XML Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Atukpa M, Wekhe A, Idris A, Recab R. Effects of ethanolic fruit extract of solanum aethiopicum (L.) on saccharin induced hyperlipidemia and sperm abnormalities in male wistar rats. Journal of Research in Applied and Basic Medical Sciences 2023; 9 (4) :215-222
URL: http://ijrabms.umsu.ac.ir/article-1-268-en.html
Nigerian Army University Biu, Borno State, Nigeria , atukpaelaigwum@gmail.com
Abstract:   (1085 Views)
Background & Aims:  Saccharin is approximately 300 times sweeter than sucrose, and since its discovery, there has been several controversies regarding its potential toxicity as chronic saccharin consumption negatively influences biochemical parameters. Subsequently, Solanum aethiopicum is a good source of bioactive compounds that can be used to treat a variety of ailments including nervous, respiratory, visual, renal, circulatory and fertility issues. The aim of this study was to investigate the effects of ethanolic fruit extract of Solanum Aethiopicum (L.) on saccharin induced hyperlipidemia and sperm abnormalities in male Wistar rats.
Materials & Methods:  In this experimental study, 16 Wistar rats were divided into four groups (Groups 1 to 4) comprising of four Wistar Rats per group. Group 1 (control) was given distilled water and feed only, group 2 was administered saccharin (10 mg), group 3 were administered saccharin (10 mg) and 50 mg of extract, while group 4 was administered saccharin (10 mg) and 100 mg of extract. The extract was administered for 21 days, then the rats were sacrificed and blood sample was collected through cardiac puncture for Lipid profile test. Also, semen analysis was conducted to assess sperm count, motility, viability, and morphology. The results were expressed as mean ± SEM. The differences between the four groups were determined using one-way analysis of variance, and results were considered to be significant at p ≤ 0.05.
Results:  The results showed that saccharin adversely affected lipid profile and sperm parameters in Wistar Rats. Also, ethanolic fruit extract of Solanum aethiopicum caused a significant dose-dependent increase of lipid profile and sperm parameters in Wistar Rats administered saccharin.
Conclusion:  Solanum aethiopicum is beneficial for treatment of sperm abnormalities and hyperlipidemia. It is recommended that the fruit be utilized as a less expensive alternative in clinical therapies for treating sperm abnormalities and hyperlipidemia.
Full-Text [PDF 299 kb]   (342 Downloads) |   |   Full-Text (HTML)  (207 Views)  
Type of Study: orginal article | Subject: General

