Dear Label_Name,

Greetings! I hope you are well.

I am writing on behalf of an international publishing house, Science and Education Publishing, USA (http://www.sciepub.com).

Science and Education Publishing (SciEP) is a multidisciplinary open access publisher of Journals covering the fields of Science, Technology and Medicine. All SciEP publications are subject to high-quality peer review, editorial and production processes and are freely available online.

Welcome to the April, 2013 edition of SciEP newsletter, providing monthly summaries of articles on science & education related topics of interest to scientist and professionals. The mission of our journals is to provide an open access forum for publishing new findings on issues pertinent to scientific and academic field. We also invite you to submit original research papers, review articles, short reports, or case studies are considered for publication in our Multidisciplinary Journals.

American Journal of Public Health Research
DOI: 10.12691/ajphr-1-1-3

The Implementation of a Tele-Homecare System with Service Oriented Architecture and HL7 Message Transmission Standard
Ching-Sung Wang

American Journal of Medical and Biological Research
DOI: 10.12691/ajmbr-1-1-2

The Influence of Ethanol on Pyruvate Kinases Activity in Vivo, in Vitro, in Silico
Lelevich Sergey Vladimirovich, Khrustalev Vladislav Victorovich, Barkovsky Eugene Victorovich, Shedogubova Tatyana Aleksandrovna

American Journal of Medical Sciences and Medicine
DOI: 10.12691/ajmsm-1-1-1

Clinical and Histological Features in Wegener Granulomatosis
Li Cavoli Gioacchino, Passantino Rita, Bono Luisa, Tortorici Calogera, Ferrantelli Angelo, Giammarresi Carlo, Rotolo Ugo

American Journal of Infectious Diseases and Microbiology
DOI: 10.12691/ajidm-1-1-2

The Curse of Lymphatic Filariasis: Would the Continual Use of Diethylcarbamazine Eliminate this Scourge in Papua New Guinea?
Anne Lanham, Lillian Mwanri

We have released issues of some journals on February 2013.
American Journal of Public Health Research
American Journal of Medical Sciences and Medicine
American Journal of Medical and Biological Research
American Journal of Pharmacological Sciences
American Journal of Clinical Medicine Research
American Journal of Nursing Research
American Journal of Cancer Prevention
American Journal of Medicine Studies
American Journal of Infectious Diseases and Microbiology
American Journal of Cardiovascular Disease Research
American Journal of Biomedical Research
American Journal of Mechanical Engineering
American Journal of Microbiological Research
Journal of Preventive Medicine
American Journal of Food and Nutrition
American Journal of Hypertension Research
American Journal of Sports Science and Medicine
Journal of Cancer Research and Treatment
American Journal of Zoological Research
Journal of Biomedical Engineering and Technology
American Journal of Microbiological Research
Biomedical Science and Engineering

We are pleased to announce that submissions are now being accepted for peer review for all the journals across all our subject areas in SciEP.

Please submit your manuscript via our online submission system:
http://www.sciepub.com/author/signin

To unsubscribe from our mailing list, please click on the following link: unsubscribe

I am looking forward to hearing from you.

Kind regards,

David Rain
Email:join@sciepub.com
Science and Education Publishing (http://www.sciepub.com)

Biochemical Studies in Experimentally Induced-hyperthyroid Rats Treated with Folic and Ascorbic Acid

Tarek M Mohamed, Ehab Tousson*, Doha M. Beltagy, Ahmed Samy El Said

Department of Zoology, Department of Chemistry, Faculty of Science, Tanta University, Egypt

Abstract: Hyperthyroidism is a relatively prevalent condition, and is one of the most common endocrine problems seen in clinical practice, high serum cholesterol and increased oxidative stress are common associated risk factors of hyperthyroidism. Multivitamin deficiencies in folate and vitamin C are also one of the hyperthyroidism complications. Individually or combined Folic acid and vitamin C were introduced to hyperthyroid induced rats. A relative enhancement in the thyroid hormones with a normal lipid profile was noticed. Previous researches confirmed that the depletion on the lipid in hyperthyroidism will be gained after treatment.

