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选定药用、草本和水生植物的抗脂解酶和脂解酶活性,以及一种抗脂解酶化合物的结构阐明。

Anti- and pro-lipase activity of selected medicinal, herbal and aquatic plants, and structure elucidation of an anti-lipase compound.

机构信息

Department of Food Science, Faculty of Food Science and Technology, University Putra Malaysia UPM, Serdang 43400, Selangor, Malaysia.

出版信息

Molecules. 2013 Nov 26;18(12):14651-69. doi: 10.3390/molecules181214651.

Abstract

Plants that help in slowing down the digestion of triacylglycerols (TAGs) in the pancreas and small intestine of humans play an important role in the reduction of obesity. On the other hand, there may be plants or plant parts that stimulate intestinal lipolytic activity, thus contributing to greater TAG assimilation. The aim of this study was to evaluate the aqueous methanolic extracts of ninety eight (98) medicinal, herbal and aquatic plant materials from Malaysia for their effect on porcine pancreatic lipase (PPL) activity and to identify the structure of an anti-lipase compound from one of the sources. The degree of inhibition was also quantified as relative to orlistat activity against PPL (orlistat equivalents). Results revealed that while 19.4% of the extracts were found to have anti-lipase activity ≥80%, 12% were actually found to promote PPL activity. Twenty two percent (22.4%) exhibited moderate inhibition (41%-80%) and 2% were neutral toward PPL activity. The ripe fruit of Averrhoa carambola and the leaves of Archidendron jiringa (Jack) I.C Nielsen L. (jering), Cynometra cauliflora (nam-nam) and Aleurites moluccana (L.) Willd (candle nut/buah keras) had the highest (100%) anti-lipase activity and are equivalent to 0.11 µg orlistat/mL. Plants that stimulated lipase activity included Pimpinella anisum L. (aniseed/jintan manis), activating the enzyme by 186.5%. Kaempferol 3-O-rhamnoside was isolated from the ethyl acetate fraction of C. cauliflora leaves and found to be an active lipase inhibitor. The structure was elucidated using 1H-NMR, 13C-NMR and 2D-NMR analyses.

摘要

有助于减缓人类胰腺和小肠中三酰基甘油(TAGs)消化的植物在肥胖减轻中起着重要作用。另一方面,可能有植物或植物部分刺激肠道脂肪酶活性,从而有助于更大程度地吸收 TAG。本研究的目的是评估来自马来西亚的 98 种药用、草药和水生植物材料的水甲醇提取物对猪胰脂肪酶(PPL)活性的影响,并从其中一种来源鉴定出一种抗脂肪酶化合物的结构。抑制程度也被量化为相对于奥利司他对 PPL 的活性(奥利司他当量)。结果表明,虽然 19.4%的提取物被发现具有≥80%的抗脂肪酶活性,但实际上有 12%的提取物促进了 PPL 活性。22%(22.4%)表现出中度抑制(41%-80%),2%对 PPL 活性呈中性。杨桃的成熟果实和阿肯德龙 jiringa(Jack)I.C Nielsen L.(jering)、Cynometra cauliflora(nam-nam)和 Aleurites moluccana(L.)Willd(candle nut/buah keras)的叶子具有最高的(100%)抗脂肪酶活性,相当于 0.11 µg 奥利司他/mL。刺激脂肪酶活性的植物包括 Pimpinella anisum L.(八角/甜八角),可使酶激活 186.5%。山奈酚 3-O-鼠李糖苷从 C. cauliflora 叶的乙酸乙酯部分中分离出来,被发现是一种有效的脂肪酶抑制剂。使用 1H-NMR、13C-NMR 和 2D-NMR 分析阐明了结构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fad/6270111/c49c141325ff/molecules-18-14651-g001.jpg

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