Kane Colston , Karen Mifsud , Nicola Rooney , Juan Manuel Grande , Irene Bueno
{"title":"非甾体抗炎药(NSAIDs)对食腐猛禽的潜在威胁:呼吁进行更广泛的研究和监测","authors":"Kane Colston , Karen Mifsud , Nicola Rooney , Juan Manuel Grande , Irene Bueno","doi":"10.1016/j.etap.2025.104817","DOIUrl":null,"url":null,"abstract":"<div><div>Asian vulture declines have been linked to the consumption of contaminated livestock carcasses with the non-steroidal anti-inflammatory (NSAID) diclofenac. Studies have suggested that the toxicity of NSAIDs to Old World vultures may be through an intronic premature termination codon (PTC) in the gene CYP2C19, encoding a cytochrome P450 enzyme thought responsible for diclofenac metabolism in vultures. However, it remains unclear whether this mechanism applies for all susceptible raptor species. We used nucleotide databases (NCBI) to compare the Cape vulture (<em>Gyps coprotheres</em>) CYP2C19 sequence to other vulture sequences to identify the presence of the intronic PTC. Our search revealed that only <em>Gyps</em> species possessed the CYP2C19 PTC. This is despite NSAID toxicity at similar contaminant levels found in non-<em>Gyps</em> accipitrid mortalities. Our findings suggest avian scavengers could be affected by additional toxicological mechanisms, including sublethal toxicity. Further research is required to establish such mechanisms and exposure risk in non-<em>Gyps</em> scavengers.</div></div>","PeriodicalId":11775,"journal":{"name":"Environmental toxicology and pharmacology","volume":"119 ","pages":"Article 104817"},"PeriodicalIF":4.2000,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Non-steroidal anti-inflammatory drugs (NSAIDs) as a hidden threat to scavenging raptors beyond Gyps: A call for wider research and surveillance\",\"authors\":\"Kane Colston , Karen Mifsud , Nicola Rooney , Juan Manuel Grande , Irene Bueno\",\"doi\":\"10.1016/j.etap.2025.104817\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Asian vulture declines have been linked to the consumption of contaminated livestock carcasses with the non-steroidal anti-inflammatory (NSAID) diclofenac. Studies have suggested that the toxicity of NSAIDs to Old World vultures may be through an intronic premature termination codon (PTC) in the gene CYP2C19, encoding a cytochrome P450 enzyme thought responsible for diclofenac metabolism in vultures. However, it remains unclear whether this mechanism applies for all susceptible raptor species. We used nucleotide databases (NCBI) to compare the Cape vulture (<em>Gyps coprotheres</em>) CYP2C19 sequence to other vulture sequences to identify the presence of the intronic PTC. Our search revealed that only <em>Gyps</em> species possessed the CYP2C19 PTC. This is despite NSAID toxicity at similar contaminant levels found in non-<em>Gyps</em> accipitrid mortalities. Our findings suggest avian scavengers could be affected by additional toxicological mechanisms, including sublethal toxicity. Further research is required to establish such mechanisms and exposure risk in non-<em>Gyps</em> scavengers.</div></div>\",\"PeriodicalId\":11775,\"journal\":{\"name\":\"Environmental toxicology and pharmacology\",\"volume\":\"119 \",\"pages\":\"Article 104817\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-09-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Environmental toxicology and pharmacology\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1382668925001929\",\"RegionNum\":3,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENVIRONMENTAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental toxicology and pharmacology","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1382668925001929","RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
Non-steroidal anti-inflammatory drugs (NSAIDs) as a hidden threat to scavenging raptors beyond Gyps: A call for wider research and surveillance
Asian vulture declines have been linked to the consumption of contaminated livestock carcasses with the non-steroidal anti-inflammatory (NSAID) diclofenac. Studies have suggested that the toxicity of NSAIDs to Old World vultures may be through an intronic premature termination codon (PTC) in the gene CYP2C19, encoding a cytochrome P450 enzyme thought responsible for diclofenac metabolism in vultures. However, it remains unclear whether this mechanism applies for all susceptible raptor species. We used nucleotide databases (NCBI) to compare the Cape vulture (Gyps coprotheres) CYP2C19 sequence to other vulture sequences to identify the presence of the intronic PTC. Our search revealed that only Gyps species possessed the CYP2C19 PTC. This is despite NSAID toxicity at similar contaminant levels found in non-Gyps accipitrid mortalities. Our findings suggest avian scavengers could be affected by additional toxicological mechanisms, including sublethal toxicity. Further research is required to establish such mechanisms and exposure risk in non-Gyps scavengers.
期刊介绍:
Environmental Toxicology and Pharmacology publishes the results of studies concerning toxic and pharmacological effects of (human and veterinary) drugs and of environmental contaminants in animals and man.
Areas of special interest are: molecular mechanisms of toxicity, biotransformation and toxicokinetics (including toxicokinetic modelling), molecular, biochemical and physiological mechanisms explaining differences in sensitivity between species and individuals, the characterisation of pathophysiological models and mechanisms involved in the development of effects and the identification of biological markers that can be used to study exposure and effects in man and animals.
In addition to full length papers, short communications, full-length reviews and mini-reviews, Environmental Toxicology and Pharmacology will publish in depth assessments of special problem areas. The latter publications may exceed the length of a full length paper three to fourfold. A basic requirement is that the assessments are made under the auspices of international groups of leading experts in the fields concerned. The information examined may either consist of data that were already published, or of new data that were obtained within the framework of collaborative research programmes. Provision is also made for the acceptance of minireviews on (classes of) compounds, toxicities or mechanisms, debating recent advances in rapidly developing fields that fall within the scope of the journal.