LEVELS OF THYROID HORMONES AND THEIR CORRELATION WITH LIPID AND LIPOPROTEIN CONCENTRATIONS IN BLOOD SERUM OF MALE CAMELS (CAMELUS DROMEDARIUS) IN THE EGYPTIAN OASIS

Document Type : Research article

Authors

1 Biochemistry Unit, Animal Health Research Institute, New-Valley.

2 Dept. of Physiology, Faculty of Medicine Assiut University, Egypt.

3 Biochemistry Unit, Animal Health Research Institute, Assiut Branch;

Abstract

Thyroid dysfunction is an endemic condition in man and animals in the Egyptian oasis due to the environmental iodine deficiency. The aim of this work was to estimate the circulating thyroid hormone concentrations and their correlation with lipid and lipoprotein profile in blood serum of male dromedary camels in the Egyptian oasis. Blood for serum collection was sampled from 92 randomly selected apparently healthy male camels (Camelus dromedarius), 2-10 years old (divided into 4 groups; 2-4, 4-6, 6-8 and 8-10 years) from their natural habitat in the periurban areas at El-Kharga oasis. The recorded over all mean values of blood serum tri-iodothyronine (T3) and thyroxine (T4) concentrations in dromedary camels were 1.179 ±0.03 nmol/l and 80.59 ±2.27 nmol/l respectively. The effect of age of camels was non significant for both   T3 (F=1.446, P=0.235) and T4 (F=2.014, P=0.096). The over all mean concentrations of blood serum lipids of camels were 369.0±7.504 mg/dl for total lipids, 0.898 ±0.028 mmol/l for total cholesterol and 0.606±0.021 mmol/l for Triglycerides. The effect of age of camels was significant for total lipids (F=3.870, P=0.016), total cholesterol (F=3.987, P=0.011) and triglycerides (F=5.626, P=0.003). It was noticed that old camels (8-10 years) had the highest mean values of these blood serum lipids. The recorded over all mean values for lipoproteins was 0.462±0.023 mmol/l for high density lipoprotein-cholesterol (HDL-C), 0.314 ±0.010 mmol/l for low density lipoprotein-cholesterol (LDL-C) and 0.121± 0.004 mmol/l for very low density lipoprotein-cholesterol (VLDL-C). The age of camels had a significant effect on the mean concentrations of blood serum HDL-C (F=4.051, P=0.009), LDL-C (F=3.698, P=0.024) and VLDL-C (F=5.584, P=0.002). Aged camels (8-10 years) showed the highest values of HDL-C and VLDL-C, whereas LDL-C was highest in camels aged 4-8 years. The linear regression analysis revealed that the regression factor (R2) and correlation coefficient (r) between the estimated blood serum T3 concentrations and lipogram in blood serum of camels was non significant. Also R2 and       r between T4 and total lipids, HDL-C and VLDL-C were non significant. On the other hand, there was significant inverse linear regression (R2) and negative correlation (r) between T4 and each of total cholesterol (R2=0.167, r = – 0.290, P=0.037), triglycerides (R2=0.193, r = – 0.375, P=0.021) and LDL-C (R2=0.196, r = – 0.397, P=0.015). It can be concluded that dromedary camels in the Egyptian oases have low values of circulating thyroid hormones. However, there were no apparent clinical signs of goiter. It seems that these camels are suffering from a state of subclinical hypothyroidism with a pronounced effect on lipid metabolism.

Keywords


Biochemistry Unit,

Animal Health Research Institute, New-Valley.

 

Levels of thyroid hormones and their correlation with lipid and lipoprotein concentrations in blood serum of male camels (Camelus dromedarius)

in the Egyptian oasis

(With 4 Tables and One Figure)

 

By

M.A. Saleh; Ibtisam M.H. El-Mileegy*

 andM. Abdel-Salam**

* Dept. of Physiology, Faculty of MedicineAssiut University, Egypt.

** Biochemistry Unit, Animal Health Research Institute, Assiut Branch;

(Received at 21/12/2006)

 

مستوى هرمونات الغدة الدرقية وارتباطها بترکيزات الدهون والبروتينات الدهنية في مصل دم ذکور الإبل (وحيدة السنم) في الواحات المصرية

 

مصطفى أحمد صالح ، إبتسام محمد المليجي ، محمد عبد السلام محمد

­­­­­­­­­­­­­­­­­­­­­­

يعتبر الخلل الوظيفي للغدة الدرقية من الحالات المتوطنة في الإنسان والحيوان في منطقة الواحات المصرية نتيجة لنقص اليود بالبيئة المحيطة. وکان الهدف من هذه الدراسة تقدير مستوى هرمونات الغدة الدرقية ومدى إرتباطها مع صورة الدهون والبروتينات الدهنية في مصل دم ذکور الإبل في هذه المنطقة. لذلک تم أخذ عينات دم لفصل المصل من عدد 92 ذکر من الإبل التي تم اختيارها بطريقة عشوائية من بيئتها الطبيعية في بعض المناطق المحيطة بالواحات الخارجة وکانت هذه الإبل سليمة ظاهريا ويتراوح أعمارها من 2 إلى 10 سنوات قسمت إلى 4 مجموعات (2-4 و 4-6 و6-8 و8-10 سنوات). وأظهرت النتائج أن المتوسط العام لترکيز هرمون التراي أيودوثيرونين (T3) والثيروکثين (T4) في مصل الدم کان 1.179 ± 0.030 مليمول/ لتر و 80.59  ± 2.274مليمول/ لتر على التوالي. ولم يؤثر العمر معنويا على هذه القيم. کما أوضحت النتائج أن المتوسط العام لترکيز الدهون في المصل کان 369.0 ±7.504 مجم/100مل بالنسبة للدهنيات الکلية و 0.898 ± 0.028 مليمول/ لتر بالنسبة للکوليستيرول الکلي و0.606 ± 0.021 مليمول/ لتر بالنسبة للترىاجليسرايد. وقد لوحظ أن قيم هذه الدهون کانت أعلى في الأعمار الکبيرة (8-10 سنوات). وقد سجلت المتوسطات العامة للبروتينات الدهنية 0.462 ±0.023 مليمول/ لتر بالنسبة للکوليستيرول عالي الکثافة (HDL-C) و0.314 ± 0.010 مليمول/ لتر بالنسبة للکوليستيرول منخفض الکثافة (LDL-C) و0.121 ± 0.004  مليمول/ لتر بالنسبة للکوليستيرول شديدة الانخفاض في الکثافة (VLDL-C). وکان للعمر تأثير معنوي على هذه الأنواع من البروتينات الدهنية حيث کانت قيمها أعلى في الإبل المعمرة (8-10 سنوات) إلا أن قيمه الکوليستيرول منخفض الکثافة کانت أعلى في الإبل التي يتراوح عمرها بين 4-8 سنوات. وقد أوضح تحليل الانحدار الخطي ومعادلة الخط المستقيم ومعامل الارتباط عدم وجود علاقة معنوية بين ترکيزات التراى أيودوثيرونين وصورة الدهون في مصل الدم. وکذلک الأمر بين ترکيز الثيروکثين وکل من الدهون الکلية و  HDL-CوVLDL-C. ولکن کانت هناک علاقة خطية عکسية وارتباط سلبي بين ترکيز الثيروکثين وکل من الکوليستيرول الکلي والتراجليسريد وLDL-C. ويمکن أن نستخلص من هذه الدراسة أن ترکيز هرمونات الغدة الدرقية منخفضة في إبل الواحات المصرية. ولکن بالرغم من ذلک لاتوجد أعراض ظاهرية لتضخم الغدة الدرقية في هذه الإبل. وبذلک يبدو أن هذه الإبل تعاني من نقص الإفراز الدرقي تحت الإکلينيکي والذي له تأثير بارز على التمثيل الغذائي للدهون.

