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依美加群靶向盘尾丝虫 SLO-1 通道,并在盘尾丝虫病牛模型中产生广泛的驱虫效果。

Emodepside targets SLO-1 channels of Onchocerca ochengi and induces broad anthelmintic effects in a bovine model of onchocerciasis.

机构信息

Institut de Recherche Agricole pour le Développement, Centre Régional de Wakwa, Ngaoundéré, Cameroun.

Bayer AG, Engineering & Technology, Applied Mathematics, Leverkusen, Germany.

出版信息

PLoS Pathog. 2021 Jun 2;17(6):e1009601. doi: 10.1371/journal.ppat.1009601. eCollection 2021 Jun.

DOI:10.1371/journal.ppat.1009601
PMID:34077488
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8202924/
Abstract

Onchocerciasis (river blindness), caused by the filarial worm Onchocerca volvulus, is a neglected tropical disease mostly affecting sub-Saharan Africa and is responsible for >1.3 million years lived with disability. Current control relies almost entirely on ivermectin, which suppresses symptoms caused by the first-stage larvae (microfilariae) but does not kill the long-lived adults. Here, we evaluated emodepside, a semi-synthetic cyclooctadepsipeptide registered for deworming applications in companion animals, for activity against adult filariae (i.e., as a macrofilaricide). We demonstrate the equivalence of emodepside activity on SLO-1 potassium channels in Onchocerca volvulus and Onchocerca ochengi, its sister species from cattle. Evaluation of emodepside in cattle as single or 7-day treatments at two doses (0.15 and 0.75 mg/kg) revealed rapid activity against microfilariae, prolonged suppression of female worm fecundity, and macrofilaricidal effects by 18 months post treatment. The drug was well tolerated, causing only transiently increased blood glucose. Female adult worms were mostly paralyzed; however, some retained metabolic activity even in the multiple high-dose group. These data support ongoing clinical development of emodepside to treat river blindness.

摘要

盘尾丝虫病(河盲症)由盘尾丝虫引起,是一种被忽视的热带病,主要影响撒哈拉以南非洲地区,导致超过 130 万人丧失生活能力。目前的控制措施几乎完全依赖伊维菌素,它可以抑制由第一阶段幼虫(微丝蚴)引起的症状,但不能杀死寿命长的成虫。在这里,我们评估了埃莫德昔佩,一种用于伴侣动物驱虫应用的半合成环八肽,以评估其对成年丝虫(即作为大环内酯类药物)的活性。我们证明了埃莫德昔佩在盘尾丝虫和其来自牛的姐妹种奥氏奥克森古虫的 SLO-1 钾通道中的活性相当。在牛中评估单次或 7 天治疗两种剂量(0.15 和 0.75mg/kg)的埃莫德昔佩,发现其对微丝蚴具有快速活性,延长了雌性虫的生殖力抑制,并在治疗后 18 个月产生了杀大环内酯类药物的效果。该药物耐受性良好,仅导致血糖短暂升高。雌性成虫大多瘫痪;然而,即使在高剂量多剂量组中,一些成虫仍保持代谢活性。这些数据支持埃莫德昔佩继续进行治疗河盲症的临床开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4325/8202924/4d836501b28f/ppat.1009601.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4325/8202924/78fb6b2c9b50/ppat.1009601.g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4325/8202924/132c6b0a7ba4/ppat.1009601.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4325/8202924/2f21a7981824/ppat.1009601.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4325/8202924/d72de2e5fdf9/ppat.1009601.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4325/8202924/a56e46cf6729/ppat.1009601.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4325/8202924/dd506bfadc43/ppat.1009601.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4325/8202924/4d836501b28f/ppat.1009601.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4325/8202924/78fb6b2c9b50/ppat.1009601.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4325/8202924/de1b3def8664/ppat.1009601.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4325/8202924/132c6b0a7ba4/ppat.1009601.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4325/8202924/2f21a7981824/ppat.1009601.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4325/8202924/d72de2e5fdf9/ppat.1009601.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4325/8202924/a56e46cf6729/ppat.1009601.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4325/8202924/dd506bfadc43/ppat.1009601.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4325/8202924/4d836501b28f/ppat.1009601.g008.jpg

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