Skip to content
2000
Volume 22, Issue 3
  • ISSN: 1573-4072
  • E-ISSN: 1875-6646

Abstract

This current review provides a thorough examination of the potential of plant-based chemicals as effective male contraceptive treatments by synthesizing results from several pre-clinical investigations. The established literature highlights the urgent requirement for male contraceptive strategies that are safe, effective, and reversible, considering the drawbacks and difficulties of current options. The need for male contraceptive research and the inherent drawbacks of available solutions are also covered in this review. It clarifies the possible benefits of plant-based contraceptives by emphasizing their natural source, expected safety profile, and low side effect rate. In this review, 49 plants evaluated for male oral contraceptive action are discussed. PubMed, Cochrane library, Embase, ScienceDirect, and Google Scholar databases are used for the literature search. This review explores the complex pathways, including hormone regulation, spermatogenesis suppression, sperm motility interference, and sperm maturation disruption, by which plant-based chemicals may have contraceptive effects. Pre-clinical investigations have examined a wide range of plant-derived substances, including flavonoids, anthraquinones, glycosides, alkaloids, phenolics, diterpenes, triterpenes, tannins, saponins, steroids, and phytosterols, among other phytochemical families. Every phytochemical is thoroughly examined, including its botanical origins, phytoconstituents, native name, and unique effects on male fertility. Results from research conducted on animals are methodically summarised in this study, including information on the effectiveness, dose, delivery methods, and reversibility of contraceptive effects. Furthermore, the discussion includes findings from research, emphasizing the possible influence on sperm parameters (sperm production, deformation, count, viability, and motility), reproductive hormones (testosterone level), thickness and diameter of seminiferous tubules (ST) as well as spermatocytes and secondary spermatocytes, Sertoli cells (SCs), and Leydig cell (LCs). According to the assessment, male contraceptives made of plants have a lot of potential as a future weapon in the arsenal of contraceptives. Pre-clinical research has shown the safety, effectiveness, and reversibility of several plant-derived drugs, which offers a solid basis for more investigation and advancement. However, there are still a lot of obstacles to overcome, like standardizing plant extracts, guaranteeing uniform effectiveness, and carrying out thorough safety evaluations. This review emphasizes the significance of undertaking well-designed clinical studies to validate pre-clinical findings, creating standardized formulations for consistent outcomes, and resolving regulatory issues as well as ethical considerations for human use to progress this subject.

Loading

Article metrics loading...

/content/journals/cbc/10.2174/0115734072346159250311050808
2025-03-24
2026-03-08
Loading full text...

Full text loading...

References

  1. World Population ClockU.S. Census Bureau Current Population.2024Available from www.census.gov/popclock/print.php?component=counter
    [Google Scholar]
  2. UNFPAState of World Population 2022: The case for action in the neglected crisis of unintended pregnancy.2022Available from: www.unfpa.org/sites/default/files/pub-pdf/EN_SWP22 report_0.pdf
    [Google Scholar]
  3. FP 2030. Integrating FP & HIV Services. 2022. Available from:https://fp2030.org/HIVintegration
  4. BearakJ. PopinchalkA. GanatraB. MollerA.B. TunçalpÖ. BeavinC. KwokL. AlkemaL. Unintended pregnancy and abortion by income, region, and the legal status of abortion: Estimates from a comprehensive model for 1990–2019.Lancet Glob. Health202089e1152e116110.1016/S2214‑109X(20)30315‑6 32710833
    [Google Scholar]
  5. KhourdajiI. ZilliouxJ. EisenfratsK. FoleyD. SmithR. The future of male contraception: A fertile ground.Transl. Androl. Urol.20187S2Suppl. 2S220S23510.21037/tau.2018.03.23 29928620
    [Google Scholar]
  6. RothM. AmoryJ. Beyond the condom: Frontiers in male contraception.Semin. Reprod. Med.201634318319010.1055/s‑0036‑1571435 26947703
    [Google Scholar]
  7. JohnsonD. SandlowJ.I. Vasectomy: Tips and tricks.Transl. Androl. Urol.20176470470910.21037/tau.2017.07.08 28904903
    [Google Scholar]
  8. KanakisG. GoulisD. Male contraception: A clinically-oriented review.Hormones (Athens)201514459861410.14310/horm.2002.1623 26732151
    [Google Scholar]
  9. ThirumalaiA. AmoryJ.K. Emerging approaches to male contraception.Fertil. Steril.202111561369137610.1016/j.fertnstert.2021.03.047 33931201
    [Google Scholar]
  10. PageS.T. AmoryJ.K. BremnerW.J. Advances in male contraception.Endocr. Rev.200829446549310.1210/er.2007‑0041 18436704
    [Google Scholar]
  11. HeinemannK. SaadF. WiesemesM. WhiteS. HeinemannL. Attitudes toward male fertility control: Results of a multinational survey on four continents.Hum. Reprod.200520254955610.1093/humrep/deh574 15608042
    [Google Scholar]
  12. FauserB.C.J.M. AdamsonG.D. BoivinJ. ChambersG.M. de GeyterC. DyerS. InhornM.C. SchmidtL. SerourG.I. TarlatzisB. Zegers-HochschildF. AshiruO. BrownS. ByeK. Calhaz-JorgeC. ColluraB. De SutterP. GianaroliL. GiudiceL. IshiharaO. MocanuE.V. OmbeletW. PaiR. PenningsG. RaymerJ. TaylorH. Declining global fertility rates and the implications for family planning and family building: An IFFS consensus document based on a narrative review of the literature.Hum. Reprod. Update202430215317310.1093/humupd/dmad028 38197291
    [Google Scholar]
  13. Reproductive Health. ANA Position Statement. 2022. Available from:https://www.nursingworld.org/practice-policy/nursing-excellence/official-position-statements/id/reproductive-health/
  14. KaurR. SharmaA. KumarR. KharbR. Rising trends towards herbal contraceptives.J. Nat. Prod. Plant Resour.201114512http://scholarsresearchlibrary.com/JNPPR-vol1-iss4/JNPPR-2011-1-4-5-12.pdf
    [Google Scholar]
  15. SinghN. SinghS.K. Citrus limon extract: Possible inhibitory mechanisms affecting testicular functions and fertility in male mice.Syst Biol Reprod Med2016621394810.3109/19396368.2015.1078422 26787324
    [Google Scholar]
  16. SoniP.K. LuhadiaG. SharmaD.K. MaliP.C. Antifertility activates of traditional medicinal plants in male with emphasis on their mode action: A review.J. Global Biosci.20154111651179
    [Google Scholar]
  17. MandalT.K. DasN.S. Testicular toxicity in cannabis extract treated mice: Association with oxidative stress and role of antioxidant enzyme systems.Toxicol. Ind. Health2010261112310.1177/0748233709354553 19942653
    [Google Scholar]
  18. SharmaR.S. RajalakshmiM. Antony JeyarajD. JeyarajD.A. Current status of fertility control methods in India.J. Biosci.2001264Suppl.39140510.1007/BF02704741 11779954
    [Google Scholar]
  19. ThirumalaiA. PageS.T. Androgens in male contraception.Best Pract. Res. Clin. Endocrinol. Metab.202236510162710.1016/j.beem.2022.101627 35249804
    [Google Scholar]
