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通过促进GABA能传递来作用于由GABA能机制介导的惊厥的药物的抗惊厥特性。

Anticonvulsant profile of drugs which facilitate GABAergic transmission on convulsions mediated by a GABAergic mechanism.

作者信息

Rastogi S K, Ticku M K

出版信息

Neuropharmacology. 1986 Feb;25(2):175-85. doi: 10.1016/0028-3908(86)90039-0.

Abstract

The effects of selected modulators of GABAergic transmission, either alone or in combination, were tested for their potency on the seizure pattern and mortality induced by convulsant drugs in rat. Pentobarbital and diazepam were effective against both tonic and clonic seizure components induced by bicuculline and picrotoxin. The anticonvulsant profile of ethanol closely resembled that of pentobarbital. Pentobarbital, diazepam and ethanol did not modify seizures induced by strychnine. In contrast, progabide, a central gamma-aminobutyric acid (GABA) receptor agonist, caused significant protection only against convulsions induced by strychnine and its lethality, but did not protect against seizures induced by bicuculline or picrotoxin. Data on interaction of drugs with subprotective doses of these agents clearly demonstrated potentiation of the anticonvulsant actions of these modulators. Thus, seizures induced by bicuculline were more sensitive to the inhibition by pentobarbital in combination with diazepam or ethanol, while pentobarbital with progabide was equally effective against convulsions induced by GABA antagonists. Diazepam, in combination with progabide, blocked only convulsions induced by picrotoxin. Ethanol, in combination with either pentobarbital or with diazepam, was effective against all the three convulsant drugs. These results are consistent with the concept that drugs which facilitate GABAergic transmission are effective against seizures related to an impairment of GABA transmission. Further, the present data indicate that tonic seizures are more susceptible to the actions of drugs than the clonic component. Smaller doses of these drugs, alone or in combination, modified the seizure patterns and mortality, whereas at larger doses, the possible involvement of a nonspecific depressant action cannot be ruled out.

摘要

对选定的γ-氨基丁酸(GABA)能传递调节剂单独或联合使用时,测试其对大鼠惊厥药物诱发的癫痫发作模式和死亡率的影响。戊巴比妥和地西泮对荷包牡丹碱和印防己毒素诱发的强直和阵挛性癫痫发作成分均有效。乙醇的抗惊厥谱与戊巴比妥相似。戊巴比妥、地西泮和乙醇不能改变士的宁诱发的癫痫发作。相比之下,中枢γ-氨基丁酸(GABA)受体激动剂普罗加比仅对士的宁诱发的惊厥及其致死性有显著保护作用,但对荷包牡丹碱或印防己毒素诱发的癫痫发作无保护作用。药物与这些药物亚保护剂量相互作用的数据清楚地表明这些调节剂的抗惊厥作用得到了增强。因此,荷包牡丹碱诱发的癫痫发作对戊巴比妥与地西泮或乙醇联合使用的抑制作用更敏感,而戊巴比妥与普罗加比联合使用对GABA拮抗剂诱发的惊厥同样有效。地西泮与普罗加比联合使用仅能阻断印防己毒素诱发的惊厥。乙醇与戊巴比妥或地西泮联合使用对所有三种惊厥药物均有效。这些结果与促进GABA能传递的药物对与GABA传递受损相关的癫痫发作有效的概念一致。此外,目前的数据表明强直发作比阵挛成分更容易受到药物作用的影响。这些药物单独或联合使用较小剂量时可改变癫痫发作模式和死亡率,而在较大剂量时,不能排除非特异性抑制作用的可能参与。

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