首页> 外文期刊>Environmental toxicology and chemistry >APPARENT TOLERANCE OF TURKEY VULTURES (CATHARTES AURA) TO THE NON-STEROIDAL ANTI-INFLAMMATORY DRUG DICLOFENAC
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APPARENT TOLERANCE OF TURKEY VULTURES (CATHARTES AURA) TO THE NON-STEROIDAL ANTI-INFLAMMATORY DRUG DICLOFENAC

机译:土耳其秃(对非甾体类抗炎药双氯芬酸的表观耐受性

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The nonsteroidal anti-inflammatory drug diclofenac is extremely toxic to Old World Gyps vultures (median lethal dose ~0.1-0.2 mg/kg), evoking visceral gout, renal necrosis, and mortality within a few days of exposure. Unintentional secondary poisoning of vultures that fed upon carcasses of dicloferiac-treated livestock decimated populations in the Indian subcontinent. Because of the widespread use of diclofenac and other cyclooxygenase-2 inhibiting drugs, a toxicological study was undertaken in turkey vultures (Cathartes aura) as an initial step in examining sensitivity of New World scavenging birds. Two trials were conducted entailing oral gavage of diclofenac at doses ranging from 0.08 to 25 mg/kg body weight. Birds were observed for 7 d, blood samples were collected for plasma chemistry (predose and 12, 24, and 48 h and 7 d postdose), and select individuals were necropsied. Diclofenac failed to evoke overt signs of toxicity, visceral gout, renal necrosis, or elevate plasma uric acid at concentrations greater than 100 times the estimated median lethal dose reported for Gyps vultures. For turkey vultures receiving 8 or 25 mg/kg, the plasma half-life of diclofenac was estimated to be 6 h, and it was apparently cleared after several days as no residues were detectable in liver or kidney at necropsy. Differential sensitivity among avian species is a hallmark of cyclooxygenase-2 inhibitors, and despite the tolerance of turkey vultures to diclofenac, additional studies in related scavenging species seem warranted.
机译:非甾体类抗炎药双氯芬酸对旧大陆秃鹰秃((中位致死剂量〜0.1-0.2 mg / kg)极具毒性,在暴露后几天内会引起内脏痛风,肾坏死和死亡。饲喂双氯芬酸处理过的牲畜尸体的秃鹰无意中毒,使印度次大陆的人口减少。由于双氯芬酸和其他抑制环氧合酶2的药物的广泛使用,因此在火鸡兀鹰(Cathartes aura)中进行了毒理学研究,作为检查新世界清除鸟类敏感性的第一步。进行了两项试验,要求对双氯芬酸进行口服管饲,剂量范围为0.08至25 mg / kg体重。观察鸟类7天,采集血样进行血浆化学分析(给药前,给药后12、24、48h和7d),并对尸体进行尸检。双氯芬酸不能引起明显的毒性,内脏痛风,肾坏死或血浆尿酸升高的迹象,其浓度大于吉普斯秃鹰的估计中值致死剂量的100倍。对于接受8或25 mg / kg的火鸡兀鹰,双氯芬酸的血浆半衰期估计为6小时,并且在尸体剖检时在肝脏或肾脏中未检测到任何残留物,因此几天后显然已清除。禽类之间的差异敏感性是环氧合酶2抑制剂的标志,尽管火鸡秃鹰对双氯芬酸具有耐受性,但有关清除物种的进一步研究似乎是必要的。

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