  20. VermaS. YadavA. Rising trends towards the development] of oral herbal male contraceptive: An insight review.Future J. Pharm. Sci.2021712310.1186/s43094‑020‑00154‑7
    [Google Scholar]
  21. Abdel-MagiedE.M. Abdel-RahmanH.A. HarrazF.M. The effect of aqueous extracts of Cynomorium coccineum and Withania somnifera on testicular development in immature Wistar rats.J. Ethnopharmacol.20017511410.1016/S0378‑8741(00)00348‑2 11282435
    [Google Scholar]
  22. BhattN. DeshpandeM. A critical review and scientific prospective on contraceptive therapeutics from ayurveda and allied ancient knowledge.Front. Pharmacol.20211262959110.3389/fphar.2021.629591 34149405
    [Google Scholar]
  23. LevinskyH. SingerR. BarnetM. SagivM. AllaloufD. Sialic acid content of human spermatozoa and seminal plasma in relation to sperm counts.Arch. Androl.1983101454610.3109/01485018308990169 6847304
    [Google Scholar]
  24. ChinoyN.J. ShrobonaB.S. Effects of chronic administration of aluminum chloride on reproductive functions of testis and some accessory sex organs of male mice. Indian.J. Env. Toxi.1997711215
    [Google Scholar]
  25. BrooksD.E. HigginsS.J. Characterization and androgen-dependence of proteins associated with luminal fluid and spermatozoa in the rat epididymis.Reproduction198059236337510.1530/jrf.0.0590363 7431293
    [Google Scholar]
  26. BedwalR.S. EdwardsM.S. KatochM. BahugunaA. DewanR. Histological and biochemical changes in testis of zinc deficient BALB/c strain of mice.Indian J. Exp. Biol.1994324243247 8088879
    [Google Scholar]
  27. BoneW. JonesN.G. KampG. YeungC.H. CooperT.G. Effect of ornidazole on fertility of male rats: Inhibition of a glycolysis-related motility pattern and zona binding required for fertilization in vitro.Reproduction2000118112713510.1530/reprod/118.1.127 10793634
    [Google Scholar]
  28. LohiyaN.K. AnsariA.S. Male contraceptive agents.Comparative Endocrinology and Reproduction; Joy,. KrishnaK.P. KrishnaA. HaldarC. New DelhiNarosa Publishing House1999260277
    [Google Scholar]
  29. ShanY. ZhaoJ. WeiK. JiangP. XuL. ChangC. XuL. ShiY. ZhengY. BianY. ZhouM. SchrodiS.J. GuoS. HeD. A comprehensive review of Tripterygium wilfordii hook. f. in the treatment of rheumatic and autoimmune diseases: Bioactive compounds, mechanisms of action, and future directions.Front. Pharmacol.202314128261010.3389/fphar.2023.1282610 38027004
    [Google Scholar]
  30. ChangZ. QinW. ZhengH. ScheggK. HanL. LiuX. WangY. WangZ. McSwigginH. PengH. YuanS. WuJ. WangY. ZhuS. JiangY. NieH. TangY. ZhouY. HitchcockM.J.M. TangY. YanW. Triptonide is a reversible non-hormonal male contraceptive agent in mice and non-human primates.Nat. Commun.2021121125310.1038/s41467‑021‑21517‑5 33623031
    [Google Scholar]
  31. WangJ. WangH. TaiF. Effects of Tripterygium wilfordii multiglycosides on sex hormones and receptors in mandarin vole Leydig cells.Anim. Biol. Leiden Neth.201262221722910.1163/157075611X618174
    [Google Scholar]
  32. Al-AssarN.B. KhattakM.N.K. MashwaniZ.R. KananS. UllahI. AliU. KhanA.A. Phytochemical profile and antiproliferative activities of acetone extracts of Asplenium polypodioides Blume. and A. dalhousiae Hook. in MDA-MB-231 breast cancer cells.Saudi J. Biol. Sci.202128116324633110.1016/j.sjbs.2021.06.098 34764753
    [Google Scholar]
  33. DavidM. AinQ. AhmadM. ZamanW. JahanS. A biochemical and histological approach to study antifertility effects of methanol leaf extract of Asplenium dalhousiae Hook. in adult male rats.Andrologia2019516e1326210.1111/and.13262 30838702
    [Google Scholar]
  34. UdosenI.R. OsuS.R. Phytochemistry, and effects of Telfairia occidentalis Leaf extracts on the growth and haematological properties of wistar albino rats.J. Appl. Sci. Environ. Manag.202226231732210.4314/jasem.v26i2.20
    [Google Scholar]
  35. NjokuR-C.C. AbarikwuS.O. UwakweA.A. Mgbudom-OkahC.J. Telfairia occidentalis supplemented diet induces changes in sperm parameters and testosterone level in rats.Andrologia2018507e1304410.1111/and.13044 29761541
    [Google Scholar]
  36. Al-SnafiA.E. The pharmacological activities of Cuminum cyminum-A review.IOSR J. Pharm.2016664665
    [Google Scholar]
  37. SaxenaP. GuptaR. GuptaR.S. Contraceptive studies of isolated fractions of Cuminum cyminum in male albino rats.Nat. Prod. Res.201529242328233110.1080/14786419.2015.1008473 25675391
    [Google Scholar]
  38. SandhirR. KhuranaM. SinghalN.K. Potential benefits of phytochemicals from Azadirachta indica against neurological disorders.Neurochem. Int.202114610502310.1016/j.neuint.2021.105023 33753160
    [Google Scholar]
  39. ShaikhM.A. NaqviS.N.H. ChaudhryM.Z. Effect of neem oil on the structure and function of the mature male albino rat testes.Braz. J. Morphol. Sci.20092614954
    [Google Scholar]
  40. OsagieO.A. IgbinogunU. OkohO.J. OriakhiK. Phytochemical composition, in vitro antioxidant and antimicrobial activities of methanol extract of cheese wood (Alstonia boonei) Leaves collected from Benin City, Nigeria.J. Appl. Sci. Environ. Manag.202327102283228910.4314/jasem.v27i10.20
    [Google Scholar]
  41. RajiY. SalmanT.M. AkinsomisoyeO.S. Reproductive functions in male rats treated with methanolic extract of Alstonia boonei stem bark.Afr. J. Biomed. Res.200587105111Available from: https://hdl.handle.net/1807/7342
    [Google Scholar]
  42. MonikaS. ThirumalM. KumarP.R. Phytochemical and biological review of Aegle marmelos Linn.Future Sci. OA202393FSO84910.2144/fsoa‑2022‑0068 37026028
    [Google Scholar]
  43. ChauhanA. AgarwalM. KushwahaS. MutrejaA. Antifertility studies of Aegle marmelos Corr., an Indian medicinal plant on male albino rats.Egypt. J. Biol.20081012835
    [Google Scholar]
  44. TuduC.K. DuttaT. GhoraiM. BiswasP. SamantaD. OleksakP. JhaN.K. KumarM. Radha ProćkówJ. Pérez de la LastraJ.M. DeyA. Traditional uses, phytochemistry, pharmacology and toxicology of garlic (Allium sativum), a storehouse of diverse phytochemicals: A review of research from the last decade focusing on health and nutritional implications.Front. Nutr.2022994955410.3389/fnut.2022.929554 36386956
    [Google Scholar]
  45. HammamiI. AmaraS. BenahmedM. El MayM.V. MauduitC. Chronic crude garlic-feeding modified adult male rat testicular markers: Mechanisms of action.Reprod. Biol. Endocrinol.2009716510.1186/1477‑7827‑7‑65 19552815
    [Google Scholar]
  46. HossenM.F. NijhuR.S. KhatunA. A phytochemical and pharmacological review on Dalbergia sissoo: A potential medicinal plant.J. Pharmacogn. Phytochem.2023121525710.22271/phyto.2023.v12.i1a.14557
    [Google Scholar]
  47. VermaH.P. SinghS.K. Effect of aqueous leaf extract of Dalbergia sissoo Roxb. on spermatogenesis and fertility in male mice.Eur. J. Contracept. Reprod. Health Care201419647548610.3109/13625187.2014.945165 25112407
    [Google Scholar]
  48. MansourR.B. WasliH. BourgouS. KhamessiS. KsouriR. Megdiche-KsouriW. CardosoS.M. Insights on Juniperus phoenicea essential oil as potential anti-proliferative, anti-tyrosinase, and antioxidant candidate.Molecules20232822754710.3390/molecules28227547 38005268
    [Google Scholar]
