Weak Anti-inflammatory and Anti-cancer Properties of Saffron

IF 1.1 Q4 PHARMACOLOGY & PHARMACY Research Journal of Pharmacognosy Pub Date : 2019-06-22 DOI:10.22127/RJP.2020.219943.1557
M. Heidari, Z. Razzaghi, M. Rostami-Nejad, Sina Rezaei-Tavirani, S. Safari, M. Rezaei-Tavirani
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引用次数: 2

Abstract

Background and objectives: Positive role of saffron in human health promotion has been investigated in widespread researches. Anticancer property, neuroprotection, protection of cardiovascular system and several positive properties are reported for saffron customers. The aim of this study was assessment of saffron weakness against light damage in rat retina. Methods: Gene profiles of control samples (C group) and light damage (L) groups were extracted from Gene Expression Omnibus (GEO) and compared with similar samples in the presence of saffron. The unprotected differentially expressed genes (DEGs) were evaluated via network analysis and pathway investigation.  The critical genes which were not protected by saffron were identified and discussed. Results: Numbers of 67 DEGs were investigated via protein-protein interaction (PPI) network analysis, pathway assessment, and action map investigation. Findings indicated that STAT1, JUN, FOS, and STAT3 were the crucial genes that were not protected by saffron against light damage in rat retina. Conclusion: It may be necessary that consumption of saffron require a suitable protocol to avoid from possible disadvantages; however, saffron is well known for its benefits in human nutrition.
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藏红花的弱抗炎和抗癌作用
背景与目的:藏红花在促进人体健康方面的积极作用已被广泛研究。据报道,藏红花具有抗癌、神经保护、心血管系统保护和一些积极的特性。本研究的目的是评估藏红花对大鼠视网膜光损伤的抵抗力。方法:从Gene Expression Omnibus (GEO)中提取对照组(C组)和光损伤组(L组)的基因图谱,并在藏红花存在的情况下与同类样品进行比较。通过网络分析和通路研究对未保护的差异表达基因(DEGs)进行评价。对不受藏红花保护的关键基因进行了鉴定和讨论。结果:通过蛋白相互作用(PPI)网络分析、通路评估和行动图调查,研究了67个deg的数量。结果表明,STAT1、JUN、FOS和STAT3是藏红花不保护大鼠视网膜免受光损伤的关键基因。结论:有必要制定合适的藏红花食用方案,以避免可能出现的不利影响;然而,藏红花以其对人体营养的益处而闻名。
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来源期刊
Research Journal of Pharmacognosy
Research Journal of Pharmacognosy PHARMACOLOGY & PHARMACY-
CiteScore
1.10
自引率
20.00%
发文量
0
审稿时长
8 weeks
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