BIO254:Pacemaker

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WIKIPEDIA BIO154/254: Molecular and Cellular Neurobiology

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Due Date: 11/20

Overview

Pacemakers are internal oscillators in organisms that control the period and phase of other oscillators. They are thus ‘master clocks’. This controlling feature distinguishes pacemakers from the many other types of oscillators that control the timing of many biological processes and functions. For a brief description of biological oscillators see the section on biological rhythm generators below. The two most commonly described pacemakers are the circadian pacemaker and the cardiac pacemaker.

Circadian pacemaker

Circadian pacemakers coordinate the timing of biological events in an organism with the day/night cycle caused by the rotation of the Earth about its axis. Circadian rhythms are found in fungi, mammals, insects, fish, bacteria, and plants (Panda, 2002). Timing these events conveys a selective advantage. For example, getting the photosynthetic machinery running in plants before the sun comes up allows the maximum amount of light to be converted to useable energy (Merrow, 2005).

Defining Characteristics

Circadian pacemakers are self-sustaining, have a characteristic period, are capable of entrainment, and are temperature compensated.

1) Self-sustaining

A defining feature of a pacemaker is that it will continue to oscillate in the absence of external cues. This is in contrast to external regulators of activity such as thermoregulation of lizard activity level by the warming of the sun.

2) Characteristic period

Circadian pacemakers have a period of approximately 24 hours, . If kept in constant darkness, some mice will have a period of activity and rest that is slightly less than 24 hours (Pittendrigh, 1993).

3) Entrainment

Despite being self-sustaining, circadian pacemakers can be entrained (synchronized) by input from external cues such as light or social activity.

These cues are often linked to physical phenomena such as the rotation of the Earth about its own axis, the orbit of the Earth around the Sun, and the tides directed by the orbit of the Moon around the Earth. Pacemakers that are linked to external phenomena are called circa and the rest are called non-circa (Hosn, 1997). Non-circa pacemakers are not synchronized to external cycles but may still be influenced by external cues. Non-circa pacemakers include the heartbeat pacemaker in the sinus node in humans. For more information on light entrainment see Term 8.1 in the BIOSCI 154/254 Wikipedia.

4) Temperature compensation

History

The earliest record of an observation of a circadian pacemaker was made by de Mairan, a French astronomer, in 1729 (Hosn, 1997). He observed that clover leaves moved even in total darkness, despite the fact that the purpose of their movement seemed to be to track the sun. Linaeus (1707-1778) introduced the concept of a ‘flower clock’. In 1914 Szymanski showed that even under constant conditions goldfish had a circadian rhythm. A genetic basis for the circadian rhythms was indicated in experiments in bean plants by Bunning in 1932. Experiments by Pittendrigh around 1954 showed that the circadian rhythm in Drosophila was temperature compensated. Experiments by Ronald J. Konopka in Seymour Benzer’s lab identified a gene in which mutations caused an alteration of the circadian pacemaker’s period, and was thus named Period abbreviated as Per. Different mutations of Per either shortened or lengthened the period, or abolished the rhythm altogether (Chandrashekaran, 1999). Since then many other genes involved in circadian pacemaker have been identified.

Biological rhythms

The biological rhythms that pacemakers control are mentioned in the Bible (Psalms) and in the writings of Aristotle (384-322 BC) (Ward, 1971), and the human heartbeat has surely been known to humans for as long as we have existed (130,000 years of anatomically modern humans).

The periods of biological rhythm generators range from sub-microsecond in the electric organ of eels (Moortgat, 1998), to 24 hours in circadian pacemakers, to 1 month in the menstrual cycle, to 12 months in hibernation, to longer than 1 year in bamboo (Fig. 1).
Figure 1. Image from (Engelmann, 2004).


Biological rhythm generators control cell division in embryogenesis, menstruation, blooming of flowers, and circadian activity level. Oscillatory processes also underlie sensory coding, attention, memory and sleep (Fontanini, 2006). Biological oscillators are found in most organisms including bacteria (Engelmann, 2004), fungi, plants, insects, and mammals.

