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Spider toxins and methods for their use as blockers of calcium channels and amino acid receptor function

机译:蜘蛛毒素及其用作钙通道和氨基酸受体功能阻滞剂的方法

摘要

Methods and compositions for blocking various channels and receptors within an organism are provided. For example, two toxins were isolated from the Agelenopsis aperta spider. The first toxin comprised a toxin having a molecular weight of from approximately 5,000 to approximately 10, 000. This toxin was found to have an irreversible effect on calcium channels within the central nervous system. A second toxin having a molecular weight of less than about 1,000 was also isolated. This toxin was found to have a reversible blocking effect on calcium channels within the central nervous system and the cardiovascular system.P PA third toxin was isolated from the Argiope aurantia spider. This toxin was found to have a reversible effect on excitatory amino acid receptors. Finally, a toxin having a molecular weight of from approximately 5,000 to approximately 7,000 daltons was isolated from the Hololena Curta spider. This toxin was found to have an irreversible effect on excitatory amino acid receptors.PP The present invention further relates to methods of treating heart and neurological diseases by applying the toxins isolated and identified. In particular, the low molecular weight toxin from Agelenopsis aperta may provide a treatment of certain heart conditions such as arrhythmia, angina, Hypertension, and congestive heart failure. In addition, the toxins may provide beneficial effects on certain neurological conditions including seizures. It is also found that the toxins having an irreversible effect are effective as tags in probing the various components within the calcium channels and excitatory amino acid receptors and are effective insecticides and anthelmintics.
机译:提供了用于阻断生物体内各种通道和受体的方法和组合物。例如,从Aperlenopsis aperta蜘蛛中分离出两种毒素。第一毒素包括分子量为约5,000至约10,000的毒素。发现该毒素对中枢神经系统内的钙通道具有不可逆的作用。还分离出分子量小于约1,000的第二毒素。已发现该毒素对中枢神经系统和心血管系统内的钙通道具有可逆的阻断作用。第三点毒素是从Argiope aurantia蜘蛛中分离出来的。发现该毒素对兴奋性氨基酸受体具有可逆作用。最后,从Holelena Curta蜘蛛中分离出分子量为约5,000至约7,000道尔顿的毒素。发现该毒素对兴奋性氨基酸受体具有不可逆的作用。本发明还涉及通过应用分离和鉴定的毒素来治疗心脏和神经系统疾病的方法。特别地,来自老龄菌的低分子量毒素可以提供对某些心脏疾病例如心律不齐,心绞痛,高血压和充血性心力衰竭的治疗。此外,毒素可能对某些神经系统疾病(包括癫痫发作)产生有益作用。还发现具有不可逆作用的毒素作为探测钙通道和兴奋性氨基酸受体内各种组分的标签是有效的,并且是有效的杀虫剂和驱虫药。

著录项

  • 公开/公告号US4925664A

    专利类型

  • 公开/公告日1990-05-15

    原文格式PDF

  • 申请/专利权人 UNIVERSITY OF UTAH;

    申请/专利号US19860921218

  • 发明设计人 THOMAS N. PARKS;J. R. HUNTER JACKSON;

    申请日1986-10-20

  • 分类号A61K35/58;

  • 国家 US

  • 入库时间 2022-08-22 06:07:31

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