a) The HOOF CAPSULE surrounds: the distal end of the middle
phalanx (C), the distal interphalangeal joint (L), and the distal pha-
lanx (coffin bone, D) with the terminations of the common dig.
extensor tendon (H) on the extensor process and the deep dig. flex-
or tendon (K) on the flexor tubercle. Also enclosed is the distal
sesamoid (navicular) bone (E), which serves as a trochlea for the
deep dig. flexor tendon. The navicular bursa (M) reduces friction
between them.
The cornified hoof capsule consists of the lamina (horny wall) with
an abaxial part, a dorsal border, and an axial part facing the inter-
digital space, as well as the horny sole and horny bulb. The capsule
has a thickness of about 10 mm in the dorsal part and about 5 mm
in the axial part. The growth of the epidermis pushes the cornified
masses distally at a rate of about 5 mm per month. After an exun-
gulation the renewal of the entire hoof capsule would require up to
20 months. Horn formation is more intensive in calves than in
adults and more active on the pelvic than on the thoracic limb. In
the last third of pregnancy and in very high milk production, horn
formation is reduced. That is shown on the superficial surface of
the hoof by the formation of semicircular grooves.
When cattle are kept on soft footing with little or no possibility of
exercise the horn grows faster than it is worn off and therefore the
hoofs must be trimmed regularly.
I. The lamina (Paries corneus) consists of external, middle, and
internal layers, which are bonded together and formed by the peri-
oplic, coronary, and wall segments respectively. The external layer
is very thin; the middle layer constitutes the bulk of the lamina; and
the internal layer bears the horny lamellae that make up the junc-
tional horn.
II. The junctional horn is part of the suspensory apparatus of the
coffin bone. This term includes all of the tissues that attach the cof-
fin bone (distal phalanx) to the inside of the lamina. The suspenso-
ry apparatus of the coffin bone consists of a connective tissue (der-
mal) part and an epidermal part. Collagenous fiber bundles
anchored in the outer zone of the coffin bone run obliquely proxi-
modorsally in the reticular layer and then in the lamellae of the der-
mis. The collagen fibers are attached to the basement membrane.
The tension is then transmitted through the living epidermal cell
layers by desmosomes and bundles of keratin filaments to the junc-
tional (lamellar) horn, which is attached to the lamina. The pres-
sure exerted on the coffin bone by the body weight is transformed
by the shock absorbing suspensory apparatus of the coffin bone
into tension; the tension is transformed in the lamina to pressure;
this pressure weighs upon the ground at the solear border of the
lamina. One part of the body weight is not transformed, but falls
directly on a support of solear and apical bulbar horn. In the basal
bulbar segment the elastic horn and the thick subcutaneous cush-
ion act as a shock absorbing mechanism of the hoof. The cham-
bered cushions work in a manner comparable to the gel cushion
system of modern running shoes. With the exception of a non-
weightbearing concavity at the axial end of the white zone, the sole
and bulb horn form a flat ground surface.
The suspensory apparatus of the coffin bone actuates the hoof
mechanism by traction on the internal surface of the lamina and by
pressure on the sole and bulb. This can be measured with strain
gauges. It concerns the elastic changes in form of the hoof capsule
that occur during loading and unloading. In weight bearing, the
space inside the lamina is reduced, while the palmar/plantar part of
the capsule expands and the interdigital space is widened. During
unloading, the horny parts return to their initial form and position.
III. The rate of horn formation differs greatly among the individual
hoof segments. In the coronary segment horn formation is very
intensive. In the proximal half of the wall segment the rate of horn
formation is low. In the distal half, on the other hand, horn is
formed in measurable amounts and at an increasing rate toward the
apex of the hoof. (The term sterile bed, used in older textbooks for
the wall segment is therefore incorrect.) Proximally in the wall seg-
ment the beginnings of the dermal lamellae bear proximal cap
papillae. From the epidermis on these papillae, nontubular proxi-
mal cap horn is produced. This is applied to the sides of the proxi-
mal parts of the horny lamellae. Distal to the cap horn, as far as the
middle of the wall, not much lamellar horn is added. In the distal
half of the wall segment the horny lamellae become markedly high-
er, up to 5 mm, and, beginning with their middle portion, become
flanked by amorphous distal cap horn that is applied cap-like over
the edges of the dermal lamellae. It is formed on the distal cap
papillae by the living epidermis there (see p. 27, right figure).
Distally on the wall-sole border the almost vertically directed der-
mal lamellae bend into horizontally directed dermal ridges of the
sole segment. At the bend the lamellae are split into terminal der-
mal papillae which have a remarkable diameter of 0.2–0.5 mm.
They are covered by living epidermis from which terminal tubular
horn is formed. As a part of the white zone the terminal horn fills
the spaces between the horny lamellae (see p. 27, right figure).
IV. The white zone (white line) consists only of horn produced by
the wall segment, and presents external, middle, and internal parts.
The external part (a) appears to the naked eye as a shining white
millimeter-wide stripe. It consists of the basal sections of the horny
lamellae and the flanking proximal cap horn, and borders the most-
ly nonpigmented inner coronary horn, which does not belong to the
zona alba. The middle part (b) of the white zone is formed by the
intermediate sections of the horny lamellae with the distal cap horn
that lies between them. The internal part (c) of the white zone con-
sists of the crests of the horny lamellae and, between them, the ter-
minal tubular horn. They cornify in the distal half of the wall or at
the wall-sole border.
The white zone has abaxial and axial crura (b", b'), which lie
between the mostly unpigmented coronary horn and the sole horn.
The axial crus ends halfway between the apex of the hoof and the
palmar/plantar surface of the bulb. The abaxial crus extends far-
ther, to the basal part of the bulb, where the end of the white zone
becomes distinctly wider and turns inward. (See p. 25 above and
text illustration.) The whole white zone and especially the wider
abaxial end are predisposed to “white line disease,” which by
ascending infection can lead to “purulent hollow wall.” The way
for ascending microorganisms is opened by crumbling cap and ter-
minal tubular horn, which technical material testing proves to be
masses of soft horn.
V. Horn quality is the sum of the characteristics of the biomaterial
horn, including hardness or elasticity, resistance to breakage, water
absorption, and resistance to chemical and microbial influences.
Horn quality is adapted to the biomechanical requirements of the
different parts of the hoof. Accordingly, hard horn is found in the
lamina; soft elastic horn in the proximal part of the bulb. Horn
quality can be determined by morphological criteria in combina-
tion with data from physicotechnical material testing.
26
7. THE HOOF (UNGULA)
a White zone
Sole:
b Body of the sole
b' Axial crus
b" Abaxial crus
Bulb of hoof:
c Basal part
c' Apical part
c'
b'
b"
Anatomie des Rindes englisch 09.09.2003 12:36 Uhr Seite 26