Purkinje Fibers of The Heart Conduction System
Purkinje Fibers of The Heart Conduction System
Purkinje Fibers of The Heart Conduction System
MEDICINE HISTORY
Eliška O.
Institute of Anatomy, 1 st Medical School, Charles University Prague
SUMMARY
It has been 160 years now since Purkinje published his findings of conduction fibers in the heart in Archiv f. Ana-
tomie u. Physiologie, and 166 years since the Polish version of this publication. Even during Purkinje’s life some
anatomists had studied the morphology of these fibers, but nobody at that time understood the great physiological
and medical importance this discovery would have for medicine. This can be seen as late as the 20th century and
even today. Purkinje’s work triggered a cascade of these discoveries, which led at the beginning of the previous cen-
tury to the formulation of the basic scheme of the conduction system. Purkinje fibers or Purkinje cardiomyocytes
are part of the whole complex of the cardiac conduction system, which is today classified as specific heart muscle
tissue responsible for the generation of the heart impulses. From the point of view of their ultrastructural composi-
tion, the cells of different parts of the cardiac conduction system are largely similar. In contrast to heart contractile
cardiomyocytes, the cells of the cardiac conduction system including Purkinje fibers have a small amount of myo-
fibrils, fewer small mitochondria and thus a light cytoplasm as well as a higher glycogen content, but their T-tubu-
lar system is tiny or absent. These cells can be detected with some morphological, histochemical methods. Howe-
ver, the cells of the conduction system are not completely uniform as they differ in size, number of nexuses-gaps,
intercalary disks and in some other features in the individual parts of the conduction system. However, these specia-
lized cells work as a whole. Nowadays morphological research concerning all parts of the cardiac conduction sys-
tem, including Purkinje fibers, is focused on ultrastructural, histochemical and genetic issues, with the aim of pre-
venting and treating disturbances of the conduction system such as arrhythmias with the increasingly popular
genetic therapy - and possibly of replacing electrical pacemakers with biological ones. If Jan Evangelista Purkinje
had lived nowadays, he would have been surprised and delighted at the degree and extent of research and the clini-
cal application his discovery induced.
Key words: Purkinje fibers, morphology, history, present time. El.
res from the contractile cardiomyocytes, are able to generate spon- Jan Evangelista Purkinje was born the 18 December 1787 in
taneous impulses and conduct them to the whole heart muscle. In Libochovice (Bohemia). In 1818 he defended his doctorate and in
the heart these specialized cells are mutually connected and form an spring 1823 he became Professor of the University in Vratislav
anatomical and physiological unit, called the heart conduction sys- (Previously: Breslau, Germany; nowadays: Wroclaw, Poland),
tem. where he worked until 1850. It was during this period in Vratislav,
between the ages of 35 and 63, that he made his most important dis-
coveries. This very age generally represents the physiological
WHAT DID J. E. PURKINJE IN THE HEART? extent of the greatest creative waves of the human being. From 1850
until his death in 1869 Purkinje worked in the Institute of Physiol-
Jan Evangelista Purkinje was the first person in the world to dis- ogy in Prague, which he had founded and built up. The acquisition
cover and describe the heart conduction system, in particular its last of the big Plösl microscope in 1835 represented an important turn-
part (from the point of view of the conduction system behavior), ing point for Purkinje’s histological and embryological research.
which is called the Purkinje fibers in his honor. The fibers of this Purkinje published his discovery of a part of the heart conduction
last part run on the interior surface of the ventricles to join the system, nowadays called Purkinje fibers – Purkinje cardiomyocytes
working cardiomyocytes. Nowadays these fibers are also called (1) in 1845 in “Archiv für Anatomie, Physiologie und wis-
Purkinje heart cells or Purkinje cardiomyocytes. senschaftliche Medicin”, in the article “Mikroskopisch – neurolo-
The paper was presented as part of the Purkinje Night at the Czech Physicians’ Club in Prague on 23 May 2005.
