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火鸡秃鹫(红头美洲鹫)对非甾体抗炎药双氯芬酸的明显耐受性。

Apparent tolerance of turkey vultures (Cathartes aura) to the non-steroidal anti-inflammatory drug diclofenac.

作者信息

Rattner Barnett A, Whitehead Maria A, Gasper Grace, Meteyer Carol U, Link William A, Taggart Mark A, Meharg Andrew A, Pattee Oliver H, Pain Deborah J

机构信息

Patuxent Wildlife Research Center, U.S. Geological Survey, Beltsville Agricultural Research Center-East, Building 308, 10300 Baltimore Avenue, Beltsville, Maryland 20705, USA.

出版信息

Environ Toxicol Chem. 2008 Nov;27(11):2341-5. doi: 10.1897/08-123.1.

Abstract

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 diclofenac-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.

摘要

非甾体抗炎药双氯芬酸对旧大陆兀鹫具有极高毒性(半数致死剂量为0.1 - 0.2毫克/千克),接触后数天内会引发内脏痛风、肾坏死并导致死亡。以双氯芬酸处理过的牲畜尸体为食的兀鹫会意外发生二次中毒,这使印度次大陆的兀鹫数量大幅减少。由于双氯芬酸和其他环氧化酶 - 2抑制药物的广泛使用,对红头美洲鹫开展了一项毒理学研究,作为研究新大陆食腐鸟类敏感性的第一步。进行了两项试验,通过口服灌胃给予双氯芬酸,剂量范围为0.08至25毫克/千克体重。对鸟类观察7天,采集血样进行血浆生化检测(给药前、给药后12、24、48小时及7天),并对部分个体进行尸检。在浓度高于报道的兀鹫估计半数致死剂量100倍以上时,双氯芬酸未引发明显的毒性迹象、内脏痛风、肾坏死,也未使血浆尿酸升高。对于接受8或25毫克/千克剂量的红头美洲鹫,双氯芬酸的血浆半衰期估计为6小时,数天后显然已被清除,因为尸检时在肝脏或肾脏中未检测到残留。鸟类物种间的敏感性差异是环氧化酶 - 2抑制剂的一个特点,尽管红头美洲鹫对双氯芬酸具有耐受性,但对相关食腐物种进行更多研究似乎是有必要的。

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