 

Summary

 

Thyroid dysfunction is an endemic condition in man and animals in the Egyptian oasis due to the environmental iodine deficiency. The aim of this work was to estimate the circulating thyroid hormone concentrations and their correlation with lipid and lipoprotein profile in blood serum of male dromedary camels in the Egyptian oasis. Blood for serum collection was sampled from 92 randomly selected apparently healthy male camels (Camelus dromedarius), 2-10 years old (divided into 4 groups; 2-4, 4-6, 6-8 and 8-10 years) from their natural habitat in the periurban areas at El-Kharga oasis. The recorded over all mean values of blood serum tri-iodothyronine (T3) and thyroxine (T4) concentrations in dromedary camels were 1.179 ±0.03 nmol/l and 80.59 ±2.27 nmol/l respectively. The effect of age of camels was non significant for both   T3 (F=1.446, P=0.235) and T4 (F=2.014, P=0.096). The over all mean concentrations of blood serum lipids of camels were 369.0±7.504 mg/dl for total lipids, 0.898 ±0.028 mmol/l for total cholesterol and 0.606±0.021 mmol/l for Triglycerides. The effect of age of camels was significant for total lipids (F=3.870, P=0.016), total cholesterol (F=3.987, P=0.011) and triglycerides (F=5.626, P=0.003). It was noticed that old camels (8-10 years) had the highest mean values of these blood serum lipids. The recorded over all mean values for lipoproteins was 0.462±0.023 mmol/l for high density lipoprotein-cholesterol (HDL-C), 0.314 ±0.010 mmol/l for low density lipoprotein-cholesterol (LDL-C) and 0.121± 0.004 mmol/l for very low density lipoprotein-cholesterol (VLDL-C). The age of camels had a significant effect on the mean concentrations of blood serum HDL-C (F=4.051, P=0.009), LDL-C (F=3.698, P=0.024) and VLDL-C (F=5.584, P=0.002). Aged camels (8-10 years) showed the highest values of HDL-C and VLDL-C, whereas LDL-C was highest in camels aged 4-8 years. The linear regression analysis revealed that the regression factor (R2) and correlation coefficient (r) between the estimated blood serum T3 concentrations and lipogram in blood serum of camels was non significant. Also R2 and       r between T4 and total lipids, HDL-C and VLDL-C were non significant. On the other hand, there was significant inverse linear regression (R2) and negative correlation (r) between T4 and each of total cholesterol (R2=0.167, r = – 0.290, P=0.037), triglycerides (R2=0.193, r = – 0.375, P=0.021) and LDL-C (R2=0.196, r = – 0.397, P=0.015). It can be concluded that dromedary camels in the Egyptian oases have low values of circulating thyroid hormones. However, there were no apparent clinical signs of goiter. It seems that these camels are suffering from a state of subclinical hypothyroidism with a pronounced effect on lipid metabolism.

 

Key words: Thyroid hormones, lipid, lipoproteins, dromedary camel, Egyptian oasis.

 

Introduction

 

Dysfunction of the thyroid gland is a common endocrine disorder (Brody, 1999; Laurberg et al., 2000 & 2001; Kelly, 2000; Markou et al., 2001 and Wu, et al. 2005). Goiter is endemic among the Egyptian population (Abdou et al., 1967). The condition is severe in human beings in the Egyptian oasis (Coble, et al. 1968 and WHO/NI, 1992). Soil, original foods and water in the Egyptian oasis are iodine deficient, which is directly reflected on the iodine concentration in human and animal populations in this area (UNICEF, 1993, Saleh, 2000 and Yousef, 2006).

Hypothyroidism is a graded phenomenon with different levels of severity and wide inter-individual range of clinical and biochemical presentation (Murray, et al. 1999). Subclinical thyroid dysfunction is viewed as a risk factor for secondary hyperlipidaemia (Catharine, et al. 2000). Half to third of hypothyroid cases in human are manifesting dyslipidaemia, therefore the lipogram panel is considered a useful diagnostic aid for thyroid dysfunction (Caraccio, et al. 2002). However, the exact underlying mechanisms, notably their effect on the quantitative and qualitative distribution of lipoproteins, remain to be explored (Walsh, et al. 2005 and Iqbal, et al. 2006).

Ibrahim, et al. (1984) found hypertriglyceridaemia in hypothyroid Nubian goats. Wasfi, et al (1987) found poor correlation between either T3 or T4 and cholesterol levels in camels in Saudi Arabia. However, Faye and Bengoumi (1994) reported that camels are more sensitive to iodine deficiency than the other domestic ruminants. Overt hypothyroidism (goiter) and subclinical hypothyroidism has a significant effect on the concentrations of circulating cholesterol and triglycerides in Sudanese camels (Abu Damir et al. 1990 and Barsham 2000).

Lipoprotein metabolism is a complicated process and is still somewhat difficult (Fernandez, 2001). Tulenko and Sumner (2002) reported that the main circulating classes of lipoproteins are chylomicrons (very high density lipoprotein cholesterol, VHDL-C), high density lipoprotein cholesterol (HDL-C), low density lipoprotein cholesterol (LDL-C) and very low density lipoprotein cholesterol (VLDL-C).

Reports on lipoproteins in camels are scarce. Nazifi, et al. (2000) found that blood serum lipids and lipoproteins in camels were lower than those reported for other animal species and they were higher in aged camels than in young individuals. Mohamed et al. (2006) found that LDL-C was positively correlated with cholesterol and negatively correlated with triglycerides in camels infected with internal parasites.

The significance of dyslipidemia in subclinical hypothyroidism in livestock remains controversial. The aim of this work was the estimation of thyroid hormone concentrations and their correlation with the lipogram in blood serum of male dromedary camels in iodine deficient areas at the Egyptian oasis.

 

Materials and methods

 

The study area: The New-Valley governorate (the Egyptian Oasis) covers most of the western Egyptian desert and represents about 46 % of the Egyptian area. This area is 77.8 m altitude and lies between 22° 30′ and 25° 40′ N latitudes and between 29° 42′ and 31° 20′ E longitudes. New-Valley is an arid inland tropical area. Soil nature is sandy limestone with low humus and low annual precipitation. The climate is arid, essentially that of the desert. There is no surface water or rivers. Rainfall is almost negligible. Watering and irrigation depend absolutely on the ground wells.

Animals and sampling: The nature of camels in Egyptian oases is nomadic. Camel owners depend mainly on natural pasture resources to feed their animals. Camels browse freely on ephemeral and perennial plants and bushes belong mainly to Acacia species, German grass (Haloxylon salicornicum), Kassla (Cyperus conglomeratus), and some times Barseem (Medicago sativa).

This study was carried out during the thermoneutral zone (September-October 2006). Ninety two apparently healthy male camels (Camelus dromedarius), 2-10 years old were randomly selected from their natural habitat in the periurban areas at El-Kharga oasis. After faecal and blood parasitological investigations as a routine work in our laboratory, only parasite free camels were selected. The selected camels were classified according to their age into 4 groups: 2-4 years, 4-6 years, 6-8 years and 8-10 years. Blood was drained from the jugular vein into 10-ml capacity vacuum tubes (Venoject, Sterile Terumo Europe, Leuven, Belgium). Blood collection was carried out from camels at the fasting state in the early morning before browsing. Clear sera were separated and kept in deep freeze at -20 °C until used.

Biochemical assay: Blood serum T3 and T4 were estimated by standard ELISA techniques using test kits (Bio-Merieux, 69280 Marcy, L’Etoile, France) according to manufacture instructions. Total serum lipid, total cholesterol (TC) and triglycerides (TG) were determined by enzymatic colorimetric assay by using commercial test kits (Sclavo diagnostics, Italy) after the methods described by Stein (1986), Zlatkis and Zak (1969) and Fletcher (1968) respectively. High-density lipoprotein cholesterol (HDL-C) was determined enzymatically in the supernatant after selective phosphotungstic acid-magnesium chloride-induced precipitation of other lipoproteins by using commercial test kits (SERA-PAK plus, Bayer diagnostics) according to Rifai and Warnick (1994). Low-density lipoprotein cholesterol (LDL-C) and Very low-density lipoprotein cholesterol (VLDL-C) were calculated by using the Friedewald formula (Friedewald, et al. 1972) as following: LDL-C = TC - (HDL-C + triglycerides/5), VLDL = triglycerides/5.

