Unit of Physiology, Department of Health Sciences, University of Jaén, 23071 Jaén, Spain.
Curr Med Chem. 2013;20(10):1313-22. doi: 10.2174/0929867311320100008.
Although the renin-angiotensin system (RAS) is already an old acquaintance, there are often exciting discoveries that improve our knowledge of it and open new therapeutic possibilities. Moreover, well-established drugs, such as angiotensin-converting enzyme inhibitors (ACEI), angiotensin receptor blockers (ARB), or beta-blockers, show that their mechanism of action may be the result of parallel pathways other than the ones initially established. A detailed analysis of the RAS can be carried out in part through the study of the enzymes, named angiotensinases, involved in its cascade, whose activity is a reflection of the functionality of their peptide substrates. The study of these enzymes offers the possibility of controlling the effects of angiotensins through various pharmacological manipulations. For example, angiotensinase inhibitors or activators are being used or have been proposed as antihypertensive agents. They have also been suggested as analgesic and antidepressant drugs or targets for drug development against different pathologies such as Alzheimer's disease, epilepsy or ischemia. On the other hand, the analysis of brain asymmetry has revealed surprising results about the laterality of central and peripheral components of the RAS. Such studies indicate that the neurovisceral integration, already proposed by Claude Bernard (1867) should also be analyzed from a bilateral perspective. In this review, the RAS and the role of various angiotensinases implicated in the cascade are revisited. Therapeutic strategies involving some components of the RAS with an unusual vision resulting from a bilateral perspective added to their study are discussed.
尽管肾素-血管紧张素系统(RAS)已经是一个老相识,但它经常有令人兴奋的发现,这些发现提高了我们对它的认识,并开辟了新的治疗可能性。此外,已被广泛应用的药物,如血管紧张素转换酶抑制剂(ACEI)、血管紧张素受体阻滞剂(ARB)或β受体阻滞剂,表明它们的作用机制可能是最初确定的途径之外的其他平行途径的结果。对 RAS 的详细分析可以部分通过研究其级联反应中涉及的酶,即血管紧张素酶来进行,其活性反映了其肽底物的功能。对这些酶的研究为通过各种药理学手段来控制血管紧张素的作用提供了可能性。例如,血管紧张素酶抑制剂或激活剂被用作或被提议作为抗高血压药物。它们还被提议作为镇痛和抗抑郁药物,或作为针对阿尔茨海默病、癫痫或缺血等不同病理的药物开发的靶点。另一方面,大脑不对称性的分析揭示了 RAS 的中枢和外周成分的偏侧性的惊人结果。这些研究表明,Claude Bernard(1867 年)提出的神经内脏整合也应该从双侧的角度进行分析。在这篇综述中,重新审视了 RAS 及其在级联反应中涉及的各种血管紧张素酶的作用。讨论了涉及 RAS 的一些成分的治疗策略,这些策略从双侧的角度来看具有不寻常的视野,并增加了对它们的研究。