{"id":19249,"date":"2018-03-25T10:18:57","date_gmt":"2018-03-25T10:18:57","guid":{"rendered":"http:\/\/biomedpharmajournal.org\/?p=19249"},"modified":"2020-04-23T05:45:48","modified_gmt":"2020-04-23T05:45:48","slug":"fluoride-toxicity-in-rabbits-and-the-role-of-calcium-in-prevention-of-fluoride-toxicity","status":"publish","type":"post","link":"https:\/\/biomedpharmajournal.org\/staging\/vol11no1\/fluoride-toxicity-in-rabbits-and-the-role-of-calcium-in-prevention-of-fluoride-toxicity\/","title":{"rendered":"Fluoride Toxicity in Rabbits and The Role of Calcium in Prevention of Fluoride Toxicity"},"content":{"rendered":"<p><strong>Introduction<\/strong><\/p>\n<p>Fluoride exerts its effect on caries and on dental fluorosis by distinct mechanisms. The action of fluoride is not only local in the oral cavity but also systemic. It is the blood fluoride concentration that influences the metabolic variables and vice versa.<sup>1,2<\/sup> For example, enamel formation is a continuous process and that the clinically visualized defects are dependent on the thickness of enamel formed under exposure to a given fluoride dose. Thus, the plasma fluoride concentration moderates the fluorosis in developing dentition.<sup>3,4,5<\/sup> The systemic effect of fluoride and the average time of exposure of ameloblasts to fluoride determines dental fluorosis.<sup>6,7<\/sup> The aim of this research is to evaluate the magnitude of dental, skeletal and non-skeletal fluorosis with the action of calcium and fluoride to reduce fluoride toxicity.<\/p>\n<p><strong>Materials and Method<\/strong><\/p>\n<p>A total number of eight colony bred rabbits (Oryctolagus Cuniculus) from different mothers were used of which 6 were males and 2 were females. The weights of the rabbits ranged from 500 grams to 1000 grams and were 6 to 8 months of age.<\/p>\n<p>These rabbits were divided into 3 groups.<\/p>\n<p>Group I: Control group &#8211; two animals were given prescribed diet.<\/p>\n<p>Group II: Study group &#8211; four animals were fed with prescribed diet and oral administration of 10mg \/kg body weight of sodium fluoride (NaF) daily for 6 months.<\/p>\n<p>Group III: Study group \u2013 two animals were fed with prescribed diet and oral administration of 10mg\/kg body weight of NaF with 250mg of calcium daily for 6 months.<\/p>\n<p><strong><em>Rabbit\u2019s Diet<\/em><\/strong><\/p>\n<p>Rabbits were fed with lab animal feed for rabbits (ration computed and supplied by TANUVAS &#8211; Veterinary University, Chennai-35) in the mornings. Green grass CO-3 was fed in the evenings. Additionally fresh carrots and cabbage leaves were fed 2-3times a weak.<\/p>\n<p><strong><em>Fluoride and Calcium<\/em><\/strong><\/p>\n<p>The fluoride used in the research for ingestion in to the rabbits to find out fluoride toxicity in different organs is sodium fluoride powder prepared by S.D fine chem limited, Mumbai- 30. Calcium that is used in the research for ingestion in to the rabbits was a calcium syrup prepared by Elders pharmaceuticals.<\/p>\n<p><strong><em>Methodology<\/em><\/strong><\/p>\n<p>Animals were preserved in the cage and normal diet was given daily. Fluoride 10mg\/kg body wt to the animals and fluoride 10mg\/kg body wt with 250 mg calcium were given orally with syringe. Sodium fluoride stock solution was taken in a 2ml syringe according to the weight of the animal and fed by inserting the syringe in the lateral diastema of rabbit\u2019s mouth. Calcium was fed with a 5 ml syringe by inserting the syringe in the lateral diastema of rabbit\u2019s mouth. This procedure was performed for 180 days.<\/p>\n<p>At the end of 180 days animals were clinically examined for structural and functional changes. Blood was drawn by heart puncture for estimation of Hemoglobin, RBC and WBC count. Then animals were sacrificed by using an overdose of ketamin and xylazene. Vertical incisions were made in the ventral aspect of the control and experimental animals to expose the thorax and abdomen. Then the skeletal and non-skeletal tissues and teeth were studied macroscopically.