Statistical analysis: General linear model analysis of variance (GLM-ANOVA) was performed on the pooled data using SPSS package V. 11.5 (SPSS, 2002). The means were compared with comparison-wise standard error (SE) rate after significant F-tests. The interactions between the four age groups were included in the model using pair-wise multiple comparison procedures (Duncan's new multiple range test). Linear regression analysis (LRA) and Pearson product moment correlation (PPMC) were performed on the arranged all-raw data of serum thyroid hormones, lipids and lipoproteins regardless to the effect of age. T3 and T4 concentrations were used as dependent variables and the lipogram as independent variables.  The data were represented by the regression equation, regression factor (R2), degree of correlation (r) and the level of significance (P) of these operations. A statistical difference was considered at probability <5%.

 

Results

 

The recorded over all mean values of blood serum tri-iodothyronine (T3) and thyroxine (T4) concentrations in dromedary camels (Table, 1) were 1.179 ±0.030 nmol/l (0.552-1.691 nmol/l) and 80.59 ±2.274 nmol/l (35.91-124.1 nmol/l) respectively. The effect of age of camels was non significant for both T3 (F=1.446, P=0.235) and T4 (F=2.014, P=0.096).

The over all mean concentrations of blood serum lipids of camels were 369.0 ±7.504 mg/dl (236.3-511.8 mg/dl) for total lipids, 0.898 ±0.028 mmol/l (0.460-1.523 mmol/l) for total cholesterol and 0.606±0.021 mmol/l (0.282-0.986 mmol/l) for triglycerides (Table, 2). The effect of age of camels was significant for total lipids (F=3.870, P=0.016), total cholesterol (F=3.987, P=0.011) and triglycerides (F=5.626, P=0.003). It was noticed that old camels (8-10 years) had the highest mean values of these blood serum lipids.

 

Table 1: Mean values of blood serum thyroid hormones in camels.

 

Thyroid

hormones

Age (years)

Over all LSM

N=92

F test

2-4

n=23

4-6

n=23

6-8

n=23

8-10

n=23

F value

P value

T3 (nmol/l)

 

 

 

 

 

 

 

Mean

1.159 a

1.261a

1.202 a

1.093 a

1.179

1.446NS

0.235

SE

0.054

0.056

0.046

0.068

0.030

 

 

Min

0.581

0.614

0.753

0.552

0.552

 

 

Max

1.609

1.691

1.568

1.596

1.691

 

 

T4 (nmol/l)

 

 

 

 

 

 

 

Mean

77.48 a

82.61 a

87.22 a

75.04 a

80.59

2.014NS

0.096

SE

3.235

4.884

4.902

4.816

2.274

 

 

Min

57.94

45.82

39.64

35.91

35.91

 

 

Max

109.2

116.1

124.1

114.0

124.1

 

 

 

NS: non significant at p<0.05. a: there are no significant difference between means in the same row.

 

 

Table 2: Mean values of blood serum lipids in camels.

Lipids

Age (years)

Over all

LSM

n=92

F test

2-4

n=23

4-6

n=23

6-8

n=23

8-10

n=23

F value

P value

Total lipids mg/dl

 

 

 

 

 

 

 

Mean

351.8 a

330.7 a

373.8 a

419.7 b

369.0

3.870*

0.016

SE

10.521

14.145

16.712

12.374

7.504

 

 

Min

259.5

236.3

276.6

294.1

236.3

 

 

Max

451.6

468.7

511.8

509.8

511.8

 

 

Cholesterol mmol/l

 

 

 

 

 

 

 

Mean

0.734 a

0.872 a

0.867 a

1.119 b

0.898

3.987*

0.011

SE

0.046

0.055

0.048

0.049

0.028

 

 

Min

0.491

0.514

0.460

0.694

0.460

 

 

Max

1.212

1.396

1.295

1.523

1.523

 

 

Triglycerides mmol/l

 

 

 

 

 

 

 

Mean

0.497 a

0.529 ab

0.618 b

0.780 c

0.606

5.626**

0.003

SE

0.028

0.038

0.032

0.045

0.021

 

 

Min

0.310

0.295

0.334

0.282

0.282

 

 

Max

0.765

0.866

0.876

0.986

0.986

 

 

 

*,** F value is significant at p<0.05 and 0.01 respectively. Means with different superscript letters (a,b,c) in the same row are significantly different at P<0.05 (Duncan's new multiple range test).

 

Table 3: Mean values of blood serum lipoproteins in camels.

Lipoproteins

Age (years)

Over all LSM

n=92

F test

2-4

n=23

4-6

n=23

6-8

n=23

8-10

n=23

F value

P value

HDL-C mmol/l

 

 

 

 

 

 

 

Mean

0.379 a

0.411 a

0.391 a

0.667 b

0.462

4.051**

0.009

SE

0.030

0.035

0.030

0.052

0.023

 

 

Min

0.191

0.215

0.184

0.260

0.184

 

 

Max

0.732

0.772

0.715

1.127

1.127

 

 

LDL-C mmol/l

 

 

 

 

 

 

 

Mean

0.255 a

0.356 b

0.353 b

0.293 a

0.314

3.698*

0.024

SE

0.018

0.018

0.019

0.019

0.010

 

 

Min

0.121

0.214

0.194

0.164

0.121

 

 

Max

0.391

0.516

0.516

0.462

0.516

 

 

VLDL-C mmol/l

 

 

 

 

 

 

 

Mean

0.099 a

0.106 a

0.124 b

0.156 c

0.121

5.584**

0.002

SE

0.005

0.006

0.006

0.011

0.004

 

 

Min

0.054

0.049

0.061

0.068

0.049

 

 

Max

0.139

0.142

0.168

0.31

0.31

 

 

 

*,** F value is significant at p<0.05 and 0.01 respectively. Means with different superscript letters (a,b,c) in the same row are significantly different at P<0.05 (Duncan's new multiple range test).

Table 4: Linear regression (R2), correlation coefficient (r) and level of significance (P) between the thyroid hormones and the lipogram in blood serum of camels.

 

 

T3

T4

 

R2

r

P

R2

r

P

Total lipid

0.012

-0.079

0.143 NS

0.077

-0.189

0.321 NS

Cholesterol

0.003

-0.044

0.521 NS

0.167

-0.290

0.037*

Triglycerides

0.002

-0.035

0.414 NS

0.193

-0.375

0.021*

HDL-C

9x10-04

-0.011

0.732 NS

0.022

-0.092

0.415 NS

LDL-C

0.020

-0.099

0.089 NS

0.196

-0.397

0.015*

VLDL-C

0.0001

-0.021

0.605 NS

0.002

-0.018

0.562 NS

 

 

 
   


NS Non significant;*Significant (P<0.05%)

 

Fig. 1: Linear regression equation, regression factor (R2) and level of significance (P) between T4 and each of total cholesterol, triglycerides and LDL-C in blood serum of camels.

The values of blood serum lipoproteins are presented in Table 3. The recorded over all mean values were 0.462±0.023 mmol/l (0.184-1.127 mmol/l) for HDL-C, 0.314 ±0.010 mmol/l (0.121-0.516 mmol/l) for LDL-C and 0.121± 0.004 mmol/l (0.049-0.31 mmol/l) for VLDL-C. The age of camels had a significant effect on the mean concentrations of blood serum HDL-C (F=4.051, P=0.009), LDL-C (F=3.698, P=0.024) and VLDL-C (F=5.584, P=0.002). Old camels (8-10 years) showed the highest values of HDL-C and VLDL-C, whereas LDL-C was higher in camels aged 4-8 years.

