Theories of Ageing Flashcards
1
Q
Theories of WHY we age:
Wear and Tear - What is it?
Adaptive Evolutionary - What is it?
Non-adaptive Evolutionary - What is Mutation accumulation and Antagonistic Pleiotropic genes?
Disposable Soma theory - What is it?
A
- We are a machine that wears out
- Ageing selectively advantageous to a species
- • Mutation accumulation - Genes expressed after reproduction are lost from evolutionary control
• Antagonistic Pleiotropic genes - Genes have an Early positive effect and a Late negative effect - Organism is a machine that transfers free energy to progeny
o Species specific longevity as they prioritise different thing - e.g. some prioritise fertility while others prioritise maintenance
2
Q
Theories of HOW we age:
System-Level Theories - What is the Neuroendocrine theory?
Cellular-Level Theories - What are the 4 aspects of it?
Genomic Stability - What are the 5 aspects of it?
A
- Functional decrease in neurons and associated hormones (Decreased HPA-axis)
- • Wear and Tear - Higher basal metabolic rate leads to shorter lifespan
• Crosslink formation - Biological molecules develop cross links over time, affecting its physical and chemical properties
• Heat Shock proteins - Produced at times of cell stress; decreased production of it with age, leading to decreased ability to cope with stress
• Hayflick Phenomena - Biological clock; Fibroblasts in culture divide a set number of times before stopping, which is due to Telomere depletion
o Telomeres shorten with each division
o HeLa cell line (Breast carcinoma) has unlimited division - • Error catastrophe - Accumulation of errors in transcription and translation leads to ageing
• Somatic mutation - Unimportant due to low occurrence rate and DNA repair
• Free Radical Theory - Highly reactive chemical compounds from reactions that damage DNA; there are many enzymes that protect the cells
• Mitochondrial Theory - Mitochondrial DNA is damaged due to O2 radicals; it has no Protein coat for protection
• Cell Senescence - Triggered by DNA damage, leading to Growth Arrest and altered gene expression; Upregulation of degrading enzymes and stimulation of pre-malignant cell growth