|Year : 2015 | Volume
| Issue : 2 | Page : 65-75
Role of some phytoestrogens in recovering bone loss: histological results from experimental ovariectomized rat models
Hafiza A Sharaf, Nermeen M Shaffie, Fatma A Morsy, Manal A Badawi, Naglaa F Abbas
Department of Pathology, National Research Centre, Cairo, Egypt
|Date of Submission||04-Oct-2015|
|Date of Acceptance||03-Nov-2015|
|Date of Web Publication||8-Feb-2016|
Nermeen M Shaffie
Assistant Professor of Histology, National Research Center, 26122 Cairo
Source of Support: None, Conflict of Interest: None
Osteoporosis is a disease characterized by a decrease in bone mass and is widely recognized as a major health problem. Ovarian hormone deficiency is a major risk factor for osteoporosis. A sharp decrease in ovarian estrogen production is the predominant cause of rapid bone loss and deterioration of bone architecture, resulting in increased bone fragility during the first decade after menopause.
Materials and methods
A total of 70 albino rats were used, divided into seven groups of 10 rats each. Group 1 was subjected to sham operation and used as a control group. In group 2, rats were ovariectomized (OVX) and used as a model of postmenopausal osteoporosis. Three months after the operation the OVX rats (group 2) were divided into six subgroups: one was considered the positive control group; another one was treated with synthetic estrogen compound; and the other four subgroups were fed a diet containing red clover, fennel, carob, and a combination of the three plants. At the end of the experiment (after 3 months' treatment) the animals were killed, and the femur shafts were extracted, decalcified, and processed into paraffin blocks. Sections were stained with hematoxylin and eosin for histopathological, image analysis, and morphometric studies. Other sections were stained with periodic acid Schiff for histochemical investigations.
The histopathological results of this study revealed that ovariectomy caused a decrease in thickness of the cortical compact bone in the middle shaft of the femur and of the trabeculae in cancellous bone in the head of the femur bone. Histochemical results showed new bone formation in sections of rats treated with plants. The best results were detected in sections of rats treated with a combination of the three plants. Red clover, fennel, and carob individually or combined have a better ameliorating effect on ovariectomy-induced osteoporosis than does synthetic estrogen compound.
Treatment of OVX rats with phytoestrogens such as red clover, fennel, and carob might improve the histopathological and histochemical changes and morphometric parameters in bone with ovariectomy-induced osteoporosis.
Keywords: carob, estrogen, fennel, osteoporosis, ovariectomy, rat, red clover
|How to cite this article:|
Sharaf HA, Shaffie NM, Morsy FA, Badawi MA, Abbas NF. Role of some phytoestrogens in recovering bone loss: histological results from experimental ovariectomized rat models. J Arab Soc Med Res 2015;10:65-75
|How to cite this URL:|
Sharaf HA, Shaffie NM, Morsy FA, Badawi MA, Abbas NF. Role of some phytoestrogens in recovering bone loss: histological results from experimental ovariectomized rat models. J Arab Soc Med Res [serial online] 2015 [cited 2021 Jan 18];10:65-75. Available from: http://www.new.asmr.eg.net/text.asp?2015/10/2/65/175880
| Introduction|| |
Osteoporosis (OP) is a bone metabolic disease characterized by low bone mineral density (BMD) with high risk for fractures. It occurs when there is an imbalance between bone resorption and bone formation during the bone remodeling process  . OP is a silent epidemic problem; it has now become a major health hazard affecting over 2000 million people worldwide  . OP is generally viewed as resulting from a combination of age-related, hormonal, dietary, lifestyle, and genetic factors, all of which can lead to reduced bone mass  .
Ovariectomy provides the most popular model for studying events associated with postmenopausal osteoporosis (PMO) with estrogen deficiency, and it has been well established that ovariectomy elicits bone loss and increases bone turnover in rats. Ovariectomized (OVX) rats are widely accepted models for PMO  . The most common type of OP is bone loss associated with ovarian hormone deficiency at menopause  , which leads to loss of bone mass  . Women are generally affected four times more than men, and fracture rates among women are approximately twice as high as that of men  .
Estrogen deficiency has been regarded as a critical cause of OP, which can result from naturally or surgically induced menopause  . Reduction in estrogen leads to increased osteoclastic activity, which enhances bone loss by stimulating bone resorption because of reduced hormonal control over osteoblast cell activity  . The osteoblasts and osteoclasts have estrogen receptors, and estrogen affects bones partly because of these receptors. It has been proposed that estrogen causes depletion in the number of osteoclasts in bone by inhibiting maturation at the cellular level while enhancing the synthesis of cytokines that play roles in bone formation  .
Loss of estrogens accelerates the effects of aging on bone by decreasing the defense against oxidative stress. Both aging and loss of sex steroids have adverse effects on skeletal homeostasis  . Lean et al.  noted that estrogen exerts beneficial actions through suppression of reactive oxygen species (ROS) that stimulate osteoclasts, the cells that resorb bone. Thus, estrogen might prevent bone loss by enhancing oxidant defenses in bone. They also found that estrogen deficiency after ovariectomy causes bone loss by lowering thiol antioxidants in osteoclasts. This directly sensitizes osteoclasts to osteoclastogenic signals and leads to ROS-enhanced expresion of cytokines that promote osteoclastic bone resorption.
Treatment with natural herbs is likely to cause fewer side effects compared with the presently used synthetic drugs  .
Phytoestrogens appear to offer the most potential for the prevention of bone loss and have attracted attention as a possible agent in preventing and treating PMO, preventing cancer, and relieving menopausal symptoms  .
Phytoestrogens are similar to mammalian estrogens both structurally and functionally  . There is evidence that diets containing high levels of phytoestrogenic isoflavones are associated with a low incidence of OP and menopausal symptoms  .
