| Vital
Cell
Observation
of Antiaging
Effects of Vital Cell in Rabbits
Materials: 20 4-month-old,
healthy purebred New Zealand rabbits, 10 males and 10 females each
weighing 2kg. (Supplied by Shanghai Laboratory Animal Center of
China Academy)
Grouping: Rabbits were divided randomly into two
groups of 10, labeled Group A (the administration group) and Group
B (the control group).
Feeding: Every rabbit in both groups is fed in
a separated cage in the same room. All are observed under room temperature.
The feeding of rabbits is strictly defined according to time and
quantity.
Method: After 2
years of treatment researchers randomly selected one male and one
female rabbit from each group (A -treatment and B-control). Researchers
also selected one male and female rabbit from a group of 6-month-old,
healthy purebred New Zealand rabbits weighing 2kg each. This group
was labeled Group C (young, healthy controls).
Researchers randomly numbered all
6 rabbits and, after etherizing them, obtained tissue samples from
for examination with both optical and electron microscopes. Tissues
were prepared for optical microscope by fixing with formalin, paraffin
section, HE staining, weight elastic fiber staining on the myocardium
and coronary arteries, and NAP staining fixed by acetone for womb
tissues.
Tissue samples for the electron microscope were fixed with 2.5%
sporicidin, embedded with expoxide resin, prepped into ultra-thin
sections and stained with acetate uranium and citrialuminum.
Observation Index:
Researchers examined tissue samples from the thymus glands, hearts,
lungs, livers, spleens, kidneys, brains, wombs and testes/womb of
the 6 rabbits from Group A, B, and C under optical microscope.
Researchers examined tissue samples
from the livers of all 6 rabbits and testes of the 3 male rabbits
from Group A, B, and C under electron microscope.
Thymus gland: The weight of the
thymus gland of the rabbits in Group A was 2g. The atrophy of the
thymus gland was relatively slight. The weight of the thymus gland
of the rabbits in Group B was 1g, the cells of the thymus gland
decreased and adipose tissues overgrew. The weight of the thymus
gland of the rabbits if Group C was 3g and the tissues and structure
remained normal.
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| Thymus
- Old rabbit
Thymus with severe atrophy,
heavy fatty infiltration |
Thymus
- Treated rabbit
Firm mass, only slight signs of atrophy |
Heart: There were very few micro-fiber
foci in the myocardium of the rabbits in Group A. The pathological
changes in the coronary arteries were not obvious, and the elastic
intima was clear. The myocardium of the rabbits in Group B was fiberized.
There were deposits of lipofuscin. The collagen fibers of the coronary
arteries overgrew, the intima became thickened irregularly and the
elastic intima split and proliferated. The myocardium and coronary
arteries of the rabbits in Group C kept normal.
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| Heart
- Old rabbit
Sclerosis of coronary artery, thickened intima, fibrosis
|
Heart
- Treated rabbit
Slight myocardial fibrosis and unclear coronary sclerosis |
Lung: There were no obvious pathological
changes in the blood vessels of the lungs of the rabbits in Group
A. The wall of the arteriole of the lungs of the rabbits in Group
B thickened and the arteriole became narrower. The blood vessels
of the lungs of the rabbits in Group C were normal.
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| Lung
- Old rabbit
Thickening of small arteries, narrowing of arterioles
|
Lung
- Treated rabbit
No thickening or damage to small artery walls |
Liver: There was a little blood
stagnation of the liver in the rabbits of Group A, but the atrophy
of the hepatic cells was not very obvious. Very little lipofuscin
was found. There was obvious blood stagnation and atrophy of the
liver and obvious atrophy of the hepatic cells in the rabbits of
Group B. Deposits of lipofuscin could be found. The livers of the
rabbits in Group C were normal.
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| Liver
- Old rabbit
Stagnant blood, lipofuscin deposits in cells |
Liver
- Treated rabbit
Absence of blood stagnation,
no lipofuscin in cells |
Spleen: There was no blood stagnation
of the spleen in Group A. The walls of the central arteries of the
splenic corpuscles thickened slightly. There was blood stagnation
of the spleen in Group B, and the walls of the central arteries
of the splenic corpuscles thickened thus causing the arteries to
become narrower. The rabbits in Group C were normal.
