Plant-derived bioactive compounds have emerged as promising therapeutic agents for enhancing male reproductive health. Arachis hypogaea (groundnut), an extensively cultivated oilseed crop, possesses rich phytochemical constituents; however, its specific effects on male reproductive parameters remain incompletely characterised. The present study aimed to evaluate the effects of Arachis hypogaea oil extract on reproductive function in male Wistar rats. Twenty male Wistar rats (180 - 200 g) were randomly assigned to four groups (n=5/group). Group 1 (control) received standard rat chow and water ad libitum, while Groups 2, 3, and 4 were administered A. hypogaea oil extract via daily oral gavage at doses of 150, 300, and 600 mg/kg, respectively, for 56 days. Serum reproductive hormones (follicle-stimulating hormone [FSH], luteinizing hormone [LH], and testosterone) were quantified using ELISA, while Sperm parameters (sperm count, motility, viability and morphology) were assessed using standard established protocols. Administration of A. hypogaea oil extract significantly elevated FSH and testosterone levels across all treatment groups compared to the control group (p<0.05). LH levels showed significant increases at 300 mg/kg (1.53 ± 0.02 mIU/mL) and 600 mg/kg (3.06 ± 0.01 mIU/mL) relative to controls (p<0.05). The 300 mg/kg and 600 mg/kg doses produced marked improvements in sperm viability, motility, and normal morphology, with sperm count more than doubling (580.00 ± 40.62 and 560.00 ± 53.40 M/mL, respectively) compared to the control, accompanied by significant reductions in dead sperm percentages (p<0.05). Evidence from the present study shows that Arachis hypogaea oil extract demonstrates dose-dependent enhancement of male reproductive function in Wistar rats, improving both hormonal profiles and sperm quality parameters. These findings support the therapeutic potential of A. hypogaea oil as a natural supplement for male reproductive health and warrant further investigation into its clinical applications and mechanistic pathways.
| Published in | Journal of Diseases and Medicinal Plants (Volume 12, Issue 3) |
| DOI | 10.11648/j.jdmp.20261203.12 |
| Page(s) | 109-116 |
| Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
| Copyright |
Copyright © The Author(s), 2026. Published by Science Publishing Group |
Arachis hypogaea, Male Infertility, Reproductive Hormones, Sperm Parameters, Wistar Rats
Control | 150mg/kg AH | 300mg/kg AH | 600mg/kg AH | |
|---|---|---|---|---|
FSH (mIU/mL) | 0.83 0.22 | 1.00 0.04* | 1.41 0.02* | 2.04 0.01* |
LH (mIU/mL) | 1.05 0.08 | 0.97 0.04 | 1.53 0.02* | 3.06 0.01* |
TEST (mIU/mL) | 2.06 0.03 | 2.38 0.07* | 2.60 0.07* | 3.11 0.04* |
TSI | 1.97 0.05 | 2.46 0.08* | 1.70 0.04* | 1.02 0.03* |
LH-FSH ratio | 1.27 0.06 | 0.98 0.07* | 1.09 0.01* | 1.50 0.04* |
Control | 150mg/kg AH | 300mg/kg AH | 600mg/kg AH | |
|---|---|---|---|---|
Viability (%) | 70.00 2.24 | 74.00 2.45 | 85.00 1.58* | 84.00 1.87* |
Normal (%) | 70.00 2.23 | 74.00 2.45 | 85.00 1.58* | 85.00 1.58* |
Abnormal (%) | 30.00 2.24 | 26.00 2.45 | 15.00 1.58* | 15.00 1.58* |
Active (%) | 65.00 1.58 | 71.00 3.32 | 81.00 2.92* | 81.00 2.92* |
Sluggish (%) | 11.00 1.00 | 10.00 0.00 | 9.00 1.00 | 9.00 1.00 |
Dead (%) | 24.00 2.44 | 19.00 4.60 | 10.00 1.58* | 10.00 1.58* |
Sperm Count (×106/mL) | 254.00 20.40 | 340.00 36.74 | 580.00 40.62* | 560 53.40* |
| [1] | Agarwal A, Gupta S, Sharma R. Acrosome Reaction Measurement. In: Agarwal A, Gupta S, Sharma R, editors. Andrological Eval Male Infertil Lab Guide [Internet]. Cham: Springer International Publishing; 2016 [cited 2023 Jan 25]. p. 143–6. |
| [2] | Agarwal A, Baskaran S, Parekh N, Cho C-L, Henkel R, Vij S, et al. Male infertility. The Lancet. 2021; 397: 319–33. |