<\/p>\n<p>After studying the macroscopical appearance of teeth, bone and other organs, soft tissues of stomach, intestine, liver, kidney, lung, artery, vein, ligament, muscle and teeth were collected for histopathological study with eosin and hematoxillin.<\/p>\n<p><strong>Results<\/strong><\/p>\n<p>Rabbits were used as an animal model to evaluate the fluoride toxicity in tooth, bone, and non-skeletal soft tissue was carried out for a period of 180 days continuously giving 10mg\/kg body wt of oral ingestion of fluoride daily to the animal. Observations were also made among the experimental animals fed with 10 mg\/kg body wt of NaF with 250mg of calcium. The observation of animals fed with NaF and animals fed with fluoride and calcium were made comparing the control animals. At the end of 180 days the animals were examined for toxic manifestation both clinically and histopathologically.<\/p>\n<p><strong><em>Clinical Observation<\/em><\/strong><\/p>\n<p>The weight of the control animal and experimental animal were recorded at the end of the experiment. It was found that weight of the each experimental animal with 10mg\/kg body wt was slightly less than the control group of animals (Table 1). Animal activities like walking, moving the head, moving the limbs were slightly restricted than compared to the control animals. On examination of teeth, there was no brown discoloration in the experimental animal fed with NaF but mild opaque color was noticed with area of destruction in few teeth. All the above recorded changes were found in those animals fed with 10 mg NaF \/ kg body weight fluoride, daily. On the contrary, examination of experimental animals fed with 10mg\/kg body wtNaF and 250mg calcium revealed no changes in loss of weight, restricted movement and tooth changes.<\/p>\n<p><strong>Table 1: Weight of the animals in kilograms.<\/strong><\/p>\n<table style=\"width: 95%;\" border=\"1\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr>\n<td style=\"text-align: center;\" width=\"223\"><strong>\u00a0<\/strong><\/td>\n<td style=\"text-align: center;\" width=\"141\"><strong>Before Experiment<\/strong><\/td>\n<td style=\"text-align: center;\" width=\"141\"><strong>After Experiment<\/strong><\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center;\" width=\"223\">Control<\/td>\n<td style=\"text-align: center;\" width=\"141\">1.045<\/td>\n<td style=\"text-align: center;\" width=\"141\">1.734<\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center;\" width=\"223\">Experimental animals fed with NaF-10mg\/Kg body weight<\/td>\n<td style=\"text-align: center;\" width=\"141\">A-1.039<\/p>\n<p>B-0.833<\/p>\n<p>C-1.387<\/p>\n<p>D-1.341<\/td>\n<td style=\"text-align: center;\" width=\"141\">A-1.531<\/p>\n<p>B-1.261<\/p>\n<p>C-1.552<\/p>\n<p>D-1.709<\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center;\" width=\"223\">Experimental animals fed with NaF-10mg\/Kg body weight and calcium<\/td>\n<td style=\"text-align: center;\" width=\"141\">M-1.007<\/p>\n<p>N-1.149<\/td>\n<td style=\"text-align: center;\" width=\"141\">M-1.673<\/p>\n<p>N-1.775<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>&nbsp;<\/p>\n<p><strong><em>Histological Changes<\/em><\/strong><\/p>\n<p>Control and experimental animals were sacrificed by injecting xylazene and ketamin. On exposure to thorax and abdomen morphological examination of organs were made. No change with reference to size, shape, color in any of the organs of the animals fed with 10mg\/kg body wt NaF and 10mg \/ kg body wt NaF and 250mg calcium were seen.(Figure 1&amp; 2).