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Increased tonic activation of presynaptic metabotropic glutamate receptors in the rat supraoptic nucleus following chronic dehydration

机译:慢性脱水后大鼠视上核中突触前代谢型谷氨酸受体的补品激活增加

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摘要

Chronic dehydration induces structural changes in the hypothalamic supraoptic nucleus (SON), including increased glutamate synapses and retraction of astroglial processes. We performed whole-cell recordings in acute hypothalamic slices to determine whether these changes increase tonic activation of presynaptic metabotropic glutamate receptors (mGluRs) by increasing ambient glutamate in the SON. Activation of presynaptic group III mGluRs caused a decrease in the frequency of miniature excitatory postsynaptic currents (mEPSCs) in SON neurones that was significantly attenuated in slices from dehydrated rats (−27.8 %) compared with untreated rats (−41.7 %), suggesting a higher basal occupancy of mGluRs by ambient glutamate during dehydration. Blocking group III mGluRs caused an increase in the frequency of mEPSCs that was significantly higher in slices from dehydrated rats (+42.8 %) than untreated rats (+31.4 %), suggesting greater tonic activation of presynaptic mGluRs by ambient glutamate during dehydration. Increasing ambient glutamate levels by inhibiting astrocyte glutamate uptake resulted in a decrease in mEPSC frequency due to increased activation of presynaptic mGluRs. This was attenuated in slices from dehydrated rats (−35.4 %) compared with slices from untreated rats (−48.8 %), suggesting diminished astrocytic glutamate uptake during dehydration. Immunochemical analyses revealed a robust expression of the GLT-1 transporter protein in the SON, which was diminished in SON punches from dehydrated rats compared with untreated controls. Thus, dehydration leads to increased tonic activation of presynaptic mGluRs on glutamate terminals, consistent with a decrease in glutamate buffering capacity. The resulting reduction in glutamate release probability may compensate for the increase in glutamate release sites that occurs during dehydration.
机译:慢性脱水引起下丘脑超视核(SON)的结构变化,包括谷氨酸突触增加和星形胶质细胞退缩。我们在急性下丘脑切片中进行了全细胞记录,以确定这些变化是否通过增加SON中的环境谷氨酸来增加突触前代谢型谷氨酸受体(mGluRs)的滋补活化。突触前组III mGluRs的激活导致SON神经元中微型兴奋性突触后电流(mEPSCs)频率的降低,与未治疗的大鼠(-41.7%)相比,脱水大鼠的切片(−27.8%)显着衰减。脱水过程中环境谷氨酸对mGluRs的基本占有率。阻断组III的mGluRs导致脱水大鼠切片中mEPSCs频率的升高(+ 42.8%)比未处理的大鼠(+ 31.4%)要高得多,这表明在脱水过程中环境谷氨酸对突触前mGluRs的补品活化作用更大。通过抑制星形胶质细胞谷氨酸的摄取来增加周围谷氨酸水平,由于突触前mGluRs的活化增加而导致mEPSC频率的降低。与未处理大鼠的切片(-48.8%)相比,脱水大鼠的切片(-35.4%)的这种衰减减弱,表明脱水过程中星形细胞谷氨酸的吸收减少。免疫化学分析显示,GLT-1转运蛋白在SON中表达强健,与未处理的对照组相比,脱水大鼠的SON打孔减少了该表达。因此,脱水导致谷氨酸末端上突触前mGluRs的补品激活增加,这与谷氨酸缓冲能力的降低相一致。导致的谷氨酸盐释放概率的降低可以补偿在脱水过程中发生的谷氨酸盐释放位点的增加。

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