| [3] | Dugule DS-G, Gana ED, Paul J. Causes, Effects and Management of Infertility Among Reproductive Women in Karim Lamido Local Government Area of Taraba State-Nigeria. Tex J Med Sci. 2023; 16: 36–49. |
| [4] | Aitken RJ, Smith TB, Jobling MS, Baker MA, De Iuliis GN. Oxidative stress and male reproductive health. Asian J Androl. Medknow; 2014; 16: 31–8. |
| [5] | Alahmar A. Role of oxidative stress in male infertility: An updated review. J Hum Reprod Sci. 2019; 12: 4. |
| [6] | Chinko BC, Umeh OU. Alterations in lipid profile and oxidative stress markers following heat stress on Wistar rats: ameliorating role of vitamin C. Biomed Sci. 2023; 9(1): 6. |
| [7] | Nansubuga K. Oxidative Stress, Hormonal Response, and the Reproductive System: Therapeutic Prospects of Antioxidant-Rich Plant Extracts. 2025; 15: 10–5. |
| [8] | Maroto M, Torvisco SN, García-Merino C, Fernández-González R, Pericuesta E. Mechanisms of hormonal, genetic, and temperature regulation of germ cell proliferation, differentiation, and death during spermatogenesis. Biomolecules. 2025 Mar 29; 15(4): 500. |
| [9] | Houda A, Nyaz S, Sobhy BM, Bosilah AH, Romeo M, Michael JP, et al. Seminiferous tubules and spermatogenesis. Male Reprod Anat. IntechOpen; 2021. |
| [10] | Wang Y, Su M, Chen Y, Huang X, Ruan L, Lv Q, et al. Research progress on the role and mechanism of DNA damage repair in germ cell development. Front Endocrinol. Frontiers Media SA; 2023; 14: 1234280. |
| [11] | Dar RA, Shahnawaz M, Ahanger MA, Majid IU. Exploring the diverse bioactive compounds from medicinal plants: a review. J Phytopharm. 2023; 12: 189–95. |
| [12] | Sepehrfar D, Sudagar M, Paknejad H, Siahkalroodi SY, Norouzitallab P. Role of phytochemicals in farmed fish reproductive performance: A review. Iran J Fish Sci. 2023; 22. |
| [13] | Tungmunnithum D, Thongboonyou A, Pholboon A, Yangsabai A. Flavonoids and other phenolic compounds from medicinal plants for pharmaceutical and medical aspects: An overview. Medicines. MDPI; 2018; 5: 93. |
| [14] | Akram NA, Shafiq F, Ashraf M. Peanut (Arachis hypogaea L.): A Prospective Legume Crop to Offer Multiple Health Benefits Under Changing Climate. Compr Rev Food Sci Food Saf. 2018; 17: 1325–38. |
| [15] | Maestri D. Groundnut and tree nuts: a comprehensive review on their lipid components, phytochemicals, and nutraceutical properties. Crit Rev Food Sci Nutr. Taylor & Francis; 2023; 1–25. |
| [16] | Toomer OT. Nutritional chemistry of the peanut ( Arachis hypogaea). Crit Rev Food Sci Nutr. 2018; 58: 3042–53. |
| [17] | Akhtar S, Khalid N, Ahmed I, Shahzad A, Suleria HAR. Physicochemical Characteristics, Functional Properties, and Nutritional Benefits of Peanut Oil: A Review. Crit Rev Food Sci Nutr. Taylor & Francis; 2014; 54: 1562–75. |
| [18] | Chinko BC, Joffa PP, Ododo AG, Igwedibia PC, Okeke JC, Ukrakpo OS, Ikete PW, Onuoha OG, Nath-Abraham C, Opurum HC. Arachis hypogaea (Peanut) Oil Supplementation Improves Haematological and Serum Lipid Profiles in Male Wistar Rats. Asian Hematology Research Journal. 2026 Apr 23; 9(2): 224-33. |
| [19] | Ododo AG, Chinko BC, Dapper DV. Proximate analysis, phytochemical profiling and GC–MS characterization of bioactive compounds of ethanolic extract and oil of Arachis hypogaea. Discover Plants. 2026 Mar 2; 3(1): 46. |
| [20] | Kyei S, Eke I, Abdul-Karim H, Darko G, Akaranta O. Phytochemicals from Peanut (Arachis hypogaea L.) Skin Extract with Potential for Pharmacological Activity. Curr Bioact Compd. 2021; 17. |
| [21] | Salas-Huetos A, Muralidharan J, Galiè S, Salas-Salvadó J, Bulló M. Effect of Nut Consumption on Erectile and Sexual Function in Healthy Males: A Secondary Outcome Analysis of the FERTINUTS Randomized Controlled Trial. Nutrients. 2019; 11: 1372. |
| [22] |
Paddock C. Men’s sexual function may benefit from daily nut consumption [Internet]. 2019 [cited 2026 Apr 27].
