Synergistic polytherapy for the broad-spectrum treatment of chemically-induced seizures in rats.

IF 3.3 3区 医学 Q2 PHARMACOLOGY & PHARMACY Toxicology and applied pharmacology Pub Date : 2024-10-28 DOI:10.1016/j.taap.2024.117137
Alex S Cornelissen, Roland M van den Berg, Steven D Klaassen, Jelle C de Koning, Jan P Langenberg, Liesbeth C M de Lange, Marloes J A Joosen
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Abstract

Chemically-induced seizures, as a result of exposure to a neurotoxic compound, present a serious health concern. Compounds can elicit seizure activity through disruption of neuronal signaling by neurotransmitters, either by mimicking, modulating or antagonizing their action at the receptor or interfering with their metabolism. Benzodiazepines, such as diazepam and midazolam, and barbiturates are the mainstay of treatment of seizures. However, chemically-induced seizures are often persistent, requiring repeated treatment and increased doses of anticonvulsants, which in turn may lead to severe adverse effects such as respiratory depression. Here, we investigated the potential of rational polytherapy consisting of the benzodiazepine midazolam and the selective a2-adrenergic agonist dexmedetomidine as an improved, generically applicable anticonvulsant treatment regimen. Therapeutic efficacy was evaluated against two experimental paradigm compounds that induce persistent seizures in rats, the rodenticide TETS and the nerve agent soman. Following exposure, both TETS and soman elicited profound seizure activity and convulsions, associated with substantial mortality. Treatment with midazolam or dexmedetomidine alone provided no or limited suppression of seizure activity and improvement of survival at 4 h. Polytherapy consisting of midazolam and dexmedetomidine showed excellent anticonvulsant efficacy. Even at low doses, polytherapy showed a profound effect that lasted for the duration of the experiment. Analysis of the dose-response relationships confirmed presence of synergy. Administration of polytherapy in non-exposed animals did not indicate aggravation of adverse effects on respiration or heart rate. Even though more research is needed for the translation to clinical use, polytherapy consisting of midazolam and dexmedetomidine shows promise for the broad-spectrum treatment of (chemically-induced) seizures in emergency situations.

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用于广谱治疗化学药物诱发的大鼠癫痫发作的协同多效疗法。
因接触神经毒性化合物而引起的化学性癫痫发作是一个严重的健康问题。化合物可以通过模仿、调节或拮抗神经递质在受体上的作用或干扰神经递质的新陈代谢,破坏神经元的信号传递,从而诱发癫痫发作。苯二氮卓类药物(如地西泮和咪达唑仑)和巴比妥类药物是治疗癫痫发作的主要药物。然而,化学药物诱发的癫痫发作往往是持续性的,需要反复治疗和增加抗惊厥药物的剂量,这反过来又可能导致严重的不良反应,如呼吸抑制。在此,我们研究了由苯二氮卓类药物咪达唑仑和选择性 a2 肾上腺素能激动剂右美托咪定组成的合理多元疗法作为一种改进的、通用的抗惊厥治疗方案的潜力。针对两种诱发大鼠癫痫持续发作的实验范例化合物(杀鼠剂 TETS 和神经毒剂索曼)进行了疗效评估。接触 TETS 和索曼后,都会引起严重的癫痫活动和抽搐,并导致大量死亡。单独使用咪达唑仑或右美托咪定治疗不会或只能有限地抑制癫痫发作活动,并能在 4 小时内改善存活率。由咪达唑仑和右美托咪定组成的复合疗法显示出卓越的抗惊厥疗效。即使是低剂量,联合疗法也能产生深远的效果,并持续整个实验过程。剂量-反应关系分析证实了协同作用的存在。对未接触过多药的动物施用多药治疗后,呼吸或心率方面的不良反应并未加剧。尽管将咪达唑仑和右美托咪定组成的综合疗法应用于临床还需要更多的研究,但这种疗法有望在紧急情况下广泛治疗(化学诱发的)癫痫发作。
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来源期刊
CiteScore
6.80
自引率
2.60%
发文量
309
审稿时长
32 days
期刊介绍: Toxicology and Applied Pharmacology publishes original scientific research of relevance to animals or humans pertaining to the action of chemicals, drugs, or chemically-defined natural products. Regular articles address mechanistic approaches to physiological, pharmacologic, biochemical, cellular, or molecular understanding of toxicologic/pathologic lesions and to methods used to describe these responses. Safety Science articles address outstanding state-of-the-art preclinical and human translational characterization of drug and chemical safety employing cutting-edge science. Highly significant Regulatory Safety Science articles will also be considered in this category. Papers concerned with alternatives to the use of experimental animals are encouraged. Short articles report on high impact studies of broad interest to readers of TAAP that would benefit from rapid publication. These articles should contain no more than a combined total of four figures and tables. Authors should include in their cover letter the justification for consideration of their manuscript as a short article.
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