Hygrophila auriculata seed extract mitigates infertility caused by streptozotocin-induced diabetes in Wistar albino rat model

Hygrophilla auriculata & infertility in Wistar albino rat

Authors

  • Gokilavani Myilraj Department of Pharmacology, Chettinad Academy of Research and Education, Chennai, Tamil Nadu, India https://orcid.org/0009-0005-1577-8725
  • Arunkumar Radhakrishnan Department of Pharmacology, Chettinad Academy of Research and Education, Chennai, Tamil Nadu, India

DOI:

https://doi.org/10.62310/liab.v6i1.299

Keywords:

Male infertility, Diabetes, Hygrophila auriculata, Antioxidant, Lipid peroxidation, DNA fragmentation

Abstract

The present study investigates the effect of an ethanolic extract of Hygrophila auriculata seeds on the male reproductive organ weights, testicular lipid peroxidation and antioxidant potential, testosterone levels, and effects on sperm quality parameters in a streptozotocin (STZ)-induced diabetic male rat model, a widely used experimental model of diabetes-associated infertility. The extract was administered orally to STZ-induced diabetic rats to evaluate its effect on reproductive parameters in terms of evaluating sperm count, motility, viability, morphology and chromatin dispersal assay along with organ weight of male reproductive organs and serum testosterone levels. Antioxidant activity in testicular extract was assessed by measuring lipid peroxidation, glutathione peroxidase, superoxide dismutase, reduced glutathione and catalase assays. The results revealed that athough the male reproductive organ weights decreased significantly in diabetic and treatment groups as compared to the control, the semen quality parameters such as sperm count, motility and viability improved significantly (p<0.05) in the treatment groups. The H. auriculata seed extract significantly (p<0.05) reduced lipid peroxidation in the testicular tissue as compared to the untreated diabetic controls. H. auriculata seed extract was not observed to have ameliorative potential against sperm DNA damage. The ethanolic extract of H. auriculata seed significantly (p<0.05) improved serum testosterone concentration as compared to the control and diabetic rat model groups implying an androgenic effect of the extract. The study provides evidence that the ethanolic extract of H. auriculata seeds protects testicular integrity and sperm quality by reducing lipid peroxidation levels in a diabetic rat model.

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References

Abhijith SP, Lathamani VS, Kshama MA. (2025). Canine diabetes mellitus: a comprehensive review of pathogenesis, diagnosis, and management strategies. Indian Journal of Veterinary and Animal Science Research 54(5): 1-20. https://doi.org/10.56093/ijvasr.v54i5.172388

Al-Khawaldeh O, Al-Dalahmeh A, Al-Sbou M, Al-Sayaydeh A, Al-Qura’n M. (2024). Rosmarinic acid attenuates testicular damage via modulating oxidative stress and apoptosis in STZ-induced diabetic albino mice. Stresses 4(3): 505-517. https://doi.org/10.3390/stresses4030032

Alzain RFA, El-Boshy ME, Gad HM, Elsayed HK. (2021). Effect of metformin, glibenclamide, sitagliptin and their combinations on male rats’ fertility. Journal of Young Pharmacists 13(2): 124–129. https://doi.org/10.5530/jyp.2021.13.25

American Diabetes Association. (2019). Classification and diagnosis of diabetes: Standards of medical care in diabetes—2019. Diabetes Care 42(1): S13–S28. https://doi.org/10.2337/dc19-S002

Anusha P, Immanuel SR. (2013). Antioxidant and antibacterial activities of leaves extract of Hygrophila auriculata (Schumach.) Heine. International Journal of Pharmacy and Pharmaceutical Sciences 5(3): 321–327.

Barkabi-Zanjani S, Ghorbanzadeh V, Aslani M, Ghalibafsabbaghi A, Chodari L. (2020). Diabetes mellitus and the impairment of male reproductive function: Possible signalling pathways. Diabetes & Metabolic Syndrome: Clinical Research & Reviews 14(6): 1907–1914. https://doi.org/10.1016/j.dsx.2020.07.031

Cheung KKT, Luk AOY, So WY, Ma RCW, Kong APS, Chow FCC, Chan JCN. (2015). Testosterone level in men with type 2 diabetes mellitus and related metabolic effects: A review of current evidence. Journal of Diabetes Investigation 6(2): 112–123. https://doi.org/10.1111/jdi.12288

