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阿朴肉桂酸的药理学:一种天然苯乙酮。

Pharmacology of apocynin: a natural acetophenone.

机构信息

Shobhaben Pratapbhai Patel School of Pharmacy & Technology Management, SVKM's NMIMS, Mumbai, India.

出版信息

Drug Metab Rev. 2021 Nov;53(4):542-562. doi: 10.1080/03602532.2021.1895203. Epub 2021 Mar 10.

DOI:10.1080/03602532.2021.1895203
PMID:33689526
Abstract

Apocynin is a naturally occurring acetophenone, found in the roots of . Various chemical and pharmaceutical modifications have been carried out to enhance the absorption and duration of action of apocynin, like, formulation of chitosan-based apocynin-loaded solid lipid nanoparticles, chitosan-oligosaccharide based nanoparticles, and biodegradable polyanhydride nanoparticles. Apocynin has been subjected to a wide range of experimental screening and has proved to be useful for amelioration of a variety of disorders, like diabetic complications, neurodegeneration, cardiovascular disorders, lung cancer, hepatocellular cancer, pancreatic cancer, and pheochromocytoma. Apocynin has been primarily reported as an NADPH oxidase (NOX) inhibitor and prevents translocation of its p47 subunit to the plasma membrane, observed in neurodegeneration and hypertension. However, recent studies highlight its off-target effects that it is able to function as a scavenger of non-radical oxidant species, which is relevant for its activity against NOX 4 mediated production of hydrogen peroxide. Additionally, apocynin has shown inhibition of eNOS-dependent superoxide production in diabetic cardiomyopathy, reduction of NLRP3 activation and TGFβ/Smad signaling in diabetic nephropathy, diminished VEGF expression and decreased retinal NF-κB activation in diabetic retinopathy, inhibition of P38/MAPK/Caspase3 pathway in pheochromocytoma, inhibition of AKT-GSK3β and ERK1/2 pathways in pancreatic cancer, and decreased FAK/PI3K/Akt signaling in hepatocellular cancer. This review aims to discuss the pharmacokinetics and mechanisms of the pharmacological actions of apocynin.

摘要

白杨素是一种天然存在的苯乙酮,存在于. 为了提高白杨素的吸收和作用持续时间,已经进行了各种化学和药物修饰,如壳聚糖基载白杨素固体脂质纳米粒、壳聚糖寡糖纳米粒和可生物降解的聚酸酐纳米粒的制剂。白杨素已经进行了广泛的实验筛选,并且已被证明对改善多种疾病(如糖尿病并发症、神经退行性疾病、心血管疾病、肺癌、肝细胞癌、胰腺癌和嗜铬细胞瘤)有用。白杨素主要被报道为 NADPH 氧化酶 (NOX) 抑制剂,可防止其 p47 亚基向质膜易位,这在神经退行性疾病和高血压中观察到。然而,最近的研究强调了其非靶标效应,即它能够作为非自由基氧化剂的清除剂发挥作用,这与其针对 NOX4 介导的过氧化氢产生的活性相关。此外,白杨素已显示在糖尿病心肌病中抑制 eNOS 依赖性超氧化物的产生,在糖尿病肾病中减少 NLRP3 激活和 TGFβ/Smad 信号转导,在糖尿病性视网膜病变中减少 VEGF 表达和降低视网膜 NF-κB 激活,在嗜铬细胞瘤中抑制 P38/MAPK/Caspase3 途径,在胰腺癌中抑制 AKT-GSK3β 和 ERK1/2 途径,以及在肝细胞癌中降低 FAK/PI3K/Akt 信号转导。本综述旨在讨论白杨素的药代动力学和药理作用机制。

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