System deceleration refers to the progressive, age-related reduction in the rate and efficiency of fundamental physiological processes across multiple organ systems, resulting in a measurable slowing of metabolic turnover and reduced adaptive capacity. This phenomenon is a hallmark of senescence, impacting critical functions like cellular repair, hormone synthesis and clearance, and overall systemic responsiveness. It reflects the body’s decreasing ability to maintain robust homeostasis against internal and external stressors.
Origin
This term is a conceptual model used in biogerontology to describe the macro-level manifestation of molecular and cellular aging, such as telomere shortening and mitochondrial dysfunction. It is a way to articulate the clinical observation that older individuals respond more slowly and less vigorously to physiological challenges. The concept provides a framework for understanding the systemic nature of aging.
Mechanism
The mechanism is multi-factorial, driven by cumulative cellular damage, including oxidative stress and glycation, leading to impaired mitochondrial function and reduced endocrine signaling. For instance, the age-related decline in thyroid hormone conversion and clearance contributes to a lower basal metabolic rate. Furthermore, reduced growth hormone secretion diminishes the pace of tissue anabolism and repair, collectively manifesting as a deceleration of systemic function.
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