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艾地苯醌对年轻和老年大鼠体内5-羟色胺释放及5-羟色胺能受体的影响。

Effect of idebenone on in vivo serotonin release and serotonergic receptors in young and aged rats.

作者信息

Scavini C, Rozza A, Lanza E, Favalli L, Racagni G, Brunello N

机构信息

Institute of Pharmacology, University of Pavia, Italy.

出版信息

Eur Neuropsychopharmacol. 1996 May;6(2):95-102. doi: 10.1016/0924-977x(95)00067-y.

Abstract

The effect of idebenone on the serotonergic system was evaluated in the aging rat by measuring the kinetic constants of 3H-5HT and 3H-ketanserin binding sites in the cerebral cortex of rats at 3, 15 and 24 months of age following acute and subchronic administration of the drug. Idebenone displayed no in vitro affinity toward any population of serotonin receptors and did not modify their kinetic parameters after a single dose of 100 mg/kg, at any age tested. A subchronic treatment with the drug for 21 days at the dose of 30 mg/kg did not induce any relevant change in 3- and 15-month-old rats, whereas it significantly increased the density of both 3H-5HT and 3H-ketanserin binding sites in 24-month-old rats, where a lower number of receptors is detected as a consequence of aging. This effect was rather specific, since under the same experimental conditions no changes were detected in the density of cortical beta-adrenergic receptors in aged animals. In microdialysis studies, acute administration with idebenone did not affect 5HT and 5HIAA release at any age. Conversely, the pattern of serotonin metabolism was significantly modified in aged rats following repeated treatment with idebenone and was partially restored to a value similar to the one observed in young animals. These results suggest that idebenone, a putative neuroprotective agent which has been shown to improve brain metabolism in ischemic conditions, might also attenuate age-associated neuronal damage, acting probably on several neurotransmitter systems which undergo selective modification during aging.

摘要

通过测量3、15和24月龄大鼠在急性和亚慢性给予艾地苯醌后大脑皮质中3H-5HT和3H-酮色林结合位点的动力学常数,评估了艾地苯醌对衰老大鼠血清素能系统的影响。在任何测试年龄,单次给予100mg/kg剂量的艾地苯醌后,其对任何血清素受体群体均无体外亲和力,也未改变其动力学参数。以30mg/kg的剂量对大鼠进行21天的亚慢性治疗,在3月龄和15月龄大鼠中未引起任何相关变化,而在24月龄大鼠中,其显著增加了3H-5HT和3H-酮色林结合位点的密度,24月龄大鼠由于衰老而检测到受体数量较少。这种作用相当特异,因为在相同实验条件下,老年动物皮质β-肾上腺素能受体的密度未检测到变化。在微透析研究中,急性给予艾地苯醌在任何年龄均不影响5HT和5HIAA的释放。相反,老年大鼠在反复给予艾地苯醌后,血清素代谢模式发生显著改变,并部分恢复到与年轻动物相似的值。这些结果表明,艾地苯醌是一种公认的神经保护剂,已被证明在缺血条件下可改善脑代谢,它可能还会减轻与年龄相关的神经元损伤,可能作用于衰老过程中发生选择性改变的几种神经递质系统。

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