The present study aimed to determine whether gill macro- and microstructure show compensatory responses in three freshwater fish differing in their sensitivity to high environmental ammonia (HEA). The highly ammonia-sensitive salmonid Oncorhynchus mykiss (rainbow trout), the less ammonia-sensitive cyprinid Cyprinus carpio (common carp) and the highly ammonia-resistant cyprinid Carassius auratus (goldfish) were used as test species and were exposed for 0 h (control), 3h, 12h, 24h, 48 h, 84 h and 180 h to 1mM ammonia (as NH4HCO3; pH 7.9). In cyprinids, dramatic alterations were initiated quickly evident by thickening of filaments and lamellae, retraction of lamellae, enlargement of interlamellar cell mass (ILCM), and increase in the water-blood diffusion distance; while in trout, these modifications were absent or developed very slowly. These reorganizations may attempt to reduce the surface area presumably protecting against the water borne ammonia; and were more pronounced in goldfish marked by momentous enlargement of ILCM volume and the presence of rudimental and almost fused lamellae. Extensive mucus production in the gills of goldfish and carp and to a limited extent in trout may have been part of general stress response and/or may have played a protective role. While goldfish and carp showed shrinkage of apical crypts of mitochondrion rich cells (MRCs), probably aiding to regulate ion status, trout showed enlarged apical crypts of MRCs. All species displayed changes in the pattern of the microridges on the surface of pavement cells (PVCs). Overall, the present results connote that the goldfish with its minimal respiratory surface area and a large population of the MRCs with small apical crypts located on the edge of ILCM is better prepared for survival in ammonia polluted water compared to carp which maintain larger lamellae and especially the trout that did not show gill remodeling.
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http://dx.doi.org/10.1016/j.aquatox.2014.06.018 | DOI Listing |
Background: Parkinson's Disease (PD) is a neurodegenerative disorder with prodromal gastrointestinal (GI) issues often emerging decades before motor symptoms. Pathologically, PD can be driven by accumulation of misfolded alpha synuclein (aSyn) protein in the brain and periphery, including the GI tract. Disease epidemiology differs by sex, with men twice as likely to develop PD.
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November 2024
Institut Curie, PSL Research University, CNRS UMR 144, F-75005 Paris, France.
Intestinal epithelial cells, which are instrumental in nutrient absorption, fluid regulation, and pathogen defense, undergo continuous proliferation and differentiation within the intestinal crypts, migrating towards the luminal surface where they are eventually shed. RAB GTPases are key regulators of intracellular vesicular trafficking and are involved in various cellular processes, including cell migration and polarity. Here, we investigated the role of RAB6 in the development and maintenance of the gut epithelium.
View Article and Find Full Text PDFFront Cardiovasc Med
September 2024
Multimodality Cardiac Imaging Section, IRCCS Policlinico San Donato, Milan, Italy.
Front Immunol
October 2024
Department of Veterinary Diagnostic and Production Animal Medicine, College of Veterinary Medicine, Iowa State University, Ames, IA, United States.
Introduction: The critical early stages of infection and innate immune responses to porcine epidemic diarrhea virus (PEDV) at the intestinal epithelium remain underexplored due to the limitations of traditional cell culture and animal models. This study aims to establish a porcine enteroid culture model to investigate potential differences in susceptibility to infection across segments of the porcine small intestine (duodenum, jejunum, and ileum).
Methods: Intestinal crypt cells from nursery pigs were cultured in Matrigel to differentiate into porcine enteroid monolayer cultures (PEMCs).
Nihon Yakurigaku Zasshi
September 2024
School of Pharmacy, Kitasato University.
Prediction of intestinal drug absorption and drug-induced intestinal toxicity is critical for the development of orally-administered drugs. However, it is difficult to accurately predict these events because of large species differences and a lack of appropriate in vitro assay. Then, we proposed the use of human crypt-derived intestinal cells for the prediction of intestinal absorption and the risk of intestinal toxicity.
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