Lecture 3 Flashcards

1
Q

What are the functional characteristics of all biological clocks (ultradian, circadian, circannual clocks, etc.)?

A

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2
Q

How have past investigators experimentally confirmed that the daily clock is indeed an
endogenous timer?

A

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3
Q

What is the experimental evidence that the SCN is an important biological clock?
What is the evidence that other extra-SCN clocks might also exist in mammals?
–in other vertebrates?

A

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4
Q

Actiwatch data in humans

A

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5
Q

Actiwatch data in humans Adult Locomoter Activity

A

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6
Q

Undergraduate Student

Locomotor Activity Data

A

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7
Q

Effect of SCN Lesions

A

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8
Q

Circadian Variations in Body Functions

A

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9
Q

Exogenous versus Endogenous

Control of Biological Clocks

A

Some behavioral rhythms have been recognized since ancient times, but they have generally been attributed to exogenous (outside the organism) factors.

Recent evidence indicates that endogenous (inside the organism) timing mechanisms mediate many of the observed rhythms in physiology and behavior.

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10
Q

Time Sense

A
  • Endogenous and exogenous clocks in Bees
  • Endogenous clock constant

• Exogenous clock depends on celestial cues
Renner (1960)

• Long Island, NY hive.
Foraged 12:54 - 2:24 EST

• Fly hive to Davis, CA
3hr and 15min time difference
Foraged 9:45 - 12:15
Jet lagged bees
Exogenous clock gradually adjusts
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11
Q

Zeitgedachtnis:

August Forel

A

In 1910, August Forel reached the conclusion that bees were able to remember things after he had a bothersome encounter with them.

He liked having breakfast outside on a patio with his family each morning, but he finally had to retreat into the house because bees kept trying to eat his food.

From inside the house, he noted that the bees continued to visit the patio each morning at the same time even though there was no longer any food for them.

How could bees remember the exact time to come each day looking for sweet jam?

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12
Q

Zeitgedachtnis

von Frisch and Beling

A

In 1929 Karl von Frisch and I. Beling developed Forel’s observations into laboratory experiments.

They fed bees sugar water at precisely the same time each day.

As Forel had observed, when they removed the food, the bees still came to feed at exactly the same time each day.

The only variable in this experiment was the presence or absence of food; the bees’
behavior remained the same.

von Frisch and Beling then repeated the experiment in a salt mine where there was no
change in light or temperature.
The variable was still food, and the environmental conditions were held constant.

The bees continued to feed at the same time each day.

What conclusions could they make if the bees continued to feed at the same time in unchanging environmental conditions?

How did the bees know what time it was?

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13
Q

Sun Compass

A

In other early experiments, Gustave Kramer trained
starlings to fly in a particular direction for its source
of food using the sun as a compass.

When placed in a laboratory where an electric light
replaced the real sun as a direction giver, hour after hour the bird added 15° of arc counter clockwise to the angle it made relative to the artificial sun.

He concluded that the bird knew that the angular velocity of the sun is on average 15° per hour and that it had access to some reliable clock to compensate for its constantly shifting ‘compass’.

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14
Q

Sun Arc Hypothesis

A

?

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15
Q

Temperature compensation of
biological clocks:

Intro

A

More often than not, chemical reaction rates depend on temperature, with a doubling of rate with every 10°C rise in temperature.

In places like Ohio, where temperature changes are quite common and sudden, a temperature dependent clock would be very unreliable.

Scientists have now suggested that the biological clock is temperature compensated, and so varies very little at different constant temperatures.

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16
Q

Temperature compensation of
biological clocks:

Bünning

A

In 1931, Bünning created a hypothesis of temperature-dependence of biological clocks.

He conducted experiments on bean plants and found them to show a change in period length of leaf movement with changes in temperature.

Bünning found that for a 10° rise in temperature, there was a 20% change in the period length of leaf movement.

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17
Q

Temperature compensation of
biological clocks

Brown & Webb

A

In contrast to this temperature-dependent hypothesis, Brown & Webb (1948) forwarded the temperature-independent hypothesis which stated that the function of the biological clock does not vary with temperature.

Their experimental subject was Fiddler crabs.

Fiddler crabs, during the daytime are dark in color, but
turn pale at night exhibiting a daily light-dark cycle.

Brown & Webb found that in these crabs, the period of the daily cycles of change in color was completely independent of temperature over a range of 20° C.

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18
Q

Temperature compensation of
biological clocks:

Pittendrigh

A

To further test this temperature independent hypothesis, Pittendrigh investigated the effect of temperature on the eclosion behavior of fruit flies.

He placed some vials of Drosophila in 26° C and some in 16° C.

Pittendrigh observed that the first emergence peak at the lower temperatures was 12hrs overdue.

However, subsequent emergence peaks showed very little deviation from those at higher temperatures.

Following these results, Pittendrigh confirmed the temperature-independent
hypothesis and stated that Bünning was misled by a ‘step-induced’ transient that does not reflect the steady-state behavior of the oscillations that drive the rhythm.

Transients are temporary cycles, usually seen during resetting.

