Citrullus colocynthis and Silbum Marian as therapeutic agent in metabolic syndrome Rrattus model

Authors

  • Abdullah Talal Al-Nuaymia College of pharmacy,University of Mosul, Iraq, College of Medicine, Ninevah Univrsity, Iraq
  • Muhammad Ahmed Ahmed Al Kataan College of Medicine, Ninevah Univrsity, Iraq https://orcid.org/0000-0002-9670-7494

DOI:

https://doi.org/10.59480/phahs.v1i2.16

Keywords:

phenolic compounds, glycemic profile, mitochondrial copies number, action potential, lactate: pyruvate ratio.

Abstract

Background: Plants represent a treasure chest with many unrevealed medical applications as hypoglycemic and antioxidant roles. A pathological condition characterized by hyperglycemia, insulin resistance, and dyslipidemia  known as metabolic syndrome.

Objectives: This work focuses on examining the hypoglycemic effect of three plants on a metabolic syndrome( MS)-induced animal model and studying the role of the extracted phenolic compounds on different mitochondrial function genomic parameters.

Methods: Citrullus colocynthis, Silbum Marian, and Rheum rhabarbarum phenolic compounds extracted and quantified using the Folin–Ciocalteu reagent, as described by Sánchez-Rangel et al. (2013).Forty albino rats were included in the work. They were divided into eight groups of five animals each as follows: negative control (normal), positive control (MS induced with fructose with no treatment), and MS treatment with Citrullus colocynthis, MS treatment with Silbum Marian, and MS treatment with Rheum rhabarbarum. Non-MS animals treated with Citrullus colocynthis Non-metabolic syndrome animals treated with Silbum Marian and non-MS animals treated with Rheum rhabarbarum. Serum glucose, Lipid profile, liver function tests, serum glucose, lactate, pyruvate, and molar lactate/pyruvate ratio. Genomic study was conducted by qPCR 

Conclusion: metabolic syndrome significantly reduce mitochondrial genome copies number. The application of the ethanolic extract of Citrullus colocynthis and Silbum Marian 

 

 

 

Author Biography

Abdullah Talal Al-Nuaymia, College of pharmacy,University of Mosul, Iraq, College of Medicine, Ninevah Univrsity, Iraq

 

 

References

Ahmed, M. (2018). Exploring the impact of hypoxia mimetic agents on multipotent stem cell biology. Keele University.

Frazier-wood, A. C., & Wang, Z. (2016). 3/6/18-Technoscience-Metabolic Syndrome. 447–459. https://doi.org/10.1007/978-3-319-11251-0

Heo, J. W., No, M. H., Cho, J., Choi, Y., Cho, E. J., Park, D. H., Kim, T. W., Kim, C. J., Seo, D. Y., Han, J., Jang, Y. C., Jung, S. J., Kang, J. H., & Kwak, H. B. (2021). Moderate aerobic exercise training ameliorates impairment of mitochondrial function and dynamics in skeletal muscle of high-fat diet-induced obese mice. FASEB Journal, 35(2). https://doi.org/10.1096/fj.202002394R

Patti, M. E., & Corvera, S. (2010). The role of mitochondria in the pathogenesis of type 2 diabetes. In Endocrine Reviews (Vol. 31, Issue 3, pp. 364–395). Oxford Academic. https://doi.org/10.1210/er.2009-0027

Prakaschandra, R., & Naidoo, D. P. (2022). The association between the hypertriglyceridaemia waist phenotype, cardiovascular risk factors and the metabolic syndrome in South African Asian-Indians. Diabetes & Metabolic Syndrome: Clinical Research & Reviews, 16(6), 102524. https://doi.org/10.1016/J.DSX.2022.102524

Ruegsegger, G. N., Creo, A. L., Cortes, T. M., Dasari, S., & Nair, K. S. (2018). Altered mitochondrial function in insulin-deficient and insulin-resistant states. In Journal of Clinical Investigation (Vol. 128, Issue 9, pp. 3671–3681). American Society for Clinical Investigation. https://doi.org/10.1172/JCI120843

Sánchez-Rangel, J. C., Benavides, J., Heredia, J. B., Cisneros-Zevallos, L., & Jacobo-Velázquez, D. A. (2013). The Folin-Ciocalteu assay revisited: Improvement of its specificity for total phenolic content determination. Analytical Methods, 5(21), 5990–5999. https://doi.org/10.1039/c3ay41125g

Sebastián, D., Hernández-Alvarez, M. I., Segalés, J., Sorianello, E., Muñoz, J. P., Sala, D., Waget, A., Liesa, M., Paz, J. C., Gopalacharyulu, P., Orešič, M., Pich, S., Burcelin, R., Palacín, M., & Zorzano, A. (2012). Mitofusin 2 (Mfn2) links mitochondrial and endoplasmic reticulum function with insulin signaling and is essential for normal glucose homeostasis. Proceedings of the National Academy of Sciences of the United States of America, 109(14), 5523–5528. https://doi.org/10.1073/PNAS.1108220109/SUPPL_FILE/PNAS.201108220SI.PDF

Sergi, D., Naumovski, N., Heilbronn, L. K., Abeywardena, M., O’Callaghan, N., Lionetti, L., & Luscombe-Marsh, N. (2019). Mitochondrial (dys)function and insulin resistance: From pathophysiological molecular mechanisms to the impact of diet. Frontiers in Physiology, 10, 532. https://doi.org/10.3389/FPHYS.2019.00532/BIBTEX

Taqa, G., Yahya, ِa., & Alkataan, M. (2022). Histological and molecular study of N-acetyl cysteine’s effects on salivary glands in fructose-induced metabolic syndrome in albino rats. Egyptian Journal of Histology, 0(0), 0–0. https://doi.org/10.21608/EJH.2022.133355.1673

Vatashchuk, M. V., Bayliak, M. M., Hurza, V. V., Storey, K. B., & Lushchak, V. I. (2022). Metabolic Syndrome: Lessons from Rodent and Drosophila Models. BioMed Research International, 2022, 5850507. https://doi.org/10.1155/2022/5850507

Published

2023-06-30

How to Cite

Al-Nuaymia, A. T., & Alkataan, M. (2023). Citrullus colocynthis and Silbum Marian as therapeutic agent in metabolic syndrome Rrattus model. InnovoMedica Journal, 2(1), 23–28. https://doi.org/10.59480/phahs.v1i2.16

Issue

Section

Research Article

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