Centre for Wildlife, Indian Veterinary Research Institute, Bareilly, Uttar Pradesh 243122, India.
RSPB Centre for Conservation Science, The Lodge, Sandy, Bedfordshire SG19 2DL, UK.
Sci Total Environ. 2022 Feb 25;809:152088. doi: 10.1016/j.scitotenv.2021.152088. Epub 2021 Nov 30.
Population declines of Gyps vultures across the Indian subcontinent were caused by unintentional poisoning by the non-steroidal anti-inflammatory drug (NSAID) diclofenac. Subsequently, a number of other NSAIDs have been identified as toxic to vultures, while one, meloxicam, is safe at concentrations likely to be encountered by vultures in the wild. Other vulture-safe drugs need to be identified to reduce the use of those toxic to vultures. We report on safety-testing experiments on the NSAID tolfenamic acid on captive vultures of three Gyps species, all of which are susceptible to diclofenac poisoning. Firstly, we estimated the maximum level of exposure (MLE) of wild vultures and gave this dose to 40 Near Threatened Himalayan Griffons G. himalayensis by oral gavage, with 15 control birds dosed with benzyl alcohol (the carrier solution for tolfenamic acid). Two birds given tolfenamic acid died with elevated uric acid levels and severe visceral gout, while the remainder showed no adverse clinical or biochemical signs. Secondly, four G. himalayensis were fed tissues from water buffaloes which had been treated with double the recommended veterinary dose of tolfenamic acid prior to death and compared to two birds fed uncontaminated tissue; none suffered any clinical effects. Finally, two captive Critically Endangered vultures, one G. bengalensis and one G. indicus, were given the MLE dose by gavage and compared to two control birds; again, none suffered any clinical effects. The death of two G. himalayensis may have been an anomaly due to i) the high dose level used and ii) the high ambient temperatures at the time of the experiment. Tolfenamic acid is likely to be safe to Gyps vultures at concentrations encountered by wild birds and could therefore be promoted as a safe alternative to toxic NSAIDs. It is manufactured in the region, and is increasingly being used to treat livestock.
整个印度次大陆的食腐秃鹫数量减少,是由于无意中摄入了非甾体抗炎药(NSAID)双氯芬酸而导致的。随后,又发现了一些其他 NSAID 对秃鹫有毒,而美洛昔康在野外秃鹫可能接触到的浓度下是安全的。需要确定其他对秃鹫安全的药物,以减少对有毒 NSAID 的使用。我们报告了对三种食腐秃鹫(Gyps 属)圈养秃鹫进行 NSAID 托芬那酸安全性测试实验的结果,这三种秃鹫均易受双氯芬酸中毒影响。首先,我们估算了野生秃鹫的最大暴露量(MLE),并通过口服灌胃的方式给 40 只近危喜马拉雅兀鹫喂食了这一剂量,同时用 15 只喂食苯甲醇(托芬那酸的载体溶液)作为对照。两只喂食了托芬那酸的秃鹫因尿酸水平升高和严重内脏痛风而死亡,其余的则没有出现任何不良的临床或生化迹象。其次,给四只喜马拉雅兀鹫喂食了生前曾接受推荐兽医剂量两倍托芬那酸治疗的水牛皮组织,并与两只喂食未受污染组织的秃鹫进行了比较;它们均未出现任何临床影响。最后,两只圈养的极危兀鹫,一只孟加拉兀鹫和一只印度兀鹫,通过灌胃给予了 MLE 剂量,并与两只对照鸟进行了比较;同样,它们均未出现任何临床影响。两只喜马拉雅兀鹫的死亡可能是由于以下两个原因导致的:i)使用的高剂量水平和 ii)实验时的高环境温度。托芬那酸在野生鸟类接触到的浓度下可能对食腐秃鹫是安全的,因此可以作为有毒 NSAID 的安全替代品进行推广。它在该地区生产,并且越来越多地用于治疗牲畜。