Chemical Composition of Camel Colostrum and Milk: The Potential Consumption in Fresh and Frozen-thawed States on Blood Glucose Values and Hematological Profiles in Mice

N
Noura Alshaibani1
A
Abd El-Nasser Ahmed Mohammed1,*
1Department of Animal and Fish Production, College of Agriculture and Food Sciences, King Faisal University, P.O. Box 402, Al-Ahsa 31982, KSA, Saudi Arabia.

Background: Camel milk has been shown to improve blood glucose value, liver and kidney functions.

Methods: Forty male albino mice were distributed over five groups; control, camel milk (CM) and camel colostrum (CC) either fresh (F) or frozen-thawed (FT). Chemical composition of camel colostrum and milk were determined through milkoscan system. Body weights (BW), rectal temperature, pulse rate and peripheral oxygen saturation (SPO2), were recorded. Blood glucose values were recorded per two days. Blood samples were collected for hematology analyses.

Result: The results showed that camel’s colostrum had higher (P<0.0001) solid not fat (SNF), protein and lactose but lower fat values compared to camel’s milk. Final body weights (g) were significantly increased in colostrum and milk groups if compared to control one. The highest blood glucose values were found in FTCC followed by FTCM groups whereas the lowest glucose values were found in FCC followed by FCM groups. Colostrum and milk groups had higher (P<0.05) red and white blood cells, hematocrite and hemoglobin if compared to control group. It could be concluded that FCC followed by FCM are potential in decreasing blood glucose levels versus frozen-thawed ones.

People living in harsh environments face numerous challenges such as malnutrition and related metabolic disorders (Machan et al., 2022). Malnutrition challenges in harsh environments include limited access to nutrient-rich foods, droughts and unpredictable weather patterns affecting food production and difficulties in storing and preserving perishable foods (Morgan and Fanzo, 2020). Additionally, the metabolic disorders include diabetes due to dietary limitations and stress, dehydration and mineral deficiencies (García-García  et al., 2020). Camels are considered the most important animal species to produce milk in the harsh environmental conditions (Djenane and Aider, 2024; Mohammed and Alshaibani, 2024). It has been reported that 2.12 million tons of camel milk were approximately produced from 5.25 million she-camels (Ramadan and Inoue-Murayama, 2017). Both camel colostrum and milk offer a unique nutritional profile and potential health benefits to both neonates and human as well (Mohammed and Alshaibani, 2024). In recent decades, numerous studies have investigated the changes in camel milk production and composition. Camel milk is a significant source of protein for people living in arid regions, particularly those who live nomadic lifestyles (Arain et al., 2024). Camel milk and colostrum have been recognized for their potential health benefits particularly in arid and semi-arid regions where she-camels are prevalent (Mohammed and Alshaibani, 2024).
       
Several studies have explored the potential health benefits of camel milk, including its therapeutic effects on certain diseases in both experimental animals and humans (Liu et al., 2023; Mohammed et al., 2025a). It has been found that camel milk is rich in a variety of bioactive components, including immunoglobulins, lactoferrin, vitamins and minerals, suggesting a wide range of therapeutic applications (Khaliq et al., 2024). Researchers are beginning to unravel the mechanisms underlying these purported benefits of camel milk, colostrum and camel milk products (Kanha, 2010; Almasri et al., 2024). Evidences from several studies indicate that camel milk is effective in treating many diseases such as diabetes, cancer, viral hepatitis and other infections (Oselu  et al., 2022; Shakeel et al., 2022).
               
People who are overweight or obese are more likely to develop insulin resistance (Fryk et al., 2021). Doctors often adjust insulin dosages based on a person’s weight (Dailey et al., 2010). Being overweight is a major risk factor for type 2 diabetes (Yashi and Daley, 2025). Due to the assumption of lowering blood glucose levels upon consuming camel milk particularly for individuals with diabetes, the aims of the current study were to explore the changes of blood glucose levels, physiological parameters, hematological profiles and plasma biochemistry values in mice consuming camel milk and colostrum (fresh and frozen-thawed) of low, medium and obese body weights.
The experimental procedures were approved by the ethical committee of King Faisal University [KFU-REC-2025-FEB-EA252]. The fresh and frozen-thawed camel colostrum and camel milk were obtained from camel farm located in Al-Ahsaa area of KSA. The experimental procedures were carried out in the experimental animal labs of Agriculture and Food Sciences College, King Faisal University of KSA.
 
Animal management and site of study
 
The present two experiments were carried out from October 2024 to January 2025 in the department of animal and fish production of King Faisal University. Forty albino male mice were used for conducting the study (body weight g 33.80± 0.66) (Fig 1).

Fig 1: Effects of ad libitum consumption of fresh and frozen-thawed camel milk and colostrum on blood glucose values, physiological parameters, hematological profiles in mice.


       
The study was designed to explore the changes of blood glucose levels, body weight gain, rectal temperature, pulse rate, SPO2, hematological profiles in mice receiving ad libitum camel milk and colostrum (fresh and frozen-thawed). Mice were kept in cage (40.0 x 24.0 x 18.0 cm) of control and the milk and colostrum groups. The mice were fed pellet diet composed of 22.0 protein, 3.20 fiber, 2.90 fat, 1.0 mixture of minerals and vitamins and energy of 3300 kcal/kg. The control group was provided ad libitum water whereas camel milk and colostrum groups were provided ad libitum camel milk and colostrum diluted with water (1:1 volume) through bottles with automated nipple. The mice consumed daily ~5.0 and ~4.0 ml of diluted milk and colostrum, respectively. This ad libitum method was chosen to allow the animals to regulate their intake according to their voluntary needs and reduces stress. The camel milk and colostrum were given fresh and frozen-thawed states. Animals had free access to diet. Mice were kept controlled under 12 h light and 12 h dark cycles starting at 8:0 a.m. The temperature (°C) and relative humidity (%) values during the study were controlled to 24.50±1.5°C and 41.0±6.0%, respectively. The duration of the experiment was sixteen days.
 
Monitoring body weight, rectal temperature, heart rate, peripheral oxygen saturation and blood glucose values
 
Body weights (g) of control and experimental groups were recorded using digital balance (Sartorius balance, Azulmart-KSA). The mice of all groups were sedated using 26.6 mg/kg BW xylazine for immediate recording of rectal temperature, pulse rate and SPO2. Rectal temperatures were recorded using clinical thermometer (Citizen) (Mohammed et al., 2012). Peripheral oxygen saturation (SPO2) and pulse rates were recorded using pulse oximeter apparatus (CMS60D-VET). Blood glucose values were recorded using blood glucose meter (ICare, Taiwan) without sedation. The tail vein of mice was punctured and 10 μl tiny blood sample put on ICare glucose strips for recording blood glucose values.
 
