Histological Effect of Antidiabetic Herbal Tea on The Spleen of Albino Rats Induced with Alloxan (Diabetes)

Authors

  • Uwuigbe M. Department of Histopathology, Faculty of Medical Laboratory Science, Ambrose Alli University Ekpoma, Edo State.
  • WISDOM OHIWEREI OHILUX GLOBAL , RESEARCH, MEDICAL AND TRAINING CENTRE, EKPOMA, EDO STATE. 2. Department of Medical Laboratory Science, Mudiame University, Irrua, Edo State
  • Ogbe O.C. Department of Anatomy, Ambrose Alli University, Ekpoma, Edo State, Nigeria
  • Obeagu E.I Department of Biomedical and Laboratory Science, Africa University Zimbabwe
  • Ohiwerei F.O. Department of Research and Training, Ohilux Global Research, Medical and Training Institute, Ekpoma, Edo State

DOI:

https://doi.org/10.56778/rjhs.v3i1.550

Keywords:

Albino rats, Alloxan, Anti-diabetic herbal tea, Diabetes mellitus, Spleen Histology

Abstract

This study investigated the effects of an anti-diabetic herbal tea on splenic histology and body weight in alloxan-induced diabetic Wistar rats. Thirty rats were divided into five groups (n=6): a positive control (Group A), a negative diabetic control (Group B), and three experimental groups (Groups C, D, and E) that received 3.4 ml, 6.7 ml, and 13 ml of the herbal tea, respectively, for 14 days. Body weight was recorded before and after treatment, and spleen tissues were analyzed histologically with H&E staining. The results showed that the diabetic control group (Group B) had a significant decrease in body weight (p=0.01), while the positive control group (Group A) showed no significant change (p=0.85). In the treatment groups, a low dose (Group C) resulted in a significant weight reduction (p=0.03), whereas higher doses (Groups D and E) showed non-significant trends toward weight loss (p=0.07 and p=0.08, respectively). Histological analysis revealed splenic infarcts and coagulative necrosis in the diabetic control group. The low-dose group (Group C) exhibited inflammatory changes and congestive splenomegaly. In contrast, the moderate-dose group (Group D) showed a near-normal splenic architecture, and the high-dose group (Group E) displayed a preserved fibroelastic capsule. These findings indicate that the anti-diabetic herbal tea has dose-dependent effects on body weight and spleen histology. Specifically, a moderate dose (6.7 ml) restored splenic structure, while a higher dose (13 ml) provided structural protection, suggesting its potential as a therapeutic agent for managing diabetes. The study underscores the importance of proper dosing to optimize therapeutic outcomes.

 

References

Araujo, J., Paradis, A., Mendes, J., Petrik, S., & De Rivera, C. (2022). Induction of Type I Diabetes Mellitus in Beagle Dogs Using Alloxan and Streptozotocin. Current Protocols, 2(11), e580. https://doi.org/10.1002/cpz1.580

Dailey, M. O. (2002). The Immune Functions of the Spleen. In A. J. Bowdler (Ed.), The Complete Spleen (pp. 51–69). Humana Press. https://doi.org/10.1007/978-1-59259-124-4_4

Gurjar, H. P. S., Irchhaiya, Dr. R., & Vermas, Dr. A. (2016). Review On Some Medicinal Plants With Antidiabetic Activity. Journal of Drug Delivery and Therapeutics, 6(2), 45–51. https://doi.org/10.22270/jddt.v6i2.1199

Hanchang, W., Wongmanee, N., Yoopum, S., & Rojanaverawong, W. (2022). Protective role of hesperidin against diabetes induced spleen damage: Mechanism associated with oxidative stress and inflammation. Journal of Food Biochemistry, 46(12). https://doi.org/10.1111/jfbc.14444

Haruna, H. M. S., Umar, H., Baba, G., & Zakari, A. (2024). Hypoglycemic and Hypolipidemic Effects of Aqueous Leaf Extract of Guiera senegalensis on Diabetic Albino Rats. Sahel Journal of Life Sciences FUDMA, 2(4), 34–39. https://doi.org/10.33003/sajols-2024-0204-06

Khan, V., Najmi, A., Mohd. Akhtar, Mohd. Aqil, Mohd. Mujeeb, & Pillai, K. (2012). A pharmacological appraisal of medicinal plants with antidiabetic potential. Journal of Pharmacy And Bioallied Sciences, 4(1), 27. https://doi.org/10.4103/0975-7406.92727

Kolay, Dr. S. R., Kumar, Dr. S., & Dubey, Dr. N. K. (Eds.). (2023). Socio-Scientific Interaction in Diabetes and Cancer and Its Management. B P International. https://doi.org/10.9734/bpi/mono/978-81-968135-7-4

