Dose-related Reversible Suppression of Spermatogenesis and Fertility in Male Laboratory Mice after Treatment with Hibiscus rosa-sinensis (Linn.)
DOI:
https://doi.org/10.17140/phoj.2026.v11.i01.pp641-653.2659Keywords:
Malvaceae, Testis, Fertility, Creatinine, LibidoAbstract
The development of an orally active, safe, reversible, and effective male contraceptive of plant origin has
long been a major research focus, owing to its ready availability, cost-effectiveness, and, most importantly,
the preservation of privacy. To evaluate the effects of oral administration of Hibiscus rosa-sinensis (H. rosa-
sinensis; family: Malvaceae) on male reproductive endpoints and fertility, 30 adult male albino mice of
proven fertility were allocated to six groups. Mice in the treated groups received the benzene leaf extract of H.
rosa-sinensis (100 and 200 mg/kg b. w. daily), whereas those in the control group received olive oil for 35 days.
H. rosa-sinensis treatment induced dose-related histological alterations in reproductive organs, including
reduced organ weights, decreased height of the seminiferous epithelium, reduced diameter of stage VII
tubules, and increased percentage of affected seminiferous tubules in the testes. Treatments adversely
affected sialic acid and fructose levels and sperm parameters; libido was not affected, but fertility was
significantly suppressed in extract-treated males compared with controls. Forty-two days after treatment
withdrawal, reproductive endpoints and fertility returned to levels comparable with controls. Furthermore,
the histoarchitecture of the liver and kidney, serum levels of ALT, AST, and creatinine, and haematological
parameters remained unaltered compared with controls. The results suggest that treatment with H. rosa-
sinensis causes dose-dependent, reversible suppression of spermatogenesis and fertility in albino mice,
without any visible toxicity. Therefore, it might be a potential candidate for herbal male contraception.
References
Chaudhury RR. The quest for a herbal contracep-tive, 1993.
Missoum A. An update review on Hibiscus rosa sinensis phytochemistry and medicinal uses. Jour-nal of Ayurvedic and Herbal Medicine, 4, 135–46 (2018).
Kapoor M, Kaur G, Kaur N, Sharma C, Batra K, Singh D. The Traditional Uses, Phytochemistry and Pharmacology of Genus Hibiscus: A Review. European Journal of Medicinal Plants, 32, 1–37 (2021).
Kumar A, Kumar S. Pharmacological Review on Hibiscus Rosa Sinensis. International Journal of Novel Research and Development, 7, 2456–4184 (2022).
Joseph KS. Phytochemicals and Biological Activi-ties of Flowers of Hibiscus x rosa-sinensis (Chinese Rose). Bioactive Compounds in Edible Flowers. CRC Press, pp.209–24 (2026).
Gupta PC. Contraceptive potential of Hibiscus rosa-sinensis (Linn.) – An update. International Journal of Pharmaceutical Research, 4, 7–9 (2012).
Jana TK, Das S, Ray A, Mandal D, Giri Jana S, Bhat-tacharya J. Study of the effects of hibiscus rosa-sinensis flower extract on the spermatogenesis of male albino rats. Journal of Physiology and Phar-macology Advances, 3, 167–71 (2013).
Julia D, Nita S. Effect of Hibiscus Rosa-Sinensis Linn. Extracts on the Amount, Motility, Morphol-ogy, Viability of Spermatozoa of Male Rats (Rattus Norvegicus). Biomedical Journal of Indonesia, 5, 34–42 (2019).
Carolin BT, Novelia S, Nita S. Effects of Hibiscus rosa-sinensis Linn. flower extract on epididymis, prostate and seminal vesicles of male rats. Inter-national Biological and Biomedical Journal, 5, 12– 7 (2019).
Verma S, Yadav A. Rising trends towards the de-velopment of oral herbal male contraceptive: an insight review. Future Journal of Pharmaceutical Sciences, 7, 1–15 (2021).