The linear regression and correlation analysis between the thyroid hormones (dependant variables) and the lipogram (in-dependant variables) are represented in Table 4 and Figure 1. The linear equation, regression factor (R2) and correlation coefficient (r) between the estimated blood serum T3 concentrations and lipogram in blood serum of camels were non significant. The interaction between T4 and total lipids, HDL-C and VLDL-C was also non significant. On the other hand, there were significant inverse linear equation and negative correlation between T4 and total cholesterol (y = –0.0033x +1.11, R2=0.167, r = –0.29, P=0.037), triglycerides (y = –0.0037x +0.943, R2=0.193, r = –0.375, P=0.021) and LDL-C (y = –0.0019x +0.455, R2=0.196, r = –0.397, P=0.015).

 

Discussion

 

Under field practice, the judgment of the thyroid state and thyroidal abnormalities in animals is depending mainly on the values of the circulating thyroid hormones (Kaneko, 1997). The thyroid hormones thyroxine (T4) and triiodothyronine (T3) increase the metabolic activities of almost all the tissues of the body (Kelly, 2000). About 90% of the hormones secreted by the thyroid gland are T4 and 10% is T3. However, most of the T4 is eventually converted to T3 in the tissues, so that both are important functionally (Huszenicza, et al. 2002 and Ganong, 2003).

The recorded mean values of blood serum T4 and T3 concentrations in dromedary camels in the Egyptian oasis were 80.59±2.274 nmol/l (35.91-124.1 nmol/l) and 1.179±0.030 nmol/l (0.552-1.691 nmol/l) respectively. These values were lower than those reported by Wasfi, et al. (1987) in Saudi Arabia who recorded values of 17.92±1.19 µg/dl (230.63±15.32 nmol/l) and 9.33±1.15 ng/ml (1.43±0.18 nmol/l) as normal camel serum total T4 and T3 levels respectively. The values were also lower than those reported by Abu Damir, et al. (1990) for normal and affected camels with clinical and subclinical goiter in the Kordofan region of the Sudan. On the other hand, the mean concentrations of T4 in the current study were similar to those reported by Barsham (2000) in goiterogenic areas in Sudan. The author found that the mean concentrations of T4 (nmol/l) in camels in Idd Elfursan and Zalingei regions in Sudan were 80.48±25.1 and 83.09±25.55 respectively. Lower values were reported by the author for camels in Nyala region which recorded a mean value of 57.37±18.30 nmol/l. Higher mean values of T3 (nmol/l) were recorded by Barsham (2000) which were 1.68±0.61, 1.62±0.65 and 1.88±1.12 respectively for camels reared in Nyala, Idd Elfursan and Zalingei regions in Sudan. The concentration of the circulating thyroid hormones in camels in this study were slightly higher than those reported in our previous work in the same area (Saleh et al. 2003) probably due to the lower number of camels in the earlier study.

Despite of the comparable low values of thyroid hormones in camels in this study with those obtained in goiterogenic areas in Sudan by Abu Damir, et al (1990) and Barsham (2000), there were no apparent clinical signs of goiter observed in camels in the Egyptian oasis. Iodine deficiency was early reported in the soil, water, food, human and sheep in the Egyptian oasis area (UNICEF, 1993, Saleh, 2000 and Yousef, 2006). It seems that camels in the Egyptian oasis are either adapted to iodine deficiency in their natural habitat or it can be suggested that these camels are suffering from a state of unapparent or subclinical hypothyroidism which is directly related to the well recognized iodine deficiency in the Egyptian oasis.

Differences in thyroid hormone concentrations within normal camel population can be expected as a result of pregnancy, lactation, season and plain of nutrition as well as dehydration or rehydration (Yagil, et al. 1978; Alfuraiji, et al. 1994; Abu Damir, 1998; Bengoumi  et al. 1999 & 2003 and Idris, et al. 2006). In the current work, age of camels had no apparent effect on the mean concentrations of thyroid hormones. Similar results were previously cited by Wasfi, et al. (1987) and Nazifi and Gheisari (2000).

The over all mean concentrations of blood serum total lipids, cholesterol and triglycerides in camels in this work were lower than those reported for other animal species (Mills and Taylaur, 1971; Bruss, 1997; Kerr, 2002 and Latimer, et al. 2003) and slightly lower than those reported previously for camels (Wasfi, et al. 1987; Abu Damir, et al. 1990; Nazifi and Maleki, 1998; Mohamed and Hussein, 1999; Barsham, 2000; Nazifi, et al., 2000 and Mohamed, et al., 2006). On the other hand the quantitative and qualitative composition of blood serum lipoproteins in the investigated camels differ than those reported by Nazifi et al. (2000), Shehata, et al. (2001) and Mohamed et al. (2006). These differences in concentrations of blood serum lipids and lipoproteins in normal camels might be related to the variation in the environment, management and feeding behaviour of camels at the different localities (Kerr, 2002 and Latimer, et al., 2003).

The mean values of blood serum lipids and lipoproteins tend to increase with the increase of age of camels except for LDL-C which increased in camels aged 4-8 years. These results agree with the findings of Nazifi, et al. (2000) who found that old camels had the highest values of blood serum lipids and lipoproteins. Nevertheless, Shehata, et al. (2001) and Baraka and Illek (2003) found that age had no effect on the circulating lipogram in camels.

Thyroid hormones influence the major metabolic pathways and play a crucial role in the regulation of mitochondrial oxidative metabolism of protein, carbohydrate and lipid by increasing the basal energy expenditure (Kaneko, 1997). With specific view to lipid metabolism, thyroid hormones affect synthesis, mobilization and degradation of lipids (Pucci, et al., 2000 and Danese, et al., 2000). The participant effects of thyroid hormones on lipid metabolism include enhanced utilization of lipid substrates, increase in the synthesis and mobilization of triglycerides stored in adipose tissue, increase in the concentration of non-esterified fatty acids and increase of lipoprotein-lipase activity (Miettinen, 1968; McGavin, et al 2001; Duntas, 2002; Frank, et al., 2003 a,b & 2004 and Shavdatuashvili, 2005).

In this work there were no regression or correlation between T3 and serum lipogram in camels Also the regression and correlation between T4 and total lipids, HDL-C and VLDL-C were non significant. On the other hand, there were significant inverse linear equation, regression factor and negative correlation between T4 and each of total cholesterol, triglycerides and LDL-C.

Frank et al. (1999; 2003a,b; 2004) reported that higher plasma triglyceride (TG), very low-density lipoprotein (VLDL), and low-density lipoprotein (LDL) concentrations were detected following thyroidectomy in horses suggesting that thyroid hormones play an important role in equine lipoprotein metabolism. On the other hand, Wasfi, et al (1987) found poor correlation between either T3 or T4 and cholesterol levels in clinically healthy camels suggesting that it is only evident under severely altered thyroid function and not the range of thyroid hormones levels seen in physiological conditions.

Bruss, (1997) reported that lipid disorders exhibit great individual variability and hypercholesterolemia occurs in about 75 percent of hypothyroid animals. The suggested possible mechanisms of hypercholesterolemia in hypothyroid individuals were the decreased conversion of cholesterol into bile acids (Efstathiadou, et al., 2001). Further studies showed that hypothyroidism depressed the synthesis of cholesterol, increased cholesterol absorption, changes in hepatic lipase activity and delayed removal of low density lipoprotein from the plasma (Abrams and Grundy 1981a,b; Danese, et al., 2000; Caraccio, et al., 2002; Walsh, et al., 2005 and Chapidze, et al., 2006).

Hypertriglyceridaemia in hypothyroid individuals is primarily the result of increased triacylglycerols production by the liver, possibly as a consequence of increased hepatic microsomal synthesis of triacylglyserols and/or of a decreased oxidation of fatty acids (Ibrahim, et al., 1984; Meier, et al., 2001; Danese, et al., 2000; Duntas, 2002 and William, et al., 2004). In addition, several studies showed that the decrease of thyroid hormone had an effect on lipoprotein lipase and seems to be of importance on the disturbance in triglyceride metabolism (Valdemarsson, et al., 1983; Duntas, 2002; Ineck and Ng, 2003 and Iqbal, et al., 2006).

