infection, use of antiretroviral therapy (ART) increases the risk of PTB. As the mechanisms remain unexplored, we conducted this study to determine whether HIV and ART were associated with placental changes that could contribute to PTB.SettingWe collected and evaluated placentas from 38 HIV-positive women on ART and 43 HIV-negative women who had preterm deliveries in Nairobi, Kenya.MethodsAnatomical features of the placentas were examined at gross and microscopic levels. Cases were matched for gestational age and compared by the investigators who were blinded to maternal HIV serostatus.ResultsAmong preterm placentas, HIV infection was significantly associated with thrombosis (P = 0.001), infarction (P = 0.032), anomalies in cord insertion (P = 0.02), gross evidence of membrane infection (P = 0.043), and reduced placental thickness (P = 0.010). Overall, preterm placentas in both groups were associated with immature villi, syncytial knotting, villitis, and deciduitis. Features of HIV-positive versus HIV-negative placentas included significant fibrinoid deposition with villus degeneration, syncytiotrophoblast delamination, red blood cell adhesion, hypervascularity, and reduction in both surface area and perimeter of the terminal villi.ConclusionsThese results imply that HIV infection and/or ART are associated with morphological changes in preterm placentas that contribute to delivery before 37 weeks. Hypervascularity suggests that the observed pathologies may be attributable, in part, to hypoxia. Further research to explore potential mechanisms will help elucidate the pathways that are involved perhaps pointing to interventions for decreasing the risk of prematurity among HIV-positive women
Comparing placentas from normal and abnormal pregnancies
This report describes work carried out at a Mathematics-in-Medicine Study Group. It is believed that placenta shape villous network characteristics are strongly linked to the placenta’s efficiency, and hence to pregnancy outcome. We were asked to consider mathematical ways to describe the shape and other characteristics of a placenta, as well as forming mathematical models for placenta development. In this report we propose a number of possible measure of placental shape, form, and efficiency, which can be computed from images already obtained. We also consider various models for the early development of placentas and the growth of the villous tree
A YY1-dependent increase in aerobic metabolism is indispensable for intestinal organogenesis
During late gestation, villi extend into the intestinal lumen to dramatically increase the surface area of the intestinal epithelium, preparing the gut for the neonatal diet. Incomplete development of the intestine is the most common gastrointestinal complication in neonates, but the causes are unclear. We provide evidence in mice that Yin Yang 1 (Yy1) is crucial for intestinal villus development. YY1 loss in the developing endoderm had no apparent consequences until late gestation, after which the intestine differentiated poorly and exhibited severely stunted villi. Transcriptome analysis revealed that YY1 is required for mitochondrial gene expression, and ultrastructural analysis confirmed compromised mitochondrial integrity in the mutant intestine. We found increased oxidative phosphorylation gene expression at the onset of villus elongation, suggesting that aerobic respiration might function as a regulator of villus growth. Mitochondrial inhibitors blocked villus growth in a fashion similar to Yy1 loss, thus further linking oxidative phosphorylation with late-gestation intestinal development. Interestingly, we find that necrotizing enterocolitis patients also exhibit decreased expression of oxidative phosphorylation genes. Our study highlights the still unappreciated role of metabolic regulation during organogenesis, and suggests that it might contribute to neonatal gastrointestinal disorders
Production of a subunit vaccine candidate against porcine post-weaning diarrhea in high-biomass transplastomic tobacco