(329)
ČAS OP I S L ÉK A ŘŮ Č ESK Ý C H , 145, 2006, N o. 4
gische Beobachtungen”. Over 15 pages the author describes neuro- clinical discoveries and papers dealing with this issue, which still
logical fibers and ganglions in various organs. Only the last two reverberates today. Owing to their localization on heart ventricles
pages deal with Purkinje heart fibers. The paper represents, as Purk- walls as described by Purkinje, these particular cardiomyocytes are
inje mentions himself, a follow-up to his previous neurohistological regarded as a final segment of the conduction system that is con-
works that had been published in Polish (2) in 1839 in Rocznik nected to normal cardiomyocytes verticular musculature and go as
wydzialu lekarskiego w uniwersytecie Jagiellonskim. Krakow, Tom far as the improper chordae tendineae. Purkinje cells have the fol-
II, pp. 44-67. Purkinje had observed the conduction fibers in lowing important morphological features: 20-70 microns of size,
sheep’s hearts. The paper was partly translated from German into spacious sarcoplasm, small amount of myofibrils localized
Czech by Professors Borovanský and Weigner in 1937 (3). Having marginally in the cell. Two years before Purkinje’s death (1867)
gone through the available literature I have not found an accurate Obermeier described three types of Purkinje cells differing in quan-
and self-contained Czech translation of this paper, so I shall take the tity of sarcoplasm and thus in compactness of myofibrils. Bigger
liberty of presenting the English (Czech) translation here. cells predominantly had a cubic shape with fewer myofibrils
marginally in the cell; they were connected to spherical cells of
The English (Czech) translation of the Journal formulation middle size having more myofibrils and finally to the cells of a long
13. Directly under the serous membrane (skin) on the interior thin shape having more striated myofibrils. He found Purkinje
walls of the sheep heart I observed firstly a network net of grey, flat fibers in hearts of sheep, horses, pigs, cows, geese and pigeons.
and gelatinous fibers that partly spreads to the papillary muscles However, he did not find them in humans, cats, hares, mice or frogs.
and to other neighboring fibrous trabeculal and that partly bridges In the heart of big animals, such as beef cattle, he observed the
furrow of the heart walls. Then, during a microscopic observation, Purkinje fibers not only under ventricle endocardium but also in the
I found these fibers are mostly formed by grains (cells) resembling ventricle muscle. (6). Obermeier suggested another name for Purk-
the cells in ganglions, which are tightly joined forming a polyedric inje fibers – Purkinje muscles chains (“Purkinje’sche Muskelket-
shape. In the interior of each grain I found one or two nuclei not of ten”). Knowledge of the conduction system and Purkinje cardio-
spherical shape, similar to the nuclei of the genuine ganglion myocytes was significantly expanded thanks to the research of
grains. In these grains I found fibers that were mutually crosswise a Japanese scientist Tawara. (7). In 1906 Sunao Tawara published
connected in the number of 5 to 10 pieces, arranged into longitudi- the results of his two and half year work in Marburg, concerning the
nal bundles of grey fibrils. Elastic tissue formed by double fibrils is conduction system, in his book: Das Reizleitungssystem des
located among the grains in the interstitium of their walls. When Säugetierherzens. Verlag Gustav Fischer, 1906 (200 pages and 10
treated with vinegar, these fibrils present transverse strips similar to color tables). Tawara’s teacher and consultant, Ludwig Aschoff
heart muscle fibrils. It is difficult to say if they represent real fibers (1866–1945) behaved very nobly as he did not mention himself as
or just contours of membranous walls which, like plant cells, sur- a co-author of the book. He had only written a foreword. Tawara
round granular contents; in my opinion the second option is more discovered the atrioventricular node (formerly called Tawara or
likely, as after crushing the grains, I could not see any similar free Aschoff Tawara node); he also histologically described in detail
fibrils. On no account can they be compared to nervous fibrils that Purkinje cells in the atrioventricular node and branches and their
may be seen in ganglions, weaving ganglion balls round, even transition to the contractile muscle. He was keen to retain the name
though it appears so at first sight. I never managed to find real ner- of Purkinje bundles and thus helped to spread the term to the whole
vous fibrils in these granular fibers, which would prove the obvious cardiologic world. He excluded some previous opinions regarding
nature of the ganglions. Purkinje fibers (cells) as a pathological structure (8). In 1908, in his
Therefore, I would incline to categorize this new tissue as carti- publication concerning the discovery of electrocardiogram,
laginous, although considering its softness, I am in doubt about its Einthoven used Tawara’s research concerning the atrioventricular
effect in the relation to a relatively huge muscle mass of the heart. conduction system, including its final bifurcation of conduction
(Thus, it is currently more likely to me to consider this tissue an fibers (or Purkinje fibers) into the heart muscle, in the interpretation
independent locomotive apparatus and to regard the membranes of the electrocardiogram (9). One of the first wax and wire recon-
surrounding the grains as muscular ones). Moreover, I found simi- structions of the atrioventricular node, branches and bifurcation of
lar granular fibers in beef, pig and horse. However, I never man- Purkinje fibers of the calf heart was effected by Lydia de Witt 1909
aged to find the same in human, dog, rabbit or hare. (10).
Although a literal translation from the German original aged 160 It has already been said that Purkinje fibers are part of the con-
years into Czech (and English afterwards) seems slightly halting duction system. Individual parts of the conduction system are locat-
from the point of view of the contemporary professional terminolo- ed in different places of the heart, e.g. in the right atrium wall, in the
gy, it is possible to deduce the following facts: interventricular septum and in the wall of both ventricles.