Dena SM, Adeleye AO, Mohlala K, Langa BC, Opuwari CS. (2025). The impact of diabetes mellitus-related oxidative stress on male fertility: A review. Journal of Diabetes 17(10): e70157. https://doi.org/10.1111/1753-0407.70157

Dhanalakshmi S, Harikrishnan N, Srinivasan N, Pandian P, Tanisha BA, Kumar MT, Lokesh V, Yuvashri N, Supriya S. (2022). A perspective overview on Hygrophila auriculata. Pharmacognosy Journal 12(6): 1748–1752. http://dx.doi.org/10.5530/pj.2020.12.237

Ghasemi A, Khalifi S, Jedi SS. (2014).Streptozotocin-nicotinamide-induced rat model of type-2 diabetes. Acta Physiologica Hungarica 101: 408-420. https://doi.org/10.1556/APhysiol.101.2014.4.2

Ghosh C, Maity R, Roy A, Mallick C. (2023). Dose-dependent protective effect of Hygrophila auriculata seeds on cyproterone acetate-induced testicular dysfunction. Reproductive Sciences 30(11): 3359–3371. https://doi.org/10.1007/s43032-023-01279-9

Ghosh C, Mallick C. (2020). Protective effect of ethanolic extract of Hygrophila auriculata seeds in sexual dysfunction in male albino rats. Andrologia 52(2): e13482. https://doi.org/10.1111/and.13482

Gokilavani M, Arunkumar R. (2026). Predicting anti-diabetic property of a compound extracted from Hygrophila auriculata seed using molecular docking for GCMS, physical characteristics, drug disposition, drug toxicity and protein ligand interaction. Advances in Bioresearch 17(1): 01-09. https://doi.org/10.15515/abr.0976-4585.17.1.19

Graziani A, Scafa R, Grande G, Ferlin A. (2024). Diabetes and male fertility disorders. Molecular Aspects of Medicine 99: 101303. https://doi.org/10.1016/j.mam.2024.101303

Huang R, Chen J, Guo B, Jiang C, Sun W. (2024). Diabetes-induced male infertility: potential mechanisms and treatment options. Molecular Medicine 30(1): 11. https://doi.org/10.1186/s10020-023-00771-x

Jalil MJ, Muhammad AS, Salman MD. (2017). Histomorphometric evaluation of mice testicular tissue fixed by two types of fixatives. Iraqi Journal of Science 58(3B): 1363–1370. https://doi.org/10.24996/ijs.2017.58.3B.1

Kotian SR, Kumar A, Mallik SB, Bhat NP, D’Souza A, Pandey AK. (2019). Effect of diabetes on the male reproductive system—A histomorphological study. Journal of Morphological Sciences 36(01): 17–23. https://doi.org/10.1055/s-0039-1683405

La Vignera S, Condorelli R, Vicari E, D'Agata R, Calogero AE. (2012). Diabetes Mellitus and Sperm Parameters. Journal of Andrology 33(2): 145–153. https://doi.org/10.2164/jandrol.111.013193

Luo H, Guo F, Li J, Ma X, Shi Y. (2025). Antidiabetic agents and male fertility: unravelling the impact of glucose-lowering therapies on sperm quality in diabetic males—a narrative review. Translational Andrology and Urology 14(2): 3387–3401. https://doi.org/10.21037/tau-24-112

Manigandan G, Subramaniyan V. (2021). Anti-diabetic activities of isolated compound beta-sitosterol from the ethanolic extract of Andrographis echioides. International Journal of Pharmaceutical Sciences and Research 12(9): 5125–5133. https://doi.org/10.13040/IJPSR.0975-8232.12(9).5125-33

Maresch CC, Stute DC, Alves MG, Oliveira PF, de Kretser DM, Linn T. (2018). Diabetes-induced hyperglycaemia impairs male reproductive function: A systematic review. Human Reproduction Update 24(1): 86–105. https://doi.org/10.1093/humupd/dmx033

Martins RVL, Silva AMS, Duarte AP, Socorro S, Correia S, Maia CJ. (2021). Natural products as protective agents for male fertility. BioChem 1(3): 122–147. https://doi.org/10.3390/biochem1030011

Ohkawa H, Ohishi N, Yagi K. (1979). Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Analytical Biochemistry 95(2): 351–358. https://doi.org/10.1016/0003-2697(79)90738-3