  49. ShkukaniH.G. SalhabA.S. DisiA.M. ShomafM.S. QuadanF.A. Antifertility effect of ethanolic extract of Juniperus phoenica (L.) in male albino rats.J. Herb. Pharmacother.200873-417918910.1080/15228940802152463 18928140
    [Google Scholar]
  50. DalviT.S. KarandeA.V. JaiswalR.S. PandeyK.K. ShahN.J. Mimusops elengi-Ethnobotanical knowledge, phytochemical studies, pharmacological aspect and future prospects.Int. J. App. Chem. Bio. Sci2022315063Available from: https://identifier.visnav.in/1.0001/ijacbs-21k-23006/
    [Google Scholar]
  51. SinghN. SinghS.K. Aqueous fruit extract of Mimusops elengi causes reversible suppression of spermatogenesis and fertility in male mice.Andrologia201648780781610.1111/and.12516 27489141
    [Google Scholar]
  52. AsifH.M. SultanaS. AkhtarN. A panoramic view on phytochemical, nutritional, ethanobotanical uses and pharmacological values of Trachyspermum ammi Linn.Asian Pac. J. Trop. Biomed.20144S545S55310.12980/APJTB.4.2014APJTB‑2014‑0242
    [Google Scholar]
  53. KumarM.S. Rameswara ReddyR.R. ManasaG. VanajaP. SirishaG. AstalakshmiN. Antifertility effect of Trachyspermum ammi (Linn) sprague fruits on male rats.Int. J. Pharm. Biol. Arch.201122705709
    [Google Scholar]
  54. SekarK. BharathiR.V. FrancoS.R.A. RadhaR. Review on the pharmacognostical, phytochemical and pharmacological aspects of Tabernaemontana coronaria.Indian J. Pharm. Sci.202486240710.36468/pharmaceutical‑sciences.1291
    [Google Scholar]
  55. JainS. JainA. PaliwalP. SolankiS.S. Antifertility effect of chronically administered Tabernaemontana divaricata leaf extract on male rats.Asian Pac. J. Trop. Med.20125754755110.1016/S1995‑7645(12)60096‑0 22647817
    [Google Scholar]
  56. GaraniyaN. BapodraA. Ethno botanical and Phytophrmacological potential of Abrus precatorius L.: A review.Asian Pac. J. Trop. Biomed.20144Suppl. 1S27S3410.12980/APJTB.4.2014C1069 25183095
    [Google Scholar]
  57. JahanS. SaeedN. IjlalF. KhanM.A. AhmadM. ZafarM. AbbasiA.M. Histomorphological study to evaluate anti-fertility effect of Abrus precatorius L. in adult male mice.J. Med. Plants Res.20093121029103310.5897/JMPR.9000705
    [Google Scholar]
  58. SinghN. JaiswalJ. TiwariP. SharmaB. Phytochemicals from citrus limon juice as potential antibacterial agents.Open Bioactive Compd. J.2020811610.2174/1874847302008010001
    [Google Scholar]
  59. PetricevichV.L. Abarca-VargasR. Allamanda cathartica: A review of the phytochemistry, pharmacology, toxicology, and biotechnology.Molecules2019247123810.3390/molecules24071238 30934947
    [Google Scholar]
  60. SinghA. SinghS.K. Reversible antifertility effect of aqueous leaf extract of Allamanda cathartica L. in male laboratory mice.Andrologia200840633734510.1111/j.1439‑0272.2008.00866.x 19032682
    [Google Scholar]
  61. GroverM. BehlT. SehgalA. SinghS. SharmaN. VirmaniT. RachamallaM. FarasaniA. ChigurupatiS. AlsubayielA.M. FelembanS.G. SandujaM. BungauS. In vitro phytochemical screening, cytotoxicity studies of Curcuma longa extracts with isolation and characterisation of their isolated compounds.Molecules20212624750910.3390/molecules26247509 34946592
    [Google Scholar]
  62. MishraR.K. SinghS.K. Reversible antifertility effect of aqueous rhizome extract of Curcuma longa L. in male laboratory mice.Contraception200979647948710.1016/j.contraception.2009.01.001 19442785
    [Google Scholar]
  63. SasikalaP. GanesanS. JayaseelanT. AzhagumadhavanS. PadmaM. SenthilkumarS. ManiP. Phytochemicals and GC–MS analysis of bioactive compounds present in ethanolic leaves extract of Taraxacum officinale (L).J. Drug Deliv. Ther.201991909410.22270/jddt.v9i1.2175
    [Google Scholar]
  64. TahtamouniL.H. AlqurnaN.M. Al-HudhudM.Y. Al-HajjH.A. Dandelion (Taraxacum officinale) decreases male rat fertility in vivo.J. Ethnopharmacol.2011135110210910.1016/j.jep.2011.02.027 21354287
    [Google Scholar]
  65. RajeV.N. YadavA.V. ShelarP.A. Coccinia indica-A phytopharmacological review.Res. J. Pharmacogn. Phytochem201351914
    [Google Scholar]
  66. VermaH.P. SinghS.K. Antifertility efficacy of Coccinia indica in male mice and its possible mechanisms of action on spermatogenesis.Gen. Comp. Endocrinol.2017241899910.1016/j.ygcen.2016.05.007 27174748
    [Google Scholar]
  67. BagliniE. SalernoS. BarresiE. RobelloM. Da SettimoF. TalianiS. MariniA.M. Multiple Topoisomerase I (TopoI), Topoisomerase II (TopoII) and Tyrosyl-DNA Phosphodiesterase (TDP) inhibitors in the development of anticancer drugs.Eur. J. Pharm. Sci.202115610559410.1016/j.ejps.2020.105594 33059042
    [Google Scholar]
  68. YangZ. YeW. WangL. GuoY. XueS. Antifertility effects of orally administration of low dose gossypol acetic acid combined with methyltestosterone plus ethinyl estradiol on male rat.Reprod. Contracept.200819420121010.1016/S1001‑7844(08)60022‑X
    [Google Scholar]
  69. NilaK.M. KarthikeyanJ. Phytochemical profiling, antibacterial potential and GC-MS analysis of methanol leaf extract of Enicostemma axillare.Int. J. Curr. Microbiol. Appl. Sci.2017672688269510.20546/ijcmas.2017.607.378
    [Google Scholar]
  70. DhanapalR. RatnaJ.V. GuptaM. SarathchandranI. Preliminary study on antifertility activity of Enicostemma axillare leaves and Urena lobata root used in Indian traditional folk medicine.Asian Pac. J. Trop. Med.20125861662210.1016/S1995‑7645(12)60127‑8 22840449
    [Google Scholar]
  71. BabuS.S. MadhuriD.B. AliS.L. A pharmacological review of Urena lobata plant.Asian J. Pharm. Clin. Res.2016922022Available from: https://journals.innovareacademics.in/index.php/ajpcr/article/view/10011
    [Google Scholar]
  72. RahulC. PankajP. SarwanS.K. MaheshJ.K. Phytochemical screening and antimicrobial activity of Albizzia lebbeck.J. Chem. Pharm. Res.201025476484Available from: http://jocpr.com/vol2-iss5-2010/JCPR-2010-2-5-476-484.pdf
    [Google Scholar]
  73. GuptaR.S. KachhawaJ.B. ChaudharyR. Antifertility effects of methanolic pod extract of Albizzia lebbeck (L.) Benth in male rats.Asian J. Androl.200462155159 15154091
    [Google Scholar]
  74. DasP. SrivastavA.K. Phytochemical extraction and characterization of the leaves of Aloe vera barbadensis for its anti-bacterial and anti-oxidant activity.Int. J. Sci. Res.201546658661Available from: https://api.semanticscholar.org/CorpusID:21658287
    [Google Scholar]
  75. OyewopoA.O. OremosuA.A. AkangE.N. NoronhaC.C. OkanlawonA.O. Effects of Aloe vera (Aloe barbadensis) aqueous leaf extract on testicular weight, sperm count and motility of adult male Sprague-Dawley rats.J. Am. Sci.2011743134Available from: https://api.semanticscholar.org/CorpusID:31281970
    [Google Scholar]
  76. SzewczykA. MarinoA. MolinariJ. EkiertH. MiceliN. Phytochemical characterization, and antioxidant and antimicrobial properties of agitated cultures of three rue species: Ruta chalepensis, Ruta corsica, and Ruta graveolens.Antioxidants202211359210.3390/antiox11030592 35326242
    [Google Scholar]
  77. SailaniM.R. MoeiniH. Effect of Ruta graveolens and Cannabis sativa alcoholic extract on spermatogenesis in the adult wistar male rats.Indian J. Urol.200723325726010.4103/0970‑1591.33720 19718326
