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(A) The programmed theory |
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(1) Programmed theory Telomere shortening theory | Aging is the result of a sequential switching of certain genes. Telomere plays a role in the genomic instability with aging. |
(2) Neuroendocrine theory | Biological clocks act through the neurohumoral system to control the pace of aging. |
(3) Immunological theory | The immune system is programmed to decline, which leads to an increased vulnerability to acute and chronic inflammation, resulting in aging and death. |
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(B) The damage or error theory (Nonprogrammed theory) |
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(1) Wear and tear theory | Cells and tissues have vital parts that wear out, that leads to aging. |
(2) Rate of living theory Metabolic theory | The greater a rate of basal oxygen metabolism, the shorter its lifespan. |
(3) Cross-linking theory Glycation theory | The accumulation of modified constituents, such as cross-linked and glycated proteins, damages cells and tissues, resulting in aging. |
(4) Free radical theory Oxidative stress theory Mitochondrial theory | Free radicals and reactive oxygen species (ROS) cause cellular damage and the accumulation of oxidative damage leads to aging. Mitochondria are a main source of ROS and also a target of ROS. |
(5) Somatic DNA damage theory | DNA damages occur continuously in living cells. Most of these damages are repaired, whereas some accumulate, resulting in cellular dysfunction and aging. In particular, damages to mitochondrial DNA lead to mitochondrial dysfunction. |
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