Red clover (Trifolium pratense) supplementation has been the subject of much interest for its role in the reduction of menopausal symptoms and conditions related to aging because of their high concentrations of phytoestrogens  . It contains four important estrogenic isoflavones (daidzein, genistein, formononetin, and biochanin A) and coumestans  . Red clover isoflavones (RCI) are being increasingly used in dietary supplements for their purported estrogenic effect in in-vivo and in-vitro assays  . Long-term administration of isoflavones was found to positively affect bone metabolism  . The positive effect of isoflavones on bone metabolism may be mediated by at least two mechanisms: the first is the impact on osteoclasts through activation of apoptosis, and the second is the inhibition of tyrosine kinase activity through modulation of membrane endoplasmic reticulum (ER) with consecutive changes in the activity of alkaline phosphatase  .
Fennel (Foeniculum vulgare Mill; Apiaceae family) is one of the most widespread annual or perennial plants with an aromatic odor. The most frequently investigated is the essential oil, which has shown antioxidant, antimicrobial, and hepatoprotective activity. Many herbs are well known to contain large amounts of phenolic antioxidants, which are mainly composed of phenolic acids and flavonoids  .
Carob (Ceratonia siliqua L.; Leguminosae family) contains a remarkable amount of condensed tannins and other polyphenols  . Carob polyphenols protect against decreased lipid peroxidation induced by cisplatin administration  . The aqueous extract of carob induces a depletion of hydrogen peroxide in the kidney, liver, and brain but not in heart tissues  . Hydrogen peroxide is an important ROS because of its ability to penetrate biological membranes. However, it may be more toxic if converted to hydroxyl radicals in the cell, leading to lipid peroxidation  and oxidative DNA damage  .
Therefore, the aim of this study was to evaluate the effectiveness of red clover, fennel, carob, and estrogen on the progression of bone loss (OP) in OVX female rats.
| Materials and methods|| |
Seventy female Sprague-Dawley rats, aged 7 weeks and weighing 170-190 g at the beginning of the experiment, were used in this study. They were housed two per cage and maintained in standard conditions under a 12 : 12 light/dark cycle, at a temperature of 22 ± 1°C and 55-60% relative humidity. Rats were fed a standard nutritionally balanced diet according to AIN-93  and drinking water ad libitum.
After a 7-day adaptation period to the controlled laboratory conditions, the animals were randomly divided into seven groups of 10 rats each.
The first group: in this group female rats (n = 10) were anesthetized with diethyl ether and subjected to sham operation.
The second group: in this group the ovaries of the remaining female rats (n = 60) were removed bilaterally according to the method described by Waynforth  and Lasota and Danowska-Klonowska  . Three months after the operation, this group was subdivided into:
2.1 (C-OVX): OVX control rats fed a standard diet devoid of any additives.
2.2 (ER-OVX): OVX rats treated with estrogen synthetic compound at a dose of 50 μg/kg/day.
2.3 (RC-OVX): OVX rats fed a diet containing 4% red clover.
2.4 (FE-OVX): OVX rats fed a diet containing 7.68% fennel.
2.5 (CA-OVX): OVX rats fed a diet containing 0.46% carob.
2.6 (COM-OVX): OVX rats fed a diet containing a mixture of all additives.
The OVX rats were subjected to the following treatments for 3 months.
At the end of the experimental period, the animals were killed and the shafts of the femur were removed, immersed in glutaraldehyde, and after 4 h were decalcified with EDTA solution for 20 days. Paraffin (5 μm) tissue sections from the middle shaft of the femur were cut using a conventional technique. Sections were stained with hematoxylin and eosin  and examined under a light microscope.
The morphometric analysis was performed at the Pathology Department, National Research Center, using a Leica Qwin 500 Image Analyzer (Leica Imaging Systems Ltd, Cambridge, UK).
To measure the mean thickness of the outer cortical bone of the middle shaft of the femur, perpendicular lines were drawn from the periosteum to the endosteum at many sites  .
Morphometric analysis is carried out on routine hematoxylin and eosin-stained slides. We count the maximum number of osteocytes in a frame area of 3905.5 μm 2 at a magnification of ×100. The results appear automatically on the monitor in the form of the distance measured in μm and area in μm 2 with the mean, SD, the minimum length, and the maximum length and area measured.
Staining with periodic acid Schiff (PAS) for demonstration of newly formed bone tissue  was performed on sections of the left femur bone of rats in all groups.
Areas of reactivity were marked and the optical density of PAS was measured using the gray image menu in 10 small measuring frames in each specimen. The image was transformed into a gray image (a grid of pixels), each representing the intensity of brightness at that point by a range of numbers.
The experiment was conducted in accordance with the National Regulations of Animal Welfare and Institutional Animal Ethical Committee (IAEC), National Research Centre.
| Results|| |
Histological and morphometric results
Histological sections of the middle shaft of femur from rats of the sham-operated control group showed that bone tissue was of the compact type, covered by two layers, the periosteum located externally, which is a dense connective tissue, and the endosteum, a thin cell-rich connective tissue, lining the internal surface of the bone facing the bone marrow cavity. Within the bone matrix, osteocytes in their lacunae were detected [Figure 1]a).
|Figure 1: Longitudinal sections of the middle shaft of femur of (a) a shamoperated rat shows an oute fi brous layer, periosteum (arrow), and an inner layer facing the marrow cavity, endosteum (arrowhead). (b) The same group shows normal cortical width of the shaft. (c) A sham-operated rat showing normal osteocytes and Haversian canals. (d) The head of the femur of a sham-operated rat showing normal architecture of the trabeculae of the inner cancellous bone and bone marrow spaces. (a) Hematoxylin and eosin-stained section; (b– d binary image morphometric measurement; ×400|
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The head of the femur bone was formed of cancellous bone. Trabeculae of the cancellous bone of control rats were composed of a network of irregular bone lamellae between which osteocytes resided in their lacunae. Bone marrow spaces were observed between trabeculae [Figure 1]b).
