Regoli D
Sem Hop. 1984 Mar 29;60(14):987-1002.
Polypeptides are endogenous agents, involved in the regulation of many physiologic functions and the pathogenesis of several diseases. Polypeptide antagonists form a group of new chemical entities which may provide valid therapeutic agents. Some polypeptides (angiotensin, kinins) are released through the action of proteolytic enzymes (renin, kallikreins) and act as hormones or autacoids; others (substance P, neurotensin) are synthetized by nervous cells to serve as neurotransmitters or neuromodulators. The main homeostatic role of the renin-angiotensin system is to uphold high systemic arterial blood pressure. Overproduction of renin and insufficient checking of renin secretion are among the most common causes of arterial hypertension. Several forms of arterial hypertension (neurovascular, idiopathic) benefit from a reduction in renin-angiotensin system activity. This is achieved either through decreasing renin secretion, by inhibiting conversion of angiotensin I into angiotensin II, or through blocking the peripheral actions (at the receptor sites) of angiotensin II. Renin secretion is very significantly reduced by beta-blocking agents (propranolol); conversion of angiotensin I into angiotensin II is inhibited by teprotide, captopril and their derivatives; peripheral actions of angiotensin II are blocked by saralasin. Bradykinin and related agents produce vasodilation, increase vascular permeability and stimulate pain fibers. Kinins thus reproduce the cardinal features of inflammation and are held to be mediators of the inflammatory reaction. The substance P neuropeptide is found in the brain and bowel; it may act as a transmitter of the sensation of pain at the spinal cord and central nervous system sites. Among other effects outside of the brain, substance P is a potent vasodilator and inhibits renin secretion. Neurotensin is a neuropeptide which produces hypothermia, muscular relaxation and analgesia. Outside of the brain, this peptide is involved in the regulation of gastric secretion, intestinal motility and insulin and glucagon secretion. The vasoactive intestinal peptide, found in certain cholinergic nerve endings, is a large peptide which inhibits gastric secretion, intestinal motility and vascular tone.
多肽是内源性物质,参与多种生理功能的调节以及多种疾病的发病过程。多肽拮抗剂构成了一类新的化学实体,可能成为有效的治疗药物。一些多肽(如血管紧张素、激肽)通过蛋白水解酶(肾素、激肽释放酶)的作用释放出来,作为激素或局部激素发挥作用;其他多肽(如P物质、神经降压素)由神经细胞合成,用作神经递质或神经调节剂。肾素-血管紧张素系统的主要稳态作用是维持较高的体循环动脉血压。肾素分泌过多以及对肾素分泌的抑制不足是动脉高血压最常见的原因之一。几种形式的动脉高血压(神经血管性、特发性)可通过降低肾素-血管紧张素系统活性而获益。这可以通过减少肾素分泌、抑制血管紧张素I转化为血管紧张素II或通过阻断血管紧张素II的外周作用(在受体部位)来实现。β受体阻滞剂(普萘洛尔)可显著减少肾素分泌;替普罗肽、卡托普利及其衍生物可抑制血管紧张素I转化为血管紧张素II;沙拉新可阻断血管紧张素II的外周作用。缓激肽及相关物质可引起血管舒张、增加血管通透性并刺激痛觉纤维。因此,激肽再现了炎症的主要特征,被认为是炎症反应的介质。P物质神经肽存在于脑和肠道中;它可能在脊髓和中枢神经系统部位作为痛觉的传递者。在脑外的其他作用中,P物质是一种强效血管舒张剂,并抑制肾素分泌。神经降压素是一种神经肽,可引起体温过低、肌肉松弛和镇痛。在脑外,这种肽参与胃分泌、肠道蠕动以及胰岛素和胰高血糖素分泌的调节。存在于某些胆碱能神经末梢的血管活性肠肽是一种大肽,可抑制胃分泌、肠道蠕动和血管张力。