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Brit. Heart J., 1965, 27, 420. AN X-RAY MICROSCOPIC STUDY OF THE BLOOD SUPPLY TO THE VALVES OF THE HUMAN HEART BY JOHN A. CLARKE Fronm the Department of Anatomy, University of Glasgow, Glasgow W.2 Received October 19, 1964 Descriptions of the presence of blood vessels in the valves of human hearts vary. Using routine histological, injection, and clearing techniques, the majority of authors have described vessels in the attached portion of the cusp, but differ on the incidence of this observation and its relation to com- pletely normal histological valve structure. Thus Gross (1921) demonstrated blood vessels in 6 per cent of normal mitral valves from birth until the ninth decade of life, and reported that this finding possibly had some relation to the incidence of endocarditis in the vascularized valves. This view was supported by several authors (Kugel and Gross, 1926; Kugel, 1928; Ritter, Gross, and Kugel, 1928; Gross and Kugel, 1931). Gross and Friedberg (1936a, b) thought that any vascularized heart valve was probably abnormal. In a critical review of the observations of previous authors and from an examination of human and animal heart valves, Gross (1937) thought that the majority of human heart valves were avascu- lar, and emphasized the need for careful interpretation of any vascularity and the presence of previous histological damage. Winternitz, Thomas, and LeCompte (1938) examined normal and diseased valves by injection and clearing techniques, and reported vessels in the normal cusps of atrio- ventricular valves, which had an endocardial origin. Harper (1945) investigated human and rabbit heart valves by injection and vital staining tech- niques; he showed that human heart valves were "largely avascular", that vessels in diseased valves were of inflammatory origin, and that new blood vessel formation could be induced in rabbits after the injection of aleuronate. The present work gives an account of the blood supply to the valves of the human heart, using the Coslett Nixon X-ray projection microscope. This technique gives an opportunity for examining small arterioles and capillary beds without histological preparation in contrast to the routine histological, injection, and clearing techniques of previous investigations. MATERIAL AND METHODS Fifty normal human hearts were obtained within 12 hours of death and examined in equally distributed 5-year groups between the 15th and 80th years. After perfusion with saline at 370 C. for 2 hours, the hearts were injected with micropaque (particulate diameter 0 5 F or less) through the ascending aorta, at manometri- cally controlled physiological pressures. X-ray projection micrographs were recorded on Ilford Contrasty Plates with an exposure time of IG minutes. The microscope was operated at 15 kV and 40 microamperes, a copper target providing the x radiation. All the valves were examined histologically after injection and radiography to exclude the presence of previous disease, even in the presence of a negative history of cardiac involvement. 420 on January 7, 2020 by guest. Protected by copyright. http://heart.bmj.com/ Br Heart J: first published as 10.1136/hrt.27.3.420 on 1 May 1965. Downloaded from

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Page 1: ANX-RAY MICROSCOPIC STUDY OF THE BLOOD SUPPLY TO ... - Heart · Brit. HeartJ., 1965, 27, 420. ANX-RAY MICROSCOPIC STUDY OF THEBLOOD SUPPLY TO THEVALVES OFTHEHUMANHEART BY JOHNA. CLARKE

Brit. Heart J., 1965, 27, 420.

AN X-RAY MICROSCOPIC STUDY OF THE BLOOD SUPPLY TOTHE VALVES OF THE HUMAN HEART

BY

JOHN A. CLARKE

Fronm the Department ofAnatomy, University of Glasgow, Glasgow W.2

Received October 19, 1964

Descriptions of the presence of blood vessels in the valves of human hearts vary. Using routinehistological, injection, and clearing techniques, the majority of authors have described vessels in theattached portion of the cusp, but differ on the incidence of this observation and its relation to com-pletely normal histological valve structure. Thus Gross (1921) demonstrated blood vessels in 6 percent of normal mitral valves from birth until the ninth decade of life, and reported that this findingpossibly had some relation to the incidence of endocarditis in the vascularized valves. This viewwas supported by several authors (Kugel and Gross, 1926; Kugel, 1928; Ritter, Gross, and Kugel,1928; Gross and Kugel, 1931). Gross and Friedberg (1936a, b) thought that any vascularizedheart valve was probably abnormal.

In a critical review of the observations of previous authors and from an examination of humanand animal heart valves, Gross (1937) thought that the majority of human heart valves were avascu-lar, and emphasized the need for careful interpretation of any vascularity and the presence ofprevioushistological damage. Winternitz, Thomas, and LeCompte (1938) examined normal and diseasedvalves by injection and clearing techniques, and reported vessels in the normal cusps of atrio-ventricular valves, which had an endocardial origin.

Harper (1945) investigated human and rabbit heart valves by injection and vital staining tech-niques; he showed that human heart valves were "largely avascular", that vessels in diseasedvalves were of inflammatory origin, and that new blood vessel formation could be induced in rabbitsafter the injection of aleuronate.