    [Google Scholar]
  78. PatilN. ChandelV. RanaA. JainM. KaushikP. Investigation of Cannabis sativa phytochemicals as anti-Alzheimer’s agents: An in silico study.Plants202312351010.3390/plants12030510 36771595
    [Google Scholar]
  79. GangaramS. NaidooY. DewirY.H. El-HendawyS. Phytochemicals and biological activities of Barleria (Acanthaceae).Plants20211118210.3390/plants11010082 35009086
    [Google Scholar]
  80. VermaP.K. SharmaA. JoshiS.C. GuptaR.S. DixitV.P. Effect of isolated fractions of Barleria prionitis root methanolic extract on reproductive function of male rats: Preliminary study.Fitoterapia200576542843210.1016/j.fitote.2005.03.007 15964711
    [Google Scholar]
  81. ShahA.J. GilaniA.H. Blood pressure lowering effect of the extract of aerial parts of Capparis aphylla is mediated through endothelium-dependent and independent mechanisms.Clin. Exp. Hypertens.201133747047710.3109/10641963.2010.549273 21978026
    [Google Scholar]
  82. SarathchandiranI. ManavalanR. AkbarshaM.A. KadalmaniB. KararP.K. Studies on spermatotoxic effect of ethanolic extract of Capparis aphylla (Roth).J. Biol. Sci.20077354454810.3923/jbs.2007.544.548
    [Google Scholar]
  83. SharmaA. SharmaR. SharmaM. KumarM. BarbhaiM.D. LorenzoJ.M. SharmaS. SamotaM.K. AtanassovaM. CarusoG. NaushadM. Radha ChandranD. PrakashP. HasanM. RaisN. DeyA. MahatoD.K. DhumalS. SinghS. SenapathyM. RajalingamS. VisvanathanM. SaleenaL.A.K. MekhemarM. Carica papaya L. leaves: Deciphering its antioxidant bioactives, biological activities, innovative products, and safety aspects.Oxid. Med. Cell. Longev.20222022112010.1155/2022/2451733 35720184
    [Google Scholar]
  84. AkinloyeO.O. MorayoO.M. Evaluation of andrological indices and testicular histology following chronic administration of aqueous extract of Carica papaya leaf in Wistar rat.Afr. J. Pharm. Pharmacol.20104252255
    [Google Scholar]
  85. VermaR.J. NambiarD. ChinoyN.J. Toxicological effects of Carica papaya seed extract on spermatozoa of mice.J. Appl. Toxicol.200626653353510.1002/jat.1173 17080407
    [Google Scholar]
  86. JiraungkoorskulW. SirinthipapornA. Wound healing property review of siam weed, Chromolaena odorata.Pharmacogn. Rev.20171121353810.4103/phrev.phrev_53_16 28503052
    [Google Scholar]
  87. YakubuM.T. AkanjiM.A. OladijiA.T. Evaluation of antiandrogenic potentials of aqueous extract of Chromolaena odoratum (L.) K. R. leaves in male rats.Andrologia200739623524310.1111/j.1439‑0272.2007.00792.x 18076423
    [Google Scholar]
  88. ZhengM.S. LiuY.S. YuanT. LiuL.Y. LiZ.Y. HuangX.L. Research progress on chemical constituents of Citrullus colocynthis and their pharmacological effects.Zhongguo Zhongyao Zazhi202045481682410.19540/j.cnki.cjcmm.20191104.201 32237481
    [Google Scholar]
  89. MaliP.C. ChaturvediM. AnsariA.S. DixitV.P. Antispermatogenic effects of an ethanol extract of Citrullus colocynthis root in male albino rats.Pharm. Biol.200139211311910.1076/phbi.39.2.113.6259
    [Google Scholar]
  90. KumarD. SinglaR.K. SharmaR. SharmaP. KumarL. KaurN. DhawanR.K. SharmaS. DuaK. Phytochemistry and polypharmacological potential of Colebrookea oppositifolia smith.Curr. Top. Med. Chem.202323533434810.2174/1568026623666221202112414 36476430
    [Google Scholar]
  91. GuptaR.S. YadavR.K. DixitV.P. DobhalM.P. Antifertility studies of Colebrookia oppositifolia leaf extract in male rats with special reference to testicular cell population dynamics.Fitoterapia200172323624510.1016/S0367‑326X(00)00311‑7 11295299
    [Google Scholar]
  92. Gonçalves PereiraR.C. Gontijo EvangelistaF.C. dos Santos JúniorV.S. de Paula SabinoA. Gonçalves MaltarolloV. de FreitasR.P. Pains DuarteL. Cytotoxic activity of triterpenoids from Cheiloclinium cognatum branches against chronic and acute leukemia cell Lines.Chem. Biodivers.20201712e200077310.1002/cbdv.202000773 33108694
    [Google Scholar]
  93. de Oliveira MaiaL. de CarvalhoR.K. dos Santos MartinsJ. PerilloM. LaversN. de SousaP.V. LiãoL.M. AndersenM.L. CostaF.O. Mazaro-CostaR. Antispermatogenic effects of Cheiloclinium cognatum (Celastraceae).Rev. Bras. Plantas Med.201820338346
    [Google Scholar]
  94. Al-SnafiA.E. The contents and pharmacology of Crotalaria juncea-A review.IOSR J. Pharm.2016667786Available from: https://api.semanticscholar.org/CorpusID:212598445
    [Google Scholar]
  95. VijaykumarB. SangamaI. SharanabasappaA. PatilS.B. Antifertility activity of various extracts of Crotalaria juncea, Linn., seeds in male mice.Philipp. J. Sci.200313213946
    [Google Scholar]
  96. ManthriS. KotaC.S. TalluriM. PradeshA. Pharmacognostic, phytochemical and pharmacological review of Dendrophthoe falcata.Rev. Am. Soc.201131825Available from: https://updatepublishing.com/journal/index.php/jp/article/view/2222
    [Google Scholar]
  97. GuptaR.S. KachhawaJ.B.S. SharmaA. Effect of methanolic extract of Dendrophthoe falcata stem on reproductive function of male albino rats.J. Herb. Pharmacother.20087211310.1080/J157v07n02_01 18285304
    [Google Scholar]
  98. OsmanA.G. AliZ. OluwasesanB.M. KamdemR.S. KhanI.A. Chemical constituents from fadogia agrestis.Planta Med.2016825PC56
    [Google Scholar]
  99. YakubuM.T. AkanjiM.A. OladijiA.T. Effects of oral administration of aqueous extract of Fadogia agrestis (Schweinf. Ex Hiern) stem on some testicular function indices of male rats.J. Ethnopharmacol.2008115228829210.1016/j.jep.2007.10.004 18023305
    [Google Scholar]
  100. ThomasS.D. Leptadenia hastata: A review of its traditional uses and its pharmacological activity.Med. Chem.2012214815010.4172/2161‑0444.1000132
    [Google Scholar]
  101. BayalaB. TelefoP.B. BassoleI.H.N. TambouraH.H. BelemtougrR.G. SawadogoL. MalpauxB. DacheuxJ.L. Anti-spermatogenic activity of Leptadenia hastata (Pers.) Decne leaf stems aqueous extracts in male Wistar rats.J. Pharma. Toxic.20116439139910.3923/jpt.2011.391.399
    [Google Scholar]
  102. MazumderP.M. JhaD. Biological, chemical and pharmacological aspects of Madhuca longifolia.Asian Pac. J. Trop. Med.201811191410.4103/1995‑7645.223528
    [Google Scholar]
  103. GopalkrishnanB. ShimpiS.N. Antifertility effect of Madhuca latifolia (ROXB.) macbride seed extract.Int. J. Appl. Biol. Pharm. Technol.2011244953
    [Google Scholar]
  104. LodhiS. JainA. JainA.P. PawarR.S. SinghaiA.K. Effects of flavonoids from Martynia annua and Tephrosia purpurea on cutaneous wound healing.Avicenna J. Phytomed.201665578591 27761428
    [Google Scholar]
  105. MaliP.C. AnsariA.S. ChaturvediM. Antifertility effect of chronically administered Martynia annua root extract on male rats.J. Ethnopharmacol.2002822-3616710.1016/S0378‑8741(02)00084‑3 12241978
    [Google Scholar]
  106. NazimM. SadiqQ-U-A. NawazA. AnjumS. AliM. MaryamH. Mentha arvensis, a medicinal and aromatic plant, has high nutritional value and several-uses: A review.Buletin Agroteknologi202012374910.32663/ba.v1i2.1180
    [Google Scholar]
  107. SharmaN. JocobD. Antifertility investigation and toxicological screening of the petroleum ether extract of the leaves of Mentha arvensis L. in male albino mice.J. Ethnopharmacol.200175151210.1016/S0378‑8741(00)00362‑7 11282436
