Hasan K M Mehedi, Rahman Md Shaifur, Arif K M T, Sobhani Mahbub E
Biotechnology and Genetic Engineering Discipline, Khulna University, Bangladesh.
Age (Dordr). 2012 Dec;34(6):1421-33. doi: 10.1007/s11357-011-9319-0. Epub 2011 Oct 5.
Psychological stress has extreme adverse consequences on health. However, the molecular mechanisms that mediate and accelerate the process of aging due to stress hormone are not well defined. This review has focused on diverse molecular paths that come out in response to chronic psychological stress via releasing of excessive glucocorticoids (GCs), involved in the aging process. GCs suppress transcription of nuclear cell adhesion molecules which impair synaptic plasticity, memory formation, and cognitive ability. Again, GCs promote muscle atrophy by means of motivating ubiquitin proteasome system and can repress muscle protein synthesis by inhibition of PI3-kinase/Akt pathway. GCs also inhibit interleukin-2 synthesis through suppressing T cell receptor signal that leads to loss of T cell activation, proliferation, and B-cell activation. Moreover, GCs increase the expression of collagenase-3, RANK ligand, and colony stimulating factor-1 that induce bone resorption. In general, stress-induced GCs can play causal role for aging and age-related disorders.
心理压力对健康有极其不利的影响。然而,介导并加速应激激素导致衰老过程的分子机制尚未完全明确。本综述聚焦于通过释放过量糖皮质激素(GCs)来应对慢性心理压力时出现的多种分子途径,这些途径参与了衰老过程。GCs抑制核细胞粘附分子的转录,这会损害突触可塑性、记忆形成和认知能力。此外,GCs通过激活泛素蛋白酶体系统促进肌肉萎缩,并可通过抑制PI3激酶/Akt途径抑制肌肉蛋白质合成。GCs还通过抑制T细胞受体信号来抑制白细胞介素-2的合成,从而导致T细胞活化、增殖以及B细胞活化的丧失。此外,GCs会增加诱导骨吸收的胶原酶-3、核因子κB受体活化因子配体(RANK ligand)和集落刺激因子-1的表达。一般来说,应激诱导的GCs可能在衰老和与年龄相关的疾病中起因果作用。