荆芥主要化合物的抗高血糖活性研究

S. Escandón-Rivera, A. Pérez-Vásquez, A. Navarrete, M. Hernandez, E. Linares, R. Bye, R. Mata
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引用次数: 13

摘要

在正常和烟酰胺/链脲霉素(NA/STZ, 40/100 mg/kg)高血糖小鼠的口服糖耐量试验(OSTT, 3 g/kg)中,输注Calea的主要成分去甲基异绿callin(1)和caleins A(4)和caleins C (5) (3.16-31.6 mg/kg, p.o.)可控制餐后葡萄糖水平。其效果与阿卡波糖(5 mg/kg)相当。在分离1、4和5的过程中,获得了4种以前未报道的植物代谢产物,即6-乙酰基-5-羟基-2-甲基-2-羟甲基- 2h -chromene (3), herniarin (6), scoparone(7)和4 ',7-dimethylapigenin(8)。此外,通过x射线分析证实了calein C(5)的结构。该物种精油的药理评价(31.6-316.2 mg/kg, p.o.)也引起了OSTT期间血糖水平的重要降低。气相色谱-质谱联用(GC-MS)对顶空固相微萃取(HS-SPME)吸附的化合物和加氢蒸馏得到的活性精油进行分析,发现其中以铬1为主要成分(19.92%);其中倍半萜类含量最高,为55.67%,分别为姜黄烯(7.10%)、匙硫酚(12.95%)和石竹烯氧化物(13.0%)。建立了一种高效液相色谱(HPLC)定量测定铬1和6-羟基乙酰基-5-羟基-2,2-二甲基- 2h -铬(2)的方法,并按标准方案进行了验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-Hyperglycemic Activity of Major Compounds from Calea ternifolia
Demethylisoencecalin (1) and caleins A (4) and C (5) (3.16–31.6 mg/kg, p.o.), the major components from an infusion of Calea ternifolia controlled postprandial glucose levels during an oral sucrose tolerance test (OSTT, 3 g/kg) in normal and nicotinamide/streptozotocin (NA/STZ, 40/100 mg/kg) hyperglicemic mice. The effects were comparable to those of acarbose (5 mg/kg). During the isolation of 1, 4, and 5, four additional metabolites not previously reported for the plant, were obtained, namely 6-acetyl-5-hydroxy-2-methyl-2-hydroxymethyl-2H-chromene (3), herniarin (6), scoparone (7), and 4′,7-dimethylapigenin (8). In addition, the structure of calein C (5) was confirmed by X-ray analysis. Pharmacological evaluation of the essential oil of the species (31.6–316.2 mg/kg, p.o.) provoked also an important decrement of blood glucose levels during an OSTT. Gas chromatography coupled with mass spectrometry (GC-MS) analysis of the headspace solid phase microextraction (HS-SPME)-adsorbed compounds and active essential oil obtained by hydrodistillation revealed that chromene 1 was the major component (19.92%); sesquiterpenes represented the highest percentage of the essential oil content (55.67%) and included curcumene (7.10%), spathulenol (12.95%) and caryophyllene oxide (13.0%). A suitable High Performance Liquid Chromatography (HPLC) method for quantifying chromenes 1 and 6-hydroxyacetyl-5-hydroxy-2,2-dimethyl-2H-chromene (2) was developed and validated according to standard protocols.
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