https://www.medicalnewstoday.com/articles/325891 (Accessed 27 Apr 2026). |
| [23] |
Richter A. Should Men Eat Peanuts? [Internet]. Healthline. 2021 [cited 2026 Apr 27].
https://www.healthline.com/nutrition/peanut-benefits-for-men (Accessed 27 Apr 2026). |
| [24] | Berean DI. Role of Antioxidants in Male Semen Preservation. Integr Male Reprod Health-Risk Mech Interv. IntechOpen; 2025. |
| [25] | Mishra R, Nikam A, Hiwarkar J, Nandgude T, Bayas J, Polshettiwar S. Flavonoids as potential therapeutics in male reproductive disorders. Future J Pharm Sci. Springer; 2024; 10: 100. |
| [26] | Kurhaluk N, Kamiński P, Tkaczenko H. Oxidative stress, antioxidants, gut microbiota and male fertility. Cell Physiol Biochem. 2025; 59: 82–123. |
| [27] | Narayana K, Prashanthi N, Nayanatara A, Kumar HHC, Abhilash K, Bairy KL. Effects of methyl parathion (o, o-dimethyl o-4-nitrophenyl phosphorothioate) on rat sperm morphology and sperm count, but not fertility, are associated with decreased ascorbic acid level in the testis. Mutat Res Toxicol Environ Mutagen. Elsevier; 2005; 588: 28–34. |
| [28] | Kaur P, Bansal MP. Effect of experimental oxidative stress on steroidogenesis and DNA damage in mouse testis. J Biomed Sci. Springer; 2004; 11: 391–7. |
| [29] | Mohamed M, Sulaiman SA, Jaafar H, Sirajudeen KNS. Antioxidant protective effect of honey in cigarette smoke-induced testicular damage in rats. Int J Mol Sci. Molecular Diversity Preservation International (MDPI); 2011; 12: 5508–21. |
| [30] | Raji Y, Udoh US, Mewoyeka OO, Ononye FC, Bolarinwa AF. Implication of reproductive endocrine malfunction in male antifertility efficacy of Azadirachta indica extract in rats. College Of Medicine, University of Ibadan, Nigeria; 2003. |
| [31] | Kısa Ü, Başar MM, Ferhat M, Yılmaz E, Başar H, Çağlayan O, et al. Testicular tissue nitric oxide and thiobarbituric acid reactive substance levels: evaluation with respect to the pathogenesis of varicocele. Urol Res. Springer; 2004; 32: 196–9. |
| [32] | Slott VL, Suarez JD, Perreault SD. Rat sperm motility analysis: methodologic considerations. Reprod Toxicol. Elsevier; 1991; 5: 449–58. |
| [33] | Hall JE, Hall ME. Guyton and Hall textbook of medical physiology e-book: Guyton and Hall textbook of medical physiology e-book. Elsevier Health Sciences; 2020. |
| [34] | Plant TM, Zeleznik AJ. Knobil and Neill’s physiology of reproduction. Academic Press; 2014. |
| [35] | Lei T, Yang Y, Yang W-X. Luteinizing hormone regulates testosterone production, leydig cell proliferation, differentiation, and circadian rhythm during spermatogenesis. Int J Mol Sci. MDPI; 2025; 26: 3548. |
| [36] | Dufau ML, Winters CA, Hattori M, Aquilano D, Baranao JLS, Nozu K, et al. Hormonal regulation of androgen production by the Leydig cell. J Steroid Biochem. Elsevier; 1984; 20: 161–73. |
| [37] | Alves MG, Rato L, Carvalho RA, Moreira PI, Socorro S, Oliveira PF. Hormonal control of Sertoli cell metabolism regulates spermatogenesis. Cell Mol Life Sci. Springer; 2013; 70: 777–93. |
| [38] | Ni F-D, Hao S-L, Yang W-X. Multiple signaling pathways in Sertoli cells: recent findings in spermatogenesis. Cell Death Dis. Nature Publishing Group UK London; 2019; 10: 541. |
| [39] | Erukainure OL, Chukwuma CI. African walnut (Plukenetia conophora) oil promotes glucose uptake while improving energy metabolism and steroidogenesis and maintaining surface architecture in rat testes. Front Nutr. Frontiers Media SA; 2024; 11: 1505453. |