Blood sample collection and analyses
 
Blood samples were collected from the orbital sinus of control mice group, fresh and frozen-thawed camel colostrum and milk mice groups at the end of experiment (Hoff, 2000). The obtained blood samples were analyzed using automatic hematology analyzer (Mythic 5Vet PRO Hematology Analyzer). The resulting blood profiles include white and red blood cells, hemoglobin and hematocrit values (Mohammed and Al-Suwaiegh, 2023).
 
Statistical analysis
 
Body weight, blood glucose, rectal temperature, SPO2, pulse rate and hematological values of control and fresh and frozen-thawed camel colostrum and milk groups were statistically analyzed using General Linear Model procedure of one way ANOVA (SAS 2008) according to the following model:
 
Yij = μ + Ti+ eij
 
Where,
μ = Mean,
Ti = Effects of fresh and frozen-thawed camel colostrum and milk consumption.
Eij = Standard error.
       
Duncan’s multiple range test (1955) was used to compare between means of control and fresh and frozen-thawed camel colostrum and milk groups.
Body weight, blood glucose, rectal temperature, SPOand pulse rate, blood and plasma profile values of control and fresh and frozen-thawed camel milk and colostrum groups are presented in (Fig 2 and 3) (Table1 and 2).

Fig 2: Chemical composition of fresh camel colostrum and camel milk. SNF, solid none fat; freez. P., freezing point.



Fig 3: Changes in blood glucose values (mg/dl) upon consumption of camel fresh colostrum in mice of medium body weight.



Table 1: Changes of body weight (g), rectal temperature (°C), pulse rate and peripheral oxygen saturation (%) in mice receiving ad libitum fresh and frozen-thawed camel milk and colostrum groups in mice.



Table 2: Changes of blood profiles of mice consuming fresh and frozen-thawed camel milk and colostrum.


 
Chemical composition of fresh camel colostrum and camel milk
 
Fresh colostrum and milk of Mejham camel breed were collected from farm located in Al-Ahsaa region. In addition, fresh camel colostrum and milk were frozen and thawed. Chemical compositions of camel colostrum and camel milk were determined through milkoscan (Fig 2).
 
Body weight, rectal temperature, SPO2 and pulse rate
 
Changes of final body weight (g), rectal temperature, pulse rate and SPO2 are presented in Table 1. Value of final body weight was significantly increased in fresh and frozen-thawed camel milk and colostrum groups compared to that of control group and no differences was found between milk and colostrum groups either fresh or frozen-thawed groups in final body weight. Additionally, rectal temperature (°C), pulse rates and SPO2 values were not differed among control, colostrum and milk groups.
 
Monitoring blood glucose levels
 
Blood glucose values per two days of medium body weight mice consuming fresh and frozen-thawed camel milk and colostrum are presented in Fig 3. There were no significant differences in blood glucose levels between any of the groups at the start of the experiment. All groups had similar starting glucose levels around 137-139 mg/dl. Over the sixteen days, the fresh colostrum group consistently showed the lowest blood glucose levels (P<0.001), while the frozen-thawed colostrum group showed the highest ones. The fresh milk group showed a decrease in glucose levels, although it remained higher than the fresh colostrum group. The control group’s glucose levels remained relatively stable over the sixteen days of experiment. Collectively, the highest (P<0.001) blood glucose values were found in frozen-thawed colostrum followed by frozen-thawed milk groups whereas the lowest (P<0.001) blood glucose values were found in fresh colostrum followed by fresh milk groups if compared to control group.
 
Hematological profiles
 
The effects of camel milk (fresh and frozen-thawed) and camel colostrum (fresh and frozen-thawed) compared to a control group on various hematological profiles are presented in Table 2. The control group had significantly lower (<0.0001) RBCs counts (7.45x106/μl l) compared to all other groups (~ 8.4-8.5 x 106/μl l). Similarly, the control group had a lower PCV (38.1%) compared to the other groups (~ 43.5 - 45.1%). In addition, the control group also had lower hemoglobin levels (13.50 g/dl) compared to the other groups (~ 14.5 - 14.6 g/dl). The control group had the lowest (P<0.0001) WBCs count (5.60 x 103/µl). The fresh colostrum group had the highest (P<0.0001) WBCs count (6.90 x 103/µl), followed by the frozen-thawed colostrum group (6.80 x 103/μl) and the fresh milk group (6.50 x 103/μl). The same trends were obtained for types of WBCs and platelets.
       
Results of the presents experiments are presented in Fig 2-3 and Table 1-2 indicating the effects of camel milk and colostrum either fresh or frozen-thawed on body weight gain, blood glucose profiles, hematological profiles in mice. Collectively, the obtained results indicated a potential effect of fresh camel colostrum followed by fresh milk in decreasing blood glucose levels versus frozen-thawed and control groups. In addition, body weight gain, hematological profiles were improved in fresh and frozen-thawed camel milk and colostrum groups compared to control one. These effects could be attributed to the ingredients in camel colostrum and milk (Fig 2). Both camel colostrum and milk contain various biological compounds, some of which can be potentially effect on blood glucose levels and body functions (Khaliq et al., 2024; Seyiti et al., 2024; Mohammed et al., 2025a). Freezing and thawing, a common method for preserving food and biological samples can have significant effects on protein structures of camel colostrum and milk. These freezing and thawing procedures of milk and colostrum can range from subtle changes in their immunoglobulins and other bioactive compounds conformation to irreversible denaturation and aggregation, ultimately influencing protein functions and stability (Wöll et al., 2023). Freezing can lead to the formation of ice crystals, which can disrupt these delicate structures, potentially causing denaturation. Freezing can also affect the stability of milk and colostrum lipids, potentially leading to oxidation or other forms of degradation (Fasse et al., 2021).
 
Body weight, rectal temperature, SPO2 and pulse rate
 
Camel milk and colostrum have been explored for a variety of potential health benefits (García-García  et al., 2020; Djenane and Aider, 2024). These benefits may include changes in body weight gain where the control group exhibited a significantly lower final body weight (38.45g) compared to all milk and colostrum supplemented groups (P<0.05) (39.35 g to 40.00 g). This suggests that milk supplementation, regardless of type (fresh or frozen-thawed milk or colostrum), promoted weight gain compared to the control. This could be attributed to the contents of camel milk and colostrum (Fig 3) (Khaliq et al., 2024; Olfa et al., 2023). The similar final body weights among the milk and colostrum supplemented groups suggest that freezing procedure and type (milk vs. colostrum) did not significantly influence body weight gain. Rectal temperatures and pulse rates remained relatively consistent across all groups. The small variations observed are not likely to be biologically significant and suggest that milk and colostrum consumption did not substantially affect these physiological parameters.
       
