Molecular Pathology Unit, Cancer Research Centre, Institute for Medical Research, National Institutes of Health, Ministry of Health Malaysia, Setia Alam, Shah Alam 40170, Malaysia.
Molecules. 2023 Jun 2;28(11):4532. doi: 10.3390/molecules28114532.
Despite many publications related to the identification of new angiotensin-I-converting enzyme (ACE) inhibitors, especially peptides from natural products, the actual reason/s for why new ACE inhibitors need to be discovered are yet to be fully understood. New ACE inhibitors are pivotal to address serious side effects caused by commercially available ACE inhibitors in hypertensive patients. Despite the effectiveness of commercial ACE inhibitors, due to these side effects, doctors often prescribe angiotensin receptor blockers (ARBs). Recent evidence has shown the benefits of ACE inhibitors over ARBs in hypertensive patients and hypertensive-diabetes mellitus patients. In order to address these side effects, the somatic ACE's enzyme structures need to be revisited. The peptides isolated from the natural products need to be verified for their stability against ACE and several important gastrointestinal enzymes. The stable peptides sequence with the presence of favourable ACE inhibitory-related amino-acids, such as tryptophan (W), at the C-terminal need to be subjected to molecular docking and dynamics analyses for selecting ACE inhibitory peptide/s with C-domain-specific inhibition instead of both C- and N-domains' inhibition. This strategy will help to reduce the accumulation of bradykinin, the driving factor behind the formation of the side effects.
尽管有许多关于鉴定新血管紧张素转化酶 (ACE) 抑制剂的出版物,特别是来自天然产物的肽,但是仍未完全了解为何需要发现新的 ACE 抑制剂。新的 ACE 抑制剂对于解决高血压患者中商业上可用的 ACE 抑制剂引起的严重副作用至关重要。尽管商业 ACE 抑制剂有效,但由于这些副作用,医生通常会开血管紧张素受体阻滞剂 (ARB)。最近的证据表明,ACE 抑制剂在高血压患者和高血压糖尿病患者中的益处优于 ARB。为了解决这些副作用,需要重新审视体细胞 ACE 的酶结构。需要验证从天然产物中分离出的肽对 ACE 和几种重要的胃肠道酶的稳定性。具有有利的 ACE 抑制相关氨基酸(如色氨酸(W))的稳定肽序列在 C 末端,需要进行分子对接和动力学分析,以选择具有 C 结构域特异性抑制而不是 C 和 N 结构域抑制的 ACE 抑制肽。这种策略将有助于减少缓激肽的积累,缓激肽是形成副作用的驱动因素。