Keywords: Hyperthyroidism, lipid profile, cortisol, oxidative stress, folic acid, vitamin C

Received November 01, 2014; Revised November 17, 2014; Accepted November 19, 2014

Citation: Tarek M Mohamed, Ehab Tousson, Doha M. Beltagy, Ahmed Samy El Said, Biochemical Studies in Experimentally Induced-hyperthyroid Rats Treated with Folic and Ascorbic Acid. Biomedicine and Biotechnology, 2 (4). 60-65. January 2014. doi:10.12691/bb-2-4-1

1. Introduction

Many websites publish information about hyperthyroidism and how to deal with it. We should be awared about its beneficial role or its hazards. Many of these remedies are prescribed for both hyperthyroidism and hypothyroidism at the same time, so we tested two of the vitamins usually prescribed and there is depletion in the information about them, the vitamin C as a natural vitamin is found in most of our food like Blackcurrants (200 mg 100 g⁻¹), Oranges (50 mg 100 g⁻¹) and Green peppers (100 mg 100 g⁻¹) [1].

Folate as a natural antioxidant vitamin occurs naturally in orange juice, strawberries, dark green leafy vegetables and peanuts [2]. Decreased hepatic stores of folic acid have been observed in experimental animals made hyperthyroid by the administration of thyroid hormone) [3]. There is a depletion of the information dealing with the effects of folic acid and vitamin C on hyperthyroid rats and their effect on the thyroid hormones and the cortisol level.

Both lipogenesis and lipolysis are increased in hyperthyroidism, but the net effect is lipolysis, as reflected by an increase in the plasma concentration of free fatty acids and glycerol and a decrease in the serum cholesterol level; triglyceride levels are usually slightly decreased. The enhanced mobilization and oxidation of free fatty acids in response to fasting or catecholamines is a result of enhancement of lipolytic pathways by thyroid hormones [4].

Natural remedies and vitamins may replace the antithyroid drugs at one day, antithyroid drugs act principally by interfering with the organification of iodine, thereby suppressing thyroid hormone levels. Methimazole (Tapazole) and propylthiouracil (PTU) are the two agents available in the United States. Remission rates vary with the length of treatment, but rates of 60 percent have been reported when therapy is continued for two years. Relapse can occur in up to 50 percent of patients who respond initially, regardless of the regimen used. A recent randomized trial indicated that relapse was more likely in patients who smoked, had large goiters, or had elevated thyroid-stimulating antibody levels at the end of therapy) [5]. Increased aspartate aminotransferase and alanine aminotransferase are observed in nearly one third of patients treated with propylthiouracil, and the rise is usually dose-related) [6]. Agranulocytosis is the most serious complication of antithyroid drug therapy and is estimated to occur in 0.1 to 0.5 percent of patients treated with these drugs [7]. This research aimed to study the protective effects of folic acid and ascorbic acid as natural vitamins in hyperthyroidism by assessing many biochemical markers as thyroid hormones, cortisol, oxidative stress markers and lipid profile.

2. Materials and Methods

The experiments were performed on 70 male albino rats (Sprague dawley) weighing 125±10 g and of 9-10 week’s age. They were obtained from our laboratory farms in the Zoology Department, Faculty of Science, Tanta University, Egypt. The rats were kept in the laboratory for one week before the experimental work and maintained on a standard rodent diet (20% casein, 15% corn oil, 55% corn starch, 5% salt mixture and 5% vitaminzed starch obtained from Egyptian Company for Oils and Soap; Kafr-Elzayat, Egypt) and water available ad libitum) [8]. The temperature in the animal room was maintained at 23±2°C with a relative humidity of 55±5%. Light was on a 12:12 hr light-dark cycle. The experimental protocol was approved by Local Ethics Committee and Animals Research and was approved by the faculty of science. The rats were randomly and equally divided into seven groups (10 animals each).

GI a: Control group in which animals never received any treatment.

GI b: Folic acid group in which animals received 8 mg/kg of body weight folic acid 2nd week to 6th week [9,10].

GI c: Vitamin C group in which animals received 240 mg/kg of body weight vitamin C daily from 2nd week to 6th week [11].

