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强心苷哇巴因和地高辛会干扰新生大鼠脑源性星形胶质细胞中谷氨酸转运体GLAST的调节。

Cardiac glycosides ouabain and digoxin interfere with the regulation of glutamate transporter GLAST in astrocytes cultured from neonatal rat brain.

作者信息

Nguyen Khoa T D, Buljan Vlado, Else Paul L, Pow David V, Balcar Vladimir J

机构信息

Discipline of Anatomy and Histology, School of Medical Sciences, Bosch Institute of Biomedical Research, Sydney Medical School, The University of Sydney, Anderson Stuart Building F 13, Sydney, NSW 2006, Australia.

出版信息

Neurochem Res. 2010 Dec;35(12):2062-9. doi: 10.1007/s11064-010-0274-4. Epub 2010 Oct 2.

Abstract

Glutamate transport (GluT) in brain is mediated chiefly by two transporters GLT and GLAST, both driven by ionic gradients generated by (Na(+), K(+))-dependent ATPase (Na(+)/K(+)-ATPase). GLAST is located in astrocytes and its function is regulated by translocations from cytoplasm to plasma membrane in the presence of GluT substrates. The phenomenon is blocked by a naturally occurring toxin rottlerin. We have recently suggested that rottlerin acts by inhibiting Na(+)/K(+)-ATPase. We now report that Na(+)/K(+)-ATPase inhibitors digoxin and ouabain also blocked the redistribution of GLAST in cultured astrocytes, however, neither of the compounds caused detectable inhibition of ATPase activity in cell-free astrocyte homogenates (rottlerin inhibited app. 80% of Pi production from ATP in the astrocyte homogenates, IC50 = 25 μM). Therefore, while we may not have established a direct link between GLAST regulation and Na(+)/K(+)-ATPase activity we have shown that both ouabain and digoxin can interfere with GluT transport and therefore should be considered potentially neurotoxic.

摘要

大脑中的谷氨酸转运(GluT)主要由两种转运体GLT和GLAST介导,二者均由(Na⁺,K⁺)依赖性ATP酶(Na⁺/K⁺-ATP酶)产生的离子梯度驱动。GLAST位于星形胶质细胞中,其功能在存在GluT底物的情况下通过从细胞质向质膜的易位来调节。这种现象被天然毒素rottlerin阻断。我们最近提出rottlerin通过抑制Na⁺/K⁺-ATP酶起作用。我们现在报告,Na⁺/K⁺-ATP酶抑制剂地高辛和哇巴因也阻断了培养的星形胶质细胞中GLAST的重新分布,然而,这两种化合物均未在无细胞的星形胶质细胞匀浆中引起可检测到的ATP酶活性抑制(rottlerin抑制星形胶质细胞匀浆中ATP产生Pi的约80%,IC50 = 25 μM)。因此,虽然我们可能尚未确立GLAST调节与Na⁺/K⁺-ATP酶活性之间的直接联系,但我们已表明地高辛和哇巴因均可干扰GluT转运,因此应被视为具有潜在神经毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f23/3002169/fc1bf5ea9c8c/11064_2010_274_Fig1_HTML.jpg

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