A) Purkinje excluded that the fibers he found were nervous fib- At this point a question arises: are all parts of the conduction
rils and ganglions. system morphologically similar or partly similar, or they are funda-
B) After some hesitation he also excluded the hypothesis of car- mentally structurally different?
tilaginous origin of the fibers.
C) He finally described the fibers as being of a muscular type
belonging to the locomotor apparatus. PARTS OF THE CONDUCTION SYSTEM –
Purkinje could not know at that time that these fibers he disco- CRONOLOGICAL DEVELOPMENT
vered and described as fibers of being a muscular type, were fibers DISCOVERIES
of the conduction system.
Purkinje’s name would possibly have gone out the window if the As it has already been said, Purkinje presented the first part of
discoverer of electric currents in the heart contraction (together the conduction system in the shape of the final network of heart fib-
with Heinrich Müller) a Swiss anatomist and physiologist Professor rils on the interior wall of sheep ventricles in 1845. The atrioven-
Rudolf Albert Kölliker (1852) had pointed these fibers out, naming tricular bundle was the second discovered part of the conduction
them Purkinje fibers. (4, 5). Since then, this term has been broadly system (11). It is called after its discoverer, an internist His Junior
accepted in international literature. The discovery of Purkinje fibers (1893), the His bundle. A similar discovery was made by Kent
launched an explosion of other morphological, physiologic and (1892–1893), who found a muscular connection between atria and
(330)
ČAS OP I S L ÉK A ŘŮ Č ESK Ý C H , 145, 2006, N o. 4
ventricles and dissected the atrioventricular node (12). However, he Atrioventricular node – AV node
was not convinced of the importance of these bundles. The last The atrioventricular node is localized between the coronary sinus
structure of the conduction system, the sino-atrial node (13), was mouth and the septal leaflet of the tricuspid valve in Koch triangle.
discovered by Keith and Flack in 1907. It can easily be revealed by dissection. It is 5–7 mm long and
So-called atrial conduction pathways, also referred to as atrial 2–5 mm wide. Its cells can be microscopically distinguished from
preferential pathways or internodal pathways connecting the sinoa- the atrial muscle. Their structure is plexiform, they are nearly of the
trial and the atrioventricular nodes, are still a matter of contention same size as atrial cells, but their cytoplasm is lighter than in atrial
(14–16). The question is whether these pathways are formed by and ventricular myocytes. They are characterized by their striated
conductive substance or just by working cardiomyocytes. These structure and intercalated disks. Inside the node we find larger
pathways were known as early as the beginning of the 20th century. amounts of elastic and collagenous connective tissue than in atrial
They consist of an anterior pathway of Bachman (1916), running and ventricular muscle, but less than in the sinoatrial node. The
from the anterior margin of the sinoatrial node, surrounding the node is divided into two zones: a superficial one, formed by transi-
vena cava superior and in the anterior part of the interatrial septum tional cells and normal cardiomyocytes and a deep (compact) one.
running to the atrioventricular node (17). The middle preferential The cells of the compact zone are similar to nodal cells. Small nodal
pathway (Wenckebach – 1907) runs from the proximal surface of cells gradually transfer to bigger Purkinje fibers of the atrioventri-
the sinoatrial node to the dorsal part of the atrial septum up to the cular bundle. The electronogrammes of nodal cells of the AV node
limbus fossae ovalis, where it joins the anterior pathway, and show a smaller number of irregularly arranged myofibrils, a poorly
together they join the atrioventricular node (18). Finally, there is the developed sarcoplasmatic reticulum and no tubular system. Cell
posterior (inferior) preferential pathway (Thorel – 1910) that junctions are formed by a lot of desmosomes and few nexuses. We
detaches from the caudaly of the sinoatrial node, running caudad can more frequently see the fasciae adherentes than in sinuatrial
along the crista terminalis and in its inferior part entering the atri- cells, but not so often than in atrial and ventricular myocytes. For
oventricular node (18). basic data about the atrioventicular junction area see citations
(32–38).
