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Effects of Tephrosia purpurea and Momordica dioica on streptozotocin-induced diabetic nephropathy in rats 紫荆、苦瓜对链脲佐菌素所致大鼠糖尿病肾病的影响
Pub Date : 2014-07-01 DOI: 10.1016/j.bionut.2014.06.003
Avijeet Jain , Alok Nahata , Santram Lodhi , Abhay K. Singhai

Present study investigated the effects of Tephrosia purpurea (TP) and Momordica dioica (MD) in streptozotocin-induced diabetic nephropathy in wistar rats. Rats were divided into 12 groups (n = 6). Diabetes was induced with a single dose of streptozotocin (55 mg/kg i.p.). Day 4 of the study was considered first day of the study as administration of ethanolic extracts of TP leaves and MD fruits were started on 4th day. In protective regimen (initial 26 days of experimental period), ethanolic extract was administered orally at 200 and 400 mg/kg/day, whereas curative regimen began after 26 days and continued up to 40 days. Diabetic control group was considered as standard for comparison. Serum glucose, urea, creatinine and urine albumin levels were significantly lower in treated groups as compared to the diabetic control. Malondialdehyde was significantly (P < 0.001) lowered in treated groups as compared to diabetic control group. Treated groups have shown significant increase (P < 0.001) in reduced glutathione level which was reduced in diabetic control group. Change in body weight was found to be non-significant in treated groups. It was concluded that TP leaf and MD fruit extracts can provide a radical cure for drug-induced diabetic nephropathy by a reduction in renal damage.

本研究探讨了紫荆(TP)和苦瓜(MD)对链脲佐菌素诱导的糖尿病大鼠肾病的作用。将大鼠分为12组(n = 6),采用单剂量链脲佐菌素(55 mg/kg i.p)诱导糖尿病。研究的第4天作为研究的第一天,第4天开始给药茶茶叶和MD果实的乙醇提取物。在保护组(实验初期26天)中,乙醇提取物以200和400 mg/kg/天的剂量口服,而治疗组在26天后开始并持续到40天。以糖尿病对照组为比较标准。与糖尿病对照组相比,治疗组的血清葡萄糖、尿素、肌酐和尿白蛋白水平显著降低。丙二醛显著(P <0.001),治疗组与糖尿病对照组相比降低。治疗组明显增加(P <0.001),而糖尿病对照组的谷胱甘肽水平降低。治疗组的体重变化不显著。综上所述,茶茶叶和茶茶果提取物对药物性糖尿病肾病具有根治作用,可减轻肾脏损害。
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引用次数: 10
Tasiamide-B a new cyanobacterial compound for treating skin cancer Tasiamide-B一种新的治疗皮肤癌的蓝藻化合物
Pub Date : 2014-07-01 DOI: 10.1016/j.bionut.2013.10.001
Subramaniyan Vijayakumar, Muniaraj Menakha

Skin cancer is caused by HSP90 receptor protein molecule. It is treated with commercial drugs, like cabazitaxel and dyclonine. The aim of the present study was to predict screen and identify the potential high efficient anti-skin cancer compounds from the marine flora of cyanobacteria. To screen the bioactive compounds against skin cancer causing protein, HSP90, Glide module (Schrodinger suite) was applied. Among the 31 bioactive compounds screened, best Glide docking score of –9.144 was found in tasiamide-B. When this tasiamide-B was compared with the commercially available drugs, like cabazitaxel and dyclonine through molecular docking, tasiamide-B was found to be more effective by interacted strongly with skin cancer causing target protein, HSP90. The results of the study support the fact that in silico molecular docking studies using Glide and Hex programs are very useful in predicting skin cancer treating drug. In this study, tasiamide-B was predicted as the best active cyanobacterial compound derived from Symploca sp.

