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噻奈普汀对中枢胆碱能系统的作用:5-羟色胺的参与

Effect of tianeptine on the central cholinergic system: involvement of serotonin.

作者信息

Bertorelli R, Amoroso D, Girotti P, Consolo S

机构信息

Istituto di Ricerche Farmacologiche Mario Negri, Milan, Italy.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1992 Mar;345(3):276-81. doi: 10.1007/BF00168687.

Abstract

The effect of tianeptine on in vivo acetylcholine (ACh) release from brain hemispheric regions of freely moving rats was investigated using the microdialysis technique coupled with a sensitive radioenzymatic method. Tianeptine, at the dose of 30 mg/kg i.p., reduced ACh release from dorsal hippocampi by 40% in 40 min, and induced a 30% decrease of ACh output from frontal cortices while at the doses of 10 and 20 mg/kg it had no effect. In striata the drug did not significantly affect ACh release although it showed a tendency to increase it. The ACh content in the three areas considered was not affected by tianeptine at above doses. The drug did not alter choline-o-acetyltransferase and acetylcholinesterase activities suggesting that it did not influence the cholinergic system through direct action on the ACh metabolism; furthermore, it did not influence the sodium-dependent high-affinity uptake of choline in striatum, cortex and hippocampus. Impairment of serotonergic (5-HT) neurotransmission by chemical lesion of the median raphe nucleus or by metergoline, a blocker of 5-HT receptors, antagonized the cholinergic effect of tianeptine. The involvement of the serotonergic system is specific because lesions of the noradrenergic dorsal bundle failed to prevent the inhibitory action of tianeptine. The present data suggest that 5-HT may mediate the effect of tianeptine on the cholinergic system in dorsal hippocampi.

摘要

采用微透析技术结合灵敏的放射酶法,研究了噻奈普汀对自由活动大鼠脑半球区域体内乙酰胆碱(ACh)释放的影响。腹腔注射30mg/kg剂量的噻奈普汀,40分钟内可使背侧海马体的ACh释放减少40%,使额叶皮质的ACh输出减少30%,而10mg/kg和20mg/kg剂量则无此作用。在纹状体中,该药物虽有增加ACh释放的趋势,但未对其释放产生显著影响。上述剂量的噻奈普汀未影响所研究的三个区域的ACh含量。该药物未改变胆碱乙酰转移酶和乙酰胆碱酯酶的活性,表明其并非通过直接作用于ACh代谢来影响胆碱能系统;此外,它也未影响纹状体、皮质和海马体中钠依赖性高亲和力胆碱摄取。通过中缝背核化学损伤或5-HT受体阻断剂美替拉酮损害5-羟色胺能(5-HT)神经传递,可拮抗噻奈普汀的胆碱能作用。5-羟色胺能系统的参与具有特异性,因为去甲肾上腺素能背束损伤未能阻止噻奈普汀的抑制作用。目前的数据表明,5-HT可能介导了噻奈普汀对背侧海马体胆碱能系统的作用。

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