GII a: Hyperthyroid group in which rats received 100 µg/Kg L-Thyroxin sodium administration as a chewable lab chow for 4 weeks [8,12].

GII b: Co-treated hyperthyroid with folic acid.

GII c: Co-treated hyperthyroid with vitamin C.

GII d: Co-treated hyperthyroid with folic acid and vitamin C.

At the end of the experimental period rats were euthanized with intravenous injection with sodium pentobarbital and subjected to a complete necropsy. Blood samples were individually collected from the inferior vena cava of each rat in non heparinized glass tubes, random blood samples were collected from rat's tail at approx 8 am for cortisol estimation. Serum was separated by centrifugation at 3000 rpm for 15 minutes. The collected serum was stored at -20°C until analysis. Serum was analyzed to determine the T3, T4, TSH, AM - Cortisol and some lipid profile levels.

1. Estimation of thyroxine (T4), triiodothyronine (T3) and thyrotropin (TSH) according to the methods of Thakur et al. [13], Maes et al. [14] and Mandel et al. [15] respectively. The kits for these hormones were obtained from Calbiotech INC (CBI), USA.

2. Determination of serum cortisol was performed in serum collected from rat's tail at approximately 8 am (from 8 to 9.45 in our experiment) and then stored at -20°C till analyzed by ELISA technique using MyBio Source, Inc. Catalog No. MBS701698 by Assay designs following the manufacturer instruction using competitive inhibition enzyme immunoassay technique.

3. Some Lipid Profile parameters were performed using Bioassay systems Kits catalog no ECCH-100 and EHDL-100 by using quantitative colorimetric determination of Cholesterol, LDL and HDL. Triglycerides was estimated by BioVision Kit catalog no k622-100.

2.1. Determination of Tissue Oxidative Stress

The adrenal glands collected at the end of the experiment and the adrenal homogenate (10%; w/v) was prepared in an ice-cold 0.067 M phosphate buffer. Then, the homogenate was centrifuged at 3000 rpm for 10 min at 4 C. The resulting supernatant was used to determine the adrenal catalase, MDA, total protein, reduced glutathione and nitric oxide.

1. Catalase activity was estimated according to the method of Xue et al. [16].

2. MDA was estimated by the method of Mesbah et al. [17].

3. Determination of total protein was performed by using Diamond Diagnostic kit using a Biuret reagent as described by Beyer [18].

4. Reduced glutathione was determined by the method of Ellman [19].

5. Nitric oxide level was determined following the procedure described by Miranda et al. [20].

2.2. Statistical Analysis

Data (n = 10) were expressed as mean values + SEM. All data were subjected to one-way ANOVA test to determine differences among groups. P values less than 0.05 were considered significant. Results were analyzed and graphed using Graphpad prism 6 software (Graphpad, San Diego, CA).

3. Results

The rat weight was measured at the beginning of the experiment and before the rat euthanasia and was expressed in Table 1 as the mean of the weight difference ± SEM. The folic acid group (GI b) and the vitamin C group (GI C) had a normal rat weight values as compared to the control group.

Table 1. Changes in the % of body weight level in different group under study

The hyperthyroid group (GII a) showed a weight loss as compared to the control group. The co treatment with folic acid (GII b) gained rats more weight as compared to the control group. The co treatment with vitamin C or both vitamins (GII c or GII d) gained rats more weights as compared to the hyperthyroid group but didn’t reach the normal value as compared to the control group.

The T3, T4 and TSH levels in different groups were shown in Table 2. T3, T4 and TSH values in the negative control groups (GI b &GI c) were at the normal values as compared to the control group.

The hyperthyroid group (GII a) showed a higher T3 &T4 values as compared to the control group. The co treatment with folic acid and / or vitamin C (GII b, GII c& GII d) reduced the T3 & T4 levels as compared to the hyperthyroid group but didn’t reach the normal values as compared to the control group.

Table 2. Changes in T4, T3 and TSH levels in different group under study. (mean ± SEM)

As in Table 2 the hyperthyroid group (GII a) showed a reduced TSH value as compared to the control group, the TSH value was slightly increased in the group treated with both vitamins (GII d).