| [40] | Ștefănescu R, Tero-Vescan A, Negroiu A, Aurică E, Vari C-E. A comprehensive review of the phytochemical, pharmacological, and toxicological properties of Tribulus terrestris L. Biomolecules. MDPI; 2020; 10: 752. |
| [41] | Jaafar NS, Jaafar IS, Noori ZS. Cressa cretica Pharmacognosy, and Pharmacology (A review). Iraqi J Pharm Sci. 2021; 30: 31–40. |
| [42] | Papadopoulos V, Garza S, Zirkin B. Cell biology and regulation of adult and aging leydig cell steroidogenesis. Leydig Cells Form Regul Funct Health Dis. Springer; 2025. p. 71–120. |
| [43] | Yatung S, Trivedi AK. Daily and seasonal changes in steroidogenic markers in the hypothalamus and testes of tree sparrow (Passer montanus). J Neuroendocrinol. Wiley Online Library; 2025; 37: e13478. |
| [44] | Strauss III JF, FitzGerald GA. Steroid Hormones: Structure and Nomenclature. Yen Jaffes Reprod Endocrinol E-Book Physiol Pathophysiol Clin Manag. Elsevier Health Sciences; 2017; 74. |
| [45] | Santi D, Spaggiari G, Furini C, Griseta V, Zizzi EA, Granata AR, Simoni M. Temporal trends in serum testosterone and luteinizing hormone levels indicate an ongoing resetting of hypothalamic-pituitary-gonadal function in healthy men: a systematic review. Journal of Endocrinological Investigation. 2025 Nov; 48(11): 2721-34. |
| [46] | Roelfsema F, Yang RJ, Liu PY, Takahashi PY, Veldhuis JD. Feedback on LH in testosterone-clamped men depends on the mode of testosterone administration and body composition. J Endocr Soc. Endocrine Society Washington, DC; 2019; 3: 235–49. |
| [47] | Lim CT, Khoo B. Normal physiology of ACTH and GH release in the hypothalamus and anterior pituitary in man. Endotext Internet. MDText.com, Inc.; 2025. |
| [48] | Shokrollahi B, Sharifi F. Dose-and time-dependent effects of intravenous Irisin administration on Gnrh, Lh, Fsh, and estrogen in Kurdish ewes during the breeding season. Res Vet Sci. Elsevier; 2025; 193: 105737. |
| [49] | Christin-Maitre S, Young J. Androgens and spermatogenesis. Ann Endocrinol. Elsevier; 2022. p. 155–8. |
| [50] | Sengupta P, Arafa M, Elbardisi H. Hormonal regulation of spermatogenesis. Mol Signal Spermatogenesis Male Infertil. CRC Press; 2019. p. 41–9. |
| [51] | Suri S, Khan SS, Naeem S, Nisa ZU, Alam N, Majeed S, et al. The beneficial effect of Allium Cepa bulb extract on reproduction of rats; A two-generation study on fecundity and sex hormones. PLoS One. Public Library of Science San Francisco, CA USA; 2024; 19: e0294999. |
| [52] | Salehi F, Zarei L, Mokhayeri Y, Rajabzadeh O. The effect of hydroalcoholic extract of salvia miltiorrhiza on hormonal and cellular parameters of spermatogenesis in male rats after the consumption of ibuprofen. Food Science & Nutrition. 2025 Aug; 13(8): e70705. |
| [53] | Shahrajabian MH, Sun W. Five important seeds in traditional medicine, and pharmacological benefits. Seeds. MDPI; 2023; 2: 290–308. |
| [54] | Al-Chalabi S, Mahmood RI, Rashaa F, Rf AL. The effect of some plants extract on hormonal and testicular function in rats. Int J Pharm Res. 2020; 12: 1223–8. |
| [55] | Mauduit C, Hamamah S, Benahmed M. Stem cell factor/c-kit system in spermatogenesis. Hum Reprod Update. Oxford University Press; 1999; 5: 535–45. |
