Hypertension and Vascular Research Division, Department of Internal Medicine, Henry Ford Hospital, Detroit, Michigan, USA.
Compr Physiol. 2011 Apr;1(2):971-93. doi: 10.1002/cphy.c100053.
Autocrine, paracrine, endocrine, and neuroendocrine hormonal systems help regulate cardio-vascular and renal function. Any change in the balance among these systems may result in hypertension and target organ damage, whether the cause is genetic, environmental or a combination of the two. Endocrine and neuroendocrine vasopressor hormones such as the renin-angiotensin system (RAS), aldosterone, and catecholamines are important for regulation of blood pressure and pathogenesis of hypertension and target organ damage. While the role of vasodepressor autacoids such as kinins is not as well defined, there is increasing evidence that they are not only critical to blood pressure and renal function but may also oppose remodeling of the cardiovascular system. Here we will primarily be concerned with kinins, which are oligopeptides containing the aminoacid sequence of bradykinin. They are generated from precursors known as kininogens by enzymes such as tissue (glandular) and plasma kallikrein. Some of the effects of kinins are mediated via autacoids such as eicosanoids, nitric oxide (NO), endothelium-derived hyperpolarizing factor (EDHF), and/or tissue plasminogen activator (tPA). Kinins help protect against cardiac ischemia and play an important part in preconditioning as well as the cardiovascular and renal protective effects of angiotensin-converting enzyme (ACE) and angiotensin type 1 receptor blockers (ARB). But the role of kinins in the pathogenesis of hypertension remains controversial. A study of Utah families revealed that a dominant kallikrein gene expressed as high urinary kallikrein excretion was associated with a decreased risk of essential hypertension. Moreover, researchers have identified a restriction fragment length polymorphism (RFLP) that distinguishes the kallikrein gene family found in one strain of spontaneously hypertensive rats (SHR) from a homologous gene in normotensive Brown Norway rats, and in recombinant inbred substrains derived from these SHR and Brown Norway rats this RFLP cosegregated with an increase in blood pressure. However, humans, rats and mice with a deficiency in one or more components of the kallikrein-kinin-system (KKS) or chronic KKS blockade do not have hypertension. In the kidney, kinins are essential for proper regulation of papillary blood flow and water and sodium excretion. B2-KO mice appear to be more sensitive to the hypertensinogenic effect of salt. Kinins are involved in the acute antihypertensive effects of ACE inhibitors but not their chronic effects (save for mineralocorticoid-salt-induced hypertension). Kinins appear to play a role in the pathogenesis of inflammatory diseases such as arthritis and skin inflammation; they act on innate immunity as mediators of inflammation by promoting maturation of dendritic cells, which activate the body's adaptive immune system and thereby stimulate mechanisms that promote inflammation. On the other hand, kinins acting via NO contribute to the vascular protective effect of ACE inhibitors during neointima formation. In myocardial infarction produced by ischemia/reperfusion, kinins help reduce infarct size following preconditioning or treatment with ACE inhibitors. In heart failure secondary to infarction, the therapeutic effects of ACE inhibitors are partially mediated by kinins via release of NO, while drugs that activate the angiotensin type 2 receptor act in part via kinins and NO. Thus kinins play an important role in regulation of cardiovascular and renal function as well as many of the beneficial effects of ACE inhibitors and ARBs on target organ damage in hypertension.
自分泌、旁分泌、内分泌和神经内分泌激素系统有助于调节心血管和肾功能。这些系统之间的平衡任何变化都可能导致高血压和靶器官损伤,无论其原因是遗传、环境还是两者的结合。内分泌和神经内分泌血管加压素激素,如肾素-血管紧张素系统(RAS)、醛固酮和儿茶酚胺,对于调节血压和高血压及靶器官损伤的发病机制非常重要。虽然血管舒张自分泌物质如激肽的作用没有那么明确,但越来越多的证据表明,它们不仅对血压和肾功能至关重要,而且可能对抗心血管系统的重塑。在这里,我们主要关注激肽,它是含有缓激肽氨基酸序列的寡肽。它们由组织(腺体)和血浆激肽释放酶等酶从激肽原产生。激肽的一些作用是通过自分泌物质介导的,如前列腺素、一氧化氮(NO)、内皮衍生超极化因子(EDHF)和/或组织纤溶酶原激活物(tPA)。激肽有助于预防心肌缺血,并在血管紧张素转换酶(ACE)和血管紧张素 1 型受体阻滞剂(ARB)的预处理以及心血管和肾脏保护作用中发挥重要作用。但是,激肽在高血压发病机制中的作用仍然存在争议。犹他州家庭的一项研究表明,一种表达为高尿激肽排泄的显性激肽释放酶基因与原发性高血压的风险降低有关。此外,研究人员已经鉴定出一种限制片段长度多态性(RFLP),它区分了在自发性高血压大鼠(SHR)中发现的激肽基因家族与正常血压的棕色挪威大鼠中的同源基因,并且在源自这些 SHR 和棕色挪威大鼠的重组近交系中,这种 RFLP 与血压升高相关。然而,缺乏激肽-激肽系统(KKS)的一个或多个成分或慢性 KKS 阻断的人类、大鼠和小鼠没有高血压。在肾脏中,激肽对于调节乳头血流和水钠排泄非常重要。B2-KO 小鼠似乎对盐的高血压生成作用更敏感。激肽参与 ACE 抑制剂的急性降压作用,但不参与其慢性作用(除了盐皮质激素诱导的高血压)。激肽似乎在关节炎和皮肤炎症等炎症性疾病的发病机制中发挥作用;它们作为炎症的介质作用于先天免疫系统,通过促进树突状细胞的成熟来促进炎症,树突状细胞激活机体的适应性免疫系统,从而刺激促进炎症的机制。另一方面,通过 NO 起作用的激肽有助于 ACE 抑制剂在新内膜形成过程中的血管保护作用。在缺血/再灌注引起的心肌梗死中,激肽有助于在预处理或 ACE 抑制剂治疗后减少梗死面积。在梗死后心力衰竭中,ACE 抑制剂的治疗效果部分通过激肽通过释放 NO 介导,而激活血管紧张素 2 受体的药物部分通过激肽和 NO 起作用。因此,激肽在心血管和肾功能的调节以及 ACE 抑制剂和 ARB 在高血压靶器官损伤中的许多有益作用中发挥重要作用。