Rectal temperatures and pulse rates remained relatively consistent across all groups. The small variations observed are not likely to be biologically significant and suggest that camel milk and colostrum consumption did not substantially affect these physiological parameters. A notable difference was observed in SPO2 levels. The control group exhibited a considerably lower SPO2 (83.2%) compared to all camel milk and colostrum supplemented groups, which ranged from 86.3% to 87.6%. This suggests that camel milk and colostrum consumption may have a positive impact on oxygen saturation. The higher SPO2 in the camel milk and colostrum groups could indicate improved respiratory function or oxygen utilization due to higher RBCs and Hb values (Table 2) (Hafen and Sharma, 2022; Mohammed et al., 2025b).
 
Blood glucose levels
 
The control group exhibits a relatively stable blood glucose level throughout the experimental period, with a slight increase towards the end. This suggests that without any milk and colostrum supplementation, blood glucose remains consistent with minor fluctuations. The fresh camel colostrum supplementation indicates the strongest hypoglycemic effect followed by fresh camel milk versus the strongest hyperglycemic effect of frozen-thawed colostrum and milk, respectively, if compared to control one. The hypoglycemic effect of camel milk has been confirmed in several studies (García-García  et al., 2020; Mohammadabadi and Jain, 2024; Mbye et al., 2025) whereas the hypoglycemic effect of camel colostrum has been not explored to the best of our knowledge earlier. Camel milk is suggested to be a suitable hypoglycemic factor in experimental animals and diabetic people (García-García  et al., 2020; AlKurd et al., 2022; Mohammadabadi and Jain 2024). Consuming camel milk lowers blood glucose value and reduces the amount of insulin required for treatment by 30-35% for patients with type I diabetes (Mirmiran et al., 2017; García-García  et al., 2020; Mohammadabadi and Jain, 2024). It has been assumed that camel milk contains insulin-like proteins that enhance health of diabetic patients (Anwar et al., 2022). With frozen-thawed procedures, such insulin-like proteins in camel colostrum and milk might be denatured and aggregated. In addition, the SNF, fat, proteins and lactose contents of camel colostrum and milk could be attributed to hyperglycemic effect of frozen-thawed colostrum and milk if compared to control group (Fig 2).
 
Hematological profiles
 
Camel colostrum and milk supplementation, regardless of whether it was fresh or frozen, appear to have a positive effect on red blood cell parameters (RBCs, PCV, Hb), white blood cell parameters (WBCs, neutrophils, lymphocytes and monocytes) and platelet counts compared to the control group (Table 2). Camel colostrum and milk supplementation seem to enhance the production or levels of red blood cells, hemoglobin and platelets. In addition, camel colostrum and milk supplementation also appear to stimulate the production of various types of white blood cells, suggesting a potential immune-modulatory effect. Furthermore, freezing the camel colostrum and milk did not seem to significantly alter its effects on these hematological parameters. The higher concentration of bioactive compounds such as lactoferrin and various immunoglobulins (IgM, IgA, IgG and IgD) are found in camel colostrum and milk, which has turned camel colostrum and milk into substances with extraordinary medicinal properties (Ho et al., 2022). The presence of high levels of these compounds along with various vitamins (C, B1, B2, E, A) (Swelum et al., 2021), lysozymes, insulin-like molecules and lactoperoxidase cause the therapeutic potential of camel milk (Behrouz et al., 2024).
Significant effects of fresh and frozen-thawed camel colostrum and milk on body weight gain, hamtological profiles. The most prominent findings of this study indicated that fresh camel colostrum supplementation gave the strongest hypoglycemic effect followed by fresh camel milk versus the strongest hyperglycemic effect of frozen-thawed colostrum and milk, respectively. Further studies are still required to explore the fresh camel milk and colostrum on diabetic experimental model animals with different body weights. 
This work was supported by the Deanship of Scientific Research, Vice Presidency for Graduate Studies and Scientific Research, King Faisal University, Saudi Arabia [Grant No. KFU253484].
 
Novelty statement
 
Fresh camel colostrum supplementation gave the strongest hypoglycemic effect compared to fresh camel milk.
 
Funding
 
Deanship of Scientific Research, Vice Presidency for Graduate Studies and Scientific Research, King Faisal University, Saudi Arabia [KFU253484].
 
Disclaimers
 
The views and conclusions expressed in this article are solely those of the authors and do not necessarily represent the views of their affiliated institutions.
 
Informed consent
 
The Ethical Committee of Deanship of Scientific Research, King Faisal University, Saudi Arabia, approved all animal experimental care (KFU253484).
 
The authors have declared no conflict of interest.

  1. AlKurd, R., Hanash, N., Khalid, N., Abdelrahim, D.N., Khan, M.A.B, Mahrous, L., Radwan, H., Naja, F., Madkour, M., Obaideen, K. (2022). Effect of camel milk on glucose homeostasis in patients with diabetes: A systematic review and meta- analysis of randomized controlled trials. Nutrients. 14: 1245.

  2. Almasri, R., Bedir, A.S., Ranneh, Y.K., El-Tarabily, K.A., Al Raish, S.M. (2024). Benefits of camel milk over cow and goat milk for infant and adult health in fighting chronic diseases: A review. Nutrients. 16(22): 3848.

  3. Anwar, I., Khan, F.B., Maqsood, S., Ayoub, M.A. (2022). Camel milk targeting insulin receptor-toward understanding the antidiabetic effects of camel milk. Frontiers in Nutrition. 8: 819278.

  4. Arain, M.A., Salman, H.M., Ali, M., Khaskheli, G.B., Barham, G.S., Marghazani, I.B., Ahmed, S. (2024). A review on camel milk composition, techno-functional properties and processing constraints. Food Science Animal Research. 44(4): 739-757. 

  5. Behrouz, S., Mohammadi, M., Sarir, H., Boskabady, M.H. (2024). The effects of camel milk in systemic inflammation and oxidative stress of cigarette smoke-induced chronic obstructive pulmonary disease model in rat. Frontiers Veterinary Science. 11: 1464432.

  6. Dailey, G., Admane, K., Mercier, F., Owens, D. (2010). Relationship of insulin dose, A1c lowering and weight in type 2 diabetes: Comparing insulin glargine and insulin detemir. Diabetes Technology Therapeutics. 12(12): 1019-1027.

  7. Djenane, D., Aider, M. (2024). The one-humped camel: The animal of future, potential alternative red meat, technological suitability and future perspectives. F1000Res. 11: 1085.

  8. Duncan, D.B. (1955). Multiple range and multiple Ftest. Biometrics. 1955. 11: 1. 

  9. Fasse, S., Alarinta, J., Frahm, B., Wirtanen, G. (2021). Bovine colostrum for human consumption-improving microbial quality and maintaining bioactive characteristics through processing. Dairy. 2(4): 556-575.