皮肤癌是由热休克蛋白90受体蛋白分子引起的。它是用商业药物治疗的,如卡巴他赛和代克隆碱。本研究的目的是预测、筛选和鉴定海洋蓝藻菌群中潜在的高效抗皮肤癌化合物。为了筛选抗皮肤癌蛋白的生物活性化合物,采用HSP90, Glide模块(薛定谔套件)。在筛选的31种生物活性化合物中,滑行对接得分最高的是tasiamide-B,得分为-9.144。通过分子对接将该他西亚胺- b与市售药物卡巴他他赛、代克隆碱等进行比较,发现他西亚胺- b与致皮肤癌靶蛋白HSP90有较强的相互作用,更有效。该研究结果支持了使用Glide和Hex程序的硅分子对接研究在预测皮肤癌治疗药物方面非常有用的事实。在本研究中,tasiamide-B被预测为从Symploca sp.中提取的活性最好的蓝藻化合物。
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引用次数: 2
Studies on chemical composition of three species of Enteromorpha 三种浒苔属植物的化学成分研究
Pub Date : 2014-07-01 DOI: 10.1016/j.bionut.2014.04.001
K. Ganesan , K. Suresh Kumar , P.V. Subba Rao , Y. Tsukui , N. Bhaskar , M. Hosokawa , K. Miyashita

Studies on proximate, mineral, fatty and amino acid composition of edible Enteromorpha species, viz. Enteromorpha compressa, Enteromorpha linza and Enteromorpha tubulosa, collected from the Northwest coast of India, revealed for species-dependent nutrient composition variation. The present study showed a higher amount of sugar (51.05 ± 1.22%), protein (19.09 ± 0.91%) and lipid content (5.56 ± 0.16%) E. tubulosa. Amongst the seventeen elements analyzed (Ca, K, Mg, Na, P, As, Cd, Co, Cu, Fe, Hg, Mn, Mo, Ni, Zn, Cr, Pb), all three species showed a higher amount of calcium content. E. compressa was obtained with rich amount of macro-elements (11.42 ± 0.017 g/100 g dry wt), while maximum micro- and trace-elements (81.51 ± 6.65 mg/100 g dry wt) were recorded in E. linza. Amino acid analysis revealed seven out of the 10 essential amino acids were present either in excess or at-par with the reference proteins. Moreover, all the three species studied possessed relatively high n-3 fatty acids; additionally they had more unsaturated fatty acids than saturate ones, except in E. compressa. Therefore, based on the present investigation, it could be stated that the three species studied could be used as food supplements to improve the nutritive value in the omnivorous diet.

对采自印度西北海岸的可食Enteromorpha compressa、Enteromorpha linza和Enteromorpha tubulosa的近缘、矿物质、脂肪和氨基酸组成进行了研究,揭示了营养成分的种类依赖性变化。本研究显示,小管棘球蚴的糖含量(51.05±1.22%)、蛋白质含量(19.09±0.91%)和脂肪含量(5.56±0.16%)较高。在17种元素(Ca、K、Mg、Na、P、As、Cd、Co、Cu、Fe、Hg、Mn、Mo、Ni、Zn、Cr、Pb)中,3种元素的钙含量均较高。其中,苦参的微量元素含量最高(81.51±6.65 mg/100 g干wt),而苦参的微量元素含量最高(11.42±0.017 g/100 g干wt)。氨基酸分析显示,10种必需氨基酸中有7种存在过量或与参考蛋白相同。此外,所研究的三个物种都具有较高的n-3脂肪酸;此外,它们含有的不饱和脂肪酸比饱和脂肪酸多,但压缩叶除外。因此,根据目前的研究,可以认为所研究的三种植物可以作为杂食性饮食的营养补充剂,以提高营养价值。
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引用次数: 16
The total antioxidant content and radical scavenging investigation on 17 phytochemical from dietary plant sources used globally as functional food 全球功能性食品植物源中17种植物化学物质的总抗氧化剂含量及自由基清除研究
Pub Date : 2014-07-01 DOI: 10.1016/j.bionut.2014.03.007
Neeraj Kumar Sethiya, Ashish Trivedi, Shrihari Mishra

In search to potent natural antioxidant from plant-based metabolites, a comparative study was designed in present investigation. The antioxidant activity of various phytochemicals listed in text was determined by using 1,1-diphenyl-2-picrylhydrazyl (DPPH), ferric reducing power assays (FRAP) and phosphomolybdenum complex method. The level of the antioxidant activity by all three used assays was significantly (P < 0.001) higher in vitamin E, ascorbic acid, curcumin, gallic acid, ellagic acid, β-carotene and ursolic acid than other. Hence, these should be regarded as a potential source of natural antioxidants and could be effectively employed as an ingredient in functional food.