<\/p>\n<table style=\"width: 70%;\" border=\"1\" cellpadding=\"5\">\n<tbody>\n<tr>\n<td>\u00a0<img decoding=\"async\" class=\"alignnone size-thumbnail wp-image-19263\" src=\"https:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig1-150x150.jpg\" alt=\"Figure 1: Physical characteristics of the animal\" width=\"150\" height=\"150\" srcset=\"https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig1-150x150.jpg 150w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig1-256x256.jpg 256w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig1.jpg 647w\" sizes=\"(max-width: 150px) 100vw, 150px\" \/><\/td>\n<td><strong>Figure 1: Physical characteristics of the animal<\/strong><\/p>\n<p>&nbsp;<\/p>\n<p><a href=\"http:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig1.jpg\" target=\"_blank\">Click here to View figure<\/a><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>&nbsp;<\/p>\n<table style=\"width: 70%;\" border=\"1\" cellpadding=\"5\">\n<tbody>\n<tr>\n<td>\u00a0<img decoding=\"async\" class=\"alignnone size-thumbnail wp-image-19264\" src=\"https:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig2-150x150.jpg\" alt=\"Figure 2: Clinical examination of the teeth\" width=\"150\" height=\"150\" srcset=\"https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig2-150x150.jpg 150w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig2-256x256.jpg 256w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig2.jpg 743w\" sizes=\"(max-width: 150px) 100vw, 150px\" \/><\/td>\n<td><strong>Figure 2: Clinical examination of the teeth<\/strong><\/p>\n<p>&nbsp;<\/p>\n<p><a href=\"http:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig2.jpg\" target=\"_blank\">Click here to View figure<\/a><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>&nbsp;<\/p>\n<p>Tissues were collected from bone, teeth, gastric mucosa, intestinal mucosa, liver, kidney, artery, vein, lung, ligament, muscle along with bone and teeth. The structural changes in the gastric mucosa were observed with a magnifying glass. (Figure 3 to 6) The gastric mucosa in experimental animals fed with 10 mg \/kg body wt showed mucosal congestion, slight erythema and mild erosion. Cut section of artery and vein showed no changes in the wall of the vessel. Intestinal mucosa had no alteration in the lumen on examination. The collected specimens from soft tissues were subjected to histopathological examination with eosin and hematoxilin stain and the observation were seen under microscope.<\/p>\n<table style=\"width: 70%;\" border=\"1\" cellpadding=\"5\">\n<tbody>\n<tr>\n<td>\u00a0<img decoding=\"async\" class=\"alignnone size-thumbnail wp-image-19266\" src=\"https:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig3-150x150.jpg\" alt=\"Figure 3: Histopathological picture of rabbit bone. 3A. Normal 3B. Amorphous sprinkling of blackish bluish granular deposits. Osteiod tissue occupying 20- 30 % of bone. 3C. No changes seen in animal fed with Fluoride and Calcium\" width=\"150\" height=\"150\" srcset=\"https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig3-150x150.jpg 150w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig3-256x256.jpg 256w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig3.jpg 722w\" sizes=\"(max-width: 150px) 100vw, 150px\" \/><\/td>\n<td><strong>Figure 3: Histopathological picture of rabbit bone. <\/strong><strong>3A. Normal\u00a0<\/strong><strong>3B. Amorphous sprinkling of blackish bluish granular deposits. Osteiod tissue occupying 20- 30 % of bone. 3C. No changes seen in animal fed with Fluoride and Calcium<\/strong><\/p>\n<p>&nbsp;<\/p>\n<p><a href=\"http:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig3.jpg\" target=\"_blank\">Click here to View figure<\/a><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>&nbsp;<\/p>\n<p>Major changes were seen in the liver. The tissues of control animal showed normal architecture and normal cytological appearance. In the experimental animals fed with 10mg\/kg body wt NaF, periportal inflammation sparse lymphocytes and hepatocytes, moderate lysosomal granules, ballooning degeneration were seen in the liver. On the other hand, animals fed\u00a0\u00a0 with\u00a0\u00a0 sodium fluoride 10mg\/kg body weight and 250 mg calcium showed normal architecture with no periportal inflammation, scanty cytoplasm granules and absence of ballooning degeneration of hepatocytes. (Figure 4)<\/p>\n<table style=\"width: 70%;\" border=\"1\" cellpadding=\"5\">\n<tbody>\n<tr>\n<td>\u00a0<img decoding=\"async\" class=\"alignnone size-thumbnail wp-image-19267\" src=\"https:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig4-150x150.jpg\" alt=\"Figure 4: Histopathological picture of rabbit liver. 