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Camel milk and microRNAs: a narrative review integrating molecular evidence, bioinformatics, and nutraceutical perspectives on metabolic diseases in the Sahel

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Published: 16 April 2026
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Camel milk is increasingly recognized as a promising nutraceutical resource for addressing the double burden of malnutrition and metabolic disease in the Sahel, within a broader context of epidemiological and nutritional transition. This narrative review synthesizes recent evidence published between 2020 and 2024 on the molecular mechanisms underlying the metabolic effects of camel milk, with particular attention to the Sahelian context and Chad. Current evidence indicates that camel milk has a distinctive nutritional profile, characterized by relatively low lactose content, a favorable proportion of unsaturated fatty acids, and the presence of stable extracellular vesicles, including exosomes, enriched in bioactive microRNAs (miRNAs). miRNAs are short non-coding RNA molecules involved in the post-transcriptional regulation of gene expression. Extracellular miRNAs have been identified in bodily fluids, suggesting that they may facilitate epigenetic communication between tissues. Furthermore, miRNAs are highly conserved molecules across animal species, especially among mammals; therefore, it is reasonable to expect that the targets of miRNAs are orthologous genes in different species. In addition to well-described miRNAs such as miR-148a, miR-30d, and miR-21, recent sequencing studies have identified additional conserved miRNAs across camel species, including let-7i-5p, let-7b-5p, miR-200a-3p, and miR-26a-5p. Integrative analysis of experimentally validated and high-confidence predicted target genes suggests convergence on pathways involved in insulin signaling, adipogenesis, inflammatory regulation, growth control, and cellular homeostasis. Preclinical studies and a limited number of clinical trials suggest that camel milk may exert antidiabetic and hypolipidemic effects. However, important challenges remain, including seasonal variability in milk composition, limited preservation infrastructure, the lack of regulatory frameworks supporting health claims, and the absence of clinical evidence generated in Sahelian populations. Overall, camel milk emerges as a biologically relevant food matrix with potential metabolic benefits in environments undergoing rapid dietary transition. Nevertheless, its proposed nutraceutical role remains to be confirmed through locally grounded translational and clinical research addressing exosome miRNA bioavailability, mechanism of action, and context-adapted valorization strategies.

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1. Global Burden of Disease Collaborative Network. Global Burden of Disease Study 2021 (GBD 2021) Results. Institute for Health Metrics and Evaluation (IHME); 2024. Available from: https://vizhub.healthdata.org/gbd-results/
2. Gouda HN, Charlson F, Sorsdahl K, et al. Burden of non-communicable diseases in sub-Saharan Africa, 1990-2017: results from the Global Burden of Disease Study 2017. Lancet Glob Health 2019;7:e1375‑87. DOI: https://doi.org/10.1016/S2214-109X(19)30374-2
