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犬恶丝虫(Dirofilaria immitis)对经典驱虫药及其他化合物的收缩活性和运动反应。

Contractile activity and motility responses of the dog heartworm Dirofilaria immitis to classical anthelmintics and other compounds.

作者信息

Bowen John M, Vitayavirasak Banjong

机构信息

College of Veterinary Medicine, University of Georgia, Athens, GA 30602-7371, USA.

出版信息

Vet Parasitol. 2005 Nov 25;134(1-2):183-8. doi: 10.1016/j.vetpar.2005.06.020. Epub 2005 Aug 1.

DOI:10.1016/j.vetpar.2005.06.020
PMID:16076531
Abstract

A variety of compounds including classical anthelmintics and avermectin analogs were screened for their effects on movements of adult heartworms (HW) (Dirofilaria immitis). Contractile activity was measured by tension recording of spontaneous movements of intact HW coil preparations (6 min compound exposure) and motility was evaluated by observation of spontaneous, free movements in culture (3 and 7 days compound exposure). Results for female HW indicated that some compounds caused spastic paralysis of contractile activity and inhibition of motility in culture (bephenium, DL-tetramisole, and pyrantel); some caused only spastic paralysis of contractile activity (methyridine and disophenol); and some caused only inhibition of motility in culture (chlorpromazine, dithiazanine, 1-ethoxycarbonylmethyl-1-methylpyrrolidinium, and 4-methyltropolone). Effects on motility in culture appeared to be lethal. The following compounds lacked effects: amprolium, 2-amino-2-thiazoline, bithionol, bitoscanate, bitriben, hexachlorophene, ivermectin, and 10 H-phenothiazine. A group of avermectin analogs was screened for effects only on motility in culture of both adult female and male HW. Several of the analogs affected motility, but the effects appeared to be non-lethal. Microfilaria release into the culture media was suppressed by two of the analogs (an aglycone and avermectin B2). The HW maintenance system used in the present study facilitated screening of compounds for effects on this parasite.

摘要

对包括经典驱虫药和阿维菌素类似物在内的多种化合物进行了筛选,以研究它们对成年犬心丝虫(HW)(犬恶丝虫)活动的影响。通过对完整HW螺旋制剂的自发运动进行张力记录来测量收缩活性(化合物暴露6分钟),并通过观察培养物中的自发自由运动来评估运动能力(化合物暴露3天和7天)。雌性HW的结果表明,一些化合物会导致收缩活性的痉挛性麻痹并抑制培养物中的运动能力(苄酚宁、DL-四咪唑和噻嘧啶);一些化合物仅导致收缩活性的痉挛性麻痹(甲噻嘧啶和双酚);还有一些化合物仅抑制培养物中的运动能力(氯丙嗪、双硫氯酚、1-乙氧羰基甲基-1-甲基吡咯烷鎓和4-甲基托酚酮)。对培养物中运动能力的影响似乎是致命的。以下化合物没有作用:氨丙啉、2-氨基-2-噻唑啉、硫双二氯酚、硝硫氰胺、乙胺嗪、六氯酚、伊维菌素和10H-吩噻嗪。对一组阿维菌素类似物仅筛选了其对成年雌性和雄性HW培养物中运动能力的影响。几种类似物影响了运动能力,但这些影响似乎并非致命。两种类似物(一种苷元阿维菌素和阿维菌素B2)抑制了微丝蚴释放到培养基中。本研究中使用的HW维持系统有助于筛选对该寄生虫有作用的化合物。

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