praziquantel

✍ dations ◷ 2025-11-13 03:11:17 #praziquantel
吡喹酮(英语:Praziquantel,或英语:Biltricide)为一种用于人类及动物的驱虫药,专门治疗绦虫及吸虫。对于血吸虫、中华肝吸虫、广节裂头绦虫(英语:Diphyllobothrium latum)特别有效,吡喹酮为世界卫生组织基本药物标准清单上的药物,为世界上对于基本公共卫生最重要的药物之一。1970年代由拜耳公司的药学部研发成功。吡喹酮可以用于治疗人类、哺乳类,以及鱼类的寄生虫病。包含肠胃道或是外部的感染,以下为其适用疾病:The majority of side effects develop due to the release of the contents of the parasites as they are killed and the consequent host immune reaction. The heavier the parasite burden, the heavier and more frequent the side effects normally are.The antibiotic rifampicin decreases plasma concentrations of praziquantel.Carbamazepine and phenytoin are reported to reduce the bioavailability of praziquantel.Chloroquine reduces the bioavailability of praziquantel.The drug cimetidine heightens praziquantel bioavailability.The mode of action is not exactly known at present, but experimental evidence indicates praziquantel increases the permeability of the membranes of schistosome cells towards calcium ions. The drug thereby induces contraction of the parasites, resulting in paralysis in the contracted state. The dying parasites are dislodged from their site of action in the host organism and may enter systemic circulation or may be destroyed by host immune reaction (phagocytosis). Additional mechanisms including focal disintegrations and disturbances of oviposition (laying of eggs) are seen in other types of sensitive parasites.Another hypothesis concerning the mechanism of action of praziquantel has been recently reported. The drug seems to interfere with adenosine uptake in cultured worms. This effect may have therapeutical relevance given that the schistosome, as the Taenia(英语:Taenia (genus)) and the Echinococcus(英语:Echinococcus) (other praziquantel-sensitive parasites), is unable to synthesize purines such as adenosine de novo.Bayer's Animal Health Division website states, "Praziquantel is active against cestodes (tapeworms). Praziquantel is absorbed, metabolized in the liver, and excreted in the bile. Upon entering the digestive tract from the bile, cestocidal activity is exhibited. Following exposure to praziquantel, the tapeworm loses its ability to resist digestion by the mammalian host. Because of this, whole tapeworms, including the scolices (plural of "scolex"), are very rarely passed after administration of praziquantel. In many instances, only disintegrated and partially digested pieces of tapeworms will be seen in the stool. The majority of tapeworms are digested and are not found in the feces."Praziquantel is administered as a racemate, but only the (R)-enantiomer is biologically active; the enantiomers may be separated using a resolution of an amine obtained from praziquantel.Praziquantel is well absorbed (about 80%) from the gastrointestinal tract. However, due to extensive first-pass metabolism, only a relatively small amount enters systemic circulation. Praziquantel has a serum half-life of 0.8 to 1.5 hours in adults with normal renal and liver function. Metabolites have a half-life of 4 to 5 hours. In patients with significantly impaired liver function (Child Pugh classes B ll///d C), the serum half-life is increased to 3 to 8 hours. Praziquantel and its metabolites are mainly excreted renally; within 24 hours after a single oral dose, 70 to 80% is found in urine, but less than 0.1% as the unchanged drug. Praziquantel is metabolized through the cytochrome P450 pathway via CYP3A4. Agents that induce or inhibit(英语:Enzyme induction and inhibition) CYP3A4 such as phenytoin, rifampin, and azole antifungals will affect the metabolism of praziquantel.Praziquantel has a particularly dramatic effect on patients with schistosomiasis. Studies of those treated have shown that within six months of receiving a dose of praziquantel, up to 90% of the damage done to internal organs due to schistosomiasis infection can be reversed.Praziquantel was developed in the laboratories for parasitological research of Bayer AG and Merck KGaA in Germany (Elberfeld and Darmstadt) in the mid 1970s.吡喹酮名列世界卫生组织基本药物标准清单之中, 是世界上对于基本公共卫生最重要的药物之一。在英国,吡喹酮并未获准在人体上使用。但在必要时可以根据在患者实名的情况下进口。在英国吡喹酮可以作为兽用驱虫药销售。在美国,吡喹酮被FDA批准用于血吸虫病及肝吸虫病的治疗,尽管它对其他种类的感染也有效。Template:Anthelmintics

相关

  • 细菌接合接合(英文:Conjugation,又译结合),又称为接合作用、细菌接合,是发生于原生动物间的现象,指的是两个细菌之间发生的一种遗传物质交换现象,属于细菌有性生殖的一个重要阶段。在接合现
  • 吸入器吸入器或吸入剂(英语:inhaler)是一种医疗设备,可协助让药品通过肺部吸收入体内,主要用来治疗哮喘和慢性阻塞性肺病。比如,用于治疗流感的扎那米韦(英语:Zanamivir)就必须通过吸入器来
  • TNF-α1A8M, 1TNF, 2AZ5, 2E7A, 2TUN, 2ZJC, 2ZPX, 3ALQ, 3IT8, 3L9J, 4TSV, 5TSW· cytokine activity · tumor necrosis factor receptor binding · protein binding · id
  • 量子生物学量子生物学是利用量子理论来研究生命科学的一门学科。该学科包含利用量子力学研究生物过程和分子动态结构。利用量子生物学研究量子水平的分子动态结构和能量转移,如果所得结
  • 腹膜炎腹膜炎,是指一种发生于腹膜的炎症反应。该反应主要由细菌感染、化学物质、物理性伤害等因素引起,且很可能因没有及时治疗而危及生命。其症状可能包含剧烈疼痛、腹部肿胀、发烧
  • 凝血血液凝固,或称为凝血指的是血液由液体状态转变为不流动的凝胶状态的过程,是生理性止血的重要环节。血液凝固的实质就是血浆中的可溶性纤维蛋白原变成不可溶的纤维蛋白的过程。
  • 自然自然(英文:Nature),是指不断运行演化的宇宙万物,包括生物界和非生物界两个相辅相成的体系。人类所能理解地自然现象有:生物界的基因模因、共识主动、意识行为、社会活动和生态系统
  • 血容量减少血容量减少,亦称血容量过低、休克,指的是体内血量减少的状况。 它表现在体内血液体积收缩和脱盐上。常见的血容量减少的原因有:
  • SUDOC大学文档系统(Système Universitaire de Documentation,简称SUDOC)是法国高等教育机构图书馆所使用的图书系统。该系统收录了法国大专院校、研究型图书馆及资源中心的联合目录
  • 马(学名:Equus ferus caballus),广泛分布于世界各地,原产于中亚草原,6000多年前就被人类驯养,最早的马匹驯养遗址于乌克兰草原发现,15世纪后,才被欧洲殖民者带到美洲和澳洲地区。马耳