3. INSEED, UNICEF. [Multiple Indicator Cluster Survey (MICS) 2019 Survey Results Report]. N’Djamena, Chad; 2020.
4. Pengpid S, Peltzer K. Prevalence and correlates of multiple non-communicable disease risk factors among adults in Zambia: results of the first national STEPS survey in 2017. Pan Afr Med J 2020;37:265. DOI: https://doi.org/10.11604/pamj.2020.37.265.25038
5. Muzamil M, Irfan M, Shoaib M, et al. A Comprehensive Review on Therapeutic Properties of Camel Milk. J Health Rehabil Res 2024;4:883‑8. DOI: https://doi.org/10.61919/jhrr.v4i1.493
6. Jimale MA, Maiolo S, Colizzi V, et al. Camel milk consumption as a natural preventive strategy against dysmetabolic disorders and implications for dairy industry development in Somalia. Somali J Sci Tec Soc 2025 17;1. DOI: https://doi.org/10.4081/sjsts.2025.581
7. Zempleni J, Aguilar-Lozano A, Sadri M, et al. Biological Activities of Extracellular Vesicles and Their Cargos from Bovine and Human Milk in Humans and Implications for Infants. J Nutr 2017;147:3‑10. DOI: https://doi.org/10.3945/jn.116.238949
8. Benmoussa A, Lee CHC, Laffont B, et al. Commercial Dairy Cow Milk microRNAs Resist Digestion under Simulated Gastrointestinal Tract Conditions. J Nutr 2016;146:2206‑15. DOI: https://doi.org/10.3945/jn.116.237651
9. Mun D, Ryu S, Lim DH, et al. Comparative miRNome analysis of colostrum- and mature milk-derived extracellular vesicles from Holstein and Jersey cows. J Anim Sci Technol 2025;67:193-207. DOI: https://doi.org/10.5187/jast.2024.e84
10. Xu YR, Zhao J, Huang HY, et al. Recent insights into breast milk microRNA: their role as functional regulators. Front Nutr 2024;11:1366435. DOI: https://doi.org/10.3389/fnut.2024.1366435
11. Shaban AM, Raslan M, Qahl SH, et al. Ameliorative Effects of Camel Milk and Its Exosomes on Diabetic Nephropathy in Rats. Membranes 2022;12:1060. DOI: https://doi.org/10.3390/membranes12111060
12. Melnik BC. Milk exosomal miRNAs: potential drivers of AMPK-to-mTORC1 switching in β-cell de-differentiation of type 2 diabetes mellitus. Nutr Metab 2019;16:85. DOI: https://doi.org/10.1186/s12986-019-0412-1
13. Perge P, Nagy Z, Decmann Á, et al. Potential relevance of microRNAs in inter-species epigenetic communication, and implications for disease pathogenesis. RNA Biol 2017;14:391-401. DOI: https://doi.org/10.1080/15476286.2016.1251001
14. Khaliq A, Mishra AK, Niroula A, et al. An updated comprehensive review of camel milk: Composition, therapeutic properties, and industrial applications. Food Biosci 2024;62:105531. DOI: https://doi.org/10.1016/j.fbio.2024.105531
15. Shuiep E, El-Zubeir I, El Owni O. Influence of season and management on composition of raw camel (Camelus dromedarius) milk in Khartoum state, Sudan. Trop Subtrop Agroecosystems 2008;8:101-6.
16. Mecocci S, Trabalza-Marinucci M, Cappelli K. Extracellular Vesicles from Animal Milk: Great Potentialities and Critical Issues. Animals 2022;12:3231. DOI: https://doi.org/10.3390/ani12233231
17. Devarajan A, Mudgil P, Aldhaheri F, et al. Camel milk-derived probiotic strains encapsulated in camel casein and gelatin complex microcapsules: Stability against thermal challenge and simulated gastrointestinal digestion conditions. J Dairy Sci 2022;105:1862‑77. DOI: https://doi.org/10.3168/jds.2021-20745
18. Wu R, Yue C, Xie Y, et al. Sequencing and analysis of micro RNAs in camel milk exosomes. Acta Vet Hung 2023. DOI: https://doi.org/10.1556/004.2023.00869
19. Ong BX, Brunmeir R, Zhang Q, et al. Regulation of Thermogenic Adipocyte Differentiation and Adaptive Thermogenesis Through Histone Acetylation. Front Endocrinol 2020;11:95. DOI: https://doi.org/10.3389/fendo.2020.00095
20. Sheedy FJ. Turning 21: Induction of miR-21 as a Key Switch in the Inflammatory Response. Front Immunol 2015;6:19. DOI: https://doi.org/10.3389/fimmu.2015.00019