(331)
ČAS OP I S L ÉK A ŘŮ Č ESK Ý C H , 145, 2006, N o. 4
astride on the ventricle septum muscle, under the membranous sep- of diameter) and are situated in the ventricular myocardium (32).
tum. The left branch runs from the bundle as a continuous layer of They are also located in the ventricular subendocardial layer and in
fibers along the whole length of bifurcation, whereas the right false chordae tendineae.
branch seems to be a direct follow-up of the ramifying bundle. The Type III. – These are present in the junction between the big
right branch passes under the septal endocardium to the musculus Purkinje cell and the myocardium cell and are bigger than working
papillaris anterior and fragments to the net of Purkinje fibers for the cardiomyocytes. They have few mitochondria and no T system. We
walls of the right ventricle. The left branch splits under the septal call them transitional form of Purkinje cell (8-12 microns of dia-
endocardium into the anterior and posterior fasciculi and both of meter).
them pass to Purkinje fibers of the ventricle. Some authors recog- The size of Purkinje fibers is also given in various forms. There
nize three rather than two fasciculi: anterior, medial and posterior. are interspecific variances, but there are also differences in data
The cells of both parts of the atrioventricular bundle and branches from different authors. The size of Purkinje fibers in whales is about
in human are smaller than the cells of the working myocardium 19–94 microns whereas in humans it is about 10–46 microns (32).
(37). However, in bigger mammals, such as cows and sheep, the Purkinje cells, as is universally accepted, contain few myofibrils.
cells of atrioventricular bundle and branches resemble larger The Z line may be larger but may be absent as well. The T system
Purkinje cells. The cells in the bundle and branches are longitudi- is absent or just poorly developed and mitochondria are small with
nally oriented and separated by collagenous fibers. James and Sherf few cristae. Myofibrils in Purkinje fibers work as passive cytoskele-
(1971) described in electronogrammes in dogs and humans that the tal components (52, 54). They are different in composition of
atrioventricular bundle consists of large cells similar to Purkinje myosin from the cells of working myocardium, as they contain not
fibers, containing few myofibrils and a light perinuclear zone (16). only two light chains but also an accessory type of myosin with an
In addition they found 2 types of transitional cells there: large ones intermediate molecular weight (53, 55). Unlike working cardio-
and narrow ones. In the proximal part of the bundle they described myocytes, where the sarcoplasmatic reticulum is joined with the
the cells identical to the sinuatrial bundle cells. Here, in the SA sarcolemma of the T tubule (interior coupling) and with the periph-
node, they called them P cells. The cells in question are nodal cells eral sarcolemma (peripheral coupling), Purkinje fibers that do not
microscopically appearing as pale. However, cardiologic literature have T tubules are joined with the peripheral sarcolemma only (56).
did not accept this term and consistently continues to use the term Purkinje fibers are PAS positive as they contain a considerable
of “nodal cells” for the SA and AV node cells. They cannot be mis- amount of glycogen, which is typical for the conduction system
taken with Purkinje fibers. Later on, James et al. (1974) described cells (50,49). A large quantity of glycogen in Purkinje fibers is
the ultrastructure of branches (47). According to them, the left metabolized by the way of anaerobic enzymes. Thanks to this pro-
branch consists of typical Purkinje fibers (cells) that are mixed with perty, these cells are more resistant to hypoxia than the ventricle
cells resembling working cardiomyocytes. The cell junctions are myocardium cells (57). An activity of acetylcholinesterase was
made of intercalated disks that contain long nexuses. The right found in the conduction system, including Purkinje cardiomy-
branch is mostly formed by working cardiomyocytes. Typical Pur- ocytes; however, no such activity was detected in working
kinje fibers (cells) were very rare in the right branch. Vassal–Adams myocardium cells (58). There is interspecific variety in connection
(1983) does not recognize these findings and considers the whole of Purkinje fibers with working ventricular cardiomyocytes, among
atrioventricular system, including the node, quite heterogeneous different animals and between animal and man as well. The differ-
(48). It cannot be clearly specified into separated cell types. All ence is in presence or absence of transitional cells between Purkin-
these heterogeneous cells are connected with intercalated disks. je fibers and working cardiomyocytes. Such a connection between
a Purkinje cardiomyocyte and a transitional cell guarantees a high
resistance of coupling and a quick conduction on the working
PURKINJE FIBERS (PURKINJE CELLS, myocardium. This arrangement is well marked in rabbits and pigs
PURKINJE CARDIOMYOCYTES, (59). On the contrary, no transitional cells were detected in human
RAMI SUBENDOCARDIALES and cattle hearts. The Purkinje fibers detected here only got smal-
ler on passage to the myocardium. In the cattle heart, Purkinje fibers
They represent the terminal part of the conduction system. They under the ventricular endocardium form a two-dimensional net that
consist of the AV bundle and branch. Under the ventricle endo- converts into a three-dimensional one on its passage to the
cardium the branches fragment into the net of fibers discovered by myocardium. At the beginning, Purkinje fibers in myocardium are
Purkinje. These are formed by cells with a small amount of fibrils surrounded by a connective tissue - which gradually disappears, so
and a great quantity of glycogen in reverse. Purkinje fibers in that a contact of the Purkinje fibers with ventricular myocytes can
human reach only the interior myocardium layer, whereas in certain be realized. Only in the area of 2 mm under the epicardium was this
animals they extend to the whole myocardium (6, 49). The fibers connection not found (60). This electrical coupling between Pur-
are connected to the working myocardial cells by intercalated disks, kinje fibers and working cardiomyocytes may be disturbed in aci-
with or without the transitional cells. One fiber transfers the dosis, hypoxia and hyperkalemia (61). Ectopic impulses, distur-
impulse on thousands of working cardiomyocytes. This arrange- bances in conduction of an impulse and reentry tachycardias can
ment guarantees a synchronous action of working cardiomyocytes emerge in Purkinje fibers in the peri-infarctuous area (62–64). The
during the contraction. electrical impulse is more quickly transferred by Purkinje fibers
There is no uniform description of Purkinje cells in the literature. (2–3 m/sec) than by ventricular cardiomyocytes (0,3–0,4 m/sec).