In the case of OVX rats, examination of the middle shaft of the femur showed marked decrease in the thickness of the compact bone of the shaft (49.01 ± 12.02) as compared with the sham-operated group (78.43 ± 5.33) and decrease in the number of osteocytes (26 vs. 79). Many osteoporotic cavities, resorption cavities, and calcified cartilage were observed in bone tissue. Erosion cavities were detected on the outer surface [Figure 2]a and [Table 1]. An increase in the mean areas of Haversian canals was observed (21.15 ± 15.69) as compared with the sham-operated group (15.34 ± 9.97) [Figure 2]b and [Table 1].
|Figure 2: Longitudinal sections of the middle shaft of (a) an overiectomized rat showing many osteoporotic cavities (star), deformation of the general architecture of the tissue, and erosion cavities on the endosteal surface (blue arrow). (b) An overiectomized rat showing widened Haversian canals. (a) Hematoxylin and eosin-stained section; (b) binary image morphometric measurement; ×400|
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|Table 1 Mean area of cortical bone thickness (shaft), mean Haversian canals' area, number of osteocytes and trabecular thickness of different groups|
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Examination of cancellous bone in the head of the femur revealed decreased mean areas of bone trabeculae (276.08 μm 2 ) as compared with the sham-operated group (1220.9 μm 2 ) [Table 1]. Also, widening of bone marrow spaces and increase in blood vascularity within the bone marrow were noticed [Figure 3].
|Figure 3: A photomicrograph of a section of trabecular bone of an ovariectomized rat showing marked reduction in trabecular thickness and widening of bone marrow spaces. Hematoxylin and eosin-stained section, ×400|
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Examination of bone sections of the middle shaft in OVX rats treated with synthetic estrogen compound showed slight increase in the thickness of the shaft cortical bone (52.52 ± 1.4 μm), compared with the OVX group (49.01 ± 12.02). The number of osteocytes was also slightly increased (n = 47), as compared with OVX rats (n = 26). Decrease in the mean areas of Haversian canals (16.74 ± 6.45 μm 2 ) was observed compared with the OVX group (21.15 ± 15.69 μm 2 ). Many osteoporotic cavities were still present. Irregular erosion of endosteal surface could be observed [Figure 4]a and [Table 1].
|Figure 4: (a) A longitudinal section of cortical bone tissue of the middle shaft of the femur of an ovariectomized rat treated with estrogen synthetic compound showing decrease in thickness in the shaft as compared with sham-operated rats; resorption cavities are still present (arrows) and an increase in the number of osteocytes is evident. (b) A section of trabecular bone of the same group showing mild increase in trabecular thickness as compared with the ovariectomized group. Hematoxylin and eosin-stained section, (a) ×200 and (b) ×400|
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In the head of the femur of this group, decreased mean areas of bone trabeculae (329.11 μm 2 ) were observed compared with the sham-operated group (1220 μm 2 ) [Table 1] and [Figure 4]b). However, slight increase in mean areas of bone trabeculae (329.11 μm 2 ) was seen compared with OVX rats (276.08 μm 2 ).
In the case of OVX rats treated with red clover, an improvement was seen in pathological changes in the form of increase in cortical bone thickness of the middle shaft (61.72 ± 1.9 μm) as compared with the OVX group (49.01 ± 12.02 μm), and the number of osteocytes returned to normal (n = 79). However, erosion cavities were still noticed on both sides of the cortical bone [Figure 5]a and [Table 1]. There was a decrease in the mean area of Haversian canals (15.34 ± 9.97) as compared with the OVX group (21.15 ± 15.69) [Table 1].
|Figure 5: (a) A longitudinal section of the middle shaft of the femur of an ovariectomized rat fed red clover showing mild increase in cortical bone thickness, although erosion cavities are observed on both sides of the bone (arrows). (b) A section of trabecular bone of the same group showing noticeable increase in trabecular area with increase in the number of osteocytes. Hematoxylin and eosin-stained section, (a) ×200 and (b) ×400|
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Decreased mean area of bone trabeculae of the femur head cancellous bone (763.25 μm 2 ) was observed compared with the sham-operated group (1220.9 μm 2 ), whereas the mean area demonstrated an increase compared with OVX rats (267.08 μm 2 ) [Table 1] and [Figure 5]b).
OVX rats treated with fennel revealed an improvement in histological changes. Examination of bone sections of the middle shaft of the femur showed increase in thickness of the cortical shaft bone (64.62 ± 3.54 μm) as compared with OVX rats (49.01 ± 12.02 μm), although it was nonuniform, and an increased number of osteocytes (n = 36 vs. 26 in OVX rats). Irregularity was detected on the endosteal surface [Table 1] and [Figure 6]a).
|Figure 6: (a) A longitudinal section of the middle shaft of the femur of an ovariectomized rat fed fennel showing nonuniform increase in thickness of the cortical bone with mild reduction in the area of Haversian canals. Irregularity of endosteal surface was observed. (b) A section of trabecular bone of the same group showing moderate increase in trabecular areas and calcified cartilage (arrow). (a) Binary image morphometric measurement; (b) hematoxylin and eosin-stained section; ×400|
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Cancellous bone of the head of the femur showed moderate increase in the mean areas of the bone trabecular surface (351.65 μm 2 ) as compared with OVX rats (276.08 μm 2 ) [Table 1] and [Figure 6]b).
Examination of the compact bone of the middle shaft of the femur of OVX rats treated with carob showed an increase in shaft cortical thickness (89.00 ± 3.23 μm) compared with untreated OVX rats(49.01 ± 12.02 μm), and an increased number of osteocytes (34 vs. 26) denoting recovery of bone tissue. The mean areas of Haversian canals were smaller in the OVX group fed carob (17.39 ± 10.51 μm 2 ) compared with untreated OVX rats (21.15 ± 15.69 μm 2 ) [Table 1] and [Figure 7]a).
|Figure 7: (a) A longitudinal section of the middle shaft of the femur of an ovariectomized rat fed carob showing marked increase in cortical bone thickness with increased number of osteocytes. No erosion or osteoporotic cavities are observed. (b) A section of trabecular bone showing marked increase in trabecular area. Hematoxylin and eosinstained section, ×400|
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Marked increase in mean areas of cancellous bone trabeculae (913.25 μm 2 ) was observed in this group compared with untreated OVX rats (276.08 μm 2 ) [Table 1] and [Figure 7]b).
