Keywords
eidolon helvum
- uterus - fiber - gravid - non-gravid
Introduction
Bats are unmistakable, as no other mammal has true wings for flight. Globally, the
order Chiroptera (from the Greek Cheiro, meaning hand, and ptera, meaning wing) is currently composed of 18 families, ∼ 174 genera and 900 species,
while some authors put it at 1,000 (Microchiroptera 825 and Megachiroptera 175) and
some at 1,100 species accounting for ∼ 20% of all mammals.[1]
[2] About 211 species live in Africa. Chiropterans are subdivided into two main suborders;
-
Megachiropterans (Old World fruit bats or flying foxes) and
-
Microchiropterans (any bat that is not a fruit bat).[1]
There are approximately 164 species of fruit bats, grouped into 41 genera in a single
family, the Pteropodidae. The Microchiroptera is the larger of the suborders, consisting
of 17 families, 133 genera and 743 species. All bats belong to the kingdom Animalia,
phylum Chordata, subphylum Vertebrata, class Mammalia and order Chiroptera.
Bats, like humans, are mammals, having hairs and giving birth to living young and
feeding them milk from mammary glands. They are most abundant in the tropics and comprise
about one fifth of all mammal species.[3]
Each of the different species differs in its breeding mode, even a particular species
may differ in its breeding habits in different climatic regions,[4]
[5] but they all have certain characteristics in common; from a review of the large
volume of work on the reproduction of bats, the following can be deduced:
First, bats breed during sharply defined seasons.[6]
[7]
[8] It is often recognized that reproductive periods of frugivorous bats are closely
linked to and may be triggered by peaks of fruit abundance.[9]
[10]
[11]
Secondly, they exhibit the phenomenon of sperm storage and delayed fertilization and/or
delayed implantation, sometimes due to alternation or intermittent periodic development
of the male and female gonads per season.[8]
[12]
[13]
Third, the uterus was classified as bicornuate and symmetrical,[4]
[8]
[14] but a publication by Odukoya et al (2009) has reclassified it as partial septate
and symmetrical.
Fourth, bats generally have a single parturition of one young per year.[15]
[16] Some have two parturitions per year or twins, some have triplets, like the hairy-tailed
bat, while Artibeus litaratus breeds throughout the year.[8]
[15]
[17]
[18]
The aim of this study was to investigate the uterus of these bats during the non-pregnant
and pregnant states for adequate information and comparison between the two states
to ascertain what histological adaptations occur during pregnancy in relation to collagen
and elastic fibers.
The African straw-colored fruit bat or African palm tree fruit bat is present in Africa,
Asia (the Arab Peninsula), in the southwest of the Arab Peninsula.[19] In Africa, they form large colonies in widely scattered locations across the central
belt of Africa. Major roost sites are known at Jinja and Kampala, in Uganda; Ile-Ife
and Lagos, in Nigeria; Accra and Nli Falls, in Ghana; Abidjan, in Ivory Coast; Dar-es-Salaam,
in Tanzania.[20] Others include Kahuzi-Biega National Park, in the Democratic Republic of Congo.[21]
The males are slightly larger than the females. The head-and-body length is reported
to be between 143 and 215 mm. The weights ranges between 230 and 350 g. The wings
are large and narrow, allowing the bats to fly long distances and not expend as much
energy trying to flap them a lot. The head is large and pointed with large eyes and
no white facial markings.[22]
The wingspan of the E. helvum averages 3 feet (a meter) and they have fox-like facial features (like all other
Megachiropterans). The hair on their body and head is straw colored, but their wings,
snout and ears have a dark brown color.[23]
Much has been published on the ovaries and ovarian cycle in this bat species.[8] The uterus was classified as bicornuate, but a more recent work by Odukoya et al
(2009) has shown that it is a partial septate type of uterus, and also published much
on the structural anatomy and the histoarchitecture of the organ [24]; therefore, this study only attempted to study its histological adaptations during
pregnancy in relation to fibers integrity.
Materials and Methods
A total of 47 female bats were used; they were harvested on the Obafemi Awolowo University
Campus at different times to assess the different stages in their reproductive cycle.
The bats were brought into the department and kept in cages in the Animal Holdings
of the Department to acclimatize for at least 24 hours before sacrifice. The bats
were fed overnight with ripe bananas and water. The animals were carefully assessed,
screened and assumed to be presumably healthy.
