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Ontogenetic aspects of hypertension development: analysis in the rat.

机译:高血压发展的个体遗传学方面:在大鼠中的分析。

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In this review, we attempt to outline the age-dependent interactions of principal systems controlling the structure and function of the cardiovascular system in immature rats developing hypertension. We focus our attention on the cardiovascular effects of various pharmacological, nutritional, and behavioral interventions applied at different stages of ontogeny. Several distinct critical periods (developmental windows), in which particular stimuli affect the further development of the cardiovascular phenotype, are specified in the rat. It is evident that short-term transient treatment of genetically hypertensive rats with certain antihypertensive drugs in prepuberty and puberty (at the age of 4-10 wk) has long-term beneficial effects on further development of their cardiovascular apparatus. This juvenile critical period coincides with the period of high susceptibility to the hypertensive effects of increased salt intake. If the hypertensive process develops after this critical period (due to early antihypertensive treatment or late administration of certain hypertensive stimuli, e.g., high salt intake), blood pressure elevation, cardiovascular hypertrophy, connective tissue accumulation, and end-organ damage are considerably attenuated compared with rats developing hypertension during the juvenile critical period. As far as the role of various electrolytes in blood pressure modulation is concerned, prohypertensive effects of dietary Na+ and antihypertensive effects of dietary Ca2+ are enhanced in immature animals, whereas vascular protective and antihypertensive effects of dietary K+ are almost independent of age. At a given level of dietary electrolyte intake, the balance between dietary carbohydrate and fat intake can modify blood pressure even in rats with established hypertension, but dietary protein intake affects the blood pressure development in immature animals only. Dietary protein restriction during gestation, as well as altered mother-offspring interactions in the suckling period, might have important long-term hypertensive consequences. The critical periods (developmental windows) should be respected in the future pharmacological or gene therapy of human hypertension.
机译:在这篇综述中,我们试图概述控制高血压系统的未成熟大鼠心血管系统结构和功能的主要系统的年龄依赖性相互作用。我们将注意力集中在在个体发育的不同阶段应用的各种药理,营养和行为干预措施对心血管的影响。在大鼠中指定了几个不同的关键时期(发育窗口),其中特定的刺激影响了心血管表型的进一步发展。显然,在青春期前和青春期(4-10周龄)使用某些降压药对遗传性高血压大鼠进行短期短暂治疗,对心血管设备的进一步发展具有长期的有益影响。这个少年关键时期与盐摄入量增加对高血压的高敏感性时期相吻合。如果在此关键时期后出现高血压过程(由于早期抗高血压治疗或某些高血压刺激(例如高盐摄入)的后期给药),则与之相比,血压升高,心血管肥大,结缔组织蓄积和终末器官损害会大大减轻在少年危急期大鼠患高血压。就各种电解质在血压调节中的作用而言,日粮Na +的降压作用和日粮Ca2 +的降压作用在未成熟动物中得到增强,而日粮K +的血管保护和降压作用几乎与年龄无关。在给定的饮食电解质摄入水平下,即使在患有高血压的大鼠中,饮食碳水化合物和脂肪摄入之间的平衡也可以改变血压,但饮食蛋白质摄入仅影响未成熟动物的血压发展。妊娠期饮食中蛋白质的限制以及哺乳期母婴间相互作用的改变可能对长期高血压产生重要影响。在人类高血压的未来药理或基因治疗中应考虑关键时期(发育期)。

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