It can be concluded that dromedary camels in the Egyptian oasis have low values of circulating thyroid hormones. However, there were no apparent clinical signs of goiter. It seems that these camels are suffering from a state of subclinical hypothyroidism with a pronounced effect on lipid metabolism.

 

REFERENCES

 

Abdou, I.A.; Ali, H.E.; Bassioni, A.B.; Nafie, A.M. and Abde-Kader, M.S. (1967): Nutritional deficiencies, goiter, dental caries and parasitic infestations among school children in rural and urban areas of Assiut and Aswan Governorates, Bulletin of Nutrition institute, Cairo, Egypt, 111: 106-110.

Abrams, J.J. and Grundy, S.M. (1981a): Cholesterol metabolism in hypothyroidism and hyperthyroidism in man. J. Lipid Res. 22: 323-338.

Abrams, J.J. and Grundy, S.M. (1981b): Metabolism of plasma triglycerides in hypothyroidism and hyperthyroidism in man. J. Lipid Res. 22: 307-322.

Abu Damir, H. (1998): Mineral deficiencies, tonicities and imbalances in the camel (Camelus dromedarius): a review. Vet. Bull. 68: 1103-1119.

Abu Damir, H.; Barri, M.E.S.; Tageldin, M.H. and Idris, O.F. (1990): Clinical and subclinical colloid goitre in adult camels (Camelus dromedarius) at Kordofan region of Sudan. Br Vet J. 146:     219-227.

Alfuraiji, M.M.; Basmaeil, S.M. and Gamil, M.H. (1994): A note on relation ship of plasma thyroxine and triiodothyronine rate to body weight in growing male camels. Animal Production 59: 460-462.

Baraka, T.A. and Illek, J. (2003): Clinical investigation of thyroid hormones profile as a diagnostic aspect in camels (Camelus dromedarius) in Egypt. J. Egypt Vet. Med. Assoc. 65: 297-309.

Barsham, M.A. (2000): Some biochemical and histopathological Alterations associated with hypothyroidism in camels (Camelus dromedarius). M.Vet Sc. Thesis, Faculty of Veterinary Science, University of Khartoum.

Bengoumi, M.; Moutaouakil, F.; De la Farge, F. and Faye, B. (1999): Thyroidal status of the dromedary camel (Camelus dromedarius): Effect of some physiological factors. Journal of Camel Practice and Research. 6: 41-43.

Bengoumi, M.; Moutaouakil, F.; De la Farge, F. and Faye, B. (2003): Seasonal variations of the plasma thyroid hormone concentrations and the body temperature in the dromedary camel. J. Camel Practice and Research. 10: 115-119.

Brody, T. (1999): Nutritional Biochemistry, 6th ed., Academic Press, New York, PP. 371.

Bruss, M.L. (1997): Lipids and ketones. In: Clinical Biochemistry of Domestic Animals. Eds. Kaneko, J. J; Harvey, J. W. and Bruss, M. L; 5th Ed. Academic press, London. pp. 83-115.

Caraccio, N.; Ferrannini, E. and Monzani, F. (2002): Lipoprotein Profile in Subclinical Hypothyroidism: Response to Levothyroxine Replacement, a Randomized Placebo-Controlled Study. J Clin Endocrinol Metab 87: 1533-1538

Catharine, J.; Scott-Moncrieff, R. and Lynn Guptill-Yoran (2000): Hypothyroidism. In: Text Book of Veterinary Internal Medicine, 5th ed. Ettinger, S.J and Feldman, E.C., WB Saunders Co., Philadelphia, London.

Chapidze, G.; Dolidze, N.; Williams, M.; Sharadze, E. and Latsabidze, N. (2006): Peculiarities of lipid profile parameters in cardiac patients with hypo- and hyperthyroidism. Georgian Med. News. 133: 44-46.

Coble, Y.; Davis, J.; Schubert, A.; Meta, F. and Awad, A.Y. (1968): Goiter and iodine deficiency in Egyptian oasis. Amer. J. Clin. Nutr. 21: 227-283.

Danese, M.D.; Ladenson, P.W.; Meinert, C.L. and Powe, N.R. (2000): Effect of Thyroxine Therapy on Serum Lipoproteins in Patients with Mild Thyroid Failure: A Quantitative Review of the Literature. The Journal of Clinical Endocrinology & Metabolism 85: 2993-3001.

Duntas, L.H. (2002): Thyroid disease and lipids. Thyroid. 12: 287-293.

Efstathiadou, Z.; Bitsis, S.; Milionis, H.J.; Kukuvitis, A.; Bairaktari, E.T.; Elisaf, M.S. and Tsatsoulis, A. (2001): Lipid profile in subclinical hypothyroidism: is L-thyroxine substitution beneficial? European Journal of Endocrinology 145: 705–710.

Faye, B. and Bengoumi, M. (1994): Trace elements status in camels. A review. Biol Trace Elem. Res. 41: 1-11.

Fernandez, M.L. (2001): Guinea Pigs as Models for Cholesterol and Lipoprotein Metabolism. J. Nutr. 131: 10–20.

Fletcher, M.J. (1968): A colorimetric method for estimating serum triglycerides. Clinica et Chimica Acta 22 393–397.

Frank, N.; Sojka, J.E. and Latour, M.A. (2003a): Effects of hypothyroidism and withholding of feed on plasma lipid concentrations, concentration and composition of very-low-density lipoprotein, and plasma lipase activity in horses. Am. J. Vet. Res. 64: 823–828.

Frank, N.; Sojka, J.E. and Latour, M.A. (2004): Effect of hypothyroidism on the blood lipid response to higher dietary fat intake in mares. J. Anim. Sci. 82: 2640–2646

Frank, N.; Sojka, J.E.; Latour, M.A.; McClure, S.R. and Polazzi, L. (1999): Effect of hypothyroidism on blood lipid concentrations in horses. Am. J. Vet. Res. 60: 730–733.

Frank, N.; Sojka, J.E.; Patterson, B.W.; Wood, K.V.; Bonham, C.C. and Latour, M.A. (2003b): Effect of hypothyroidism on kinetics of metabolism of very-low-density lipoprotein in mares. Am. J. Vet. Res. 64:1052–1058.

 

Friedewald, W.T.; Levy, R.I. and Fredrickson D.S. (1972): Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clinical Chemistry 18: 499–502.

Ganong, W.F. (2003): Review of medical physiology. 19th ed. Appleton & Long. Libraire Du Liban.

Huszenicza, Gy.; Kulcsar, M. and Rudas, P. (2002): Clinical endocrinology of thyroid gland function in ruminants. Vet. Med. Czech, 47: 199–210.

Ibrahim, R.E.; Maglad, M.A.; Adam, S.E.; Mirghani, T.E. and Wasfi, I.A. (1984): The effect of altered thyroid status on lipid metabolism in Nubian goats. Comp. Biochem. Physiol.; 77B: 507-512.

Idris, O.F.; Mohamedein, N.M. and Abdel-Rahman, S.H. (2006): Effect of water deprivation on thyroid hormones in extreme climatic conditions in camels (Camelus dromedaries). Proceedings of the 12th Sci. Cong., 10-12 Dec. 2006. Fac. Vet. Med., Assist Univ. Egypt. pp. 11-15.

Ineck, B.A. and Ng, T.M. (2003): Effects of subclinical hypothyroidism and its treatment on serum lipids. Ann Pharmacother.       37:725-730.

Iqbal, A.; Jorde, R. and Figenschau, Y. (2006): Serum lipid levels in relation to serum thyroid-stimulating hormone and the effect of thyroxine treatment on serum lipid levels in subjects with subclinical hypothyroidism: the Tromso Study J. Intern Med. 260: 53-61.

