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治疗浓度的丙戊酸钠可改变钙离子反应,并伴有其对人星形细胞瘤细胞中蛋白激酶C的微弱抑制作用。

Sodium valproate at therapeutic concentrations changes Ca2+ response accompanied with its weak inhibition of protein kinase C in human astrocytoma cells.

作者信息

Kurita Masatake, Nishino Satoshi, Ohtomo Kouji, Rai Mayumi, Shirakawa Hisayoshi, Mashiko Hirobumi, Niwa Shin-Ichi, Nakahata Norimichi

机构信息

Department of Neuropsychiatry, School of Medicine, Fukushima Medical University, 1 Hikarigaoka, Fukushima 960-1295, Japan.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 2007 Apr 13;31(3):600-4. doi: 10.1016/j.pnpbp.2006.11.019. Epub 2007 Jan 25.

Abstract

Sodium valproate (VPA) has been used clinically for treatment of not only epilepsy but also mood disorder. Although VPA is effective for treatment of epilepsy via inhibition of gamma-aminobutyric acid transaminase, it remains unknown why VPA is effective for the treatment of mood disorder. The authors examined the effect of VPA at therapeutic concentrations (300 and 600 microM) on the elevation of intracellular free calcium concentration (Ca(2+)) induced by carbachol, a muscarinic receptor agonist, in 1321N1 human astrocytoma cells. Treatment of the cells with 300 and 600 microM VPA for 2 min did not change the carbachol-induced Ca(2+) elevation. Treatment with 300 and 600 microM VPA for 48 h, however, reduced the elevation. Since we have shown that Li(+) reduced carbachol-induced Ca(2+) elevation in protein kinase C (PKC)-downregulated 1321N1 cells [Kurita, M., Mashiko, H., Rai, M., Kumasaka, T., Kouno, S., Niwa, S., Nakahata, N., 2002. Lithium chloride at a therapeutic concentration reduces Ca(2+)response in protein kinase C down-regulated human astrocytoma cells, Eur. J. Pharmacol. 442, 17-22.], the activity of PKC was examined. Treatment with VPA at the same concentrations for 24 or 48 h weakly reduced protein kinase C activity in membrane and cytosol fractions from the cells. On the other hand, the treatment of the cells with 600 microM VPA for 24 or 48 h slightly increased the B(max) value, but not the K(d) value, in the binding of [(3)H]quinuclidinyl benzylate, a muscarinic receptor ligand, to the membranes, suggesting that the number or affinity of muscarinic receptor did not decrease after VPA treatment. These results indicate that VPA at therapeutic concentrations slightly decreases the PKC activity and inhibits muscarinic receptor-mediated Ca(2+) elevation probably through change in the intracellular signaling pathway. VPA-induced reduction of PKC activity and Ca(2+) elevation may play a role in the treatment of mood disorder.

摘要

丙戊酸钠(VPA)在临床上不仅用于治疗癫痫,还用于治疗情绪障碍。尽管VPA通过抑制γ-氨基丁酸转氨酶对癫痫治疗有效,但其对情绪障碍治疗有效的原因仍不清楚。作者研究了治疗浓度(300和600微摩尔)的VPA对毒蕈碱受体激动剂卡巴胆碱诱导的1321N1人星形细胞瘤细胞内游离钙浓度([Ca(2+)]i)升高的影响。用300和600微摩尔VPA处理细胞2分钟,并未改变卡巴胆碱诱导的[Ca(2+)]i升高。然而,用300和600微摩尔VPA处理48小时,则降低了这种升高。由于我们已经表明Li(+)降低了蛋白激酶C(PKC)下调的1321N1细胞中卡巴胆碱诱导的[Ca(2+)]i升高[栗田,M.,益子,H., Rai,M.,熊坂,T.,河野,S.,丹羽,S.,中畑,N.,2002。治疗浓度的氯化锂降低蛋白激酶C下调的人星形细胞瘤细胞中的Ca(2+)反应,欧洲药理学杂志。442,17 - 22。],因此检测了PKC的活性。用相同浓度的VPA处理24或48小时,可轻微降低细胞中膜和胞质溶胶部分的蛋白激酶C活性。另一方面,用600微摩尔VPA处理细胞24或48小时,可使毒蕈碱受体配体[(3)H]喹核醇基苄酯与膜的结合中的B(max)值略有增加,但K(d)值未增加,这表明VPA处理后毒蕈碱受体的数量或亲和力并未降低。这些结果表明,治疗浓度的VPA可轻微降低PKC活性,并可能通过改变细胞内信号通路抑制毒蕈碱受体介导的[Ca(2+)]i升高。VPA诱导的PKC活性降低和[Ca(2+)]i升高可能在情绪障碍的治疗中起作用。

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