Graph 1 shows the AM – cortisol values of different groups, The group treated with vitamin C (GI c) and the group treated with folic acid (GII b) slightly reduced the AM – cortisol value as compared to the control group.

Figure 1. Changes in AM- cortisol level in different group under study. aSignificantly different from control (GI a) (P < 0.05). bSignificantly different from hyperthyroid (GII a) (P < 0.05).

The hyperthyroid group (GII a) had a more AM – cortisol value as compared to the control group. The co treatment with folic acid or vitamin C (GII b or GII c) increased the AM – cortisol value as compared to the hyperthyoid group and the co treatment with both vitamins (GII d) reduced the AM – cortisol value as compared to the hyperthyroid group but it did’t reach the normal value as compared to the control group.

Table 3 shows the total cholesterol, LDL, TG and HDL in different groups. Treatment with folic acid (GI b) or vitamin C (GI c) reduced the total cholesterol level as compared to the control group; treatment with vitamin C reduced the total cholesterol value more than the treatment with folic acid. Hyperthyroid group (GII a) had less cholesterol level as compared to the control level, co treatment with folic acid (GII b) or vitamin C (GII c) increased the total cholesterol value as compared to the hyperthyroid group but it didn't reach the normal value as compared to the control group. Co treatment with both vitamins (GII d) reduced the cholesterol level as compared to the control level or the hyperthyroid group.

The groups treated with folic acid (GI b) or vitamin C (GI c) had higher TG values as compared to the control group. The hyperthyroid group (GII a) had less TG value as compared to the control group. The co treatment with folic acid (GII b) increased the TG level as compared to the hyperthyroid group but it didn't reach the normal level as in the control group. The co treatment with vitamin C (GII c) or both vitamins (GII d) reduced the TG value as compared to the hyperthyroid group or the control group.

The folic acid treated group (GI b) had a nearly normal LDL level as compared to the control group. The treatment with vitamin C (GI c) reduced the LDL value as compared to the control group. The hyperthyroid group (GII a) had less LDL value as compared to the control group. The co treated groups with folic acid (GII b) or both vitamins (GIII d) showed increased LDL value as compared to the hyperthyroid group but only co treatment with both vitamins (GII d) exceeded the normal value and the other groups was below the normal value as compared to the control group.

Serum HDL value in folic acid group (GI b) or vitamin C group (GI c) was lower than the normal value as compared to the control group. The HDL value of the hyperthyroid group was lower than the control group. Co treatment with folic acid (GII b) or vitamin C (GII c) increased the HDL value as compared to the hyperthyroid group and exceeded the normal value. The co treatment with both vitamins (GII d) reduced the HDL value as compared to the hyperthyroid or the control group. The co treatment with vitamin C (GII c) had a higher value than the co treatment with folic acid (GII b).

Table 3. Determination of some lipid profile parameters in induced hyperthyroid rats as well as those treated with folic acid and / or vitamin C as compared to control (mean ± SEM)

Graph 2 a represents the adrenal total protein, 2-b represents the adrenal MDA, 2-c represents the adrenal reduced glutathione, 2-d represents the adrenal catalase, 2-e represents the adrenal nitric oxide in induced hyperthyroid rats as well as those treated with folic acid and / or vitamin C. aSignificantly different from control (GI a) (P < 0.05). bSignificantly different from hyperthyroid (GII a) (P < 0.05).

Graphs 2-a, 2-b, 2-c, 2-d and 2-e represents total protein, MDA, reduced glutathione, catalase and nitric oxide in the adrenal gland tissue.

There was no significant change in total protein levels in the adrenal gland tissue as shown in graph 2-a.

In graph 2-b, the hyperthyroid group shows an increased MDA level as compared with the control groups. Treatment with folic acid during the hyperthyroid state reduced the MDA level in a more sufficient way than treatment with vitamin C but treatment with both vitamins reduced the MDA level more sufficiently than the individual treatment.