4A. Normal 4B. Liver changes: Periportal inflammation, Sparse lymphocytes, Ballooning degeneration, Lysosomal granules are seen in Fluoride fed animal. 4C. No changes seen in animal fed with Fluoride and Calcium\" width=\"150\" height=\"150\" srcset=\"https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig4-150x150.jpg 150w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig4-256x256.jpg 256w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig4.jpg 675w\" sizes=\"(max-width: 150px) 100vw, 150px\" \/><\/td>\n<td><strong>Figure 4: Histopathological picture of rabbit liver. 4A. Normal 4B. Liver changes: Periportal inflammation, Sparse lymphocytes, Ballooning degeneration, Lysosomal granules are seen in Fluoride fed animal. 4C. No changes seen in animal fed with Fluoride and Calcium<\/strong><\/p>\n<p>&nbsp;<\/p>\n<p><a href=\"http:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig4.jpg\" target=\"_blank\">Click here to View figure<\/a><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>&nbsp;<\/p>\n<p><strong><em>Bone Changes<\/em><\/strong><\/p>\n<p>Control animal showed no deposits in the bone and the bone structure was normal. In animals fed With Sodium Fluoride-10mg\/Kg Body Weight, the Section of bone showed\u00a0\u00a0 amorphous sprinkling of blackish blue granular deposits within the osteoid. These deposits were patchy and occupied 20% to 30% of the bone area. The marrow spaces were normal. These findings\u00a0 clearly\u00a0 indicates\u00a0 that the\u00a0 structure\u00a0 of\u00a0 bone\u00a0 reacts\u00a0 abnormally with the\u00a0 fluoride action.\u00a0 The presence of 20 to 30% of osteoid tissue in the structure of bone suggests that the mineralization of the bone was affected in presence of excess fluoride in the body. These changes in the structure of bone were not seen in those animals fed with NaF 10mg\/kg body wt along with 250mg of calcium. (Figure 3)<\/p>\n<p><strong><em>Tooth Changes<\/em><\/strong><\/p>\n<p>In control animals, the tooth was normal. However, in animals fed with sodium fluoride-10mg\/kg body weight, the central capillaries in the teeth were calcified. The outer enamel showed concentric deposits of calcium in the form ring of bluish black granules. \u00a0From the above observation it is clear that fluoride disturbs the calcified area making irregular calcifications and calcified capillaries. But\u00a0 these\u00a0 type\u00a0 of\u00a0 alterations were not recorded\u00a0 in the\u00a0 tooth\u00a0 of\u00a0 animals\u00a0 fed with 10mg \/kg body wt of\u00a0 sodium fluoride and calcium. (Figure 5)<\/p>\n<table style=\"width: 70%;\" border=\"1\" cellpadding=\"5\">\n<tbody>\n<tr>\n<td>\u00a0<img decoding=\"async\" class=\"alignnone size-thumbnail wp-image-19268\" src=\"https:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig5-150x150.jpg\" alt=\"Figure 5: Histopathological picture of rabbit teeth. 5A. Normal 5B. Presence of concentric deposits of calcium in the form of ring like bluish black granules. Core shows central capillaries are calcified. 5C. No changes seen in animal fed with Fluoride and Calcium\" width=\"150\" height=\"150\" srcset=\"https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig5-150x150.jpg 150w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig5-256x256.jpg 256w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig5.jpg 671w\" sizes=\"(max-width: 150px) 100vw, 150px\" \/><\/td>\n<td><strong>Figure 5: Histopathological picture of rabbit teeth. 5A. Normal 5B. Presence of concentric deposits of calcium in the form of ring like bluish black granules. Core shows central capillaries are calcified. 