21. Bianchi-Smiraglia A, Wolff DW, Marston DJ, et al. Regulation of local GTP availability controls RAC1 activity and cell invasion. Nat Commun 2021;12:6091. DOI: https://doi.org/10.1038/s41467-021-26665-2
22. Rhee C, Lee BK, Beck S, et al. Arid3a is essential to execution of the first cell fate decision via direct embryonic and extraembryonic transcriptional regulation. Genes Dev 2014;28:2219‑32. DOI: https://doi.org/10.1101/gad.247163.114
23. Kramer DA, Piper HK, Chen B. WASP Family Proteins: Molecular Mechanisms and Implications in Human Disease. Eur J Cell Biol 2022;101:151244. DOI: https://doi.org/10.1016/j.ejcb.2022.151244
24. Dykes SS, Gray AL, Coleman DT, et al. The Arf-like GTPase Arl8b is essential for three-dimensional invasive growth of prostate cancer in vitro and xenograft formation and growth in vivo. Oncotarget 2016;7:31037‑52. DOI: https://doi.org/10.18632/oncotarget.8832
25. Xu Z, Hu H, Fang D, et al. The deubiquitinase USP38 promotes cell proliferation through stabilizing c-Myc. Int J Biochem Cell Biol 2021;137:106023. DOI: https://doi.org/10.1016/j.biocel.2021.106023
26. Li Y, Deng X, Zeng X, Peng X. The Role of Mir-148a in Cancer. J Cancer 2016;7:1233‑41. DOI: https://doi.org/10.7150/jca.14616
27. Zhang Y, Fu Y, Zhang F, Liu J. Destabilization of Akt promotes the death of myeloma cell lines. Biomed Res Int 2014;2014:190629. DOI: https://doi.org/10.1155/2014/190629
28. Zheng B, Liang L, Wang C, et al. MicroRNA-148a suppresses tumor cell invasion and metastasis by downregulating ROCK1 in gastric cancer. Clin Cancer Res Off J Am Assoc Cancer Res 2011;17:7574‑83. DOI: https://doi.org/10.1158/1078-0432.CCR-11-1714
29. Patel K, Kollory A, Takashima A, et al. MicroRNA Let-7 Downregulates STAT3 Phosphorylation in Pancreatic Cancer Cells by Increasing SOCS3 Expression. Cancer Lett 2014;347:54‑64. DOI: https://doi.org/10.1016/j.canlet.2014.01.020
30. Sampson VB, Rong NH, Han J, et al. MicroRNA let-7a down-regulates MYC and reverts MYC-induced growth in Burkitt lymphoma cells. Cancer Res 2007;67:9762‑70. DOI: https://doi.org/10.1158/0008-5472.CAN-07-2462
31. Popkin BM. Measuring the nutrition transition and its dynamics. Public Health Nutr 24:318‑20. DOI: https://doi.org/10.1017/S136898002000470X
32. Husseini Z, Gilbert C. Milk‐Derived Extracellular Vesicles and microRNAs: Potential Modulators of Intestinal Homeostasis. FASEB J 2025;39:e70947. DOI: https://doi.org/10.1096/fj.202501630R
33. Zheng Y, Wu F, Zhang M, et al. Hypoglycemic effect of camel milk powder in type 2 diabetic patients: A randomized, double‐blind, placebo‐controlled trial. Food Sci Nutr 2021;9:4461‑72. DOI: https://doi.org/10.1002/fsn3.2420
34. He J, Guo K, Chen Q, et al. Camel milk modulates the gut microbiota and has anti-inflammatory effects in a mouse model of colitis. J Dairy Sci 2022;105:3782-93. DOI: https://doi.org/10.3168/jds.2021-21345
35. Arab L. Effect of Heat Treatments on the Constituents of Camel Milk. Pak J Zool 2021;54. DOI: https://doi.org/10.17582/journal.pjz/20190422190446
36. Smits M, Joosten H, Faye B, Burger PA. The Flourishing Camel Milk Market and Concerns about Animal Welfare and Legislation. Anim Open Access J MDPI 2022;13:47. DOI: https://doi.org/10.3390/ani13010047
37. Mohamed E, Mustafa A. Fatty Acids Content in Milk of Dromedary Camel (Camelus dromedarius) from Farming and Pastoral Systems in Sudan. Int J Sci Res 2016;5:570-3. DOI: https://doi.org/10.21275/v5i6.NOV164095
38. Lai CY, Yeh KY, Liu BF, et al. MicroRNA-21 Plays Multiple Oncometabolic Roles in Colitis-Associated Carcinoma and Colorectal Cancer via the PI3K/AKT, STAT3, and PDCD4/TNF-α Signaling Pathways in Zebrafish. Cancers (Basel) 2021;13:5565. DOI: https://doi.org/10.3390/cancers13215565

How to Cite



Camel milk and microRNAs: a narrative review integrating molecular evidence, bioinformatics, and nutraceutical perspectives on metabolic diseases in the Sahel. (2026). Sahelian Journal of Responsible One Health, 2(1). https://doi.org/10.4081/sjroh.2026.619