Kaneko, J.J. (1997): Thyroid function, In: Clinical Biochemistry of Domestic Animals. Eds. Kaneko, J. J; Harvey, J. W. and Bruss, M. L; 5th Ed. Academic press, London. pp. 571-588.

Kelly, G. (2000): Peripheral Metabolism of Thyroid Hormones: A Review. Altern Med. Rev. 5: 306-333.

Kerr, M.G. (2002): Veterinary Laboratory Medicine 2nd ed. Blackwell Science, UK.

Latimer, K.S.; Prasse, K.W. and Mahaffey, E.A. (2003): Proteins, lipids and carbohydrates. In Veterinary laboratory Medicine: Clinical Pathology. 4th ed. Ames, Lowa State Univ Press. pp. 162-192.

Laurberg, P.; Bulow, Pedersen I.; Knudsen, N.; Ovesen, L. and Andersen, S. (2001): Environmental iodine intake affects the type of nonmalignant thyroid disease. Thyroid, 11: 457-69

 

Laurberg, P.; Nohr, S.B.; Pedersen, K.M.; Hreidarsson, A.B.; Andersen, S.; Bulow, Pedersen I.; Knudsen, N.; Perrild, H.; Jorgensen, T. and Ovesen, L. (2000): Thyroid disorders in mild iodine deficiency. Thyroid, 10: 951-963.

Markou, K.; Georgopoulos, N.; Kyriazopoulou, V. and Vagenakis, A.G. (2001): Iodine-Induced hypothyroidism, Thyroid, 11: 501-510.

McGavin, M.D.; Carleton, W.W. and Zachary, J.F. (2001): Thyroid gland, In: Special Veterinary Pathology, 3rd ed., Mosby Co., St Lois, London, Philadelphia. Pp 295-305.

Meier, C.; Staub, J.J.; Roth, C.B.; Guglielmetti, M.; Kunz, M.; Miserez, A.R.; Drewe, J.; Huber, P.; Herzog, R. and Muller, B. (2001): TSH-Controlled L-Thyroxine Therapy Reduces Cholesterol Levels and Clinical Symptoms in Subclinical Hypothyroidism: A Double Blind, Placebo-Controlled Trial (Basel Thyroid Study). J Clin Endocrinol Metab 86: 4860-4866. 

Miettinen, T.A. (1968): Mechanism of serum cholesterol reduction by thyroid hormones in hypothyroidism. J. Lab. Clin. Med. 4:   537-547.

Mills, G.L. and Taylaur, C.E. (1971): The distribution and composition of serum lipoproteins in eighteen animals. Comp. Bioch. and Physiol. 40B: 489-501.

Mohamed, A.M.; Abd Ellah, M.R.; Abou El-Ella, Gh.A. and Osman, F.A. (2006): The influence of some nematode parasitism on lipid metabolism and lipoprotein profile in dromedary camel (Camelus dromedaries). Proceedings of the 12th Sci. Cong.,    10-12 Dec. 2006. Fac. Vet. Med., Assist Univ. Egypt. 265-275.

Mohamed, H.A. and Hussein, A.N. (1999): Studies on normal haemtological and serum biochemical values of the ‘Hijin’ racing camels (Camelus dromedarius) in Kuwait. Veterinary Research Communications, 23: 241-248.

Murray, R.K.; Granner, D.K.; Mayes, P.A. and Rodwell, V.W. (1999): Harper's Biochemistry. 25th ed. Appleton and Lange. Norwalk, Connecticut/San Mateo, California.

Nazifi, S. and Gheisari, H.R. (2000): Observations on comparative values of thyroxin (T4), triiodothyronine (T3), T3 uptake and free thyroxin index (FTI) in serum and cerebrospinal fluid of camel (Camelus dromedaries) Journal of Camel Practice and Research. 7: 53-55.

Nazifi, S. and Maleki, K. (1998): Biochemical analysis of serum and cerebrospinal fluid in clinically normal adult camel (Camelus dromedaries). Research in Veterinary Science, 65: 83-84.

Nazifi, S.; Gheisari, H.R.; Abbasali Poorkabir, M. and Saadatfar, S. (2000): Serum lipids and lipoproteins in clinically healthy male camels (Camelus dromedaries). Veterinary Research Communications, 24: 527-531.

Pucci, E.; Choate, L. Pinchera, A. (2000): Thyroid and lipid metabolism. International Journal of Obesity and Related Metabolic Disorders. 24 Suppl 2: S109-S112.

Rifai, N. and Warnick, G.R. (1994): Laboratory measurement of lipids, lipoproteins and apolipoproteins. AACC press. Washington, DC.

Saleh, M.A. (2000): Prevalence, causes and types of iodine deficiency disorders (IDD) in Egyptian oasis sheep. Egyptian J. of Agric. Res. 78: 167-174.

Saleh, M.A.; Abdel-Salam, M.; El-Mileegy, I.M.H. and El-Sokkary, G.H. (2003): Electrolytes and protein homeostasis in Bedouin camels (Camelus dromedarius) during dry thermal stress in the Egyptian oasis. The 7th Sci. Cong., Egyptian Soc. for Cattle Diseases. 7-9 Dec.pp. 319-329.

Shavdatuashvili, T. (2005): Lipoprotein profile and endothelial function in patients with subclinical and overt hypothyroidism. Georgian Medical News. 129: 57-60.

Shehata, Y.M.; El-Dawy, Kh.; Abde El-Razik, M.S.Z. and Helal, F.G. (2001): Influence of sex and age on some biochemical constituents of camels (Camelus dromedaries). The 2nd International Sci. Conf. Mansora 8-9 April. pp 85-103.

SPSS (2002): Sample Power Statistics, SPSS 11.5, Syntax Reference Guide for SPSS Base. SPSS Inc., 233 South Wacker Drive, Chicago, IL.

Stein, E.A. (1986): Quantitative enzymatic clorimetric test for determination of plasma total lipid and cholesterol. In Tietz, N.W. (ed.) Test book of clinical chemistry. W.B. Saunders, Philadelphia. pp. 879-886.

Tulenko, T.N. and Sumner, A.E. (2002): The physiology of lipoproteins. J. Nucl. Cardiol. 9: 638-649.

UNICEF (1993): Report on assessment of the prevalence of iodine deficiency disorders in New-Valley Governorate, UNICEF– High Institute of Public Health, 1993, Alexandria, Egypt.

Valdemarsson, S.; Hansson, P.; Hedner, P. and Nilsson-Ehle, P. (1983): Relations between thyroid function, hepatic and lipoprotein lipase activities, and plasma lipoprotein concentrations. Acta Endocrinol (Copenh) 104: 50-56

Walsh, J.P.; Bremner, A.P.; Bulsara, M.K.; O'leary, P.; Leedman, P.J.; Feddema, P. and Michelangeli, V. (2005): Thyroid dysfunction and serum lipids: a community-based study. Clin Endocrinol (Oxf). 63: 670-675.

Wasfi, I.A.; Hafez, A.M.; El-Tayeb, F.A.A. and El-Taher, A.Y. (1987): Thyroid hormones, cholesterol and triglycerides level in the camel. Res. Vet. Sci.; 42: 418.

WHO/NI (1992): Report on prevalence of IDD among school children in Egypt, WHO–Nutrition Institute, Cairo.

William, J.; Hueston, M.D.; William, S. and Pearson, M.H.A. (2004): Subclinical Hypothyroidism and the Risk of Hypercholesterolemia. Annals of Family Medicine. 2: 351-355.

Wu, S.Y.; Green, W.L.; Huang, W.S.; Hays, M.T. and Chopra, I.J. (2005): Alternate pathways of thyroid hormone metabolism. Thyroid.15: 943-958.

Yagil, R.; Etzion, Z. and Ganadi, J. (1978): Camel thyroid metabolism: effect of season and dehydration. J. Appl. Physiol. 45: 540-544.