Thus, in the paper of Obermeier already, a description of three types That is thanks to a group of proteins – connexins C40,C43, C45. If
of Purkinje cells (see the chapter about history) may be found. the connexins are knockouted, a disturbance appears in conduction
Another description of 3 types of Purkinje cells was given in of impulses through the AV node and Purkinje fibers, including the
1973 and 1987 (50, 51): spatial conduction of impulses (65, 66). A confocal laser micro-
Type I. – The cells of this type are situated in the area of the scope is used in mapping normal and abnormal dynamics of Ca2+ in
atrioventricular bundle bifurcation and in the proximal part of Purkinje conduction cells (67). An accumulation of Ca2+ in the
branches. They contain a small amount of myofibrils and the cells cytosol in the present of cardiotonic agens leads to tachyarrhyth-
are smaller (6 microns of diameter) than in type II. mias in the Purkinje cells but not in the working ventricular car-
Type II. – These are the biggest Purkinje fibers (10–20 microns diomyocytes (68). Lately, the genes influencing the development of
(332)
ČAS OP I S L ÉK A ŘŮ Č ESK Ý C H , 145, 2006, N o. 4
(333)
ČAS OP I S L ÉK A ŘŮ Č ESK Ý C H , 145, 2006, N o. 4
L I TE R A TU R E 31. Bharati, S., Lev, M.: Morphology of the sinus and atrioventricular
nodes and their innervation. In: Electrophysiology of the Sinoatrial and
1. Purkyně, J. E.: Mikroskopisch-neurologische Beobachtungen. Arch. Atrioventricular nodes, Alan R. Liss, Inc., 1988, pp. 3-14.
f. Anat. Physiol. wiss. Med. 1845, 12, pp. 281-295. 32. Truex, R. C.: Comparative anatomy and functional considerations of
2. Purkyně, J. E.: Nowe spostrzezenia i badania przedmiocie Fizyologii the cardiac connecting system . In: de Carvalho, A. P., de Mello, W. C.:
i drobnowidzowéj Anatomii udzielone przez naszego Czlonka korres- The specialized tissues of the heart. Elsevier Publish. Company, 1961,
pondenta Dr. J. E. Purkiniego. Rocznik wydzialu lekarskiego w uni- pp. 22-43.
wersytecie Jagiellonskim. Krakow. 1839, Tom II, pp. 44-67. 33. Truex, R. C., Smythe, M. Q.: Recent observation on the human car-
3. Borovanský, L., Weigner, K.: Anatomické práce Jana Ev. Purkyně. diac connecting system , with special considerations of the atrioventri-
Sborník „Jan Ev. Purkyně 1787–1937“ pp. 3-31. Praha, Edice Purky- cular node and bundle. In: Taccardi, B.,Marchetti, G., eds. Electrophy-
ňova společnost, 1937. In Czech. siology of the heart. Symposium Publications Div. Pergamon Press,
4. Kölliker, A. : Mikroskopische Anatomie oder Gewebelehre des Men- 1965, pp. 177-198.
schen. Bd. II, 1854, p. 494. 34. Truex, R. C.: Anatomical considerations of the human atrioventricu-
5. Chodounský, K.: Jan Evang. Purkyně, působení jeho pro rozvoj čes- lar junction. In: Dreifus, L.S., Likoff, W., eds. Mechanisms and thera-
ké kultury. Praha, Nakladatelství české akademie věd a umění, 1927. py of cardiac arrythmias. New York, Grune and Stratton, 1966, pp.
In Czech. 333-340.
6. Obermeier, H.: Ueber Structur und Textur der Purkinje’schen Fäden. 35. Truex, R. C., Smythe, M. Q.: Reconstruction of the human atrioven-
Archiv f. Anat. Physiol. u. wiss. Med., 1867, pp. 358-386. tricular node. Anat. Rec., 1967, 158, pp. 11-20.
