Department of Pharmacology and Therapeutics, Faculty of Pharmacy, Health Sciences Center, Kuwait University, P.O. Box 24923, 13110, Safat, Kuwait.
Inflammopharmacology. 2013 Feb;21(1):1-9. doi: 10.1007/s10787-012-0137-5. Epub 2012 Apr 17.
Cardiovascular diseases are the prime cause of death in the world. The kallikrein-kinin system has been implicated in the pathophysiology of the vascular smooth muscle and cardiac dysfunctions. In recent years, numerous observations obtained from clinical and experimental models of diabetes, hypertension, cardiac failure, ischemia, myocardial infarction and left ventricular hypertrophy, have suggested that the reduced activity of the local kallikrein-kinin system may be instrumental for the induction of cardiovascular-related diseases. The cardioprotective actions of the angiotensin-converting enzyme inhibitors are primarily dependent on protecting the kinin-forming components, which may cause regression of the left ventricular hypertrophy in hypertensive situations. The ability of kallikrein gene delivery to produce a wide spectrum of beneficial effects makes it an excellent candidate in treating hypertension, cardiovascular and renal diseases. In addition, stable kinin agonists may also be available in the future as therapeutic agents for cardiovascular and renal disorders.
心血管疾病是世界上主要的死亡原因。激肽释放酶-激肽系统与血管平滑肌和心脏功能障碍的病理生理学有关。近年来,从糖尿病、高血压、心力衰竭、缺血、心肌梗死和左心室肥厚的临床和实验模型中获得的大量观察结果表明,局部激肽释放酶-激肽系统活性降低可能是诱导心血管相关疾病的原因。血管紧张素转换酶抑制剂的心脏保护作用主要依赖于保护形成激肽的成分,这可能导致高血压情况下左心室肥厚的消退。激肽原基因传递产生广泛有益作用的能力使其成为治疗高血压、心血管和肾脏疾病的理想候选药物。此外,稳定的激肽激动剂也可能在未来作为心血管和肾脏疾病的治疗药物。