为了从植物代谢产物中寻找有效的天然抗氧化剂,本研究设计了一项比较研究。本文采用1,1-二苯基-2-吡啶肼(DPPH)法、铁还原力法(FRAP)和磷钼配合物法测定了所列植物化学物质的抗氧化活性。三种方法的抗氧化活性水平均显著(P <0.001)维生素E、抗坏血酸、姜黄素、没食子酸、鞣花酸、β-胡萝卜素和熊果酸的含量高于其他。因此,这些应被视为天然抗氧化剂的潜在来源,可以有效地用作功能性食品的成分。
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引用次数: 41
Isolation and molecular recognization of 6-prenyl apigenin towards MAO-A as the active principle of seeds of Achyranthes aspera
Pub Date : 2014-07-01 DOI: 10.1016/j.bionut.2014.03.003
Shoban Janet Beula , V. Bhaskar Anada Raj , Bijo Mathew

Purpose

The present study was undertaken to isolate the bioactive flavonoid compound from the seeds of Achyranthes aspera and establish its molecular interaction towards monoamine oxidase-A enzyme.

Materials and methods

The structure of the isolated flavonoid was ascertained by UV, 1H NMR, 13C NMR, DEPT 90, DEPT 135 and ESI-MS. Molecular level interaction was studied through molecular docking simulation carried out with AutoDock 4.2 in the catalytic portion of MAO-A.

Results

5, 7-dihydroxy-2-(4-hydroxyphenyl)-6-(3-methylbut-2-en-1-yl)-4H-chromen-4-one was isolated by chromatographic techniques. The docking study revealed that the structure of the isolated flavonoid showed to be a potent monoamine oxidase-A inhibitor with a docking score of −8.06 and calculated inhibition constant of about 1.23 μM.

Conclusion

On the basis of molecular docking study, we propose that isolated flavonoid can successfully dock into the inhibitor-binding pocket of human monoamine oxidase-A isoform with appreciable predicted affinity. The results therefore suggest that 6-prenyl apigenin can be a promising lead for developing novel monoamine oxidase-A inhibitors.

目的从牛膝种子中分离出具有生物活性的黄酮类化合物,并确定其与单胺氧化酶- a酶的分子相互作用。材料与方法采用紫外光谱(UV)、1H NMR、13C NMR、DEPT 90、DEPT 135、ESI-MS等方法对分离得到的黄酮类化合物进行结构鉴定。结果通过色谱分离得到5,7 -二羟基-2-(4-羟基苯基)-6-(3-甲基-2-en-1-基)- 4h - chromen4 -one。对接研究表明,分离得到的黄酮类化合物是一种有效的单胺氧化酶a抑制剂,对接分数为−8.06,计算出的抑制常数约为1.23 μM。结论在分子对接研究的基础上,我们提出分离的黄酮类化合物可以成功对接到人单胺氧化酶- a异构体的抑制剂结合口袋中,并具有可观的预测亲和力。因此,6-烯丙基芹菜素可能是开发新型单胺氧化酶- a抑制剂的有希望的先导物。
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引用次数: 7
Antidiabetic, hypolipidemic and histopathological analysis of Gymnema sylvestre (R. Br) leaves extract on streptozotocin induced diabetic rats 匙羹藤叶提取物对链脲佐菌素诱导的糖尿病大鼠的降糖、降血脂和组织病理学分析
Pub Date : 2014-07-01 DOI: 10.1016/j.bionut.2014.03.008
Srinivasan Prabhu, Subramaniyan Vijayakumar

Objective

To investigate antidiabetic, hypolipidemic histopathological analysis of Gymnema sylvestre methanolic extract (GSME) in streptozotocin induced diabetic rat by administering oral doses (100, 200 and 400 mg/kg body weight).

Methods

Blood glucose levels were measured using blood glucose test strips with elegance glucometer on weekly intervals till the end of study (i.e. four weeks). Blood glucose, urine sugar, triglycerides (TG), low density lipoprotein (LDL), high density lipoprotein (HDL) and very low density lipoprotein (VLDL) were determined in normal and streptozotocin induced diabetic rats after oral administration of the extract for 28 days. Histopathological changes in diabetic rat organs (pancreas, liver, and kidney) were also observed after extract treatment.

Results

Daily oral administration GSME (100, 200 and 400 mg/kg body weight) and glibenclamide (5 mg/kg) showed beneficial effects on blood glucose level (P < 0.01) and hyperlipidaemia due to diabetes. The extract treatment also showed to enhance serum insulin level and body weight of diabetic rats as compared to diabetic control group. Furthermore, the extract has a favorable effect on the histopathological studies, in streptozotocin induced diabetes.