5C. No changes seen in animal fed with Fluoride and Calcium<\/strong><\/p>\n<p>&nbsp;<\/p>\n<p><a href=\"http:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig5.jpg\" target=\"_blank\">Click here to View figure<\/a><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>&nbsp;<\/p>\n<table style=\"width: 70%;\" border=\"1\" cellpadding=\"5\">\n<tbody>\n<tr>\n<td><img decoding=\"async\" class=\"alignnone size-thumbnail wp-image-19269\" src=\"https:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig6-150x150.jpg\" alt=\"Figure 6: Histopathological picture of other organs of the rabbit.\" width=\"150\" height=\"150\" srcset=\"https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig6-150x150.jpg 150w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig6-256x256.jpg 256w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig6.jpg 558w\" sizes=\"(max-width: 150px) 100vw, 150px\" \/><\/td>\n<td><strong>Figure 6: Histopathological picture of other organs of the rabbit.<\/strong><\/p>\n<p>&nbsp;<\/p>\n<p><a href=\"http:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2018\/03\/Vol11No1_Flu_Pri_fig6.jpg\" target=\"_blank\">Click here to View figure<\/a><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>&nbsp;<\/p>\n<p><strong>Discussion<\/strong><\/p>\n<p>In the present study, the clinical parameters such as weight loss, reduction of movement, hair loss and changes in the teeth were present in those animals fed with 10 mg NaF \/ kg body weight fluoride. On the contrary, the experimental animals fed with NaF and calcium showed no changes in the above mentioned parameters. Paul et al<sup>8<\/sup> in their study found inhibitory action of NaF on motor activity along with diminished activity of AchE in the central nervous system. This could be attributed to the lack of motor movement in NaF treated animals. Mullenix et al<sup>9<\/sup> found similar results in their study as well.<\/p>\n<p>Opit et al<sup>10<\/sup> found out that in NaF treated animals, protein synthesis was inhibited by fluoride by blocking the Na-K activated ATPase pump. Also the activity of the AchE was inhibited by fluoride leading to muscle weakness and poor activity at the neuromuscular junction. Susheela et al<sup>11<\/sup> in their study found substantial increase in the serum fluoride level on oral intake of NaF which could be due to absorption of fluoride in the gastrointestinal tract. On the other hand Schiffl et al<sup>12<\/sup> in their study found elevated fluoride serum levels resulting from decreased urinary excretion of fluoride.<\/p>\n<p>In the present study, the gastric mucosa of the animals fed with 10 mg \/kg body wt NaF showed mucosal congestion, slight erythema and mild erosion. While those fed with NaF and Calcium showed no changes in the gastric mucosa. Das et al<sup>13<\/sup> in their study found atrophy of the gastric mucosa in NaF treated animals.<\/p>\n<p>In the present study animals fed with NaF only showed significant histopathological changes in the liver and bone tissues when compared to the control animals. In the present study, the animals fed with NaF only showed reduction in Hemoglobin values and the total WBC count. While those fed with NaF and Calcium showed no changes in the haematological parameters.<\/p>\n<p>Boink et al<sup>14<\/sup> and Farley et al<sup>15<\/sup> in their study found significant hypocalcemia in NaF treated animals. Fluorapatite is poorly soluble form of calcium causing hypocalcaemic states. Calcium prevents absorption of fluoride from the gastrointestinal tract. Thus if calcium supplements are given along with NaF, hypocalcaemic state can be countered.<\/p>\n<p>Chinoy and Sequeria<sup>16<\/sup> in their study have concluded that in animals treated with NaF, there is depletion of body protein along with accumulation of glycogen in the body. This could be an indication for the changes in the locomotory activity of NaF treated animals.