Key Laboratory of Targeted Intervention of Cardiovascular Disease, Collaborative Innovation Center for Cardiovascular Disease Translational Medicine, Department of Physiology, Nanjing Medical University, Nanjing, Jiangsu, 211166, China.
Emergency Department, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, 210011, China.
J Physiol Biochem. 2024 Aug;80(3):585-598. doi: 10.1007/s13105-024-01034-x. Epub 2024 Jul 15.
Isoleucine-proline-proline (Ile-Pro-Pro, IPP) is a natural food source tripeptide that inhibits angiotensin-converting enzyme (ACE) activity. The aim of this study was to determine the central and peripheral roles of IPP in attenuating sympathetic activity, oxidative stress and hypertension. Male Sprague-Dawley rats were subjected to sham-operated surgery (Sham) or two-kidney one-clip (2K1C) surgery to induce renovascular hypertension. Renal sympathetic nerve activity and blood pressure were recorded. Bilateral microinjections of IPP to hypothalamic paraventricular nucleus (PVN) attenuated sympathetic activity (-16.1 ± 2.5%, P < 0.001) and hypertension (-8.7 ± 1.5 mmHg, P < 0.01) in 2K1C rats by inhibiting ACE activity and subsequent angiotensin II and superoxide production in the PVN. Intravenous injections of IPP also attenuated sympathetic activity (-15.1 ± 2.1%, P < 0.001) and hypertension (-16.8 ± 2.3 mmHg, P < 0.001) via inhibiting ACE activity and oxidative stress in both PVN and arteries of 2K1C rats. The duration of the effects of the intravenous IPP was longer than those of the PVN microinjection, but the sympatho-inhibitory effect of intravenous injections occurred later than that of the PVN microinjection. Intraperitoneal injection of IPP (400 pmol/day for 20 days) attenuated hypertension and vascular remodeling via inhibiting ACE activity and oxidative stress in both PVN and arteries of 2K1C rats. These results indicate that IPP attenuates hypertension and sympathetic activity by inhibiting ACE activity and oxidative stress. The sympathoinhibitory effect of peripheral IPP is mainly caused by the ACE inhibition in PVN, and the antihypertensive effect is related to the sympathoinhibition and the arterial ACE inhibition. Long-term intraperitoneal IPP therapy attenuates hypertension, oxidative stress and vascular remodeling.
异亮氨酸-脯氨酸-脯氨酸(Ile-Pro-Pro,IPP)是一种天然的食物来源三肽,可抑制血管紧张素转换酶(ACE)的活性。本研究旨在确定 IPP 在减轻交感神经活性、氧化应激和高血压中的中枢和外周作用。雄性 Sprague-Dawley 大鼠接受假手术(Sham)或双肾一夹(2K1C)手术以诱导肾血管性高血压。记录肾交感神经活性和血压。IPP 双侧下丘脑室旁核(PVN)微量注射可通过抑制 ACE 活性和随后 PVN 中血管紧张素 II 和超氧化物的产生,减轻 2K1C 大鼠的交感神经活性(-16.1±2.5%,P<0.001)和高血压(-8.7±1.5mmHg,P<0.01)。静脉注射 IPP 还可通过抑制 ACE 活性和 2K1C 大鼠 PVN 和动脉中的氧化应激,减轻交感神经活性(-15.1±2.1%,P<0.001)和高血压(-16.8±2.3mmHg,P<0.001)。静脉注射 IPP 的作用持续时间长于 PVN 微量注射,但静脉注射的交感神经抑制作用发生时间晚于 PVN 微量注射。腹腔注射 IPP(400pmol/天,持续 20 天)可通过抑制 2K1C 大鼠 PVN 和动脉中的 ACE 活性和氧化应激,减轻高血压和血管重塑。这些结果表明,IPP 通过抑制 ACE 活性和氧化应激来减轻高血压和交感神经活性。外周 IPP 的交感神经抑制作用主要是由 PVN 中的 ACE 抑制引起的,降压作用与交感神经抑制和动脉 ACE 抑制有关。长期腹腔内 IPP 治疗可减轻高血压、氧化应激和血管重塑。