  10. Fryk, E., Olausson, J., Mossberg, K., Strindberg, L., Schmelz, M., Brogren, H., Gan, L.M., Piazza, S., Provenzani, A., Becattini, B., Lind, L., Solinas, G., Jansson, P.A. (2021). Hyperinsulinemia and insulin resistance in the obese may develop as part of a homeostatic response to elevated free fatty acids: A mechanistic case-control and a population-based cohort  study. EBioMedicine. 65: 103264. 

  11. García-García, F.J., Monistrol-Mula, A., Cardellach, F. Garrabou, G. (2020). Nutrition, bioenergetics and metabolic syndrome. Nutrients. 12(9): 2785.

  12. Hafen, B.B., Sharma, S. (2022). Oxygen Saturation. [Updated (2022) Nov 23]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan-. (2022). Available from: https://www.ncbi.nlm.nih.gov/ books/NBK525974/.

  13. Ho, T.M., Zou, Z., Bansal, N. (2022). Camel milk: a review of its nutritional value, heat stability and potential food products.  Food Research International. 153: 110870.

  14. Hoff, J. (2000). Methods of blood collection in the mouse. Laboratory Animal. 29: 47-5353.

  15. Kanha, H.A. (2010). Compositional, technological and nutritional aspect of dromedary camel milk. International Dairy Journal. 20(12): 811-821.

  16. Khaliq, A., Mishra, A.K., Niroula, A., Baba, W.N., Shaukat, M.N., Rabbani, A. (2024). An updated comprehensive review of camel milk: Composition, therapeutic properties and industrial applications. Food Bioscience. 62: 105531.

  17. Liu, C., Liu, L.-X., Yang, J., Liu, Y.G. (2023). Exploration and analysis of the composition and mechanism of efficacy of camel milk. Food Bioscience. 53: 102564.

  18. Machan, S.N., Agwata, J.F., Oguge, N.O. (2022). Environmental factors influencing the sustenance of the camel milk value Chain in Isiolo County, Northern Kenya. Resources. 11(3): 27.

  19. Mbye, M., Ali, A.H. Kamal-Eldin, F.A. Banat, F. (2025). The impact of camel milk and its products on diabetes mellitus management: A review of bioactive components and therapeutic potential. NFS Journal. 38: 100204.

  20. Mirmiran, P., Ejtahed, H.S., Angoorani, P., Eslami, F., Azizi, F. (2017). camel milk has beneficial effects on diabetes mellitus: A systematic review. International Journal Endocrinology Metabolism. 15(2): e42150.

  21. Mohammadabadi, T., Jain, R. (2024). Camel milk; A potent superfood for diabetes complications. Food Science and Nutrition Therapy. 10(1): 035-43.

  22. Mohammed, A.A., Abdelnabi, M.A., Modlinski, J.A. (2012). Evaluation of anesthesia and reproductive performance upon diazepam and xylazine injection in rats. Animal Science Paper  Reports. 30(3): 285-202.

  23. Mohammed, A.A., Almuyidi, A., Almarri, H., Alkhalifah, H., Alhmad, A., Alali, H., AlHuwaish, O., AlKhawaher, M. (2025a). Unique characteristics of camel body systems: Adaptation to harsh conditions, productive and reproductive performances: A review. Indian Journal Animal Research. doi: 10. 18805/IJAR.BF-1922.

  24. Mohammed, A.A., Alshaibani, N. (2024). Camel milk yield and composition and its adjuvant potential impacts on health of consumers: A review. Indian Journal Animal Research. 59(2): 177-184.  doi: 10.18805/IJAR.BF-1872.

  25. Mohammed, A.A., Al-Suwaiegh, S. (2023). Impacts of nigella sativa  inclusion during gestation and lactation on ovarian follicle development, as well as the blood and metabolic profiles of ardi goats in subtropics. Agriculture. 13: 674.

  26. Mohammed, A.A., Al-Suwaiegh, S., Al-Suwaiegh, S. (2024). Potential impacts of dried green coleus forskolin leaves on changes of body and liver weight, glucose and body temperature, serum profiles in mice. Indian Journal Animal Research. 58(12): 2132-2137. doi: 10.18805/IJAR.BF-1839.

  27. Mohammed, A.A., Sayed, M.S.E., AlGherair, I., Al-Suwaiegh, S. (2025b). The potential influence of coleus forskolii, green coffee and green tea on body weight, reproductive performance, hematological profiles in mice. Indian Journal Animal Research. 59(8): 1295-1302. doi: 10.18805/IJAR.BF-1916.

  28. Morgan, A.E., Fanzo, J. (2020). Nutrition transition and climate risks in Nigeria: Moving towards food systems policy coherence. Current Environmental Health Reports. 7(4): 392-403.

  29. Olfa, O., Zeineb, J., Halima, E.H. (2023). Enzymatic hydrolysates from camel colostrum and milk proteins display inhibitory activity toward a key enzyme related to obesity. Acta Alimentaria. 52(3): 480-489. 

  30. Oselu, S., Ebere, R., Arimi, J.M. (2022). Camel milk and camel milk product situation in Kenya in relation to the world. International Journal of Food Science. 2022: 1237423.

  31. Ramadan, S., Inoue-Murayama, M. (2017). Advances in camel genomics and their applications: A review. Journal Animal Genetics. 45: 49-58.

  32. SAS. (2008). SAS User’s Guide: Basics. Statistical Analysis System Institute, Inc., 2008, Cary, NC, USA.

  33. Seyiti, S., Kelimu, A., Yusufu, G. (2024). Bactrian camel milk: Chemical composition, bioactivities, processing techniques and economic potential in China. Molecules. 29(19): 4680.

  34. Shakeel, K., Rabail, R., Iahtisham-Ul-Haq, S., Nawaz, A., Manzoor, M.F., Walayat, N., Socol, C.T., Maerescu, C.M., Aadil, R.M. (2022). Camel milk protectiveness toward multiple liver disorders: A review. Frontiers in Nutrition. 9: 944842. 

  35. Swelum, A.A., El-Saadony, M.T., Abdo, M., Ombarak, R.A., Hussein, E.O.S., Suliman, G., Alhimaidi, A.R., Ammari, A.A., Ba- Awadh, H., Taha, A.E., El-Tarabily, K.A., Abd El-Hack, M.E. (2021). Nutritional, antimicrobial and medicinal properties of Camel’s milk: A review. Saudi Journal Biological Science. 28(5): 3126-3136.

  36. Wöll, A.K., Desombre, M., Enghauser, L., Hubbuch, J. (2023). A phase diagram-based toolbox to assess the impact of freeze/thaw ramps on the phase behavior of proteins. Bioprocess and Biosystems Engineering. 43(2): 179-192.

  37. Yashi, K., Daley, S.F. (2025). Obesity and Type 2 Diabetes. In: Stat Pearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan-. Available from: https://www.ncbi.nlm.nih. gov/books /NBK592412/.

