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为什么慢性肾脏病会进展?进化适应性与适应不良。

Why is chronic kidney disease progressive? Evolutionary adaptations and maladaptations.

作者信息

Chevalier Robert L

机构信息

Department of Pediatrics, The University of Virginia, Charlottesville, Virginia, United States.

出版信息

Am J Physiol Renal Physiol. 2023 Nov 1;325(5):F595-F617. doi: 10.1152/ajprenal.00134.2023. Epub 2023 Sep 7.

Abstract

Despite significant advances in renal physiology, the global prevalence of chronic kidney disease (CKD) continues to increase. The emergence of multicellular organisms gave rise to increasing complexity of life resulting in trade-offs reflecting ancestral adaptations to changing environments. Three evolutionary traits shape CKD over the lifespan: ) variation in nephron number at birth, ) progressive nephron loss with aging, and ) adaptive kidney growth in response to decreased nephron number. Although providing plasticity in adaptation to changing environments, the cell cycle must function within constraints dictated by available energy. Prioritized allocation of energy available through the placenta can restrict fetal nephrogenesis, a risk factor for CKD. Moreover, nephron loss with aging is a consequence of cell senescence, a pathway accelerated by adaptive nephron hypertrophy that maintains metabolic homeostasis at the expense of increased vulnerability to stressors. Driven by reproductive fitness, natural selection operates in early life but diminishes thereafter, leading to an exponential increase in CKD with aging, a product of antagonistic pleiotropy. A deeper understanding of the evolutionary constraints on the cell cycle may lead to manipulation of the balance between progenitor cell renewal and differentiation, regulation of cell senescence, and modulation of the balance between cell proliferation and hypertrophy. Application of an evolutionary perspective may enhance understanding of adaptation and maladaptation by nephrons in the progression of CKD, leading to new therapeutic advances.

摘要

尽管肾脏生理学取得了重大进展,但慢性肾脏病(CKD)的全球患病率仍在持续上升。多细胞生物的出现导致生命复杂性不断增加,从而产生了反映祖先对不断变化环境适应的权衡。在整个生命周期中,有三个进化特征塑造了CKD:1)出生时肾单位数量的差异,2)随着年龄增长肾单位逐渐丧失,以及3)对肾单位数量减少的适应性肾脏生长。尽管细胞周期在适应不断变化的环境中提供了可塑性,但它必须在可用能量所规定的限制范围内发挥作用。通过胎盘获得的能量的优先分配会限制胎儿肾发生,这是CKD的一个危险因素。此外,随着年龄增长肾单位的丧失是细胞衰老的结果,而适应性肾单位肥大加速了这一过程,这种肥大以增加对应激源的易感性为代价维持代谢稳态。受生殖适应性驱动,自然选择在生命早期起作用,但此后会减弱,导致CKD随着年龄呈指数增长,这是拮抗性多效性的产物。对细胞周期进化限制的更深入理解可能会导致对祖细胞更新与分化之间平衡的操纵、细胞衰老的调控以及细胞增殖与肥大之间平衡的调节。应用进化观点可能会增强对CKD进展过程中肾单位适应和适应不良的理解,从而带来新的治疗进展。

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