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Glucocorticoids are active players and therapeutic targets in atherosclerotic cardiovascular disease

机译:糖皮质激素是动脉粥样硬化心血管疾病的活跃球员和治疗靶标

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Adrenal-derived glucocorticoids mediate the physiological response to stress. Chronic disturbances in glucocorticoid homeostasis, i.e. in Addison's and Cushing's disease patients, predispose to the development of atherosclerotic cardiovascular disease. Here we review preclinical and clinical findings regarding the relation between changes in plasma glucocorticoid levels and the atherosclerosis extent. It appears that, although the altered glucocorticoid function can in most cases be restored in the different patient groups, current therapies do not necessarily reverse the associated risk for atherosclerotic cardiovascular disease. In our opinion much attention should therefore be given to the development of a Cushing's disease mouse model that can (1) effectively replicate the effect of hypercortisolemia on atherosclerosis outcome observed in humans and (2) be used to investigate, in a preclinical setting, the relative impact on atherosclerosis susceptibility of already available (e.g. metyrapone) and potentially novel (i.e. SR-BI activity modulators) therapeutic agents that target the adrenal glucocorticoid output.
机译:肾上腺素衍生的糖皮质激素介导对压力的生理反应。糖皮质激素稳态的慢性紊乱,即在Addison和Cushing的疾病患者中,易于动脉粥样硬化心血管疾病的发展。在这里,我们审查了关于血浆糖皮质激素水平和动脉粥样硬化程度之间的关系的临床前和临床调查结果。似乎,尽管在大多数情况下,在大多数情况下可以在不同的患者组中恢复改变的糖皮质激素功能,但目前的疗法不一定逆转动脉粥样硬化心血管疾病的相关风险。因此,在我们看来,应注意,在临床前,可以有效地赋予含有(1)的缓冲疾病小鼠模型的疾病小鼠模型的发展,以(1)在人类和(2)中观察到的人类粥样硬化症的影响,以临床前设置,对已经可用的动脉粥样硬化易感性的相对影响(例如梅罗布酮)和潜在的新(即SR-BI活性调节剂)治疗剂,其靶向肾上腺激素输出。

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