Gupta PC, Yadav L. Effect of Hibiscus-Rosa-Sinensis (Linn.) on the Reproductive Endpoints and Fertility in Male Albino Mice. Journal of Chem-ical Health Risks, 14, 3220–33 (2024).
World Health Organisation. WHO Chemical Guide-lines, CG-03, 1001A/Ip. (1986).
CPCSEA. Guidelines on the regulation of scientific experiments on animals. Government of India, New Delhi, (2007).
Gupta PC. Evaluation of Antifertility Potential of Ficus bengalensis (Linn.) in Male Albino Mice. In-ternational Journal of Pharmacy Research and Technology, 4, 69–73 (2014).
World Health Organisation. WHO Laboratory Man-ual for the Examination of Human Semen and Sperm-Cervical Mucus Interaction. Vol. 19, Cam-bridge University Press, (1996).
Wyrobek AJ, Bruce WR. Chemical induction of sperm abnormalities in mice. Proceedings of the National Academy of Sciences, 72, 4425–9 (1975).
Warren L. The thiobarbituric acid assay of sialic acids. J Biol Chem, 234, 1971–5 (1959).
Lindner HR, Mann T. Relationship between the content of androgenic steroids in the testes and the secretory activity of the seminal vesicles in the bull. Journal of Endocrinology, 21, 341–NP (1960).
Ghai C. A Textbook of Practical Physiology. JP Med-ical Ltd, (2013).
Reitmann S, Frankel S. A colorimetric method for the determination of serum glutamic oxalacetic and glutamic pyruvic transaminases. American Journal of Clinical Pathology, 28, 56–63 (1957).
Salewski E. Färbemethode zum makroskopischen Nachweis von Implantationsstellen am Uterus der Ratte. Naunyn-Schmiedebergs Archiv für Experi-mentelle Pathologie und Pharmakologie, 247, 367 (1964).
Russell LD, Ettlin RA, Hikim APS, Clegg ED. Histo-logical and Histopathological Evaluation of the Testis, Wiley Online Library, 1993.
Abe K, Takano H. Response of the Mouse Epididy-mal Duct to the Disappearance and Reappear-ance of Spermatozoa Induced by Temporal Cryp-torchidism. Archivum Histologicum Japonicum, 50, 315–24 (1987).
Gupta RS, Kachhawa JBS, Chaudhary R. Antisper-matogenic, antiandrogenic activities of Albizia lebbeck (L.) Benth bark extract in male albino rats. Phytomedicine, 13, 277–83 (2006).
Mishra RK, Singh SK. Reversible antifertility effect of aqueous rhizome extract of Curcuma longa L. in male laboratory mice. Contraception, 79, 479–87 (2009).
Singh A, Singh SK. Evaluation of antifertility po-tential of Brahmi in male mouse. Contraception, 79, 71–9 (2009).
Singh N, Singh SK. Citrus limon extract: Possible inhibitory mechanisms affecting testicular func-tions and fertility in male mice. Systems Biology in Reproductive Medicine, 62, 39–48 (2016).
Verma HP, Singh SK. Antifertility efficacy of Coc-cinia indica in male mice and its possible mecha-nisms of action on spermatogenesis. General and Comparative Endocrinology, 241, 89–99 (2017).
Kadalmani B, Niranjana R, Natarajan UA, Chandi-ran IS. Antifertility and Antioxidant Activities of Ethanolic Extract of Leonotis nepetifolia in Male Albino Rats. J. Basic Clin. Appl. Health, 3, 115–21 (2020).
Gupta PC, Yadav L. Evaluation of antispermato-genic and antifertility properties of Terminalia chebula (Retz.) in albino mice. Int J Reprod Con-tracept Obstet Gynecol, 13, 1774–84 (2024).
Hess RA, Schaeffer DJ, Eroschenko VP, Keen JE. Frequency of the stages in the cycle of the semi-niferous epithelium in the rat. Biology of Repro-duction, 43, 517–24 (1990).
