首页> 外文期刊>Journal of Neuroscience Research >Effect of chronic gestational treatment with the adenosine A1 receptor agonist R-phenylisopropyladenosine on metabotropic glutamate receptors/phospholipase C pathway in maternal and fetal brain.
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Effect of chronic gestational treatment with the adenosine A1 receptor agonist R-phenylisopropyladenosine on metabotropic glutamate receptors/phospholipase C pathway in maternal and fetal brain.

机译:腺苷A1受体激动剂R-苯基异丙基腺苷对妊娠和孕产妇和胎儿脑代谢型谷氨酸受体/磷脂酶C通路的影响。

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Pregnant Wistar rats were orally treated with the adenosine receptor agonist R-phenylisopropyladenosine (R-PIA) throughout the gestational period, and the status of the metabotropic glutamate (mGlu) receptor/phospholipase C transduction pathway from maternal and fetal brain was analyzed. In mothers' brains, radioligand binding assays revealed a significant decrease in the Bmax value, without any significant alteration in Kd value. Similar results were observed in the steady-state level of mGlu(1) and mGlu(5) receptors assayed by Western blot, suggesting that both receptor subtypes were modulated by chronic R-PIA treatment. mRNA coding mGlu(1) or mGlu(5) receptors was not altered, suggesting a posttranscriptional modulation as a possible mechanism of the loss of mGlu(1) and mGlu(5) receptors at the membrane surface. Moreover, phospholipase C stimulated by (R,S)-3,5-dihydroxyphenylglycine (DHPG), a selective agonist of group I mGlu receptors, was also significantly decreased after R-PIA treatment, suggesting a heterologous desensitization of group I mGlu/PLC pathway in maternal brain. Western blot and RT-PCR assays showed that neither alphaG(q/11) nor PLCbeta(1) was affected by R-PIA treatment. In fetal brain, no significant differences in mGlu receptors/PLC transduction pathway were observed after R-PIA treatment. These results suggest that chronic R-PIA intake during pregnancy modulates group I mGlu receptor signalling pathway in maternal brain, promoting a down-regulation of mGlu(1) and mGlu(5) receptors and a heterologous desensitization of the mGlu/PLC system.
机译:在整个妊娠期,对怀孕的Wistar大鼠进行口服腺苷受体激动剂R-苯基异丙基腺苷(R-PIA)治疗,并分析了来自母体和胎儿脑的代谢型谷氨酸(mGlu)受体/磷脂酶C的转导途径。在母亲的大脑中,放射性配体结合测定显示Bmax值显着下降,而Kd值没有任何显着变化。通过蛋白质印迹法检测到的mGlu(1)和mGlu(5)受体稳态水平观察到相似的结果,表明这两种受体亚型均受慢性R-PIA处理的调节。编码mGlu(1)或mGlu(5)受体的mRNA并未改变,表明转录后调节是膜表面上mGlu(1)和mGlu(5)受体丢失的可能机制。此外,R-PIA治疗后,由(R,S)-3,5-二羟基苯基甘氨酸(DHPG)(I组mGlu受体的选择性激动剂)刺激的磷脂酶C也显着降低,表明I组mGlu / PLC的异源脱敏产妇大脑中的通路。 Western印迹和RT-PCR分析表明,R-PIA处理均不影响alphaG(q / 11)和PLCbeta(1)。在胎儿脑中,R-PIA治疗后在mGlu受体/ PLC传导途径上没有观察到显着差异。这些结果表明,怀孕期间长期摄入R-PIA会调节母体脑中的I类mGlu受体信号传导途径,促进mGlu(1)和mGlu(5)受体的下调以及mGlu / PLC系统的异源脱敏。

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