In graph 2-c the rate of reduced glutathione in the hyperthyroid group was lower than the negative control groups, co vitamin C or co treatment with both vitamins increased the glutathione level as compared to the hyperthyroid group.

In graph 2-d, the catalase activity was increased in the hyperthyroid group more than the control group. The treatment with folic acid or vitamin C reduced the catalase activity as compared to hyperthyroid group. Treatment with both vitamins reduced the enzyme activity more efficiently than the single vitamin treatment.

In graph 2-e, the nitric oxide level in the hyperthyroid group was higher than all other folic acid and /or vitamin C treated groups.

Graph 2 a represents the adrenal total protein, 2-b represents the adrenal MDA, 2-c represents the adrenal reduced glutathione, 2-d represents the adrenal catalase, 2-e represents the adrenal nitric oxide in induced hyperthyroid rats as well as those treated with folic acid and / or vitamin C. aSignificantly different from control (GI a) (P < 0.05). bSignificantly different from hyperthyroid (GII a) (P < 0.05).

4. Discussion

Hyperthyroidism is reported to cause high oxidative stress and to decreased anti-oxidant metabolites in hyperthyroid patients, these changes are corrected in euthyroidism, without any influence of thyrostatic drugs per se. Nutritional support with antioxidant agents, which are defective during hyperthyroidism, is warranted [21,22].

As markedly from the results obtained in Table 1, Hyperthyroid rats (GII a) were the only rats that showed decreased body weight. This decrease can be explained by the concept stated that hyperthyroidism is commonly associated with increased food consumption, parallel with a loss of body weight and decreased serum cholesterol level and increased the levels of lipid peroxidation products in metabolically active tissues [23,24].

Interestingly, from the data obtained in Table 2 hyperthyroid rats (GII a) showed elevation in T3 & T4 levels by incredible increases reach to about 3 and 2 folds, respectively. While TSH concentration showed a dramatic significant decrease reaches to about 20% of the negative control concentration, we may conclude that the TSH level was decreased as a result of negative feedback inhibition mechanism. T3 level might be increased as a result of deiodinase enzyme which converts T4 into T3 [25]. The treatment with folic acid and/or vitamin C managed to reduce the T4& T3 levels but the TSH level was still below the normal value, suggesting an ameliorating potential of these vitamins in hyperthyroidism.

Hyperthyroidism was reported by Gallagher et al. [26] to increase the cortisol level and increase cortisol clearance, he reported that there was an almost certain increased functional adrenal capacity to nearly double normal as evident from greater cortisol production per unit time. In Table 3 there is increased AM- cortisol level which is consistent with the previous paper. We may assume that the use of folic acid or vitamin C as a co treatment affected the cortiol production/clearance balance in the hyperthyroid state and increased the cortisol level. The use of both treatments as a co treatment decreased the cortisol level.

The hyperthyroid state established in the selected group decreased the body weight gain in the hyperthyroid group and treatment with vitamins increased the body weight gain.

Thyroid hormone is reported to increase HMG-CoA reductase which is an integral membrane protein of the smooth ER, it is the major point of regulating the pathway of cholesterol synthesis, and much of the cholesterol synthesis in vertebrates takes place in the liver. A small fraction of the cholesterol made there is incorporated into the membranes of hepatocytes, but most of it is exported in one of three forms: biliary cholesterol, bile acids, or cholesteryl esters. Cholesterol and cholesteryl esters, like triacylglycerols and phospholipids, are essentially insoluble in water, yet must be moved from the tissue of origin to the tissues in which they will be stored or consumed. They are carried in the blood plasma as plasma lipoproteins [27]. The total cholesterol level in the hyperthyroid group is lower than the cholesterol level of negative control group or the folic acid group; we may suppose that the thyroid hormone may increase both cholesterol synthesis and cholesterol degradation as a result of the high total body catabolic rate of the hyperthyroidism. Hyperthyroidism is reported to decrease the HDL level and after treatment the HDL level increases [28] and these findings is consistent with our results.