Examination of bone sections of the middle shaft of the femur in OVX rats treated with a combination of red clover, fennel, and carob showed an improvement in the pathological changes in the form of increased thickness of the cortical shaft bone (100.93 ± 4.59 μm) compared with untreated OVX rats (49.01 ± 12.02 μm), as well as increased number of osteocytes (n = 42 vs. 26) and narrowing in the mean area of Haversian canals (8.70 ± 3.48 vs. 21.15 ± 15.69) [Table 1] and [Figure 8]a).
|Figure 8: (a) A longitudinal section of the middle shaft of the femur of an ovariectomized rat fed a combination of the three plants showing normalization of the cortical bone thickness the numbers shown in the figure are the numbers of measuring lines used by image analyzer system. (b) A section of trabecular bone of the same group shows considerable amelioration of trabecular thickness. (a) Binary image morphometric measurement, (b) hematoxylin and eosin-stained section; ×400|
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By examining the head of the femur of this group, increase in mean areas of cancellous bone trabeculae (1850 μm 2 ) was observed compared with the sham-operated group (1220.90 μm 2 ) and the untreated OVX group (276.08 μm 2 ) [Table 1] and [Figure 8]b).
Sections of bone in the sham-operated group showed PAS-stained areas in cement lines in the shaft compact bone [Figure 9]a) and trabeculae [Figure 9]b). In the case of OVX rats cement lines were unapparent in PAS-stained sections in the shaft and in bone trabeculae [Figure 10]a and b. The gray level of PAS staining of this group was markedly reduced when compared with the sham-operated group (0.07 vs. 0.3) [Figure 16].
|Figure 9: A longitudinal section of cortical bone of the middle shaft of femur (a) and trabecular bone (b) of sham-operated rats showing periodic acid Schiff (PAS)-positive reaction in cement lines. PAS reaction, ×400|
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|Figure 10: A longitudinal section of the middle shaft of the femur (a) and trabecular bone (b) of ovariectomized rats showing unapparent periodic acid Schiff (PAS)-stained section. PAS reaction, ×400|
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The bone of OVX rats treated with synthetic estrogen compound exhibited faint PAS reaction in cement lines in both cortical and trabecular bone [Figure 11]a and b). The gray level of the staining of this group showed slight increase when compared with OVX (0.1 vs. 0.07) [Figure 16]). Bone sections in the OVX group treated with red clover exhibited an intense PAS-positive reaction in cement lines [Figure 12]a and b). The gray level of staining in OVX rats treated with red clover returned to normal levels (0.3) [Figure 16]). The bone of OVX rats treated with fennel showed distinct PAS-positive reaction in cement lines of the shaft and bone trabeculae [Figure 13]a and b), whereas sections from OVX rats fed carob showed moderate PAS-positive reaction in the cement lines of shaft and bone trabeculae [Figure 14]a and b). The gray levels of staining in these two groups were nearly normal (0.33 and 0.25, respectively) [Figure 16]). Examination of bone sections of OVX rats treated with a combination of red clover, fennel, and carob exhibited very intense distinct PAS-positive reaction in the cement lines in the shaft and trabeculae [Figure 15]a and b), which was markedly increased when compared with OVX rats (0.4 vs. 0.07) and the sham-operated group (0.4 vs. 0.3) [Figure 16]).
|Figure 11: A longitudinal section of the middle shaft of the femur (a) and trabecular bone (b) of ovariectomized rats treated with synthetic estrogen compound showing very slight periodic acid Schiff (PAS)-positive reaction in cement lines. PAS reaction, ×400|
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|Figure 12: A longitudinal section of the middle shaft of the femur (a) and trabecular bone (b) of ovariectomized rats fed red clover exhibiting intense periodic acid Schiff (PAS)-positive reaction in cement lines (arrow). PAS reaction, ×400|
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|Figure 13: A longitudinal section of the middle shaft of the femur (a) and trabecular bone (b) of ovariectomized rats fed fennel exhibiting intense periodic acid Schiff (PAS)-positive reaction in cement lines. PAS reaction, ×400|
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|Figure 14: A longitudinal section of the middle shaft of the femur (a) and trabecular bone (b) of ovariectomized rats fed with carob exhibited moderate periodic acid reaction in cement lines positive reaction. PAS reaction, ×400|
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|Figure 15: A longitudinal section of the middle shaft of femur (a) and trabecular bone (b) of ovariectomized rats fed a combination of the three plants exhibiting very intense distinct periodic acid Schiff (PAS)-positive|
reaction in cement lines. PAS reaction, ×400
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|Figure 16: A chart showing the mean gray level of periodic acid Schiff (PAS) stain in different groups|
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| Discussion|| |
OP is characterized by decrease in bone mass and is widely recognized as a major health problem. It is a multifactorial process and is associated with demographic and lifestyle factors, morbidity, drug use, medical history, and altered hormonal profile  . Worldwide, OP is considered second only to cardiovascular disease as a leading health problem  . Estrogens play an important role in skeletal homeostasis. A sharp decrease in ovarian estrogen production is the predominant cause of rapid bone loss and deterioration of bone architecture, resulting in increased bone fragility during the first decade after menopause  .
In the present study, ovariectomy of rats induced a decrease in thickness of the shaft cortical bone and decrease in the number of osteocytes. Many osteoporotic cavities were also seen. The results of the present work are in agreement with those of Weber et al.  , Park et al.  , and Kalleny  , who reported that histomorphometric and statistical results of the outer cortical bone of OVX rats revealed significant decrease in the mean outer cortical bone thickness (28% loss) compared with sham-operated control rats.
The cortical bone of OVX rats also showed resorption cavities and irregularly eroded endosteal surface containing osteoclasts  and reduction in the cortical and trabecular bone thickness  .
