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1.
J Small Anim Pract ; 61(3): 156-162, 2020 Mar.
Article in English | MEDLINE | ID: mdl-31867733

ABSTRACT

OBJECTIVES: To describe the use of a xenotransfusion protocol, the outcome of xenotransfusion in recipient cats and to assess owner memory of the xenotransfusion. MATERIALS AND METHODS: Cats administered xenotransfusions in two hospitals between January 2016 and July 2018 were included. Adherence to xenotransfusion protocol, cause of anaemia, blood type, packed cell volume (PCV), transfusion volume, transfusion reactions, PCV 12 hours after transfusion and survival to discharge were recorded. Owners of surviving cats were questioned to assess if they remembered that a xenotransfusion had been performed. RESULTS: Forty-nine cats underwent the xenotransfusion protocol. The most common causes of anaemia were surgical blood loss (n = 17), immune-mediated haemolytic anaemia (n = 14) and neoplasia (n = 14). Median PCV before transfusion was 10%. Six cats (12%) had febrile non-haemolytic transfusion reactions. Median PCV 12 hours after transfusion was 25%. Ten cats (20%) died or were euthanased within 24 hours of xenotransfusion. A delayed haemolytic transfusion reaction occurred in 25 of 39 (64%) cats manifesting as icterus in 15 cats after a median of 1.9 days and haemolytic serum in 19 cats after a median of 2 days. Of the 18 cats alive at 1 week after discharge, 15 (83%) were still alive at a median of 173 days after xenotransfusion. All owners contacted remembered that their cats had received a xenotransfusion. CLINICAL SIGNIFICANCE: Xenotransfusion of canine packed red blood cells to cats is possible but haemolysis should be expected between 1 and 6 days after transfusion.


Subject(s)
Cat Diseases , Transfusion Reaction/veterinary , Animals , Blood Grouping and Crossmatching/veterinary , Blood Transfusion/veterinary , Cats , Dogs , Hematocrit/veterinary
2.
Mar Pollut Bull ; 101(1): 334-348, 2015 Dec 15.
Article in English | MEDLINE | ID: mdl-26555795

ABSTRACT

Despite their representativeness and importance in coastal waters, subtidal rocky bottom habitats have been under-studied. This has resulted in a lack of available indicators for subtidal hard substrate communities. However, a few indicators using subtidal macroalgae have been developed in recent years for the purpose of being implemented into the Water Framework Directive (WFD). Accordingly, a quality index of subtidal macroalgae has been defined as a French assessment tool for subtidal rocky bottom habitats in coastal waters. This approach is based on 14 metrics that consider the depth penetration, composition (sensitive, characteristic and opportunistic) and biodiversity of macroalgae assemblages and complies with WFD requirements. Three ecoregions have been defined to fit with the geographical distribution of macroalgae along the French coastline. As a test, QISubMac was used to assess the water quality of 20 water bodies. The results show that QISubMac may discriminate among different quality classes of water bodies.


Subject(s)
Ecosystem , Environmental Monitoring/methods , Seawater/chemistry , Seaweed/growth & development , Water Pollution/analysis , Water Quality , Ecology , Environmental Monitoring/legislation & jurisprudence , European Union , Government Regulation
3.
Toxicol Lett ; 124(1-3): 47-58, 2001 Oct 15.
Article in English | MEDLINE | ID: mdl-11684357

ABSTRACT

Methyl t-butyl ether (MTBE), ethyl t-butyl ether (ETBE), and t-amyl methyl ether (TAME) are three alkoxyethers added to gasoline to improve combustion and thereby to reduce the level of carbon monoxide and aromatic hydrocarbons in automobile exhaust. Oxidative demethylation of MTBE and TAME and deethylation of ETBE by CYP enzymes results in the formation of tertiary alcohols and aldehydes, both potentially toxic. The metabolism of these three alkoxyethers was studied in a panel of 12 human liver microsomes. The relatively low apparent Km(1) was 0.25+/-0.17 (mean+/-SD), 0.11+/-0.08 and 0.10+/-0.07 mM and the high apparent Km(2) was 2.9+/-1.8, 5.0+/-2.7 and 1.7+/-1.0 mM for MTBE, ETBE and TAME, respectively. Kinetic data, correlation studies, chemical inhibition and metabolism by heterologously expressed human CYPs support the assertion that the major enzyme involved in MTBE, ETBE and TAME metabolisms is CYP2A6, with a minor contribution of CYP3A4 at low substrate concentration.


Subject(s)
Air Pollutants/metabolism , Cytochrome P-450 Enzyme System/metabolism , Ethyl Ethers/metabolism , Methyl Ethers/metabolism , Air Pollutants/pharmacokinetics , Cell Culture Techniques , Ethyl Ethers/pharmacokinetics , Humans , Kinetics , Methyl Ethers/pharmacokinetics , Microsomes, Liver/enzymology , Oxidation-Reduction
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