天然产物研究与开发 ›› 2025, Vol. 37 ›› Issue (6): 1096-1103.doi: 10.16333/j.1001-6880.2025.6.013 cstr: 32307.14.1001-6880.2025.6.013

• 开发研究 • 上一篇    下一篇

恰玛古不同极性萃取部位体外抗氧化及护肝活性研究

梁钦兰1,胡梦颖2,陈 莉1,王 凡1,王欣茹1,杨晓君1*,哈木拉提·哈斯木2*   

  1. 1新疆农业大学食品科学与药学学院,乌鲁木齐830052;2新疆维吾尔自治区药物研究院,乌鲁木齐830034
  • 出版日期:2025-06-25 发布日期:2025-06-25
  • 基金资助:
    自治区重点研发计划(2022B02037-2)

Antioxidant and hepatoprotective activities of different polar parts of Brassica rapa L. in vitro and in vivo

LIANG Qin-lan1,HU Meng-ying2,CHEN Li1,WANG Fan1,WANG Xin-ru1,YANG Xiao-jun1*,HASIMU Hamulati2*    

  1. 1School of Food Science and Pharmacy,Xinjiang Agricultural University,Urumqi 830052,China;2 Xinjiang Institute of Materia Medica,Urumqi 830034,China
  • Online:2025-06-25 Published:2025-06-25

摘要:

研究恰玛古不同极性萃取部位体内外抗氧化及肝保护活性,并初步评价其安全性,从而筛选最佳活性部位,为恰玛古的开发利用提供科学参考。本研究通过检测DPPH、ABTS自由基清除能力以及总抗氧化能力(total antioxidative capability,T-AOC);建立四氯化碳(CCl4,0.15%,0.06 mL/10 g)致小鼠肝损伤模型,测定血清中天门冬氨酸氨基转移酶(aspartate transaminase,AST)、丙氨酸氨基转移酶(alanine aminotransferase,ALT)与肝脏匀浆中超氧化物歧化酶(superoxide dsmutase,SOD)、谷胱甘肽过氧化物酶(glutathione peroxidase,GSH-Px)活性,考察恰玛古不同极性萃取部位的体外和体内抗氧化及护肝活性;通过给予小鼠不同极性萃取部位浸膏溶液,连续观察14 d小鼠体征与死亡情况,在实验结束时统计小鼠体重增长,并解剖观察各脏器,评价其毒性反应。结果显示,不同极性萃取部位DPPH、ABTS自由基清除率的IC50值大小顺序为:水混悬萃取部位>石油醚萃取部位>正丁醇萃取部位>乙酸乙酯萃取部位。铁离子抗氧化能力法测定乙酸乙酯与正丁醇萃取部位T-AOC最强。体内实验结果表明,乙酸乙酯和正丁醇萃取部位可明显降低CCl4致小鼠肝损伤模型血清中AST、ALT水平(P<0.05,P<0.01),可显著提高小鼠体内SOD、GSH-Px活性,与模型组比较有显著性差异(P<0.05),病理结果显示,阳性药(联苯双酯滴丸)、乙酸乙酯和正丁醇萃取部位能有效减轻CCl4导致的小鼠急性肝损伤。且小鼠给予恰玛古不同极性萃取部位后,未见急性毒性,提示安全无毒。综上所述,恰玛古不同极性萃取部位中,正丁醇与乙酸乙酯萃取部位体外抗氧化活性较好,且具有良好的体内外抗氧化及护肝效果。

关键词: 恰玛古, 不同极性萃取部位, 抗氧化活性, 护肝活性, 四氯化碳肝损伤

Abstract:

This study aims to investigate the antioxidant and hepatoprotective activities of different polar extraction parts of Brassica rapa L. in vitro and in vivo, and to preliminarily evaluate its safety, so as to screen the best active parts and provide scientific reference for the development and utilization of B. rapa. DPPH, ABTS free radical scavenging ability and total antioxidant capacity (T-AOC) were detected; a mouse model of liver injury induced by carbon tetrachloride (CCl4, 0.15%,0.06 mL/10 g) was established. The activities of aspartate transaminase (AST) and alanine aminotransferase (ALT) in serum and superoxide dsmutase (SOD) and glutathione peroxidase (GSH-Px) in liver homogenate were determined, and the antioxidant and hepatoprotective activities of different polar extracts of B. rapa in vitro and in vivo were investigated. The signs and death of mice were observed continuously for 14 days by giving the extract solution of different polar extraction parts of mice. At the end of the experiment, the weight gain of mice was counted, and the organs were dissected and observed to evaluate their toxic reactions. The results showed that the order of IC50 values of DPPH and ABTS free radical scavenging rates of different polar extraction parts was: water suspension extraction part > petroleum ether extraction part > n-butanol extraction part > ethyl acetate extraction part. Ferric reducing ability of plasma method was used to determine the T-AOC of ethyl acetate and n-butanol extracts. The results of in vivo experiments showed that the ethyl acetate and n-butanol extracts could significantly reduce the levels of AST and ALT in the serum of mice with liver injury induced by CCl4 (P < 0.05,P < 0.01), and significantly increase the activities of SOD and GSH-Px in mice. Compared with the model group, there was a significant difference (P < 0.05). The pathological results showed that the positive drug (bifendate dropping pills), ethyl acetate and n-butanol extracts could effectively reduce the acute liver injury induced by CCl4 in mice. After mice were given different polar extraction parts of B. rapa, no acute toxicity was observed, suggesting that it was safe and non-toxic. In summary, among the different polar extracts of B. rapa, n-butanol and ethyl acetate extracts have better antioxidant activity in vitro, and have good antioxidant and liver protection effects in vivo and in vitro.

Key words: Brassica rapa L., different polar fractions, antioxidant activity, hepatoprotective activity, CCl4-induced liver injury

中图分类号:  R151