    [Google Scholar]
  108. WatchoP. DefoP.B.D. Wankeu-NyaM. Carro-JuarezM. NguelefackT.B. KamanyiA. Mondia whitei (Periplocaceae) prevents and Guibourtia tessmannii (Caesalpiniaceae) facilitates fictive ejaculation in spinal male rats.BMC Complement. Altern. Med.2013131410.1186/1472‑6882‑13‑4 23295154
    [Google Scholar]
  109. WatchoP. KamtchouingP. SokengS. MoundipaP.F. TantchouJ. EssameJ.L. KouetaN. Reversible antispermatogenic and antifertility activities of Mondia whitei L. in male albino rat.Phytother. Res.2001151262910.1002/1099‑1573(200102)15:1<26::AID‑PTR679>3.0.CO;2‑N 11180518
    [Google Scholar]
  110. AdeleyeO.O. AyeniO.J. AjamuM.A. Traditional and medicinal uses of Morinda lucida.J. Med. Plants Stud.201862249254
    [Google Scholar]
  111. RajiY. AkinsomisoyeO.S. SalmanT.M. Antispermatogenic activity of Morinda lucida extract in male rats.Asian J. Androl.20057440541010.1111/j.1745‑7262.2005.00051.x 16281089
    [Google Scholar]
  112. BorahR. BiswasS.P. Tulsi (Ocimum sanctum), excellent source of phytochemicals.Int. J. Environ. Agric. Biotechnol.20183526525810.22161/ijeab/3.5.21
    [Google Scholar]
  113. SethiJ. YadavM. SoodS. DahiyaK. SinghV. Effect of tulsi (Ocimum Sanctum Linn.) on sperm count and reproductive hormones in male albino rabbits.Int. J. Ayurveda Res.20101420821010.4103/0974‑7788.76782 21455446
    [Google Scholar]
  114. KumarS.S. PaulyS. GS. Phytochemical screening of inflorescence of Piper betle.Int. J. Curr. Pharm. Res.2020126899210.22159/ijcpr.2020v12i6.40299
    [Google Scholar]
  115. SarkarM. GangopadhyayP. BasakB. ChakrabartyK. BanerjiJ. AdhikaryP. ChatterjeeA. The reversible antifertility effect of Piper betle Linn. on Swiss albino male mice.Contraception200062527127410.1016/S0010‑7824(00)00177‑3 11172798
    [Google Scholar]
  116. ZahinM. BokhariN.A. AhmadI. HusainF.M. AlthubianiA.S. AlruwaysM.W. PerveenK. ShalawiM. Antioxidant, antibacterial, and antimutagenic activity of Piper nigrum seeds extracts.Saudi J. Biol. Sci.20212895094510510.1016/j.sjbs.2021.05.030 34466087
    [Google Scholar]
  117. MishraR.K. SinghS.K. Antispermatogenic and antifertility effects of fruits of Piper nigrum L. in mice.Indian J. Exp. Biol.2009479706714 19957882
    [Google Scholar]
  118. BalkrishnaA. SinghS. SrivastavaD. MishraS. RajputS.K. AryaV. Quassia amara L.: A comprehensive review of its ethnomedicinal uses, phytochemistry, pharmacology and toxicity.J. Phytopharmacol.202211319419910.31254/phyto.2022.11310
    [Google Scholar]
  119. ParveenS. DasS. KundraC.P. PereiraB.M. A comprehensive evaluation of the reproductive toxicity of Quassia amara in male rats.Reprod. Toxicol.2003171455010.1016/S0890‑6238(02)00080‑1 12507657
    [Google Scholar]
  120. KamliM.R. SharafA.A.M. SabirJ.S.M. RatherI.A. Phytochemical screening of Rosmarinus officinalis L. as a potential anticholinesterase and antioxidant-medicinal plant for cognitive decline disorders.Plants202211451410.3390/plants11040514 35214846
    [Google Scholar]
  121. NusierM.K. BatainehH.N. DaradkahH.M. Adverse effects of rosemary (Rosmarinus officinalis L.) on reproductive function in adult male rats.Exp. Biol. Med. (Maywood)2007232680981310.3181/00379727‑232‑2320809 17526773
    [Google Scholar]
  122. BurbureV.S. BahetiA.M. DeshmukhC.D. WaniM.S. MaitreyeeD. Phytochemical and pharmacological profile of cassia tora.J. Hosp. Pharm202015472
    [Google Scholar]
  123. KhanS. MaliP.C. Reversible antifertility effect of Cassia tora Linn in male rats. Int. J. Life-Sci.Sci. Res.2017351415142310.21276/ijlssr.2017.3.5.26
    [Google Scholar]
  124. AnandM. BasavarajuR. A review on phytochemistry and pharmacological uses of Tecoma stans (L.) Juss. ex Kunth.J. Ethnopharmacol.202126511327010.1016/j.jep.2020.113270 32822823
    [Google Scholar]
  125. MathurN. JainG.C. PandeyG. Effect of Tecoma stans leaves on the reproductive system of male albino rats.Int. J. Pharmacol.20106215215610.3923/ijp.2010.152.156
    [Google Scholar]
  126. SobehM. MahmoudM.F. HasanR.A. AbdelfattahM.A.O. OsmanS. RashidH. El-ShazlyA.M. WinkM. Chemical composition, antioxidant and hepatoprotective activities of methanol extracts from leaves of Terminalia bellirica and Terminalia sericea (Combretaceae).PeerJ20197e632210.7717/peerj.6322 30834179
    [Google Scholar]
  127. PatilS.J. SatishagoudaS. VishwanathaT. PatilS.B. Effect of Terminalia bellirica barks extracts on activities of accessory reproductive ducts in male rats.Int. J. Pharm. Sci. Rev. Res.2010127579http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/3548
    [Google Scholar]
  128. BaoJ. DaiS.M. A Chinese herb Tripterygium wilfordii Hook F in the treatment of rheumatoid arthritis: Mechanism, efficacy, and safety.Rheumatol. Int.20113191123112910.1007/s00296‑011‑1841‑y 21365177
    [Google Scholar]
  129. MatlinS.A. BelenguerA. StaceyV.E. QlanS.Z. XuY. ZhangJ.W. SandersJ.K.M. AmorS.R. PearceC.M. Male antifertility compounds from Tripterygium wilfordii Hook F.Contraception199347438740010.1016/0010‑7824(93)90036‑7 8508668
    [Google Scholar]
  130. LomenickB. HaoR. JonaiN. ChinR.M. AghajanM. WarburtonS. WangJ. WuR.P. GomezF. LooJ.A. WohlschlegelJ.A. VondriskaT.M. PelletierJ. HerschmanH.R. ClardyJ. ClarkeC.F. HuangJ. Target identification using drug affinity responsive target stability (DARTS).Proc. Natl. Acad. Sci. USA200910651219842198910.1073/pnas.0910040106 19995983
    [Google Scholar]
  131. ZhangM. MengM. LiuY. QiJ. ZhaoZ. QiaoY. HuY. LuW. ZhouZ. XuP. ZhouQ. Triptonide effectively inhibits triple-negative breast cancer metastasis through concurrent degradation of Twist1 and Notch1 oncoproteins.Breast Cancer Res.202123111610.1186/s13058‑021‑01488‑7 34922602
    [Google Scholar]
  132. SmithG.F. Designing drugs to avoid toxicity.Prog. Med. Chem.20115014710.1016/B978‑0‑12‑381290‑2.00001‑X 21315927
    [Google Scholar]
  133. AbbasM. DavidM. Qurat-Ul-Ain AhmadM. JahanS. In vitro evaluation of contraceptive efficacy of Asplenium dalhousiae Hook. and Mentha longifolia L. on testicular tissues of adult male mice. Austin Pharmacol Pharm., 2019, 4(1), 1020. Available from:https://austinpublishinggroup.com/pharmacology-pharmaceutics/fultext/app-v4-id1020.pdf
    [Google Scholar]
  134. RadhikaN.K. SreejithP.S. AshaV.V. Cytotoxic and apoptotic activity of Cheilanthes farinosa (Forsk.) Kaulf. against human hepatoma, Hep3B cells.J. Ethnopharmacol.2010128116617110.1016/j.jep.2010.01.002 20064591
    [Google Scholar]
  135. NjokuR.C.C. AbarikwuS.O. Antifertility and profertility effects of the leaves and seeds of fluted pumpkin: Sperm quality, hormonal effects and histomorphological changes in the testes of experimental animal models.J. Integr. Med.202119210411010.1016/j.joim.2021.01.007 33518482
    [Google Scholar]
  136. Gagandeep; Dhanalakshmi, S.; Méndiz, E.; Rao, A.R.; Kale, R.K. Chemopreventive effects of Cuminum cyminum in chemically induced forestomach and uterine cervix tumors in murine model systems.Nutr. Cancer200347217118010.1207/s15327914nc4702_10 15087270
    [Google Scholar]