Conclusions

G. sylvestre possesses antidiabetic property as well improve body weight, and total lipid levels. GSME has also favorable effect to inhibit the histopathological changes in streptozotocin-induced diabetes.

目的观察链脲佐菌素诱导的糖尿病大鼠口服100、200、400 mg/kg体重的木门醇提物(GSME)对糖尿病的降糖、降血脂作用。方法采用带雅致血糖仪的血糖试纸每周一次测量血糖水平,直至研究结束(即四周)。对正常及链脲佐菌素诱导的糖尿病大鼠口服提取物28 d后的血糖、尿糖、甘油三酯(TG)、低密度脂蛋白(LDL)、高密度脂蛋白(HDL)和极低密度脂蛋白(VLDL)进行测定。提取物处理后,糖尿病大鼠胰腺、肝脏和肾脏的组织病理学改变也被观察到。结果每日口服GSME(100、200和400 mg/kg体重)和格列本脲(5 mg/kg体重)对血糖水平有良好的影响(P <0.01)和糖尿病引起的高脂血症。与糖尿病对照组相比,该提取物还能提高糖尿病大鼠的血清胰岛素水平和体重。此外,该提取物对链脲佐菌素诱导的糖尿病有良好的组织病理学研究作用。西尔维斯特具有抗糖尿病的特性,以及改善体重,和总脂质水平。GSME对链脲佐菌素诱导糖尿病的组织病理改变也有良好的抑制作用。
{"title":"Antidiabetic, hypolipidemic and histopathological analysis of Gymnema sylvestre (R. Br) leaves extract on streptozotocin induced diabetic rats","authors":"Srinivasan Prabhu,&nbsp;Subramaniyan Vijayakumar","doi":"10.1016/j.bionut.2014.03.008","DOIUrl":"10.1016/j.bionut.2014.03.008","url":null,"abstract":"<div><h3>Objective</h3><p><span>To investigate antidiabetic<span>, hypolipidemic histopathological analysis of </span></span><span><em>Gymnema sylvestre</em></span><span> methanolic extract (GSME) in streptozotocin induced diabetic rat by administering oral doses (100, 200 and 400</span> <!-->mg/kg body weight).</p></div><div><h3>Methods</h3><p><span>Blood glucose levels<span> were measured using blood glucose<span> test strips with elegance glucometer on weekly intervals till the end of study (</span></span></span><em>i.e</em><span><span>. four weeks). Blood glucose, urine sugar<span>, triglycerides<span> (TG), low density lipoprotein (LDL), </span></span></span>high density lipoprotein<span> (HDL) and very low density lipoprotein<span><span> (VLDL) were determined in normal and streptozotocin induced diabetic rats after oral administration of the extract for 28 days. Histopathological changes in diabetic rat organs (pancreas, liver, and kidney) were also observed after extract </span>treatment.</span></span></span></p></div><div><h3>Results</h3><p>Daily oral administration GSME (100, 200 and 400<!--> <span>mg/kg body weight) and glibenclamide (5</span> <!-->mg/kg) showed beneficial effects on blood glucose level (<em>P</em> <!-->&lt;<!--> <span><span>0.01) and hyperlipidaemia due to diabetes. The extract treatment also showed to enhance </span>serum insulin level<span> and body weight of diabetic rats as compared to diabetic control group. Furthermore, the extract has a favorable effect on the histopathological studies, in streptozotocin induced diabetes.</span></span></p></div><div><h3>Conclusions</h3><p><em>G. sylvestre</em><span> possesses antidiabetic property as well improve body weight, and total lipid levels. GSME has also favorable effect to inhibit the histopathological changes in streptozotocin-induced diabetes.</span></p></div>","PeriodicalId":100182,"journal":{"name":"Biomedicine & Preventive Nutrition","volume":"4 3","pages":"Pages 425-430"},"PeriodicalIF":0.0,"publicationDate":"2014-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.bionut.2014.03.008","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91252745","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 12
Protective effect of betaine on protein, glycoproteins and amino acids in isoprenaline-induced myocardial infarction in albino rats 甜菜碱对异丙肾上腺碱诱导的白化大鼠心肌梗死中蛋白质、糖蛋白和氨基酸的保护作用
Pub Date : 2014-07-01 DOI: 10.1016/j.bionut.2014.06.005
Balakrishnan Meena , Lawrance Anbu Rajan , Rangasamy Anandan

