Riaz Ammara, Rasul Azhar, Hussain Ghulam, Zahoor Muhammad Kashif, Jabeen Farhat, Subhani Zinayyera, Younis Tahira, Ali Muhammad, Sarfraz Iqra, Selamoglu Zeliha
Department of Zoology, Faculty of Life Sciences, Government College University, Faisalabad 38000, Pakistan.
Department of Physiology, Faculty of Life Sciences, Government College University, Faisalabad 38000, Pakistan.
Adv Pharmacol Sci. 2018 May 2;2018:9794625. doi: 10.1155/2018/9794625. eCollection 2018.
Natural products, an infinite treasure of bioactive chemical entities, persist as an inexhaustible resource for discovery of drugs. This review article intends to emphasize on one of the naturally occurring flavonoids, astragalin (kaempferol 3-glucoside), which is a bioactive constituent of various traditional medicinal plants such as . This multifaceted compound is well known for its diversified pharmacological applications such as anti-inflammatory, antioxidant, neuroprotective, cardioprotective, antiobesity, antiosteoporotic, anticancer, antiulcer, and antidiabetic properties. It carries out the aforementioned activities by the regulation and modulation of various molecular targets such as transcription factors (NF-B, TNF-, and TGF-1), enzymes (iNOS, COX-2, PGE2, MMP-1, MMP-3, MIP-1, COX-2, PGE-2, HK2, AChe, SOD, DRP-1, DDH, PLC1, and GPX), kinases (JNK, MAPK, Akt, ERK, SAPK, IB, PI3K, and PKC2), cell adhesion proteins (E-cadherin, vimentin PAR-2, and NCam), apoptotic and antiapoptotic proteins (Beclin-1, Bcl-2, Bax, Bcl-x, cytochrome c, LC3A/B, caspase-3, caspase-9, procaspase-3, procaspase-8, and IgE), and inflammatory cytokines (SOCS-3, SOCS-5, IL-1, IL-4, IL-6, IL-8, IL-13, MCP-1, CXCL-1, CXCL-2, and IFN-). Although researchers have reported multiple pharmacological applications of astragalin in various diseased conditions, further experimental investigations are still mandatory to fully understand its mechanism of action. It is contemplated that astragalin could be subjected to structural optimization to ameliorate its chemical accessibility, to optimize its absorption profiles, and to synthesize its more effective analogues which will ultimately lead towards potent drug candidates.
天然产物是生物活性化学实体的无尽宝库,仍然是药物发现的取之不尽的资源。这篇综述文章旨在强调一种天然存在的黄酮类化合物——紫云英苷(山奈酚3 - 葡萄糖苷),它是多种传统药用植物的生物活性成分,如……这种多面性的化合物因其多种药理应用而闻名,如抗炎、抗氧化、神经保护、心脏保护、抗肥胖、抗骨质疏松、抗癌、抗溃疡和抗糖尿病特性。它通过调节和调控各种分子靶点来发挥上述活性,这些分子靶点包括转录因子(NF - B、TNF - 、TGF - 1)、酶(iNOS、COX - 2、PGE2、MMP - 1、MMP - 3、MIP - 1、COX - 2、PGE - 2、HK2、AChe、SOD、DRP - 1、DDH、PLC1和GPX)、激酶(JNK、MAPK、Akt、ERK、SAPK、IB、PI3K和PKC2)、细胞粘附蛋白(E - 钙粘蛋白、波形蛋白PAR - 2和NCam)、凋亡和抗凋亡蛋白(Beclin - 1、Bcl - 2、Bax、Bcl - x、细胞色素c、LC3A/B、caspase - 3、caspase - 9、procaspase - 3、procaspase - 8和IgE)以及炎性细胞因子(SOCS - 3、SOCS - 5、IL - 1、IL - 4、IL - 6、IL - 8、IL - 13、MCP - 1、CXCL - 1、CXCL - 2和IFN - )。尽管研究人员已经报道了紫云英苷在各种疾病条件下的多种药理应用,但仍需要进一步的实验研究来充分了解其作用机制。可以设想,紫云英苷可以进行结构优化,以改善其化学可及性,优化其吸收情况,并合成更有效的类似物,这最终将导向有潜力的候选药物。