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作 者:陈钟伦[1] 刘甘泉[1] 姚愈忠[1] 陈培熹[1]
机构地区:[1]中山医科大学生理教研室
出 处:《广东药学院学报》1995年第2期79-81,共3页Academic Journal of Guangdong College of Pharmacy
基 金:美国中华医学基金
摘 要:用Wistar大鼠在氨基甲酸乙酯麻醉下研究微电泳5-羟色胺(5-HT)和5-HT2受体拮抗剂赛庚啶对大脑皮层第一体感区诱发单位放电(SI-EUD)有无明显影响。结果表明5-HT在5-20nA时对SI-EUD无明显影响;40-160nA时,有抑制或易化作用,以抑制作用为主;赛庚啶可拮抗5-HT对SI-EUD的抑制作用。提示5-HT2受体可能参与5-HT对SI-EUD单位的抑制作用。The effects of microiontophoretically applled 5-hydroxyptamine(5-HT)andcyprohetadine on evoked unit discharges of primary somatosensory cortex(SI-EUD) in Wistar ratsanesthetized with urethane were investigated. The results showed that:(1) When 5-20nA of 5- HT was applied,no obvious effect of 5-HT on SI-EUD was found.When 40-16onA of 5-HTwas applied,both inhibitory and faeilitating effects of 5-HT on SI-EUD were observed , the majoteffect being inhibitory.(2)The inhibitory effect of 5-HT on SI-EUD could be bloked by Cypro-heptamine(antagonist of 5-HT2 receptors).It is suggested that 5-HT2 receptors may be inxolvedin medicating the 5-HT inhibitory effect on SI-EUD.
分 类 号:R338.25[医药卫生—人体生理学]
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