Lee, S.-J., Cho, K. H., Kim, J. C., Choo, H. J., Hwang, J.-Y., Cho, H. C., & Hah, Y.-S. (2024). Comparative analysis of anti-obesity effects of green, fermented, and γ-aminobutyric acid teas in a high-fat diet-induced mouse model. Applied Biological Chemistry, 67(1), 36. https://doi.org/10.1186/s13765-024-00888-5

Lenzen, S. (2008). The mechanisms of alloxan- and streptozotocin-induced diabetes. Diabetologia, 51(2), 216–226. https://doi.org/10.1007/s00125-007-0886-7

Moscow State Academy of Veterinary Medicine and Biotechnology – MVA by K. I. Skryabin”, Moscow, Russia, & Gildikov, D. I. (2024). Multiple organ pathology in rats with experimental alloxan diabetes. Veterinariya, Zootekhniya i Biotekhnologiya, 5(126), 39–47. https://doi.org/10.36871/vet.zoo.bio.202405004

National Cancer Institute. (2020). Splenomegaly. In Definitions. Qeios. https://doi.org/10.32388/8KC967

Özerkan, D., Özsoy, N., Cebesoy, S., & Özer, Ç. (2021). Distribution of spleen connective tissue fibers in diabetic and vitamin C treated diabetic rats. Biotechnic & Histochemistry, 96(5), 347–353. https://doi.org/10.1080/10520295.2020.1795718

Pernar, L. I. M., & Tavakkoli, A. (2019). Anatomy and Physiology of the Spleen. In Shackelford’s Surgery of the Alimentary Tract, 2 Volume Set (pp. 1591–1597). Elsevier. https://doi.org/10.1016/B978-0-323-40232-3.00136-9

Rashid, K., Bhattacharya, S., & Sil, P. C. (2012). Protective role of D-saccharic acid-1,4-lactone in alloxan induced oxidative stress in the spleen tissue of diabetic rats is mediated by suppressing mitochondria dependent apoptotic pathway. Free Radical Research, 46(3), 240–252. https://doi.org/10.3109/10715762.2011.650694

Sarma, S., Kashyap, A., Chakrabarti, A., & Singh, S. S. (2024). Quercetin Ameliorated Diabetic Stress through Upregulation of Antioxidant Enzymes and the Nrf-2/HO-1 Axis in the Spleen of Mice. International Journal of Pharmaceutical Sciences and Drug Research, 1004–1012. https://doi.org/10.25004/IJPSDR.2024.160611

Scridon, A., Perian, M., Marginean, A., Fisca, C., Vantu, A., Ghertescu, D., Chevalier, P., & Serban, R. C. (2015). Wistar rats with long-term streptozotocin-induced type 1 diabetes mellitus replicate the most relevant clinical, biochemical, and hematologic features of human diabetes / Sobolanii Wistar cu diabet zaharat tip 1 indus cu streptozotocina reproduc cele mai relevante caracteristici clinice, biochimice si hematologice ale diabetului uman. Revista Romana de Medicina de Laborator, 23(3), 263–274. https://doi.org/10.1515/rrlm-2015-0028

Soares, P. H. L., Borges, G. M., Alves, M. L. F. S., Costa, L. M., & Vieira, C. C. L. D. R. (2024). Esplenomegalia: Principais Causas Em Uma Revisão Da Literatura. Revista Ibero-Americana de Humanidades, Ciências e Educação, 10(5), 6151–6157. https://doi.org/10.51891/rease.v10i5.14336

Vasu, S., McClenaghan, N. H., & Flatt, P. R. (2016). Molecular Mechanisms of Toxicity and Cell Damage by Chemicals in a Human Pancreatic Beta Cell Line, 1.1B4. Pancreas, 45(9), 1320–1329. https://doi.org/10.1097/MPA.0000000000000645

Zhong, X., Zhang, T., Liu, Y., Wei, X., Zhang, X., Qin, Y., Jin, Z., Chen, Q., Ma, X., Wang, R., & He, J. (2015). Short-term weight-centric effects of tea or tea extract in patients with metabolic syndrome: A meta-analysis of randomized controlled trials. Nutrition & Diabetes, 5(6), e160–e160. https://doi.org/10.1038/nutd.2015.10

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Published

2025-08-31

How to Cite

Uwuigbe, M., OHIWEREI, W., Ogbe, C., Obeagu, E., & Ohiwerei, F. (2025). Histological Effect of Antidiabetic Herbal Tea on The Spleen of Albino Rats Induced with Alloxan (Diabetes). RADINKA JOURNAL OF HEALTH SCIENCE, 3(1), 458–469. https://doi.org/10.56778/rjhs.v3i1.550