The animals were sacrificed by cervical dislocation after intramuscular pentobarbital
sodium (40 mg/kg b/w) administration. Abdominopelvic incisions were made to expose
and excise their uteri. These uteri were immediately washed in physiological saline
and blotted dry using filter paper before being weighted on a Mettler Toledo sensitive
weighing balance (Mettler-Toledo, LLC, Columbus, OH, USA).
Histological Procedures
Paraffin Tissue Processing
The uteri were immediately fixed in a 10% formal saline solution limiting the postmortem
time to ∼ 2 minutes. Tissues were fixed for period of 24 hours before further processing.
The tissues were dehydrated with graded alcohol, cleared in xylene and infiltrated
with molten paraffin wax. The tissues were embedded in paraffin wax and sectioned
at a thickness of 5 µm using a rotary microtome. The sections were placed on glass
slides and dried at 37°C until they were ready for the staining procedures.
Verhoeff-Van Gieson Staining Procedure
The sections were dewaxed in xylene and rehydrated, and then stained for elastic and
collagen fibers using the modified differential Verhoeff-van Gieson method according
to Verhoeff, 1908. Elastic fibers stained black, while collagen fibers stained red,
and muscle stained yellow.
Results
The fiber type is a mixture of both elastic and collagen fibers, and the predominant
fiber being the elastic type in the non-pregnant state. During pregnancy, however,
there is a gradual transition of the fiber type from elastic to predominantly collagen
fibers. After parturition, as the integrity of the uterine muscularis returns to normal,
the elastic fibers are also gradually regenerated, and once again become predominant.
[Figs. 1], [2], [3], [4], [5], [6], [7]
Fig. 1 The uterine muscularis in the non-pregnant state, showing an admixture of collagen
(red) and elastic (brown/black) fibers. Verhoeff-van Gieson stain, (X 400).
Fig. 2 Cross section of the uterine body during the non-pregnant state, showing an admixture
of elastic and collagen fibers, but predominantly elastic fibers. Verhoeff-van Gieson
stain, (X 200).
Fig. 3 Cross section of the non-pregnant limb at the initial stage of pregnancy showing
the deeply stained, predominant elastic fibers. Verhoeff-van Gieson stain, (X 250).
Fig. 4 Cross section of the pregnant limb at the initial stage of pregnancy showing more
elastic fibers than collagen fibers. The pregnant limb showed more collagen fibers
than both the non-pregnant limb and the non-pregnant uterus. Verhoeff-van Gieson stain,
(X 200).
Fig. 5 The fibers type in the non-pregnant limb completely changed from predominantly elastic
to exclusively collagen fibers (bright red stain) type during pregnancy. It shows
no trace of elastic fibers. Verhoeff-van Gieson stain, (X 200).
Fig. 6 The pregnant limb at an advanced stage in pregnancy shows a transition from the predominant
elastic fibers to exclusively collagen fibers, and more smooth muscle fibers stained
yellow. Verhoeff-van Gieson stain, (X 250).
Fig. 7 The uterine body after parturition displaying elastic fibers regeneration. It depicts
a fine distribution of both elastic and collagen fibers. Verhoeff-van Gieson stain,
(X 250).
Discussion
This study has been able to show that there is interplay of elastic and collagen fibers
during the non-pregnant and the pregnant states, specifically in the uterus of the
E. helvum. During pregnancy, the elastic fibers, which are predominant during the non-pregnant
state, are replaced by collagen fibers, which are able to withstand the stretch pressure
exerted on the uterus. Hooke's law states that an elastic body will stretch and return
to its normal state until the elastic limit is exceeded, and the yield point is reached
when the elastic body can no longer return to its normal state, any further stretch
at this point will take it to the breaking point.
It can thus be inferred that, during pregnancy, the elastic fibers are stretched beyond
the elastic limit; they reached the yield point and degenerated, gradually giving
way to the collagen fibers that are well able to withstand the stretch pressure exerted
on the uterus by the developing fetus, until parturition, when the elastic fibers
are regenerated.
Conclusion
Elastic fibers tend to obey Hooke's law during pregnancy in the uterus of the frugivorous
bat E. helvum, which signifies a form of histomorphological response or adaptation to pregnancy
in the uterus of this bat species.