Myocardial infarction is emerging as a foremost public health concern in most parts of the world even in developing countries still afflicted by infectious diseases, under nutrition and other illnesses related to poverty. There has been increasing recognition that certain natural substances have the potential to reduce the detrimental effect of a number of cardiovascular risk factors. In the present study, we have investigated the protective effect of betaine administration on changes in the levels of protein, glycoproteins and amino acids was studied in isoprenaline-induced myocardial infarction in rats as an animal model of myocardial infarction in man. Oral pre-treatment with betaine significantly attenuated (P < 0.01) the isoprenaline-induced rise in the levels of troponin-T and creatine phosphokinase [CPK]. Oral supplementation of betaine also significantly (P < 0.01) counteracted the isoprenaline-induced alterations in the levels of amino acids [taurine, aspartate, glutamate, arginine, hydroxy proline and homocysteine], protein content, glycoprotein components [hexose and hexosamine] and lipid peroxidation in the heart tissue and maintained their levels comparable to that of control animals. The results indicated that the overall cardioprotective effect of betaine was probably related to its ability to strengthen the myocardial membrane by its membrane stabilizing action or to a counteraction of free radicals by its antioxidant property.

在世界大多数地区,甚至在仍然受传染病、营养不良和其他与贫穷有关的疾病困扰的发展中国家,心肌梗塞正在成为一个最重要的公共卫生问题。人们越来越认识到,某些天然物质有可能减少一些心血管危险因素的有害影响。在本研究中,我们研究了甜菜碱对异丙肾上腺碱诱导的大鼠心肌梗死中蛋白质、糖蛋白和氨基酸水平变化的保护作用,作为人类心肌梗死的动物模型。口服甜菜碱预处理显著减毒(P <0.01)异丙肾上腺素诱导的肌钙蛋白- t和肌酸磷酸激酶[CPK]水平升高。口服补充甜菜碱也显著(P <0.01)抵消了异丙肾上腺碱引起的心脏组织中氨基酸(牛磺酸、天冬氨酸、谷氨酸、精氨酸、脯氨酸和同型半胱氨酸)、蛋白质含量、糖蛋白组分(己糖和己糖)和脂质过氧化水平的变化,并保持与对照动物相当的水平。结果表明,甜菜碱的整体心脏保护作用可能与其通过稳定心肌膜来增强心肌膜的能力或通过抗氧化作用来对抗自由基有关。
{"title":"Protective effect of betaine on protein, glycoproteins and amino acids in isoprenaline-induced myocardial infarction in albino rats","authors":"Balakrishnan Meena ,&nbsp;Lawrance Anbu Rajan ,&nbsp;Rangasamy Anandan","doi":"10.1016/j.bionut.2014.06.005","DOIUrl":"10.1016/j.bionut.2014.06.005","url":null,"abstract":"<div><p><span><span>Myocardial infarction is emerging as a foremost public health<span> concern in most parts of the world even in developing countries still afflicted by infectious diseases, under nutrition and other illnesses related to poverty. There has been increasing recognition that certain natural substances have the potential to reduce the detrimental effect of a number of cardiovascular risk factors. In the present study, we have investigated the protective effect of betaine administration on changes in the levels of protein, </span></span>glycoproteins and amino acids was studied in isoprenaline-induced myocardial infarction in rats as an animal model of myocardial infarction in man. Oral pre-treatment with betaine significantly attenuated (</span><em>P</em> <!-->&lt;<!--> <span>0.01) the isoprenaline-induced rise in the levels of troponin-T and creatine phosphokinase [CPK]. Oral supplementation of betaine also significantly (</span><em>P</em> <!-->&lt;<!--> <span><span><span><span>0.01) counteracted the isoprenaline-induced alterations in the levels of amino acids [taurine, aspartate, glutamate, arginine, </span>hydroxy proline and homocysteine], protein content, glycoprotein components [hexose and hexosamine] and </span>lipid peroxidation in the heart tissue and maintained their levels comparable to that of control animals. The results indicated that the overall cardioprotective effect of betaine was probably related to its ability to strengthen the </span>myocardial membrane<span> by its membrane stabilizing action or to a counteraction of free radicals by its antioxidant property.</span></span></p></div>","PeriodicalId":100182,"journal":{"name":"Biomedicine & Preventive Nutrition","volume":"4 3","pages":"Pages 403-409"},"PeriodicalIF":0.0,"publicationDate":"2014-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.bionut.2014.06.005","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88270879","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Polychlorinated biphenyl (PCBs)-induced oxidative stress plays a role on vertebral antioxidant system: Ameliorative role of vitamin C and E in male Wistar rats 多氯联苯(PCBs)诱导的氧化应激对雄性Wistar大鼠椎体抗氧化系统的影响:维生素C和E的改善作用
Pub Date : 2014-07-01 DOI: 10.1016/j.bionut.2014.04.004
Subramanian Karthikeyan, Muthusamy Sridhar, Govindan Ramajayam, Ramadoss Lavanya, Jagadeesan Arunakaran, Narasimhan Srinivasan