19
Q

Transients

A

temporary cycles, usually seen during resetting

20
Q

Early resistance to the notion of
endogenous clocks:

Arhenius

A

Arhenius, proposed an alternative view which stated that the clock of an organism comprises an “Open System” and timing of the periods persisting in ‘constant conditions’ is derived through its geographical environment.

21
Q

Early resistance to the notion of
endogenous clocks…

Brown

A

In 1959, Brown suggested that there are diurnal fluctuations in the air pressure and slight periodic fluctuations in gravity associated with the rotation
of the earth in relation to the sun and moon.

Brown conducted experiments on the metabolic rate on Fiddler crabs and potatoes.

These organisms showed daily fluctuations of metabolic rates, exhibiting a maximum in the morning and a minimum in the evening.

Brown concluded the daily metabolic rhythms in both the crab and potato are imposed daily from the external physical environment.

He stated that “short of the demonstration that biological cycles of the natural geographical cycles can still persist in organisms traveling in space well outside of the earth’s rhythmic field of influence, there is no logical basis on which this hypothesis can be rejected”.

22
Q

Early resistance to the notion of
endogenous clocks…

Hammer

A

K.C. Hammer and colleagues in the 1960’s carried out experiments which contradicted Brown’s hypothesis.

They conducted experiments at the South Pole (1 of the 2 geographical poles where all diurnal variables can virtually be eliminated).

23
Q

Evidence resolves early

resistance to endogenous clocks

A

The running activity of the hamster, the rhythmic activity of the cockroach, growth rhythms of Neurospora, eclosion of Drosophila and leaf movements of bean plants were recorded when the organisms were placed on turntables which were revolved counter to the earth’s rotation, once every 24 hrs.

This rotation once every 24hrs counter to the earth’s rotation, would completely eliminate the effects of diurnal variables.

The results obtained showed external variables of a diurnal nature associated with the rotation of the earth had no detectable influence on the basic mechanisms of the
biological clock.

They concluded that, although it was possible that some external periodic stimulus may
regulate the biological clock, it does not arise from any factor associated with the Earth’s
rotation.

24
Q

Brown:

The Lamark of Chronobiology?

A

With the recent advancement in biological experiments in space, Brown’s theory of geographical effects was further proven to be wrong.

In the bread mould Neurospora crasa a clock controls the switch from vegetative to asexual reproduction.

When this bread mould was launched in to space it continued to show a circadian rhythm of vegetative spore production with a period close to 22hrs.

This confirmed that the free running period persisted in space and was not influenced by any geophysical factors.

25
Q

Evolution of Biological Clocks:

Temporal Organization

A

They control an organisms’ behavior and activities so that they occur at the “right time”.

For example, clocks coordinate when males & females of the same species become fertile so that the period of maximum fertility coincides, thus establishing a breeding season.

In cyanobacteria (blue-green algae), there is both photosynthesis and nitrogen fixation, but nitrogen fixation can’t occur in the presence of oxygen.
These processes, therefore, need to be separated.
Under the control of a biological clock, these 2 processes are temporally segregated: photosynthesis occurs during the day,
fixation during the night.

26
Q

Evolution of Biological Clocks:

Temporal Organization between Species.

A

Biological clocks function such that certain species are active, for example, during the day, while others are active during the night.

If a prey species is active during the night, then the clock of its predator will ensure it “wakes up” so it does not miss out on a potential meal.

In the same way, prey species may become active at times when the predators are usually not active (to avoid becoming a meal!)

27
Q

Evolution of Biological Clocks:

Anticipation of an Organism’s Environment.

A

By registering local time and events (such as high & low tide), biological clocks allow organisms to prepare for and anticipate their environment.

Predictive Homeostasis is a good example of this –
• An organism can activate certain systems preempting the
changes that will occur in the environment.
E.g., In humans, cortisol levels are raised before we wake up, increasing the metabolic rate so we have the energy necessary for the day ahead.

28
Q

Rho (ρ)

A

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29
Q

α

A

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30
Q

Free-running period (τ)

A

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31
Q

LL

A

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32
Q

After-Effects or Transients

A

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33
Q

Δφ

A

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34
Q

φ

A

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35
Q

Double-plotted 24h and 20h “days” for WT and tau mutant mice

A

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36
Q

Constructing a Phase Response

Curve

A

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37
Q

Tau does not equal 24 h

A

Problem when tau is exactly the period of
geophysical cycle (could be driven by hidden
zeitgeber)
Not easy to entrain to changing day lengths
Species-specificity affects tau
Individuality affects tau
Taus are innate and persist for many cycles

38
Q

Deer Mouse Activity under LD, DD, and LL

A

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39
Q

DD

A

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40
Q

LD

A

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41
Q

Aschoff’s rule

A
  1. Nocturnal animals have DD taus less than LL taus, diurnal animals have DD taus greater than LL taus.
  2. Period of tau shortens as light intensity increases in diurnal (day-active) animals
    and lengthens as light intensity increases in nocturnal (night-active) animals.
42
Q

Aschoff’s Rule in Various Vertebrates

A

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43
Q

Voles and DD

A

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