Biological rhythm generators use different mechanisms that can roughly be grouped according to the length of their periods (Fig. 2)
Figure 2. Image from (Buhusi, 2006).


Mechanisms

1) Mammals

In mammals, the suprachiasmatic nuclus of the hypothalamus is the circadian pacemaker. Circadian pacemakers control circulating hormone levels, cognitive and locomotor activity levels,

The SCN controls circadian oscillators in the retina, liver, heart, lung (Peirson, 2006), and kidney (Merrow, 2005). Thus the mean level of heart rate seemsto be independent of the circadian period. ROBERTO REFINETTI AND MICHAEL MENAKER Independence of heart rate and circadian period in the golden hamster Am J Physiol Regulatory Integrative Comp Physiol 264:235-238, 1993.


Circadian pacemakers make use of a transcription/translation feedback loop. Several experiments in which single cells are isolated have shown that single cells can generate circadian rhythms of gene expression and circadian pacemakers are thus

2) Insects

3) Fish

Many of the clock genes in mammals have homologs in zebrafish and the interactions are largely similar with a few differences (Cahill, 2002).

4)

Cardiac pacemakers

There are actually two cardiac pacemakers, a primary and secondary; the secondary acts as a backup in case the primary ceases to function. The cardiac pacemaker uses a different mechanism than the circadian pacemaker, which makes sense since they have very different periods. The cardiac pacemaker is similar to the circadian pacemaker in that it controls many other oscillators: specifically, the cells of the heart, each of which has the ability to generate spontaneous rhythmic depolarization. Only the cardiac pacemaker cells in the sinoatrial node control the heart rate because they have a faster rhythm than the other cells in the heart, and thus their signal causes the other cells to depolarize before they get a chance to depolarize. The primary cardiac pacemaker is in the sinoatrial node, and the secondary cardiac pacemaker, which is a backup in case the primary pacemaker fails, is in the atrioventricular node. The mechanisms that causes spontaneous depolarization is based on the unique properties of the potassium, sodium, and calcium channels in the pacemaker cells of the heart. The cells spontaneously depolarize due to a feedback mechanism in which the rate of potassium efflux decreases as the cell depolarizes, depolarizing it further, and due to the ‘funny current’ which is due to sodium leaking in.

Artificial pacemakers

Artificial pacemakers are currently made useing microelectronics however genetically engineered pacemakers may begin to replace microelectronic pacemakers (Boink, 2006).

Cardiac

Artificial pacemakers made with microelectronics are used in patients with deficient pacemakers, for example when the sinus node of the heart does not function correctly.

Neural

Micoelectronic pacemakers implanted in the brain of epilepsy patients at the precise (with 1 mm accuracy) locations that are the origins of seizures in a given patient create signals that help prevent seizures (http://www.clevelandclinic.org/health/health-info/docs/1900/1937.asp?index=8782).

Other pacemakers

It is likely that many of the other biological rhythms described in Fig. 2 are controlled by oscillators that have the defining characteristics of pacemakers listed above, however it has not been common to refer to them as pacemakers. For example, a few articles refer to a pacemaker for the menstrual cycle (), but most do not use this terminology.

References

Boink GJ, Seppen J, de Bakker JM, Tan HL (2006) .Gene therapy to create biological pacemakers.Med Biol Eng Comput. Oct 18; [Epub ahead of print]

Cahill GM (2002) Clock mechanisms in zebrafish. Cell Tissue Res. 2002 Jul;309(1):27-34. Epub 2002 May 25.

Fontanini A, Bower JM.Slow-waves in the olfactory system: an olfactory perspective on cortical rhythms.Trends Neurosci. 2006 Aug;29(8):429-37. Epub 2006 Jul 13.

Moortgat KT, Clifford H. Keller§, Theodore H. Bullock, and Terrence J. Sejnowski (1998) Submicrosecond pacemaker precision is behaviorally modulated: The gymnotiform electromotor pathway. PNAS Vol. 95, Issue 8, 4684-4689.