References
1. Kearns ML, MacAindriu F, Reynolds CM. The impact of non-caloric sweeteners on male fertility: A systematic review and narrative synthesis in rodent models. Front Nutr 2022;9:854074. Available from: http://dx.doi.org/10.3389/fnut.2022.854074. [DOI:10.3389/fnut.2022.854074] [PMID] []
2. Helal EG, Al-Shamrani A, Abdelaziz MA, El-Gamal MS. Comparison between the effect of sucralose and sodium saccharin on some physiological parameters in male albino Rats. Egyp J Hosp Med 2019a;74(7):1552-8. [DOI:10.21608/ejhm.2019.28025]
3. Meldgaard M, Brix N, Gaml-Sørensen A, Ernst A, Ramlau-Hansen CH, Tøttenborg SS, et al. Consumption of sugar-sweetened or artificially sweetened beverages and Semen Quality in young men: A cross-sectional study. Int J Environ Res Public Health 2022;19(2):682. Available from: http://dx.doi.org/10.3390/ijerph19020682. [DOI:10.3390/ijerph19020682] [PMID] []
4. Magnuson BA, Carakostas MC, Moore NH, Poulos SP, Renwick AG. Biological fate of low-calorie sweeteners. Nutr Rev 2016;74(11):670-89. Available from: http://dx.doi.org/10.1093/nutrit/nuw032. [DOI:10.1093/nutrit/nuw032] [PMID]
5. Singh Z. Toxicological aspects of saccharin. Food Biology. 2013;2(1):4-7. [Google Scholar]
6. Andrejić BM, Mijatović VM, Samojlik IN, Horvat OJ, Ćalasan JD, Đolai MA. The influence of chronic intake of saccharin on rat hepatic and pancreatic function and morphology: gender differences. Bosn J Basic Med Sci 2013;13(2):94-9. Available from: http://dx.doi.org/10.17305/bjbms.2013.2372. [DOI:10.17305/bjbms.2013.2372] [PMID] []
7. Musavi H, Tabnak M, Alaei Sheini F, Hasanzadeh Bezvan M, Amidi F, Abbasi M. Effect of garlic (Allium sativum) on male fertility: a systematic review. J Herbmed Pharmacol 2018;7(4):306-12. Available from: http://dx.doi.org/10.15171/jhp.2018.46. [DOI:10.15171/jhp.2018.46]
8. Chen B, Wan C, Mehmood MA, Chang JS, Bai F, Zhao X. Manipulating environmental stresses and stress tolerance of microalgae for enhanced production of lipids and value-added products-A review. Bioresour Technol 2017;244(Pt 2):1198-206. Available from: http://dx.doi.org/10.1016/j.biortech.2017.05.170. [DOI:10.1016/j.biortech.2017.05.170] [PMID]
9. Zabbey VZ, Adienbo OM, Ojeka SO, Dapper DV. Evaluation of the Hydroethanolic Fruit Extract of Solanum aethiopicum (Garden Egg) on the Concentration of Reproductive Hormones, Sperm Parameters and Histology of the Testis of Male Wistar Rats. Greener J Med Sci 2021;11(2):249-56. [Google Scholar]
10. Ekweogu CN, Ude VC, Nwankpa P, Emmanuel O, Ugbogu EA. Ameliorative effect of aqueous leaf extract of Solanum aethiopicum on phenylhydrazine-induced anaemia and toxicity in rats. Toxicol Res 2020;36(3):227-38. Available from: http://dx.doi.org/10.1007/s43188-019-00021-5. [DOI:10.1007/s43188-019-00021-5] [PMID] []
11. Faraone I, Lela L, Ponticelli M, Gorgoglione D, De Biasio F, Valentão P, et al. New insight on the bioactivity of Solanum aethiopicum Linn. Growing in Basilicata Region (Italy): Phytochemical characterization, liposomal incorporation, and antioxidant effects. Pharmaceutics 2022;14(6):1168. Available from: http://dx.doi.org/10.3390/pharmaceutics14061168. [DOI:10.3390/pharmaceutics14061168] [PMID] []
12. Abubakar AR, Sani IH, Malami S. Quantitative Determination of Secondary Metabolites of Fractions Obtained from Solanum aethiopicum (L). L) Fruit Dutse J Pure App Sci 2020;6(3):25-33. [Google Scholar]
13. Han M, Opoku KN, Bissah NAB, Su T. Solanum aethiopicum: The nutrient-rich vegetable crop with great economic, genetic biodiversity and pharmaceutical potential. Horticulturae 2021;7(6):126. Available from: http://dx.doi.org/10.3390/horticulturae7060126. [DOI:10.3390/horticulturae7060126]
14. Okafor HK, Odugbemi AI, Okezie CB, Achebe MK. Antidiabetic and hypolipidemic effects of garden egg (Solanum aethiopicum) leaf extract in beta-cells of streptozotocin induced diabetic male Wistar Rats. Ann Res Rev Biol 2016;1-11. [DOI:10.9734/ARRB/2016/26841]
15. Eze SO, Kanu CQ. Phytochemical and nutritive composition analysis of Solanum aethopicum L. J Pharm Sci Innov 2014;3(4):358-62. Available from: http://dx.doi.org/10.7897/2277-4572.034172. [DOI:10.7897/2277-4572.034172]
