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垂体腺苷酸环化酶激活肽(PACAP)是神经元中前强啡肽 mRNA 表达的上游调节剂。

Pituitary adenylate cyclase-activating polypeptide (PACAP) is an upstream regulator of prodynorphin mRNA expression in neurons.

机构信息

Department of Biological Chemistry, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Sugitani 2630, Toyama 930-0194, Japan.

出版信息

Neurosci Lett. 2010 Nov 5;484(3):174-7. doi: 10.1016/j.neulet.2010.08.044. Epub 2010 Aug 20.

Abstract

Although dynorphins are widely involved in the control of not only nociceptive neurotransmission but also a variety of brain functions such as memory and emotion, no natural regulator for inducing the mRNA expression of prodynorphin (Pdyn), a precursor protein of dynorphins, is known. Using primary cultures of rat cortical neurons, we found that pituitary adenylate cyclase-activating polypeptide (PACAP), a member of the vasoactive intestinal polypeptide (VIP)/secretin/glucagon neuropeptide family, markedly induces Pdyn mRNA expression. PACAP was much more effective than VIP, indicating a major role for PAC1 in the PACAP-induced Pdyn mRNA expression. The increase in Pdyn mRNA expression was independent of de novo protein synthesis. Administration of forskolin, an activator for adenylate cyclase/protein kinase A (PKA), but not TPA, an activator for protein kinase C (PKC), induced Pdyn mRNA expression, suggesting a major role for PKA. The involvement of PKA was supported by the inhibition of PACAP-induced Pdyn mRNA expression upon addition of H89, an inhibitor for PKA. The PACAP-induced potentiation of NMDA-R was involved in the mRNA expression of Bdnf or c-fos but not Pdyn. These results suggest PACAP to be an upstream regulator for inducing Pdyn mRNA expression through PKA.

摘要

尽管强啡肽广泛参与不仅伤害性神经传递的控制,而且还参与各种大脑功能,如记忆和情绪,但目前还不知道诱导强啡肽前体蛋白(Pdyn)mRNA 表达的天然调节剂。使用大鼠皮质神经元的原代培养物,我们发现垂体腺苷酸环化酶激活肽(PACAP),一种血管活性肠肽(VIP)/分泌素/胰高血糖素神经肽家族的成员,显著诱导 Pdyn mRNA 表达。PACAP 比 VIP 更有效,表明 PAC1 在 PACAP 诱导的 Pdyn mRNA 表达中起主要作用。Pdyn mRNA 表达的增加与新蛋白质合成无关。腺嘌呤核苷环化酶/蛋白激酶 A(PKA)的激活剂forskolin 的给药,而不是蛋白激酶 C(PKC)的激活剂 TPA,诱导 Pdyn mRNA 表达,表明 PKA 的主要作用。PKA 抑制剂 H89 的加入抑制了 PACAP 诱导的 Pdyn mRNA 表达,这支持了 PKA 的参与。PACAP 诱导的 NMDA-R 增强参与了 Bdnf 或 c-fos 的 mRNA 表达,但不参与 Pdyn。这些结果表明 PACAP 通过 PKA 成为诱导 Pdyn mRNA 表达的上游调节剂。

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