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一种新型抗精神病喹啉酮衍生物(OPC-14597)对伏隔核神经元活动多巴胺能抑制的拮抗作用。

Antagonizing effects of a novel antipsychotic quinolinone derivative (OPC-14597) on dopaminergic inhibition of neuronal activities in the nucleus accumbens.

作者信息

Amano T, Matsubayashi H, Momiyama T, Ishihara K, Todo N, Sasa M

机构信息

Department of Pharmacology, Hiroshima University School of Medicine, Japan.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 1995 Jan;19(1):105-16. doi: 10.1016/0278-5846(94)00114-w.

Abstract
  1. The effects of a newly synthesized quinolinone derivative, 7-(4-[4-(2,3-dichlorophenlyl)-1-piperazinyl]butyloxy)-3,4-di hydro-2-(1H)- quinolinone (OPC-14597), an antipsychotic drug, on neuronal activities of the nucleus accumbens (Acc) were investigated in rats anesthetized with chloral hydrate using a microiontophoretic method. 2. Spikes elicited by stimulation of the parafascicular nucleus (Pf) of the thalamus were extracellularly recorded in the Acc neuron of chloral hydrate-anesthetized adult Wistar rats using a glass microelectrode attached along a seven-barreled micropipette, each of which was filled with dopamine, OPC-14597, SKF 38393 (D1 receptor agonist), quinpirole (D2 receptor agonist) and 2M NaCl. The drugs were microiontophoretically applied to the target neurons recorded. 3. Effects of the drugs on the Acc neurons activated monosynaptically by stimulation of the Pf were examined. Spikes elicited by Pf stimulation were inhibited by iontophoretic application of dopamine, SKF 38393 and quinpirole in a dose-dependent manner. 4. Microiontophoretic application of OPC-14597 alone affected the spikes elicited by the Pf stimulation in none of 26 neurons tested. However, the dopamine-, SKF 38393- and quinpirole-induced inhibition of the spike generation in the Acc neurons was antagonized during simultaneous application of OPC-14597. 5. The firing induced by iontophoretically applied glutamate was inhibited by dopamine, SKF 38393 and quinpirole, but not by OPC-14597. However, the dopamine-, SKF 38393- and quinpirole-induced inhibition of the glutamate-induced firing was also antagonized during simultaneous application of OPC-14597 in a dose-dependent manner in all neurons tested. 6. These findings suggest that OPC-14597 blocks dopaminergic inhibition of the Acc neurons receiving input from the Pf by acting on both D1 and D2 receptors located on the neurons.
摘要
  1. 采用微离子电泳法,研究了一种新合成的喹啉酮衍生物7-(4-[4-(2,3-二氯苯基)-1-哌嗪基]丁氧基)-3,4-二氢-2-(1H)-喹啉酮(OPC-14597),一种抗精神病药物,对水合氯醛麻醉大鼠伏隔核(Acc)神经元活动的影响。2. 使用沿着七管微吸管连接的玻璃微电极,在水合氯醛麻醉的成年Wistar大鼠的Acc神经元中细胞外记录丘脑束旁核(Pf)刺激引发的尖峰,每个微吸管中分别填充多巴胺、OPC-14597、SKF 38393(D1受体激动剂)、喹吡罗(D2受体激动剂)和2M NaCl。将这些药物通过微离子电泳法施加到记录的目标神经元上。3. 研究了药物对由Pf刺激单突触激活的Acc神经元的影响。Pf刺激引发的尖峰被多巴胺、SKF 38393和喹吡罗的离子电泳施加以剂量依赖的方式抑制。4. 单独微离子电泳施加OPC-14597对26个测试神经元中Pf刺激引发的尖峰均无影响。然而,在同时施加OPC-14597期间,多巴胺、SKF 38393和喹吡罗对Acc神经元中尖峰产生的抑制作用被拮抗。5. 离子电泳施加谷氨酸诱导的放电被多巴胺、SKF 38393和喹吡罗抑制,但不被OPC-14597抑制。然而,在所有测试神经元中,同时施加OPC-14597期间,多巴胺、SKF 38393和喹吡罗对谷氨酸诱导放电的抑制作用也以剂量依赖的方式被拮抗。6. 这些发现表明,OPC-14597通过作用于神经元上的D1和D2受体,阻断了接受来自Pf输入的Acc神经元的多巴胺能抑制。

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