The present work gives an account of the blood supply to the valves of the human heart, usingthe Coslett Nixon X-ray projection microscope. This technique gives an opportunity for examiningsmall arterioles and capillary beds without histological preparation in contrast to the routinehistological, injection, and clearing techniques of previous investigations.

MATERIAL AND METHODSFifty normal human hearts were obtained within 12 hours of death and examined in equally distributed

5-year groups between the 15th and 80th years. After perfusion with saline at 370 C. for 2 hours, the heartswere injected with micropaque (particulate diameter 0 5 F or less) through the ascending aorta, at manometri-cally controlled physiological pressures.

X-ray projection micrographs were recorded on Ilford Contrasty Plates with an exposure time of IGminutes. The microscope was operated at 15 kV and 40 microamperes, a copper target providing thex radiation.

All the valves were examined histologically after injection and radiography to exclude the presence ofprevious disease, even in the presence of a negative history of cardiac involvement.

420

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BLOOD SUPPLY TO VALVES OF HUMAN HEART

RESULTSIt was clear from the micrographs that the arterial supply to the atrio-ventricular, aortic, and

pulmonary valves originated from terminal atrial and ventricular branches of the coronary arteries.Atrio-ventricular Valves. (a) Tricuspid Valve. Of the 50 tricuspid valves examined, only 8

were shown to have vessels in their attached margin, and came from the age-group of 35-50 years.The picture was the same in these 8 cases: arterioles 40-80 V. in diameter lay in the attached marginof all the cusps and divided to distribute a capillary network in the proximal 3 mm. of the cusp(Fig. 1). In this group no vessels could be demonstrated arising from the endocardial surfaceor along the chordc tendinee from the papillary muscles. It was found that when a cusp wasvascularized, the adjacent cusps showed equal vascularity.

(b) Mitral Valve. Of the 50 mitral valves examined, 5 were shown to have vessels in theirattached margins, and all these specimens came from hearts in which the tricuspid valve was vas-cularized. Both cusps were equally supplied, the picture consisting of arterioles, 30-60 ,x in diameter,which distributed a capillary plexus to the proximal 2 mm. of the cusps (Fig. 2). No vessels werefound in the chordc tendineae.

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DD

FIG. I.-Micrograph* of the septal cusp of the tricuspidvalve from a subject aged 35 years. Note thearterioles (a) at the attachment of the cusp (b)dividing to distribute a capillary plexus (p) to theproximal part of the cusp (P). Distal part of thecusp (D) is avascular. (x 47.)

FIG. 2.-Micrograph of the anterior cusp of the mitralvalve from a subject aged 40 years. Note thearterioles (a) at the attachment of the cusp (b)dividing to distribute a capillary plexus (p) to theproximal part of the cusp (P). Distal part (D) isavascular. ( x 55.)

* All micrographs are of full thickness specimens. Long axis of valve cusp and papillary muscle (1-a).

(c) Aortic Valve. In this group, 12 of the 50 aortic valves examined were shown to have ablood supply, all the specimens coming from the 20-40 year age-group. In each case arterioles,30-40 p in diameter, lay at the attached margin and distributed a capillary network to the proximal3 mm. of the valve cusps (Fig. 3). The distribution was equal in all the cusps.

(d) Pulmonary Valve. Twelve specimens had vessels in the cusps of the pulmonary valve, andcame from the same hearts in which the aortic valve was vascularized. In each case arterioles,20-30 F in diameter, lay at the attached margin of the cusps and divided to supply the proximal3 mm. ofthe cusp with a capillary plexus (Fig. 4).

(e) Papillary Muscles. In all the specimens examined the papillary muscles were vascularized.

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JOHN A. CLARKE

b-

D D

FIG. 3.-Micrograph of the aortic valve from a subjectaged 25 years. Note the arterioles (a) at theattachment of the cusp (b) dividing to distribute acapillary plexus (p) to the proximal part of thecusp (P). Distal part (D) is avascular. (x 70.)

.

FIG. 5.-Micrograph of the papillary muscle attachedto the anterior cusp of the mitral valve from asubject aged 40 years. Note the parallel arterioles(a) in the papillary muscle (p) ending in a "hair-pin" fashion (b), and the avascular chordatendinea (c). (x 17.)

...

rp

D D

FIG. 4.-Micrograph of the pulmonary valve from asubject aged 30 years. Note the arterioles (a) atthe attachment of the cusp (b) dividing to supply acapillary plexus (p) to the proximal part of thecusp (P). Distal part (D) is avascular. ( x 70.)

