IMPACT OF AGAVE EXTRACT ON ATHEROSCLEROSIS IN RAT MODEL: ASSESSING ITS THERAPEUTIC POTENTIAL, ELUCIDATING ITS MECHANISMS, IMPLICATIONS FOR CARDIOVASCULAR HEALTH, AND ENHANCING TREATMENT OPTIONS

Main Article Content

Ghanwa Amjad
Aneeza Masood
Maria Zahid
Andleeb Zahra
Syed Khalil Ullah
Sania Riaz

Keywords

Abstract

Atherosclerosis is the deposition of fat within the wall of arteries. Risk factors include increased consumption of saturated fat. In this study, a rat model of atherosclerosis was established using high fat diet, the effect of Agave sisalana L. was analyzed on the experimental model and results were compared with standard drug by biochemical analysis which included lipid profile test and liver function tests. Rats were divided into five groups, all groups except control were given high fat for 8 weeks followed by a treatment for 6 weeks; control (normal rat feed),positive control (high fat diet 1ml/day), drug treated (high fat 1ml/day for 8 weeks + Lipiget 1ml/day for 6 weeks), extract treated (high fat 1ml/day for 8 weeks+ Agave sisalana L. extract 0.5ml/day for 6 weeks) and combined group (high fat 1ml/day for 8 weeks+ Lipiget 0.5ml/day and agave extract 0.25ml/ day for 6 weeks) respectively. Weights were observed on daily basis and a significant increase in weight was observed in all groups fed with high fat diet. After 8 weeks, treatment was given and a decrease in weights were observed in drug treated, extract treated and combined group. Upon biochemical analysis, triglycerides were seen to be high in positive control due to consumption of high fat diet and were decreased in drug, extract and combined groups which shows that both drug and extract have positive effects in reducing atherosclerosis. ALT concentration was low in positive control group and shown to be increased in all treatment groups. Bilirubin was in high concentration in positive control group as compared to other groups. No significant difference was observed in other parameters. Hence, we conclude that consumption of Agave sisalana L. by high fat diet fed rats attenuates the progression of atherosclerotic lesions.

Abstract 160 | PDF Downloads 69

References

1. Aziz, M., & Yadav, KS. (2016). Pathogenesis of atherosclerosis a review. Medical & Clinical Reviews, 2(3). https://doi.org/10.21767/2471-299x.1000031.
2. Gaziano T, Reddy KS, Paccaud F, et al. Cardiovascular Disease. In: Jamison DT, Breman JG, Measham AR, et al., editors. Disease Control Priorities in Developing Countries. 2nd edition. Washington (DC): The International Bank for Reconstruction and Development / The World Bank; 2006. Chapter 33. Available from: https://www.ncbi.nlm.nih.gov/books/NBK11767/ Co-published by Oxford University Press, New York.
3. Getz, G. S., & Reardon, C. A. (2012). Animal models of atherosclerosis. Arteriosclerosis, thrombosis, and vascular biology, 32(5), 1104–1115.
https://doi.org/10.1161/ATVBAHA.111.23769.
4. Ilyas, I., Little, P. J., Liu, Z., Xu, Y., Kamato, D., Berk, B. C., Weng, J., & Xu, S. (2022). Mouse models of atherosclerosis in Translational Research. Trends in Pharmacological Sciences, 43(11), 920–939. https://doi.org/10.1016/j.tips.2022.06.009.
5. López-Romero, J. C., Ayala-Zavala, J. F., González-Aguilar, G. A., Peña-Ramos, E. A., & González-Ríos, H. (2018). Biological activities of Agave by-products and their possible applications in food and pharmaceuticals. Journal of the science of food and agriculture, 98(7), 2461–2474. https://doi.org/10.1002/jsfa.8738.
6. Misra, A. K., Varma, S. K., & Kumar, R. (2018). Anti-inflammatory Effect of an Extract of Agave americana on Experimental Animals. Pharmacognosy research, 10(1), 104–108. https://doi.org/10.4103/pr.pr_64_17.
7. Pagliaro, B., Santolamazza, C., Simonelli, F., & Rubattu, S. (2015). Phytochemical Compounds and Protection from Cardiovascular Diseases: A State of the Art. BioMed research international, 2015, 918069. https://doi.org/10.1155/2015/918069.
8. Pérez-Zavala, M. L., Hernández-Arzaba, J. C., Bideshi, D. K., & Barboza-Corona, J. E. (2020). Agave: a natural renewable resource with multiple applications. Journal of the science of food and agriculture, 100(15), 5324–5333. https://doi.org/10.1002/jsfa.10586.
9. Perlman R. L. (2016). Mouse models of human disease: An evolutionary perspective. Evolution, medicine, and public health, 2016(1), 170–176. https://doi.org/10.1093/emph/eow014.
10. Pineda, D.T.S., Alacron, N.C., Godinez, M.E.M., Toress, M.D.P.N., Hernandez, J.P., Fitz, P.A. (2017). Antibacterial and anti inflammatory activity of extracts and fractions from Agave cupreata. International Journel of Pharmacology, 13 (8), 1063-1070. DOI: 10.3923/ijp.2017.1063.1070.
11. Sarwar, M.B., Ahmad, Z., Anicet, B.A., Sajid, M., Rashid, B., Hassan, S., Ahmed, M., Husnain, T. (2020). Identification and validation of superior housekeeping gene (s) for qRT-PCR data normalization in Agave sisalana (a CAM-plant) under abiotic stresses. Physiol Mol Biol Plant, 4 (1-8).
12. Shahzad, S., Hussain, M., Munir, H., Arfan, M. (2017). Proximate Composition and Spatio-Temporal Heterogeneity of Phytochemicals in Agave sisalana adapted in Different Zones of Punjab, Pakistan. Research Square, DOI: https://doi.org/10.21203/rs.3.rs-181255/v1
13. Shokouh, P., Jeppesen, P., Hermansen, K., Nørskov, N., Laustsen, C., Jacques Hamilton-Dutoit, S., Qi, H., et al. (2017). A Combination of Coffee Compounds Shows Insulin-Sensitizing and Hepatoprotective Effects in a Rat Model of Diet-Induced Metabolic Syndrome. Nutrients, 10(1), 6. MDPI AG. Retrieved from http://dx.doi.org/10.3390/nu10010006.
14. Singh, P., Tanwar, N., Saha, T., Gupta, A., Sargam, V. (2018). Phytochemical screening and analysis of Carica papaya, Agave americana and Piper nigrum. International Journal of Current Microbiology and Applied Sciences, 7 (2), 1786-1794.
15. Tewari, D., Tripathi, Y.C., Anjum, N. (2014). Agave sisalana: A plant with high chemical diversity and medicinal importance. World Journal of Pharmaceutical Research, 3 (8).
16. Vasanthi, H.R., ShriShriMal, N., Das, D.K., Retraction Notice: Phytochemicals from plants to combat cardiovascular disease. Curr Med Chem. 2012;19(14):2242-51. doi: 10.2174/092986712800229078. Retraction in: Curr Med Chem. 2020;27(32):5444. PMID: 22414106.
17. Vogel, M. E., Idelman, G., Konaniah, E. S., & Zucker, S. D. (2017). Bilirubin prevents atherosclerotic lesion formation in low‐density lipoprotein receptor‐deficient mice by inhibiting endothelial VCAM‐1 and ICAM‐1 signaling. Journal of the American Heart Association, 6(4). https://doi.org/10.1161/jaha.116.004820.

Most read articles by the same author(s)