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内皮素-1 和 -3 通过大鼠下丘脑后区的多种信号通路调节神经元去甲肾上腺素转运体。

Endothelin-1 and -3 modulate the neuronal norepinephrine transporter through multiple signalling pathways in the rat posterior hypothalamus.

机构信息

Cátedra de Fisiología e Instituto de la Química y Metabolismo del Fármaco (IQUIMEFA-CONICET), Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín 956, Piso 7, 1113AAD Buenos Aires, Argentina.

出版信息

Neurochem Int. 2010 Oct;57(3):306-13. doi: 10.1016/j.neuint.2010.06.009. Epub 2010 Jun 25.

Abstract

We have previously reported that endothelin-1 and -3 modulate different steps of noradrenergic transmission in the hypothalamus. We showed that endothelins modify neuronal norepinephrine transport activity through the regulation of the kinetic constant and internalization. In the present work we sought to define the endothelin receptors and intracellular mechanisms involved in the down-regulation of neuronal norepinephrine uptake induced by endothelin-1 and -3 in the rat posterior hypothalamic region. Results showed that endothelin-1 reduced norepinephrine uptake through ET(B) receptors, whereas endothelin-3 through a non-conventional or atypical endothelin receptor. In both cases, the effect on norepinephrine uptake was coupled to protein kinase A and C as well as nitric oxide pathways. However, neither protein kinase G nor intracellular or extracellular calcium and calcium/calmodulin-dependent protein kinase II were involved. In addition, the same intracellular mechanisms participated in the reduction of nisoxetine binding (norepinephrine transporter internalization index) induced by both endothelins. Present findings reveal the underlying mechanisms involved in the regulation of the neuronal norepinephrine transporter by endothelins and further support the role of these peptides in the modulation of noradrenergic transmission at the presynaptic nerve endings in the posterior hypothalamus.

摘要

我们之前曾报道过内皮素-1 和 -3 调节下丘脑去甲肾上腺素能传递的不同步骤。我们表明,内皮素通过调节动力学常数和内化来改变神经元去甲肾上腺素的转运活性。在本工作中,我们试图确定参与内皮素-1 和 -3 诱导大鼠下丘脑后区神经元去甲肾上腺素摄取下调的内皮素受体和细胞内机制。结果表明,内皮素-1 通过 ET(B)受体减少去甲肾上腺素摄取,而内皮素-3 通过非传统或非典型的内皮素受体。在这两种情况下,对去甲肾上腺素摄取的影响都与蛋白激酶 A 和 C 以及一氧化氮途径有关。然而,蛋白激酶 G 以及细胞内或细胞外钙和钙/钙调蛋白依赖性蛋白激酶 II 均不参与。此外,相同的细胞内机制参与了内皮素诱导的去甲肾上腺素转运体(去甲肾上腺素转运体内化指数)结合减少。目前的研究结果揭示了内皮素调节神经元去甲肾上腺素转运体的潜在机制,并进一步支持这些肽在调节下丘脑后区突触前神经末梢去甲肾上腺素能传递中的作用。

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