7. Tawara, S.: Das Reizleitungssystem des Säugetierherzens. Eine ana- 36. James, T. N., Sherf, L.: Ultrastructure of the human atrioventricular
tomisch-histologische studie über das Atrioventricularbündel und die node. Circulation, 1968, 37, pp. 1049-1070.
Purkinjeschen Fäden. Jena, Verlag v. Gustav Fischer, 1906. 37. Anderson, R. H., Becker, A. E., Brechenmacher, C.: The human
8. Suma, K.: Sunao Tawara: a father of modern cardiology. PACE, 2001, atrioventricular junction area. A morphological study of the AV node
24, pp. 88-96. and bundle. Europ. J. Cardiol., 1975, 3, pp. 11-25.
9. Einthoven, W.: Weiteres über das Elektrokardiogram. Pflüger 38. Truex, R. C., Marino, T. A., Marino, D. R.: Observations on the
Archiv.ges. Physiol., 1908, 122, pp. 517-584. development of the human atrioventricular node and bundle. Anat.
10. DeWitt, L.: Observations of the sino-ventricular connecting system of Rec., 1978, 192, pp. 337-350.
the mammalian heart. Anat. Rec., 1909, 3, pp. 475-497. 39. Sherf, L., James, T. N.: Fine structure of cells and their histologic
11. His, W. Jr.: Die Thätigkeit des embryonalen Herzens und deren Bede- organization within internodal patways of the heart: clinical and elect-
utung für die Lehre von der Herzbewegung beim Erwachsenen. Arbe- rocardiographic implications. Am. J. Cardiol., 1979, 44, pp. 345-369.
iten aus der med. Klinik zu Leipzig 1893, pp. 14-49. 40. Anderson, R. H., Yen, H. S., Smith, A., Becker, A. E.: The interno-
12. Kent A.F.S.: Researches on the structure and function of the mamma- dal atrial myocardium. Anat. Rec., 1981, 201, pp. 75-82.
lian heart. J. Physiol., 1893, 14, pp. 233-254. 41. Ayetty, A. S., Navaratnem, V., Yates, R. D.: Ultrastructure of the
13. Keith A.,Flack M.: The form and nature of the muscular connections internodal myocardium in the rat. J. Anat., 1988, 158, pp. 77-90.
between primary divisions of the vertebrate heart. J. Anat. Physiol., 41, 42. Anderson, R. H, Christoffels, V.M., Moorman, A. F. M.: Controve-
1907, pp. 172-189. sies concerning the anatomical definition of the connecting system .
14. James T.N.: The connecting pathways between the sinus node and A- Anat. Rec. (Part B: New Anat.) , 2004, 280 B, pp. 8-14.
V node and between the right and left atrium in the human heart. Am. 43. Aschoff, L.: Referat über die Herzstörungen in ihren Beziehungen zu
Heart J., 1963, 66, pp. 498-508. den spezifischen Muskelsystemen des Herzens. Verhandlungen der
15. Meredith J., Titus J.L.: The anatomic atrial connections between the deutsch. pathol. Gesellschaft, 1910, 14, pp. 3-35.
sinus and AV node. Circulation, 1968, 37, pp. 566-579. 44. Mönckeberg, J. G.: Beiträge zur normalen und pathologischen Ana-
16. James, T. N., Sherf, L.: Specialized tissues and preferential conduc- tomie des Herzens.Verhandlungen deutsch. pathol. Gesellschaft, 1910,
tion in the atria of the heart. Am. J. Cardiol., 1971, 28, pp. 414-427. 14, pp. 64-71.
17. Bachman, G.: The interatrial time interval. Am. J. Physiol., 1916, 41, 45. Emberson, J. W., Challice, C. E: Studies on the impulse conducting
pp. 309-320. patways in the atrium of the mammalian heart. Am. Heart J., 1970, 79,
18. Wenckebach, K. F.: Beiträge zur Kenntnis der menschlichen Herz- pp. 653-667.
tätigkeit. Arch. Anat. Physiol. (Lpz), Physiol. Abt., 1907, 1, pp. 1-2. 46. Bojsen-Moller, F., Tranum-Jensen, J.: Rabbit heart nodal tissue
19. Thorel, Ch.: Über die supraventrikulären Abschnitt des sog. Reizlei- sinuatrial ring bundle and atrioventricular connexions identified as
tungssystems. Verhandlungen der deutsch. pathol. Gesellschaft, 1910, a neuromuscular system. J. Anat., 1972, 112, pp. 367-382.