Yousef, E.M. (2006): Some minerals profile in sheep serum in new-valley governorate, M. Vet. Sci. Fac. Vet. Med. Assiut Univ.

Zlatkis, A. and Zak, B. (1969): Study of a new cholesterol reagent. Analytical Biochemistry 29: 143–148.

 

Abdou, I.A.; Ali, H.E.; Bassioni, A.B.; Nafie, A.M. and Abde-Kader, M.S. (1967): Nutritional deficiencies, goiter, dental caries and parasitic infestations among school children in rural and urban areas of Assiut and Aswan Governorates, Bulletin of Nutrition institute, Cairo, Egypt, 111: 106-110.
Abrams, J.J. and Grundy, S.M. (1981a): Cholesterol metabolism in hypothyroidism and hyperthyroidism in man. J. Lipid Res. 22: 323-338.
Abrams, J.J. and Grundy, S.M. (1981b): Metabolism of plasma triglycerides in hypothyroidism and hyperthyroidism in man. J. Lipid Res. 22: 307-322.
Abu Damir, H. (1998): Mineral deficiencies, tonicities and imbalances in the camel (Camelus dromedarius): a review. Vet. Bull. 68: 1103-1119.
Abu Damir, H.; Barri, M.E.S.; Tageldin, M.H. and Idris, O.F. (1990): Clinical and subclinical colloid goitre in adult camels (Camelus dromedarius) at Kordofan region of Sudan. Br Vet J. 146:     219-227.
Alfuraiji, M.M.; Basmaeil, S.M. and Gamil, M.H. (1994): A note on relation ship of plasma thyroxine and triiodothyronine rate to body weight in growing male camels. Animal Production 59: 460-462.
Baraka, T.A. and Illek, J. (2003): Clinical investigation of thyroid hormones profile as a diagnostic aspect in camels (Camelus dromedarius) in Egypt. J. Egypt Vet. Med. Assoc. 65: 297-309.
Barsham, M.A. (2000): Some biochemical and histopathological Alterations associated with hypothyroidism in camels (Camelus dromedarius). M.Vet Sc. Thesis, Faculty of Veterinary Science, University of Khartoum.
Bengoumi, M.; Moutaouakil, F.; De la Farge, F. and Faye, B. (1999): Thyroidal status of the dromedary camel (Camelus dromedarius): Effect of some physiological factors. Journal of Camel Practice and Research. 6: 41-43.
Bengoumi, M.; Moutaouakil, F.; De la Farge, F. and Faye, B. (2003): Seasonal variations of the plasma thyroid hormone concentrations and the body temperature in the dromedary camel. J. Camel Practice and Research. 10: 115-119.
Brody, T. (1999): Nutritional Biochemistry, 6th ed., Academic Press, New York, PP. 371.
Bruss, M.L. (1997): Lipids and ketones. In: Clinical Biochemistry of Domestic Animals. Eds. Kaneko, J. J; Harvey, J. W. and Bruss, M. L; 5th Ed. Academic press, London. pp. 83-115.
Caraccio, N.; Ferrannini, E. and Monzani, F. (2002): Lipoprotein Profile in Subclinical Hypothyroidism: Response to Levothyroxine Replacement, a Randomized Placebo-Controlled Study. J Clin Endocrinol Metab 87: 1533-1538
Catharine, J.; Scott-Moncrieff, R. and Lynn Guptill-Yoran (2000): Hypothyroidism. In: Text Book of Veterinary Internal Medicine, 5th ed. Ettinger, S.J and Feldman, E.C., WB Saunders Co., Philadelphia, London.
Chapidze, G.; Dolidze, N.; Williams, M.; Sharadze, E. and Latsabidze, N. (2006): Peculiarities of lipid profile parameters in cardiac patients with hypo- and hyperthyroidism. Georgian Med. News. 133: 44-46.
Coble, Y.; Davis, J.; Schubert, A.; Meta, F. and Awad, A.Y. (1968): Goiter and iodine deficiency in Egyptian oasis. Amer. J. Clin. Nutr. 21: 227-283.
Danese, M.D.; Ladenson, P.W.; Meinert, C.L. and Powe, N.R. (2000): Effect of Thyroxine Therapy on Serum Lipoproteins in Patients with Mild Thyroid Failure: A Quantitative Review of the Literature. The Journal of Clinical Endocrinology & Metabolism 85: 2993-3001.
Duntas, L.H. (2002): Thyroid disease and lipids. Thyroid. 12: 287-293.
Efstathiadou, Z.; Bitsis, S.; Milionis, H.J.; Kukuvitis, A.; Bairaktari, E.T.; Elisaf, M.S. and Tsatsoulis, A. (2001): Lipid profile in subclinical hypothyroidism: is L-thyroxine substitution beneficial? European Journal of Endocrinology 145: 705–710.
Faye, B. and Bengoumi, M. (1994): Trace elements status in camels. A review. Biol Trace Elem. Res. 41: 1-11.
Fernandez, M.L. (2001): Guinea Pigs as Models for Cholesterol and Lipoprotein Metabolism. J. Nutr. 131: 10–20.
Fletcher, M.J. (1968): A colorimetric method for estimating serum triglycerides. Clinica et Chimica Acta 22 393–397.
Frank, N.; Sojka, J.E. and Latour, M.A. (2003a): Effects of hypothyroidism and withholding of feed on plasma lipid concentrations, concentration and composition of very-low-density lipoprotein, and plasma lipase activity in horses. Am. J. Vet. Res. 64: 823–828.
Frank, N.; Sojka, J.E. and Latour, M.A. (2004): Effect of hypothyroidism on the blood lipid response to higher dietary fat intake in mares. J. Anim. Sci. 82: 2640–2646
Frank, N.; Sojka, J.E.; Latour, M.A.; McClure, S.R. and Polazzi, L. (1999): Effect of hypothyroidism on blood lipid concentrations in horses. Am. J. Vet. Res. 60: 730–733.
Frank, N.; Sojka, J.E.; Patterson, B.W.; Wood, K.V.; Bonham, C.C. and Latour, M.A. (2003b): Effect of hypothyroidism on kinetics of metabolism of very-low-density lipoprotein in mares. Am. J. Vet. Res. 64:1052–1058.
 
Friedewald, W.T.; Levy, R.I. and Fredrickson D.S. (1972): Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clinical Chemistry 18: 499–502.
Ganong, W.F. (2003): Review of medical physiology. 19th ed. Appleton & Long. Libraire Du Liban.
Huszenicza, Gy.; Kulcsar, M. and Rudas, P. (2002): Clinical endocrinology of thyroid gland function in ruminants. Vet. Med. Czech, 47: 199–210.
Ibrahim, R.E.; Maglad, M.A.; Adam, S.E.; Mirghani, T.E. and Wasfi, I.A. (1984): The effect of altered thyroid status on lipid metabolism in Nubian goats. Comp. Biochem. Physiol.; 77B: 507-512.
Idris, O.F.; Mohamedein, N.M. and Abdel-Rahman, S.H. (2006): Effect of water deprivation on thyroid hormones in extreme climatic conditions in camels (Camelus dromedaries). Proceedings of the 12th Sci. Cong., 10-12 Dec. 2006. Fac. Vet. Med., Assist Univ. Egypt. pp. 11-15.
Ineck, B.A. and Ng, T.M. (2003): Effects of subclinical hypothyroidism and its treatment on serum lipids. Ann Pharmacother.       37:725-730.
Iqbal, A.; Jorde, R. and Figenschau, Y. (2006): Serum lipid levels in relation to serum thyroid-stimulating hormone and the effect of thyroxine treatment on serum lipid levels in subjects with subclinical hypothyroidism: the Tromso Study J. Intern Med. 260: 53-61.
Kaneko, J.J. (1997): Thyroid function, In: Clinical Biochemistry of Domestic Animals. Eds. Kaneko, J. J; Harvey, J. W. and Bruss, M. L; 5th Ed. Academic press, London. pp. 571-588.
Kelly, G. (2000): Peripheral Metabolism of Thyroid Hormones: A Review. Altern Med. Rev. 5: 306-333.
Kerr, M.G. (2002): Veterinary Laboratory Medicine 2nd ed. Blackwell Science, UK.
Latimer, K.S.; Prasse, K.W. and Mahaffey, E.A. (2003): Proteins, lipids and carbohydrates. In Veterinary laboratory Medicine: Clinical Pathology. 4th ed. Ames, Lowa State Univ Press. pp. 162-192.
Laurberg, P.; Bulow, Pedersen I.; Knudsen, N.; Ovesen, L. and Andersen, S. (2001): Environmental iodine intake affects the type of nonmalignant thyroid disease. Thyroid, 11: 457-69
 