16. World Medical Association, American Physiological Society. Guiding principles for research involving animals and human beings. Am J Physiol Regul Integr Comp Physiol 2002a;283(2):R281-3. Available from: http://dx.doi.org/10.1152/ajpregu.00279.2002. [DOI:10.1152/ajpregu.00279.2002]
17. Akunna GG, Ogunmodede OS, Saalu CL, Ogunlade B, Bello AJ, Salawu EO. Ameliorative effect of Moringa oleifera (drumstick) leaf extracts on chromium-induced testicular toxicity in rat testes. World J Life Sci Med Res 2012;2(1). [Google Scholar]
18. Hosseini A, Shahrani M, Asgharian S, Anjomshoa M, Rostamzadeh A, Lorigooini Z, et al. Ameliorative effect of Allium atroviolaceum on sperm quality in cyclophosphamide-treated mice. Futur J Pharm Sci 2021;7(1). Available from: http://dx.doi.org/10.1186/s43094-021-00234-2. [DOI:10.1186/s43094-021-00234-2]
19. Abdullahi HM, Atiku MK, Abdulmumin Y, Sadiya WH. Effect of honey and intensity of swimming exercise on semen parameters of male albino Wistar rats. Trop J Obstet Gynaecol 2019;36(2):258. Available from: http://dx.doi.org/10.4103/tjog.tjog_5_19. [DOI:10.4103/TJOG.TJOG_5_19]
20. Kolawole T. Ameliorative effects of the methanolic extract of the rind of Citrullus lanatus on lead acetate induced toxicity on semen parameters and reproductive hormones of male albino wistar rats. European J Med Plants 2014;4(9):1125-37. Available from: http://dx.doi.org/10.9734/ejmp/2014/11011. [DOI:10.9734/EJMP/2014/11011]
21. Azeez OH, Alkass SY, Persike DS. Long-term saccharin consumption and increased risk of obesity, diabetes, hepatic dysfunction, and renal impairment in rats. Medicina (Kaunas) 2019;55(10):681. Available from: http://dx.doi.org/10.3390/medicina55100681. [DOI:10.3390/medicina55100681] [PMID] []
22. Hall IH, Voorstad PJ, Chapman JM Jr, Cocolas GH. Antihyperlipidemic activity of saccharin analogues in rodents. J Pharm Sci 1983;72(10):1192-8. Available from: http://dx.doi.org/10.1002/jps.2600721022. [DOI:10.1002/jps.2600721022] [PMID]
23. Eletta OAA, Orimolade BO, Oluwaniyi OO, Dosumu OO. Evaluation of proximate and antioxidant activities of Ethiopian eggplant (Solanum aethiopicum L) and Gboma eggplant (Solanum macrocarpon L). J App Sci Env Manag 2017;21(5):967-72. [DOI:10.4314/jasem.v21i5.25]
24. Adewoyin M, Ibrahim M, Roszaman R, Isa M, Alewi N, Rafa A, et al. Male infertility: The effect of natural antioxidants and phytocompounds on seminal oxidative stress. Diseases 2017;5(1):9. Available from: http://dx.doi.org/10.3390/diseases5010009. [DOI:10.3390/diseases5010009] [PMID] []
25. Adelakun SA, Ukwenya VO, Akingbade GT, Omotoso OD, Aniah JA. Interventions of aqueous extract of Solanum melongena fruits (garden eggs) on mercury chloride induced testicular toxicity in adult male Wistar rats. Biomed J 2020;43(2):174-82. Available from: http://dx.doi.org/10.1016/j.bj.2019.07.004. [DOI:10.1016/j.bj.2019.07.004] [PMID] []
26. Durairajanayagam D. Physiological role of reactive oxygen species in male reproduction. In: Oxidants, Antioxidants and Impact of the Oxidative Status in Male Reproduction. Elsevier; 2019. p. 65-78. [DOI:10.1016/B978-0-12-812501-4.00008-0]
27. Zabbey VZ, Adienbo OM, Ojeka SO. Interventions of the hydroethanolic fruit extract of Solanum aethiopicum on lead-induced testicular toxicity in adult male Wistar rats. Zenodo 2022. Available from: http://dx.doi.org/10.5281/ZENODO.6599228. [Google Scholar]
28. Tunwagun DA, Akinyemi OA, Ayoade TE, Oyelere SF. Qualitative analysis of the phytochemical contents of different anatomical parts of ripe Solanum aethiopicum Linneaus fruits. J Complement Altern Med Res 2020;14-22. Available from: http://dx.doi.org/10.9734/jocamr/2020/v9i330142. [DOI:10.9734/jocamr/2020/v9i330142]
29. Doostabadi MR, Hassanzadeh-Taheri M, Asgharzadeh M, Mohammadzadeh M. Protective effect of vitamin E on sperm parameters, chromatin quality, and DNA fragmentation in mice treated with different doses of ethanol: An experimental study. Int J Reprod Biomed (Yazd) 2021;19(6):525-36. Available from: http://dx.doi.org/10.18502/ijrm.v19i6.9374. [DOI:10.18502/ijrm.v19i6.9374] [PMID] []

Add your comments about this article : Your username or Email:
CAPTCHA

Send email to the article author


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2024 CC BY-NC 4.0 | Journal of Research in Applied and Basic Medical Sciences

Designed & Developed by : Yektaweb