14, pp. 71-90. 47. James, T. N., Sherf, L., Urthaler, F. : Fine structure of the bundle-
20. Opthof, T.: The mammalian sino-atrial node. Cardiovasc. Drugs The- branches. Br. Heart J., 1974, 36, pp. 1-18.
rapy, 1988, 1, pp. 573-597. 48. Vassall–Adams, P. R. : Ultrastructure of the human atrioventricular
21. Söderström, N.: Myocardial infarction and mural thrombosis in the conduction tissues. Europ. Heart J., 1983, 4, pp. 449-460.
atria of the heart. Acta Med. Scand., 1948, 217, pp. 1-114. 49. Hondeghem, L. M., Stroobandt, R.: Purkinje fibers of sheep papilla-
22. Viragh, S., Porte, A.: The fine structure of the conducting system of ry muscle: occurrence of discontinuous fibers. Am. J. Anat., 1973, 141,
the monkey heart (Macaca mulatta). I. The sino-atrial node and inter- pp. 251-262.
nodal connections. Z. Zellforsch. Mikrosk. Anat., 1973, 145, pp. 191- 50. Viragh, S. Challice, C. E.: The impulse generation and conduction
211. system of the heart. In: Ultrastructure in biological systems, V 6. Ult-
23. Hudson, R. E.: The human pacemaker and its pathology. Br. Heart J., rastructure of the mammalian heart. New York, London, Academic
1960, 22, pp. 153-167. Press, 1973, pp. 43-89.
24. James, T. N.: Anatomy of the human sinus node. Anat. Rec., 1961, 51. Viragh, S., Stoeckel, M. E., Porte, A.: Light and electron microsco-
141, pp. 109-139. pic structure of the cardiac Purkinje fibers. Physiologia Bohemoslova-
25. James, T. N.: The sinus node. Reviews. Amer. J. Cardiol., 1977, 40, ca, 1987, 36, pp. 233-242.
pp. 965-986. 52. Thornell, L. E., Sjöstrom, M., Anderson, K. E.: The relationship
26. Sano, T., Mizuhira, V., Matsuda, K.: Electrophysiology and ultra- between mechanical stress and myofibrillar organization in heart Pur-
structure of the heart. Grune Stratton Inc., 1967, kinje fibers. J. Mol. Cell Cardiol., 1976, 8, pp. 689-695.
27. Truex, R. C., Smythe, M. Q., Taylor, M. J.: Reconstruction of the 53. Thornell, L. E., Eriksson, A., Stigbrand T., Sjöström, M.: Structu-
human sinoatrial node. Anat. Rec., 1967, 159, pp. 371-78. ral proteins in cow Purkinje and ordinary ventricular fibres - a marked
28.. Davies, M. J.: Pathology of conducting tissue of the heart. London, difference. J. Mol. Cell Cardiol., 1978, 10, pp. 605-616.
Butterworth, 1971. 54. Thornell, L. E., Eriksson, A.: Filament systems in the Purkinje fibres
29. Bonke, F. I. M.: The sinus node. Structure, function and clinical rele- of the heart. Am. J. Physiol., 1981, 241, pp. H291-H305.
vance. Martinus Nijhoff Med. Div., 1978. 55. Thornell, L. E., Forsgren, S.: Myocardial cell heterogenity in the
30. Canale, E. D., Smolich, J. J., Campbell, J. H.: Cardiac muscle. Ber- human heart with respect to myosin ATPase activity. Histochem. J.,
lin, Heidelberg, New York, Tokyo, SpringerVerlag, 1986. 1982, 14, pp. 479-490.
(334)
ČAS OP I S L ÉK A ŘŮ Č ESK Ý C H , 145, 2006, N o. 4
56. Sommer, J. R., Johnson, E. A.: Cardiac muscle. A comparative stu- 69. Rentschler, PP.,Vaidya, D. M., Tamaddon, H. et al.: Visualization
dy of Purkinje fibers and ventricular fibers. J. Cell Biol., 1968, 36, pp. and functional characterization of the developing murine cardiac con-
497-526. duction system. Development, 2001, 128, pp. 1785-1792.
57. Friedman, P. L.,Stewart, J. R.,Fenoglio, J. J. Jr., Wit, A. L.: Sur- 70. Rosen, M. R., Brink, P. R, Cohen, I. S., Robinson, R. B.: Genes,
vival of subendocardial Purkinje fibers after extensive myocardial stem cells and biological pacemakers. Cardiovascular Res. 2004, 64,
infarction in dogs. Circ. Res., 1973, 33, pp. 597-611. pp. 12-23.