Post-weaning diarrhea (PWD) in piglets is a major problem in piggeries worldwide and results in severe economic losses. Infection with Enterotoxigenic Escherichia coli (ETEC) is the key culprit for the PWD disease. F4 fimbriae of ETEC are highly stable proteinaceous polymers, mainly composed of the major structural subunit FaeG, with a capacity to evoke mucosal immune responses, thus demonstrating a potential to act as an oral vaccine against ETEC-induced porcine PWD. In this study we used a transplastomic approach in tobacco to produce a recombinant variant of the FaeG protein, rFaeG(ntd/dsc), engineered for expression as a stable monomer by N-terminal deletion and donor strand-complementation (ntd/dsc). The generated transplastomic tobacco plants accumulated up to 2.0 g rFaeG(ntd/dsc) per 1 kg fresh leaf tissue (more than 1% of dry leaf tissue) and showed normal phenotype indistinguishable from wild type untransformed plants. We determined that chloroplast-produced rFaeG(ntd/dsc) protein retained the key properties of an oral vaccine, i.e. binding to porcine intestinal F4 receptors (F4R), and inhibition of the F4-possessing (F4+) ETEC attachment to F4R. Additionally, the plant biomass matrix was shown to delay degradation of the chloroplast-produced rFaeG(ntd/dsc) in gastrointestinal conditions, demonstrating a potential to function as a shelter-vehicle for vaccine delivery. These results suggest that transplastomic plants expressing the rFaeG(ntd/dsc) protein could be used for production and, possibly, delivery of an oral vaccine against porcine F4+ ETEC infections. Our findings therefore present a feasible approach for developing an oral vaccination strategy against porcine PWD
Effects of Clostridium perfringens iota toxin in the small intestine of mice
Iota toxin is a binary toxin solely produced by Clostridium perfringens type E strains, and is structurally related to CDT from C. difficile and CST from C. spiroforme. As type E causes hemorrhagic enteritis in cattle, it is usually assumed that associated diseases are mediated by iota toxin, although evidence in this regard has not been provided. In the present report, iota toxin intestinal effects were evaluated in vivo using a mouse model. Histological damage was observed in ileal loops treated with purified iota toxin after 4 h of incubation. Luminal iota toxin induced fluid accumulation in the small intestine in a dose dependent manner, as determined by the enteropooling and the intestinal loop assays. None of these changes were observed in the large intestine. These results suggest that C. perfringens iota toxin alters intestinal permeability, predominantly by inducing necrosis and degenerative changes in the mucosal epithelium of the small intestine, as well as changes in intestinal motility. The obtained results suggest a central role for iota toxin in the pathogenesis of C. perfringens type E hemorrhagic enteritis, and contribute to remark the importance of clostridial binary toxins in digestive diseases.Fil: Redondo, Leandro Martin. Instituto Nacional de Tecnología Agropecuaria. Centro de Investigación en Ciencias Veterinarias y Agronómicas. Instituto de Patobiología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Redondo, Enzo Alejandro. Instituto Nacional de Tecnología Agropecuaria. Centro de Investigación en Ciencias Veterinarias y Agronómicas. Instituto de Patobiología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Dailoff, Gabriela Cecilia. Instituto Nacional de Tecnología Agropecuaria. Centro de Investigación en Ciencias Veterinarias y Agronómicas. Instituto de Patobiología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Leiva, Carlos Leónidas. Instituto Nacional de Tecnología Agropecuaria. Centro de Investigación en Ciencias Veterinarias y Agronómicas. Instituto de Patobiología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Díaz Carrasco, Juan María. Instituto Nacional de Tecnología Agropecuaria. Centro de Investigación en Ciencias Veterinarias y Agronómicas. Instituto de Patobiología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Bruzzone, Octavio Augusto. Instituto Nacional de Tecnología Agropecuaria. Centro Regional Patagonia Norte. Estación Experimental Agropecuaria San Carlos de Bariloche; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Cangelosi, Adriana. Dirección Nacional de Instituto de Investigación. Administración Nacional de Laboratorio e Instituto de Salud “Dr. C. G. Malbrán”; ArgentinaFil: Geoghegan, Patricia. Dirección Nacional de Instituto de Investigación. Administración Nacional de Laboratorio e Instituto de Salud “Dr. C. G. Malbrán”; ArgentinaFil: Fernandez Miyakawa, Mariano Enrique. Instituto Nacional de Tecnología Agropecuaria. Centro de Investigación en Ciencias Veterinarias y Agronómicas. Instituto de Patobiología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentin
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