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多巴胺负荷导致音猬因子信号通路失活,引发轻微肝性脑病认知功能下降。

Dopamine Burden Induced the Inactivation of Sonic Hedgehog Signaling to Cognitive Decline in Minimal Hepatic Encephalopathy.

作者信息

Ding Saidan, Yang Jianjing, Huang Xueli, Liu Leping, Hu Jiangnan, Xu Zhu, Zhuge Qichuan

机构信息

1Zhejiang Provincial Key Laboratory of Aging and Neurological Disease Research, Department of Surgery Laboratory, the First Affiliated Hospital, Wenzhou Medical University, Zhejiang 325000, China.

2Department of Neurosurgery, the First Affiliated Hospital, Wenzhou Medical University, Zhejiang 325000, China.

出版信息

Aging Dis. 2017 Jul 21;8(4):442-457. doi: 10.14336/AD.2016.1123. eCollection 2017 Jul.

Abstract

Minimal hepatic encephalopathy (MHE) is induced by elevated intracranial dopamine (DA). The relationship of the Shh pathway with memory loss in MHE, however, is elusive. In the current study, rats with MHE induced with DA displayed downregulation of the Shh pathway. Additionally, injection of Shh into MHE/DA-treated rats reversed downregulation of BDNF/NT3, whereas administration of cyclopamine (Cyc) enhanced the inhibition of expression of BDNF/NT3. Furthermore, naringin (Nrg) substantially prevented cognitive impairment in MHE/DA-treated rats and upregulated the Shh pathway, paralleling the elevated expression of BDNF/NT3. Overall, our results indicate that the Shh pathway can induce the expression of BDNF/NT3, and DA causes memory loss by inactivation of Shh pathway signaling to BDNF/NT3 in MHE rats, which is reversed by Nrg. Our study may provide new theory basis of pathogenesis and therapeutic target of MHE.

摘要

轻微肝性脑病(MHE)由颅内多巴胺(DA)升高所致。然而,在MHE中,Shh信号通路与记忆丧失之间的关系尚不明确。在本研究中,用DA诱导产生MHE的大鼠表现出Shh信号通路的下调。此外,向经MHE/DA处理的大鼠注射Shh可逆转脑源性神经营养因子(BDNF)/神经营养素-3(NT3)的下调,而给予环杷明(Cyc)则增强了对BDNF/NT3表达的抑制。此外,柚皮苷(Nrg)显著预防了经MHE/DA处理大鼠的认知障碍,并上调了Shh信号通路,这与BDNF/NT3表达升高相平行。总体而言,我们的结果表明,Shh信号通路可诱导BDNF/NT3的表达,DA通过使MHE大鼠中向BDNF/NT3的Shh信号通路失活而导致记忆丧失,而Nrg可逆转这种情况。我们的研究可能为MHE的发病机制和治疗靶点提供新的理论依据。

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