Chemical Composition of Camel Colostrum and Milk: The Potential Consumption in Fresh and Frozen-thawed States on Blood Glucose Values and Hematological Profiles in Mice

N
Noura Alshaibani1
A
Abd El-Nasser Ahmed Mohammed1,*
1Department of Animal and Fish Production, College of Agriculture and Food Sciences, King Faisal University, P.O. Box 402, Al-Ahsa 31982, KSA, Saudi Arabia.

Background: Camel milk has been shown to improve blood glucose value, liver and kidney functions.

Methods: Forty male albino mice were distributed over five groups; control, camel milk (CM) and camel colostrum (CC) either fresh (F) or frozen-thawed (FT). Chemical composition of camel colostrum and milk were determined through milkoscan system. Body weights (BW), rectal temperature, pulse rate and peripheral oxygen saturation (SPO2), were recorded. Blood glucose values were recorded per two days. Blood samples were collected for hematology analyses.

Result: The results showed that camel’s colostrum had higher (P<0.0001) solid not fat (SNF), protein and lactose but lower fat values compared to camel’s milk. Final body weights (g) were significantly increased in colostrum and milk groups if compared to control one. The highest blood glucose values were found in FTCC followed by FTCM groups whereas the lowest glucose values were found in FCC followed by FCM groups. Colostrum and milk groups had higher (P<0.05) red and white blood cells, hematocrite and hemoglobin if compared to control group. It could be concluded that FCC followed by FCM are potential in decreasing blood glucose levels versus frozen-thawed ones.

People living in harsh environments face numerous challenges such as malnutrition and related metabolic disorders (Machan et al., 2022). Malnutrition challenges in harsh environments include limited access to nutrient-rich foods, droughts and unpredictable weather patterns affecting food production and difficulties in storing and preserving perishable foods (Morgan and Fanzo, 2020). Additionally, the metabolic disorders include diabetes due to dietary limitations and stress, dehydration and mineral deficiencies (García-García  et al., 2020). Camels are considered the most important animal species to produce milk in the harsh environmental conditions (Djenane and Aider, 2024; Mohammed and Alshaibani, 2024). It has been reported that 2.12 million tons of camel milk were approximately produced from 5.25 million she-camels (Ramadan and Inoue-Murayama, 2017). Both camel colostrum and milk offer a unique nutritional profile and potential health benefits to both neonates and human as well (Mohammed and Alshaibani, 2024). In recent decades, numerous studies have investigated the changes in camel milk production and composition. Camel milk is a significant source of protein for people living in arid regions, particularly those who live nomadic lifestyles (Arain et al., 2024). Camel milk and colostrum have been recognized for their potential health benefits particularly in arid and semi-arid regions where she-camels are prevalent (Mohammed and Alshaibani, 2024).
       
Several studies have explored the potential health benefits of camel milk, including its therapeutic effects on certain diseases in both experimental animals and humans (Liu et al., 2023; Mohammed et al., 2025a). It has been found that camel milk is rich in a variety of bioactive components, including immunoglobulins, lactoferrin, vitamins and minerals, suggesting a wide range of therapeutic applications (Khaliq et al., 2024). Researchers are beginning to unravel the mechanisms underlying these purported benefits of camel milk, colostrum and camel milk products (Kanha, 2010; Almasri et al., 2024). Evidences from several studies indicate that camel milk is effective in treating many diseases such as diabetes, cancer, viral hepatitis and other infections (Oselu  et al., 2022; Shakeel et al., 2022).
               
People who are overweight or obese are more likely to develop insulin resistance (Fryk et al., 2021). Doctors often adjust insulin dosages based on a person’s weight (Dailey et al., 2010). Being overweight is a major risk factor for type 2 diabetes (Yashi and Daley, 2025). Due to the assumption of lowering blood glucose levels upon consuming camel milk particularly for individuals with diabetes, the aims of the current study were to explore the changes of blood glucose levels, physiological parameters, hematological profiles and plasma biochemistry values in mice consuming camel milk and colostrum (fresh and frozen-thawed) of low, medium and obese body weights.
The experimental procedures were approved by the ethical committee of King Faisal University [KFU-REC-2025-FEB-EA252]. The fresh and frozen-thawed camel colostrum and camel milk were obtained from camel farm located in Al-Ahsaa area of KSA. The experimental procedures were carried out in the experimental animal labs of Agriculture and Food Sciences College, King Faisal University of KSA.
 
Animal management and site of study
 
The present two experiments were carried out from October 2024 to January 2025 in the department of animal and fish production of King Faisal University. Forty albino male mice were used for conducting the study (body weight g 33.80± 0.66) (Fig 1).

Fig 1: Effects of ad libitum consumption of fresh and frozen-thawed camel milk and colostrum on blood glucose values, physiological parameters, hematological profiles in mice.


       
The study was designed to explore the changes of blood glucose levels, body weight gain, rectal temperature, pulse rate, SPO2, hematological profiles in mice receiving ad libitum camel milk and colostrum (fresh and frozen-thawed). Mice were kept in cage (40.0 x 24.0 x 18.0 cm) of control and the milk and colostrum groups. The mice were fed pellet diet composed of 22.0 protein, 3.20 fiber, 2.90 fat, 1.0 mixture of minerals and vitamins and energy of 3300 kcal/kg. The control group was provided ad libitum water whereas camel milk and colostrum groups were provided ad libitum camel milk and colostrum diluted with water (1:1 volume) through bottles with automated nipple. The mice consumed daily ~5.0 and ~4.0 ml of diluted milk and colostrum, respectively. This ad libitum method was chosen to allow the animals to regulate their intake according to their voluntary needs and reduces stress. The camel milk and colostrum were given fresh and frozen-thawed states. Animals had free access to diet. Mice were kept controlled under 12 h light and 12 h dark cycles starting at 8:0 a.m. The temperature (°C) and relative humidity (%) values during the study were controlled to 24.50±1.5°C and 41.0±6.0%, respectively. The duration of the experiment was sixteen days.
 
Monitoring body weight, rectal temperature, heart rate, peripheral oxygen saturation and blood glucose values
 
Body weights (g) of control and experimental groups were recorded using digital balance (Sartorius balance, Azulmart-KSA). The mice of all groups were sedated using 26.6 mg/kg BW xylazine for immediate recording of rectal temperature, pulse rate and SPO2. Rectal temperatures were recorded using clinical thermometer (Citizen) (Mohammed et al., 2012). Peripheral oxygen saturation (SPO2) and pulse rates were recorded using pulse oximeter apparatus (CMS60D-VET). Blood glucose values were recorded using blood glucose meter (ICare, Taiwan) without sedation. The tail vein of mice was punctured and 10 μl tiny blood sample put on ICare glucose strips for recording blood glucose values.
 