PCB are still prevalent in the environment despite the fact that they have been banned in many countries for several decades, have wide range of adverse effects in various organ systems including bone. The present study aimed at evaluating the effects of PCB on vertebral bone and the ameliorative role of vitamin C or E in the adult male Wistar rats. Group-I rats received vehicle (corn oil) intraperitoneally (i.p), group-II received Aroclor [1254] 2 mg/kg bwt/day (i.p), group-III received Aroclor [1254] (i.p) and simultaneously vitamin C 100 mg/kg bwt/day (orally), group-IV received Aroclor [1254] (i.p) and simultaneously vitamin E 50 mg/kg bwt/day (orally). After 30 days, rats were euthanized and vertebrae were dissected. The osteoblast functional markers (ALP and Collagen), osteoclast functional marker (TRAP), antioxidant enzymes (SOD, GPx and GST) and lipid peroxidation (LPO) were assessed in the vertebral bone of control and experimental animals. A significant decrease the ALP, collagen enzyme activity and increase the TRAP activity were observed in PCBs (Aroclor 1254) treated rats. SOD and GPx were increased in the PCB treated rats. Vitamin C or E given along with PCB, prevented the effects of PCB on ALP and TRAP. GST activity was effective in simultaneous administration of vitamin C treated group. LPO was altered in PCB treatment and animals remaining were not altered. PCB induces oxidative stress and stimulates osteoclast activity but suppresses osteoblast function and it perturbs the antioxidant system. Vitamin C or vitamin E was able to prevent the effects of PCB.

尽管PCB在许多国家已经被禁止了几十年,但它在环境中仍然普遍存在,对包括骨骼在内的各种器官系统有广泛的不利影响。本研究旨在评估多氯联苯对成年雄性Wistar大鼠椎骨的影响以及维生素C或E的改善作用。ⅰ组大鼠腹腔灌胃玉米油,ⅱ组大鼠灌胃Aroclor [1254] 2 mg/kg bwt/d (i.p),ⅲ组大鼠灌胃Aroclor [1254] 1 mg/kg bwt/d同时灌胃维生素C 100 mg/kg bwt/d(口服),ⅳ组大鼠灌胃Aroclor [1254] 1 mg/kg bwt/d同时灌胃维生素E 50 mg/kg bwt/d(口服)。30天后,对大鼠实施安乐死并解剖椎骨。测定对照动物和实验动物椎骨中成骨细胞功能标志物(ALP、Collagen)、破骨细胞功能标志物(TRAP)、抗氧化酶(SOD、GPx、GST)和脂质过氧化(LPO)水平。多氯联苯(Aroclor 1254)处理后大鼠ALP、胶原酶活性显著降低,TRAP活性显著升高。多氯联苯处理大鼠SOD和GPx均升高。与多氯联苯同时给予维生素C或E,可阻止多氯联苯对ALP和TRAP的影响。同时给予维生素C处理组GST活性有效。PCB处理改变了LPO,其余动物没有改变。多氯联苯诱导氧化应激,刺激破骨细胞活性,但抑制成骨细胞功能,扰乱抗氧化系统。维生素C或维生素E能够防止多氯联苯的影响。
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引用次数: 2
Amino acid composition and nutritional quality of gonad from jellyfish Rhopilema esculentum 水母性腺氨基酸组成及营养品质研究
Pub Date : 2014-07-01 DOI: 10.1016/j.bionut.2014.04.007
Huahua Yu, Rongfeng Li, Song Liu, Rong-e Xing, Xiaolin Chen, Pengcheng Li

In the present study, amino acid compositions of two jellyfish gonad samples were determined and the nutritional value was evaluated by the amino acid score method recommend by WHO/FAO and fuzzy recognition method. The two samples were abundant in amino acids. The major amino acids were both glutamic acid, lysine, glycine, aspartic acid and leucine and the contents of these amino acids were 51.47% and 52.52% of the total amino acids, respectively. The essential amino acids were 42.89% and 40.70%, the flavor amino acids were 47.39% and 50.12% and the medicinal amino acids were 66.55% and 66.92% of the total amino acids, respectively. μ (a, μi) values of the two samples were respectively 0.91 and 0.94 and SRC values were respectively 70.89 and 69.96, indicating that the essential amino acids of jellyfish gonad were well-balanced and the nutritional value of jellyfish gonad was high.