Also, Khattab et al.  found that the femur cortical bone of OVX untreated rats showed osteoporotic regions with bone destruction, loss of normal Haversian system pattern, numerous resorption cavities, and distinct changes in femur cortical bone, as well as splitting and the presence of osteoclast cells.
Similarly NAMS  observed that estrogen deficiency triggers osteoclasts, which enhance bone loss by stimulating bone resorption.
In the present study, the group of OVX rats showed marked decrease in the thickness of the bone trabeculae compared with sham-operated controls. The results of the present work are in agreement with those of Kalleny  who revealed that the group of OVX rats showed significant decrease in the mean trabecular bone volume (nearly 48% loss compared with controls) causing widening of the bone marrow spaces as a result of the increase in the intertrabecular distance. Moreover, these bone trabeculae showed loss of normal architecture in which some trabeculae were observed as islands of widely separated specules, whereas other trabeculae appeared thinned out.
The mechanism of ovariectomy-induced bone effect has been explained by Kimble et al.  , who postulated that interleukin-1, a cytokine produced by bone marrow cells and bone cells, has a role in the pathogenesis of PMO because of its potent stimulatory effects on bone resorption in vitro and in vivo. Oktem et al.  have clarified that the pathogenesis of OP generates a free radical contributing to the imbalance between bone formation and resorption caused by estrogen depletion.
Reduction in estrogen leads to increased osteoclastic activity because of reduced hormonal control over osteoblast cell activity  . In the estrogen-deficient state, such as in menopause, the balance between bone resorption and bone formation shifts toward an increasing level of bone resorption, with more resorption than formation; this results in loss of bone mass and deterioration of trabecular bone microarchitecture  .
In the present study, examination of bone sections of OVX rats treated with synthetic estrogen compound showed slight increase in the thickness of the cortical bone of the shaft, whereas the mean areas of Haversian canals were still reduced compared with that in OVX rats. Many osteoporotic cavities were still present. This may be explained by the findings of Li et al.  , who reported that the reduction in the activation found with antiresorptive therapies with a transient increase in bone mass is due to the fill in of the resorption cavities.
The results of the present work are in disagreement with those of Hayashi et al.  , who reported that histomorphometric indices of bone turnover were suppressed by treatment with estrogen.
Estrogen activation of osteoblasts stimulates expression of special proteins and growth factors  . Similarly, da Paz et al.  noted that estrogen had an independent anabolic effect on the osteoblastic function. Both ER activation and AR activation have the capacity to preserve trabecular bone mass  .
Phytoestrogens are plant-derived nonestradiol phenolic compounds that are believed to protect against cardiovascular diseases, OP, and hormone-related disorders  . Phytoestrogens can be easily metabolized and eliminated. Many investigations have shown lower prevalence of OP and hip fracture among Asian women consuming high amounts of phytoestrogens  .
Many types of phytoestrogens  are known to be antioxidant as they suppress the formation of ROS and prevent the release of cytochrome c from mitochondria. As previously known, OVX is associated with increase in free radicals  . These free radicals are responsible for causing physiological damage to many organs.
In the present study, the treatment of OVX rats with red clover resulted in an increase in cortical bone thickness as compared with the OVX group, and a noticeable increase in the number of osteocytes and decrease in the mean area of Haversian canals. No osteoporotic cavities or resorption cavities were recorded. The results of the present work are in agreement with those of Wronski and Yen  , who reported that red clover is hypothesized to have a positive effect on BMD as women age. Similarly, Khattab et al.  found that the treatment of OVX with red clover resulted in protection from osteoporotic changes induced by OVX in a dose-dependent manner. The protective role of RCI may be attributed to its phytoestrogen effect on bone formation, and a consequence of a genomic and estrogen receptor-mediated effect  . In addition, Occhiuto et al.  found that treatment with isoflavones significantly reduced the number of osteoclasts compared with that in OVX control rats. These findings suggest that RCI are effective in reducing bone loss induced by ovariectomy, probably by reducing bone turnover through inhibition of bone resorption.
In addition, Sabudak and Guler  observed that red clover botanical dietary supplements have received a lot of attention recently for their potential use in the maintenance and improvement of bone health. It contains four important estrogenic isoflavones (daidzein, genistein, formononetin, and biochanin A) and coumestans. The red clover-induced improvement in bone histology has been explained by Polkowski and Mazurek  , who postulated that the positive effect of isoflavones on bone metabolism may be mediated by at least two mechanisms: the first is the impact on osteoclasts through activation of apoptosis, and the second is the inhibition of tyrosine kinase activity through modulation of membrane ER with consecutive changes in the activity of alkaline phosphatase.
In the present study the treatment of OVX rats with fennel resulted in some improvement in histological changes in the form of increase in thickness of the shaft cortical bone and increase in the number of osteocytes, compared with OVX rats. The improvement in pathological changes in the present work may be due to the estrogenic potency of fennel. According to Oktay et al.  , fennel seed extract has been shown to have estrogenic, antioxidant, and antihirsutism activities. Fennel extract is a rich source of phytochemicals, and many of these compounds have beneficial effects on human health. Jung et al.  demonstrated the role of estrogen as an antiosteoporotic agent. The effects of estrogen on osteoblasts and osteoclasts are mediated by binding to intracellular estrogen receptor and modulating the production of target proteins.
In addition, Djeridane et al.  reported that many of these phytochemicals possess significant antioxidant capacities that are associated with lower occurrence and lower mortality rates of several human diseases. The radical scavenging activity of the extracts could be related to the nature of phenolics and their hydrogen-donating ability. According to Yang et al. , scavenging of OH− is an important antioxidant activity of fennel because of its very high reactivity, which can easily cross the cell membranes at specific sites, react with most biomolecules, and cause tissue damage and cell death. Thus, removal of OH− is very important for the protection of the living system. According to Chatterjee et al.  the ability of fennel seed extracts to quench hydroxyl radicals seems to be directly related to the prevention of propagation of the lipid peroxidation process, and to being good scavengers of active oxygen species, thus reducing the rate of chain reaction.
