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Aging Midterm
| Question | Answer |
|---|---|
| What is senescence? | A deteriorative change that causes increased mortality |
| What is hormesis? | stimulatory effects of low doses of substances known to be toxic at higher doses |
| What do adaptive theories of the evolution of aging say? | propose that senescence leading to death provides a selective advantage to the species |
| What do non-adaptive theories of the evolution of aging say? | propose that senescence is detrimental to fitness and is outside the force of natural selection |
| What is antagonistic pleiotropy? | when a gene is beneficial to the organism's fitness early on in life and is detrimental to the organism's fitness later on due to a decline in the force of natural selection |
| “Rate of living” Pearl 1928, Rubner 1908, Weismann 1889. | Life span inversely proportional to metabolic rate. Many exceptions (e.g., bats, humming birds), |
| Somatic mutation theory (Szilard 1959). | DO NOT CONFUSE WITH “MUTATION ACCUMULATION” EVOLUTIONARY THEORY! Genetic mutations accumulate with time leading to functional failure. |
| What is the Hayflick limit? | the limited number of cell divisions that human fibroblasts and other cell types will undergo in cultur |
| What are the products of glycolysis? | pyruvate, NADH, ATP |
| Where do the products of glycolysis go and why? | the mitochondria to support the Krebs cycle and oxidative phosphorylation/ETC |
| What does the Krebs cycle produce? | reducing equivalents and building blocks for macromolecules |
| What does the ETC do? | reduce oxygen and use the energy to convert ADP to ATP |
| be able to draw ATP! | ok. |