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Ipomoea batatas L. Lam. 通过抑制炎症介质来改善急性和慢性炎症,采用体外和体内模型进行了全面探讨。

Ipomoea batatas L. Lam. ameliorates acute and chronic inflammations by suppressing inflammatory mediators, a comprehensive exploration using in vitro and in vivo models.

机构信息

Department of Pharmacy, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, 45320, Pakistan.

Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, 45320, Pakistan.

出版信息

BMC Complement Altern Med. 2018 Jul 13;18(1):216. doi: 10.1186/s12906-018-2279-5.

DOI:10.1186/s12906-018-2279-5
PMID:30005651
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6045844/
Abstract

BACKGROUND

Ipomoea batatas L. Lam. is a functional food and belongs to family Convolvulaceae. It is used as an antiinflammatory, aphrodisiac, antiasthmatic, anticonvalescent, antitumor, antanemic and antidiabetic agent by local communities. This study has been planned to evaluate its antiinflammatory and antiarthritic potentials.

METHODS

Dry powder of I. batatas tuber and roots were extracted with ethyl acetate (IPT-EA, IPR-EA) and methanol (IPT-M, IPR-M), respectively. These extracts were tested for total phenolic and flavonoid contents (TPC and TFC), HPLC finger printing, multidimensional in vitro and in vivo antioxidant potential and albumin denaturation inhibition. Carrageenan-induced paw edema, croton oil-induced ear and anal edema inhibition and Complete Freund's Adjuvant (CFA)-induced antiarthritic assays were executed at a dose of 300 mg/kg body weight on Sprague-Dawley rats. Serum levels of interleukins IL-1β and IL-6 and nitric oxide (NO) were assessed to measure the inhibition of inflammation.

RESULTS

Maximal TPC (319.81 ± 14.20 μg GAE/mg dry extract) and TFC (208.77 ± 9.09 μg QE/mg DE) were estimated in IPR-EA extract. IPT-EA and IPR-EA yielded the maximum amounts of rutin (7.3 ± 1.12 and 4.5 ± 0.55), caffeic acid (1.60 ± 0.25 and 2.17 ± 0.26) and myricetin (2.7 ± 0.14 and 1.01 ± 0.08 μg/mg DE), respectively in HPLC-DAD analysis. All extracts showed dose dependent response in in vitro antioxidant assays. Best inhibition (76.92 ± 3.07%) of albumin denaturation was shown by IPT-EA in comparison to ibuprofen (79.48 ± 4.71%). IPR-EA exhibited highest edema inhibition in models of carrageenan-induced paw edema (79.11 ± 5.47%) and croton oil-induced ear and anal edema (72.01 ± 7.80% and 70.80 ± 4.94%, respectively). Significant inhibition of CFA-induced arthritic edema and arthritic score were observed by IPR-EA as compared to ibuprofen. Suppression of pro-inflammatory cytokines (IL-1β, IL-6) and NO levels was shown by IPR-EA and IPT-EA, respectively.

CONCLUSION

These results depict that richness of polyphenols and phytoconstituents in I. batatas ameliorates oxidative stress and inflammation of acute and chronic nature. Dose dependent antioxidant potential and inhibition of inflammatory edema, pro-inflammatory cytokines and hematological, biochemical and histological changes prove I. batatas therapeutic potential as an antiinflammatory and antiarthritic agent.

摘要

背景

Ipomoea batatas L. Lam. 是一种功能性食品,属于旋花科。当地社区将其用作抗炎、壮阳、抗哮喘、滋补、抗肿瘤、抗贫血和抗糖尿病药物。本研究旨在评估其抗炎和抗关节炎潜力。

方法

干燥的 I. batatas 块茎和根粉末分别用乙酸乙酯(IPT-EA、IPR-EA)和甲醇(IPT-M、IPR-M)提取。测试这些提取物的总酚和类黄酮含量(TPC 和 TFC)、HPLC 指纹图谱、多维体外和体内抗氧化潜力以及白蛋白变性抑制。在 Sprague-Dawley 大鼠上以 300mg/kg 体重的剂量进行角叉菜胶诱导的爪肿胀、巴豆油诱导的耳和肛门肿胀抑制以及完全弗氏佐剂(CFA)诱导的抗关节炎测定。评估血清白细胞介素 IL-1β 和 IL-6 以及一氧化氮(NO)水平,以衡量炎症抑制程度。

结果

IPR-EA 提取物中 TPC(319.81±14.20μg GAE/mg 干提取物)和 TFC(208.77±9.09μg QE/mg DE)含量最高。IPT-EA 和 IPR-EA 分别产生芦丁(7.3±1.12 和 4.5±0.55μg/mg DE)、咖啡酸(1.60±0.25 和 2.17±0.26μg/mg DE)和杨梅素(2.7±0.14 和 1.01±0.08μg/mg DE)的最大量。所有提取物在体外抗氧化测定中均表现出剂量依赖性反应。与布洛芬(79.48±4.71%)相比,IPT-EA 对白蛋白变性的抑制作用最好(76.92±3.07%)。IPR-EA 在角叉菜胶诱导的爪肿胀模型(79.11±5.47%)和巴豆油诱导的耳和肛门肿胀(72.01±7.80%和 70.80±4.94%)中表现出最高的肿胀抑制作用。与布洛芬相比,IPR-EA 对 CFA 诱导的关节炎肿胀和关节炎评分有显著抑制作用。IPR-EA 和 IPT-EA 分别显示出对促炎细胞因子(IL-1β、IL-6)和 NO 水平的抑制作用。

结论

这些结果表明,Ipomoea batatas 中多酚和植物成分的丰富度可改善急性和慢性炎症的氧化应激和炎症。剂量依赖性抗氧化潜力以及抑制炎症性水肿、促炎细胞因子以及血液学、生化和组织学变化证明了 I. batatas 作为抗炎和抗关节炎药物的治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73eb/6045844/5baa02a0c6dd/12906_2018_2279_Fig9_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73eb/6045844/5baa02a0c6dd/12906_2018_2279_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73eb/6045844/5502b8a7954d/12906_2018_2279_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73eb/6045844/63aa445ba464/12906_2018_2279_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73eb/6045844/a123da5ae648/12906_2018_2279_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73eb/6045844/a0d20c8bfb95/12906_2018_2279_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73eb/6045844/5baa02a0c6dd/12906_2018_2279_Fig9_HTML.jpg

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