Vielee Samuel T, Wise John P
Pediatrics Research Institute, Department of Pediatrics, University of Louisville, Louisville, KY 40202, USA.
Department of Pharmacology and Toxicology, University of Louisville, Louisville, KY 40202, USA.
Brain Sci. 2023 Mar 16;13(3):500. doi: 10.3390/brainsci13030500.
Advancements in modern medicine have improved the quality of life across the globe and increased the average lifespan of our population by multiple decades. Current estimates predict by 2030, 12% of the global population will reach a geriatric age and live another 3-4 decades. This swelling geriatric population will place critical stress on healthcare infrastructures due to accompanying increases in age-related diseases and comorbidities. While much research focused on long-lived individuals seeks to answer questions regarding how to age healthier, there is a deficit in research investigating what aspects of our lives accelerate or exacerbate aging. In particular, heavy metals are recognized as a significant threat to human health with links to a plethora of age-related diseases, and have widespread human exposures from occupational, medical, or environmental settings. We believe heavy metals ought to be classified as a class of gerontogens (i.e., chemicals that accelerate biological aging in cells and tissues). Gerontogens may be best studied through their effects on the "Hallmarks of Aging", nine physiological hallmarks demonstrated to occur in aged cells, tissues, and bodies. Evidence suggests that cellular senescence-a permanent growth arrest in cells-is one of the most pertinent hallmarks of aging and is a useful indicator of aging in tissues. Here, we discuss the roles of heavy metals in brain aging. We briefly discuss brain aging in general, then expand upon observations for heavy metals contributing to age-related neurodegenerative disorders. We particularly emphasize the roles and observations of cellular senescence in neurodegenerative diseases. Finally, we discuss the observations for heavy metals inducing cellular senescence. The glaring lack of knowledge about gerontogens and gerontogenic mechanisms necessitates greater research in the field, especially in the context of the global aging crisis.
现代医学的进步提高了全球的生活质量,并使人类的平均寿命延长了数十年。目前的估计预测,到2030年,全球12%的人口将达到老年,并再活3至4十年。由于与年龄相关的疾病和合并症的增加,这一不断膨胀的老年人口将给医疗基础设施带来巨大压力。虽然许多针对长寿个体的研究试图回答如何更健康地衰老的问题,但在研究我们生活中的哪些方面会加速或加剧衰老方面却存在不足。特别是,重金属被认为是对人类健康的重大威胁,与大量与年龄相关的疾病有关,并且在职业、医疗或环境环境中广泛存在于人类接触中。我们认为重金属应该被归类为一类老年源(即加速细胞和组织生物衰老的化学物质)。通过研究老年源对“衰老标志”的影响可能是最好的研究方法,这九个生理标志已被证明会出现在衰老的细胞、组织和身体中。有证据表明,细胞衰老——细胞的永久性生长停滞——是衰老最相关的标志之一,也是组织衰老的一个有用指标。在这里,我们讨论重金属在大脑衰老中的作用。我们首先简要讨论一般的大脑衰老,然后详细阐述重金属对与年龄相关的神经退行性疾病的影响。我们特别强调细胞衰老在神经退行性疾病中的作用和观察结果。最后,我们讨论重金属诱导细胞衰老的观察结果。由于对老年源和老年源机制的了解明显不足,因此该领域需要更多的研究,特别是在全球老龄化危机的背景下。