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咯利普兰对大鼠脑内[3H]奎宁环基苯甲酸酯和[3H]佛波醇12,13 - 二丁酸酯结合的年龄相关影响。

Age-related effects of rolipram on [3H]quinuclidinyl benzilate and [3H]phorbol 12,13-dibutyrate binding in the rat brain.

作者信息

Chen T, Kato H, Araki T, Itoyama Y, Kogure K

机构信息

Department of Neurology, Tohoku University School of Medicine, Sendai, Japan.

出版信息

Tohoku J Exp Med. 1998 Jun;185(2):107-18. doi: 10.1620/tjem.185.107.

Abstract

Cholinergic neurotransmission and protein kinase C (PKC) in the brain play important roles in the processes of cognitive function. In this study, we examined the effect of chronic treatment with rolipram, a 3',5'-cyclic adenosine monophosphate (cyclic AMP)-selective phosphodiesterase inhibitor, on age-related changes in [3H]quinuclidinyl benzilate (QNB) and [3H]phorbol 12,13-dibutyrate (PDBu) binding, which labeled brain muscarinic cholinergic receptors and PKC, respectively. Rolipram was administered per os to young (15 weeks old) and old (80 weeks old) Wistar rats at dosage of 0.01 mg/kg and 0.1 mg/kg once a day over 4 weeks. Then, quantitative in vitro autoradiography was performed. Control old rats showed elevations in [3H]PDBu binding in the hippocampus and the cerebellum compared to young rats, but [3H]QNB binding was largely unchanged. Chronic treatment of the old rats with the higher dose of rolipram led to reductions in [3H]QNB and [3H]PDBu binding in many brain regions. However, the same treatment of the young rats induced no or minimal effect. Thus, the response of the brain to rolipram was different between young and old rats. These results suggest that the cyclic AMP-selective phosphodiesterase system in the brain is modified during aging, modulating subsequently cholinergic neurotransmission and PKC activity exclusively in old rat brains.

摘要

大脑中的胆碱能神经传递和蛋白激酶C(PKC)在认知功能过程中发挥着重要作用。在本研究中,我们检测了用咯利普兰(一种3',5'-环磷酸腺苷(环磷腺苷)选择性磷酸二酯酶抑制剂)进行长期治疗对[3H]喹核醇基苯甲酸酯(QNB)和[3H]佛波醇12,13-二丁酸酯(PDBu)结合的年龄相关变化的影响,这两种物质分别标记了脑毒蕈碱胆碱能受体和PKC。将咯利普兰以0.01 mg/kg和0.1 mg/kg的剂量经口给予年轻(15周龄)和老年(80周龄)的Wistar大鼠,每天一次,持续4周。然后,进行体外定量放射自显影。与年轻大鼠相比,对照老年大鼠海马和小脑中的[3H]PDBu结合增加,但[3H]QNB结合基本未变。用高剂量咯利普兰对老年大鼠进行长期治疗导致许多脑区中[3H]QNB和[3H]PDBu结合减少。然而,对年轻大鼠进行相同治疗未产生或仅产生最小影响。因此,年轻和老年大鼠大脑对咯利普兰的反应不同。这些结果表明,大脑中的环磷腺苷选择性磷酸二酯酶系统在衰老过程中发生改变,随后仅在老年大鼠大脑中调节胆碱能神经传递和PKC活性。

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