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南极磷虾尾肉水解物中降压肽的分离与鉴定

Isolation and identification of antihypertensive peptides from antarctic krill tail meat hydrolysate.

作者信息

Hatanaka Akimasa, Miyahara Hiroko, Suzuki Ken Ichi, Sato Seizo

机构信息

Central Research Laboratories of Nippon Suisan Kaisha Ltd., 559-6 Kitano-Machi, Hachioji, Tokyo 192-0906, Japan.

出版信息

J Food Sci. 2009 May-Jul;74(4):H116-20. doi: 10.1111/j.1750-3841.2009.01138.x.

Abstract

Antarctic krill (Euphausia superba) obtained from the huge biomass in Antarctic waters is an important food product in Japan. Antarctic krill peptide powder (AKPP) prepared from the tail meat by enzymatic hydrolysis significantly decreased the systolic blood pressure in spontaneously hypertensive rats by a single oral administration (1, 10, or 100 mg). Presumably, the effect of AKPP was through inhibition of the conversion of angiotensin, which mediates blood pressure elevation, from its inactive propeptide to the mature angiotensin. Two potent angiotensin I-converting enzyme (ACE) inhibitory peptides were isolated from AKPP by high-performance liquid chromatography (HPLC) and identified as Val-Trp (IC(50)= 2.75 microg/mL; 12.9 microM) and Leu-Lys-Tyr (IC(50)= 4.26 microg/mL; 10.1 microM). Val-Trp and Leu-Lys-Tyr comprised 0.025%+/- 0.0023% (w/w) and 0.018%+/- 0.0023% (w/w) of AKPP, respectively, as measured by electrospray ionization mass spectrometry (ESI-MS). The contributions of Val-Trp and Leu-Lys-Tyr to the ACE inhibitor activity of AKPP were 17.7%+/- 1.60% and 8.04%+/- 1.03%, respectively, suggesting that these 2 peptides constitute a substantial portion of the overall ACE inhibitor potential of AKPP.

摘要

从南极海域庞大生物量中获取的南极磷虾(Euphausia superba)是日本一种重要的食品。通过酶解从尾肉制备的南极磷虾肽粉(AKPP)单次口服给药(1、10或100毫克)可显著降低自发性高血压大鼠的收缩压。据推测,AKPP的作用是通过抑制介导血压升高的血管紧张素从无活性前体肽转化为成熟血管紧张素。通过高效液相色谱(HPLC)从AKPP中分离出两种有效的血管紧张素I转换酶(ACE)抑制肽,鉴定为Val-Trp(IC50 = 2.75微克/毫升;12.9微摩尔)和Leu-Lys-Tyr(IC50 = 4.26微克/毫升;10.1微摩尔)。通过电喷雾电离质谱(ESI-MS)测定,Val-Trp和Leu-Lys-Tyr分别占AKPP的0.025%±0.0023%(w/w)和0.018%±0.0023%(w/w)。Val-Trp和Leu-Lys-Tyr对AKPP的ACE抑制活性的贡献分别为17.7%±1.60%和8.04%±1.03%,表明这两种肽构成了AKPP总体ACE抑制潜力的很大一部分。

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