In the present experiment the treatment of OVX rats with carob induced an increase in shaft cortical thickness compared with OVX rats, and increase in the number of osteocytes denoting recovery of bone tissue. The mean areas of Haversian canals were still smaller in the OVX rats subjected to carob treatment as compared with untreated OVX rats. Increased ROS lead to oxidative stress and a degenerative signaling cascade triggered by oxidation of vital cellular components, which induced cellular damage and cell death  . Oxidative stress is characterized by depletion from intracellular stores of endogenous antioxidants or by rapid alteration in antioxidant enzymes such as superoxide dismutase, catalase, and glutathione peroxidase, resulting in increased lipoperoxidation  . The improvement in pathological changes observed in this group may be due to the antioxidant activity of carob. According to Rodrigo and Bosco  and Seifried et al.  the antioxidant capacity of carob extracts is mainly related to their higher level of phenolic compounds in this fraction. These compounds are well known for their ability to scavenge free radicals such as superoxide radical (O 2 ), hydroxyl radical (OH), and other ROS. Also, Rice-Evans et al.  reported that the ability of plant extracts to scavenge H 2 O 2 may be attributed to their phenolic compounds, which donate electrons to H 2 O 2 and reduce it to water. Sebai et al.  reported that C. siliqua L. pods (carob) contain antioxidants and vitamin E, and can help to improve bone fractures because the seeds are rich in phosphorus and calcium.
The richness of carob fruit  or leaf in polyphenols  is the basis of its antioxidant ability, scavenging free radicals such as hydroxyl radical (OH), which is the major cause of lipid peroxidation  .
In the present study, the osteoporotic bone of OVX rats showed no signs of new bone deposition from the subperiosteal area, and the bone matrix did not show PAS-positive reaction as compared with control. The results of the present work are in agreement with those of Kalleny  , who reported that the bone of OVX rats showed no signs of subperiosteal bone deposition, and its matrix did not exhibit intense PAS-positive reaction compared with controls.
The compact and trabecular bones of OVX rats treated with red clover or fennel and/or carob exhibited intense PAS-positive reaction as compared with the bone of OVX rats. Chayanupatkul et al.  clarified that the newly formed bone takes on a distinctive magenta color from PAS reagent because the type of collagen matrix that is formed is type III, which is the emergency type, and a good candidate for repairing bone matrix. Type III collagen will then be replaced by the more permanent type I collagen matrix, which is the most stable because of its very strong cross-links allowing more stability for the new bone. In agreement with Ono et al.  , who stated that collagen plays an important role in binding calcium in bone, it is suggested that the red clover, fennel, and carob treatment used in this study prevents the loss of BMD by upregulating collagen synthesis from osteoblasts of compact and trabecular bone. The area showing subperiosteal bone deposition as a distinct basophilic cement line also exhibited intense PAS-positive reaction.
| Conclusion|| |
Treatment of OVX rats with phytoestrogens such as red clover, fennel, and carob resulted in an improvement in the histopathological and histochemical changes and morphometric parameters in ovariectomy-induced OP. Thus, these phytoestrogens may contribute to the development of a new form of medicinal plant therapy in place of hormonal replacement therapy for menopause-induced OP.
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Conflicts of interest
There are no conflicts of interest.
| References|| |
Nazrun AS, Norazlina M, Norliza M, Nirwana SI. The anti-inflammatory role of vitamin e in prevention of osteoporosis. Adv Pharmacol Sci 2012; 2012.
Abdulameer SA, Sulaiman SA, Hassali MA, Subramaniam K, Sahib MN. Osteoporosis and type 2 diabetes mellitus: what do we know, and what we can do?. Patient Prefer Adherence 2012; 6:435-448.
Compston J. Osteoporosis. In: Warrell DA, Benz EJ, Cox TM, Firth JD, Edward JR, Benz MD editors Oxford textbook of medicine
. 4th ed. Oxford Press: 2004. 3.
Bouxsein ML. Mechanisms of osteoporosis therapy: a bone strength perspective, Clin Cornerstone 2003; Suppl 2-21.
Occhiuto F, Pasquale RD, Guglielmo G, Palumbo DR, Zangla G, Samperi S, et al.
Effects of phytoestrogenic isoflavones from red clover (Trifolium pratense
L.) on experimental osteoporosis. Phytother Res 2007; 21:130-134.
Gronholz MJ. Prevention, diagnosis, and management of osteoporosis-related fracture: a multifactoral osteopathic approach. J Am Osteopath Assoc 2008; 108:575-585.
Kanis JA, McCloskey EV, Johansson H, Strom O, Borgstrom F, Oden A. National Osteoporosis Guideline Group. Case finding for the management of osteoporosis with FRAX - assessment and intervention thresholds for the UK. Osteoporos Int 2008; 19:1395-1408.
Das UN. Nitric oxide as the mediator of the antiosteoporotic actions of estrogen, statins, and essential fatty acids, Exp Biol Med (Maywood) 2002; 227:88-93.
Tielens S, Wymeersch F, Declercq H, Cornelissen M. Effect of 17beta-estradiol on the in vitro
differentiation of murine embryonic stem cells into the osteogenic lineage. In Vitro
Cell Dev Biol Anim 2008; 44:368-378.
Inada M, Miyaura C. Cytokines in bone diseases. Cytokine and postmenopausal osteoporosis. Clin Calcium 2010; 20:1467-1472.
Almeida M, Han L, Martin-Millan M, Plotkin LI, Stewart SA, Roberson PK, et al
. Skeletal involution by age-associated oxidative stress and its acceleration by loss of sex steroids. J Biol Chem 2007; 282:27285-27297.
Lean JM, Davies JT, Fuller K, Jagger CJ, Kirstein B, Partington GA, et al.
A crucial role for thiol antioxidants in estrogen-deficiency bone loss. J Clin Invest 2003; 112:915-923.
Tenpe CR, Yeole PG. Comparative evaluation of anti-diabetic activity of some marketed poly herbal formulations in alloxan induced diabetic rats. Int J Pharm Tech Res 2009; 1:43-49.
