Betulinic acid increases brain-derived neurotrophic factor expression via the PKA, NMDA receptor, and calcineurin pathways in cultured cortical neurons

IF 2.6 4区 医学 Q3 CHEMISTRY, MEDICINAL
Mamoru Fukuchi, Natsumi Maeda, Sachie Hoshino, Gegentuya Huanood, Kazuki Watanabe
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引用次数: 0

Abstract

Brain-derived neurotrophic factor (BDNF) is a crucial neurotrophin that plays a vital role in neuronal survival, synaptic plasticity, and cognitive function. Reduced BDNF expression has been implicated in neurodegenerative and neuropsychiatric disorders. Thus, compounds that enhance Bdnf expression may have therapeutic potential for these disorders. In this study, we screened 48 compounds, including those from Morus alba L. (Moraceae) branches and structurally similar compounds, for their ability to induce Bdnf expression in primary cultured cortical neurons derived from Bdnf-Luciferase transgenic mice. M. alba-derived compounds failed to increase Bdnf expression; however, among the structurally similar compounds, betulinic acid (BA), moronic acid, and oleanolic acid elevated Bdnf mRNA levels. Further mechanistic analysis, particularly focusing on BA, revealed that the BA-induced Bdnf expression was inhibited by the protein kinase A (PKA) inhibitor H89, N-methyl-d-aspartate receptor (NMDAR) antagonist APV, and the calcineurin inhibitor FK506. Furthermore, BA promoted the nuclear translocation of cAMP-response element-binding protein (CREB)-regulated transcriptional coactivator 1 (CRTC1), which translocates to the nucleus upon dephosphorylation by calcineurin. The BA-induced nuclear translocation of CRTC1 was completely inhibited by H89, APV, and FK506. Although BA also increased CREB phosphorylation, the phosphorylation was prevented by H89 and APV, but not by FK506. These results suggest that CREB phosphorylation and CRTC1 nuclear translocation contribute to BA-induced Bdnf expression. Our findings indicate that BA enhances Bdnf expression in a manner dependent on PKA, NMDAR, and calcineurin signaling pathways, highlighting its potential as a modulator of activity-dependent BDNF transcription.

Graphical abstract

The alternative text for this image may have been generated using AI.

Abstract Image

白桦酸通过PKA、NMDA受体和钙调磷酸酶途径增加脑源性神经营养因子在培养皮层神经元中的表达。
脑源性神经营养因子(BDNF)是一种重要的神经营养因子,在神经元存活、突触可塑性和认知功能中起着至关重要的作用。BDNF表达减少与神经退行性疾病和神经精神疾病有关。因此,增强Bdnf表达的化合物可能具有治疗这些疾病的潜力。在本研究中,我们筛选了48种化合物,包括来自桑科桑科植物分支的化合物和结构相似的化合物,以检测它们在原代培养的Bdnf-荧光素酶转基因小鼠皮质神经元中诱导Bdnf表达的能力。M. alba衍生化合物不能增加Bdnf的表达;然而,在结构相似的化合物中,白桦酸(BA)、白痴酸和齐墩果酸升高了Bdnf mRNA水平。进一步的机制分析,特别是针对BA,发现BA诱导的Bdnf表达受到蛋白激酶A (PKA)抑制剂H89、n -甲基-d-天冬氨酸受体(NMDAR)拮抗剂APV和钙调磷酸酶抑制剂FK506的抑制。此外,BA促进cAMP-response element-binding protein (CREB)-regulated transcriptional coactivator 1 (CRTC1)的核易位,而CRTC1在calcalineurin的去磷酸化作用下易位到核中。ba诱导的CRTC1核易位被H89、APV和FK506完全抑制。虽然BA也增加了CREB的磷酸化,但磷酸化被H89和APV阻止,而不被FK506阻止。这些结果表明CREB磷酸化和CRTC1核易位有助于ba诱导的Bdnf表达。我们的研究结果表明,BA以依赖于PKA、NMDAR和钙调磷酸酶信号通路的方式增强Bdnf的表达,突出了其作为活性依赖性Bdnf转录调节剂的潜力。图形抽象此图像的替代文本可能是使用AI生成的。
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来源期刊
CiteScore
6.90
自引率
3.00%
发文量
79
审稿时长
1.7 months
期刊介绍: The Journal of Natural Medicines is an international journal publishing original research in naturally occurring medicines and their related foods and cosmetics. It covers: -chemistry of natural products -biochemistry of medicinal plants -pharmacology of natural products and herbs, including Kampo formulas and traditional herbs -botanical anatomy -cultivation of medicinal plants. The journal accepts Original Papers, Notes, Rapid Communications and Natural Resource Letters. Reviews and Mini-Reviews are generally invited.
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