| [56] | Oduwole OO, Huhtaniemi IT, Misrahi M. The roles of luteinizing hormone, follicle-stimulating hormone and testosterone in spermatogenesis and folliculogenesis revisited. Int J Mol Sci. MDPI; 2021; 22: 12735. |
| [57] | Abruzzese GA, Sanchez‐Rodriguez A, Roldan ER. Sperm metabolism. Mol Reprod Dev. Wiley Online Library; 2024; 91: e23772. |
| [58] | Amaral A. Energy metabolism in mammalian sperm motility. WIREs Mech Dis. Wiley Online Library; 2022; 14: e1569. |
| [59] | Ramaswamy S, Weinbauer GF. Endocrine control of spermatogenesis: Role of FSH and LH/testosterone. Spermatogenesis. Taylor & Francis; 2014; 4: e996025. |
| [60] | Narayan B, Miyashita K, Hosakawa M. Physiological effects of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA)—A review. Food Rev Int. Taylor & Francis; 2006; 22: 291–307. |
| [61] | Yuan C, Wang J, Lu W. Regulation of semen quality by fatty acids in diets, extender, and semen. Front Vet Sci. Frontiers Media SA; 2023; 10: 1119153. |
| [62] | Esmaeili V, Shahverdi AH, Moghadasian MH, Alizadeh AR. Dietary fatty acids affect semen quality: a review. Andrology. Wiley Online Library; 2015; 3: 450–61. |
| [63] | Van Tran L, Malla BA, Kumar S, Tyagi AK. Polyunsaturated fatty acids in male ruminant reproduction—a review. Asian-Australas J Anim Sci. 2017; 30: 622–37. |
| [64] | Nnenna O, Uchendu CN, Obidike RI. Aphrodisiac Effect of Peanut Extract in Male [Internet]. In Review; 2022 Aug. |
| [65] | Ajayi AF, Akhigbe RE. Staging of the estrous cycle and induction of estrus in experimental rodents: an update. Fertil Res Pract. 2020; 6: 5. |
| [66] | Iqbal S, Omara T, Kahwa I, Mir Khan U. Protective effects of Sphaeranthus indicus floral extract against BPS-induced testicular damage in rats occurs through downregulation of RIPK1/3-MLK-driven necroptosis and Fas-FasL-mediated apoptosis. Adv Tradit Med. 2025; 25: 579–95. |
APA Style
Ododo, A. G., Chinko, B. C., Dapper, D. V. (2026). Arachis hypogaea Oil Extract Enhances Male Reproductive Hormone Profiles and Sperm Parameters in Wistar Rats. Journal of Diseases and Medicinal Plants, 12(3), 109-116. https://doi.org/10.11648/j.jdmp.20261203.12
ACS Style
Ododo, A. G.; Chinko, B. C.; Dapper, D. V. Arachis hypogaea Oil Extract Enhances Male Reproductive Hormone Profiles and Sperm Parameters in Wistar Rats. J. Dis. Med. Plants 2026, 12(3), 109-116. doi: 10.11648/j.jdmp.20261203.12
@article{10.11648/j.jdmp.20261203.12,
author = {Avwerosuoghene Great Ododo and Bruno Chukwuemeka Chinko and Datonye Victor Dapper},
title = {Arachis hypogaea Oil Extract Enhances Male Reproductive Hormone Profiles and Sperm Parameters in Wistar Rats},
journal = {Journal of Diseases and Medicinal Plants},
volume = {12},
number = {3},
pages = {109-116},
doi = {10.11648/j.jdmp.20261203.12},
url = {https://doi.org/10.11648/j.jdmp.20261203.12},
eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.jdmp.20261203.12},