Adjacent to the attachment of the chordaetendinem to the papillary muscles, arterioles,60-80 V. in diameter, lay along the long axis ofthe papillary muscle in closely assembled parallelgroups. On reaching the apex of the papillarymuscle, the arterioles looped back on their coursein a "hairpin" manner, an occasional vesselbeing distributed from the convexity of the loopfor a short distance. This pattern was unchangedin the specimens showing vessels in the heartvalves (Fig. 5).

DISCUSSIONStaining methods are particularly suitable

for investigating adaptive changes in vascularpatterns under varying conditions, giving a truepicture of the actual physiological state of thecirculation at that time. Injection methods, incontrast, present the vascular pattern at itsmaximum capacity, and are suitable for purelyanatomical investigations. Consequently, withthe technical advantages of x-ray microscopy,the blood supply to the valves was studied bythis method.

On the other hand, techniques that require staining of red cells depend upon the uniform fillingof the capillaries with red cells at the time of death, and failure to demonstrate vessels by Pickworth'smethod (sodium nitroprusside and benzidene stain) may be due to lack of blood within the vessels.Demonstration of vessels by showing alkaline phosphatase in endothelial cells (Scharrer, 1950) doesnot allow the pattern of the vessels to be appreciated, in contrast to the routine x-ray micrograph.

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BLOOD SUPPLY TO VALVES OF -HUMAN HEART

The present study has shown that the atrio-ventricular, aortic, and pulmonary valves, may haveblood vessels in their cusps.

As indicated by the x-ray microscope 16 per cent of the tricuspid valve cusps were vascularized,10 per cent of the mitral, 24 per cent of the aortic and 24 per cent of the pulmonary valve cusps.

The criterion for regarding an area as avascular was the repeated failure to introduce the injectionmedium into vessels when capillary beds were filled elsewhere in the same specimen under similarconditions.

In any interpretation of a valve cusp being vascularized care must be taken to ensure that thereis no histological abnormality in the specimen. In this series the cusps that were reported as vascularcame from hearts with a negative clinical history, and where there was no histological evidence ofthe various degrees of healing that may occur after valvular endocarditis.

The observation by Winternitz et al. (1938) that vessels may originate from the endocardialsurface of the valve cusps was not confirmed.

In contrast to the estimate by Gross (1921) that 6 per cent of the cusps of mitral valves werevlscularized, this series has shown that 10 per cent of mitral cusps possess blood vessels. The twofigures are reasonably close, and it is suggested that the improved technique of x-ray microscopy maybe demonstrating more vessels in contrast to the routine histological, injection, and clearing tech-niques used previously.

The "hairpin" pattern of the arterioles in the papillary muscles was characteristic. Though anoccasional vessel arose from the convexity of the loop and approached the chord& tendineae for ashort distance, no vessels could be demonstrated in the chordae.

As indicated by the x-ray microscope there was no evidence of alteration in the pattern of thevessels in the cusps that were vascularized with age.

SUMMARYThe blood supply to the valves of the heart and great vessels was studied by the Coslett Nixon

X-ray projection microscope.Vascularization was found in 16 per cent of the cusps in the tricuspid valve, in 10 per cent of the

mitral cusps, and in 24 per cent of the aortic and pulmonary cusps.A characteristic arteriolar pattern, which was "hairpin" in nature, was described in the papillary

muscles.

I am indebted to the Medical Research Council who gave the X-ray microscope to the Anatomy Department,University of Glasgow.

REFERENCESGross, L. (1921). The Blood Supply to the Heart in its Anatomical and Clinical Aspects. Hoeber, New York.

(1937). Significance of blood vessels in human heart valves. Amer. Heart J., 13, 275.and Friedberg, C. K. (1936a). Lesions of the cardiac valve rings in rheumatic fever. Amer. J. Path., 12,469.and (1936b). Lesions of the cardiac valves in rheumatic fever. Amer. J. Path., 12, 855.

- ,and Kugel, M. A. (1931). Topographic anatomy and histology of the valves in the human heart. Amer. J.Path., 7, 445.

Harper, W. F. (1945). The structure of the heart valves, with special reference to their blood supply and the genesis ofendocarditis. J. Path. Bact., 57, 229.

Kugel, M. A. (1928). Anatomical studies on the coronary arteries and their branches. I. Arteria anastomoticaauricularis magna. Amer. Heart J., 3, 260.and Gross, L. (1926). Gross and microscopical anatomy of the blood vessels in the valves of the human heart.Amer. Heart J., 1, 304.

Ritter, S. A., Gross, L., and Kugel, M. A. (1928). Blood vessels in the valves of normal human hearts. Amer.Heart J., 3, 433.

Scharrer, E. (1950). A technique for the demonstration of the blood vessels in the developing central nervous system.Anat. Rec., 107, 319.

Wintemitz, M. C., Thomas, R. M., and LeCompte, P. M. (1938). The Biology ofArteriosclerosis. Charles Thomas,Springfield, Illinois.

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