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| Spleen
- Old rabbit
Vessel wall thickening of central arteries in splenic
corpuscle |
Spleen
- Treated rabbit
No vessel wall thickening of arteries in splenic
corpuscle |
Kidney: There was no obvious
unit decrease of the kidney of the rabbits in Group A. Under the
view of 10 lower diameters, 300 glomeruli could be found. However,
there was unit decrease of the kidney of the rabbits in Group B.
Under the view of 10 lower diameters, some 230 glomeruli could be
found. The walls of arteriole in the kidney thickened and became
narrower. In the rabbits of Group C, about 330 glomeruli were found
under the view of 10 lower diameters.
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| Kidney
- Old rabbit
Decrease in nephrons with
few glomeruli |
Kidney
- Treated rabbit
Slight decrease in nephrons |
Brain: The soft meninx of the
rabbits in Group A did not thicken. The blood vessels expanded,
but there was no obvious blood stagnation. The soft meninx of the
rabbits in Group B, thickened, and the blood vessels of the lower
part of the arachnid membrane expanded. There was evidence of blood
stagnation. Part of the blood vessels of the brain became spuriously
calcified. The rabbits in Group C were normal.
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| Brain
- Old rabbit
Calcification of arterial vessels, thickening of
soft meninx |
Brain
- Treated rabbit
No thickening of soft meninx, slight expansion of
vessels |
Uterus: There was the enlargement
of uterus in the rabbits of Group A, and the intima thickened. AKP
staining showed (-) for the rabbits of Group A. There was atrophy
of the womb in the rabbits of Group B. The womb became narrower,
and the intima was thinner. AKP staining showed (+).
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|
| Uterus
- Old rabbit
Thinning oftunica intima of the uterine lining |
Uterus
- Treated rabbit
No thinning of tunica intima |
Testis: There was no obvious
atrophy of the spermaduct in the rabbits of Group A, and there was
a large amount of sperm. There was atrophy of the spermaducts in
the rabbits of Group B and the sperm cells of various kinds were
degenerated, reducing the number of sperm.
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| Testis
- Old rabbit
Atrophy of the seminiferous tubules, reduced sperm |
Testis
- Treated rabbit
No atrophy of the seminiferous tubules, healthy sperm |
Liver: In Group
A, the nuclei were either circular or oval, while the nuclear membrane
was clear. The nucleoli had a thread-like structure. The nuclear
chromatin was well distributed. The shape and volume of the mitochondria
in Group A were similar to those in the healthy young rabbits. They
were thick with numerous endoplasmic reticulum. Reticulation enlargement
was not apparent.
In Group B, the nuclei had an irregular
shape. The nucleoli were separated and had lost their thread-like
structure. Around the nucleoli, the chromatin had increased. Cytoplasmic
mitochondria were swollen and shortened, and their shape was irregular.
The dilatation of endoplasmic reticulum decreased. Lipofuscin deposits
could be observed.
In Group C, the mitochondria were
slightly enlarged. Their other structures were normal.
Testis: In Group
A, no atrophy of convoluted tubule was observed, and there were
no apparent degenerative changes in spermatoblasts of different
levels. The nuclei or cell organs had a clear structure.
In Group B, the convoluted tubule
was found to have shrunk. Spermatoblasts of different levels and
sterol cells showed degenerative changes. Nuclear chromatin condensed.
Denaturation of intracytoplasmic cell organs and their obscure structure
could be observed.
In Group B, thymus glands, womb and
testis displayed noticeable shrinkage. Coronary sclerosis, myocardial
focal fibrosis, lipofuscin deposits and nephronal decrease were
common. The use of an electron microscope revealed patent degenerative
changes in the nucleoli and mitochondria of hepatic cells and convoluted
tubule cells, accompanied by lipofuscin deposits.
In Group A, fewer pathologic changes
were apparent. In comparison to Group C, the organic functions in
Group A were normal.
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