Yatkin E, Daglioglu S. Evaluation of the estrogenic effects of dietary perinatal Trifolium pratense
. J Vet Sci 2011; 12:121-126.
Catthareeya T, Pittaya P, Suthida C, Sajeera K. Talinum paniculatum
(JACQ.) Gertn: a medicinal plant with potential estrogenic activity in ovariectomized rat. Int J Pharm Pharm Sci 2013; 5:478-485.
Beck V, Rohr U, Jungbauer A. Phytoestrogens derived from red clover: an alternative to estrogen replacement therapy? J Steroid Biochem Mol Biol 2005; 94:499-518.
Sabudak T, Guler N. Trifolium pratense
: a review on its phytochemical and pharmacological profile. Phytother Res 2009; 23:439-446.
Engelmann NJ, Reppert A, Yousef G, Rogers RB, Lila MA. In vitro
production of radio labeled red clover (Trifolium pratense
L.) isoflavones. Plant Cell Tissue Organ Cult 2009; 98:147-156.
Arjmandi BH, Alekel L, Hollis BW, Amin D, Stacewicz-Sapuntzakis M, Guo P, Kukreja SC. Dietary soybean protein prevents bone loss in an ovariectomized rat model of osteoporosis. J Nutr 1996; 126:161-167.
Polkowski K, Mazurek AP. Biological properties of genistein. A review of in vitro
and in vivo
data. Acta Pol Pharm 2000; 57:135-155.
Madsen HL, Bertelesn G. Spices as antioxidants, Trends Food Sci Technol 1995; 6:271-277.
Haber B. Carob fiber benefits and applications. Cereal Foods World 2002; 47:365-369.
Ahmed MM. Biochemical studies on nephroprotective effect of carob Ceratonia siliqua
L. growing in Egypt. Nat Sci 2010; 8:41-47.
Hasouna AB, Saoudi M, Trigui M, Jamoussi K, Boudawara T, Jaoua S, Feki AE. Characterization of bioactive compounds and ameliorative effects of Ceratonia siliqua
leaf extract against CCl 4
induced hepatic oxidative damage and renal failure in rats. Food Chem Toxicol 2011; 49:3183-3191.
Gulcin I, Oktay M, Kirecci E, Kufrevioglu OI. Screening of antioxidant and Antimicrobial activities of anise (Pimpinella anisum
L) seed extracts. Food Chem 2003; 83:371-382.
Khan N, Sultana S. Chemomodulatory effect of Ficus racemosa
extract against chemically induced renal carcinogenesis and oxidative damage response in Wistar rats. Life Sci 2005; 77:1194-1210.
Reeves PG, Nielsen FH, Fahey GC Jr. AIN-93 purified diets for laboratory rodents: final report of the American Institute of Nutrition ad hoc writing committee on the reformulation of the AIN-76A rodent diet. J Nutr 1993; 123:51-67.
Waynforth HB. Experimental and surgical technique in the rat
. 1980: Academic Press Inc.; 1980.
Lasota A, Danowska-Klonowska D. Experimental osteoporosis - different methods of ovariectomy in female white rats. Rocz Akad Med Bialymst 2004; 49:129-131.
Drury RAB, Wallington FA. Corleton's histological technique.
4th ed. Oxford, New York, Toronto: Oxford University Press; 1980.
Surve VV, Andersson N, Lehto-Axtelius D, Håkanson R. Comparison of osteopenia after gastrectomy, ovariectomy and prednisolone treatment in the young female rat. Acta Orthop Scand 2001; 72:525-532.
Bancroft JD, Cook HC, Turner DR. Manual of histological techniques and their diagnostic application
. 2nd ed. USA: Churchill Livingstone; 1994.
Lock CA, Lecouturier J, Mason JM, Dickinson HO. Lifestyle interventions to prevent osteoporotic fractures: a systematic review. Osteoporos Int 2006; 17:20-28.
International Osteoporosis Foundation. The facts about osteoporosis and its impact.
Nyon, Switzerland: IOF; 2003.1-3.
Blum SC, Heaton SN, Bowman BM, Hegsted M, Miller SC. Dietary soy protein maintains some indices of bone mineral density and bone formation in aged ovariectomized rats. J Nutr 2003; 133:1244-1249.
Weber K, Kaschig C, Erben RG. 1a-Hydroxyvitamin D2 and 1a-hydroxyvitaminD 3 have anabolic effects on cortical bone, but induce intracortical remodeling at toxic doses in ovariectomized rats. Bone 2004; 35:704-710.
Park JA, Ha SK, Kang TH, Oh MS, Cho MH, Lee SY, et al.
Protective effect of apigenin on ovariectomy-induced bone loss in rats. Life Sci 2008; 82:1217-1223.
Kalleny N. Histological and morphometric studies on the effect of alpha-lipoic acid on postovariectomy osteoporosis induced in adult female albino rats. Egypt J Histol 2011; 34:139-155.
Ahmed HH, Hamza AH. Potential role of arginine, glutamine and taurine in ameliorating osteoporotic biomarkers in ovariectomized rats. Rep Opin 2009; 1:24-35.
Khattab HAH, Ardawi MS, Ateeq RAM. Effect of phytoestrogens derived from red clover (Trifolium pratense
L) in ovariectomized rats. Life Sci J 2013; 10:1-11.
NAMS. Management of postmenopausal osteoporosis: position statement of the North American Menopause Society. Menopause 2002; 9:84-101.
Kimble RB, Vannice JL, Bloedow DC, Thompson RC, Hopfer W, Kung VT, et al
. Interleukin-1 receptor antagonist decreases bone loss and bone resorption in ovariectomized rats. J Clin Invest 1994; 93:1959-1967.
Oktem G, Uslu S, Vatansever SH, Aktug H, Yurtseven ME, Uysal A. Evaluation of the relationship between inducible nitric oxide synthase (iNOS) activity and effects of melatonin in experimental osteoporosis in the rat. Surg Radiol Anat 2006; 28:157-162.
