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Inhibition by Nitric Oxide of the Uptake of [3H] Serotonin into Rat Brain Synaptosomes

机译:一氧化氮对大鼠脑突触小体中[3H]血清素摄取的抑制作用

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References(28) Cited-By(13) [3H]Serotonin (5-HT) uptake by synaptosomes of rat brain was dose-dependently inhibited by nitric oxide (NO) donors such as sodium nitroprusside (SNP), 3-(2-hydroxy-1-methyl-2-nitrosohydrazino)-N-methyl-1-propanamine, 3-morpholinosydnonimine and S-nitroso-L-cysteine (NO-CYS). The inhibitory effect was blocked by reduced hemoglobin. The effect was not mimicked by ferrocyanide and ferricyanide. 8-Bromoguanosine 3'', 5''-cyclic monophosphate (8-bromo cGMP) did not affect [3H]5-HT uptake into rat cortical synaptosomes. The reduced activity of [3H]5-HT uptake into the cortical synaptosomes pretreated with NO-CYS was partially reversed by washing the preparation after the treatment. Kinetic analysis showed that NO-CYS (100 μM) decreased the Vmax value without any change in the Km value. NO-CYS did not affect the specific binding of [3H]paroxetine, a ligand that binds to the 5-HT transporter, in membranes. NO-CYS and SNP, like iodoacetic acid and sodium cyanide, decreased the ATP content in cortical synaptosomes, but the effect on ATP content was not related to that on [3H]5-HT uptake. These findings suggest that NO inhibits reversibly [3H]5-HT uptake into rat brain synaptosomes without affecting the recognition site of the 5-HT transporter in a cGMP-independent manner, and the observed effect is not due to its metabolic effect.
机译:参考文献(28)一氧化氮(NO)供体(如硝普钠(SNP))3-(2-)对大鼠脑的突触小体对By(13)[3H] 5-羟色胺(5-HT)的摄取具有剂量依赖性的抑制作用。羟基-1-甲基-2-亚硝基肼基)-N-甲基-1-丙胺,3-吗啉代亚胺和S-亚硝基-L-半胱氨酸(NO-CYS)。抑制作用被减少的血红蛋白阻断。亚铁氰化物和铁氰化物没有模仿该效果。 8-溴鸟苷3'',5''-环一磷酸(8-溴cGMP)不会影响[3H] 5-HT摄取到大鼠皮质突触小体中。通过用NO-CYS预处理的皮质突触体中[3H] 5-HT摄取的活性降低,可以通过在处理后清洗制剂来部分逆转。动力学分析表明,NO-CYS(100μM)降低了Vmax值,而Km值没有任何变化。 NO-CYS不会影响[3H] paroxetine(与5-HT转运蛋白结合的配体)在膜中的特异性结合。 NO-CYS和SNP像碘乙酸和氰化钠一样,可降低皮层突触小体中的ATP含量,但对ATP含量的影响与[3H] 5-HT的吸收无关。这些发现表明,NO可逆地抑制大鼠脑突触体中的[3H] 5-HT摄取,而不会以cGMP独立的方式影响5-HT转运蛋白的识别位点,并且观察到的效果不是由于其代谢作用。

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