Vitamin C is important in 7α-HYDROXYLASE activity and the 7α hydroxylation of cholesterol is the first and principal regulatory step in the biosynthesis and degradation of cholesterol, 7α-HYDROXYLASE activity is also enhanced by the thyroid hormone, vitamin C deficiency would deactivate this step [29,30]. In our results, the cholesterol level in the vitamin C group was lower than the control group or the hyperthyroid group. We may suppose that the co treatment with folic acid or vitamin C would reduce the T3 & T4 levels so the cholesterol level is slightly more elevated than the hyperthyroid group.

It was reported that there is a relation between hyperthyroidism and deteriorations of free radicals and antioxidant systems that increase lipid peroxidation and oxidative stress [22]. The present study indicated that, by showing a highly significant increase in MDA, catalase and NO and a noticeable decrease in and GSH levels in the hyperthyroid rats group in comparing to the control group. Treatment with folic acid and / or vitamin C managed to reduce the oxidative stress in the adrenal gland as shown in graph 2-b, 2-c, 2-d and 2-e, the hyperthyroid group showed increased MDA, catalase, and nitric oxide and decreased adrenal reduced glutathione which indicates that there is increased oxidative stress in the adrenal tissue as compared to the control group, by treatment with vitamins the oxidative stress was reduced as compared to the hyperthyroid group.

In conclusion, folic and ascorbic acids especially if co-administered together have highly protective effects on hyperthyroidism.

