Article Paper 3 Flashcards

(35 cards)

1
Q

What is torpor? (2)

A
  • a state in which an animal reduces its body temperature and metabolic rate to conserve energy.
  • It is a key part of hibernation.
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2
Q

How does hibernation differ from normal sleep?

A

hibernation is a prolonged period of torpor, where an animal reduces activity, body temperature and metabolism to survive cold and food shortages whereas normal sleep is controlled by the brain

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3
Q

What metabolic changes occur during hibernation?

A

Decrease in metabolism, body temperature, heart rate, and oxygen consumption.

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4
Q

What chemical is linked to sleep and potentially triggers torpor?

A

Adenosine — it slows brain activity and is linked to both sleep and torpor regulation.

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5
Q

Q: Why does body temperature drop during hibernation (link to enzymes)?

A

A: Reduced temperature slows enzyme activity, conserving energy by decreasing biochemical reaction rates.

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6
Q

Q: How does reduced metabolism during hibernation relate to respiration rate?

A

A: Slower metabolism means lower respiration rate, conserving energy and oxygen.

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7
Q

Q: Explain how homeostasis is still maintained during hibernation.

A

A: Core physiological processes like minimal heart rate and respiration are stabilised at low levels to maintain internal balance.

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8
Q

Q: How can comparing hibernators and non-hibernators’ genomes help medicine?

A

A: It helps identify genes linked to disease resistance or metabolic suppression, which may be useful for human therapies.

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9
Q

Q: Explain how the activation of certain genes leads to reduced metabolism during torpor.

A

A: Transcription factors activate genes that suppress metabolism, producing proteins that reduce ATP production and heat production.

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10
Q

Q: Describe how differences in gene expression lead to changes in cell function in hibernating animals.

A

A: Genes for energy conservation are expressed more, while genes for active metabolism are expressed less, altering cell function.

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11
Q

Q: Suggest how environmental factors like day length or temperature affect gene expression in hibernators.

A

A: Environmental cues like day length affect hormone levels such as melatonin, which affect hypothalamic control of gene expression for torpor.

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12
Q

Q: Explain how regulation of gene expression allows entry and exit from torpor.

A

A: External stimuli like cold activate transcription factors that switch on/off metabolic genes, enabling reversible metabolic suppression.

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13
Q

Q: What survival advantages does hibernation give animals?

A

A: Conserves energy in cold or food-scarce environments, and may offer protection against conditions like stroke or heart attack.

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14
Q

Q: Which human diseases might benefit from hibernation-based treatments?

A

A: Heart disease, stroke, Alzheimer’s disease.

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15
Q

Q: Describe how hibernator genetics could help develop treatments for stroke or heart disease.

A

A: Genes that protect tissues in torpor could be used to design drugs that prevent damage during strokes or cardiac events.

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15
Q

Q: Explain how hibernation research could help develop stroke treatments.

A

A: Lowered metabolism during torpor protects brain cells during periods of low oxygen, which is useful in strokes.

16
Q

Q: What is one ethical concern with inducing torpor in mammals for research?

A

A: Potential for distress or harm to animals during experimental procedures.

17
Q

Q: Explain how hormonal signals could contribute to torpor.

A

A: Hormones like melatonin or cortisol influence gene expression via the hypothalamus, helping initiate metabolic suppression and torpor.

18
Q

Q: Explain the role of the hypothalamus in controlling body temperature during hibernation.

A

A: The hypothalamus detects body temperature changes and sends signals to suppress thermogenesis while maintaining low, stable temperatures.

19
Q

Q: Design an investigation to test the effect of temperature on adenosine pathway activation.

A

A: Use two groups of mammals exposed to different temperatures. Administer adenosine. Measure changes in metabolic rate or core body temperature. Control variables like species, age, and drug dosage.

20
Q

Q: What is one risk if metabolic rate drops too low during experimental torpor?

A

A: Risk of organ failure or death due to insufficient energy supply.

21
Q

Q: Suggest improvements for an experiment on hypothalamus thermoregulation.

A

A: Increase sample size; use non-invasive imaging techniques; include proper control groups.

