The papillary muscles (FM) of the heart have been the subject of numerous s
tructural and functional studies. However, despite the importance of the co
llagenous compartment of the heart in the mechanical and electrical propert
ies of the myocardium, little information is available on the structural or
ganization of collagen within the PM. We study here the structural organiza
tion of collagen within the mitral papillary muscles (PM) of the human hear
t. Fragments of human mitral PM from normal and hypertensive subjects were
macerated in NaOH to eliminate the cellular components. Macerated and nonma
cerated samples were then studied with the scanning electron microscope (SE
M).
SEM shows that cardiac myocytes and endomysial capillaries are ensheathed i
n a layer of collagenous tissue. The myocyte sheath wall is formed by thin
collagen fibers oriented at right angles to the main cell axis. These sheat
hs are open structures, collagen fibers continuing into adjacent sheaths at
the points of lateral communications. Thick perimysial septa do not divide
the PM tissue into separate compartments. Hypertensive hearts show perivas
cular and interstitial fibrosis. In addition, the lumen of the coronary ves
sels is reduced or obliterated, and large areas of the myocardium are subst
ituted by densely packed collagen. Endomysial sheaths constitute a continuo
us collagenous layer that replicates the myocyte network. The endomysium sh
ould play a complex role in myocardial mechanics, assuring the equal distri
bution of force during the cardiac cycle. The absence of insulating boundar
ies should facilitate lateral propagation of excitation. Fibrosis in hypert
ensive hearts appears to be both reactive and reparative. The increase in t
he amount of collagen should greatly impair contractile capabilities and el
ectrical conductance, severely compromise heart function, and contribute to
development of heart failure. Anat. Rec. 252:509-518, 1998. (C) 1998 Wiley
-Liss, Inc.