  137. YanJ.H. TangK.W. ZhongM. DengN.H. Determination of chemical components of volatile oil from Cuminum cyminum L. by gas chromatography-mass spectrometry.Se Pu2002206569572 12683011
    [Google Scholar]
  138. GuptaR.S. SaxenaP. GuptaR. KachhawaJ.B.S. Evaluation of reversible contraceptive activities of Cuminum cyminum in male albino rats.Contraception20118419810710.1016/j.contraception.2010.10.013 21664518
    [Google Scholar]
  139. Janika SitasiwiA. IsdadiyantoS. Muflichatun, Mardiati, S. Effect of ethanolic Neem (Azadirachta indica) leaf extract as an herb contraceptive on Hepato-somatic Index of the male mice (Mus musculus). IOP Conf. Series: J. Physics: Conf. Series,201810.1088/1742‑6596/1025/1/012043
    [Google Scholar]
  140. PatilS.M. ShirahattiP.S. v BC.K. RamuR. M NN.P. Azadirachta indica A. Juss (neem) as a contraceptive: An evidence-based review on its pharmacological efficiency.Phytomedicine20218815359610.1016/j.phymed.2021.153596 34092456
    [Google Scholar]
  141. EvansW.C. Trease and Evans Pharmacognosy.15th edEdinburghSaunders2002249
    [Google Scholar]
  142. OzeG. OnyezeG.O. OjiakoO. AbanobiS. OzimsS. OhiriA. Raised serum estrogen and progesterone concentrations in female rats treated with extract of Alstonia boonei (De wild).Int. Res. J. Biochem. Bioinform201226135141
    [Google Scholar]
  143. NwezeE.I. OkaforJ.I. NjokuO. Antimicrobial activities of methanolic extracts of Trema guineensis (Schumm and Thorn) and Morinda lucida Benth used in Nigerian.Bio-Research200421394610.4314/br.v2i1.28540
    [Google Scholar]
  144. BrijeshS. DaswaniP. TetaliP. AntiaN. BirdiT. Studies on the antidiarrhoeal activity of Aegle marmelos unripe fruit: Validating its traditional usage.BMC Complement. Altern. Med.2009914710.1186/1472‑6882‑9‑47 19930633
    [Google Scholar]
  145. BansalY. BansalG. Analytical methods for standardization of Aegle marmelos: A review.J. Pharm. Educ. Res.20112237
    [Google Scholar]
  146. AgrawalS.S. KumarA. GullaiyaS. DubeyV. NagarA. TiwariP. DharP. SinghV. Antifertility activity of methanolic bark extract of Aegle marmelos (l.) in male wistar rats.Daru20122019410.1186/2008‑2231‑20‑94 23351957
    [Google Scholar]
  147. ChauhanA. AgarwalM. Reversible changes in the antifertility induced by Aegle marmelos in male albino rats.Syst Biol Reprod Med200854624024610.1080/19396360802516856 19052962
    [Google Scholar]
  148. D’SouzaU.J. NarayanaK. Induction of seminiferous tubular atrophy by single dose of 5-fluorouracil (5-FU) in Wistar rats.Indian J. Physiol. Pharmacol.20014518794 11211576
    [Google Scholar]
  149. ReiterE. McNamaraM. ClossetJ. HennenG. Expression and functionality of luteinizing hormone/chorionic gonadotropin receptor in the rat prostate.Endocrinology1995136391792310.1210/endo.136.3.7867600 7867600
    [Google Scholar]
  150. BedfordJ.M. Significance of the need for sperm capacitation before fertilization in eutherian mammals.Biol. Reprod.198328110812010.1095/biolreprod28.1.108 6338941
    [Google Scholar]
  151. LohiyaN.K. GoyalR.B. Antifertility investigations on the crude chloroform extract of Carica papaya Linn. seeds in male albino rats.Indian J. Exp. Biol.1992301110511055 1293029
    [Google Scholar]
  152. AmagaseH. PeteschB.L. MatsuuraH. KasugaS. ItakuraY. Intake of garlic and its bioactive components.J. Nutr.20011313955S962S10.1093/jn/131.3.955S 11238796
    [Google Scholar]
  153. MeistrichM.L. SamuelsR.C. Reduction in sperm levels after testicular irradiation of the mouse: A comparison with man.Radiat. Res.1985102113814710.2307/3576437 3983368
    [Google Scholar]
  154. EwingL.L. DavisJ.C. ZirkinB.R. Regulation of testicular function: A spatial and temporal view.Int. Rev. Physiol.19802241115 6248479
    [Google Scholar]
  155. ChaseD.J. KarleJ.A. FoggR.E. Maintenance or stimulation of steroidogenic enzymes and testosterone production in rat Leydig cells by continuous and pulsatile infusions of luteinizing hormone during passive immunization against gonadotrophin-releasing hormone.Reproduction199295365766710.1530/jrf.0.0950657 1404082
    [Google Scholar]
  156. CooperT.G. The epididymis as a site of contraceptive attack. In: Spermatogenesis, Fertilization, Contraception. Molecular, cellular and endocrine events in male reproduction. Schering Foundation Workshop 4; Nieschlag, E.; Habenicht, U.-F., Eds.; Springer Verlag: Berlin, 1992, P. 419-460.10.1007/978‑3‑662‑02815‑5_18
    [Google Scholar]
  157. RaoM.V. Antifertility effects of alcoholic seed extract of Abrus precatorius Linn. in male albino rats.Acta Eur. Fertil.1987183217220 3439410
    [Google Scholar]
  158. SinghA. SinghS.K. Evaluation of antifertility potential of Brahmi in male mouse.Contraception2009791717910.1016/j.contraception.2008.07.023 19041444
    [Google Scholar]
  159. CampêloL.M.L. de AlmeidaA.A.C. de FreitasR.L.M. CerqueiraG.S. de SousaG.F. SaldanhaG.B. FeitosaC.M. de FreitasR.M. Antioxidant and antinociceptive effects of Citrus limon essential oil in mice.BioMed Res. Int.20112011167867310.1155/2011/678673 21660140
    [Google Scholar]
  160. JohannS. OliveiraV.L. PizzolattiM.G. SchripsemaJ. Braz-FilhoR. BrancoA. SmâniaA. Jr Antimicrobial activity of wax and hexane extracts from Citrus spp. peels.Mem. Inst. Oswaldo Cruz2007102668168510.1590/S0074‑02762007000600004 17923995
    [Google Scholar]
  161. KulkarniT.R. BodhankarS.L. SahasrabudheR.A. Reversible anti-fertility effects of lemon seeds (Citrus limonum) in female albino rats.National J. Basic Med. Sci.201223287300
    [Google Scholar]
  162. MishraR.K. SinghS. SinghS.K. Natural products in regulation of male fertility.Indian J. Med. Res.2018148Suppl. 1S107S11410.4103/ijmr.IJMR_1968_17 30964087
    [Google Scholar]
  163. NoraH. Rajuddin Hafizudin SuhandaR. IndirayaniI. Curcumin, a potential oral herbal male contraceptive: A review article.Bali Med. J.2022121828610.15562/bmj.v12i1.3937
    [Google Scholar]
  164. NazR.K. Can curcumin provide an ideal contraceptive?Mol. Reprod. Dev.201178211612310.1002/mrd.21276 21337449
    [Google Scholar]
  165. NazR.K. The effect of curcumin on intracellular pH (pHi), membrane hyperpolarization and sperm motility.J. Reprod. Infertil.20141526270 24918078
    [Google Scholar]
  166. SoleimanzadehA. SaberivandA. Effect of curcumin on rat sperm morphology after the freeze-thawing process.Vet. Res. Forum201343185189 25653795
    [Google Scholar]
  167. TahtamouniL.H. Al-KhateebR.A. AbdellatifR.N. Al-MazaydehZ.A. YasinS.R. Al-GharabliS. ElkarmiA.Z. Anti-spermatogenic activities of Taraxacum officinale whole plant and leaves aqueous extracts.Vet. Res. Forum2016728997 27482352
    [Google Scholar]
  168. OranS.A. Al-EisawiD.M. Check-list of medicinal plants in Jordan.Dirasat Med. Biol. Sci.199825284112
    [Google Scholar]
  169. MontanariT. de CarvalhoJ.E. DolderH. Antispermatogenic effect of Achillea millefolium L. in mice.Contraception199858530931310.1016/S0010‑7824(98)00107‑3 9883387
    [Google Scholar]
  170. KirtikarK.R. BasuB.D. Indian Medicinal Plants.Lalit Mohan Publication: Allahabad1935II13471348
    [Google Scholar]
