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耳部给药载体及地塞米松浓度对小型健康犬肝脏酶活性和肾上腺功能的影响。

The effect of otic vehicle and concentration of dexamethasone on liver enzyme activities and adrenal function in small breed healthy dogs.

作者信息

Aniya Jennifer S, Griffin Craig E

机构信息

Animal Allergy Specialists, San Diego, CA 92111, USA.

出版信息

Vet Dermatol. 2008 Aug;19(4):226-31. doi: 10.1111/j.1365-3164.2008.00680.x.

Abstract

Dexamethasone 0.1% in propylene glycol vehicle has been shown to cause adrenal suppression and increased liver enzyme concentrations in normal dogs. The objectives of this study were to determine if these effects are concentration or vehicle dependent and to evaluate a dexamethasone 0.01% solution. Twenty-one privately owned normal dogs were included in this double-blinded study. Chemistry panels and adrenocorticotropin hormone (ACTH) stimulation tests were performed on day 0 and 15. Dogs were randomly assigned treatment with dexamethasone 0.01% in saline, 0.1% in saline, or 0.1% in a commercial preparation (Tresaderm: Merial, Duluth, GA, USA) in each ear twice daily for 2 weeks. Nineteen dogs completed the study. After 2 weeks of treatment, all dogs receiving dexamethasone 0.01% in saline had normal ACTH stimulation tests and liver enzyme values. In contrast, four of seven dogs (57.14%) receiving dexamethasone 0.1% in saline experienced adrenal suppression, and four of six dogs (66.67%) receiving Tresaderm experienced adrenal suppression with three of those dogs (50%) experiencing marked adrenal suppression. No dogs receiving dexamethasone 0.1% in saline had increased liver enzyme concentration, while one of six dogs (16.67%) experienced a slight elevation in alkaline phosphatase. In conclusion, it appears that adrenal suppression caused by otic dexamethasone is concentration and perhaps vehicle dependent. Veterinarians who formulate dexamethasone 0.1% otic solutions should be cognizant of potential adrenal suppression similar to that seen with Tresaderm although not to the same degree. Dexamethasone at 0.01% did not cause adrenal suppression or liver enzyme alterations after 2 weeks of treatment.

摘要

已证实,丙二醇载体中的0.1%地塞米松会导致正常犬出现肾上腺抑制和肝酶浓度升高。本研究的目的是确定这些影响是否取决于浓度或载体,并评估0.01%地塞米松溶液。本双盲研究纳入了21只私人饲养的正常犬。在第0天和第15天进行了血液生化检查和促肾上腺皮质激素(ACTH)刺激试验。犬被随机分配接受以下治疗:每天两次,在每只耳朵中滴注0.01%地塞米松盐水溶液、0.1%地塞米松盐水溶液或0.1%市售制剂(Tresaderm:美国默克动物保健公司,佐治亚州德卢斯),持续2周。19只犬完成了研究。治疗2周后,所有接受0.01%地塞米松盐水溶液的犬ACTH刺激试验和肝酶值均正常。相比之下,7只接受0.1%地塞米松盐水溶液的犬中有4只(57.14%)出现肾上腺抑制,6只接受Tresaderm的犬中有4只(66.67%)出现肾上腺抑制,其中3只(50%)出现明显肾上腺抑制。接受0.1%地塞米松盐水溶液的犬中没有肝酶浓度升高的情况,而6只犬中有1只(16.67%)碱性磷酸酶略有升高。总之,耳部使用地塞米松引起的肾上腺抑制似乎取决于浓度,也可能取决于载体。配制0.1%耳部地塞米松溶液的兽医应认识到可能存在类似于Tresaderm所见的潜在肾上腺抑制,尽管程度不同。0.01%地塞米松治疗2周后未引起肾上腺抑制或肝酶改变。

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