References

[1]   | Bender DA. Vitamin C: Physiology, Dietary Sources, and Requirements. Encyclopedia of Human Nutrition (Third Edition) 2013; 363-369
[2]   | Suitor CW, Bailey LB. Dietary folate equivalents: interpretation and application. J Am Diet Assoc 2000; 100: 88-94.
[3]   | Noronha JM, Sreenivasan A. Formate metabolism in the vitamin B12-deficient rat. Biochem J 1959; 73: 732-735.
[4]   | Silva JE. The thermogenic effect of thyroid hormone and its clinical implications. Ann Intern Med 2003; 139:205-213.
[5]   | Nedrobo BG, Holm PA, Uhlving S, Sorheim JI, Skeie S, Eide GE, et al. Predictors of outcome and comparison of different drug regimens for the prevention of relapse in patients with Grave's disease. Eur J Endocrinol. 2002; 147: 583-9.
[6]   | Williams KV, Nayak S, Becker D, Reyes J, Burmeister LA. Fifty years of experience with propylthiouracil-associated hepatotoxicity: what have we learned? J Clin Endocrinol Metab 1997; 82: 1727-1733.
[7]   | Cooper DS. Antithyroid drugs N Engl J Med. 2005; 352: 905-917
[8]   | Tousson E, Hafez E , Massoud A. , Sweef O, Atta N. Protective role of folic acid in thyroxine-induced cardiac hypertrophy in hyperthyroid rat. Biomed Aging Path 2013; 3: 89-95.
[9]   | Tousson E, Ali EM, Ibrahim W, Mansour MA. Proliferating Cell Nuclear Antigen as a Molecular Biomarker for Spermatogenesis in PTU-Induced Hypothyroidism of Rats. Reprod Sci 2011; 18: 679-686.
[10]   | Tousson E, El-Gerbed MSA, Shaleby S. Effects of maturity on histopathological alteration after a growth promoter boldenone injection in rabbits. J American Science 2011; 7: 1074-1080.
[11]   | Petrova S, Mikhaĭlova A, Donchev N. The effect of elevated amounts of ascorbic acid on the status of the vitamin and lung disorders in guinea pigs inhaling styrene. Probl Khig 1992; 17: 137-145.
[12]   | Caminos JE, Seoane LM, Tovar SA, Casanueva FF, Dieguez C. Influence of thyroid status and growth hormone deficiency on ghrelin. Eur J Endocrinol 2002; 147: 159-163.
[13]   | Thakur C, Saikia TC, Yadav RN. Total serum levels of triiodothyronine (T3), thyroxine (T4) and thyrotropin (TSH) in school going children of Dibrugarh district: An endemic goiter region of Assam. Indian J Physiol Pharmacol 1997; 41: 167-170.
[14]   | Maes M, Mommen K, Hendrickx D, Peeters D, D’Hondt P, Ranjan R, De Meyer F, Scharpe S. Components of biological variation, including seasonality, in blood concentrations of TSH, TT3, FT4, PRL, cortisol and testosterone in healthy volunteers. Clin Endocrinol (Oxford) 1997; 46: 587-598.
[15]   | Mandel SJ, Brent GA, Larsen PR. Levothyroxine therapy in patients with thyroid disease. Ann. Intern. Med. 1993; 119: 492-502.
[16]   | Xue JB, Yuan XF and Lang PZ. Determination of catalase activity and catalase inhibition by ultraviolet spectrophotometry. Chinese Environ. Chem. 1997; 16: 73-76.
[17]   | Mesbah L, Soraya B, Narimane S, Jean PF. Protective effect of flavonoides against the toxicity of vinblastine cyclophosphamide and paracetamol by inhibition of lipid-peroxidation and increase of liver glutathione. Haema 2004; 7: 59-67.
[18]   | Beyer RE. Rapid biuret assay for protein of whole fatty tissues. Biochem 1983; 129: 483-485.
[19]   | Ellman GL. Tissue sulfhydryl groups. Arch Bio chem Biophys 1959; 82: 70-77.
[20]   | Miranda KM, Espey MG, Wink DA. A rapid simple spectrophotometric method for simultaneous detection of nitrate and nitrite. Nitric Oxide 2001; 5: 67-71.
[21]   | Villanueva I, Alva-Sánchez C, Pacheco-Rosado J. The Role of Thyroid Hormones as Inductors of Oxidative Stress and Neurodegeneration. Oxid Med Cell Longev 2013; 1-15.
[22]   | Bianchi G, Solaroli E, Zaccheroni V, Grossi G, Bargossi AM, Melchionda N, Marchesini G. Oxidative stress and anti-oxidant metabolites in patients with hyperthyroidism: effect of treatment. Horm Metab Res 1999; 31 (11): 620-624.
[23]   | O’Brien T., Dinneen SF, O’Brien PC, Palumbo PJ. 1993. Hyperlipidemia in patients with primary and secondary hypothyroidism. Mayo Clin Proc 1993; 68 (9): 860-866.
[24]   | Venditti P, Balestrieri M, Di Meo S, De Leo T. Effect of thyroid state on lipid peroxidation, antioxidant defences, and susceptibility to oxidative stress in rat tissues, J Endocrinol 1997; 155: 151-157.
[25]   | Mansourian AR. Metabolic pathways of tetraidothyronine and triidothyronine production by thyroid gland: a review of articles. Pak J Biol Sci 2011; 14: 1-12.
[26]   | Gallagher TF, Hellman L, Finkelstein J, Yoshida K, Weitzman ED, Roffwarg HD, Fukushima DK. Hyperthyroidism and Cortisol Secretion in Man. J Clin Endocrinol Metab 1972; 34 (6): 919-927.
[27]   | Murray RK, Bender DA, Botham KM, Kennelly PJ, Rodwell VW, Weil PA. Harper's Illustrated Biochemistry, 28e McGraw-Hill Medical; 28 edition (June 12, 2009) ASIN: B002TGNJ1K. Copyright © The McGraw-Hill Companies. Page 462 chapter 26.
[28]   | O'Brien T, Katz K, Hodge D, Nguyen TT, Kottke BA, Hay ID. The effect of the treatment of hypothyroidism and hyperthyroidism on plasma lipids and apolipoproteins AI, AII and E. Clin Endocrinol (Oxf). 1997 Jan; 46 (1): 17-20.
[29]   | Björkhem I, Kallner A. Hepatic 7alpha-hydroxylation of cholesterol in ascorbate-deficient and ascorbate-supplemented guinea pigs. J Lipid Res. 1976; 17 (4): 360-365.
[30]   | Murray RK, Bender DA, Botham KM, Kennelly PJ, Rodwell VW, Weil PA. Harper's Illustrated Biochemistry, 26e McGraw-Hill Medical; 26 edition (2003) ASSN: 1043-9811. Copyright © The McGraw-Hill Companies. Page 226 chapter 26.