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1-(2',5'-二羟基苯基)-3-(2-氟-4-羟基苯基)-1-丙酮(RGM079):一种具有镇痛和神经保护活性的α7 烟碱型乙酰胆碱受体正向变构调节剂。

1-(2',5'-Dihydroxyphenyl)-3-(2-fluoro-4-hydroxyphenyl)-1-propanone (RGM079): A Positive Allosteric Modulator of α7 Nicotinic Receptors with Analgesic and Neuroprotective Activity.

机构信息

Instituto de Química Médica , IQM-CSIC , Juan de la Cierva 3 , Madrid 28006 , Spain.

Instituto Teófilo Hernando, Department of Pharmacology , Universidad Autónoma de Madrid , Arzobispo Morcillo 4 , Madrid 28029 , Spain.

出版信息

ACS Chem Neurosci. 2019 Aug 21;10(8):3900-3909. doi: 10.1021/acschemneuro.9b00364. Epub 2019 Aug 2.

DOI:10.1021/acschemneuro.9b00364
PMID:31322853
Abstract

Acetylcholine α7 nicotinic receptors are widely expressed in the brain, where they are involved in the central processing of pain as well as in neuropsychiatric, neurodegenerative, and inflammatory processes. Positive allosteric modulators (PAMs) show the advantage of allowing the selective regulation of different subtypes of acetylcholine receptors without directly interacting with the agonist binding site. Here, we report the preparation and biological activity of a fluoro-containing compound, 1-(2',5'-dihydroxyphenyl)-3-(2-fluoro-4-hydroxyphenyl)-1-propanone (, ), that behaves as a potent PAM of the α7 receptors and has a balanced pharmacokinetic profile and antioxidant properties comparable or even higher than well-known natural polyphenols. In addition, compound shows neuroprotective properties in Alzheimer's disease (AD)-toxicity related models. Thus, it causes a concentration-dependent neuroprotective effect against the toxicity induced by okadaic acid (OA) in the human neuroblastoma cell line SH-SY5Y. Similarly, in primary cultures of rat cortical neurons, is able to restore the cellular viability after exposure to OA and amyloid peptide Aβ, with cell death almost completely prevented at 10 and 30 μM, respectively. Finally, compound shows analgesic activity in the complete Freund's adjuvant (CFA)-induced paw inflammation model after intraperitoneal administration.

摘要

乙酰胆碱 α7 烟碱型受体广泛表达于脑内,在中枢疼痛处理以及神经精神疾病、神经退行性疾病和炎症过程中发挥作用。正变构调节剂(PAMs)的优势在于可以选择性调节不同亚型的乙酰胆碱受体,而无需直接与激动剂结合位点相互作用。在此,我们报告了一种含氟化合物 1-(2',5'-二羟基苯基)-3-(2-氟-4-羟基苯基)-1-丙酮(, )的制备和生物学活性,该化合物作为 α7 受体的有效 PAM,具有平衡的药代动力学特征和抗氧化特性,与知名天然多酚相当甚至更高。此外,化合物 在阿尔茨海默病(AD)相关毒性模型中表现出神经保护作用。因此,它在人神经母细胞瘤 SH-SY5Y 细胞系中对冈田酸(OA)诱导的毒性具有浓度依赖性的神经保护作用。同样,在原代培养的大鼠皮质神经元中,化合物 能够在暴露于 OA 和淀粉样肽 Aβ 后恢复细胞活力,分别在 10 和 30 μM 时几乎完全阻止细胞死亡。最后,化合物 在腹腔注射完全弗氏佐剂(CFA)诱导的爪炎症模型中表现出镇痛活性。

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