Blood sample collection and analyses
 
Blood samples were collected from the orbital sinus of control mice group, fresh and frozen-thawed camel colostrum and milk mice groups at the end of experiment (Hoff, 2000). The obtained blood samples were analyzed using automatic hematology analyzer (Mythic 5Vet PRO Hematology Analyzer). The resulting blood profiles include white and red blood cells, hemoglobin and hematocrit values (Mohammed and Al-Suwaiegh, 2023).
 
Statistical analysis
 
Body weight, blood glucose, rectal temperature, SPO2, pulse rate and hematological values of control and fresh and frozen-thawed camel colostrum and milk groups were statistically analyzed using General Linear Model procedure of one way ANOVA (SAS 2008) according to the following model:
 
Yij = μ + Ti+ eij
 
Where,
μ = Mean,
Ti = Effects of fresh and frozen-thawed camel colostrum and milk consumption.
Eij = Standard error.
       
Duncan’s multiple range test (1955) was used to compare between means of control and fresh and frozen-thawed camel colostrum and milk groups.
Body weight, blood glucose, rectal temperature, SPOand pulse rate, blood and plasma profile values of control and fresh and frozen-thawed camel milk and colostrum groups are presented in (Fig 2 and 3) (Table1 and 2).

Fig 2: Chemical composition of fresh camel colostrum and camel milk. SNF, solid none fat; freez. P., freezing point.



Fig 3: Changes in blood glucose values (mg/dl) upon consumption of camel fresh colostrum in mice of medium body weight.



Table 1: Changes of body weight (g), rectal temperature (°C), pulse rate and peripheral oxygen saturation (%) in mice receiving ad libitum fresh and frozen-thawed camel milk and colostrum groups in mice.



Table 2: Changes of blood profiles of mice consuming fresh and frozen-thawed camel milk and colostrum.


 
Chemical composition of fresh camel colostrum and camel milk
 
Fresh colostrum and milk of Mejham camel breed were collected from farm located in Al-Ahsaa region. In addition, fresh camel colostrum and milk were frozen and thawed. Chemical compositions of camel colostrum and camel milk were determined through milkoscan (Fig 2).
 
Body weight, rectal temperature, SPO2 and pulse rate
 
Changes of final body weight (g), rectal temperature, pulse rate and SPO2 are presented in Table 1. Value of final body weight was significantly increased in fresh and frozen-thawed camel milk and colostrum groups compared to that of control group and no differences was found between milk and colostrum groups either fresh or frozen-thawed groups in final body weight. Additionally, rectal temperature (°C), pulse rates and SPO2 values were not differed among control, colostrum and milk groups.
 
Monitoring blood glucose levels
 
Blood glucose values per two days of medium body weight mice consuming fresh and frozen-thawed camel milk and colostrum are presented in Fig 3. There were no significant differences in blood glucose levels between any of the groups at the start of the experiment. All groups had similar starting glucose levels around 137-139 mg/dl. Over the sixteen days, the fresh colostrum group consistently showed the lowest blood glucose levels (P<0.001), while the frozen-thawed colostrum group showed the highest ones. The fresh milk group showed a decrease in glucose levels, although it remained higher than the fresh colostrum group. The control group’s glucose levels remained relatively stable over the sixteen days of experiment. Collectively, the highest (P<0.001) blood glucose values were found in frozen-thawed colostrum followed by frozen-thawed milk groups whereas the lowest (P<0.001) blood glucose values were found in fresh colostrum followed by fresh milk groups if compared to control group.
 
Hematological profiles
 
The effects of camel milk (fresh and frozen-thawed) and camel colostrum (fresh and frozen-thawed) compared to a control group on various hematological profiles are presented in Table 2. The control group had significantly lower (<0.0001) RBCs counts (7.45x106/μl l) compared to all other groups (~ 8.4-8.5 x 106/μl l). Similarly, the control group had a lower PCV (38.1%) compared to the other groups (~ 43.5 - 45.1%). In addition, the control group also had lower hemoglobin levels (13.50 g/dl) compared to the other groups (~ 14.5 - 14.6 g/dl). The control group had the lowest (P<0.0001) WBCs count (5.60 x 103/µl). The fresh colostrum group had the highest (P<0.0001) WBCs count (6.90 x 103/µl), followed by the frozen-thawed colostrum group (6.80 x 103/μl) and the fresh milk group (6.50 x 103/μl). The same trends were obtained for types of WBCs and platelets.
       
Results of the presents experiments are presented in Fig 2-3 and Table 1-2 indicating the effects of camel milk and colostrum either fresh or frozen-thawed on body weight gain, blood glucose profiles, hematological profiles in mice. Collectively, the obtained results indicated a potential effect of fresh camel colostrum followed by fresh milk in decreasing blood glucose levels versus frozen-thawed and control groups. In addition, body weight gain, hematological profiles were improved in fresh and frozen-thawed camel milk and colostrum groups compared to control one. These effects could be attributed to the ingredients in camel colostrum and milk (Fig 2). Both camel colostrum and milk contain various biological compounds, some of which can be potentially effect on blood glucose levels and body functions (Khaliq et al., 2024; Seyiti et al., 2024; Mohammed et al., 2025a). Freezing and thawing, a common method for preserving food and biological samples can have significant effects on protein structures of camel colostrum and milk. These freezing and thawing procedures of milk and colostrum can range from subtle changes in their immunoglobulins and other bioactive compounds conformation to irreversible denaturation and aggregation, ultimately influencing protein functions and stability (Wöll et al., 2023). Freezing can lead to the formation of ice crystals, which can disrupt these delicate structures, potentially causing denaturation. Freezing can also affect the stability of milk and colostrum lipids, potentially leading to oxidation or other forms of degradation (Fasse et al., 2021).
 
Body weight, rectal temperature, SPO2 and pulse rate
 
Camel milk and colostrum have been explored for a variety of potential health benefits (García-García  et al., 2020; Djenane and Aider, 2024). These benefits may include changes in body weight gain where the control group exhibited a significantly lower final body weight (38.45g) compared to all milk and colostrum supplemented groups (P<0.05) (39.35 g to 40.00 g). This suggests that milk supplementation, regardless of type (fresh or frozen-thawed milk or colostrum), promoted weight gain compared to the control. This could be attributed to the contents of camel milk and colostrum (Fig 3) (Khaliq et al., 2024; Olfa et al., 2023). The similar final body weights among the milk and colostrum supplemented groups suggest that freezing procedure and type (milk vs. colostrum) did not significantly influence body weight gain. Rectal temperatures and pulse rates remained relatively consistent across all groups. The small variations observed are not likely to be biologically significant and suggest that milk and colostrum consumption did not substantially affect these physiological parameters.
       
