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Protective effect of the inhibition of the renin-angiotensin system on aging.

机译:抑制肾素-血管紧张素系统对衰老的保护作用。

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Experimental studies indicate that chronic long-term inhibition of the renin-angiotensin system (RAS) can prevent most of the deleterious effects due to aging in the cardiovascular system and in the kidney of the normal mouse and rat. In this review, all the information available on this subject provided by several studies performed by our research group during the last years is been described. Treatment was initiated either after weaning or at 12 months of age that is about half the normal life span of the rat. A converting enzyme inhibitor: enalapril or an angiotensin II type 1 (AT1) receptor blocker: losartan were used to inhibit the RAS. Cognitive behaviour, emotionality, and locomotor activity were also determined at 10 and 18 months of age in treated since weaning and untreated control rats to elucidate the participation of angiotensin II in memory disfunction. A similar observation was obtained in animals treated from 12 to 18 months of age. Results have demonstrated a significant protective effect on the function and the structure of the cardiovascular system, the kidney and the brain in all the treated animals. Damage observed at 12 months of age was not very significant, but treatment stop further deterioration that was evident in untreated animals. The similarity of the results detected with either enalapril or losartan treatment, clearly indicates that most of the effects are exerted through AT1 receptors. Analysis of the nitric oxide and antioxidant enzymes systems suggest that the protective effect is related to an antioxidant action of the RAS inhibitors and a reduced formation of reactive oxygen species. AngII inhibition might produce changes in the mechanisms of oxidative stress specially at the mitochondrial level. Prevention of mitochondrial decrease and/or damage would be related with the delay of the normal aging process.
机译:实验研究表明,长期抑制肾素-血管紧张素系统(RAS)可以预防由于正常小鼠和大鼠的心血管系统以及肾脏中的衰老而引起的大部分有害作用。在这篇综述中,描述了由我们的研究小组在过去几年中进行的几项研究提供的关于该主题的所有可用信息。在断奶后或在12个月大时开始治疗,大约是大鼠正常寿命的一半。使用转化酶抑制剂:依那普利或1型血管紧张素II(AT1)受体阻滞剂:氯沙坦来抑制RAS。自断奶和未治疗的对照大鼠阐明血管紧张素II参与记忆障碍以来,在治疗的10个月和18个月时还确定了认知行为,情感和运动能力。在12至18个月大的动物中也获得了类似的观察结果。结果表明,在所有治疗的动物中,其对心血管系统,肾脏和大脑的功能和结构具有显着的保护作用。在12个月大时观察到的损害不是很明显,但是治疗阻止了进一步恶化,这在未治疗的动物中很明显。用依那普利或氯沙坦治疗检测到的结果相似,清楚地表明,大多数作用是通过AT1受体发挥的。对一氧化氮和抗氧化酶系统的分析表明,保护作用与RAS抑制剂的抗氧化作用和活性氧物种的形成减少有关。 AngII抑制可能会导致氧化应激机制的改变,特别是在线粒体水平上。防止线粒体减少和/或损伤与正常衰老过程的延迟有关。

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