期刊文献+

海洋生物来源血管紧张素转换酶抑制肽的研究进展 被引量:4

Review on angiotensin converting enzyme inhibitory peptides from marine organisms
下载PDF
导出
摘要 血管紧张素转化酶(angiotensin converting enzyme,ACE)抑制剂通过抑制ACE活性能够降低血压。目前人工合成ACE抑制药物已开发并应用到降血压的治疗中,但会带来多种副作用。食源性ACE抑制肽与合成抑制剂相比因其副作用小、安全性高等特点,成为ACE抑制肽研究的热点。由于独特的生活环境与巨大的存在数量,海洋生物具有与陆地生物截然不同的化学结构及丰富的生物活性成分。海洋生物来源ACE抑制肽的研究为食源性ACE抑制肽的筛选提供了基础。本文结合海洋生物来源ACE抑制肽的作用机制及制备流程,对鱼类、软体动物、虾类、藻类及海绵、海蜇、粗刺参等不同生物来源的ACE抑制肽制备工艺进行了综述,并对海洋生物的综合开发利用进行了概括。 Angiotensin converting enzyme(ACE) inhibitors can reduce blood pressure by inhibiting ACE activity. At present, synthetic ACE inhibitors have been developed and applied to the treatment of blood pressure lowering, but will bring many side effects. Compared with synthetic inhibitors, foodborne ACE inhibitory peptides have become a hotspot in the research of ACE inhibitory peptides because of their less side-effects and high safety. Because of its unique living environment and large number of living organisms, marine organisms have distinct chemical structures and abundant bioactive components from terrestrial organisms. The study of ACE inhibitory peptides from marine organisms provides a basis for the screening of foodborne ACE inhibitory peptides. Based on the mechanism and preparation process of ACE inhibitory peptides from marine organisms, this paper reviewed the preparation process of ACE inhibitory peptides from different biological sources, such as fish, molluscs, shrimp, algae and sponges, jellyfish, sea cucumber, etc, and the comprehensive development and utilization of marine organisms were summarized.
作者 颜泽 姜燕蓉 刘畅 熊笑妍 张猛 孙志远 闫玉莹 赵慧 YAN Ze;JIANG Yan-Rong;LIU Chang;XIONG Xiao-Yan;ZHANG Meng;SUN Zhi-Yuan;YAN Yu-Ying;ZHAO Hui(College of Food Science and Engineering, Dalian Ocean University, Dalian 116021, China)
出处 《食品安全质量检测学报》 CAS 2018年第8期1743-1749,共7页 Journal of Food Safety and Quality
基金 国家海洋公益性行业科研专项(201505030-4)~~
关键词 血管紧张素转化酶抑制肽 制备 降血压 angiotensin converting enzyme inhibitory peptide preparation lowering blood pressure
  • 相关文献

参考文献8

二级参考文献105

共引文献56

同被引文献33

引证文献4

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部