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一种来自广东紫珠的苯乙醇苷类化合物,此前尚未被描述,可作为 Na/K-ATP 酶信号转导通路的激动剂。

A previously undescribed phenylethanoid glycoside from Callicarpa kwangtungensis Chun acts as an agonist of the Na/K-ATPase signal transduction pathway.

机构信息

Marshall Institute for Interdisciplinary Research, Marshall University, Huntington, WV, 25701, United States.

Department of Natural Medicinal Chemistry, China Pharmaceutical University, Nanjing, 210009, PR China; Jiangsu Food and Pharmaceutical Science College, Huai'an, 223003, PR China.

出版信息

Phytochemistry. 2021 Jan;181:112577. doi: 10.1016/j.phytochem.2020.112577. Epub 2020 Nov 12.

DOI:10.1016/j.phytochem.2020.112577
PMID:33190100
Abstract

The new concept that Na/K-ATPase acts as a receptor prompted us to look for new ligands from Callicarpa kwangtungensis Chun. Using column chromatography, an undescribed phenethyl alcohol glycoside, callicarpanoside A, and an undescribed benzyl alcohol glycoside, callicarpanoside B, along with twelve known polyphenols were isolated from Callicarpa kwangtungensis Chun. All the isolated compounds were evaluated for their Na/K-ATPase (NKA) inhibitory activities. Using our NKA technology platform-based screening assay protocols, callicarpanoside B was identified as an undescribed Na/K-ATPase agonist. In particular, the newly identified benzyl alcohol glycoside was found to bind NKA and activate the receptor NKA/Src complex, resulting in the activation of protein kinase cascades. These cascades included extracellular signal-regulated kinases and protein kinase C epsilon, as well as NKA α1 endocytosis at nanomolar concentrations. Unlike the class of cardiotonic steroids, callicarpanoside B showed less inhibition of NKA activity and caused less cellular toxicity. Moreover, callicarpanoside B was found to bind NKA at a different site other than the cardiotonic steroids binding site. Thus, we have identified an undescribed NKA α1 agonist that may be used to enhance the physiological processes of NKA α1 signaling.

摘要

新的概念认为 Na/K-ATP 酶作为受体,这促使我们从黄皮中寻找新的配体。使用柱层析,从黄皮中分离出一种未描述的苯乙醇糖苷,即黄皮苷 A,和一种未描述的苄基醇糖苷,即黄皮苷 B,以及 12 种已知的多酚。所有分离出的化合物均评估了其对 Na/K-ATP 酶 (NKA) 的抑制活性。使用我们基于 NKA 技术平台的筛选测定方案,鉴定出黄皮苷 B 是一种未描述的 NKA 激动剂。特别是,新发现的苄基醇糖苷被发现与 NKA 结合并激活受体 NKA/Src 复合物,从而激活蛋白激酶级联。这些级联包括细胞外信号调节激酶和蛋白激酶 C ɛ,以及 NKAα1 在纳摩尔浓度下内吞。与强心甾类化合物不同,黄皮苷 B 对 NKA 活性的抑制作用较弱,细胞毒性较小。此外,发现黄皮苷 B 与 NKA 的结合位点不同于强心甾类化合物的结合位点。因此,我们已经鉴定出一种未描述的 NKAα1 激动剂,它可能被用于增强 NKAα1 信号转导的生理过程。

相似文献

1
A previously undescribed phenylethanoid glycoside from Callicarpa kwangtungensis Chun acts as an agonist of the Na/K-ATPase signal transduction pathway.一种来自广东紫珠的苯乙醇苷类化合物,此前尚未被描述,可作为 Na/K-ATP 酶信号转导通路的激动剂。
Phytochemistry. 2021 Jan;181:112577. doi: 10.1016/j.phytochem.2020.112577. Epub 2020 Nov 12.
2
Phenylethanoid glycosides of Callicarpa kwangtungensis Chun exert cardioprotective effect by weakening Na-K-ATPase/Src/ERK1/2 pathway and inhibiting apoptosis mediated by oxidative stress and inflammation.岗梅中苯乙醇苷类成分通过减弱 Na-K-ATP 酶/Src/ERK1/2 通路和抑制氧化应激及炎症介导的细胞凋亡发挥心肌保护作用。
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Natural phenylethanoid glycosides isolated from Callicarpa kwangtungensis suppressed lipopolysaccharide-mediated inflammatory response via activating Keap1/Nrf2/HO-1 pathway in RAW 264.7 macrophages cell.从广东紫珠中分离得到的天然苯乙醇苷类化合物通过激活 RAW 264.7 巨噬细胞中的 Keap1/Nrf2/HO-1 通路抑制脂多糖介导的炎症反应。
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Proinflammatory Effects of Cardiotonic Steroids Mediated by NKA α-1 (Na+/K+-ATPase α-1)/Src Complex in Renal Epithelial Cells and Immune Cells.强心甾类通过肾上皮细胞和免疫细胞中 NKAα-1(Na+/K+-ATPaseα-1)/Src 复合物介导的促炎作用。
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Rapid identification of chemical compositions in callicarpa kwangtungensis Chun by ultra-high-performance liquid chromatography with Q Exactive hybrid quadrupole orbitrap high-resolution accurate mass spectrometry.采用超高效液相色谱- Q Exactive 混合四极杆轨道阱高分辨精确质量质谱法快速鉴定岗梅中的化学成分。
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引用本文的文献

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Cardiac Oxidative Signaling and Physiological Hypertrophy in the Na/K-ATPase α1α2 Mouse Model of High Affinity for Cardiotonic Steroids.心脏氧化信号和生理肥大在高亲和力心脏毒素甾体的 Na/K-ATPase α1α2 小鼠模型中。
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3
Biased Effect of Cardiotonic Steroids on Na/K-ATPase-Mediated Signal Transduction.
强心甾体对 Na/K-ATPase 介导的信号转导的偏倚效应。
Mol Pharmacol. 2021 Mar;99(3):217-225. doi: 10.1124/molpharm.120.000101. Epub 2021 Jan 25.