Laurberg, P.; Nohr, S.B.; Pedersen, K.M.; Hreidarsson, A.B.; Andersen, S.; Bulow, Pedersen I.; Knudsen, N.; Perrild, H.; Jorgensen, T. and Ovesen, L. (2000): Thyroid disorders in mild iodine deficiency. Thyroid, 10: 951-963.
Markou, K.; Georgopoulos, N.; Kyriazopoulou, V. and Vagenakis, A.G. (2001): Iodine-Induced hypothyroidism, Thyroid, 11: 501-510.
McGavin, M.D.; Carleton, W.W. and Zachary, J.F. (2001): Thyroid gland, In: Special Veterinary Pathology, 3rd ed., Mosby Co., St Lois, London, Philadelphia. Pp 295-305.
Meier, C.; Staub, J.J.; Roth, C.B.; Guglielmetti, M.; Kunz, M.; Miserez, A.R.; Drewe, J.; Huber, P.; Herzog, R. and Muller, B. (2001): TSH-Controlled L-Thyroxine Therapy Reduces Cholesterol Levels and Clinical Symptoms in Subclinical Hypothyroidism: A Double Blind, Placebo-Controlled Trial (Basel Thyroid Study). J Clin Endocrinol Metab 86: 4860-4866. 
Miettinen, T.A. (1968): Mechanism of serum cholesterol reduction by thyroid hormones in hypothyroidism. J. Lab. Clin. Med. 4:   537-547.
Mills, G.L. and Taylaur, C.E. (1971): The distribution and composition of serum lipoproteins in eighteen animals. Comp. Bioch. and Physiol. 40B: 489-501.
Mohamed, A.M.; Abd Ellah, M.R.; Abou El-Ella, Gh.A. and Osman, F.A. (2006): The influence of some nematode parasitism on lipid metabolism and lipoprotein profile in dromedary camel (Camelus dromedaries). Proceedings of the 12th Sci. Cong.,    10-12 Dec. 2006. Fac. Vet. Med., Assist Univ. Egypt. 265-275.
Mohamed, H.A. and Hussein, A.N. (1999): Studies on normal haemtological and serum biochemical values of the ‘Hijin’ racing camels (Camelus dromedarius) in Kuwait. Veterinary Research Communications, 23: 241-248.
Murray, R.K.; Granner, D.K.; Mayes, P.A. and Rodwell, V.W. (1999): Harper's Biochemistry. 25th ed. Appleton and Lange. Norwalk, Connecticut/San Mateo, California.
Nazifi, S. and Gheisari, H.R. (2000): Observations on comparative values of thyroxin (T4), triiodothyronine (T3), T3 uptake and free thyroxin index (FTI) in serum and cerebrospinal fluid of camel (Camelus dromedaries) Journal of Camel Practice and Research. 7: 53-55.
Nazifi, S. and Maleki, K. (1998): Biochemical analysis of serum and cerebrospinal fluid in clinically normal adult camel (Camelus dromedaries). Research in Veterinary Science, 65: 83-84.
Nazifi, S.; Gheisari, H.R.; Abbasali Poorkabir, M. and Saadatfar, S. (2000): Serum lipids and lipoproteins in clinically healthy male camels (Camelus dromedaries). Veterinary Research Communications, 24: 527-531.
Pucci, E.; Choate, L. Pinchera, A. (2000): Thyroid and lipid metabolism. International Journal of Obesity and Related Metabolic Disorders. 24 Suppl 2: S109-S112.
Rifai, N. and Warnick, G.R. (1994): Laboratory measurement of lipids, lipoproteins and apolipoproteins. AACC press. Washington, DC.
Saleh, M.A. (2000): Prevalence, causes and types of iodine deficiency disorders (IDD) in Egyptian oasis sheep. Egyptian J. of Agric. Res. 78: 167-174.
Saleh, M.A.; Abdel-Salam, M.; El-Mileegy, I.M.H. and El-Sokkary, G.H. (2003): Electrolytes and protein homeostasis in Bedouin camels (Camelus dromedarius) during dry thermal stress in the Egyptian oasis. The 7th Sci. Cong., Egyptian Soc. for Cattle Diseases. 7-9 Dec.pp. 319-329.
Shavdatuashvili, T. (2005): Lipoprotein profile and endothelial function in patients with subclinical and overt hypothyroidism. Georgian Medical News. 129: 57-60.
Shehata, Y.M.; El-Dawy, Kh.; Abde El-Razik, M.S.Z. and Helal, F.G. (2001): Influence of sex and age on some biochemical constituents of camels (Camelus dromedaries). The 2nd International Sci. Conf. Mansora 8-9 April. pp 85-103.
SPSS (2002): Sample Power Statistics, SPSS 11.5, Syntax Reference Guide for SPSS Base. SPSS Inc., 233 South Wacker Drive, Chicago, IL.
Stein, E.A. (1986): Quantitative enzymatic clorimetric test for determination of plasma total lipid and cholesterol. In Tietz, N.W. (ed.) Test book of clinical chemistry. W.B. Saunders, Philadelphia. pp. 879-886.
Tulenko, T.N. and Sumner, A.E. (2002): The physiology of lipoproteins. J. Nucl. Cardiol. 9: 638-649.
UNICEF (1993): Report on assessment of the prevalence of iodine deficiency disorders in New-Valley Governorate, UNICEF– High Institute of Public Health, 1993, Alexandria, Egypt.
Valdemarsson, S.; Hansson, P.; Hedner, P. and Nilsson-Ehle, P. (1983): Relations between thyroid function, hepatic and lipoprotein lipase activities, and plasma lipoprotein concentrations. Acta Endocrinol (Copenh) 104: 50-56
Walsh, J.P.; Bremner, A.P.; Bulsara, M.K.; O'leary, P.; Leedman, P.J.; Feddema, P. and Michelangeli, V. (2005): Thyroid dysfunction and serum lipids: a community-based study. Clin Endocrinol (Oxf). 63: 670-675.
Wasfi, I.A.; Hafez, A.M.; El-Tayeb, F.A.A. and El-Taher, A.Y. (1987): Thyroid hormones, cholesterol and triglycerides level in the camel. Res. Vet. Sci.; 42: 418.
WHO/NI (1992): Report on prevalence of IDD among school children in Egypt, WHO–Nutrition Institute, Cairo.
William, J.; Hueston, M.D.; William, S. and Pearson, M.H.A. (2004): Subclinical Hypothyroidism and the Risk of Hypercholesterolemia. Annals of Family Medicine. 2: 351-355.
Wu, S.Y.; Green, W.L.; Huang, W.S.; Hays, M.T. and Chopra, I.J. (2005): Alternate pathways of thyroid hormone metabolism. Thyroid.15: 943-958.
Yagil, R.; Etzion, Z. and Ganadi, J. (1978): Camel thyroid metabolism: effect of season and dehydration. J. Appl. Physiol. 45: 540-544.
Yousef, E.M. (2006): Some minerals profile in sheep serum in new-valley governorate, M. Vet. Sci. Fac. Vet. Med. Assiut Univ.
Zlatkis, A. and Zak, B. (1969): Study of a new cholesterol reagent. Analytical Biochemistry 29: 143–148.