Rectal temperatures and pulse rates remained relatively consistent across all groups. The small variations observed are not likely to be biologically significant and suggest that camel milk and colostrum consumption did not substantially affect these physiological parameters. A notable difference was observed in SPO2 levels. The control group exhibited a considerably lower SPO2 (83.2%) compared to all camel milk and colostrum supplemented groups, which ranged from 86.3% to 87.6%. This suggests that camel milk and colostrum consumption may have a positive impact on oxygen saturation. The higher SPO2 in the camel milk and colostrum groups could indicate improved respiratory function or oxygen utilization due to higher RBCs and Hb values (Table 2) (Hafen and Sharma, 2022; Mohammed et al., 2025b).
 
Blood glucose levels
 
The control group exhibits a relatively stable blood glucose level throughout the experimental period, with a slight increase towards the end. This suggests that without any milk and colostrum supplementation, blood glucose remains consistent with minor fluctuations. The fresh camel colostrum supplementation indicates the strongest hypoglycemic effect followed by fresh camel milk versus the strongest hyperglycemic effect of frozen-thawed colostrum and milk, respectively, if compared to control one. The hypoglycemic effect of camel milk has been confirmed in several studies (García-García  et al., 2020; Mohammadabadi and Jain, 2024; Mbye et al., 2025) whereas the hypoglycemic effect of camel colostrum has been not explored to the best of our knowledge earlier. Camel milk is suggested to be a suitable hypoglycemic factor in experimental animals and diabetic people (García-García  et al., 2020; AlKurd et al., 2022; Mohammadabadi and Jain 2024). Consuming camel milk lowers blood glucose value and reduces the amount of insulin required for treatment by 30-35% for patients with type I diabetes (Mirmiran et al., 2017; García-García  et al., 2020; Mohammadabadi and Jain, 2024). It has been assumed that camel milk contains insulin-like proteins that enhance health of diabetic patients (Anwar et al., 2022). With frozen-thawed procedures, such insulin-like proteins in camel colostrum and milk might be denatured and aggregated. In addition, the SNF, fat, proteins and lactose contents of camel colostrum and milk could be attributed to hyperglycemic effect of frozen-thawed colostrum and milk if compared to control group (Fig 2).
 
Hematological profiles
 
Camel colostrum and milk supplementation, regardless of whether it was fresh or frozen, appear to have a positive effect on red blood cell parameters (RBCs, PCV, Hb), white blood cell parameters (WBCs, neutrophils, lymphocytes and monocytes) and platelet counts compared to the control group (Table 2). Camel colostrum and milk supplementation seem to enhance the production or levels of red blood cells, hemoglobin and platelets. In addition, camel colostrum and milk supplementation also appear to stimulate the production of various types of white blood cells, suggesting a potential immune-modulatory effect. Furthermore, freezing the camel colostrum and milk did not seem to significantly alter its effects on these hematological parameters. The higher concentration of bioactive compounds such as lactoferrin and various immunoglobulins (IgM, IgA, IgG and IgD) are found in camel colostrum and milk, which has turned camel colostrum and milk into substances with extraordinary medicinal properties (Ho et al., 2022). The presence of high levels of these compounds along with various vitamins (C, B1, B2, E, A) (Swelum et al., 2021), lysozymes, insulin-like molecules and lactoperoxidase cause the therapeutic potential of camel milk (Behrouz et al., 2024).
Significant effects of fresh and frozen-thawed camel colostrum and milk on body weight gain, hamtological profiles. The most prominent findings of this study indicated that fresh camel colostrum supplementation gave the strongest hypoglycemic effect followed by fresh camel milk versus the strongest hyperglycemic effect of frozen-thawed colostrum and milk, respectively. Further studies are still required to explore the fresh camel milk and colostrum on diabetic experimental model animals with different body weights. 
This work was supported by the Deanship of Scientific Research, Vice Presidency for Graduate Studies and Scientific Research, King Faisal University, Saudi Arabia [Grant No. KFU253484].
 
Novelty statement
 
Fresh camel colostrum supplementation gave the strongest hypoglycemic effect compared to fresh camel milk.
 
Funding
 
Deanship of Scientific Research, Vice Presidency for Graduate Studies and Scientific Research, King Faisal University, Saudi Arabia [KFU253484].
 
Disclaimers
 
The views and conclusions expressed in this article are solely those of the authors and do not necessarily represent the views of their affiliated institutions.
 
Informed consent
 
The Ethical Committee of Deanship of Scientific Research, King Faisal University, Saudi Arabia, approved all animal experimental care (KFU253484).
 
The authors have declared no conflict of interest.

  1. AlKurd, R., Hanash, N., Khalid, N., Abdelrahim, D.N., Khan, M.A.B, Mahrous, L., Radwan, H., Naja, F., Madkour, M., Obaideen, K. (2022). Effect of camel milk on glucose homeostasis in patients with diabetes: A systematic review and meta- analysis of randomized controlled trials. Nutrients. 14: 1245.

  2. Almasri, R., Bedir, A.S., Ranneh, Y.K., El-Tarabily, K.A., Al Raish, S.M. (2024). Benefits of camel milk over cow and goat milk for infant and adult health in fighting chronic diseases: A review. Nutrients. 16(22): 3848.

  3. Anwar, I., Khan, F.B., Maqsood, S., Ayoub, M.A. (2022). Camel milk targeting insulin receptor-toward understanding the antidiabetic effects of camel milk. Frontiers in Nutrition. 8: 819278.

  4. Arain, M.A., Salman, H.M., Ali, M., Khaskheli, G.B., Barham, G.S., Marghazani, I.B., Ahmed, S. (2024). A review on camel milk composition, techno-functional properties and processing constraints. Food Science Animal Research. 44(4): 739-757. 

  5. Behrouz, S., Mohammadi, M., Sarir, H., Boskabady, M.H. (2024). The effects of camel milk in systemic inflammation and oxidative stress of cigarette smoke-induced chronic obstructive pulmonary disease model in rat. Frontiers Veterinary Science. 11: 1464432.

  6. Dailey, G., Admane, K., Mercier, F., Owens, D. (2010). Relationship of insulin dose, A1c lowering and weight in type 2 diabetes: Comparing insulin glargine and insulin detemir. Diabetes Technology Therapeutics. 12(12): 1019-1027.

  7. Djenane, D., Aider, M. (2024). The one-humped camel: The animal of future, potential alternative red meat, technological suitability and future perspectives. F1000Res. 11: 1085.

  8. Duncan, D.B. (1955). Multiple range and multiple Ftest. Biometrics. 1955. 11: 1. 

  9. Fasse, S., Alarinta, J., Frahm, B., Wirtanen, G. (2021). Bovine colostrum for human consumption-improving microbial quality and maintaining bioactive characteristics through processing. Dairy. 2(4): 556-575.

