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Phosphatidylinositol 4,5-bisphosphate induced flunitrazepam sensitive-GABAA receptor increase in synaptosomes from chick forebrain.

机译:磷脂酰肌醇4,5-二磷酸酯诱导的氟尼西epa敏感性GABAA受体在鸡前脑突触体中增加。

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The flunitrazepam sensitive-GABA(A) receptor density was increased by cytochalasins C and D at 37 degrees C suggesting that microfilament depolymerization induces exposure to the radioligand of a GABA(A) receptor in synaptosomes (Pharm Biochem Behav 72 (2002) 497). Similarly, phosphatidylinositol-4,5-bisphosphate (1-5 microM), but not a mixture of phospholipids, induced an increase of GABA(A) receptors in synaptosomes. Furthermore, N-ethyl maleimide, an inactivator of the sensitive fusion protein, which interacts with GABA(A) receptor, abolished the receptor increase induced by phosphatidylinositol-4,5-bisphosphate. Together, the results suggest that phosphatidylinositol-4,5-bisphosphate, acts via microfilament depolymerization increasing the binding of the radioligand to receptors possibly by modulation of their interaction with proteins involved in trafficking and docking mechanisms.
机译:在37摄氏度时,细胞松弛素C和D增加了氟硝西sensitive敏感性GABA(A)受体的密度,这表明微丝解聚诱导突触体中GABA(A)受体的放射性配体暴露(Pharm Biochem Behav 72(2002)497)。同样,磷脂酰肌醇-4,5-双磷酸酯(1-5 microM),而不是磷脂的混合物,在突触小体中诱导GABA(A)受体的增加。此外,与GABA(A)受体相互作用的灵敏融合蛋白的灭活剂N-乙基马来酰亚胺消除了磷脂酰肌醇-4,5-双磷酸酯诱导的受体增加。在一起,结果表明磷脂酰肌醇-4,5-二磷酸通过微丝解聚起作用,增加了放射性配体与受体的结合,可能是通过调节它们与涉及运输和对接机制的蛋白质的相互作用。

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