58. Tanaka, H., Hamamoto, T., Takamata, T.: Toward integrated under- 71. Thakur, R. K., Klein, G. J., Sivaram, Ch. A. et al.: Anatomic sub-
standing of the Purkinje fibers in the heart: the functional and morp- strate for idiopathic left ventricular tachycardia. Circulation, 1996, 93,
hological inteconnection between the Purkinje fibers and ventricular pp. 497-501.
muscle. Acta Histochem. Cytochem., 2005, 38, pp. 257-265. 72. Fiala, M., Heinc, P., Lukl, J.: „Focal“ atrial fibrillation: initial expe-
59. Tranum-Jensen, J.,Wilde, A. A., M.,Vermeulen, J. T., Janse, M. rience with endocardial electrographic pictures and long term results
J.: Morphology of electrophysiologically identifed junctions between after radiofrequency catheter ablation. Cor Vasa, 2001, 43, pp. 11-16.
Purkinje fibers and ventricular muscle in rabbit and pig heart. Circ. 73. Munclinger, M. J., Pillay, R. G., Patel, J. J., Mitha, A. S.: Unusual
Res., 1991, 69, pp. 429-437. location of the substrate of fascicular idiopathic left ventricular tachy-
60. Oosthoek, P. W., Viragh, S., Lamers, W. H., Moorman, A. F. M.: cardia. Cor. Vasa, 2002, 44, pp. 87-90.
Immunohistochemical delineation of the conduction system. II. The 74. Ouyang, F., Fotuhi, P., Masahiko, G. et al.: Ventricular tachycardia
atrioventricular node and Purkinje fibers. Circ Res., 1993, 73, pp. 482- around the tricuspid annulus in right ventricular dysplasia. Circulation,
491. 2001, 103, pp. 913-914.
61. Gilmour, R. F., Evans, J. J., Zipes, D.: Purkinje-muscle and endo- 75. Kholová, I., Kautzner, J.: Anatomic characteristic of extensions of
cardial response to hyperkalemia, hypoxia and acidosis. Am. J. Physi- atrial myocardium into the pulmonary veins in subjects with and wit-
ol, 1984, 247, pp. H303-H311. hout atrial fibrilation. PACE, 2003, 26, pp. 1348-1355.
62. Sasyniuk, B. I., Mendez, C.: A mechanism of reentry in canine ven- 76. Patterson, E., Po, S. S., Scherlag, B. J., Lazzaram R.: Triggered
tricular tissue. Circ. Res., 1971, 28, pp. 3-15. firing in pulmonary veins initiated by in vitro autonomic nerve stimu-
63. Spach, M. S., Kootsey, J. M.: The nature of electrical propagation in lation. Hearth Rhythm., 2005, 2, pp. 624-631.
cardiac muscle. Am. J. Phys., 1983, 244, pp. H3-H22. 77. Šteiner, I.: Neznámá priorita Jana Ev. Purkyně: myokardialní rukávce
64. Kleber, A. G., Rieber, A. G., Janse, M. J.: Electrical uncoupling and plicních žil – příspěvek k patogenezi fibrilace síní. Čas. Lék. čes.,
increase of extracellular resistance after induction of ischemia in iso- 2005, 144, pp. 709-710. In Czech.
lated, arterially perfused rabbit papillary muscle. Circ. Res., 1987,61, 78. Ho, S. Y, Cabrera, J. A., Tran, V. H. et al.: Architecture of the pul-
pp. 271-279. monary veins relavence to radiofrequency ablation. Heart, 2001, 86,
65. Simon, A. M., Goodenough, D. A., Paul, D. L.: Mice lacking conne- pp. 265-270.
xin 40 have cardiac conduction abnormalities characteristic of atrio- 79. Eliška, O., Elišková, M.: Morphology of the coronary sinus in respect
ventricular and bundle branch block. Curr. Biol., 1998, 8, pp. 295-298. to coronary sinus rhythm. Inter. J. Cardiol., 1990, 29, pp. 141-153.
66. van Veen, T. A. B., van Rijen, H. V. M., van Kempen, M. J. A. et 80. Eliška, O., Elišková, M.: Subsidiární rytmy krajiny sinus coronarius.
al.: Discontinouous conduction in mouse bundle branches is caused by Čs. Fysiol., 1991, 40, pp. 273-282. In Czech.
bundle-branch architecture. Circulation, 2005, 112, pp. 2235-2244.
67. Tanaka, H., Takamatsu, T.: Spatiotemporal visualization of intracel-
lular Ca2+ in living heart muscle cells viewed by confocal laser scan-
ning microscopy. Acta Histochem. Cytochem., 2003, 36, pp. 193-204. The paper was supported by the research plan - MSM 0021620807.
68. Lee, F..Y., Wei, J., Wang, J. J. et al.: Electromechanical properties
of Purkinje fiber strands isolated from human ventricular endocardi- Translation: A. Hejčl
um. J. Heart Lung Transplantation, 2004, 23, pp. 737-744.
(335)