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海马胆碱能神经刺激肽对海马胆碱能活性的直接增强作用。

Direct Enhancement Effect of Hippocampal Cholinergic Neurostimulating Peptide on Cholinergic Activity in the Hippocampus.

机构信息

Department of Neurology, Nagoya City University, 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya 467-8601, Japan.

出版信息

Int J Mol Sci. 2023 May 17;24(10):8916. doi: 10.3390/ijms24108916.

Abstract

The cholinergic efferent network from the medial septal nucleus to the hippocampus is crucial for learning and memory. This study aimed to clarify whether hippocampal cholinergic neurostimulating peptide (HCNP) has a rescue function in the cholinergic dysfunction of HCNP precursor protein (HCNP-pp) conditional knockout (cKO). Chemically synthesized HCNP or a vehicle were continuously administered into the cerebral ventricle of HCNP-pp cKO mice and littermate floxed (control) mice for two weeks via osmotic pumps. We immunohistochemically measured the cholinergic axon volume in the stratum oriens and functionally evaluated the local field potential in the CA1. Furthermore, choline acetyltransferase (ChAT) and nerve growth factor (NGF) receptor (TrkA and p75NTR) abundances were quantified in wild-type (WT) mice administered HCNP or the vehicle. As a result, HCNP administration morphologically increased the cholinergic axonal volume and electrophysiological theta power in HCNP-pp cKO and control mice. Following the administration of HCNP to WT mice, TrkA and p75NTR levels also decreased significantly. These data suggest that extrinsic HCNP may compensate for the reduced cholinergic axonal volume and theta power in HCNP-pp cKO mice. HCNP may function complementarily to NGF in the cholinergic network in vivo. HCNP may represent a therapeutic candidate for neurological diseases with cholinergic dysfunction, e.g., Alzheimer's disease and Lewy body dementia.

摘要

内侧隔核到海马的胆碱能传出网络对于学习和记忆至关重要。本研究旨在阐明海马胆碱能神经刺激肽(HCNP)是否对 HCNP 前体蛋白(HCNP-pp)条件敲除(cKO)的胆碱能功能障碍具有挽救作用。通过渗透压泵,将化学合成的 HCNP 或载体连续给予 HCNP-pp cKO 小鼠和同窝 floxed(对照)小鼠的脑室两周。我们通过免疫组织化学测量了 HCNP-pp cKO 和对照小鼠 CA1 区的 CA1 层中的胆碱能轴突体积,并在功能上评估了局部场电位。此外,在给予 HCNP 或载体的野生型(WT)小鼠中定量了胆碱乙酰转移酶(ChAT)和神经生长因子(NGF)受体(TrkA 和 p75NTR)的丰度。结果,HCNP 给药在 HCNP-pp cKO 和对照小鼠中形态上增加了胆碱能轴突体积和电生理θ功率。在给予 WT 小鼠 HCNP 后,TrkA 和 p75NTR 水平也显著降低。这些数据表明,外源性 HCNP 可能补偿了 HCNP-pp cKO 小鼠中胆碱能轴突体积和θ功率的减少。HCNP 可能在体内胆碱能网络中与 NGF 互补发挥作用。HCNP 可能是具有胆碱能功能障碍的神经退行性疾病(如阿尔茨海默病和路易体痴呆)的治疗候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e2/10218987/b5ac68fa0236/ijms-24-08916-g001.jpg

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