Ettinger B, Ensrud KE, Wallace R, Johnson KC, Cummings SR, Yankov V, et al.
Effects of ultralow-dose transdermal estradiol on bone mineral density: a randomized clinical trial, Obstet Gynecol 2004; 104:443-451.
Novack DV. Estrogen and bone: osteoclasts take center stage. Cell Metab 2007; 6:254-256.
Li M, Mosekilde L, Søgaard CH, Thomsen JS, Wronski TJ. Parathyroid hormone monotherapy and cotherapy with antiresorptive agents restore vertebral bone mass and strength in aged ovariectomized rats. Bone 1995; 16:629-635.
Hayashi T, Yamamuro T, Okumura H, Kasai R, Tado K. Effect of (Asui,7)-eel calcitonin on the prevention of osteoporosis induced by combination of immobilization and ovariectomy in the rat. Bone 1998; 10:25-28.
da Paz LH, de Falco V, Teng NC, dos Reis LM, Pereira RM, Jorgetti V. Effect of 17beta-estradiol or alendronate on the bone densitometry, bone histomorphometry and bone metabolism of ovariectomized rats. Braz J Med Biol Res 2001; 34:1015-1022.
Lindberg MK, Movérare S, Skrtic S, Alatalo S, Halleen J, Mohan S, et al
. Two different pathways for the maintenance of trabecular bone in adult male mice. J Bone Miner Res 2002; 17:555-562.
Horiuchi T, Onouchi T, Takahashi M, Ito H, Orimo H. Effect of soy protein on bone metabolism in postmenopausal Japanese women. Osteoporos Int 2000; 11:721-724.
Hsu JT, Hsu WL, Ying C.
Dietary phytoestrogen regulates estrogen receptor gene expression in human mammary carcinoma cells. Nut Res 1999; 19:1447-1457.
King TS, Steger RW, Morgan WW. Effect of ovarian steroids to stimulate region-specific hypothalamic 5-hydroxytryptamine synthesis in ovariectomized rats. Neuroendocrinology 1986; 42:344-350.
Shively CA, Mirkes SJ, Lu NZ, Henderson JA, Bethea CL. Soy and social stress affect serotonin neurotransmission in primates. Pharmacogenomics J 2003; 3:114-121.
Wronski TJ, Yen CF. The ovariectomized rat as an animal model for postmenopausal bone loss. Cells Mater 1991; (suppl 1): 69-74.
Kuiper GG, Carlsson B, Grandien K, Enmark E, Häggblad J, Nilsson S, Gustafsson JA. Comparison of the ligand binding specificity and transcript tissue distribution of estrogen receptors alpha and beta. Endocrinology 1997; 138:863-870.
Oktay M, Gülcin I, Küfrevioðlu OI. Determination of in-vitro
antioxidant activity of fennel (Foeniculum vulgare
) seed extracts, LWT Food Sci Technol 2003; 36:263-271.
Jung EM, Choi KC, Yu FH, Jeung EB. Effects of 17beta-estradiol and xenoestrogens on mouse embryonic stem cells. Toxicol In Vitro
Djeridane A, Yousfi M, Nadjemi B, Boutassouma B, Stocker P, Vidal N. Antioxidant activity of some Algerian medicinal plants extracts containing phenolic compounds. Food Chem 2006; 97:654-660.
Yang J, Guo J, Yuan J. In vitro
antioxidant properties of rutin. LWT Food Sci Technol 2008; 41:1060-1066.
Chatterjee S, Goswami N, Bhatnag P. Estimation of phenolic components and in vitro
antioxidant activity of fennel (Foeniculum vulgare
) and Ajwain (Trachyspermum ammi
) seeds. Adv Biores 2012; 3:109-118.
Farrugia G, Balzan R. Oxidative stress and programmed cell death in yeast. Front Oncol 2012; 2:1-21.
Ikeda M, Nakabayashi K, Shinkai M, Hara Y, Kizaki T, Oh-ishi S, Ohno H. Supplementation of antioxidants prevents oxidative stress during a deep saturation dive. Tohoku J Exp Med 2004; 203:353-357.
Rodrigo R, Bosco C. Oxidative stress and protective effects of polyphenols: comparative studies in human and rodent kidney. A review. Comp Biochem Physiol C Toxicol Pharmacol 2006; 142: 317-327.
Seifried HE, Anderson DE, Fisher EI, Milner JA. A review of the interaction among dietary antioxidants and reactive oxygen species. J Nutr Biochem 2007; 18:567-579.
Rice-Evans CA, Miller NJ, Paganga G. Antioxidant properties of phenolic compounds. Trends Plant Sci 1997; 2:152-159.
Sebai H, Souli A, Chehimi L, Rtibi K, Amri M, El-Benna J, Sakly M. In vitro
and in vivo
antioxidant properties of Tunisian carob (Ceratonia siliqua
L.). J Med Plants Res 2013; 7:85-90.
Papagiannopoulos M, Wollseifen HR, Mellenthin A, Haber B, Galensa R. Identification and quantification of polyphenols in carob fruits (Ceratonia siliqua L.) and derived products by HPLC-UV-ESI/MSn. J Agric Food Chem 2004; 52:3784-3791.
Kumazawa S, Taniguchi M, Suzuki Y, Shimura M, Kwon MS, Nakayama T. Antioxidant activity of polyphenols in carob pods. J Agric Food Chem 2002; 50:373-377.
Chayanupatkul A, Rabie AB, Hägg U. Temporomandibular response to early and late removal of bite-jumping devices. Eur J Orthod 2003; 25:465-470.
Ono Y, Fukaya Y, Imai S, Yamakuni T. Beneficial effects of Ajuga decumbens
on osteoporosis and arthritis. Biol Pharm Bull 2008; 31:1199-1204.
[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6], [Figure 7], [Figure 8], [Figure 9], [Figure 10], [Figure 11], [Figure 12], [Figure 13], [Figure 14], [Figure 15], [Figure 16]