abstract = {Plant-derived bioactive compounds have emerged as promising therapeutic agents for enhancing male reproductive health. Arachis hypogaea (groundnut), an extensively cultivated oilseed crop, possesses rich phytochemical constituents; however, its specific effects on male reproductive parameters remain incompletely characterised. The present study aimed to evaluate the effects of Arachis hypogaea oil extract on reproductive function in male Wistar rats. Twenty male Wistar rats (180 - 200 g) were randomly assigned to four groups (n=5/group). Group 1 (control) received standard rat chow and water ad libitum, while Groups 2, 3, and 4 were administered A. hypogaea oil extract via daily oral gavage at doses of 150, 300, and 600 mg/kg, respectively, for 56 days. Serum reproductive hormones (follicle-stimulating hormone [FSH], luteinizing hormone [LH], and testosterone) were quantified using ELISA, while Sperm parameters (sperm count, motility, viability and morphology) were assessed using standard established protocols. Administration of A. hypogaea oil extract significantly elevated FSH and testosterone levels across all treatment groups compared to the control group (pArachis hypogaea oil extract demonstrates dose-dependent enhancement of male reproductive function in Wistar rats, improving both hormonal profiles and sperm quality parameters. These findings support the therapeutic potential of A. hypogaea oil as a natural supplement for male reproductive health and warrant further investigation into its clinical applications and mechanistic pathways.},
year = {2026}
}
TY - JOUR T1 - Arachis hypogaea Oil Extract Enhances Male Reproductive Hormone Profiles and Sperm Parameters in Wistar Rats AU - Avwerosuoghene Great Ododo AU - Bruno Chukwuemeka Chinko AU - Datonye Victor Dapper Y1 - 2026/08/22 PY - 2026 N1 - https://doi.org/10.11648/j.jdmp.20261203.12 DO - 10.11648/j.jdmp.20261203.12 T2 - Journal of Diseases and Medicinal Plants JF - Journal of Diseases and Medicinal Plants JO - Journal of Diseases and Medicinal Plants SP - 109 EP - 116 PB - Science Publishing Group SN - 2469-8210 UR - https://doi.org/10.11648/j.jdmp.20261203.12 AB - Plant-derived bioactive compounds have emerged as promising therapeutic agents for enhancing male reproductive health. Arachis hypogaea (groundnut), an extensively cultivated oilseed crop, possesses rich phytochemical constituents; however, its specific effects on male reproductive parameters remain incompletely characterised. The present study aimed to evaluate the effects of Arachis hypogaea oil extract on reproductive function in male Wistar rats. Twenty male Wistar rats (180 - 200 g) were randomly assigned to four groups (n=5/group). Group 1 (control) received standard rat chow and water ad libitum, while Groups 2, 3, and 4 were administered A. hypogaea oil extract via daily oral gavage at doses of 150, 300, and 600 mg/kg, respectively, for 56 days. Serum reproductive hormones (follicle-stimulating hormone [FSH], luteinizing hormone [LH], and testosterone) were quantified using ELISA, while Sperm parameters (sperm count, motility, viability and morphology) were assessed using standard established protocols. Administration of A. hypogaea oil extract significantly elevated FSH and testosterone levels across all treatment groups compared to the control group (pArachis hypogaea oil extract demonstrates dose-dependent enhancement of male reproductive function in Wistar rats, improving both hormonal profiles and sperm quality parameters. These findings support the therapeutic potential of A. hypogaea oil as a natural supplement for male reproductive health and warrant further investigation into its clinical applications and mechanistic pathways. VL - 12 IS - 3 ER -