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Biomed Res Int. 2013;2013:417928. doi: 10.1155/2013/417928. Epub 2013 Oct 29.
2
DNA fragmentation and apoptosis induced by safranal in human prostate cancer cell line.藏红花醛诱导人前列腺癌细胞系中的DNA片段化和细胞凋亡。
Indian J Urol. 2013 Jul;29(3):177-83. doi: 10.4103/0970-1591.117278.
3
Safranal treatment improves hyperglycemia, hyperlipidemia and oxidative stress in streptozotocin-induced diabetic rats.苦藏花醛处理可改善链脲佐菌素诱导的糖尿病大鼠的高血糖、高血脂和氧化应激。
J Pharm Pharm Sci. 2013;16(2):352-62. doi: 10.18433/j3zs3q.
4
Safranal ameliorates antioxidant enzymes and suppresses lipid peroxidation and nitric oxide formation in aged male rat liver.藏红花醛可改善老年雄性大鼠肝脏抗氧化酶活性,抑制脂质过氧化和一氧化氮形成。
Biogerontology. 2013 Feb;14(1):63-71. doi: 10.1007/s10522-012-9409-0. Epub 2012 Nov 22.
5
Cardiovascular effects of saffron: an evidence-based review.藏红花的心血管效应:一项基于证据的综述。
J Tehran Heart Cent. 2011 Spring;6(2):59-61. Epub 2011 May 31.
6
Use of in vitro assays to assess the potential antiproliferative and cytotoxic effects of saffron (Crocus sativus L.) in human lung cancer cell line.利用体外试验评估藏红花(番红花)对人肺癌细胞系的潜在抗增殖和细胞毒性作用。
Pharmacogn Mag. 2010 Oct;6(24):309-14. doi: 10.4103/0973-1296.71799.
7
Efficacy and safety of incretin-based therapies in patients with type 2 diabetes mellitus.
Eur J Intern Med. 2009 Jul;20 Suppl 2:S309-18. doi: 10.1016/j.ejim.2009.05.011. Epub 2009 Jun 21.
8
The effect of alpha-lipoic acid on NOS dispersion in the lung of streptozotocin-induced diabetic rats.α-硫辛酸对链脲佐菌素诱导的糖尿病大鼠肺组织中一氧化氮合酶分布的影响。
J Diabetes Complications. 2008 Jan-Feb;22(1):56-61. doi: 10.1016/j.jdiacomp.2006.08.004.
9
Crocetin, dimethylcrocetin, and safranal bind human serum albumin: stability and antioxidative properties.西红花酸、二甲基西红花酸和藏红花醛与人血清白蛋白结合:稳定性和抗氧化特性。
J Agric Food Chem. 2007 Feb 7;55(3):970-7. doi: 10.1021/jf062638l.
10
Botanical dietary supplements and the treatment of diabetes: what is the evidence?植物性膳食补充剂与糖尿病治疗:证据何在?
Curr Diab Rep. 2005 Oct;5(5):391-8. doi: 10.1007/s11892-005-0099-8.

评估肺和支气管肺泡灌洗液氧化应激指标以评价藏红花醛对糖尿病大鼠呼吸窘迫的预防作用。

Evaluation of lung and bronchoalveolar lavage fluid oxidative stress indices for assessing the preventing effects of safranal on respiratory distress in diabetic rats.

作者信息

Samarghandian Saeed, Afshari Reza, Sadati Aghdas

机构信息

Department of Basic Medical Sciences, Neyshabur Medical Faculty of Sciences, Neyshabur, Iran ; Health Strategic Research Center, Neyshabur Medical Faculty of Sciences, Neyshabur, Iran.

Addiction Research Centre, Mashhad University of Medical Sciences, Mashhad, Iran.

出版信息

ScientificWorldJournal. 2014 Feb 20;2014:251378. doi: 10.1155/2014/251378. eCollection 2014.

DOI:10.1155/2014/251378
PMID:24701146
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3950999/
Abstract

We investigated the effects of antioxidant activity of safranal, a constituent of Crocus sativus L., against lung oxidative damage in diabetic rats. The rats were divided into the following groups of 8 animals each: control, diabetic, and three diabetic + safranal-treated (0.25, 0.50, and 0.75 mg/kg/day) groups. Streptozotocin (STZ) was injected intraperitoneally (i.p.) at a single dose of 60 mg/kg for diabetes induction. Safranal was administered (i.p.) from 3 days after STZ administration to the end of the study. At the end of the 4-week period, malondialdehyde (MDA), nitric oxide (NO) and reduced glutathione (GSH) contents, activity of superoxide dismutase (SOD), and catalase (CAT) were measured in the bronchoalveolar lavage fluid (BALF) and lung tissue. Safranal in the diabetic groups inhibited the level of MDA and NO in BALF supernatant and lung homogenate. The median effective dose (ED50) values were 0.42, 0.58, and 0.48, 0.71 mg/kg, respectively. Safranal in the diabetic groups increased the level of GSH and the activity of CAT and SOD in BALF supernatant and lung homogenate. The ED50 values were 0.25, 0.33, 0.26 in BALF and 0.33, 0.35, 0.46 mg/kg in lung, respectively. Thus, safranal may be effective to prevent lung distress by amelioration oxidative damage in STZ diabetic rats.

摘要

我们研究了藏红花的成分藏红花醛对糖尿病大鼠肺氧化损伤的抗氧化活性作用。将大鼠分为以下几组,每组8只动物:对照组、糖尿病组和三个糖尿病 + 藏红花醛治疗组(0.25、0.50和0.75毫克/千克/天)。腹腔注射链脲佐菌素(STZ),单次剂量为60毫克/千克以诱导糖尿病。从注射STZ后3天开始至研究结束,腹腔注射藏红花醛。在4周实验期结束时,测量支气管肺泡灌洗液(BALF)和肺组织中的丙二醛(MDA)、一氧化氮(NO)和还原型谷胱甘肽(GSH)含量、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性。糖尿病组中的藏红花醛抑制了BALF上清液和肺匀浆中MDA和NO的水平。半数有效剂量(ED50)值分别为0.42、0.58,以及0.48、0.71毫克/千克。糖尿病组中的藏红花醛提高了BALF上清液和肺匀浆中GSH的水平以及CAT和SOD的活性。BALF中的ED50值分别为0.25、0.33、0.26,肺中的ED50值分别为0.33、0.35、0.46毫克/千克。因此,藏红花醛可能通过改善STZ糖尿病大鼠的氧化损伤来有效预防肺部窘迫。