  10. Fryk, E., Olausson, J., Mossberg, K., Strindberg, L., Schmelz, M., Brogren, H., Gan, L.M., Piazza, S., Provenzani, A., Becattini, B., Lind, L., Solinas, G., Jansson, P.A. (2021). Hyperinsulinemia and insulin resistance in the obese may develop as part of a homeostatic response to elevated free fatty acids: A mechanistic case-control and a population-based cohort  study. EBioMedicine. 65: 103264. 

  11. García-García, F.J., Monistrol-Mula, A., Cardellach, F. Garrabou, G. (2020). Nutrition, bioenergetics and metabolic syndrome. Nutrients. 12(9): 2785.

  12. Hafen, B.B., Sharma, S. (2022). Oxygen Saturation. [Updated (2022) Nov 23]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan-. (2022). Available from: https://www.ncbi.nlm.nih.gov/ books/NBK525974/.

  13. Ho, T.M., Zou, Z., Bansal, N. (2022). Camel milk: a review of its nutritional value, heat stability and potential food products.  Food Research International. 153: 110870.

  14. Hoff, J. (2000). Methods of blood collection in the mouse. Laboratory Animal. 29: 47-5353.

  15. Kanha, H.A. (2010). Compositional, technological and nutritional aspect of dromedary camel milk. International Dairy Journal. 20(12): 811-821.

  16. Khaliq, A., Mishra, A.K., Niroula, A., Baba, W.N., Shaukat, M.N., Rabbani, A. (2024). An updated comprehensive review of camel milk: Composition, therapeutic properties and industrial applications. Food Bioscience. 62: 105531.

  17. Liu, C., Liu, L.-X., Yang, J., Liu, Y.G. (2023). Exploration and analysis of the composition and mechanism of efficacy of camel milk. Food Bioscience. 53: 102564.

  18. Machan, S.N., Agwata, J.F., Oguge, N.O. (2022). Environmental factors influencing the sustenance of the camel milk value Chain in Isiolo County, Northern Kenya. Resources. 11(3): 27.

  19. Mbye, M., Ali, A.H. Kamal-Eldin, F.A. Banat, F. (2025). The impact of camel milk and its products on diabetes mellitus management: A review of bioactive components and therapeutic potential. NFS Journal. 38: 100204.

  20. Mirmiran, P., Ejtahed, H.S., Angoorani, P., Eslami, F., Azizi, F. (2017). camel milk has beneficial effects on diabetes mellitus: A systematic review. International Journal Endocrinology Metabolism. 15(2): e42150.

  21. Mohammadabadi, T., Jain, R. (2024). Camel milk; A potent superfood for diabetes complications. Food Science and Nutrition Therapy. 10(1): 035-43.

  22. Mohammed, A.A., Abdelnabi, M.A., Modlinski, J.A. (2012). Evaluation of anesthesia and reproductive performance upon diazepam and xylazine injection in rats. Animal Science Paper  Reports. 30(3): 285-202.

  23. Mohammed, A.A., Almuyidi, A., Almarri, H., Alkhalifah, H., Alhmad, A., Alali, H., AlHuwaish, O., AlKhawaher, M. (2025a). Unique characteristics of camel body systems: Adaptation to harsh conditions, productive and reproductive performances: A review. Indian Journal Animal Research. doi: 10. 18805/IJAR.BF-1922.

  24. Mohammed, A.A., Alshaibani, N. (2024). Camel milk yield and composition and its adjuvant potential impacts on health of consumers: A review. Indian Journal Animal Research. 59(2): 177-184.  doi: 10.18805/IJAR.BF-1872.

  25. Mohammed, A.A., Al-Suwaiegh, S. (2023). Impacts of nigella sativa  inclusion during gestation and lactation on ovarian follicle development, as well as the blood and metabolic profiles of ardi goats in subtropics. Agriculture. 13: 674.

  26. Mohammed, A.A., Al-Suwaiegh, S., Al-Suwaiegh, S. (2024). Potential impacts of dried green coleus forskolin leaves on changes of body and liver weight, glucose and body temperature, serum profiles in mice. Indian Journal Animal Research. 58(12): 2132-2137. doi: 10.18805/IJAR.BF-1839.

  27. Mohammed, A.A., Sayed, M.S.E., AlGherair, I., Al-Suwaiegh, S. (2025b). The potential influence of coleus forskolii, green coffee and green tea on body weight, reproductive performance, hematological profiles in mice. Indian Journal Animal Research. 59(8): 1295-1302. doi: 10.18805/IJAR.BF-1916.

  28. Morgan, A.E., Fanzo, J. (2020). Nutrition transition and climate risks in Nigeria: Moving towards food systems policy coherence. Current Environmental Health Reports. 7(4): 392-403.

  29. Olfa, O., Zeineb, J., Halima, E.H. (2023). Enzymatic hydrolysates from camel colostrum and milk proteins display inhibitory activity toward a key enzyme related to obesity. Acta Alimentaria. 52(3): 480-489. 

  30. Oselu, S., Ebere, R., Arimi, J.M. (2022). Camel milk and camel milk product situation in Kenya in relation to the world. International Journal of Food Science. 2022: 1237423.

  31. Ramadan, S., Inoue-Murayama, M. (2017). Advances in camel genomics and their applications: A review. Journal Animal Genetics. 45: 49-58.

  32. SAS. (2008). SAS User’s Guide: Basics. Statistical Analysis System Institute, Inc., 2008, Cary, NC, USA.

  33. Seyiti, S., Kelimu, A., Yusufu, G. (2024). Bactrian camel milk: Chemical composition, bioactivities, processing techniques and economic potential in China. Molecules. 29(19): 4680.

  34. Shakeel, K., Rabail, R., Iahtisham-Ul-Haq, S., Nawaz, A., Manzoor, M.F., Walayat, N., Socol, C.T., Maerescu, C.M., Aadil, R.M. (2022). Camel milk protectiveness toward multiple liver disorders: A review. Frontiers in Nutrition. 9: 944842. 

  35. Swelum, A.A., El-Saadony, M.T., Abdo, M., Ombarak, R.A., Hussein, E.O.S., Suliman, G., Alhimaidi, A.R., Ammari, A.A., Ba- Awadh, H., Taha, A.E., El-Tarabily, K.A., Abd El-Hack, M.E. (2021). Nutritional, antimicrobial and medicinal properties of Camel’s milk: A review. Saudi Journal Biological Science. 28(5): 3126-3136.

  36. Wöll, A.K., Desombre, M., Enghauser, L., Hubbuch, J. (2023). A phase diagram-based toolbox to assess the impact of freeze/thaw ramps on the phase behavior of proteins. Bioprocess and Biosystems Engineering. 43(2): 179-192.

  37. Yashi, K., Daley, S.F. (2025). Obesity and Type 2 Diabetes. In: Stat Pearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan-. Available from: https://www.ncbi.nlm.nih. gov/books /NBK592412/.
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