  171. LiuG.Z. Clinical study of gossypol as a male contraceptive.Reproduccion198153189193 6793420
    [Google Scholar]
  172. WeinbauerG.F. RovanE. FrickJ. Toxicity of gossypol at antifertility dosages in male rats: Statistical analysis of lethal rates and body weight responses.Andrologia198315321322110.1111/j.1439‑0272.1983.tb00361.x 6881556
    [Google Scholar]
  173. CoutinhoE.M. Gossypol: A contraceptive for men.Contraception200265425926310.1016/S0010‑7824(02)00294‑9 12020773
    [Google Scholar]
  174. RajS. Chand MaliS. TrivediR. Green synthesis and characterization of silver nanoparticles using Enicostemma axillare (Lam.) leaf extract.Biochem. Biophys. Res. Commun.201850342814281910.1016/j.bbrc.2018.08.045 30100057
    [Google Scholar]
  175. FagbohunE.D. AsareR.R. EgbebiA.O. Chemical composition and antimicrobial activities of Urena lobata L. (Malvaceae).J. Med. Plants Res.20126122256226010.5897/JMPR09.233
    [Google Scholar]
  176. HandayaniN. GofurA. Effect of Pulutan (Urena lobata l) leaves decoction on the hormone testosterone levels of Balb C Mice (Mus musculus). BIO Web of Conferences,20241170104810.1051/bioconf/202411701048
    [Google Scholar]
  177. HandayaniN. TenzerA. The potency of the decoction of pulutan (Urena lobata l) leaves simplicia as antifertility material based on its effect on uterine development of mice (Mus musculus) Balb C. In: Prosiding 1st National Research Symposium; Universitas Negeri Malang: Malang,2014253257
    [Google Scholar]
  178. HandayaniN. GofurA. The potency of pulutan (Urena lobata l.) Leaves decoction as antifertility based on its effect on uterine development of balb c mice (Mus musculus).J. Kedokt. Hewan (Banda Aceh)201811415315510.21157/j.ked.hewan.v11i4.6261
    [Google Scholar]
  179. HartwellJ.L. Plants used against cancer. A survey.Lloydia1971344386425 5173435
    [Google Scholar]
  180. KastureV.S. ChopdeC.T. DeshmukhV.K. Anticonvulsive activity of Albizzia lebbeck, Hibiscus rosa sinesis and Butea monosperma in experimental animals.J. Ethnopharmacol.2000711-2657510.1016/S0378‑8741(99)00192‑0 10904147
    [Google Scholar]
  181. GuptaR.S. ChaudharyR. YadavR.K. VermaS.K. DobhalM.P. Effect of saponins of Albizia lebbeck (L.) Benth bark on the reproductive system of male albino rats.J. Ethnopharmacol.2005961-2313610.1016/j.jep.2004.07.025 15588647
    [Google Scholar]
  182. BisenP. KarimF. DhurveyV. Impact of Aloe vera consumption on reproductive system: A review.J. Xi’an Univer. Archit. Technol.2024161574580
    [Google Scholar]
  183. MahrousE. AhmedH. Impact of Aloe vera gel aqueous extract-supplemented yogurt on reproductive performance of male rats. SVU-Inter.J. Vet. Sci.202141405310.21608/svu.2021.56520.1096
    [Google Scholar]
  184. McPartlandJ.M. PruittP.L. Side effects of pharmaceuticals not elicited by comparable herbal medicines: The case of tetrahydrocannabinol and marijuana.Altern. Ther. Health Med.1999545762 10394675
    [Google Scholar]
  185. FriedP.A. WatkinsonB. WillanA. Marijuana use during pregnancy and decreased length of gestation.Am. J. Obstet. Gynecol.19841501232710.1016/S0002‑9378(84)80103‑9 6332536
    [Google Scholar]
  186. ChangM.C. BerkeryD. SchuelR. LaychockS.G. ZimmermanA.M. ZimmermanS. SchuelH. Evidence for a cannabinoid receptor in sea urchin sperm and its role in blockade of the acrosome reaction.Mol. Reprod. Dev.199336450751610.1002/mrd.1080360416 8305215
    [Google Scholar]
  187. SinghK.A. GuptaR.S. Antifertility activity of β-sitosterol isolated from Barleria prionitis (L.) roots in male albino rats.Int. J. Pharm. Pharm. Sci.2016858896
    [Google Scholar]
  188. GuptaR.S. KumarP. DixitV.P. DobhalM.P. Antifertility studies of the root extract of the Barleria prionitis Linn in male albino rats with special reference to testicular cell population dynamics.J. Ethnopharmacol.200070211111710.1016/S0378‑8741(99)00150‑6 10771200
    [Google Scholar]
  189. PradhanD.K. MishraM.N. MishraA. PandaA.K. BeheraR.K. JhaS. ChoudhuryS. A comprehensive review of plants used as contraceptives.Int. J. Pharm. Sci. Res.201341148155
    [Google Scholar]
  190. SinghR. KakarS. ShahM. JainR. Some medicinal plants with anti-fertility potential: A current status.J. Basic Clin. Reprod. Sci.201871719
    [Google Scholar]
  191. ChinoyN.J. PadmanP. Antifertility investigations on the benzene extract of Carica papaya seeds in male albino rats.Curr. Res. Med. Aromat. Plants1996183489494
    [Google Scholar]
  192. PrasadM.R. RajalakshmiM. Spermatogenesis and accessory gland secretions.Textbook of Biochemistry and Human Biology19892883
    [Google Scholar]
  193. GanongW.F. Review of medical physiology.Dynamics of Blood and Lymph Flow199530525541
    [Google Scholar]
  194. DuaA. VaidyaS.R. Sperm motility and morphology as changing parameters linked to sperm count variations.J. Postgrad. Med.19964249396 9715307
    [Google Scholar]
  195. BamisayeF.A. AjaniE.O. NurainI.O. MinariJ.B. Medico-botanical investigation of siam weed (Chromolaena odorata) used among the “Ijebu” people of Ogun state, Nigeria.J. Med. Med. Sci.201451202410.14303/jmms.2013.128
    [Google Scholar]
  196. YakubuM.T. Effect of a 60-day oral gavage of a crude alkaloid extract from Chromolaena odorata leaves on hormonal and spermatogenic indices of male rats.J. Androl.20123361199120710.2164/jandrol.111.016287 22653963
    [Google Scholar]
  197. ChaturvediM. MaliP.C. AnsariA.S. Induction of reversible antifertility with a crude ethanol extract of Citrullus colocynthis Schrad fruit in male rats.Pharmacology2003681384810.1159/000068727 12660478
    [Google Scholar]
  198. YadavD.K. Pharmacognostical, phytochemical and pharmacological profile of Colebrookea oppositifolia Smith.J. Drug Deliv. Ther.201996-s23323710.22270/jddt.v9i6‑s.3745
    [Google Scholar]
  199. CarvalhoP.R.F. SilvaD.H.S. BolzaniV.S. FurlanM. Antioxidant quinonemethide triterpenes from Salacia campestris.Chem. Biodivers.20052336737210.1002/cbdv.200590016 17191985
    [Google Scholar]
  200. AllisonA.C. CacabelosR. LombardiV.R.M. ÁlvarezX.A. VigoC. Celastrol, a potent antioxidant and anti-inflammatory drug, as a possible treatment for Alzheimer’s disease.Prog. Neuropsychopharmacol. Biol. Psychiatry20012571341135710.1016/S0278‑5846(01)00192‑0 11513350
    [Google Scholar]
  201. MannowetzN. MillerM.R. LishkoP.V. Regulation of the sperm calcium channel CatSper by endogenous steroids and plant triterpenoids.Proc. Natl. Acad. Sci. USA2017114225743574810.1073/pnas.1700367114 28507119
    [Google Scholar]
  202. VijaykumarB. SangammaI. SharanabasappaA. PatilS.B. Antispermatogenic and hormonal effects of Crotalaria juncea Linn. seed extracts in male mice.Asian J. Androl.2004616770 15064837
    [Google Scholar]
  203. 2 The Wealth of India. Raw Materials; PID (CSIR): New Delhi1952334
  204. ChopraR.N. NayarS.L. Glossary of Indian medicinal plants; Coun. Sci. Ind. Res.,1956
    [Google Scholar]
  205. GuptaR.S. KachhawaJ.B.S. Evaluation of contraceptive activity of methanol extract of Dendrophthoe falcata stem in male albino rats.J. Ethnopharmacol.2007112121521810.1016/j.jep.2007.02.022 17446020
