Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: UNIPROT:A7KAX9 (grit)
1,275 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Among the waterfowl affected by white phosphorus (P4) at a military base in Alaska are tundra (Cygnus columbianus) and trumpeter (C. buccinator) swans. To estimate the toxicity of P4 to swans and compare the toxic effects to those of mallards (Anas platyrhynchos), we dosed 30 juvenile mute swans (C. olor) with 0 to 5.28 mg P4/kg body weight. The calculated LD50 was 3.65 mg/kg (95% CI: 1.40 to 4. 68 mg/kg). However, many of the swans still had P4 in their gizzards after dying, as determined by "smoking gizzards" and characteristic odor, and a lower LD50 might be calculated if all of the P4 had passed into the small intestines. We attribute the retention of P4 in swans to the possibility that P4 pellets were mistaken for the similarly sized grit in their gizzards. Most swans took 1 to 4.5 days to die in contrast to the few hours normally required in mallards and death appeared to be related more to liver dysfunction than to hemolysis. White phosphorus affected several plasma constituents, most notably elevated aspartate aminotransferase, blood urea nitrogen, lactate dehydrogenase, and alanine aminotransferase.
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PMID:Acute toxicity and sublethal effects of white phosphorus in mute swans, Cygnus olor. 1004

Cellulose nanofibers (CNFs) are an emerging engineered nanomaterial that are utilized in a variety of applications, including as a replacement for urea-formaldehyde, and other adhesives, as the binding agent in manufactured fiber and particle boards. To ensure the health and well-being of those producing, installing, or otherwise using cellulose nanofiber boards (CNFBs) it is imperative that the particulate matter (PM) produced during CNFB manipulation be evaluated for toxicity. We developed and internally verified a generation system to examine the PM produced by sanding CNFB using aluminum oxide sandpaper. With 80-grit sandpaper our system produced a low dispersity aerosol, as determined by a scanning mobility particle sizer and an optical particle counter, with a geometric mean of 28 nm (GSD = 1.60). ICP-MS evaluation showed little difference in metal concentrations between CNFB PM and nonsanded CNFB stock. We then used the system to simultaneously generate and expose both male and female C57BL/6J mice acutely for 4 hours at a concentration of 7.9 mg/m3. Sham-exposed controls were treated similarly but without sanding the CNFB. Analysis of bronchoalveolar lavage (BAL) fluid biomarkers showed no signs of inflammatory response at either 4- or 24-hours post exposure. Further, BAL cell viability, number of total cells, and pulmonary cellular recruitment were not significantly changed between the sham-exposed controls and CNFB-exposed mice. Histology further confirmed no pulmonary toxicity as a result of CNFB PM inhalation. We conclude that inhalation of a high concentration of the PM from manipulation of a CNFB did not produce acute toxic responses within 24 hours of exposure.
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PMID:Acute in vivo pulmonary toxicity assessment of occupationally relevant particulate matter from a cellulose nanofiber board. 3296 99