Peña-Rangel M T, Mercado R, Hernández-Rodríguez J
Facultad de Ciencias Naturales, U.A.Q., México, DF, México.
Neurochem Res. 1999 May;24(5):643-9. doi: 10.1023/a:1021048308232.
The purpose of the present study was the characterization of the receptors participating in the regulatory mechanism of glial Na+/K+-ATPase by serotonin (5-HT) in rat brain. The activity of the Na+ pump was measured in four brain regions after incubation with various concentrations of serotoninergic agonists or antagonists. A concentration-dependent increase in enzyme activity was observed with the 5-HT1A agonist R (+)-2-dipropylamino-8-hydroxy-1,2,3, 4-tetrahydronaphthalene hydrobromide (8-OH-DPAT) in homogenates or in glial membrane enriched fractions from cerebral cortex and in hippocampus. Spiperone, a 5-HT1A antagonist, completely inhibited the response to 8-OH-DPAT but had no effect on Na+/K+-ATPase activity in cerebellum where LSD, a 5-HT6 agonist, elicited a dose-dependent response similar to that of 5-HT. In brainstem, a lack of response to 5-HT and other agonists was confirmed. Altogether, these results show that serotonin modulates glial Na+/K+-ATPase activity in the brain, apparently not through only one type of 5-HT receptor. It seems that the receptor system involved is different according to the brain region. In cerebral cortex, the response seems to be mediated by 5-HT1A as well as in hippocampus but not in cerebellum where 5-HT6 appears as the receptor system involved.
本研究的目的是表征参与大鼠脑中5-羟色胺(5-HT)对神经胶质Na+/K+-ATP酶调节机制的受体。在与不同浓度的5-羟色胺能激动剂或拮抗剂孵育后,在四个脑区测量Na+泵的活性。在大脑皮层和海马体的匀浆或富含神经胶质膜的组分中,5-HT1A激动剂R(+)-2-二丙基氨基-8-羟基-1,2,3,4-四氢萘氢溴酸盐(8-OH-DPAT)使酶活性呈浓度依赖性增加。5-HT1A拮抗剂螺哌隆完全抑制了对8-OH-DPAT的反应,但对小脑的Na+/K+-ATP酶活性没有影响,而5-HT6激动剂麦角酰二乙胺(LSD)在小脑中引起了与5-HT类似的剂量依赖性反应。在脑干中,证实了对5-HT和其他激动剂无反应。总之,这些结果表明,5-羟色胺调节脑中神经胶质Na+/K+-ATP酶的活性,显然不是仅通过一种类型的5-HT受体。似乎根据脑区不同,所涉及的受体系统也不同。在大脑皮层中,反应似乎由5-HT1A介导,在海马体中也是如此,但在小脑中不是,在小脑中5-HT6似乎是所涉及的受体系统。