口服从鲣鱼肠中提取的肽通过抑制血管紧张素转换酶来降低自发性高血压大鼠的血压。

H Karaki, M Kuwahara, S Sugano, C Doi, K Doi, N Matsumura, T Shimizu
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引用次数: 0

摘要

1. 从鱼肝和肠自溶产物中提取的肽C111 (gly - val - tyrr - pro - his - lys)和C112 (Ile-Arg-Pro-Val-Gln)在体外抑制血管紧张素转换酶(ACE)活性,ic50分别为1.6微米和1.4微米。我们研究了口服这些肽对血压的影响。2. 在Sprague-Dawley大鼠中,口服这些肽(每个500 mg kg-1体重)可抑制静脉注射血管紧张素I的加压作用。3.在自发性高血压大鼠中,口服这些肽(100-200 mg kg-1体重)显示出抑制作用。4. 这些结果表明,肽C111和C112是口服有效的ACE抑制剂,具有降压作用。
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Oral administration of peptides derived from bonito bowels decreases blood pressure in spontaneously hypertensive rats by inhibiting angiotensin converting enzyme.

1. Peptides C111 (Gly-Val-Tyr-Pro-His-Lys) and C112 (Ile-Arg-Pro-Val-Gln), extracted from the autolysis product of bonito liver and intestine, have been shown to inhibit angiotensin converting enzyme (ACE) activity in vitro with IC50s of 1.6 microM and 1.4 microM, respectively. We examined the effects of oral administration of these peptides on blood pressure. 2. Oral administration of these peptides (500 mg kg-1 body weight each) inhibited the pressor effect of intravenously administered angiotensin I in Sprague-Dawley rats. 3. In spontaneously hypertensive rats, oral administration of these peptides (100-200 mg kg-1 body weight) showed depressor effects. 4. These results suggest that the peptides, C111 and C112, are orally effective ACE inhibitors with hypotensive effect.

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