\u00a0 However, in animals treated with calcium supplements and NaF, no depletion of locomotor behaviour or any other parameter was observed. This proves the fact that calcium supplements help to decrease the fluoride burden in the body thus counteracting the toxicity of excess fluoride in the body.<\/p>\n<p>In the present study, the animals fed with NaF only demonstrated concentric\u00a0\u00a0 deposits of calcium in the form of ring like bluish black granules in the outer enamel layer. However these findings were not consistent with the animals fed with NaF and calcium.<\/p>\n<p>Ekstrand &amp; Oliveby<sup>17<\/sup> in their study found out that low salivary calcium levels occurring due to NaF consumption caused dental lesions in NaF treated animals. Shupe et al<sup>18<\/sup> concluded that the dental lesions may be the reason for animals to inadequately masticate and swallow the food causing weight loss. It has been proved that the biochemical, behavioural and the dental impairments can be reverted back significantly after 2 months of fluoride exposure.<\/p>\n<p>Trivedi et al<sup>19<\/sup> have reported reversal of endemic fluorosis after changing fluoride containing drinking water. Catani et al<sup>20<\/sup> in their study found that animals chronically exposed to symmetrically oscillating fluoride doses can cause dental fluorosis.<\/p>\n<p><strong>Conclusion<\/strong><\/p>\n<p>In conclusion, it is found that adding calcium along with fluoride is beneficial to nullify the action of fluoride toxicity as evidenced by the fact of non involvement of toxic manifestations in the tissues in the animals fed with calcium and fluoride. The present study gives support to the epidemiological observation that increased fluoride concentration in the body causes deposition of fluoride within the tooth which may lead to dental fluorosis.<\/p>\n<p><strong>Acknowledgement<\/strong><\/p>\n<p>First and foremost I thank the Almighty for all His mercy and blessings bestowed throughout my life and career.<\/p>\n<p>It is with supreme humility, I express my sincere thanks and heartfelt gratitude to my most respected Professor and Head of the Department, Dr. N.Gnanasundaram, M.D.S., for his constant encouragement, unrelenting support and valuable guidance rendered in the preparation of this Dissertation.<\/p>\n<p>My sincere and heartfelt thanks to the Director Dr.B.Jayachandran Dare, MVSc,Ph.D, and Mr.Praveen M.Sc, of Biomedical Research unit and Laboratory Animal Center Saveetha University, Chennai for their guidance and\u00a0 cooperation throughout the\u00a0 study.<\/p>\n<p>I also express my sincere thanks to my teacher Dr. M Arvind &amp; my dear friends Dr.Sangeetha D and Dr. Atul Anand Bajoria for their constant cooperation, support and encouragement.<\/p>\n<p>I am thankful to my Madam Dr. Meera Govindarajan, M.D., Pathologist and the other staff members for the guidance, cooperation in providing laboratory facilities for me.<\/p>\n<p><strong>Conflict of Interest<\/strong><\/p>\n<p>There is no conflict of interest<\/p>\n<p><strong>References<\/strong><\/p>\n<ol>\n<li>Cury J. A., Tenuta L. M. How to maintain a cariostatic fluoride concentration in the oral environment. <em>Adv Dent Res<\/em>. 2008;20:13-16.<br \/>\n<a href=\"https:\/\/doi.org\/10.1177\/154407370802000104\" target=\"_blank\">CrossRef<\/a><\/li>\n<li>Bronckers A. L., Lyaruu D. M., DenBesten P. K. The impact of fluoride on ameloblasts and the mechanisms of enamel fluorosis.<em> J Dent Res.<\/em> 2009;88:877-893.<br \/>\n<a href=\"https:\/\/doi.org\/10.1177\/0022034509343280\" target=\"_blank\">CrossRef<\/a><\/li>\n<li>Ekstrand J.\u00a0 Fluorides metabolism. In: Fluoride in dentistry. Fejerskov O., Ekstrand J., Burt B (Editors). Copenhagen: Munksgaard. 1996;55-68.<\/li>\n<li>Angmar-M\u00e5nsson B., Whitford G. M. Plasma fluoride levels and enamel fluorosis in the rat. <em>Caries Res<\/em>. 1982;16:334-339.<br \/>\n<a href=\"https:\/\/doi.org\/10.1159\/000260617\" target=\"_blank\">CrossRef<\/a><\/li>\n<li>Aoba T., Fejerskov O. 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