Öztaş E, Yılmaz TE, Güzel E, Sezer Z, Okyar A, Özhan G. (2019). Gliclazide alone or in combination with atorvastatin ameliorated reproductive damage in streptozotocin-induced type 2 diabetic male rats. Saudi Pharmaceutical Journal 27(3): 422–431. https://doi.org/10.1016/j.jsps.2019.01.003

Rastogi A, Shankar S, Mahalingam G. (2014). Antidiabetic activity of methanolic extract of Hygrophila auriculata in adult male Wistar rats. Journal of Pharmaceutical Sciences and Research 7(3): 98–102.

Samaha G, Beatty J, Wade CM, Haase B. (2019). The Burmese cat as a genetic model of type 2 diabetes in humans. Animal Genetics 50(4) 319-325. https://doi.org/10.1111/age.12799

Santi D, Spaggiari G, Simoni M. (2018). Sperm DNA fragmentation index as a promising predictive tool for male infertility diagnosis and treatment management - meta-analyses. Reproductive BioMedicine Online 37(3): 315–326. https://doi.org/10.1016/j.rbmo.2018.06.023

Sethiya NK, Ahmed NM, Shekh RM, Kumar V, Singh PK, Kumar V. (2018). Ethnomedicinal, phytochemical and pharmacological updates on Hygrophila auriculata (Schum.) Heine: An overview. Journal of Integrative Medicine 16(5): 299–311. https://doi.org/10.1016/j.joim.2018.07.002

Simon L, Zini A, Dyachenko A, Ciampi A, Carrell DT. (2017). A systematic review and meta-analysis to determine the effect of sperm DNA damage on in vitro fertilization and intracytoplasmic sperm injection outcome. Asian Journal of Andrology 19(1): 80–90. https://doi.org/10.4103/1008-682x.182822

Sun H, Saeedi P, Karuranga S, Pinkepank M, Ogurtsova K, Duncan BB, Chan JCN, Mbanya JC, Pavkov ME, Ramachandaran A, Wild SH, James S, Herman WH, Zhang P, Bommer C, Kuo S, Boyko EJ, Magliano DJ. (2022). IDF Diabetes Atlas: Global, regional and country-level diabetes prevalence estimates for 2021 and projections for 2045. Diabetes Research and Clinical Practice 183: 109119. https://doi.org/10.1016/j.diabres.2021.109119

Vernet P, Fulton N, Wallace C, Aitken RJ. (2001). Analysis of reactive oxygen species generating systems in rat epididymal spermatozoa. Biology of Reproduction 65(4): 1102–1113. https://doi.org/10.1095/biolreprod65.4.1102

Vijayakumar M, Govindarajan R, Rao GMM, Rao CV, Shirwaikar A, Mehrotra S, Pushpangadan P. (2006). Action of Hygrophila auriculata against streptozotocin-induced oxidative stress. Journal of Ethnopharmacology 104(3): 356-361. https://doi.org/10.1016/j.jep.2005.09.030

Wolf E, Ali A, Blasi M, Blutke A, Deeg CA, Fröhlich T, Hinrichs A, Hristov H, Jaudas F, Kemter E, Keßler B, Klymiuk N, Kurome M, Matiasek K, Nagashima H, Renner S, Zakhartchenko V. (2026). Translational pig models for human diseases. Reproduction, Fertility and Development 38(1): RD25164. https://doi.org/10.1071/RD25164

Zegers-Hochschild F, Adamson GD, Dyer S, Racowsky C, de Mouzon J, Sokol R, Rienzi L, Sunde A, Schmidt L, Cooke ID, Simpson JL, van der Poel S. (2017). The international glossary on infertility and fertility care, 2017. 114(3): 333–345. https://doi.org/10.1016/j.fertnstert.2017.06.005

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Published

28-02-2026

How to Cite

Myilraj, G., & Radhakrishnan, A. (2026). Hygrophila auriculata seed extract mitigates infertility caused by streptozotocin-induced diabetes in Wistar albino rat model: Hygrophilla auriculata &amp; infertility in Wistar albino rat. Letters In Animal Biology, 6(1), 33–40. https://doi.org/10.62310/liab.v6i1.299

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Section

Research Articles
Recieved 2025-12-07
Accepted 2026-02-23
Published 2026-02-28