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METHODS FOR REDUCING ANESTHETIC-INDUCIBLE EPILEPTOGENIC AND NEUROTOXIC EFFECTS

机译:减少麻醉性致痫和神经毒性作用的方法

摘要

The disclosure encompasses methods of reducing a neural activity in an animal or human subject. The neural activity may be a seizure that may be, but is not necessarily, an inducible side-effect of an anesthetic in an animal or human subject. The methods include administering to an animal or human subject an anesthetic together with a therapeutic agent selected from an inhibitor of the Na+-K+-2Cl- symport ion co-transporter 1 (NKCC1)agent, a mineralcorticoid receptor (MR) antagonist, or an agonist of an oxytocin receptor or a derivative thereof. The therapeutic agent can be be administered before or with an anesthetic, thereby reducing the likelihood of the onset of a non-anesthesizing effect of the anesthetic or the severity thereof. A suitable mineralcorticoid receptor (MR) antagonist can be 17-spironolactone, and the oxytocin receptor agonist can be, but not limited to, oxytocin, carbetocin, and the like. The neural activity reduced by the methods of the disclosure can include the onset or level of a seizure, a neurotoxicity, a behavioral effect, a cognitive effect.
机译:本公开内容包括减少动物或人类受试者中神经活动的方法。神经活动可以是癫痫发作,其可以是但不一定是动物或人类受试者中麻醉剂的可诱导的副作用。该方法包括向动物或人类对象施用麻醉剂以及选自Na + -K + -2Cl -抑制剂的治疗剂。超共离子共转运蛋白1(NKCC1)药剂,盐皮质激素受体(MR)拮抗剂或催产素受体或其衍生物的激动剂。可以在麻醉剂之前或与麻醉剂一起施用治疗剂,从而降低了麻醉剂开始非麻醉作用的可能性或其严重性。合适的盐皮质激素受体(MR)拮抗剂可以是17-螺内酯,催产素受体激动剂可以是但不限于催产素,卡贝托星等。通过本公开的方法减少的神经活动可以包括发作的发作或水平,神经毒性,行为作用,认知作用。

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