首页> 外文期刊>Journal of hypertension >The lactotripeptides isoleucine-proline-proline and valine-proline-proline do not inhibit the N-terminal or C-terminal angiotensin converting enzyme active sites in humans.
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The lactotripeptides isoleucine-proline-proline and valine-proline-proline do not inhibit the N-terminal or C-terminal angiotensin converting enzyme active sites in humans.

机译:Lactaphe肽异氨酸 - 脯氨酸 - 脯氨酸和缬氨酸 - 脯氨酸 - 脯氨酸不抑制人类中的N-末端或C末端血管紧张素转化酶活性位点。

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BACKGROUND: The potential blood pressure lowering effect of fermented milk may involve inhibition of angiotensin-converting enzyme (ACE) by dairy lactotripeptides generated during milk fermentation, such as isoleucine-proline-proline (IPP) and valine-proline-proline (VPP). These peptides are weak ACE inhibitors in vitro but it remains unclear whether they inhibit ACE in vivo in humans. OBJECTIVE: To assess in vivo ACE inhibition in individuals given fermented milk over a 7-day period. DESIGN AND METHODS: Twelve healthy normotensive men were given 330 ml of fermented milk once daily from day 1 to day 7 (IPP: 4.5 mg and VPP: 6.6 mg) and a single dose of 50 mg captopril on day 8. ACE inhibition was assessed in vivo by measuring plasma and urine AcSDKP and plasma active renin and in vitro by measuring plasma ACE activity using hippuryl-histidine-leucine. Plasma IPP/VPP concentrations were measured by LC/MS/MS. RESULTS: Plasma IPP concentrations increased slightly and very transiently after fermented milk administration. Plasma VPP concentrations were below the limit of quantification. Fermented milk had no effect on plasma AcSDKP, ACE activity or active renin concentrations on days 1 or 7. Urine AcSDKP excretion underwent a small transient increase. In contrast, plasma and urine AcSDKP increased 7.7-fold and 70-fold, respectively, and plasma ACE activity decreased by 82.3 +/- 16.1% following captopril administration; plasma active renin concentration increased four-fold. CONCLUSION: IPP and VPP were poorly absorbed and rapidly eliminated. They did not inhibit plasma or endothelial ACE in vivo at the selected doses and had no specific effect on the N-terminal or C-terminal ACE domains.
机译:背景:发酵牛奶的潜在血压降低效果可能涉及通过在牛奶发酵过程中产生的乳酸酯素转换酶(ACE)抑制血管紧张素转换酶(ACE),例如异氨酸 - 脯氨酸 - 脯氨酸(IPP)和缬氨酸 - 脯氨酸 - 脯氨酸(VPP)。这些肽是体外弱ACE抑制剂,但仍然尚不清楚它们是否抑制人类体内的王牌。目的:评估在7天内给予发酵牛奶的个体体内ACE抑制。设计和方法:每天1日至第7天(IPP:4.5mg和VPP:6.6mg)和每次给予330毫升发酵牛奶,每次给予120毫升发酵牛奶和第8天的单剂量抑制通过使用Hippulyl组氨酸 - 亮氨酸测量等离子体ACE活性来测量血浆和尿液ACSDKP和血浆活性肾素和体外。通过LC / MS / MS测量血浆IPP / VPP浓度。结果:血浆IPP浓度在发酵牛奶给药后略微且非常瞬时瞬时增加。血浆VPP浓度低于定量限。发酵牛奶对第1或7天的血浆ACSDKP,ACE活性或活性肾素浓度没有影响。尿ACSDKP排泄出现小的瞬态增加。相比之下,血浆和尿液ACSDKP分别增加7.7倍,70倍,血浆ACE活性在卡托普利给药后减少了82.3 +/- 16.1%;血浆活性肾素浓度增加了四倍。结论:IPP和VPP吸收不良,迅速消除。它们在选定剂量上没有抑制体内的血浆或内皮αce,对N-末端或C末端Ace结构域没有具体作用。

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