本研究采用WHO/FAO推荐的氨基酸评分法和模糊识别法对两种海蜇性腺样品的氨基酸组成进行测定,并对其营养价值进行评价。这两个样品中氨基酸含量丰富。主要氨基酸为谷氨酸、赖氨酸、甘氨酸、天冬氨酸和亮氨酸,分别占总氨基酸的51.47%和52.52%。其中必需氨基酸占总氨基酸的42.89%、40.70%,风味氨基酸占47.39%、50.12%,药用氨基酸占66.55%、66.92%。两种样品的μ (a, μi)值分别为0.91和0.94,SRC值分别为70.89和69.96,说明海蜇性腺必需氨基酸平衡良好,营养价值较高。
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引用次数: 25
Isolation of chemical constituents from Spilanthes calva DC: Toxicity, anthelmintic efficacy and in silico studies 小红花化学成分的分离:毒性、驱虫功效及硅片研究
Pub Date : 2014-07-01 DOI: 10.1016/j.bionut.2014.04.002
P. Jayaraj , B. Mathew , C. Mani , R. Govindarajan

Aqueous and ethanol extracts of this Spilanthes calva DC is widely used in folk medicine in South India for treating various parasitic diseases. In vitro anthelmintic activities of crude aqueous and alcoholic extract of aerial parts of the plant was investigated to provide experimental evidence for its use in folk medicine. Investigations of in vitro anthelmintic efficacy were evaluated separately on adult Pheretima posthuma and Ascaridia galli compared with Albendazole. Ethanol extract showed more anthelmintic activity than aqueous extract. Six compounds were isolated from ethanol extract compounds 3, 4 and 6 showed significant anthelmintic activity with LC50 values of 12, 11, 9.9 and 11.47, 10.56, 8.35 respectively against both the worms. The oral LD50 of the aqueous and ethanol extracts estimated in mice is greater than 5000 mg/kg. Molecular docking studies were carried out for compound 6 by using ArgusLab 4.0.1. and Molegrow 2012.2.5.0 generated the enzyme binding interaction which suggested the lactone ring attained a non-coplanar conformation with benzisoxazole can contribute two significant hydrogen bonding interaction with Tyr 50 and Gln 134. This could be attributed to the slight structural resemblance with Albendazole and hydrogen bonding, π-π and non-polar interactions towards the inhibitor-binding cavity of the β-tubulin enzyme. Our study shows ingredients in S. calva DC ethanol extract contains an effective anthelmintic composition that could potentially developed as a promising plant origin anthelmintic.

水萃取物和乙醇萃取物在印度南部的民间医药中被广泛用于治疗各种寄生虫病。研究了该植物地上部水提物和醇提物的离体驱虫活性,为其在民间医学中的应用提供实验依据。分别与阿苯达唑进行体外驱虫实验,比较其对成虫后腹假蝇和加利蛔虫的驱虫效果。乙醇提取物的驱虫活性高于水提取物。从乙醇提取物中分离得到6个化合物,其中化合物3、4和6对两种线虫的LC50值分别为12、11、9.9和11.47、10.56、8.35。水提物和乙醇提物对小鼠的口服LD50均大于5000mg /kg。利用ArgusLab 4.0.1对化合物6进行分子对接研究。Molegrow 2012.2.5.0产生的酶结合相互作用表明,与苯并恶唑形成非共面构象的内酯环可以与Tyr 50和Gln 134产生两个显著的氢键相互作用。这可能是由于β-微管蛋白酶的抑制结合腔与阿苯达唑和氢键、π-π和非极性相互作用的结构相似。我们的研究表明,牛蒡子乙醇提取物的成分中含有一种有效的驱虫药成分,有可能成为一种有前途的植物源驱虫药。
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引用次数: 4
期刊
Biomedicine & Preventive Nutrition
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