Hess RA, De Franca LR. Spermatogenesis and cy-cle of the seminiferous epithelium. Advances in Experimental Medicine and Biology, 636, 1–15 (2008).
Ramaswamy S, Weinbauer GF. Endocrine control of spermatogenesis: Role of FSH and LH/testos-terone. Spermatogenesis, 4, e996025 (2014).
Yadav A, Sharma S, Wani SN, Kaushal K, Sharma P. Development of Oral Herbal Male Contraceptive. Current Aspects in Pharmaceutical Research and Development Vol. 8, 77–88 (2022).
Elkin ND. Evaluation of Biomarkers for Testicular Toxicity. (2010).
Singh A, Singh SK. Reversible antifertility effect of aqueous leaf extract of Allamanda cathartica L. in male laboratory mice. Andrologia, 40, 337–45 (2008).
Mishra RK, Singh SK. Antispermatogenic and an-tifertility effects of fruits of Piper nigrum L. in mice. Indian Journal of Experimental Biology, 47, 706 (2009).
Shojaeepour S, Dabiri S, Dabiri B, Imani M, Abadi MFS, Hashemi F. Histopathological findings of tes-ticular tissue following cadmium toxicity in rats. Iranian Journal of Pathology, 16, 348 (2021).
D’Souza UJA. Tamoxifen induced multinucleated cells (symplasts) and distortion of seminiferous tubules in rat testis. Asian Journal of Andrology, 5, 217–20 (2003).
Mishra RK, Singh SK. Safety assessment of Syzy-gium aromaticum flower bud (clove) extract with respect to testicular function in mice. Food and Chemical Toxicology, 46, 3333–8 (2008).
Verma HP, Singh SK. Effect of aqueous leaf extract of Dalbergia sissoo Roxb. on spermatogenesis and fertility in male mice. The European Journal of Contraception & Reproductive Health Care, 19, 475–86 (2014).
Gupta PC. Reversible Contraceptive Potential of Harad in Male Albino Mice. International Jour-nal of Pharmacy and Pharmaceutical Sciences, 9, 288–96 (2017).
Gupta PC. A Preliminary Study on Effects of Leaf Extract of Ficus bengalensis (Linn.) on Spermato-genesis and Fertility in Albino Mice. International Journal of PharmTech Research, 4, 226 (2012).
Abe K, Takano H, Ito T. Response of epididymal duct to the temporary depletion of spermato-zoa induced by testicular irradiation in mice. The Anatomical Record, 207, 17–24 (1983).
Wang C, Barratt CLR, Blithe DL. Contraceptive effi-cacy: Determining the threshold for effective sup-pression based on sperm concentration, motility, and morphology. Andrology, 12, 1574–84 (2024).
Khole V. Epididymis as a target for contraception. (2003).
Hinton BT, Cooper TG. The epididymis as a tar-get for male contraceptive development. Hand-book of Experimental Pharmacology, 198, 117–37 (2010).
Cornwall GA. Epididymis: Sperm Maturation and Motility. Encyclopedia of Reproduction: Volume 1-6, Second Edition. Vol. 1, pp.292–7 (2018).
Shah M, Singh R, Shah R, Kakar S. An overview of the current methodologies used for evaluation of anti-fertility agents. Asian Pacific Journal of Reproduction, 5, 175–8 (2016).
Khan S, Mali PC. Evaluation of Antiandrogenic Ef-fects in Castrated Rats Treated with Cassia tora Extract. SSR Institute of International Journal of Life Sciences, 5, 2259–68 (2019).
Basal WT, Ahmed ART, Mahmoud AA, Omar AR. Lufenuron induces reproductive toxicity and genotoxic effects in pregnant albino rats and their fetuses. Scientific Reports, 10, 1–24 (2020).
Risbridger GP, Taylor RA. Physiology of the male accessory sex structures: the prostate gland, sem-inal vesicles, and bulbourethral glands. Knobil and Neill’s Physiology of Reproduction. Elsevier, pp.1149–72 (2006).
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