21
Q

The article mentions that Arctic ground squirrels can survive core temperatures below 0°C. Suggest two physiological adaptations that might allow this. (4 marks)

A
  • Presence of antifreeze proteins to prevent ice crystal formation inside cells.
  • Accumulation of glucose or urea to lower the freezing point of body fluids.
  • Stabilisation of cell membranes at low temperatures.
  • Efficient vasoconstriction to protect vital organs from freezing.
22
Q

Evaluate how hibernation research could contribute to extending human lifespan. (6 marks)

A

Hibernation reduces metabolic rate, lowering oxidative stress.

Enhances DNA repair and reduces accumulation of damage.

Mimics caloric restriction, linked to increased lifespan.

Potential to reduce risk of age-related diseases.

Challenges include ethical concerns and lack of full human applicability.

More research is needed to ensure safety and long-term benefits.

23
Outline one way gene expression during hibernation can be studied and why timing is important. (3 marks)
Use transcriptomics to measure mRNA levels in tissue samples. Take samples during different torpor stages: entry, maintenance, arousal. Gene expression changes rapidly, so timing ensures accurate data collection
24
Describe how the neurotransmitter adenosine may be involved in inducing torpor. (4 marks)
Adenosine binds to receptors in the hippocampus to slow brain activity. This binding induces sleepiness and reduces neural firing. Activation of adenosine pathways reduces body temperature and metabolism. Drugs that mimic adenosine can induce torpor in animals like squirrels and rats.
25
Evaluate the reliability of tissue samples collected across hibernation periods. (4 marks)
Reliability depends on consistent collection times. Proper storage conditions prevent RNA degradation. Replication across individuals increases confidence. External variables must be controlled (e.g. age, environment).
25
Using the information in the article and your own knowledge, discuss the potential benefits and limitations of inducing torpor in humans for long-term space travel. (9 marks)
Benefits: Conserves food, oxygen, and water by lowering metabolism. Preserves bone and muscle mass in microgravity. Reduces radiation damage during deep-space travel. May protect against cognitive and cardiovascular decline. Limitations: Humans lack proven torpor mechanisms. Safety and ethical concerns with long-term suppression of consciousness. Unknown long-term effects of repeated torpor cycles. Difficult to control body temperature/metabolism in space reliably. Conclusion: Promising application, but more research is needed before human use.
26
Explain the role of adenosine in neural signalling and compare its role in sleep vs torpor. (4 marks)
Adenosine slows brain activity by binding to receptors. In sleep, it promotes drowsiness and rest. In torpor, it induces deeper metabolic suppression. Both involve reduced brain activity, but torpor is longer and more intense.
27
Compare the physiological responses to cold in hibernators and non-hibernators. (3 marks)
Non-hibernators maintain body temp via shivering and vasoconstriction. Hibernators allow body temp to drop significantly. Hibernators reduce metabolism instead of trying to generate heat.
28
Discuss the evolutionary advantages of hibernation and what it suggests about mammalian ancestry. (4 marks)
Enables survival in food-scarce or cold environments. Reduces energy demand and exposure to predators. Widely distributed among mammals — likely in common ancestor. Suggests torpor pathways are conserved across evolution.
29
Explain how urea recycling conserves resources during torpor. (3 marks)
Urea is reabsorbed instead of excreted. Used to synthesise amino acids or other compounds. Conserves nitrogen and reduces energy use.
30
Discuss the potential ethical implications of using synthetic torpor in humans. (4 marks)
Risks around consciousness suppression and long-term effects. Informed consent and safety must be ensured. Could raise issues of fairness and accessibility. Misuse in vulnerable groups or for cost-cutting purposes.
31
Evaluate the usefulness of hibernating species as models for understanding human disease. (4 marks)
Provide insight into metabolic control, neuroprotection, and cardiovascular resilience. Can identify therapeutic targets from gene comparisons. Animal physiology differs from humans — limits direct application. More testing needed before clinical use.
32
To what extent do findings in animals like rats or squirrels translate to human biology? (6 marks)
Rats share similar brain structures and pathways with humans. Squirrels show useful metabolic adaptations. Results in animals may suggest mechanisms present in humans. However, humans may lack full pathways to enter torpor. Ethical and physiological constraints limit translation. Animal models provide useful leads but aren’t fully representative.