{"title":"作用于钙通道的药物可影响右美托咪定的催眠麻醉效果。","authors":"G Horváth, M Kovács, M Szikszay, G Benedek","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The effects of chronic administration of the calcium channel antagonist verapamil on the anesthetic effects of a novel specific alpha 2-receptor agonist (dexmedetomidine) were studied in rats. It is presumed that this agonist acts on both pre- and postsynaptic alpha 2-adrenoceptors. To determine whether the central postsynaptic receptors are involved in the anesthetic interactions between these drugs, rats were treated with DSP-4 to deplete endogenous norepinephrine. Loss of the righting reflex was used to determine the presence of anesthesia and the duration of hypnosis. Chronic treatment with verapamil (1 or 5 mg/kg) significantly increased the duration of the hypnotic-anesthetic effect of dexmedetomidine. Neither acute treatment with verapamil nor the calcium channel agonist BAY K 8644 (0.5 or 1 mg/kg) influenced the dexmedetomidine-induced hypnosis after DSP-4 treatment. The results seem to support the idea that the hypnotic action of dexmedetomidine can be affected via modulation of the transmembraneous calcium movement in the central nervous system. Further, the data on catecholamine-depleted rats with DSP-4 suggest that the interactions between verapamil and dexmedetomidine may be mediated through presynaptic or homoreceptors on noradrenergic neurons.</p>","PeriodicalId":77479,"journal":{"name":"Acta biochimica et biophysica Hungarica","volume":"26 1-4","pages":"75-81"},"PeriodicalIF":0.0000,"publicationDate":"1991-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Drugs acting at calcium channels can influence the hypnotic-anesthetic effect of dexmedetomidine.\",\"authors\":\"G Horváth, M Kovács, M Szikszay, G Benedek\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The effects of chronic administration of the calcium channel antagonist verapamil on the anesthetic effects of a novel specific alpha 2-receptor agonist (dexmedetomidine) were studied in rats. It is presumed that this agonist acts on both pre- and postsynaptic alpha 2-adrenoceptors. To determine whether the central postsynaptic receptors are involved in the anesthetic interactions between these drugs, rats were treated with DSP-4 to deplete endogenous norepinephrine. Loss of the righting reflex was used to determine the presence of anesthesia and the duration of hypnosis. Chronic treatment with verapamil (1 or 5 mg/kg) significantly increased the duration of the hypnotic-anesthetic effect of dexmedetomidine. Neither acute treatment with verapamil nor the calcium channel agonist BAY K 8644 (0.5 or 1 mg/kg) influenced the dexmedetomidine-induced hypnosis after DSP-4 treatment. The results seem to support the idea that the hypnotic action of dexmedetomidine can be affected via modulation of the transmembraneous calcium movement in the central nervous system. Further, the data on catecholamine-depleted rats with DSP-4 suggest that the interactions between verapamil and dexmedetomidine may be mediated through presynaptic or homoreceptors on noradrenergic neurons.</p>\",\"PeriodicalId\":77479,\"journal\":{\"name\":\"Acta biochimica et biophysica Hungarica\",\"volume\":\"26 1-4\",\"pages\":\"75-81\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1991-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta biochimica et biophysica Hungarica\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta biochimica et biophysica Hungarica","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
研究了钙通道拮抗剂维拉帕米对一种新型特异性α 2受体激动剂右美托咪定麻醉作用的影响。据推测,这种激动剂作用于突触前和突触后的α 2-肾上腺素受体。为了确定中枢突触后受体是否参与这些药物之间的麻醉相互作用,用DSP-4治疗大鼠以消耗内源性去甲肾上腺素。翻正反射的丧失被用来确定麻醉的存在和催眠的持续时间。维拉帕米慢性治疗(1或5 mg/kg)显著增加右美托咪定催眠麻醉作用的持续时间。急性治疗维拉帕米和钙通道激动剂BAY K 8644(0.5或1 mg/kg)对spd -4治疗后右美托咪定诱导的催眠均无影响。这些结果似乎支持右美托咪定的催眠作用可以通过调节中枢神经系统的跨膜钙运动来影响。此外,对具有DSP-4的儿茶酚胺缺失大鼠的数据表明,维拉帕米和右美托咪定之间的相互作用可能通过去甲肾上腺素能神经元上的突触前受体或同受体介导。
Drugs acting at calcium channels can influence the hypnotic-anesthetic effect of dexmedetomidine.
The effects of chronic administration of the calcium channel antagonist verapamil on the anesthetic effects of a novel specific alpha 2-receptor agonist (dexmedetomidine) were studied in rats. It is presumed that this agonist acts on both pre- and postsynaptic alpha 2-adrenoceptors. To determine whether the central postsynaptic receptors are involved in the anesthetic interactions between these drugs, rats were treated with DSP-4 to deplete endogenous norepinephrine. Loss of the righting reflex was used to determine the presence of anesthesia and the duration of hypnosis. Chronic treatment with verapamil (1 or 5 mg/kg) significantly increased the duration of the hypnotic-anesthetic effect of dexmedetomidine. Neither acute treatment with verapamil nor the calcium channel agonist BAY K 8644 (0.5 or 1 mg/kg) influenced the dexmedetomidine-induced hypnosis after DSP-4 treatment. The results seem to support the idea that the hypnotic action of dexmedetomidine can be affected via modulation of the transmembraneous calcium movement in the central nervous system. Further, the data on catecholamine-depleted rats with DSP-4 suggest that the interactions between verapamil and dexmedetomidine may be mediated through presynaptic or homoreceptors on noradrenergic neurons.