    [Google Scholar]
  206. YakubuM.T. AkanjiM.A. OladijiA.T. Aphrodisiac potentials of the aqueous extract of Fadogia agrestis (Schweinf. Ex Hiern) stem in male albino rats.Asian J. Androl.20057439940410.1111/j.1745‑7262.2005.00052.x 16281088
    [Google Scholar]
  207. YakubuM.T. OladijiA.T. AkanjiM.A. Evaluation of biochemical indices of male rat reproductive function and testicular histology in wistar rats following chronic administration of aqueous extract of Fadogia agrestis (Schweinf. Ex Heirn) stem.Afr. J. Biochem. Res.200717156163
    [Google Scholar]
  208. BayalaB. Pellicer-RM.T. BassoleI.H.N. BelemtougrR. TambouraH.H. MalpauxB. Effects of aqueous extracts of Leptadenia hastata (Pers.) Decne. (Asclepediaceae) on male reproductive functions using castrated immature rats.Res. J. Med. Plant20115218018810.3923/rjmp.2011.180.188
    [Google Scholar]
  209. ShivabasavaiahS. RamH.K. PavanaT. RamyashreeM. RamyaM.C. ManjunathR. Antifertility effects of Madhuca indica leaves in male Swiss albino rats.J. Pharm. Res.201142323326
    [Google Scholar]
  210. DaniyalM. AkramM. Antifertility activity of medicinal plants.J. Chin. Med. Assoc.201578738238810.1016/j.jcma.2015.03.008 25921562
    [Google Scholar]
  211. TreaseG.E. EvansW.C. Pharmacognosy, 12th ed; Elsevier Health Sciences London: Balliere Tindal,1983
    [Google Scholar]
  212. ThawkarB.S. Phytochemical and pharmacological review of Mentha arvensis.Int. J. Green Pharm.201610210.22377/ijgp.v10i2.643
    [Google Scholar]
  213. SharmaN. JacobD. Assessment of reversible contraceptive efficacy of methanol extract of Mentha arvensis L. leaves in male albino mice.J. Ethnopharmacol.200280191310.1016/S0378‑8741(01)00364‑6 11891081
    [Google Scholar]
  214. MathurR. Fructolysis effect of 50% ethanolic extract of Mentha arvensis Linn. (leaves) in seminal vesicles of rat.Acta Eur. Fertil.1991224219220 1844325
    [Google Scholar]
  215. KanjanapothiD. SmitasiriY. PanthongA. TaesotikulT. RattanapanoneV. Postcoital antifertility effect of.Contraception198124555956710.1016/0010‑7824(81)90059‑7 7318436
    [Google Scholar]
  216. AustinC.R. ShortR.V., Eds.; Hormonal control of reproduction.Cambridge University Press19847690
    [Google Scholar]
  217. DixitV.P. BhargavaS.K. Reversible contraception like activity of embelin in male dogs (Canis indicus Linn).Andrologia198315548649410.1111/j.1439‑0272.1983.tb00174.x 6316811
    [Google Scholar]
  218. MabongaC. KamauD. KagiraJ. AlkizimF. NandwaA. Effects of Mondia Whitei ‘Mukombero’ on Sperm Parameters in Male Albino Rats.Africa Environ. Rev. J.201932586910.2200/aerj.v3i2.168
    [Google Scholar]
  219. KhannaS. GuptaS.R. GroverJ.K. Effect of long term feeding of tulsi (Ocimum sanctum Linn) on reproductive performance of adult albino rats.Indian J. Exp. Biol.1986245302304 3770821
    [Google Scholar]
  220. KasinathanS. RamakrishnanS. BasuS.L. Antifertility effect of Ocimum sanctum L.Indian J. Exp. Biol.19721012325 4344433
    [Google Scholar]
  221. SethS.D. JohriN. SundaramK.R. Antispermatogenic effect of Ocimum sanctum.Indian J. Exp. Biol.19811910975976 7309144
    [Google Scholar]
  222. ReddyP.R.K. RaoJ.M. Reversible antifertility action of testosterone propionate in human males.Contraception19725429530110.1016/0010‑7824(72)90068‑6 4650654
    [Google Scholar]
  223. MadhumitaM. GuhaP. NagA. Extraction of betel leaves (Piper betle L.) essential oil and its bio-actives identification: Process optimization, GC-MS analysis and anti-microbial activity.Ind. Crops Prod.201913811157810.1016/j.indcrop.2019.111578
    [Google Scholar]
  224. TewariP.V. ChaturvediC. DixitS.N. Antifertility effect of betal leaf stalk (Tambul patrabrint): A preliminary experimental study.J. Res. Indian Med.197042143151 12305561
    [Google Scholar]
  225. SharmaJ.D. SharmaL. YadavP. Antifertility efficacy of Piper betle Linn. (Petiole) on female albino rats.Asian J. Exp. Sci.2007211145150
    [Google Scholar]
  226. BiswalS. Phytochemical analysis and a study on the antiestrogenic antifertility effect of leaves of Piper betel in female albino rat.Anc. Sci. Life2014341162210.4103/0257‑7941.150770 25737606
    [Google Scholar]
  227. ShahS.K. JhadeD.N. Evaluation of antifertility potential of Piper betle (Petiole) on female wistar rats “rising approaches of herbal contraception”.Biochem. Biophys. Rep.2018159710210.1016/j.bbrep.2018.08.001 30128361
    [Google Scholar]
  228. AminS.A. BhattacharyaP. BasakS. GayenS. NandyA. SahaA. Pharmacoinformatics study of Piperolactam A from Piper betle root as new lead for non steroidal anti fertility drug development.Comput. Biol. Chem.20176721322410.1016/j.compbiolchem.2017.01.004 28160639
    [Google Scholar]
  229. ZodapeG.V. GaikwadV.S. Effect of Piper Nigrum (Linn.) on infertility induced by ethionamide and para amino salicylic acid in female sprague –dawley rats.Biomed. Pharmacol. J.20201321029103510.13005/bpj/1972
    [Google Scholar]
  230. KanediM. The effect of fruit extracts of black pepper on the fertility potential of male albino rats.American J. Med. Biol. Res.2016311410.12691/ajmbr‑4‑1‑1
    [Google Scholar]
  231. Duke’s Phytochemical and Ethnobotanical Databases. 2024. Available from:https://phytochem.nal.usda.gov/phytochem/plants/show/6452
  232. FaisalK. ParveenS. RajendranR. GirijaR. PeriasamyV.S. KadalmaniB. PuratchikodyA. RuckmaniK. PereiraB.M. AkbarshaM.A. Male reproductive toxic effect of Quassia amara: Observations on mouse sperm.J. Endocrinol. Reprod.20061016669Available from:https://www.informaticsjournals.com/index.php/jer/article/view/61
    [Google Scholar]
  233. NjarV. AlaoT. OkogunJ. RajiY. BolarinwaA. NdukaE. Antifertility activity of Quassia amara: Quassin inhibits the steroidogenesis in rat Leydig cells in vitro.Planta Med.199561218018210.1055/s‑2006‑958044 7753928
    [Google Scholar]
  234. RajiY. BolarinwaA.F. Antifertility activity of Quassia amara in male rats - in vivo study.Life Sci.199761111067107410.1016/S0024‑3205(97)00615‑2 9307052
    [Google Scholar]
  235. Ali HasanS. Al-RikabyA.A. Evaluating the influence of Rosemary Leaves extract on hormonal and histopathological alterations in male rabbits exposed to cypermethrin.Arch. Razi Inst.202378379780510.22092/ari.2022.359859.2487 38028826
    [Google Scholar]
  236. KhanS. MaliP.C. Evaluation of antiandrogenic effects in castrated rats treated with Cassia tora extract.SSR Inst. Int. J. Life Sci.2019522259226810.21276/SSR‑IIJLS.2019.5.2.8
    [Google Scholar]
  237. Anish BabuV.B. AntonyV.T. BinuT. Ethno-pharmacological potentialities of some ornamental plants in the family Bignoniaceae.J. Med. Plants Stud.201535135140
    [Google Scholar]
  238. SatishgoudS. SharangoudaV.T. PatilS.B. Contraceptive effect of Terminalia bellirica (Bark) extract on male albino rats.Pharmacologyonline2009212781289Available from: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4705
    [Google Scholar]
/content/journals/cbc/10.2174/0115734072346159250311050808
Loading
/content/journals/cbc/10.2174/0115734072346159250311050808
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test